加速Cu2O/MoO2光电阴极电荷分离用于光电催化析氢

IF 9.4 1区 化学 Q1 CHEMISTRY, PHYSICAL
Mengmeng Zhang , Hui Xue , Xiaopeng Han , Zhijia Zhang , Yong Jiang , Yida Deng , Wenbin Hu
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引用次数: 0

摘要

光电催化减水是建设绿色可持续社会的一种潜在途径。Cu2O作为基准光电阴极备受关注,但存在严重的电荷复合和光腐蚀问题。本工作通过原位电沉积法制备了优异的Cu2O/MoO2光电阴极。系统的理论和实验研究表明,MoO2不仅作为助催化剂能有效钝化Cu2O的表面态,加速反应动力学,还能促进光生电荷的定向迁移和分离。正如预期的那样,所构建的光电阴极具有高度增强的光电流密度和吸引人的能量转换效率。重要的是,MoO2可以通过形成的内部电场抑制Cu2O中Cu+的还原,并表现出优异的光电稳定性。这些发现为设计具有高稳定性的高活性光电阴极铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Accelerate charge separation in Cu2O/MoO2 photocathode for photoelectrocatalytic hydrogen evolution

Accelerate charge separation in Cu2O/MoO2 photocathode for photoelectrocatalytic hydrogen evolution

Photoelectrocatalyzing water reduction is a potential approach to building a green and sustainable society. As a benchmark photocathode, Cu2O receives much attention but faces serious charge recombination and photocorrosion. This work prepared an excellent Cu2O/MoO2 photocathode via in situ electrodeposition. A systematical study of theory and experiment demonstrates that MoO2 not only effectively passivates the surface state of Cu2O as well as accelerates reaction kinetics as a cocatalyst, but also promotes the directional migration and separation of photogenerated charge. As expected, the constructed photocathode exhibits a highly enhanced photocurrent density and an appealing energy transformation efficacy. Importantly, MoO2 can inhibit the reduction of Cu+ in Cu2O via a formed internal electric field and shows excellent photoelectrochemical stability. These findings pave the way to designing a high-activity photocathode with high stability.

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来源期刊
CiteScore
16.10
自引率
7.10%
发文量
2568
审稿时长
2 months
期刊介绍: The Journal of Colloid and Interface Science publishes original research findings on the fundamental principles of colloid and interface science, as well as innovative applications in various fields. The criteria for publication include impact, quality, novelty, and originality. Emphasis: The journal emphasizes fundamental scientific innovation within the following categories: A.Colloidal Materials and Nanomaterials B.Soft Colloidal and Self-Assembly Systems C.Adsorption, Catalysis, and Electrochemistry D.Interfacial Processes, Capillarity, and Wetting E.Biomaterials and Nanomedicine F.Energy Conversion and Storage, and Environmental Technologies
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