An Er-doped TiO2 phase junction as an electron transport layer for efficient perovskite solar cells fabricated in air

被引:42
|
作者
Ren, Ziqiu [1 ]
Wu, Jinde [1 ]
Wang, Na [1 ]
Li, Xin [1 ,2 ]
机构
[1] Harbin Inst Technol, Sch Chem & Chem Engn, Harbin 150001, Heilongjiang, Peoples R China
[2] Harbin Inst Technol, State Key Lab Urban Water Resource & Environm, Harbin 150001, Heilongjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
PHOTOCATALYTIC ACTIVITY; HIGH-PERFORMANCE; UP-CONVERSION; STRUCTURAL TRANSFORMATION; CHARGE SEPARATION; INTERFACE; STABILITY; GEL; ENHANCEMENT; NANOPARTICLES;
D O I
10.1039/c8ta04444a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Current perovskite solar cells (PSCs) often use high-purity single-crystal metal oxides prepared by complex growth processes as electron transport layers (ETLs). In particular, TiO2, as an ETL, can deteriorate the stability of PSCs under illumination. Here, we report a passivation strategy using Er-doped TiO2 synthesized with a one-step hydrothermal method as an ETL. Notably, the oxygen-induced defects in TiO2 have decreased to an acceptable level for PSCs due to the introduction of Er3+ ions. More interestingly, we find that a phase junction can be formed in the mixed crystalline rutile/anatase phase of TiO2, and this TiO2 phase junction can achieve efficient charge separation and accelerate internal electron transfer of the ETL. Taking advantage of these facts, we obtain TiO2-based PSCs through a two-step sequential deposition method in ambient air, whose best efficiency increases by 45.8%. Moreover, the Er-doped device exhibits remarkable ultraviolet resistance ability, whose efficiency is maintained over 90% even after 500 hour ultraviolet irradiation. We believe that this demonstrated strategy provides an effective way for preparing efficient and ultraviolet resistant PSCs in air.
引用
收藏
页码:15348 / 15358
页数:11
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