In situ construction of Co-CoO heterostructures on rGO-modified nickel foam for high-performance anode catalysts in direct borohydride-hydrogen peroxide fuel cells

IF 13.1 1区 化学 Q1 Energy
Yimin Gao, Wei Meng, Yi Lv, Yimeng Li, Zijian Geng, Jia Niu, Jiaxin Yao, Jun Yan, Kai Zhu, Dianxue Cao, Guiling Wang
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引用次数: 0

Abstract

Direct borohydride hydrogen peroxide fuel cells (DBHPFCs) are emerging as a transformative technology for sustainable energy conversion. Despite their potential, their efficiency is largely hindered by the limitations of the anode catalyst. In response to this challenge, we have developed a novel series of Co-based heterojunction metal–organic framework (MOF) derivatives, supported on reduced graphene oxide (rGO)-modified nickel foam (NF), to enhance borohydride electrooxidation performance. Our synthesis involves the thermal transformation of a ZIF67-Co(OH)2-rGO/NF precursor within a controlled temperature between 300 and 750 °C, yielding distinct phase heterostructures and pristine Co and CoO, verified by X-ray diffraction (XRD) and transmission electron microscopy (TEM) analyses. Additionally, the Ultraviolet photoelectron spectroscopy and theoretical calculation result further validate the formation of the heterojunction and direction of electron transfer along the interface as well as the BH4 adsorption behavior across the heterointerface. Notably, the catalyst annealed at 600 °C, designated Co-CoO@C-rGO/NF-600, exhibits an exceptional oxidation current density of 2.5 A·cm−2 at 0 V vs. Ag/AgCl in an electrolyte containing 2 mol·L−1 NaOH and 0.4 mol·L−1 NaBH4 Furthermore, the Co-CoO@C-rGO/NF-600 catalyst demonstrates remarkable performance as the anode catalyst in a DBHPFC assembly, achieving a peak power density of 385.73 mW·cm−2 and demonstrating the enduring operational stability. The superior electrocatalytic performance is primarily attributed to the synergistic effects of Co-CoO nanoparticles rich in active heterointerfaces and the superior electron mobility afforded by the rGO scaffold. These results not only deepen our understanding of anode catalyst design for DBHPFCs but also pave the way for breakthroughs in electrocatalytic technologies, driving forward the quest for sustainable energy solutions.

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来源期刊
Journal of Energy Chemistry
Journal of Energy Chemistry CHEMISTRY, APPLIED-CHEMISTRY, PHYSICAL
CiteScore
19.10
自引率
8.40%
发文量
3631
审稿时长
15 days
期刊介绍: The Journal of Energy Chemistry, the official publication of Science Press and the Dalian Institute of Chemical Physics, Chinese Academy of Sciences, serves as a platform for reporting creative research and innovative applications in energy chemistry. It mainly reports on creative researches and innovative applications of chemical conversions of fossil energy, carbon dioxide, electrochemical energy and hydrogen energy, as well as the conversions of biomass and solar energy related with chemical issues to promote academic exchanges in the field of energy chemistry and to accelerate the exploration, research and development of energy science and technologies. This journal focuses on original research papers covering various topics within energy chemistry worldwide, including: Optimized utilization of fossil energy Hydrogen energy Conversion and storage of electrochemical energy Capture, storage, and chemical conversion of carbon dioxide Materials and nanotechnologies for energy conversion and storage Chemistry in biomass conversion Chemistry in the utilization of solar energy
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