钝化
硫化铅
量子点
材料科学
卤化物
配体(生物化学)
硫化物
红外线的
离子
光电子学
无机化学
纳米技术
化学
光学
有机化学
受体
冶金
物理
图层(电子)
生物化学
作者
Yong Xia,TaiMing Ji,Lu Yu,Pengfei Xiang,Zhixu Wu,Xiaokun Yang,Hui Deng
出处
期刊:Solar RRL
[Wiley]
日期:2023-11-21
卷期号:8 (2)
被引量:4
标识
DOI:10.1002/solr.202300804
摘要
Tandem solar cells are regarded as an effective way to break through the theoretical efficiency of the Shockley–Queisser limit, and large‐size lead sulfide quantum dots (PbS QDs) are considered ideal infrared (IR) photovoltaic materials for absorbing low‐energy IR photons in the bottom subcells of tandem solar cells due to their tunable bandgaps and multiexciton generation effects. However, the exposed (100) surface of large‐size PbS QDs leads to poor passivation during the ligand‐exchange process, resulting in degraded device performance. Herein, a mixed halide ions ligand passivation strategy is developed to synergistically passivate the (111) and (100) facets of large‐size QDs. Particularly, a gradual dropwise addition of lead chloride salts dissolved in dimethyl sulfoxide for achieving precisely proportional surface passivation of Cl ions in the ligand exchange is proposed, which enhances the quality of the QD solids and obtains excellent control of the surface trap states. Additionally, optical and electrical characterization results show that the passivated IR PbS QD solids have higher carrier mobility, longer carrier lifetime, and lower defect density, which increases the IR efficiency of IR PbS QD solar cells to 1.25%.
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