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用于高效电催化析氧反应的RuO-CoO复合材料的合成

Synthesis of RuO-CoO Composite for Efficient Electrocatalytic Oxygen Evolution Reaction.

作者信息

Zhang Jingchao, Bu Yingping, Hao Jia, Zhang Wenjun, Xiao Yao, Zhao Naihui, Zhang Renchun, Zhang Daojun

机构信息

Henan Key Laboratory of New Optoelectronic Functional Materials, College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang 455000, China.

College of Chemistry, Zhengzhou University, Zhengzhou 450001, China.

出版信息

Nanomaterials (Basel). 2025 Sep 3;15(17):1356. doi: 10.3390/nano15171356.

DOI:10.3390/nano15171356
PMID:40938034
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12429896/
Abstract

Among various H production methods, splitting water using renewable electricity for H production is regarded as a promising approach due to its high efficiency and zero carbon emissions. The oxygen evolution reaction (OER) is an important part of splitting water, but also the main bottleneck. The anodic oxygen evolution reaction (OER) for water electrolysis technology involves multi-electron/proton transfer and has sluggish reaction kinetics, which is the key obstacle to the overall efficiency of electrolyzing water. Therefore, it is necessary to develop highly efficient and cheap OER electrocatalysts to drive overall water splitting. Herein, a series of efficient RuO-CoO composites were synthesized via a straightforward three-step process comprising solvothermal synthesis, ion exchange, and calcination. The results indicate that using 10 mg of RuCl·xHO and 15 mg of Co-MOF precursor in the second ion exchange step is the most effective way to acquire the CoO-RuO-10 (RCO-10) composite with the largest specific area and the best electrocatalytic performance after the calcination process. The optimal CoO-RuO-10 composite powder catalyst displays low overpotential ( = 272 mV), a small Tafel slope (64.64 mV dec), and good electrochemical stability in alkaline electrolyte; the overall performance of CoO-RuO-10 surpasses that of many related cobalt-based oxide catalysts. Furthermore, through integration with a carbon cloth substrate, CoO-RuO-10/CC can be directly used as a self-supporting electrode with high stability. This work presents a straightforward method to design CoO-RuO composite array catalysts for high-performance electrocatalytic OER performance.

摘要

在各种制氢方法中,利用可再生电力分解水制氢因其高效率和零碳排放而被视为一种很有前景的方法。析氧反应(OER)是分解水的重要组成部分,也是主要瓶颈。水电解技术中的阳极析氧反应涉及多电子/质子转移,反应动力学缓慢,这是影响水电解整体效率的关键障碍。因此,有必要开发高效且廉价的OER电催化剂来驱动整体水分解。在此,通过溶剂热合成、离子交换和煅烧这一简单的三步过程合成了一系列高效的RuO-CoO复合材料。结果表明,在第二步离子交换步骤中使用10 mg的RuCl·xHO和15 mg的Co-MOF前驱体是获得煅烧后具有最大比表面积和最佳电催化性能的CoO-RuO-10(RCO-10)复合材料的最有效方法。最佳的CoO-RuO-10复合粉末催化剂在碱性电解质中显示出低过电位(= 272 mV)、小塔菲尔斜率(64.64 mV dec)和良好的电化学稳定性;CoO-RuO-10的整体性能超过了许多相关的钴基氧化物催化剂。此外,通过与碳布基底集成,CoO-RuO-10/CC可直接用作具有高稳定性的自支撑电极。这项工作提出了一种设计用于高性能电催化OER性能的CoO-RuO复合阵列催化剂的简单方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bb/12429896/039e2f48d36c/nanomaterials-15-01356-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bb/12429896/b22dbbceb820/nanomaterials-15-01356-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bb/12429896/c6e147a1336f/nanomaterials-15-01356-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bb/12429896/031f78b53008/nanomaterials-15-01356-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bb/12429896/df0a3fee3992/nanomaterials-15-01356-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bb/12429896/0c501a843961/nanomaterials-15-01356-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bb/12429896/f6760b3256a1/nanomaterials-15-01356-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bb/12429896/85c222e5debd/nanomaterials-15-01356-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bb/12429896/b3651995c371/nanomaterials-15-01356-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bb/12429896/039e2f48d36c/nanomaterials-15-01356-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bb/12429896/b22dbbceb820/nanomaterials-15-01356-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bb/12429896/c6e147a1336f/nanomaterials-15-01356-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bb/12429896/031f78b53008/nanomaterials-15-01356-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bb/12429896/df0a3fee3992/nanomaterials-15-01356-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bb/12429896/0c501a843961/nanomaterials-15-01356-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bb/12429896/f6760b3256a1/nanomaterials-15-01356-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bb/12429896/85c222e5debd/nanomaterials-15-01356-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bb/12429896/b3651995c371/nanomaterials-15-01356-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bb/12429896/039e2f48d36c/nanomaterials-15-01356-g009.jpg

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本文引用的文献

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