Integration of Alloy Segregation and Surface CoO Hybridization in Carbon‐Encapsulated CoNiPt Alloy Catalyst for Superior Alkaline Hydrogen Evolution

Author:

Pan Yangdan1,Gao Junkuo1ORCID,Lv Enjun1,Li Tongtong1,Xu Hui2,Sun Lu3,Nairan Adeela1,Zhang Qichun4ORCID

Affiliation:

1. Institute of Functional Porous Materials The Key Laboratory of Advanced Textile Materials and Manufacturing Technology of Ministry of Education School of Materials Science and Engineering Zhejiang Sci‐Tech University Hangzhou 310018 P. R. China

2. College of Materials Science and Engineering China Jiliang University Hangzhou 310018 P. R. China

3. Institute of Modern Optics Tianjin Key Laboratory of Micro‐scale Optical Information Science and Technology Nankai University Tianjin 300350 P. R. China

4. Department of Materials Science and Engineering Department of Chemistry, & Center of Super‐Diamond and Advanced Films (COSDAF) City University of Hong Kong Hong Kong 999077 P. R. China

Abstract

AbstractConstructing an efficient alkaline hydrogen evolution reaction (HER) catalyst with low platinum (Pt) consumption is crucial for the cost reduction of energy devices, such as electrolyzers. Herein, nanoflower‐like carbon‐encapsulated CoNiPt alloy catalysts with composition segregation are designed by pyrolyzing morphology‐controlled and Pt‐proportion‐tuned metal–organic frameworks (MOFs). The optimized catalyst containing 15% CoNiPt NFs (15%: Pt mass percentage, NFs: nanoflowers) exhibits outstanding alkaline HER performance with a low overpotential of 25 mV at a current density of 10 mA cm−2, far outperforming those of commercial Pt/C (47 mV) and the most advanced catalysts. Such superior activity originates from an integration of segregation alloy and Co‐O hybridization. The nanoflower‐like hierarchical structure guarantees the full exposure of segregation alloy sites. Density functional theory calculations suggest that the segregation alloy components not only promote water dissociation but also facilitate the hydrogen adsorption process, synergistically accelerating the kinetics of alkaline HER. In addition, the activity of alkaline HER is volcanically distributed with the surface oxygen content, mainly in the form of Co3dO2p hybridization, which is another reason for enhanced activity. This work provides feasible insights into the design of cost‐effective alkaline HER catalysts by coordinating kinetic reaction sites at segregation alloy and adjusting the appropriate oxygen content.

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

National Synchrotron Radiation Laboratory

City University of Hong Kong

State Key Laboratory of Supramolecular Structure and Materials

Publisher

Wiley

Subject

Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials

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