异质结
钝化
钙钛矿(结构)
轨道能级差
费米能级
带隙
材料科学
电子能带结构
电离能
凝聚态物理
光电子学
半导体
纳米技术
电离
化学
物理
结晶学
电子
量子力学
离子
有机化学
图层(电子)
分子
作者
Nan Chen,Deying Luo,Peng Chen,Shunde Li,Juntao Hu,Dengke Wang,Rui Zhu,Zheng‐Hong Lu
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-02-06
卷期号:8 (3): 1313-1321
被引量:18
标识
DOI:10.1021/acsenergylett.2c02856
摘要
In contrast with the band alignment rule governing conventional semiconductor heterojunctions, the Fermi level position (i.e., work function, ϕpsk) of the perovskite and the differences in ionization energies of the organics are shown to dictate the band alignment and band offsets at perovskite/organic heterojunction interfaces. The experimental data show that the interface band alignments follow a universal alignment rule with three different energy windows: pinning of unoccupied molecular orbital states (LUMO) to the perovskite Fermi level, band offsets mediated by perovskite work functions, and pinning of occupied molecular orbital states (HOMO) to the perovskite Fermi level. The surface-passivated perovskites and several common native perovskites are all found to follow the same band alignment rule. Data scattering in measured band offsets, however, is observed on the same type of perovskites without proper surface passivation treatment. Solar cells made on the perovskites without surface passivation are also found to exhibit a large dispersive distribution in energy conversion efficiencies.
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