Entropy-driven strategy stabilizes photoactive halide perovskites for inverted solar cells

熵驱动策略可稳定用于反式太阳能电池的光活性卤化物钙钛矿

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Abstract

The phase instability of perovskite materials remains a significant obstacle to their practical application in photovoltaics. Herein, we present a high-configurational-entropy strategy based on formamidinium ion (FA(+)) to fabricate the photoactive phase-stable halide perovskites through incorporating 2-amino-1,3,4-thiadiazole (2NTD). 2NTD optimally balances interactions with the [PbI(6)](4-) octahedral frameworks while enhancing the rotational freedom of FA(+). This synergistic effect amplifies FA(+) anisotropy and elevates configurational entropy. Moreover, 2NTD effectively inhibits the formation of I(2)/I(3)(-) species and passivates the associated trap-state, thereby reducing the self-degradation behavior within perovskite films caused by undesirable iodine species. This improvement significantly enhances the crystallization and phase-stability of the perovskites under I(2)-rich conditions. Consequently, efficiencies of 26.63% (certified 26.40%) for a 0.09-cm(2) inverted PSCs, 25.34% for a 1-cm(2) device, and 23.08% for a 12.96-cm(2) mini-module were obtained. Moreover, the target device exhibits a minimized non-radiative voltage loss of 69 mV and an improved long-term operational stability.

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