钝化
光伏
钙钛矿(结构)
量子点
配体(生物化学)
材料科学
工程物理
光电子学
纳米技术
光伏系统
化学工程
化学
工程类
电气工程
图层(电子)
生物化学
受体
作者
Seon Joong Kim,Muhammad Ahsan Saeed,Tae Hyuk Kim,George E. Ham,Hochan Song,Hyungju Ahn,Hyosung Choi,Jea Woong Jo,Yunsang Kim,Hyojung Cha,Jae Won Shim
标识
DOI:10.1016/j.cej.2024.151154
摘要
The advancement of perovskite photovoltaic (PePV) systems for harnessing indoor light energy has been accelerated by the advent of the Internet of Things (IoT). However, the commercialization of these systems is impeded by moisture instability and restricted carrier lifetimes. Perovskite quantum dots (PQDs) offer viable solutions for increasing stability despite the potential effects of their organic ligands on efficiency. In this study, a ligand passivation strategy was employed in PQD photovoltaics (PQDPVs) to enhance the carrier lifetime. The inclusion of 2-phenyl-4-(1,2,2-triphenylvinyl) quinazoline (2PACz) in the PQD film effectively reduced surface defects and suppressed trap-assisted charge recombination, resulting in a prolonged carrier lifetime. The charge carrier lifetimes in passivated PQDPVs increased by 35 %. Additionally, the matching of the energy level of the PQD changed after 2PACz passivation engineering with that of the 2PACz showed an advantage for hole transport. PQDPVs fabricated using 2PACz-passivated PQDs showed an impressive output power density (Pout) of 123.3 µW/cm2 (power conversion efficiency of 41.1 %) under a fluorescent lamp (0.30 mW/cm2; 1000 lx) owing to improved open-circuit voltage and fill factor. Moreover, the device maintained more than 80 % of its initial efficiency for 500 h in an ambient atmosphere. These findings highlight the potential of PQDPVs to compete with conventional PePVs for application in self-powered optoelectronic devices under dim illumination.
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