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用于甲酸氧化和氧还原的电化学脱合金辅助表面工程钯基双功能电催化剂

Electrochemical Dealloying-Assisted Surface-Engineered Pd-Based Bifunctional Electrocatalyst for Formic Acid Oxidation and Oxygen Reduction.

作者信息

Mondal Siniya, Raj C Retna

机构信息

Functional Materials and Electrochemistry Lab, Department of Chemistry , Indian Institute of Technology, Kharagpur , Kharagpur 721302 , India.

出版信息

ACS Appl Mater Interfaces. 2019 Apr 17;11(15):14110-14119. doi: 10.1021/acsami.9b00589. Epub 2019 Apr 3.

DOI:10.1021/acsami.9b00589
PMID:30912919
Abstract

Synthesis of non-Pt bifunctional electrocatalyst for the anodic oxidation of liquid fuel and cathodic reduction of oxygen is of great interest in the development of energy conversion devices. We demonstrate a facile room-temperature synthesis of surface-engineered trimetallic alloy nanoelectrocatalyst based on Co, Cu, and Pd by thermodynamically favorable transmetallation reaction and electrochemical dealloying. The quasi-spherical Co Cu Pd trimetallic catalysts were synthesized by the thermodynamically favorable reaction of KPdCl with sheetlike Co Cu bimetallic alloy nanostructure. The surface engineering of Co Cu Pd was achieved by electrochemical dealloying. The surface-engineered alloy electrocatalyst exhibits excellent bifunctional activity toward formic acid oxidation reaction (FAOR) and oxygen reduction reaction (ORR) at same pH. The elemental composition and lattice strain control the electrocatalytic performance. The elemental composition-dependent compressive strain weakens the adsorption of oxygen-containing species and favors the facile electron transfer for FAOR and ORR. The engineered alloy electrocatalyst of CoCuPd composition is highly durable and delivers high mass-specific activity for ORR and FAOR. It delivers mass-specific activities of 1.50 and 0.202 A/mg for FAOR and ORR, respectively, in acidic pH. The overall performance is superior to that of as-synthesized Pd and dealloyed bimetallic CoPd and CuPd nanoelectrocatalysts.

摘要

合成用于液体燃料阳极氧化和氧气阴极还原的非铂双功能电催化剂在能量转换装置的开发中备受关注。我们通过热力学有利的金属转移反应和电化学脱合金化,展示了一种基于钴、铜和钯的表面工程化三金属合金纳米电催化剂的简便室温合成方法。准球形的CoCuPd三金属催化剂是通过KPdCl与片状CoCu双金属合金纳米结构的热力学有利反应合成的。CoCuPd的表面工程通过电化学脱合金化实现。这种表面工程化的合金电催化剂在相同pH值下对甲酸氧化反应(FAOR)和氧还原反应(ORR)表现出优异的双功能活性。元素组成和晶格应变控制着电催化性能。元素组成依赖性的压缩应变减弱了含氧物种的吸附,并有利于FAOR和ORR的 facile电子转移。CoCuPd组成的工程化合金电催化剂具有高度的耐久性,并且对ORR和FAOR具有高的质量比活性。在酸性pH值下,它对FAOR和ORR的质量比活性分别为1.50和0.202 A/mg。整体性能优于合成的钯以及脱合金化的双金属CoPd和CuPd纳米电催化剂。

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