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Engineering a local acid-like environment in alkaline medium for efficient hydrogen evolution reaction

Tuning the local reaction environment is an important and challenging issue for determining electrochemical performances. Herein, we propose a strategy of intentionally engineering the local reaction environment to yield highly active catalysts. Taking Pt(δ−) nanoparticles supported on oxygen vacanc...

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Detalles Bibliográficos
Autores principales: Tan, Hao, Tang, Bing, Lu, Ying, Ji, Qianqian, Lv, Liyang, Duan, Hengli, Li, Na, Wang, Yao, Feng, Sihua, Li, Zhi, Wang, Chao, Hu, Fengchun, Sun, Zhihu, Yan, Wensheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019087/
https://www.ncbi.nlm.nih.gov/pubmed/35440547
http://dx.doi.org/10.1038/s41467-022-29710-w
Descripción
Sumario:Tuning the local reaction environment is an important and challenging issue for determining electrochemical performances. Herein, we propose a strategy of intentionally engineering the local reaction environment to yield highly active catalysts. Taking Pt(δ−) nanoparticles supported on oxygen vacancy enriched MgO nanosheets as a prototypical example, we have successfully created a local acid-like environment in the alkaline medium and achieve excellent hydrogen evolution reaction performances. The local acid-like environment is evidenced by operando Raman, synchrotron radiation infrared and X-ray absorption spectroscopy that observes a key H(3)O(+) intermediate emergence on the surface of MgO and accumulation around Pt(δ−) sites during electrocatalysis. Further analysis confirms that the critical factors of the forming the local acid-like environment include: the oxygen vacancy enriched MgO facilitates H(2)O dissociation to generate H(3)O(+) species; the F centers of MgO transfers its unpaired electrons to Pt, leading to the formation of electron-enriched Pt(δ−) species; positively charged H(3)O(+) migrates to negatively charged Pt(δ−) and accumulates around Pt(δ−) nanoparticles due to the electrostatic attraction, thus creating a local acidic environment in the alkaline medium.