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Metal–Organic Framework-Derived Electrocatalysts Competent for the Conversion of Acrylonitrile to Adiponitrile

过电位 材料科学 电催化剂 塔菲尔方程 法拉第效率 化学工程 纳米孔 催化作用 电化学 电解质 无机化学 金属有机骨架 电极 纳米技术 有机化学 化学 吸附 工程类 物理化学
作者
Yi‐Ching Wang,Jia-Hui Yen,Chi-Wei Huang,Tzu‐En Chang,Youliang Chen,Yu‐Hsiu Chen,Chia‐Yu Lin,Chung‐Wei Kung
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:14 (31): 35534-35544 被引量:10
标识
DOI:10.1021/acsami.2c07060
摘要

Electrochemical conversion of acrylonitrile (AN) to produce adiponitrile (ADN), the raw material for the production of Nylon 66, has become a crucial process owing to the increasing market demand of Nylon 66. Although the metallic Pb or Cd electrodes are commonly used for this reaction, the use of electrocatalysts or electrodes modified with catalysts has been barely investigated. In this study, nanoporous and electrically conductive metal-organic framework (MOF)-derived materials composed of Pb, PbO, and carbon are synthesized by carbonizing a Pb-based MOF through thermal treatments, and these MOF-derived materials are served as electrocatalysts for the electrosynthesis of ADN. The crystallinity, morphology, elemental composition, porosity, electrical conductivity, and electrochemically active surface area of each MOF-derived material are investigated. Mass-transport-corrected Tafel analysis is used to probe the enhanced kinetics for the electrochemical reduction of AN occurring at the electrode modified with the MOF-derived material. Electrolytic experiments at various applied potentials are conducted to quantify the production rate and Faradaic efficiency toward ADN, and the result shows that the MOF-derived materials can act as electrocatalysts to initiate the electrochemical reduction of AN to produce ADN at a reduced overpotential. The optimal MOF-derived electrocatalyst can achieve a Faradaic efficiency of 67% toward ADN at an applied potential of -0.85 V versus reversible hydrogen electrode─a much lower overpotential compared to that typically required for this reaction without the use of catalysts. Findings here shed light on the design and development of advanced electrocatalysts to boost the performances for the electrosynthesis of ADN.
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