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首页> 外文期刊>Catalysis science & technology >Efficient hydrogen production from MIL-53(Fe) catalyst-modified Mo: BiVO4 photoelectrodes
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Efficient hydrogen production from MIL-53(Fe) catalyst-modified Mo: BiVO4 photoelectrodes

机译:从MIL-53高效制氢(Fe)catalyst-modified莫:BiVO4光电极

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摘要

Photoelectrochemical (PEC) water splitting to produce hydrogen energy has attracted considerable attention for solving current energy and environmental crises. However, the intrinsically high electron-hole recombination and low charge mobility greatly diminish the PEC efficiency. Herein, we demonstrated that metal organic framework MIL-53(Fe) could serve as an efficient hole-transfer co-catalyst to significantly improve the PEC performance of Mo-doped BiVO4 photoanodes toward water oxidation under solar irradiation, which is much higher than that of the traditional FeOOH co-catalyst under the same conditions. More specifically, owing to the unique 3D interlinked nanochannel and confinement effect of Fe atom sites, the charge separation, hole transport at the interface, and interactions with H2O molecules have been effectively facilitated, which thus allows for enhancing PEC water oxidation properties.
机译:光电化学(压电)水分裂生产氢能源吸引了为解决当前能源相当大的关注和环境危机。本质上高电子空穴的复合和低电荷流动大大削弱了压电陶瓷效率。有机框架MIL-53 (Fe)可以作为高效hole-transfer co-catalyst来显著改善压电陶瓷的性能对水氧化Mo-doped BiVO4光电阳极在太阳照射下,高得多比传统FeOOH co-catalyst在相同的条件下。由于独特的3 d纳米通道相通铁原子站点和约束效应,运输的电荷分离,洞接口,与水分子的相互作用有效地促进,因此哪一个允许提高压电陶瓷水氧化属性。

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