光伏
钙钛矿(结构)
结晶
结晶度
带隙
材料科学
开路电压
卤化物
制作
电压
光伏系统
光电子学
能量转换效率
纳米技术
化学工程
电气工程
无机化学
化学
工程类
复合材料
病理
替代医学
医学
作者
Nakita K. Noel,Martina Congiu,Alexandra J. Ramadan,Sarah Fearn,David P. McMeekin,Jay B. Patel,Michael B. Johnston,Bernard Wenger,Henry J. Snaith
出处
期刊:Joule
[Elsevier BV]
日期:2017-10-01
卷期号:1 (2): 328-343
被引量:151
标识
DOI:10.1016/j.joule.2017.09.009
摘要
Summary
Impressive power conversion efficiencies coupled with the relative ease of fabrication have made perovskite solar cells a front runner for next-generation photovoltaics. Although perovskite films and optoelectronic devices have been widely studied, relatively little is known about the chemistry of the precursor solutions. Here, we present a study on the hydrolysis of N,N-dimethylformamide, correlating how pH changes related to its degradation affect the crystallization of MAPbI3−xClx perovskite films. By careful manipulation of the pH, and the resulting colloid distribution in precursor solutions, we fabricate perovskite films with greatly improved crystallinity, which when incorporated into photovoltaic devices reproducibly yield efficiencies of over 18%. Extending this method to the mixed cation, mixed halide perovskite FA0.83MA0.17Pb(I0.83Br0.17)3, we obtain power conversion efficiencies of up to 19.9% and open-circuit voltages of 1.21 V for a material with a bandgap of 1.57 eV, achieving the lowest yet reported loss in potential from bandgap to a VOC of only 360 mV.
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