量子点
钙钛矿(结构)
介孔材料
钝化
材料科学
图层(电子)
光伏系统
电子传输链
电子迁移率
纳米技术
钙钛矿太阳能电池
能量转换效率
化学工程
光电子学
化学
催化作用
电气工程
生物化学
工程类
作者
Juntian Zhou,Mei Lyu,Jun Zhu,Guannan Li,Yitong Li,Suzhe Jin,Jialei Song,Haihong Niu,Jinzhang Xu,Ru Zhou
标识
DOI:10.1021/acsaem.1c03681
摘要
As a revolutionary photovoltaic technology, the perovskite solar cell has received enormous attention, owing to excellent electronic and optical properties of perovskite materials. The mesoporous TiO2 (m-TiO2) framework is extensively used as an electron transport layer (ETL) to construct high-performance perovskite solar cells (PSCs), showing efficient electron extraction capability, owing to the enlarged perovskite/ETL interface. However, the TiO2 ETL usually involves high-density oxygen vacancies, low electron mobility, and relatively high photocatalytic activity toward perovskite materials. To address such issues, herein, we demonstrate the successful construction of SnO2 quantum dot (QD)-modified m-TiO2 as an effective ETL for PSCs. It is revealed that the SnO2 QD-modified m-TiO2 ETL affords more favorable electron extraction and transport characteristics and suppressed charge recombination, resulting from the interfacial passivation and the enhanced conductivity of ETLs. Furthermore, the ultrathin SnO2 QD layer incorporated at the m-TiO2/perovskite interface effectively lowers the photocatalytic activity of TiO2 toward perovskite materials, thereby improving the long-term device stability. Eventually, the MAPbI3- and FAPbI3-based PSCs utilizing the SnO2 QD-modified m-TiO2 ETLs obtained appreciable power conversion efficiencies of 19.09 and 20.09%, respectively, higher than those of counterpart devices based on the conventional m-TiO2 and SnO2 ETLs.
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