钝化
钙钛矿(结构)
材料科学
纳米棒
无定形固体
原子层沉积
外延
图层(电子)
分解水
氧化物
化学工程
纳米技术
金属
光电子学
化学
冶金
光催化
结晶学
催化作用
生物化学
工程类
作者
Ning Wei,Yuetian Chen,Xingtao Wang,Miao Kan,Taiyang Zhang,Yixin Zhao
标识
DOI:10.1016/j.fmre.2021.11.038
摘要
Perovskite oxides with unique crystal structures and high defect tolerance are promising as atomic surface passivation layers for photoelectrodes for efficient and stable water splitting. However, controllably depositing and crystalizing perovskite-type metal oxides at the atomic level remains challenging, as they usually crystalize at higher temperatures than regular metal oxides. Here, we report a mild solution chemistry approach for the quasi-epitaxial growth of an atomic CaTiO3 perovskite layer on rutile TiO2 nanorod arrays. The high-temperature crystallization of CaTiO3 perovskite is overcome by a sequential hydrothermal conversion of the atomic amorphous TiOx layer to CaTiO3 perovskite. The atomic quasi-epitaxial CaTiO3 layer passivated TiO2 nanorod arrays exhibit more efficient interface charge transfer and high photoelectrochemical performance for water splitting. Such a mild solution-based approach for the quasi-epitaxial growth of atomic metal oxide perovskite layers could be a promising strategy for both fabricating atomic perovskite layers and improving their photoelectrochemical properties.
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