非阻塞I/O
钙钛矿(结构)
材料科学
氧化物
反应性(心理学)
氧化镍
化学稳定性
化学工程
降级(电信)
氧化锡
热稳定性
锡
镍
化学物理
化学反应
图层(电子)
热的
活化能
工作(物理)
能量学
无机化学
能量转换效率
光伏系统
萃取(化学)
分子
氧化铟锡
纳米结构
过渡金属
氧化钛
异质结
保形涂层
作者
Chenchao Xie,Shuai You,Melissa Davis,Ross A. Kerner,Kelly Schutt,Ryan A. DeCrescent,Tianran Liu,Manuel A. Rodriguez,Rosemary C. Bramante,Christian Velez,Mirzo Mirzokarimov,Marc Migliozzi,Todd Russell,Adam Lorenz,Benjia Dou,Michael Owen‐Bellini,Axel F. Palmstrom,Duong Nguyen Minh,Michael D. McGehee,Joseph J. Berry
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2026-09-24
卷期号:393 (6818): 1364-1368
被引量:1
标识
DOI:10.1126/science.aei2836
摘要
Nickel oxide (NiO x ) is a common hole transport layer (HTL) in perovskite photovoltaics, but the chemical reactivity of NiOx surfaces accelerates degradation when contacting perovskites. We developed an ultrathin, conformal tin oxide (SnO x ) interlayer to suppress interfacial reactivity between NiO x and perovskite. SnO x is typically an electron transport layer, but we show that the energy alignment can be modified for hole extraction using molecules with dipoles. This synergy yielded high efficiency in perovskite photovoltaic devices and showed an ~10x improvement in T 90 lifetime in open-circuit conditions under AM1.5G at 65°C. This structure also improves resilience to thermomechanical durability, as minimodules retained 95.7% of their initial performance after 1000 thermal cycles (−65° to 85°C), highlighting the importance of interfaces for robust perovskite photovoltaic modules.
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