光热治疗
钙钛矿(结构)
太阳能电池
材料科学
钙钛矿太阳能电池
纳米技术
理论(学习稳定性)
化学工程
化学
光电子学
结晶学
计算机科学
工程类
机器学习
作者
Xinwen Zhang,Zikun Cao,Lening Shen,Kelsey Garden,Nilave Chakraborty,Pramod Baral,Luisa Whittaker‐Brooks,Xiong Gong,Joseph M. Luther,He Wang
标识
DOI:10.1021/acsenergylett.4c02325
摘要
In halide perovskite solar cells, certain compositions, especially those with a high mixture of anions, degrade rapidly. Here, a degradation study compares the photo (exposure to light), thermal (exposure to elevated temperatures), and photo-plus-thermal (combination) stability of three representative perovskite compositions chosen for their relatively high performance and to independently test anion versus cation effects. Based upon experience and reports, the compositions studied are triple cation with a high Br ratio (Cs0.05(FA0.98MA0.02)0.95Pb(I0.5Br0.5)3), all iodide with a moderately high Cs ratio (FA0.8Cs0.2PbI3), and FA-dominated triple cation (Cs0.05(FA0.98MA0.02)0.95Pb(I0.98Br0.02)3). Cs0.05(FA0.98MA0.02)0.95Pb(I0.98Br0.02)3 displayed the best combined photo-plus-thermal stability. Degradation mechanisms were investigated by comparing the morphology, surface composition, and bulk and interface carrier dynamics. Under the harshest aging conditions (photo-plus-thermal), phase segregation and vaporization of organic cations occurred, along with the appearance of high-energy states indicating the interaction with C60. The findings were verified on perovskite films blade-coated in air used in devices (FTO/NiOx/SAM/Perovskite/C60/BCP/Cu), achieving an efficiency of 21.9% alongside correlated stability.
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