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超快沉积 NiFe 金属有机框架催化剂助力 BiVO 光阳极高效太阳能水分解。

Ultrafast Deposition of NiFe Metal-organic Framework Catalysts Boosts BiVO Photoanode for Efficient Solar Water Splitting.

机构信息

College of Chemistry and Chemical Engineering, College of Energy Material and Chemistry, Inner Mongolia University, Hohhot, 010021, China.

出版信息

Chem Asian J. 2023 Jun 15;18(12):e202300197. doi: 10.1002/asia.202300197. Epub 2023 May 12.

Abstract

The severe photocorrosion of BiVO limits its application in solar energy conversion in the long-term photoelectrochemical stability test. Herein, we synthesized a Fe@Ni-MOFs/BiVO photoanode by a simple ultrasonic method and ultrafast deposition, which avoids the problems of damaging the surface structure of photoelectrode. The Fe@Ni-MOFs/BiVO shows a photocurrent density of 4.89 mA cm at 1.23 V with an onset potential of 0.25 V under one sun illumination. Importantly, a stability over 30 h at 0.7 V can be obtained, which is so far the best stability character for MOFs-based cocatalysts decorated on BiVO . During operation, Fe@Ni-MOFs transforms into a homogeneous and active hydroxide layer covering the surface, which exposes more active sites for OER reactions. This work demonstrates a simple strategy for MOFs co-catalysts to obtain fast hole transfer capability and reduce carrier recombination, thereby improving PEC performance.

摘要

在长期光电化学稳定性测试中,BiVO 的严重光腐蚀限制了其在太阳能转换中的应用。在此,我们通过简单的超声法和超快沉积合成了 Fe@Ni-MOFs/BiVO 光阳极,避免了损坏光电极表面结构的问题。Fe@Ni-MOFs/BiVO 在 1 个太阳光照下的起始电位为 0.25 V 时,光电流密度为 4.89 mA/cm。重要的是,在 0.7 V 下可以获得超过 30 h 的稳定性,这是迄今为止 MOFs 基共催化剂在 BiVO 上修饰的最佳稳定性特征。在操作过程中,Fe@Ni-MOFs 转化为覆盖表面的均匀且活性的氢氧化物层,为 OER 反应暴露更多的活性位点。这项工作展示了一种用于 MOFs 共催化剂的简单策略,以获得快速空穴转移能力并减少载流子复合,从而提高 PEC 性能。

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