Recent Advances in Visible-Light-Driven Heterogeneous Photocatalysis

A special issue of Catalysts (ISSN 2073-4344). This special issue belongs to the section "Photocatalysis".

Deadline for manuscript submissions: closed (31 October 2021) | Viewed by 19498

Special Issue Editor


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Guest Editor
1. Center for Materials, Architectures and Integration of Nanomembranes (MAIN), Chemnitz University of Technology, Rosenbergstraße 6, 09126 Chemnitz, Germany
2. Semiconductor Physics, Institute of Physics, Chemnitz University of Technology, Reichenhainer Str. 70, 09126 Chemnitz, Germany
Interests: photocatalysis; organic synthesis; solar energy materials; photoelectrocatalysis; TiO2; thin films; semiconductor nanoparticles
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Special Issue Information

Dear Colleagues,

The consumption of non-renewable resources and the rapid growth of chemical industries are causing serious energy and environmental problems. Highly efficient systems for converting and storing solar energy are therefore required in order to tackle global energy and environmental problems. The use of sunlight and heterogeneous catalysts to drive chemical reactions is an environmentally sustainable synthesis process that leads to the basic principle of green chemistry. This concept calls for chemists to establish new methodologies for the development of sustainable chemicals, the conversion of water into molecular hydrogen fuel, and the decomposition of environmental contaminants. However, the lack of development of the most active heterogeneous photocatalysts in practical applications may probably be due to their broad bandgap energy, which only allows them to be excited by UV light. The design of visible light-responsive photocatalytic systems is therefore a primary goal of scientists.

The objective of this Special Issue is to assemble original research articles, reviews, and comments on the challenges raised by state-of-the-art visible-light-driven photocatalytic systems, as well as the mechanistic investigations of existing ones, namely:

Perovskites
g-C3N4
Band-gap engineering of UV active photocatalysts, i.e., TiO2, ZnO, niobates, etc.
Dye-sensitization
Ligant to metal charge transfer (LMCT)
Mechanistic investigations
Surface plasmon resonance (SPR) effect

Dr. Narmina O. Balayeva
Guest Editor

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Keywords

  • Band gap engineering
  • Organic synthesis
  • Pollutant degradations
  • Water splitting
  • Fuel conversions
  • NOx, acetaldehyde, and formaldehyde degradation
  • Visible-light-responsive nanocomposites
  • Surface plasmonic-assisted photocatalysis
  • LMCT
  • MLCT
  • Semiconductors
  • Electrophotocatalysis

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Published Papers (4 papers)

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Research

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14 pages, 4257 KiB  
Article
Thermal Treatment of Polyvinyl Alcohol for Coupling MoS2 and TiO2 Nanotube Arrays toward Enhancing Photoelectrochemical Water Splitting Performance
by Tho Truong Nguyen, Thi Minh Cao, Narmina O. Balayeva and Viet Van Pham
Catalysts 2021, 11(7), 857; https://doi.org/10.3390/catal11070857 - 17 Jul 2021
Cited by 17 | Viewed by 3528
Abstract
Solar-driven photoelectrochemical (PEC) water splitting, using semiconductor photoelectrodes, is considered a promising renewable energy source and solution for environmental sustainability. Herein, we report polyvinyl alcohol (PVA) as a binder material for combining MoS2 and TiO2 nanotube arrays (TNAs) to improve PEC [...] Read more.
Solar-driven photoelectrochemical (PEC) water splitting, using semiconductor photoelectrodes, is considered a promising renewable energy source and solution for environmental sustainability. Herein, we report polyvinyl alcohol (PVA) as a binder material for combining MoS2 and TiO2 nanotube arrays (TNAs) to improve PEC water splitting ability. By a thermal treatment process, the formation of the π conjunction in the PVA structure enhanced the PEC performance of MoS2/TNAs, exhibiting linear sweeps in an anodic direction with the current density over 65 μA/cm2 at 0 V vs. Ag/AgCl. Besides, the photoresponse ability of MoS2/TNAs is approximately 6-fold more significant than that of individual TNAs. Moreover, a Tafel slope of 140.6 mV/decade has been obtained for the oxygen evolution reaction (OER) of MoS2/TNAs materials. Full article
(This article belongs to the Special Issue Recent Advances in Visible-Light-Driven Heterogeneous Photocatalysis)
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13 pages, 2208 KiB  
Article
Heterogeneous Photo-Fenton Reaction for Olive Mill Wastewater Treatment—Case of Reusable Catalyst
by Cristina Agabo-García, Naima Calderón and Gassan Hodaifa
Catalysts 2021, 11(5), 557; https://doi.org/10.3390/catal11050557 - 27 Apr 2021
Cited by 13 | Viewed by 2588
Abstract
Heterogeneous catalysts can be an efficient and economical option for olive mill wastewater (OMW) treatment by an advanced oxidation process if they could be reused. In this work, OMW was treated using a heterogeneous photo-Fenton reaction (artificial ultraviolet light/H2O2/HFeO [...] Read more.
Heterogeneous catalysts can be an efficient and economical option for olive mill wastewater (OMW) treatment by an advanced oxidation process if they could be reused. In this work, OMW was treated using a heterogeneous photo-Fenton reaction (artificial ultraviolet light/H2O2/HFeO2). For this purpose, different concentrations of HFeO2 were tested: 0.04; 0.3; 0.8; 5.0; 10.0; 20.0; 30.0, and 50.0 g/L. The following operational conditions were chosen: pH = 3.0, temperature = 20 °C, agitation rate = 700 rpm. The experimental results showed high removal percentages of the main OMW characterization parameters at 50 g/L of HFeO2: %CODremoval = 62.8%; %total phenolic compounds (TPCs) = 88.9%. These results were also compared with those of other control oxidation systems, i.e., UV, H2O2, and UV/H2O2, which provided 35.5 and 56.1%; 46.2 and 74.0%; 48.0 and 76.8% removal, respectively. In addition, the catalyst was reused three times, recovering more than 90.5% of it. Full article
(This article belongs to the Special Issue Recent Advances in Visible-Light-Driven Heterogeneous Photocatalysis)
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17 pages, 4212 KiB  
Article
A Selective Synthesis of TaON Nanoparticles and Their Comparative Study of Photoelectrochemical Properties
by Vijay Khanal, Eric Soto-Harrison, Dhanesh Chandra, Narmina O. Balayeva, Detlef W. Bahnemann and Vaidyanathan (Ravi) Subramanian
Catalysts 2020, 10(10), 1128; https://doi.org/10.3390/catal10101128 - 1 Oct 2020
Cited by 9 | Viewed by 3490
Abstract
A simplified ammonolysis method for synthesizing single phase TaON nanoparticles is presented and the resulting photoelectrochemical properties are compared and contrasted with as-synthesized Ta2O5 and Ta3N5. The protocol for partial nitridation of Ta2O5 [...] Read more.
A simplified ammonolysis method for synthesizing single phase TaON nanoparticles is presented and the resulting photoelectrochemical properties are compared and contrasted with as-synthesized Ta2O5 and Ta3N5. The protocol for partial nitridation of Ta2O5 (synthesis of TaON) offers a straightforward simplification over existing methods. Moreover, the present protocol offers extreme reproducibility and enhanced chemical safety. The morphological characterization of the as-synthesized photocatalysts indicate spherical nanoparticles with sizes 30, 40, and 30 nm Ta2O5, TaON, and Ta3N5 with the absorbance onset at ~320 nm, 580 nm, and 630 nm respectively. The photoactivity of the catalysts has been examined for the degradation of a representative cationic dye methylene blue (MB) using xenon light. Subsequent nitridation of Ta2O5 yields significant increment in the conversion (ζ: Ta2O5 < TaON < Ta3N5) mainly attributable to the defect-facilitated adsorption of MB on the catalyst surface and bandgap lowering of catalysts with Ta3N5 showing > 95% ζ for a lower (0.1 g) loading and with a lamp with lower Ultraviolet (UV) content. Improved Photoelectrochemical performance is noted after a series of chronoamperometry (J/t), linear sweep voltammetry (LSV), and electrochemical impedance spectroscopy (EIS) measurements. Finally, stability experiments performed using recovered and treated photocatalyst show no loss of photoactivity, suggesting the photocatalysts can be successfully recycled. Full article
(This article belongs to the Special Issue Recent Advances in Visible-Light-Driven Heterogeneous Photocatalysis)
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Review

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36 pages, 4792 KiB  
Review
Metal Sulfide Photocatalysts for Hydrogen Generation: A Review of Recent Advances
by Zamin Mamiyev and Narmina O. Balayeva
Catalysts 2022, 12(11), 1316; https://doi.org/10.3390/catal12111316 - 27 Oct 2022
Cited by 74 | Viewed by 8539
Abstract
Metal-sulfide nanostructures have piqued the interest of researchers for decades due to their intriguing optoelectronic properties. Indeed, significant advances and improvements have been made in various fundamental aspects for cutting-edge applications, such as water splitting and hydrogen production. Furthermore, rising demand for low-dimensional [...] Read more.
Metal-sulfide nanostructures have piqued the interest of researchers for decades due to their intriguing optoelectronic properties. Indeed, significant advances and improvements have been made in various fundamental aspects for cutting-edge applications, such as water splitting and hydrogen production. Furthermore, rising demand for low-dimensional materials due to lower material consumption and improved performance due to quantum size effects has spurred research on semiconducting metal sulfides. Consequently, size-controllable nanostructures with diverse morphologies have been fabricated and studied for potential applications. However, the photocatalytic hydrogen evolution rate is still limited mainly by fast recombination rate, poor solar energy utilization and lack of surface-active sites for H2 reduction. This review will highlight particularly recent findings in metal-sulfide-based photocatalysts for hydrogen evolution reactions, considering the swift development and excellent research in this field. Following a brief overview of fundamental properties, we will explore state-of-the-art strategies for enhancing H2 generation efficiencies over the pristine, heterostructured and co-catalayzed metal-sulfide photocatalysts. Full article
(This article belongs to the Special Issue Recent Advances in Visible-Light-Driven Heterogeneous Photocatalysis)
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