钝化
结晶
钙钛矿(结构)
盐(化学)
抗坏血酸
钠
化学
钠盐
化学工程
无机化学
材料科学
结晶学
纳米技术
食品科学
有机化学
图层(电子)
工程类
作者
Yaling Han,Hongru Ma,Jing Liu,Qingshun Dong,Pengfei Wang,Siao Li,Tao Feng,Mingzhu Pei,Jiazhen Wei,Yantao Shi,Minhuan Wang,Jiming Bian
标识
DOI:10.1021/acs.jpclett.5c01590
摘要
The two-step sequential deposition process has been widely employed to fabricate perovskite solar cells (PSCs). However, the random orientation of lead iodide (PbI2) template and undesirable PbI2 residues resulting from the rapid and unregulated solid-liquid reaction poses a significant challenge to achieving high performance and long-term stability of two-step processed PSCs. Here, l-ascorbic acid sodium salt (l-AASS) was introduced into the lead iodide (PbI2) precursor solution to delicately control the FAPbI3 crystallization kinetics behavior via manipulating the arrangement mode of mesoporous PbI2 template, which provides a more favorable foundation for the subsequent infiltration and reaction of organic salts. Comprehensive characterization demonstrates that the interaction between l-AASS and PbI2 promotes the preferential orientation and a significant reduction in residual PbI2 due to the formation of the l-AASS/PbI2 complex, further enabling rapid formation of high-quality α-FAPbI3 perovskite films with larger grains at an earlier stage. Additionally, l-AASS effectively passivated the uncoordinated Pb2+ defects and reduced the nonradiative recombination sites in perovskite films. These synergistic factors holistically contribute to the remarkable improvement in PSCs performance; an encouraging power conversion efficiency (PCE) of 25.23% was achieved with impressive stability. Moreover, a PCE of 20% was obtained for large-area (65 cm2) modules, confirming the upscale potential of current premodulating PbI2 precursor strategy for industrial commercialization.
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