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The Enhancing Effect of Stable Oxygen Functional Groups on Porous-Carbon-Supported Pt Catalysts for Alkaline Hydrogen Evolution

HIGHLIGHTS: What are the main findings? The HCl treatment of porous carbon can generate abundant hydroxyl and carboxyl groups, while the further heat treatment can transform into thermally stable carbonyl and ether groups. Carbonyl and ether groups within porous carbon supports is beneficial to the...

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Detalles Bibliográficos
Autores principales: Luo, Xianyou, Yuan, Ping, Luo, Junhui, Xiao, Haoming, Li, Junyi, Zheng, Heng, Du, Baodong, Li, De, Chen, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10145733/
https://www.ncbi.nlm.nih.gov/pubmed/37111000
http://dx.doi.org/10.3390/nano13081415
Descripción
Sumario:HIGHLIGHTS: What are the main findings? The HCl treatment of porous carbon can generate abundant hydroxyl and carboxyl groups, while the further heat treatment can transform into thermally stable carbonyl and ether groups. Carbonyl and ether groups within porous carbon supports is beneficial to the improvement of HER performance of catalysts. What is the implication of the main finding? The surface properties of porous carbon supports can be well tuned via a HCl treatment followed by an appropriate heat treatment. The feasible improvement of HER performance by regulating surface oxygen functional groups of porous carbon supports. ABSTRACT: The oxygen functionalization of carbon materials has widely been employed to improve the catalytic performance of carbon-supported Pt (Pt/C) catalysts. Hydrochloric acid (HCl) has often been employed to clean carbons during the preparation of carbon materials. However, the effect of oxygen functionalization through a HCl treatment of porous carbon (PC) supports on the performance of the alkaline hydrogen evolution reaction (HER) has rarely been investigated. Herein, the impact of HCl combined with the heat treatment of PC supports on the HER performance of Pt/C catalysts has been comprehensively investigated. The structural characterizations revealed similar structures of pristine and modified PC. Nevertheless, the HCl treatment resulted in abundant hydroxyl and carboxyl groups and the further heat treatment formed thermally stable carbonyl and ether groups. Among the catalysts, Pt loading on the HCl-treated PC followed by a heat treatment at 700 °C (Pt/PC-H-700) exhibited elevated HER activity with a lower overpotential of 50 mV at 10 mA cm(−2) when compared to the unmodified Pt/PC (89 mV). Pt/PC-H-700 also exhibited better durability than the Pt/PC. Overall, novel insights into the impact of the surface chemistry properties of porous carbon supports on the HER performance of Pt/C catalysts were provided, which were useful for highlighting the feasible improvement of HER performances by regulating the surface oxygen species of porous carbon supports.