铂负载的氧化铟锡催化剂在双电子水氧化反应中高效生产H2O2

IF 11.3 1区 化学 Q1 CHEMISTRY, PHYSICAL
Kiran Srinivasan Hamkins, Lauren Vallez, Xiaolin Zheng
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引用次数: 0

摘要

双电子水氧化反应(2e - WOR)作为一种有潜力的电化学水裂解现场生产过氧化氢(H2O2)的方法,受到了越来越多的关注。然而,尽管人们正在努力寻找更有效的2e - WOR电催化剂,但用单一催化剂材料同时获得良好的活性、选择性和稳定性仍然是一个挑战。在热催化领域,金属氧化物载体已被用于调整负载金属催化剂的催化性能。受这种支撑效应的启发,本文探索了使用逆结构──金属支撑的金属氧化物双分子层──作为2e - WOR的电催化剂。金属下层通过形成莫特-肖特基结来改变上层金属氧化物的催化性能,其中内置电位影响电子传输。我们研究了几种半导体金属氧化物催化剂和不同的金属载体材料,观察到金属基质对金属氧化物催化活性的强烈影响。我们发现,由一层铂(Pt)支撑的薄层氧化铟锡(ITO)对2e - WOR的催化能力最好,其活性和稳定性明显高于未负载的ITO催化剂,其H2O2产率也高于文献中报道的大多数单组分电催化剂。金属衬底的方法为这种电化学反应的未来催化剂的创造提供了一条途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Platinum-Supported Indium Tin Oxide Catalyst for Efficient H2O2 Production via Two-Electron Water Oxidation Reaction

Platinum-Supported Indium Tin Oxide Catalyst for Efficient H2O2 Production via Two-Electron Water Oxidation Reaction
The two-electron water oxidation reaction (2e WOR) has drawn growing attention as a potential method of producing hydrogen peroxide (H2O2) on-site through electrochemical water splitting. Nevertheless, despite ongoing efforts to identify more effective electrocatalysts for 2e WOR, it remains a challenge to simultaneously achieve good activity, selectivity, and stability with a single catalyst material. In the field of thermocatalysis, metal oxide supports have been used to tune the catalytic properties of the supported metal catalysts. Inspired by this support effect, herein, we explore using the inverse structure─a metal-supported metal oxide bilayer─as the electrocatalyst for 2e WOR. The metal underlayer modifies the top metal oxide catalytic properties by forming a Mott–Schottky junction, where the built-in potential influences the electron transport. We investigated several semiconducting metal oxide catalysts and different metal support materials and observed a strong metal substrate effect on the metal oxide catalytic activity. We found that a thin layer of indium tin oxide (ITO) supported by a layer of platinum (Pt) shows the best catalytic ability toward 2e WOR, which is significantly more active and stable than the unsupported ITO catalyst, and its H2O2 production rates are also greater than most reported single component electrocatalysts in the literature. The method of metal underlayer provides a pathway to create future catalysts for this electrochemical reaction.
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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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