工作职能
钙钛矿(结构)
偶极子
光电流
材料科学
能量转换效率
单层
光电子学
开路电压
图层(电子)
化学物理
基质(水族馆)
氧化物
开尔文探针力显微镜
化学工程
电压
化学
纳米技术
结晶学
物理
有机化学
工程类
地质学
冶金
海洋学
原子力显微镜
量子力学
作者
Huimin Pang,Mingxuan Guo,Xingtong Chen,Xueqing Xia,Xiaojuan Sun,Wenlin Xia,Hengfei Shi,Yu Chen,Song Chen
标识
DOI:10.1021/acsmaterialslett.3c00241
摘要
Forming an interface dipole moment pointing from the absorber to the oxide substrate can improve the open-circuit voltage (VOC) of perovskite solar cells (PSCs) without affecting photocurrent. In past studies, however, interface dipole layers were generally formed using organic self-assembled monolayers or polyelectrolytes, which raises concerns about intrinsic stability. Meanwhile, perovskites’ substrate-dependent electronic properties question the apparent correlation between the oxide’s work function and the built-in voltage. In this work, we propose an interface dipole layer based on solution-processable metal halides, which increases the built-in voltage of the n–i–p diode by simultaneously reducing the electron transport layer’s work function and strengthening the n-type characteristics of the perovskite absorber. The n–i–p-structured PSCs with the SbX3 dipole layer achieve substantially enhanced VOC (1.171 V) and power conversion efficiency (23.11%). Further experiments and calculations confirm that the proposed dipole model can explain the VOC enhancement qualitatively and quantitatively.
科研通智能强力驱动
Strongly Powered by AbleSci AI