Perovskite Materials for Energy and Environmental Applications. Группа авторов

Читать онлайн.
Название Perovskite Materials for Energy and Environmental Applications
Автор произведения Группа авторов
Жанр Техническая литература
Серия
Издательство Техническая литература
Год выпуска 0
isbn 9781119763352



Скачать книгу

can be obtained. The bandgap of CH3NH3SnI3−xBr can be modulated from 1.30 to 2.15 eV by substitution of Pb with tin and partially substitution of I (iodine) with Br (bromine)x [42]. A linearity behavior is observed between bandgap and ratio of I/Br. Efficiency is achieved up to 5.23% when CH3NH3SnI3 is used as a light absorber in the solar cell [42]. On optimizing iodine and bromine ratio in CH3NH3SnIBr2, a way better PSC can be produced.

      2.5.5 Rapidly Increasing Efficiency

      The power conversion efficiency of PSCs has raised from 3.8% [3] in 2009 to 22.10% in 2016. For cells having square area aperture greater than 1 cm2 has shown a verified efficiency of 19.6%. This efficiency is almost equal to efficiency obtained in 2017 by thin film CIGS and CdTe which is 21% [43]. Because of tunable band gaps in the solar cell, it can be optimized accordingly to the solar spectrum. Shockley–Queisser efficiency limit can be approached by this solar cell which is about 31% for a 1.55-eV band gap [44].

      1. Pb-free alternatives/toxicity of Pb

      As we know, Pb is highly toxic and harmful to nature and the environment. Lead harms the microorganisms, which are present in the soil; hence, it is a potential threat to the ecosystem. Lead-based PSCs give high light power conversion efficiencies but to prevent the toxicity issues, we have to find alternatives to Pb. We can use tin as it is safe to replace Pb. In 2014, Pb-free perovskite cells were reported. Here, tin was used (MASnI3) in replacement of Pb, and it achieved power conversion efficiency of 5% to 6% when made with mesoporous TiO2 scaffolds [45, 46]. Cons of tin-based PSCs is that they are not stable in air, and even if they are prepared in an inert environment, they quickly degrade. The main problem is oxidation of tin from +2 to +4 because of self-doping. So the metal which can be stabilized in +2 oxidation state, then that could be used as an alternative to Pb [47].

      2. Stability

      The power conversion efficiency of PSCs has risen due to considerable amount of research and focus on architectures, compositions, and manufacturing techniques. For commercialization of perovskite cell technology, it should be able to survive at minimum 25 years without degradation in yield in an external environment. In a controlled environment, high-efficiency solar cells are synthesized but when they are exposed to the ambient atmosphere, efficiency drops rapidly. Light absorbers are very fragile/sensitive to water, because of this, solar cells are unstable [38]. The degradation also depends on oxygen, UV radiation, and temperatures.

      The rate of degradation of perovskite is very rapid (few minutes) when there is presence of water. The products formed after the degradation of perovskite are CH3NH3I and PbI2. So to increase the lifetime of PSCs it should be kept away from moisture. An HTM with long alkyl chain was used, which would help to prevent water from passing from HTM to perovskite [48]. A carbon material layer of 10 μm thick was used as back contact to retain water. After these arrangements, the stability got increased and power conversion efficiency remained as it is for 1008 hours [49].

      To some extent, the stability of the PSC has increased but it is still far away from long-term use and commercialization. For improving the stability the stability of PSCs, it is necessary to understand the degradation mechanisms and find out the state at which degradation reactions originated or accelerated [52].

      The efficiency of the PSC in the laboratory has reached 23.1%, which is comparable to the single crystalline solar cell. Because of high achievable efficiency, the researchers of different backgrounds of science have contributed in the investigation of PSCs. The higher efficiency of PSCs has been achieved due to high coefficient of absorption and long diffusion lengths. Perovskite solar cell has desired properties, enormous potential, low cost, and high efficiency. Despite achieving high efficiency, there is much difference between the stability of PSCs (1000 hours) and silicon solar cells (20– 25 years). The future challenge is to increase stability. Another drawback is it has toxic material, like Pb, which is very harmful for human beings, as well as the environment. There are some problems that are not solved yet, such as the materials, to increase the scalability, processing of materials, and so on [38].

      In total, there are three major concerns, which should be overcome before its commercialization. First, the degradation mechanism should be explored as humidity, heat, and UV light are the main reasons for degradation and brings instability in perovskite. Second, Pb is very harmful to nature, hence it should be replaced with some safer option. Third, PSCs has very high efficiency in small areas of 0.1 cm2, so this area must be increased such that efficiency and stability remains the same so that we can perform high scale [53]. Researches need to focus and improve on the perovskite and electron-hole transport materials in the future, so that we can use PSCs in place of the conventional solar cell. If these problems are solved, surely perovskite material is projected to have a significant part of the solar cell industry.

      The authors acknowledge the Chemical Engineering Department of Nirma University for providing the necessary help, infrastructure, and support for the preparation of this chapter/work.

      1. Snaith, H.J., Perovskites: The emergence of a new era for low-cost, high-efficiency solar cells. J. Phys. Chem. Lett., 4, 21, 3623–3630, 2013.

      2. Mathew, S. et al., Dye-sensitized solar cells with 13% efficiency achieved through the molecular engineering of porphyrin sensitizers. Nat. Chem., 6, 3, 242–247, 2014.

      3. Kojima, A., Teshima, K., Shirai, Y., Miyasaka, T., Organometal halide perovskites as visible-light sensitizers for photovoltaic cells. J. Am. Chem. Soc, 131, 17, 6050–6051, 2009.

      4. Kim, H. et al., All-Solid-State Submicron Thin Film. Sci. Rep., 2, 1, 1–7, 2012.

      5. Yang, W.S. et al., High-performance photovoltaic perovskite layers fabricated through intramolecular exchange. Science, 348, 6240, 1234–1237, 2015.

      6. Ma, Y. et al., Recent Research Developments of Perovskite Solar Cells. Chin. J. Chem., 32, 10, 957–963, 2014.

      7. Cheng, Z. and Lin, J., Layered organic-inorganic hybrid perovskites: Structure, optical properties, film preparation, patterning and templating engineering. CrystEngComm, 12, 10, 2646–2662, 2010.

      8. Li, X. et al., Improved performance and stability of perovskite solar cells by crystal crosslinking with alkylphosphonic acid ω-ammonium chlorides. Nat. Chem., 7, 9, 703–711, 2015.

      9.