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Article

The Photoluminescence and Vibrational Properties of Black Phosphorous Sheets Chemically/Electrochemically Functionalized in the Presence of Diphenylamine

by
Mihaela Baibarac
*,
Teodora Burlanescu
,
Malvina Stroe
,
Ion Smaranda
and
Catalin Negrila
National Institute of Materials Physics, R077125 Bucharest, Romania
*
Author to whom correspondence should be addressed.
Polymers 2022, 14(21), 4479; https://doi.org/10.3390/polym14214479
Submission received: 25 July 2022 / Revised: 12 October 2022 / Accepted: 12 October 2022 / Published: 22 October 2022
(This article belongs to the Special Issue Recent Development of Polymer Additives)
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Abstract

:
In this work, new information concerning the optical properties of black phosphorus (BP) sheets chemically/electrochemically functionalized with diphenyl amine (DPA) and its macromolecular compound (poly(diphenylamine) (PDPA)) in the absence/presence of phosphotungstic acid (PTA) is reported. Raman scattering and FTIR spectroscopy studies indicate that the interaction of BP with PTA leads to the elimination of the PxOy layer onto the surface of the BP sheets. In the case of the chemical interaction of BP with DPA, the reaction product corresponds to DPA chemically functionalized BP sheets having an imino-phosphorane (IP) structure. The electrochemical oxidation of BP sheets chemically functionalized with DPA in the presence of PTA leads to an increase in the weight of P-N bonds as a consequence of the generation of PDPA doped with the PTA heteropolyanions, as shown by FTIR spectroscopy and Raman scattering. This process is evidenced by a shift of the Raman line from 362 cm−1 to 378 cm−1, assigned to the A1g mode. This change was explained by taking into account the compression of the layers containing P atoms, which is induced by PDPA macromolecular chains. The decrease in the intensity of the PL spectra of DPA as well as PDPA, in the presence of BP, indicates that BP acts as a PL quenching agent for these compounds. A preferential orientation of the PDPA doped with the PTA heteropolyanions on the surface of BP sheets is highlighted by the variation of the binding angle of the PDPA on the surface of BP sheets from 44.7° to 39.9°.

1. Introduction

Phosphorene (P) has been receiving the attention of researchers since 2014 [1]. The main methods of synthesis of P are (i) the mechanical cleavage of black phosphorus (BP) [1]; (ii) exfoliation by ultrasonic processes in the liquid phase [2,3]; (iii) plasma-assisted synthesis [4]; and (iv) the passivation of BP with Nafion [5]. An issue with using BP mono- and few-layer nanosheets is their instability in ambient oxygen, leading to oxidative degradation, as reported in [6,7,8,9,10]. In order to avoid this problem, two functionalization processes are often used, i.e., non-covalent functionalization with electron-withdrawing molecules [11], such as ionic liquids [12,13] or 2D sheet polymers [14], and covalent functionalization with monovalent hydrogen- or fluorine-type addends when in the P lattice, with sp3-hybridization occurring in regions in which P atoms have undergone sp2-hybridization [14]. The addition of the electrophiles carbenes, oxygen, Lewis acid or nitrenes to BP has allowed the generation of the addition compounds phosphonium ylid, phosphinoxide, Lewis acid adducts and imino-phosphorane [14].
A sustained effort has been made in recent years to prepare new composite materials with both insulating polymers (e.g., polystyrene [15]) and conducting polymers (e.g., poly (3,4-ethylenedioxythiophene) [16]) as the host matrix and guest structures of BP or phosphorene (P), which are reported to have a high stability. Other composites based on P and conjugated polymers that have attracted attention have been poly (3-hexyl thiophene) [17] and polyaniline [18]. Recent studies have demonstrated that the interaction of BP with PANI leads to p-π conjugated structures and π-π heterostructures [18]. Despite these efforts, a less studied aspect is the interaction of the monomers of conjugated polymers with BP sheets [19]. In order to exemplify the importance of knowing the nature of the interactions between BP sheets and monomers, in this paper new information on the interaction of BP sheets with poly(diphenylamine) (PDPA) monomers is reported.
The first study looking at the interaction of BP with compounds having amine functional groups was reported by S. Li et al., who investigated BP surface functionalization with amines (BP-NH2) (secondary alkylamine (diethylenetriamine), primary arylamine (p-phenylenediamine) and cyclamine (4-amino-2,2,6,6-tetramethylpiperidine)) using FTIR spectroscopy, Raman scattering and X-ray photoelectron spectroscopy (XPS) [20]. In contrast with Ref. [20], the attention in this work will be focused on the interaction of the BP sheets with the secondary arylamine diphenylamine (DPA). According to the studies presented below, the BP sheets functionalized with DPA will be used to obtain new BP-functionalized composites with the polymer derived from DPA, i.e., PDPA. According to the studies presented below, the BP sheets functionalized with DPA will be used to obtain new BP-functionalized composites with the polymer derived from DPA, i.e., PDPA. As shown in this paper, the synthesis method of these can be cyclic voltammetry, involving the electrochemical oxidation of BP sheets chemically functionalized with DPA in the presence of phosphotungstic acid (PTA).
The development of the synthesis methods of P or BP and their composites have allowed new applications to be developed in the fields of: (i) information storage [21]; (ii) delaying flame ignition [22]; (iii) cancer therapy [23]; (iv) rechargeable Li and Na batteries [24,25]; (v) photocatalysis [26]; (vi) gas sensors [27]; and (vii) field effect transistors [28].
Compared to this progress, in this work our attention will be focused on the chemical interaction of BP with DPA and phosphotungstic acid (PTA), as well as the electrochemical oxidation of DPA chemically functionalized BP sheets, highlighting their optical properties.

2. Materials and Methods

DPA (≥99%), H3PW12O40 x H2O (99.995% trace metals basis, PTA), HCl (37%) and N, N-dimethylformamide (DMF, anhydrous, 99.8%) were purchased from Sigma-Aldrich, St. Louis, MO, USA. BP crystal (99.995%) was purchased from NanoIntegris.
In the case of the chemical interaction of DPA with BP, the concentration of BP in the mass of the DPA/BP mixture prepared in solid state was varied from 0 wt.% to 0.5 wt.% and 1 wt.%.
The chemical interaction of BP with PTA was carried out when the concentration of BP in the mass of the BT/PTA mixture was equal to 1.7 wt.%.
DPA electrochemical oxidation was performed using cyclic voltammetry, with the synthesized solution consisting of 10−2 M DPA, 10−3 M PTA, and 1M HCl in the semi-aqueous solution of dimethylformamide (DMF) and H2O, having a volumetric ratio of 1:1. In order to obtain composites containing BP sheets and macromolecular compounds of DPA, in the above reaction mixture BP sheets (0.1, 0.2 and 0.5 mg/mL) were added. In the absence of BP, the electrochemical oxidation of DPA leads to the formation of a film of poly(diphenylamine) (PDPA) doped with PTA heteropolyanions on the working electrode surface [29]. Before DPA electrochemical oxidation, BP was exfoliated in DMF using an ultrasonication process for 20 min. The potential range used for recording the first five cyclic voltammograms was (+100; +960) mV vs. Ag/AgCl, with the scanning rate of the potential being equal to 50 mV/s. The electrochemical cell was connected to a Voltalab 80 potentiostat/galvanostat from Radiometer Analytical.
The information about the products resulting from the interactions of BP with DPA and PTA, as well as from the electrochemical oxidation of DPA in the presence of BP, PTA and HCl was obtained by Raman scattering and FTIR spectroscopy.
The Raman spectra of BP, DPA, PTA, and the BP sheets chemically/electrochemically functionalized with DPA or their macromolecular compounds were recorded with a FTRaman spectrophotometer, MultiRam model, from Bruker.
The IR spectra of the samples prepared in this work were recorded with an FTIR spectrophotometer, Vertex 80 model, from Bruker (Billerica, MA, USA).
The photoluminescence (PL) spectra of the DPA chemically/electrochemically functionalized BP sheets were recorded with a Fluorolog spectrophotometer (3.2.2.1) from Horiba Jobin Yvon with a right-angle geometry. All PL spectra were recorded at room temperature, having slides of 3 nm both at excitation and emission. For the measurements of the anisotropic PL, before recording the PL spectra in the polarized light of the PDPA electrochemically functionalized BP sheets and PDPA, a checking polarizer alignment was carried out using a Ludox sample.
The X-ray photoelectron spectroscopy (XPS) spectra of PDPA, BP and PDPA electrochemically functionalized BP sheets were recorded with a SPECS spectrometer having a Phoibos 150 electrone energy analyzer, a monochromatic X-ray source of the type AlKa 1486.74 eV (SPECS Surface Nano Analysis GmbH, Berlin, Germany) and Spectral Data Processor SDPv7.0 software (XPS International, Mountain View, CA, USA).

3. Results and Discussion

3.1. Optical Evidence for the Interaction of BP with PTA and DPA

According to Figure 1a, the Raman spectrum of PTA is characterized by an intense line with a maximum at 1013 cm−1, having a shoulder at 989 cm−1, which accompanies another two Raman lines of low intensity at 523 cm−1 and 218–237 cm−1. The Raman lines of PTA peaked at 1013 cm−1 and 989 cm−1 and were assined to the vbirational modes of the P-O bond in the PO4 sites and the W=O bond in PTA [30].
The Raman lines at 523 cm−1 and 218-237 cm−1 were attributed to the vibrational mode of bending W-O-W and stretching W=O [31]. According to Figure 1b, the Raman spectrum of BP shows three lines with maxima at 362 cm−1, 440 cm−1 and 467 cm−1, which were attributed to the A1g, B2g and A2g vibrational modes, respectively [32]. The interaction of BP with PTA led to the following changes shown in Figure 1c: (i) a downshift of the Raman lines of PTA from 1013 cm−1 and 989 cm−1 (Figure 1a) to 1009 cm−1 and 980 cm−1, respectively (Figure 1c); (ii) a change in the ratio between the intensities of the Raman lines of PTA in the spectral ranges 200–300 cm−1 and 900–1050 cm−1 from 0.35 (Figure 1a) to 0.45 (Figure 1c); and (iii) a downshift of the Raman line of BP from 362 cm−1, 440 cm−1 and 467 cm−1 (Figure 1b) to 360 cm−1, 434 cm−1 and 461 cm−1, respectively (Figure 1c), accompanied by a change in the ratio between the intensities of the Raman line of BP, which peaked at 362 cm−1 and 467 cm−1 from 1.38 (Figure 1b) to 0.63 (Figure 1c). At present, it is well known that the A1g/A2g ratio provides information about the oxidation state of BP [33]. The decrease in the A1g/A2g ratio up to the value 0.63 is a consequence of the interaction of the oxidized BP from the interface the BP few-layer surface with the water molecules existing in H3PW12O40 x H2O. Previous studies have demonstrated that the interaction with the PxOy layer at the BP surface involves the transformation of PxOy into H3PO4 and PH3 [34]. In our case, Scheme 1 describes the interaction of BP having a PxOy layer with H3PW12O40 x H2O.
The adsorption of H3PW12O40 onto the BP surfaces induces a red-shift of the Raman lines, assigned to the vibrational modes A1g, B2g and A2g with ~2 cm−1, 6 cm−1 and 6 cm−1, respectively. An explanation of this must take into account the fact that there is a hindrance of the oscillations of the P atoms belonging to BP. A consequence of this is the decrease in energy of Raman scattering, which induces the red-shift of the Raman lines of the A1g, B2g and A2g vibrational modes.
Additional information about the reaction of BP having a PxOy layer with H3PW12O40 x H2O is shown in Figure 2, obtained using FTIR spectroscopy. Figure 2a shows the main IR bands of PTA situated at 523 cm−1, 594 cm−1, 797 cm−1, 891 cm−1, 982 cm−1, 1080 cm−1, 1605 cm−1 and 3383–3601 cm−1, being assigned to the vibrational modes of the deformation of the O-P-O bond, symmetrical stretching of the W-O-W bond, W-Oc-W stretching mode (Oc corresponds to corner oxygen atoms), W-Oe-W stretching mode (Oe corresponds to edge oxygen atoms), anti-symmetrical stretching of the W=O bond, P-O-W stretching mode, the deformation vibrational mode of water molecules and the stretching mode of hydroxyl groups in water molecules, respectively [35,36].
The interaction of BP having a PxOy layer with PTA induces the following changes, shown in Figure 2: (i) a shift of the IR band from 797 cm−1 to 800 cm−1, simultaneously with an increase in its absorbance; (ii) a change in the ratio between the absorbance of the IR bands, peaking at 982–984 cm−1 and 1080 cm−1 from 1.21 (Figure 2a) to 1.47 (Figure 2b); (iii) the disappearance of the IR bands at 3383–3601 cm−1; and (iv) the decrease in the absorbance of the IR band localized in the spectral range 1550–1650 cm−1, the variation of which was accompanied by a shift from 1605 cm−1 (Figure 2a) to 1610 cm−1 (Figure 2b). These results confirm once more that the changes reported in Figure 1 originate from the interaction of PxOy with the water from PTA.
In order to illustrate the interaction of BP with DPA, Figure 3 shows the PL spectra of DPA and the mixture of DPA:BP when the BP concentration is equal to 0.5 wt.%. and 1 wt.%.
In all three cases, the PL spectra are characterized by a band with maximums at 348 nm, 347 nm and 346 nm, and with intensities equal to 1.51 × 106 counts/sec (Figure 3a), 9.57 × 105 counts/s (Figure 3b) and 6.68 × 104 counts/s (Figure 3c), respectively. The lower intensity of the PL spectra in Figure 3b,c in comparison with Figure 3a indicates a quenching process of the DPA PL induced by BP sheets. According to Figure 4, the IR spectrum of DPA is characterized by bands with maxima at ~691–744 cm−1, 876 cm−1, 1173 cm−1, 1242 cm−1, 1317 cm−1, 1415 cm−1, 1456–1493–1518 cm−1, 1595 cm−1 and 3383 cm−1, attributed to the vibrational modes: the out-of-plane deformation of the benzene ring, deformation of the benzene ring, C-H bond, stretching of the C-N bond, C-H bond, N-H bond + C-H bond, C-C + C-H + N-H stretching, C-C bond stretching in the benzene ring and N-H bond, respectively [37]. In the presence of BP, gradual decreases in the absorbance of the IR bands localized at 691–744 cm−1 and 876 cm−1 were observed.
In our opinion, the decrease in the absorbance of the IR bands localized at 691–744 cm−1 and 876 cm−1 can be explained by the interaction of BP with DPA, when during the chemical interaction a covalent functionalization of the BP layers with DPA takes place, which leads to an intercalation of DPA between the BP layers, with a part of BP layers thus being exfoliated. The reaction product corresponds to the iminophosphorene-type structure [14], according to Scheme 2.
Summarizing the above results, we conclude that: (i) the interaction of BP@PxOy with PTA leads to a decrease in the oxidation state of BP and (ii) the interaction of BP with DPA leads to the generation of the DPA chemically functionalized BP sheets, which have an iminophosphorene-type structure.

3.2. Electrochemical Oxidation of the DPA Chemically Functionalized BP Sheets Determined by Correlated Studies of Photoluminescence, Raman Scattering, FTIR Spectroscopy and X-ray Photoelectron Spectroscopy

In order to show the vibrational properties of the composites resulting from the electrochemical oxidation of the DPA chemically functionalized BP sheets, the studies of Raman scattering and IR spectroscopy are shown here. The main Raman lines observed in Figure 5a–c have maxima at ~415–498 cm−1, 621–825 cm−1, 906–1003 cm−1, 1184 cm−1, 1331 cm−1, 1367 cm−1, 1497 cm−1, 1581 cm−1 and 1614 cm−1, belonging to macromolecular compound of DPA, i.e., PDPA doped with PTA heteropolyanions. These Raman lines are attributed to the vibrational modes caused by the deformation of the benzene ring, out-of-side of the benzene plane, P-O in the PO4 structures of the heteropolyanion, of C-H bond in the benzene ring, C aromatic ring - N in the radical cation type structural units N, N′-diphenyl benzidine, C-C stretching in the benzene ring + C-H bond in the benzene ring, C=N stretching, C=C stretching in the quinoid ring and C-C stretching in the benzene ring, respectively [37,38,39,40].
The decrease in the weight of the BP sheets in the reaction mixture induces: (i) a shift in the Raman lines from 1184 and 1497 cm−1 to 1176 and 1491 cm−1, respectively; (ii) an increase in the intensity of the Raman line from 1614 cm−1; and (iii) a change in the ratio between the intensities of the Raman lines located in the spectral range 1300–1380 cm−1. This fact suggests that: (i) the macromolecular compound contains a higher proportion of quinoid rings, with the Raman spectrum being characterized in the spectral range 1550–1650 cm−1, only by the line at 1581 cm−1 (Figure 5a), and (ii) the electrochemical oxidation of the DPA chemically functionalized BP sheets induces changes in the vibrational mode of the C=N bonds as a consequence of the reactions at the electrode/electrolyte interface when the C=N bonds are transformed into C-N bonds. This variation can explain the change in the position of the Raman line from 1176 cm−1 (Figure 5c) to 1184 cm−1 (Figure 5a). In Figure 5a, one can see a Raman line at 378 cm−1, which does not belong to DPA or its polymer. A puzzling fact is that a shift of the A1g vibrational mode of BP sheets from 362 cm−1 to 378 cm−1 was reported when the sheets containing P atoms were compressed [41]. In our case, the variation of the Raman line attributed to the A1g vibrational mode from 362 cm−1 to 378 cm−1 can be explained by taking into account the compression of the layers containing P atoms, which is induced by PDPA. In Figure 6d, it can be seen that the IR spectrum of PDPA doped with the PTA heteropolyanions is characterized by the IR bands having maxima at 696 cm−1, 748 cm−1, 812 cm−1, 874 cm−1, 922 cm−1, 1022 cm−1, 1074 cm−1, 1176 cm−1, 1315 cm−1, 1454 cm−1, 1499 cm−1 and 1595 cm−1, attributed to the vibrational modes of the inter-ring deformation, ring deformation, W-Oc-W (Oc corresponds to oxygen from the corner of the heteropolyanion structure), W-Oe-W (Oe corresponds to oxygen from the side of the heteropolyanion structure), W=O, the deformation of the quinoid ring, the stretching of the P-O-W bond, the C-H bond in the benzene (B) ring, C aromatic - N, the stretching of the C=N + C-H bond in the benzene ring, the stretching of the C-C bond in the benzene (B) ring + the stretching vibration of the C=C bond in the quinoid ring (Q) and the stretching of the C=C bond in the -NH+=Q=Q=NH+- structure, respectively [37,38,39].
Figure 6a–c highlight the following changes in the case of the composite resulting from the electrochemical oxidation of the DPA chemically functionalized BP sheets: (i) a shift of the maximum of the IR band from 812 cm−1 to 823 cm−1; (ii) an increase in the absorbance of the IR bands located at 1022 cm−1 and 1072–1076 cm−1; and (iii) a shift of the IR band from 1454 cm−1 to 1470 cm−1 simultaneously with the change in the ratio between the absorbances of the IR bands from 1454 to 1470 cm−1 and 1499 cm−1. These variations can be explained by taking into account the increase in the number of covalent bonds between the BP sheets and DPA-type structural units, when steric hindrance affects both the quinoid rings and the PTA heteropolyanions, which compensates the existing positive charges on the PDPA macromolecular chain. In order to understand the chemical structures of composites resulting from the electrochemical oxidation of DPA chemically functionalized BP sheets, Scheme 3 shows the reactions that allow the macromolecular chain growth, i.e., of dimers, tetramers and PDPA.
According to Scheme 3, reaction (1) leads to a radical of the DPA chemically functionalized BP sheets, which is instable and this will interact with another radical, leading to a dimer (reaction (2)). Next, the oxidation reaction of the dimer will lead to a diradical (reaction (2)) which, being unstable, will interact with another dimer, leading to the compound shown in reaction (3). Reaction (4) shows the oxidation reaction of the tetramer, when a composite of the type of BP layers functionalized with DPA tetramers doped with PTA heteropolyanions results. Further growth of the macromolecular chain through oxidation reactions leads to a composite made of PDPA electrochemically functionalized BP sheets.
In order to show additional experimental evidence for the PDPA electrochemically functionalized BP sheets, in Figure 7, Figure 8 and Figure 9 the XPS spectra of PDPA, BP and the PDPA electrochemically functionalized BP sheets are shown.
Figure 7 shows the case of PDPA doped with PTA heteropolyanions in: (i) the XPS C1s spectrum, a peak of high intensity at 284.37 eV, accompanied by another four peaks at 284.9 eV, 285.6 eV, 286.3 eV and 291.35 eV, which were assigned to sp2 C atoms in the benzene ring, the C-C and C-H bonds, C-N bond, the C-O and C-N+ bonds and π-π* transitions of sp2 C atoms [42]; (ii) the XPS N1s-Mo3p3/2 spectrum, with three peaks at 398.09 eV, 399.56 eV and 401.65 eV assigned to Mo3 p3/2 (where the Mo oxidized state is Mo6+), N1s of the amine groups and NH+ [43,44]; (iii) the XPS P2p spectrum, with a peak of low intensity corresponding to the TPA heteropolyanions [43,44]; and (iv) XPS O1s, which reveals an intense peak at 530.71 eV accompanied of two peaks at 531.86 eV and 533.05 eV, attributed to the O-Mo bond, adsorbed O and the C-O bonds [43,44].
The deconvolution of Figure 8 illustrates six peaks at 129.99 eV–130.83 eV, 130.86 eV–131.73 eV and 133.67 eV–134.5 eV, which were assigned the P2p doublet of BP, doublet P2p of P very low oxidized having the oxidation state P3+ and P2p doublet of P strong oxidized having the oxidized state P5+ [45]. The ratio between the intensities of the peaks at 129.99 eV and 133.63 eV is equal to 1.57.
Figure 9 shows the case of PDPA electrochemically functionalized BP sheets in: (i) XPS C1s, with the four peaks at 284.37 eV, 284.91 eV, 285.57 eV and 286.36 eV assigned to sp2 C atoms, the C-C and C-H bonds, the C-N bond and the C-O and C-N+ [42]; (ii) XPS N1s, with two peaks at 399.94 eV and 402.14 eV, assigned to the P=N bond [46,47,48] and protonated N (C-N+) [42]; (iii) XPS O1s, with two peaks at 532.04 eV and 533.38 eV, attributed to adsorbed molecular oxygen and the C-O bond; and (iv) XPS P2p, with four peaks at 134.06 eV–134.93 eV and 129.85 eV–130.71 eV, assigned to P=N bond and the P-P bond in BP [46,47,48]. The ratio between the intensities of the peaks at 129.99 eV and 133.63 eV is equal to 0.92. The smaller value of the ratio between the intensity of the peaks at 129.99 eV and 133.63 eV in the case of the PDPA electrochemically functionalized BP sheets in contrast with BP clearly confirms the decrease in the weight of P-P bonds and the increase in the weight of P=N bonds.
The electrochemical oxidation of DPA in the absence of the BP sheets, when the recording of the first five cyclic voltammograms on the Au electrode surface took place, led to films that are characterized by spectra of photoluminescence (PL (Figure 10(a1))) and photoluminescence excitation (PLE, Figure 10(a2)), having the following characteristics: (i) the PL spectrum of the sample of PDPA shows four emission bands with maxima at ~416 nm, 432 nm, 462 nm and 504 nm and (ii) the PLE spectrum highlights a band with the maximum at 368 nm. As the concentration of the BP sheets in the synthesis mixture increases, a gradual decrease in the intensity of the PL spectra of the macromolecular compound resulting from the electrochemical oxidation of the DPA chemically functionalized BP sheets was observed from 9.62 × 105 counts/s (Figure 10(a2)) to 5.16 × 105 counts/s (Figure 10(b2)), 1 × 105 counts/s (Figure 10(c2)) and 5.5 × 104 counts/sec (Figure 10(d2)). A decrease in the intensity of the PLE spectra was also observed in the case of Figure 10(a1–10d1). These variations are due to the electrochemical oxidation of the DPA chemically functionalized BP sheets, when are generated dimers, tetramers, oligomers and macromolecular compound. Taking into account the behavior of PL spectra, shown in Figure 10, these highlight the role of the BP sheets as a PL quenching agent of macromolecular compounds of DPA doped with PTA heteropolyanions.
In order to understand the adsorption mode of macromolecular compounds of DPA doped with PTA heteropolyanions on the surface of the BP sheets, in Figure 11 are shown the PL spectra in polarized light of PDPA doped with the PTA heteropolyanions and of its composites based on macromolecular compounds of DPA and the BP sheets. To calculate the PL anisotropy, the following equation was used: r = (IVV − (IHV/IHH) × IVH)/(IVV + 2(IHV/IHH) × IVH) [39,49]. IVV and IHH correspond to the PL intensity when the excitation and emission polarizers are in the vertical and horizontal positions, respectively; IVH and IHV correspond to the PL intensity when the excitation and emission polarizers are in the vertical and horizontal positions and vice versa, respectively. The r values in the case of PDPA doped with PTA heteropolyanions and the composites of the type of the BP sheets electrochemically functionalized in the presence of DPA, when in the reaction mixture the concentrations of BP sheets are 0.1, 0.2 and 0.5 mg/mL, equal to 0.109, 0.103, 0.153 and 0.127, respectively. The wrapping angle of the BP sheets with macromolecular compounds of DPA—in other words, the adsorption angle of the polymer on the surface of the BP layers ((θPL)—was calculated with the relation r = 0.4[3cos2θPL − 1)/2] [39,49], having values in the case of PDPA and the composites containing BP sheets equal to 44.1°, 44.7°, 42.4° and 39.9° when the concentrations of BP layers in the reaction mixture are 0, 0.1, 0.2 and 0.5 mg/mL, respectively. These values of the adsorption angle of the polymer on the surface of the BP layers indicate that the excitation and emission transition dipoles of macromolecular compounds are not parallel to the basal plane of the BP sheets.

4. Conclusions

In this work, new results are reported regarding the optical properties of the composite materials resulting from the electrochemical oxidation of the BP sheets chemically functionalized with DPA. The following conclusions can be drawn:
(i) The chemical interaction of the BP sheets with DPA involves a process of covalent functionalization that takes place with the formation of an iminophosphorene-type structure, which induces a decrease in the absorbance of the IR bands localized at 691–744 cm−1 and 876 cm−1. The formation of iminophosphorane groups on the BP surface was also reported through the interaction of black phosphorus with 4-benzoic acid azide [50].
(ii) The chemical interaction of the BP sheets having a PxOy layer with PTA leads to a decrease in the oxidation state of the BP sheets, as a consequence of the interaction of PxOy with water from H3PW12O40 x H2O.
(iii) The electrochemical oxidation of the DPA chemically functionalized BP sheets leads to the generation of dimers, tetramers and polymers when steric hindrance effects are highlighted by the increase in the absorbance of the IR bands peaking at 1022 cm−1 and 1072–1076 cm−1, attributed to vibrational modes of the deformation of the quinoid rings and stretching of the P-O-W bond; according to Raman spectroscopy studies, the composites resulting from the electrochemical oxidation of the DPA chemically functionalized BP sheets are characterized by an intense line at 1581 cm−1, which indicates a greater weight of quinoid rings compared to benzene rings in the macromolecular compound. The smaller ratio between the intensity of the XPS peaks at 129.99 eV and 133.63 eV in the case of the PDPA electrochemically functionalized BP sheets in contrast with BP clearly confirms the decrease in the weight of P-P bonds and the increase in the weight of P=N bonds.
(iv) The decrease in the intensity of the PL spectrum of DPA in the presence of the BP sheets highlights the role of the quenching agent of BP in the case of the PL spectra of DPA; the BP sheets play the role of a quenching agent of the PL spectra of the composites resulting from the electrochemical oxidation of the DPA chemically functionalized BP sheets in the presence of PTA.
(v) The value of the wrapping angle of the BP sheets with macromolecular compounds of DPA, when the concentrations of the BP layers in the reaction mixture are 0, 0.1, 0.2 and 0.5 mg/mL, ranging from 44.1° to 44.7°, 42.4° and 39.9°, respectively.
This study provides new opportunities for the use of BP sheets functionalized with PDPA doped with PTA heteropolyanions as an electrode active material in supercapacitor cells and rechargeable Li batteries as well as a flame-retardant agent. In this context, we point out that PDPA is one of the CPs that have been used for both supercapacitors and batteries (e.g., [51,52]), while in the case of BP, the applications in the field of energy storage have exploited the large size of the interlayer channel of 3.08 Å, which ensured a fast diffusion of ions [53]. Concerning the applications of BP as well as their composites as a flame-retardant agent, a recently study focused on BP functionalized with amine compounds for epoxy resin [20]. Risks that can lead to the fires and explosions of batteries as well as safety strategies have been reported in various reviews (e.g., [54]). One of the strategies adopted in it takes into account preventive measures by adding flame retardants in order to increase the thermal stability of the batteries. Considering this progress, in the particular case of PDPA-functionalized BP sheets, we anticipate that (i) the presence of BP sheets will facilitate an increase in ion diffusion, improving the discharge capacity of the supercapacitors and the specific capacity of the rechargeable Li batteries and (ii) an increase in the fire stability of rechargeable Li batteries, which use PDPA-functionalized BP sheets as the active electrode material, will occur.

Author Contributions

Conceptualization, M.B.; investigation, M.B., T.B., M.S., I.S. and C.N.; writing—original draft preparation, M.B., writing—review and editing, M.B.; supervision, M.B. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by a grant of the Romanian National Authority for Scientific Research and Innovation—PN18-110101 project (Core Programme).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

References

  1. Mack, S.C.; Witt, H.; Piro, R.M.; Gu, L.; Zuyderduyn, S.D.; Stutz, A.M.; Wang, X.; Gallo, M.; Garzia, L.; Zayne, K.; et al. Epigenomic alterations define lethal CIMP-positive ependymomas of infancy. Nature 2014, 506, 445–450. [Google Scholar] [CrossRef] [Green Version]
  2. Brent, J.R.; Savjani, N.; Lewis, E.A.; Haigh, S.J.; Lewis, D.J.; O’Brien, P. Production of few-layer phosphorene by liquid exfoliation of black phosphorus. Chem. Commun. 2014, 50, 13338–13341. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Gui, R.; Jin, H.; Wang, Z.; Li, J. Black phosphorus quantum dots: Synthesis, properties, functionalized modification and applications. Chem. Soc. Rev. 2018, 47, 6795–6823. [Google Scholar] [CrossRef]
  4. Kou, L.; Chen, C.; Smith, S.C. Phosphorene: Fabrication, Properties, and Applications. J. Phys. Chem. Lett. 2015, 6, 2794–2805. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Kumar, A. Controlled nanostructures and simultaneous passivation of black phosphorus (phosphorene) with Nafion. J. Mater. Res. 2020, 35, 141–152. [Google Scholar] [CrossRef]
  6. Island, J.; Steele, G.A.; van der Zant, H.S.J.; Castellanos-Gomez, A. Environmental instability of few-layer black phosphorus. 2D Mater. 2015, 2, 011002. [Google Scholar] [CrossRef] [Green Version]
  7. Favron, A.; Gaufrès, E.; Fossard, F.; Phaneuf-L’Heureux, A.-L.; Tang, N.Y.-W.; Levesque, P.; Loiseau, A.; Leonelli, R.; Francoeur, S.; Martel, R. Photooxidation and quantum confinement effects in exfoliated black phosphorus. Nat. Mater. 2015, 14, 826–832. [Google Scholar] [CrossRef]
  8. Woomer, A.H.; Farnsworth, T.W.; Hu, J.; Wells, R.A.; Donley, C.L.; Warren, S.C. Phosphorene: Synthesis, Scale-Up, and Quantitative Optical Spectroscopy. ACS Nano 2015, 9, 8869–8884. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  9. Yasaei, P.; Kumar, B.; Foroozan, T.; Wang, C.; Asadi, M.; Tuschel, D.; Indacochea, J.E.; Klie, R.F.; Salehi-Khojin, A. High-Quality Black Phosphorus Atomic Layers by Liquid-Phase Exfoliation. Adv. Mater. 2015, 27, 1887–1892. [Google Scholar] [CrossRef] [PubMed]
  10. Kang, J.; Wood, J.D.; Wells, S.A.; Lee, J.-H.; Liu, X.; Chen, K.-S.; Hersam, M.C. Solvent Exfoliation of Electronic-Grade, Two-Dimensional Black Phosphorus. ACS Nano 2015, 9, 3596–3604. [Google Scholar] [CrossRef]
  11. Abellán, G.; Lloret, V.; Mundloch, U.; Marcia, M.; Neiss, C.; Görling, A.; Varela, M.; Hauke, F.; Hirsch, A. Noncovalent Functionalization of Black Phosphorus. Angew. Chem. Int. Ed. 2016, 55, 14557–14562. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Abellán, G.; Wild, S.; Lloret, V.; Scheuschner, N.; Gillen, R.; Mundloch, U.; Maultzsch, J.; Varela, M.; Hauke, F.; Hirsch, A. Fundamental Insights into the Degradation and Stabilization of Thin Layer Black Phosphorus. J. Am. Chem. Soc. 2017, 139, 10432–10440. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Zhao, W.; Xue, Z.; Wang, J.; Jiang, J.; Zhao, X.; Mu, T. Large-Scale, Highly Efficient, and Green Liquid-Exfoliation of Black Phosphorus in Ionic Liquids. ACS Appl. Mater. Interfaces 2015, 7, 27608–27612. [Google Scholar] [CrossRef]
  14. Hirsch, A.; Hauke, F. Post-Graphene 2D Chemistry: The Emerging Field of Molybdenum Disulfide and Black Phosphorus Functionalization. Angew. Chem. Int. Ed. 2018, 57, 4338–4354. [Google Scholar] [CrossRef] [PubMed]
  15. Passaglia, E.; Cicogna, F.; Lorenzetti, G.; Legnaioli, S.; Caporali, M.; Serrano-Ruiz, M.; Ienco, A.; Peruzzini, M. Novel polystyrene-based nanocomposites by phosphorene dispersion. RSC Adv. 2016, 6, 53777–53783. [Google Scholar] [CrossRef] [Green Version]
  16. Zhang, J.; Ding, W.; Zhang, Z.; Xu, J.; Wen, Y. Preparation of black phosphorus-PEDOT:PSS hybrid semiconductor composites with good film-forming properties and environmental stability in water containing oxygen. RSC Adv. 2016, 6, 76174–76182. [Google Scholar] [CrossRef]
  17. Sun, M.M.; Wang, W.; Lv, W.; Lu, M.X.; Yan, S.H.; Liang, L.Y.; Ling, Q.D. Synthesis of regular D-A1-D-A2 copolymers via direct arylation polycondensation and application in solar cells. Synth. Met. 2015, 209, 412–418. [Google Scholar] [CrossRef]
  18. Fonsaca, J.; Domingues, S.H.; Orth, E.S.; Zarbin, A.J.G. Air stable black phosphorous in polyaniline-based nanocomposite. Sci. Rep. 2017, 7, 10165. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  19. Wu, Z.; Liang, L.; Zhu, S.; Guo, Y.; Yao, Y.; Yang, Y.; Gu, S.; Zhou, Z. High Sensitivity of Ammonia Sensor through 2D Black Phosphorus/Polyaniline Nanocomposite. Nanomaterials 2021, 11, 3026. [Google Scholar] [CrossRef] [PubMed]
  20. Liu, S.; Tao, B.; Zhao, X.; Chen, G.; Wang, D.Y. Surface functionalization of black phosphorus via amine compounds and its impacts on the flame retardancy and thermal decomposition behaviors of epoxy resin. Polymers 2021, 13, 3635. [Google Scholar]
  21. Cao, Y.; Tian, X.; Gu, J.; Liu, B.; Zhang, B.; Song, S.; Fan, F.; Chen, Y. Covalent Functionalization of Black Phosphorus with Conjugated Polymer for Information Storage. Angew. Chem. Int. Ed. 2018, 57, 4543–4548. [Google Scholar] [CrossRef] [PubMed]
  22. Ren, X.; Mei, Y.; Lian, P.; Xie, D.; Yang, Y.; Wang, Y.; Wang, Z. A Novel Application of Phosphorene as a Flame Retardant. Polymers 2018, 10, 227. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Luo, M.; Cheng, W.; Zeng, X.; Mei, L.; Liu, G.; Deng, W. Folic Acid-Functionalized Black Phosphorus Quantum Dots for Targeted Chemo-Photothermal Combination Cancer Therapy. Pharmaceutics 2019, 11, 242. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Wang, D.; Guo, G.-C.; Wei, X.-L.; Liu, L.-M.; Zhao, S.-J. Phosphorene ribbons as anode materials with superhigh rate and large capacity for Li-ion batteries. J. Power Sources 2016, 302, 215–222. [Google Scholar] [CrossRef]
  25. Luo, W.; Shen, F.; Bommier, C.; Zhu, H.; Ji, X.; Hu, L. Na-Ion Battery Anodes: Materials and Electrochemistry. Accounts Chem. Res. 2016, 49, 231–240. [Google Scholar] [CrossRef] [PubMed]
  26. Rahman, M.Z.; Kwong, C.W.; Davey, K.; Qiao, S.Z. 2D phosphorene as a water splitting photocatalyst: Fundamentals to applications. Energy Environ. Sci. 2016, 9, 709–728. [Google Scholar] [CrossRef]
  27. Cui, S.; Pu, H.; Wells, S.A.; Wen, Z.; Mao, S.; Chang, J.; Hersam, M.C.; Chen, J. Ultrahigh sensitivity and layer-dependent sensing performance of phosphorene-based gas sensors. Nat. Commun. 2015, 6, 8632. [Google Scholar] [CrossRef] [Green Version]
  28. Lee, J.; Seo, J.; Oh, J.H.; Shin, M. Nonorthogonal tight-binding parameterization of single-layer phosphorene under biaxial strain and application to FETs. Nanotechnology 2016, 27, 245202. [Google Scholar] [CrossRef]
  29. Smaranda, I.; Benito, A.M.; Maser, W.K.; Baltog, I.; Baibarac, M. Electrochemical Grafting of Reduced Graphene Oxide with Polydiphenylamine Doped with Heteropolyanions and Its Optical Properties. J. Phys. Chem. C 2014, 118, 25704–25717. [Google Scholar] [CrossRef]
  30. Guo, Y.; Li, K.; Yu, X.; Clark, J.H. Mesoporous H3PW12O40-silica composite: Efficient and reusable solid acid catalyst for the synthesis of diphenolic acid from levulinic acid. Appl. Catal. B Environ. 2008, 81, 182–191. [Google Scholar] [CrossRef]
  31. Legagneux, N.; Basset, J.-M.; Thomas, A.; Lefebvre, F.; Goguet, A.; Sá, J.; Hardacre, C. Characterization of silica-supported dodecatungstic heteropolyacids as a function of their dehydroxylation temperature. Dalton Trans. 2009, 12, 2235–2240. [Google Scholar] [CrossRef] [PubMed]
  32. Kim, J.; Lee, J.-U.; Lee, J.; Park, H.J.; Lee, Z.; Lee, C.; Cheong, H. Anomalous polarization dependence of Raman scattering and crystallographic orientation of black phosphorus. Nanoscale 2015, 7, 18708–18715. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Mitrović, A.; Wild, S.; Lloret, V.; Fickert, M.; Assebban, M.; Márkus, B.G.; Simon, F.; Hauke, F.; Abellán, G.; Hirsch, A. Interface Amorphization of Two-Dimensional Black Phosphorus upon Treatment with Diazonium Salts. Chem. A Eur. J. 2020, 27, 3361–3366. [Google Scholar] [CrossRef]
  34. Edmonds, M.T.; Tadich, A.; Carvalho, A.; Ziletti, A.; O’Donnell, K.M.; Koenig, S.P.; Coker, D.F.; Özyilmaz, B.; Neto, A.H.C.; Fuhrer, M.S. Creating a Stable Oxide at the Surface of Black Phosphorus. ACS Appl. Mater. Interfaces 2015, 7, 14557–14562. [Google Scholar] [CrossRef] [PubMed]
  35. Pires, L.H.; de Oliveira, A.N.; Monteiro, O.V., Jr.; Angélica, R.S.; Costa, C.; Zamian, J.R.; Nascimento, L.D.; Filho, G.N.D.R. Esterification of a waste produced from the palm oil industry over 12-tungstophosforic acid supported on kaolin waste and mesoporous materials. Appl. Catal. B Environ. 2014, 160–161, 122–128. [Google Scholar] [CrossRef]
  36. Essayem, N.; Holmqvist, A.; Gayraud, P.; Vedrine, J.; Ben Taarit, Y. In Situ FTIR Studies of the Protonic Sites of H3PW12O40 and Its Acidic Cesium Salts MxH3−xPW12O40. J. Catal. 2001, 197, 273–280. [Google Scholar] [CrossRef]
  37. Quillard, S.; Louarn, G.; Lefrant, S.; Macdiarmid, A.G. Vibrational analysis of polyaniline: A comparative study of leucoemeraldine, emeraldine, and pernigraniline bases. Phys. Rev. B 1994, 50, 12496–12508. [Google Scholar] [CrossRef] [PubMed]
  38. Baibarac, M.A.; Radu, A.; Cristea, M.; Cercel, R.; Smaranda, I. UV Light Effect on Cationic Photopolymerization of the SU8 Photoresist and Its Composites with Carbon Nanotubes: New Evidence Shown by Photoluminescence Studies. J. Phys. Chem. C 2020, 124, 7467–7476. [Google Scholar] [CrossRef]
  39. Kuo, C.-T.; Chiou, W.-H. Field-effect transistor with polyaniline thin film as semiconductor. Synth. Met. 1997, 88, 23–30. [Google Scholar] [CrossRef]
  40. de Santana, H.; Temperini, M.L.A.; Rubim, J. In situ resonance Raman and reflectance spectroscopic study of the electrochemical oxidation of diphenylamine. J. Electroanal. Chem. 1993, 356, 145–155. [Google Scholar] [CrossRef]
  41. Fei, R.; Yang, L. Lattice vibrational modes and Raman scattering spectra of strained phosphorene. Appl. Phys. Lett. 2014, 105, 083120. [Google Scholar] [CrossRef]
  42. Wu, M.-S.; Wen, T.-C.; Gopalan, A. Electrochemical Copolymerization of Diphenylamine and Anthranilic Acid with Various Feed Ratios. J. Electrochem. Soc. 2001, 148, D65–D73. [Google Scholar] [CrossRef]
  43. Nadaf, S.N.; Patil, S.S.; Kalantre, V.A.; Mali, S.S.; Hong, C.K.; Mane, S.R.; Bhosale, P.M. Optimization and com-parative analysis of Cs ion intercalated H3PMo12O40 photocathode: One-step hydrothermal strategy. J. Mater. Sci. Mater. Electron. 2021, 32, 22921–22935. [Google Scholar] [CrossRef]
  44. Chen, C.; Peng, J.; Shen, Y.; Chen, D.; Zhang, H.; Meng, C. Fabrication and Characterization of LuminescentMul-tilayer Films Based on Polyoxometalates and Fuchsin Basic. Z. Nat. B 2011, 66, 43–48. [Google Scholar]
  45. Luo, W.; Zemlyanov, D.Y.; Milligan, C.A.; Du, Y.; Yang, L.; Wu, Y.; Ye, P.D. Surface chemistry of black phosphorus under a controlled oxidative environment. Nanotechnology 2016, 27, 434002. [Google Scholar] [CrossRef] [Green Version]
  46. Luaña, V.; Pendás, A.A.M.; Costales, A.; And, G.A.C.; García-Alonso, F.J. Topological Analysis of Chemical Bonding in Cyclophosphazenes. J. Phys. Chem. A 2001, 105, 5280–5291. [Google Scholar] [CrossRef]
  47. Vassileva, P.; Krastev, V.; Lakov, L.; Peshev, O. XPS determination of the binding energies of phosphorus and nitrogen in phosphazenes. J. Mater. Sci. 2004, 39, 3201–3202. [Google Scholar] [CrossRef]
  48. Dake, L.; Baer, D.; Ferris, K.; Friedrich, D. Ligand and structure effects on the N-P bonds of phosphazenes. J. Electron. Spectrosc. Relat. Phenom. 1990, 51, 439–457. [Google Scholar] [CrossRef]
  49. Shea, M.J.; Mehlenbacher, R.D.; Zanni, M.T.; Arnold, M.S. Experimental Measurement of the Binding Configuration and Coverage of Chirality-Sorting Polyfluorenes on Carbon Nanotubes. J. Phys. Chem. Lett. 2014, 5, 3742–3749. [Google Scholar] [CrossRef]
  50. Liu, Y.; Gao, P.; Zhang, T.; Zhu, X.; Zhang, M.; Chen, M.; Du, P.; Wang, G.; Ji, H.; Yang, J.; et al. Azide Passivation of Black Phosphorus Nanosheets: Covalent Functionalization Affords Ambient Stability Enhancement. Angew. Chem. Int. Ed. 2018, 58, 1479–1483. [Google Scholar] [CrossRef]
  51. Baibarac, M.; Baltog, I.; Lefrant, S.; Gomez-Romero, P. Polydiphenylamine/carbon nanotube composites for applications in rechargeable lithium batteries. Mater. Sci. Eng. B 2011, 176, 110–120. [Google Scholar] [CrossRef]
  52. Baibarac, M.; Baltog, I.; Frunza, S.; Magrez, A.; Schur, D.; Zaginaichenko, S.Y. Single-walled carbon nanotubes functionalized with polydiphenylamine as active materials for applications in the supercapacitors field. Diam. Rel. Mater. 2013, 32, 72–82. [Google Scholar] [CrossRef]
  53. Zhang, H.; Wang, X.; Ma, H.; Xue, M. Recent Progresses on Applications of Conducting Polymers for Modifying Electrode of Rechargeable Batteries. Adv. Energy Sustain. Res. 2021, 2, 2100088. [Google Scholar] [CrossRef]
  54. Kong, L.; Li, C.; Jiang, J.; Pecht, M.G. Li-Ion Battery Fire Hazards and Safety Strategies. Energies 2018, 11, 2191. [Google Scholar] [CrossRef]
Polymers 14 04479 g001 550
Figure 1. Raman spectra of PTA (a), BP (b) and BP when interacting with PTA (c).
Figure 1. Raman spectra of PTA (a), BP (b) and BP when interacting with PTA (c).
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Polymers 14 04479 sch001 550
Scheme 1. The reaction of BP having a PxOy layer (BP@ PxOy) with H3PW12O40 x H2O.
Scheme 1. The reaction of BP having a PxOy layer (BP@ PxOy) with H3PW12O40 x H2O.
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Polymers 14 04479 g002 550
Figure 2. The IR spectra of PTA (a) and BP when interacting with PTA (b).
Figure 2. The IR spectra of PTA (a) and BP when interacting with PTA (b).
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Polymers 14 04479 g003 550
Figure 3. The PL spectra of DPA before (a) and after the interaction with BP 0.5 wt.% (b) and 1 wt.% (c), when the excitation wavelength is 275 nm.
Figure 3. The PL spectra of DPA before (a) and after the interaction with BP 0.5 wt.% (b) and 1 wt.% (c), when the excitation wavelength is 275 nm.
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Polymers 14 04479 g004 550
Figure 4. The IR spectra of DPA before (black curve) and after the interaction with BP; the BP concentration in the DPA:BP mixture is equal to 0.5 wt.% (red curve) and 1 wt.% (blue curve).
Figure 4. The IR spectra of DPA before (black curve) and after the interaction with BP; the BP concentration in the DPA:BP mixture is equal to 0.5 wt.% (red curve) and 1 wt.% (blue curve).
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Polymers 14 04479 sch002 550
Scheme 2. The interaction of DPA with BP.
Scheme 2. The interaction of DPA with BP.
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Figure 5. Raman spectra of the composites resulting from the electrochemical oxidation of the DPA chemically functionalized BP sheets when the concentration of BP in DMF in the synthesis mixture is 0.5 mg/mL (a), 0.2 mg/mL (b) and 0.1 mg/mL (c).
Figure 5. Raman spectra of the composites resulting from the electrochemical oxidation of the DPA chemically functionalized BP sheets when the concentration of BP in DMF in the synthesis mixture is 0.5 mg/mL (a), 0.2 mg/mL (b) and 0.1 mg/mL (c).
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Polymers 14 04479 g006 550
Figure 6. IR spectra of the composite resulting from the electrochemical oxidation of the DPA chemically functionalized BP sheets when the concentration of BP in DMF in the synthesis mixture is 0.5 mg/mL (a), 0.2 mg/mL (b) and 0.1 mg/mL (c). Figure (d) shows the IR spectrum of PDPA doped with the PTA heteropolyanions.
Figure 6. IR spectra of the composite resulting from the electrochemical oxidation of the DPA chemically functionalized BP sheets when the concentration of BP in DMF in the synthesis mixture is 0.5 mg/mL (a), 0.2 mg/mL (b) and 0.1 mg/mL (c). Figure (d) shows the IR spectrum of PDPA doped with the PTA heteropolyanions.
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Polymers 14 04479 sch003 550
Scheme 3. The reactions describing the electrochemical oxidation reactions of the DPA chemically functionalized BP sheets, which leads to composites with BP sheets electrochemically functionalized with macromolecular compounds having repeating units made through doping DPA with PTA heteropolyanions (X- corresponds to the PTA heteropolyanion).
Scheme 3. The reactions describing the electrochemical oxidation reactions of the DPA chemically functionalized BP sheets, which leads to composites with BP sheets electrochemically functionalized with macromolecular compounds having repeating units made through doping DPA with PTA heteropolyanions (X- corresponds to the PTA heteropolyanion).
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Polymers 14 04479 g007 550
Figure 7. X-ray photoelectron spectroscopy (XPS) C1s (a), N1s-Mo3p3/2 (b), O1s (c) and P2p (d) spectra of PDPA doped with TPA heteropolyanions. Red and blue curves correspond to experimental results and their deconvolution.
Figure 7. X-ray photoelectron spectroscopy (XPS) C1s (a), N1s-Mo3p3/2 (b), O1s (c) and P2p (d) spectra of PDPA doped with TPA heteropolyanions. Red and blue curves correspond to experimental results and their deconvolution.
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Figure 8. The XPS P2p spectra of BP. Red and blue curves correspond to experimental results and their deconvolution.
Figure 8. The XPS P2p spectra of BP. Red and blue curves correspond to experimental results and their deconvolution.
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Polymers 14 04479 g009 550
Figure 9. The XPS C1s (a), N1s (b), O1s (c) and P2p (d) spectra of PDPA electrochemically functionalized BP sheets. Red and blue curves correspond to experimental results and their deconvolution.
Figure 9. The XPS C1s (a), N1s (b), O1s (c) and P2p (d) spectra of PDPA electrochemically functionalized BP sheets. Red and blue curves correspond to experimental results and their deconvolution.
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Figure 10. PLE and PL spectra of PDPA (a1,a2) and the DPA chemically functionalized and electrochemically oxidized BP sheets, with the synthesis mixture containing 0.1 mg/mL (b1,b2), 0.2 mg/mL (c1,c2) and 0.5 mg/mL (d1,d2) BP in DMF. PL spectra were recorded using an excitation wavelength equal to 350 nm. PLE spectra were recorded under an emission wavelength equal to 490 nm.
Figure 10. PLE and PL spectra of PDPA (a1,a2) and the DPA chemically functionalized and electrochemically oxidized BP sheets, with the synthesis mixture containing 0.1 mg/mL (b1,b2), 0.2 mg/mL (c1,c2) and 0.5 mg/mL (d1,d2) BP in DMF. PL spectra were recorded using an excitation wavelength equal to 350 nm. PLE spectra were recorded under an emission wavelength equal to 490 nm.
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Polymers 14 04479 g011 550
Figure 11. Anisotropic photoluminescence of PDPA (a) and composites resulting from the electrochemical oxidation of DPA chemically functionalized BP sheets, when the synthesis mixture contains the BP sheets in DMF having a concentration equal to 0.1 mg/mL (b), 0.2 mg/mL (c) and 0.5 mg/mL (d).
Figure 11. Anisotropic photoluminescence of PDPA (a) and composites resulting from the electrochemical oxidation of DPA chemically functionalized BP sheets, when the synthesis mixture contains the BP sheets in DMF having a concentration equal to 0.1 mg/mL (b), 0.2 mg/mL (c) and 0.5 mg/mL (d).
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Baibarac, M.; Burlanescu, T.; Stroe, M.; Smaranda, I.; Negrila, C. The Photoluminescence and Vibrational Properties of Black Phosphorous Sheets Chemically/Electrochemically Functionalized in the Presence of Diphenylamine. Polymers 2022, 14, 4479. https://doi.org/10.3390/polym14214479

AMA Style

Baibarac M, Burlanescu T, Stroe M, Smaranda I, Negrila C. The Photoluminescence and Vibrational Properties of Black Phosphorous Sheets Chemically/Electrochemically Functionalized in the Presence of Diphenylamine. Polymers. 2022; 14(21):4479. https://doi.org/10.3390/polym14214479

Chicago/Turabian Style

Baibarac, Mihaela, Teodora Burlanescu, Malvina Stroe, Ion Smaranda, and Catalin Negrila. 2022. "The Photoluminescence and Vibrational Properties of Black Phosphorous Sheets Chemically/Electrochemically Functionalized in the Presence of Diphenylamine" Polymers 14, no. 21: 4479. https://doi.org/10.3390/polym14214479

APA Style

Baibarac, M., Burlanescu, T., Stroe, M., Smaranda, I., & Negrila, C. (2022). The Photoluminescence and Vibrational Properties of Black Phosphorous Sheets Chemically/Electrochemically Functionalized in the Presence of Diphenylamine. Polymers, 14(21), 4479. https://doi.org/10.3390/polym14214479

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