结晶
钙钛矿(结构)
异步通信
串联
卤化物
材料科学
基质(水族馆)
相(物质)
纳米技术
化学
计算机科学
光电子学
能量转换效率
催化作用
化学工程
作者
Taomiao Wang,Fei Wang,Shuangbiao Xia,Yutao Wang,Yumeng Shi,Haoran Lin,Yonghua Chen,Mingjian Yuan,Liping Zhang,Haizhe Zhong,Hanlin Hu
标识
DOI:10.1021/acsenergylett.6c02301
摘要
Abstract Wide-bandgap perovskites are essential for high-efficiency perovskite/silicon tandem solar cells but are limited by halide segregation and a narrow crystallization temperature window. Although temperature is known to influence perovskite film formation, its role in driving asynchronous crystallization between I-rich and Br-rich domains—and thus the extent of phase segregation—remains insufficiently understood. Here, we reveal that substrate temperature critically regulates these asynchronous crystallization pathways and propose an additive-engineering strategy to overcome this bottleneck. By introducing 2-mercapto-4-(trifluoromethyl) pyrimidine (2-MTP), the strong PbX2 coordination regulates DMSO–PbX2 intermediates, substantially broadening the processing temperature window. This controlled coordination modulates precursor conversion kinetics, mitigates asynchronous halide-rich domains crystallization, and effectively suppresses phase segregation in wide-bandgap perovskite films. As a result, 2-MTP-modified wide-bandgap devices achieve PCEs of 23.79% (1.67 eV; certified 23.02%) and 19.81% (1.84 eV). When implemented in perovskite/silicon tandem architectures, additive-regulated crystallization delivers 32.48% PCE (certified 31.60%) and markedly improved operational stability.
科研通智能强力驱动
Strongly Powered by AbleSci AI