通过常压 X 射线光电子能谱揭示等离子体 Ni@NiO/NiCO3 光催化剂中太阳光驱动的原子和电子转变

IF 4.4 3区 化学 Q2 CHEMISTRY, PHYSICAL Catalysis Science & Technology Pub Date : 2024-06-04 DOI:10.1039/d4cy00204k
Manoj Kumar Ghosalya , Parisa Talebi , Harishchandra Singh , Alexander Klyushin , Esko Kokkonen , Mohammed Alaoui Mansouri , Marko Huttula , Wei Cao , Samuli Urpelainen
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引用次数: 0

摘要

这项研究利用环境压力 X 射线光电子能谱(APXPS)深入研究了核壳 Ni@NiO/NiCO3 光催化剂的原子和电子转变,这是用于水分离制氢的可见光活性等离子体光催化剂的模型系统。这种催化剂在水蒸气和太阳模拟光的作用下表现出可逆的结构和电子变化。在这项研究中,我们在 1 毫巴水蒸气压力下获得了 APXPS 光谱,并利用带有 AM 1.5 滤光片的太阳模拟器测量了可见光照射下的光谱数据。原位 APXPS 光谱表明,金属镍核吸收光,激发等离子体,并产生热电子,这些电子随后通过热电子注入被 NiCO3 在氢进化反应(HER)中利用。此外,数据还显示,在水蒸气和光的作用下,NiO 会发生可逆氧化,生成 NiOOH。本研究还探讨了碳酸盐的贡献及其在光催化反应机理中的参与,从而揭示了光催化中这一鲜为人知的方面。APXPS 的结果突显了碳酸盐在光化学作用下还原成 -COOH,从而导致光催化剂失活。这项工作证明了 APXPS 在近乎真实的条件下检测潜在光催化剂的光化学反应、电荷转移动力学和中间产物方面的功效。
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Solar light driven atomic and electronic transformations in a plasmonic Ni@NiO/NiCO3 photocatalyst revealed by ambient pressure X-ray photoelectron spectroscopy†

This work employs ambient pressure X-ray photoelectron spectroscopy (APXPS) to delve into the atomic and electronic transformations of a core–shell Ni@NiO/NiCO3 photocatalyst – a model system for visible light active plasmonic photocatalysts used in water splitting for hydrogen production. This catalyst exhibits reversible structural and electronic changes in response to water vapor and solar simulator light. In this study, APXPS spectra were obtained under a 1 millibar water vapor pressure, employing a solar simulator with an AM 1.5 filter to measure spectral data under visible light illumination. The in situ APXPS spectra indicate that the metallic Ni core absorbs the light, exciting plasmons, and creates hot electrons that are subsequently utilized through hot electron injection in the hydrogen evolution reaction (HER) by NiCO3. Additionally, the data show that NiO undergoes reversible oxidation to NiOOH in the presence of water vapor and light. The present work also investigates the contribution of carbonate and its involvement in the photocatalytic reaction mechanism, shedding light on this seldom-explored aspect of photocatalysis. The APXPS results highlight the photochemical reduction of carbonates into –COOH, contributing to the deactivation of the photocatalyst. This work demonstrates the APXPS efficacy in examining photochemical reactions, charge transfer dynamics and intermediates in potential photocatalysts under near realistic conditions.

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来源期刊
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
期刊介绍: A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis. Editor-in-chief: Bert Weckhuysen Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
期刊最新文献
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