首页|Controllable defect engineering based on cobalt metal-organic framework for boosting oxygen evolution reaction

Controllable defect engineering based on cobalt metal-organic framework for boosting oxygen evolution reaction

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Defect engineering on metal-organic frameworks(MOFs)provides high flexibility to rationally design advanced oxygen evolution reaction(OER)catalysts with low overpotential and high stability.However,fundamental understanding the effect of defect concentration on catalytic OER activity is still quite ambiguous.Herein,the Co-MOF-Dx catalysts with regulated oxygen defects concentration are deliberately constructed via coupling one-pot solvothermal synthesis with NaBH4 chemical reduction process.Experimental findings propose that the oxygen defect concentration within Co-MOF-Dx gradually increases with raising the NaBH4 content,which could provide a flexible platform to tailor the electronic structure around active Co site and optimize adsorption/desorption capacity of oxygen intermediates.When the introduction content of NaBH4 is up to 5 mg,the resulting abundant unsaturated coordination defects could endow the Co-MOF-D5 catalyst with optimized electronic structure and more exposed active sites for improving charge transfer and adsorption/desorption capacity.It is found that the optimized Co-MOF-D5 can drive the current density of 10 mA cm-2 only at a low overpotential of 300 mV with the small Tafel slope of 53.1 mV dec-1 in alkaline medium.This work sheds light on the way for the development of high-performance MOF catalysts via modulating defect concentration.

Defect engineeringUnsaturated coordination defectMetal-organic frameworksOxygen evolution reaction

Tengjia Ni、Xianbiao Hou、Huanlei Wang、Lei Chu、Shuixing Dai、Minghua Huang

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School of Materials Science and Engineering,Ocean University of China,Qingdao,266100,China

国家自然科学基金国家自然科学基金山东省自然科学基金Qingdao New Energy Shandong Laboratory Open Project

5226114570022279124ZR2022ZD30QNESL OP202307

2024

结构化学
中国化学会 中国科学院福建物质结构研究所

结构化学

影响因子:0.44
ISSN:0254-5861
年,卷(期):2024.43(1)
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