材料科学
钙钛矿(结构)
钝化
能量转换效率
光伏系统
卤化物
光电子学
带隙
兴奋剂
热稳定性
磁滞
纳米技术
化学工程
无机化学
电气工程
图层(电子)
化学
工程类
物理
量子力学
作者
Sawanta S. Mali,Jyoti V. Patil,Sachin R. Rondiya,Nelson Y. Dzade,Julian A. Steele,Mohammad Khaja Nazeeruddin,P.S. Patil,Chang Kook Hong
标识
DOI:10.1002/adma.202203204
摘要
Realizing photoactive and thermodynamically stable all-inorganic perovskite solar cells (PSCs) remains a challenging task within halide perovskite photovoltaic (PV) research. Here, a dual strategy for realizing efficient inorganic mixed halide perovskite PV devices based on a terbium-doped solar absorber, that is, CsPb1-x Tbx I2 Br, is reported, which undertakes a bulk and surface passivation treatment in the form of CsPb1-x Tbx I2 Br quantum dots, to maintain a photoactive γ-phase under ambient conditions and with significantly improved operational stability. Devices fabricated from these air-processed perovskite thin films exhibit an air-stable power conversion efficiency (PCE) that reaches 17.51% (small-area devices) with negligible hysteresis and maintains >90% of the initial efficiency when operating for 600 h under harsh environmental conditions, stemming from the combined effects of the dual-protection strategy. This approach is further examined within large-area PSC modules (19.8 cm2 active area) to realize 10.94% PCE and >30 days ambient stability, as well as within low-bandgap γ-CsPb0.95 Tb0.05 I2.5 Br0.5 (Eg = 1.73 eV) materials, yielding 19.01% (18.43% certified) PCE.
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