CuAg-PEO纳米粒子系综中复杂相互作用的成像增强CO2还原

IF 1.8 4区 物理与天体物理 Q2 SPECTROSCOPY Journal of Electron Spectroscopy and Related Phenomena Pub Date : 2023-05-01 DOI:10.1016/j.elspec.2023.147331
Xinye Yuan , Tatiana Morin Caamano , Tianxiao Sun , Elena A. Baranova , Yaser Abu-Lebdeh , Jigang Zhou , Jian Wang , Huaidong Jiang
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引用次数: 0

摘要

二氧化碳电化学还原(CO2ER)是一项很有前途的技术,它可以将二氧化碳转化为有用的化学物质和燃料,同时减少温室气体的排放。铜纳米颗粒催化剂具有优异的导电性和催化活性,是CO2ER的最佳选择。在这项研究中,我们结合扫描透射x射线显微镜(STXM)和光谱技术,研究了CO2ER前后CuAg纳米催化剂的化学和电子结构变化。我们观察到具有相同价态的Cu种自聚集成不同的相。对于CO2ER后的废CuAg纳米催化剂,大部分Cu(I)和Cu(0)种被氧化为Cu(II), CuO转化为未确定的Cu(II)种。我们认为这些机制是导致CuAg纳米催化剂失去催化活性的关键原因。这些信息对于理解铜纳米颗粒催化CO2ER具有重要的价值。
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Imaging the complex interactions in CuAg-PEO nanoparticles ensemble for enhanced CO2 reduction

CO2 electrochemical reduction (CO2ER) is a promising technology that can convert CO2 into useful chemicals and fuels with simultaneously reducing greenhouse gas emissions. Cu nanoparticles-based catalysts are an optimal choice of CO2ER due to its excellent conductivity and catalytic activity. In this study, we combined scanning transmission X-ray microscopy (STXM) and spectro-ptychography to investigate the chemical and electronic structural changes of the CuAg nanocatalysts before and after CO2ER. We observed that Cu species with the same valence state self-aggregate into separated phases. For the spent CuAg nanocatalysts after CO2ER, most Cu(I) and Cu(0) species are oxidized to Cu(II) together with CuO transforming into undetermined Cu(II) species. We believe these mechanisms are the key reason why the CuAg nanocatalysts lost catalytic activity. Such information will be highly valuable for understanding Cu nanoparticles catalyzed CO2ER.

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来源期刊
CiteScore
3.30
自引率
5.30%
发文量
64
审稿时长
60 days
期刊介绍: The Journal of Electron Spectroscopy and Related Phenomena publishes experimental, theoretical and applied work in the field of electron spectroscopy and electronic structure, involving techniques which use high energy photons (>10 eV) or electrons as probes or detected particles in the investigation.
期刊最新文献
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