Mittal Mona, Garg Rahul, Jana Atanu
Department of Applied Sciences (Chemistry), Galgotias College of Engineering and Technology, Knowledge Park I, Greater Noida, Uttar Pradesh 201310, India.
Department of Chemical Engineering, Indian Institute of Technology Ropar, Nangal Rd, Hussainpur, Rupnagar, Punjab 140001, India.
Dalton Trans. 2023 Aug 29;52(34):11750-11767. doi: 10.1039/d3dt01581e.
All-inorganic and organic-inorganic hybrid perovskite solar cells (PSCs) have taken a quantum leap owing to their high performance and low-cost solution processability. Their efficiency has been dramatically increased up to ∼26%, matching the conventional inorganic photovoltaics like monocrystalline Si (26.1%), polycrystalline Si (21.6%), CdTe (22.1%), and CIGS (22.3%). Such outstanding performance has been achieved due to their excellent optoelectronic properties, such as a direct bandgap in the visible region, a very high absorption coefficient, a long charge-carrier diffusion length, and ambipolar carrier transport characteristics. FAPbI (FA = formamidinium) and CsPbI perovskites among the pool of perovskites are recommended for solar cell applications because they meet all the requirements for photovoltaic applications. However, the fundamental problem of these perovskites is that their photoactive black phase is highly unstable under ambient conditions due to small and large sizes of Cs and FA ions, respectively. The instability of the black phase of these perovskites hinders their applications in photovoltaic devices as a high-quality light absorber layer. Several approaches have been employed to prevent the formation of the photo-inactive yellow phase or to enhance the stability of the black phase of perovskites, such as dimensional and compositional engineering, the addition of external additives, and dimensional engineering. This perspective summarizes the various methods for stabilizing the black phase of CsPbI and FAPbI perovskites at room temperature as well as their application in photovoltaic devices.
全无机及有机-无机杂化钙钛矿太阳能电池(PSCs)因其高性能和低成本的溶液可加工性实现了巨大飞跃。其效率已大幅提高至约26%,与传统无机光伏材料如单晶硅(26.1%)、多晶硅(21.6%)、碲化镉(22.1%)和铜铟镓硒(22.3%)相当。之所以能取得如此出色的性能,是因为它们具有优异的光电特性,如在可见光区域的直接带隙、非常高的吸收系数、长的电荷载流子扩散长度以及双极性载流子传输特性。在众多钙钛矿材料中,甲脒铅碘(FA = 甲脒)和铯铅碘钙钛矿因其满足光伏应用的所有要求而被推荐用于太阳能电池应用。然而,这些钙钛矿的根本问题在于,由于铯离子和甲脒离子尺寸大小不同,它们的光活性黑相在环境条件下高度不稳定。这些钙钛矿黑相的不稳定性阻碍了它们作为高质量光吸收层在光伏器件中的应用。人们已采用多种方法来防止光惰性黄相的形成或提高钙钛矿黑相的稳定性,如维度和成分工程、添加外部添加剂以及维度工程。本文综述了在室温下稳定铯铅碘和甲脒铅碘钙钛矿黑相的各种方法及其在光伏器件中的应用。