We try to answer the three research questions as a subsection of a larger pre-/post study in an experimental-/control-group design. For the subject matter of the study, we chose three different topics of organic chemistry. These are stereochemistry, carbonyl-chemistry, and pericyclic reactions. We selected these three topics with care, concerning the research questions, because they demand for sophisticated mental rotation abilities.
2.4. Instruments
In order to conduct the study as described, we developed three different learning materials and AR-apps, each one for the topic stereochemistry, carbonyl-chemistry, and pericyclic reactions as well as corresponding test items.
All learning materials provide the topics’ contents by external representations, namely by a combination of texts and pictures. Concerning the dual coding theory by Paivio [
34] and the Cognitive Theory of Multimedia Learning by Mayer [
23], we paid much attention on a content wise fitting of texts and pictures in the learning materials, to avoid an increase of extraneous cognitive load. The pictures in the learning materials serve as markers to trigger the AR. The learning material for stereochemistry provides 22 AR-markers, the material for carbonyl-chemistry 24 AR-markers and the material for pericyclic reactions 19 AR-markers.
Additionally to the learning materials, we developed an iOS-based app called Augmented Reality Chemistry (short ARC) with the software Unity-3D and the Vuforia-Framework. In the app, pictures, which are printed two-dimensionally in the learning materials, are linked with 3D models or 3D animations. These 3D models and animations are self-developed with the software Blender. The app was provided in the study on Apple iPads (6th generation). The participants can scan the markers in the learning materials with the iPad’s camera, to trigger the AR. All displayed models or animations on screen allow user interaction in real time, e.g., scaling or rotating. All animations are played in a continuous loop. The AR-models in the app, present the specific three-dimensional information given in the learning materials by text and pictures only two-dimensionally.
Figure 2 shows an example of the self-developed learning material, in this case for stereochemistry. The text describes the differences of organic molecules in ecliptic or staggered formation, which are both illustrated in wedge-dash-notation for the ethane molecule below. The red letters “AR” under the pictures invite the participants to scan this figure with the iPad’s camera to trigger the AR. In this case, a 3D animation of the ethane molecule appears in wedge-dash-notation on screen, which switches in a continuous loop from the ecliptic into the staggered formation and backwards. In this manner the effects of ecliptic and staggered formation can be clarified three-dimensionally.
In
Figure 3 the app ARC can be seen in use in combination with the learning material. The ball-and-stick-model of a hypothetical molecule on screen shall be rotated around its axes. This can be done by finger-gestures in real time on screen. The learning goal of this task is to illustrate and self-experience the principle of chirality, where two structural identical molecules behave like image and reflection but do not provide the same chemical characteristics.
Figure 3 shows illustrative how the virtual three-dimensional object on screen seems to coexist with the two-dimensional picture on the paper.
As well as the pictures and the text in the learning materials, also the AR-models were developed according to typical textbooks for organic chemistry [
35].
To present not only static objects in the app,
Figure 4 shows another screenshot of the AR-app in use. This time, the app displays a chemical reaction from the learning material of the topic pericyclic reactions. The three-dimensional virtual objects on the screen play an animation in a continuous loop of the so-called Diels–Alder-reaction. During the 15 s lasting animation, both chemical educts accumulate to the chemical product of the reaction. In order to obtain the reactions’ product, the so-called orbitals of several atoms have to be considered (red and blue shapes in
Figure 4), which is why understanding the reaction is cognitive demanding. The big advantage of the AR-app here is that it does not only present the initial-state as well as the product-state of the reaction, but also the way from the educts to the product, which might be very useful for a reasonable understanding of the reactions concept.
Additionally to the descriptions of how the app ARC works,
Supplemental Materials are offered. Via QR-codes at the end of this paper, two short video clips can be accessed, which illustrate the examples from
Figure 3 and
Figure 4 in use.
In order to answer research question one, we measured the students’ perceived cognitive load. Therefore, we used a 9-item questionnaire on a 6-point Likert-scale by Klepsch and colleagues [
36]. This questionnaire is based on a self-assessment and distinguishes the cognitive load in three types. The intrinsic cognitive load describes the amount of load that learners need to invest to actively process the learning subject. In other words, the learning subject brings a specific complexity, which cannot be reduced without removing aspects. The second part of cognitive load is called extraneous cognitive load. It describes the cognitive effort needed to comprehend the learning material by its layout and design. An example for extraneous load is already given by Mayer [
23] in his spatial contiguity principle. If a text and a related picture are placed on different pages of a book, a lot more extraneous cognitive load is necessary, to transfer the information from the text towards the picture and vice versa, compared to presenting text and picture spatially close to each other. The third component of cognitive load is the germane load. Under estimation that the cognitive capacity is limited, this is the part of cognitive capacity, a learner can invest in meaningful learning activities individually.
Concerning research question two, the participants rated the app-usability on the System-usability scale by Brooke [
37]. This questionnaire was developed to evaluate the usability of several complex technical systems and has proven to be inexpensive, effective and highly reliable [
38]. It consists of 10 items, each 5 with positive and negative statements alternating, which ask for agreement on a five-point Likert-scale from strongly agree to strongly disagree. Out of these 10 items a usability score for each participant can be calculated. This score covers a scale from zero, which indicates a very bad usability to 100, which means a perfect usability. Bangor, Kortum, and Miller [
38] added an adjective description to the questionnaire, to make the usability score more interpretable. Depending on the peculiarity of the individual usability score, seven adjective ratings range from worst imaginable to best imaginable.
To measure the participants’ performance in pre- and post-tests, we developed test items for each of the three topics. All these items are in a multiple choice single-select format. Each item has one correct answer and three distractors for choice.
For the topic of stereochemistry, six items ask to rotate a given molecule around its bonding-axis in wedge-dash-notation or in Newman-projection. In four items the participants have to rotate molecules represented as ball-and-stick-models on one axis and in another four items on two axes. In another two items each, the same has to be done with molecules presented in wedge-dash-notation. Furthermore, the test includes two items to mirror a molecule and two items to determine the correct so-called absolute configuration of a molecule in the wedge-dash-notation.
We also developed 17 items to test the participants’ knowledge in carbonyl-chemistry. The first two items present ball-and-stick-models, where the participants shall name the correct corresponding orbitals and an electrostatic potential map. The next three items are presented as ball-and-stick-models, where possible areas where reactants can accumulate in case of carbonyl chemical reactions have to be selected. Six items ask to identify the correct geometry of typical carbonyl-molecules or intermediates presented in wedge-dash-notations. Another six items show first steps of carbonyl-reactions. The participants shall predict the correct product of the reaction, depending on the three-dimensional geometry, e.g., of the reactants or the intermediates of the reaction.
Six of the 15 items for the topic of pericyclic reactions ask to name the correct orbital matching of two reactants of pericyclic reactions. Three items of them are each in two-dimensional and three-dimensional representation in the wedge-dash-notation. Nine items aim to predict the correct product of pericyclic reactions. Three items of them present two-dimensional structure formulas and another six items show the task in three-dimensional wedge-dash-notations.
For measuring the participants’ general prior knowledge in organic chemistry, we used 10 items of the organic chemistry expertise test by Dickmann et al. [
24]. The mental rotation abilities were measures with 12 items of the PURDUE Visualization of Rotations Test [
39].