光催化
材料科学
半导体
分解水
电子
金属
还原(数学)
化学工程
纳米技术
结晶学
化学物理
催化作用
化学
光电子学
冶金
物理
几何学
数学
有机化学
量子力学
工程类
作者
Lifang Liu,Shiwen Du,Yejun Xiao,Xiangyang Guo,Shengye Jin,Guosheng Shao,Fuxiang Zhang
标识
DOI:10.1016/j.apcatb.2023.123094
摘要
Facets-dependent photocatalytic H2 evolution rates of inorganic semiconductors have been well recognized, but it remains unclear for metal-organic frameworks (MOFs). Herein, we controllably prepared a series of NH2-MIL-125(Ti) MOF sheets with different ratios of {001}/{111} facets exposure, on which the photocatalytic H2 evolution rates from water are demonstrated to be almost linearly increased with enhanced proportion of {001} facets. Notably, the optimized activity of ca. 2640 μmol h-1 g-1 is by far superior to all the NH2-MIL-125(Ti)-based photocatalysts reported. The discovery of facets-dependent photocatalytic water splitting performance (i.e. facets effect) was unravelled to mainly result from their distinct charge separation abilities according to the experimental facts that the saturated six-coordinated Ti atoms (Ti6c) in the {001} facets can more efficiently accept and store the photogenerated electrons by the reduction of Ti4+ into Ti3+ with respect to the low-coordinated Ti atoms (Ti4c and Ti5c) in the {111} facets.
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