Xu Hongzhe, Guo Zhaochen, Chen Peng, Wang Songcan
Australian Institute for Bioengineering and Nanotechnology and School of Chemical Engineering, The University of Queensland, St Lucia, Brisbane, QLD 4072, Australia.
Frontiers Science Center for Flexible Electronics, Xi'an Institute of Flexible Electronics (IFE), Northwestern Polytechnical University, 127 West Youyi Road, Xi'an 710072, China.
Chem Commun (Camb). 2024 Oct 22;60(85):12287-12301. doi: 10.1039/d4cc04000g.
Organic-inorganic metal halide perovskite solar cells (PSCs) have attracted extensive attention from the photovoltaic (PV) community due to their fast-growing power conversion efficiency from 3.8% to 26.7% in only 15 years. However, these organic-inorganic hybrid PSCs suffer from inferior long-term operational stability under thermal and light stress, due to the fragile hydrogen bonds between organic cations and inorganic slabs. This motivates the exploration of more robust all-inorganic alternatives against external stimuli, by substituting inorganic cesium (Cs) cations for volatile organic cations. Despite reinforced ionic interaction between Cs cations and metal halide frameworks, these Cs-based all-inorganic perovskites tend to undergo spontaneous phase transition from photoactive black phases to non-perovskite yellow phases at room temperature, significantly deteriorating their optoelectronic performance. Thus, tremendous efforts have been made to stabilize the black phase of CsPbI, while the phase instability issue of the tin-based analogue of CsSnI has not been resolved yet. This highlight article summarizes the empirical advances in stabilizing the metastable phases of CsPbI, aiming to provide useful guidelines to accelerate the development of phase-stable CsSnI for durable lead-free PV applications. Finally, the remaining challenges and future research opportunities are outlined, providing a road map to realize efficient and durable all-inorganic perovskite solar cells towards practical applications.
有机-无机金属卤化物钙钛矿太阳能电池(PSCs)在短短15年内功率转换效率从3.8%快速增长到26.7%,因此吸引了光伏(PV)领域的广泛关注。然而,由于有机阳离子和无机板层之间脆弱的氢键,这些有机-无机混合PSCs在热和光应力下长期运行稳定性较差。这促使人们探索通过用无机铯(Cs)阳离子替代挥发性有机阳离子来获得更稳定的抗外部刺激的全无机替代品。尽管Cs阳离子与金属卤化物骨架之间的离子相互作用增强,但这些基于Cs的全无机钙钛矿在室温下往往会自发地从光活性黑色相转变为非钙钛矿黄色相,显著降低其光电性能。因此,人们已经做出了巨大努力来稳定CsPbI的黑色相,而CsSnI的锡基类似物的相稳定性问题尚未得到解决。这篇亮点文章总结了稳定CsPbI亚稳相的经验进展,旨在提供有用的指导方针,以加速用于耐用无铅光伏应用的相稳定CsSnI的开发。最后,概述了剩余的挑战和未来的研究机会,提供了一条实现高效耐用的全无机钙钛矿太阳能电池实际应用的路线图。