材料科学
钙钛矿(结构)
成核
光伏
电子
电子传输链
能量转换效率
光电子学
化学工程
纳米技术
光伏系统
化学
生物化学
物理
量子力学
工程类
生态学
有机化学
生物
作者
Yao Wang,Yuheng Li,Chi Li,Li Wang,Qin Zhou,Lusheng Liang,Zilong Zhang,Chunming Liu,Wei Yu,Xuteng Yu,Peng Gao
出处
期刊:Small
[Wiley]
日期:2024-05-10
被引量:1
标识
DOI:10.1002/smll.202402531
摘要
Abstract The efficacy of electron transport layers (ETLs) is pivotal for optimizing the device performance of perovskite photovoltaic applications. However, colloidal dispersions of SnO 2 are prone to aggregation and possess structural defects, such as terminal‐hydroxyls (OH T ) and oxygen vacancies (V O s), which can degrade the quality of ETLs, impede charge extraction and transport, and affect the nucleation and growth processes of the perovskite layer. In this study, the Sb(OH) 4 − ions hydrolyzed from SbCl 3 in colloidal dispersion can bind to defect sites and effectively stabilize the SnO 2 nanocrystals are demonstrated. Upon oxidative annealing, a Sb 2 O 5 @SnO 2 composite film is formed, in which the Sb 2 O 5 not only mitigates the aforementioned defects but also broadens the energy range of unoccupied states through its dispersed conduction band. The increased electron affinity (EA) facilitates more efficient capture of photoexcited electrons from the perovskite layer, thus augmenting electron extraction and minimizing electron‐hole recombination. As a result, a significant improvement in power conversion efficiency (PCE) from 22.60% to 24.54% is achieved, with an open circuit voltage ( V OC ) of up to 1.195 V, along with excellent stability of unsealed devices under various conditions. This study provides valuable insights for the understanding and design of ETLs in perovskite photovoltaic applications.
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