锌基金属有机骨架在碱性介质中氧还原反应(ORR)过程中过氧化氢(H2O2)的生成

D. Das, V. Raut
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引用次数: 4

摘要

开发高性能、廉价、非贵重和非耐用的铂基阴极氧还原反应电催化剂是燃料电池商业化技术中的一个重要问题。本文介绍了MOF1, 1,3,5 -三羧酸(H3BTC)和锌金属基金属有机骨架,它们在碱性溶液中作为一种明确的,可调的氧还原电催化剂。采用RRDE技术测试了MOF1电催化剂在碱性电解液中对ORR的催化活性。MOF1在碱性介质中表现出良好的ORR活性和稳定性,随后通过双电子还原途径生成过氧化氢,环电极上的过氧化氢氧化电流随着循环而增大。研究结果与Koutecky-Levich图和伏安图相一致。开发高性能、廉价、非贵重和非耐用的铂基阴极氧还原反应电催化剂是燃料电池商业化技术中的一个重要问题。本文介绍了MOF1, 1,3,5 -三羧酸(H3BTC)和锌金属基金属有机骨架,它们在碱性溶液中作为一种明确的,可调的氧还原电催化剂。采用RRDE技术测试了MOF1电催化剂在碱性电解液中对ORR的催化活性。MOF1在碱性介质中表现出良好的ORR活性和稳定性,随后通过双电子还原途径生成过氧化氢,环电极上的过氧化氢氧化电流随着循环而增大。研究结果与Koutecky-Levich图和伏安图相一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hydrogen peroxide (H2O2) production in oxygen reduction reaction (ORR) proceeding in alkaline medium employing zinc based metal-organic framework
Developing high-performance, less expensive, non-precious and nondurable platinum-based electrocatalysts for oxygen reduction reaction (ORR) at the cathode side is an important issue in commercialization fuel cell technology. Here we introduce MOF1, 1, 3, 5-tricarboxylic acid (H3BTC) and zinc metal-based metal-organic framework which functions as a well-defined, tunable oxygen reduction electrocatalyst in alkaline solution. The catalytic activity of the MOF1 electrocatalyst toward the ORR in an alkaline electrolyte is tested using RRDE technique. MOF1 in alkaline media shows excellent activity and stability for ORR followed by the two-electron reduction pathway to the generation of hydrogen peroxide and the peroxide oxidation current on the ring electrode increases with cycling. The results are in support with Koutecky-Levich plots and the voltammograms.Developing high-performance, less expensive, non-precious and nondurable platinum-based electrocatalysts for oxygen reduction reaction (ORR) at the cathode side is an important issue in commercialization fuel cell technology. Here we introduce MOF1, 1, 3, 5-tricarboxylic acid (H3BTC) and zinc metal-based metal-organic framework which functions as a well-defined, tunable oxygen reduction electrocatalyst in alkaline solution. The catalytic activity of the MOF1 electrocatalyst toward the ORR in an alkaline electrolyte is tested using RRDE technique. MOF1 in alkaline media shows excellent activity and stability for ORR followed by the two-electron reduction pathway to the generation of hydrogen peroxide and the peroxide oxidation current on the ring electrode increases with cycling. The results are in support with Koutecky-Levich plots and the voltammograms.
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