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Biologically templated formation of Cobalt-Phosphide-Graphene hybrids with charge redistribution for efficient hydrogen evolution.

作者信息

Zhou Xingchen, Gong Lanqian, Wu Chunxia, Peng Yujie, Cao Bingying, Yang Huan, Wu Daoxiong, Jiang Xueliang, Xia Bao Yu

机构信息

Hubei Key Laboratory of Plasma Chemistry and Advanced Materials, School of Materials Science and Engineering, Key Laboratory of Green Chemical Engineering Process of Ministry of Education, Wuhan Institute of Technology, No. 206 Guanggu 1st Road, Wuhan 430205, China.

Key Laboratory of Material Chemistry for Energy Conversion and Storage, School of Chemistry and Chemical Engineering, Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, 1037 Luoyu Road, Wuhan 430074, China.

出版信息

J Colloid Interface Sci. 2024 Sep;669:787-793. doi: 10.1016/j.jcis.2024.05.047. Epub 2024 May 9.

DOI:10.1016/j.jcis.2024.05.047
PMID:38744156
Abstract

Developing highly efficient and sustainable hydrogen evolution reaction (HER) electrocatalysts is important for the practical application of emerging energy technologies. The spherical structure and phosphorus-rich properties of Chlorella can facilitate the construction of comparable transition metal phosphide electrocatalysts. Here, a microorganism template strategy is proposed to construct a cobalt-phosphide-graphene hybrid. Chlorella can absorb metal ions, and the generated rough spherical nanoparticles are uniformly distributed around the reduced graphene oxide nanosheets. This designed catalyst has comparable HER performance in acidic electrolytes and needs an overpotential of only 153 mV at a current density of 10 mA cm. The experimental and density functional theory results imply that the charge redistribution between CoP and pyrrole-N is the key factor in enhancing the HER activity. The induced electron aggregation at the N and P sites can serve as a key active site for absorbing the adsorbed hydrogen atom intermediate to accelerate the HER process, contributing to the active sites of CoP- and pyrrole-N-doped carbon with 0 eV hydrogen adsorption free energy. This work provides a broad idea for synthesizing advanced catalysts by a biological template approach, facilitating the innovative integration of biology and emerging electrochemical energy technologies.

摘要

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