Chloroformamidine hydrochloride as a molecular linker towards efficient and stable perovskite solar cells

被引:6
|
作者
Li, Hui [1 ,2 ]
Fu, Ping [1 ]
Lu, Ruixue [1 ,3 ]
Guo, Junxue [1 ,4 ]
Guo, Xin [1 ]
Li, Rengui [1 ]
Li, Can [1 ,2 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian Natl Lab Clean Energy, Dalian 116023, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Fudan Univ, iChEM Collaborat Innovat Ctr Chem Energy Mat, Dept Chem, Shanghai 200438, Peoples R China
[4] Univ Sci & Technol China, Sch Chem & Mat Sci, Hefei 230026, Peoples R China
基金
中国国家自然科学基金;
关键词
ELECTRON TRANSPORTING LAYER; HIGH-PERFORMANCE; PASSIVATION;
D O I
10.1039/d3tc00637a
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Interface engineering has become one of the important subjects in developing efficient and stable perovskite solar cells (PSCs). Herein, an interfacial molecular linker, chloroformamidine hydrochloride (CFA), is introduced to modify the properties of electron transport layers (ETLs) and modulate the interaction between the ETL and perovskite (PVK) layer via coordination/electrostatic coupling. It is found that the CFA molecular linker can passivate the oxygen vacancies/interfacial defects of SnO2 and construct an improved energetic alignment between the ETL and PVK layer. Consequently, a power conversion efficiency (PCE) of 23.47% with an open-circuit voltage (V-OC) of 1.17 V for the target device is achieved. Moreover, unencapsulated PSCs based on CFA-modified SnO2 (CFA@SnO2) ETLs show enhanced thermal and moisture stability compared with PSCs without CFA modification. This work provides a feasible strategy to tune the interface between the ETL and PVK for efficient and stable PSCs.
引用
收藏
页码:5039 / 5044
页数:6
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