非阻塞I/O
X射线光电子能谱
异质结
材料科学
蒸发
表征(材料科学)
氢
太阳能电池
分解水
光电子学
纳米
能量转换效率
化学工程
纳米技术
化学
催化作用
复合材料
有机化学
工程类
物理
热力学
光催化
生物化学
作者
Chao Feng,Zhi Liu,Huanxin Ju,Andraž Mavrič,Matjaž Valant,Jie Fu,Beibei Zhang,Yanbo Li
标识
DOI:10.1038/s41467-024-50893-x
摘要
The buried interface tens of nanometers beneath the solid-liquid junction is crucial for photocarrier extraction, influencing the overall efficiency of photoelectrochemical devices. Precise characterization of the interfacial properties is essential for device optimization but remains challenging. Here, we directly probe the in situ transformation of a CuxO interlayer at the NiO/n-Si interface by hard X-ray photoelectron spectroscopy. It is found that Cu(I) in the CuxO interlayer gradually transforms to Cu(II) with air exposure, forming an energetically more favorable interface and improving photoanode's efficiency. Based on this finding, a reactive e-beam evaporation process is developed for the direct deposition of a CuO interlayer, achieving a half-cell solar-to-hydrogen efficiency of 4.56% for the optimized NiO/CuO/n-Si heterojunction photoanode. Our results highlight the importance of precision characterization of interfacial properties with advanced hard X-ray photoelectron spectroscopy in guiding the design of efficient solar water-splitting devices. The buried interface beneath the solid-liquid junction is crucial for photoelectrochemical device efficiency and requires precise characterization for optimization. Here the authors probe the in situ transformation of a CuxO interlayer at the NiO/n-Si interface by hard X-ray photoelectron spectroscopy and improve solar-to-hydrogen efficiency to 4.56%.
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