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This study evaluated the electrochemical performance of organic oxidation and anode-derived gas reduction through electrochemical measurements, gas chromatography (GC) tests, and experiments on in-situ CO2 reduction coupled with organic oxidation, and systematically analyzed the mechanisms by which key factors influenced the synergistic system. Electrochemical tests revealed that the Pt electrode exhibited optimal catalytic activity for glycerol (C3H8O3) in a 0.1mol/L Na2SO4 electrolyte, and anodically generated CO2 could be efficiently reduced at the cathode. Synergistic experimental results showed that at a Na2SO4 concentration of 0.1mol/L and a cathode potential of -1.8V (vs. SCE), the CO2 produced by anodic oxidation was converted to formic acid with maximum efficiency, achieving a carbon utilization efficiency (Uc) of 79.24%. The specific electrical energy consumption for formic acid production in the synergistic system decreased by 45.6%, and relative to the separate systems for electrocatalytic oxidation of C3H8O3 and CO2 reduction, the overall energy consumption was 65% lower. Analysis of the results indicated that operational parameters regulated the selectivity of anodic and cathodic reactions by modulating the current density and the supply of CO2 and H+.

, authors=Ming-ming YIN1, Chong CHEN2, Hao-ran SUN1, Jun-wei XIANG1, Shuo WANG1, Zhi-jing WANG2, Li-zhang WANG1, *, authorsList=Ming-ming YIN, Chong CHEN, Hao-ran SUN, Jun-wei XIANG, Shuo WANG, Zhi-jing WANG, Li-zhang WANG, authorCompany=null, correspAuthors=Li-zhang WANG, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1314918540013040327, articleId=1314918537915888325, tenantId=1146029695717560320, journalId=1234093305789726721, language=CN, title=有机物电催化氧化协同CO2原位还原机理研究, columnId=1234106386565624579, journalTitle=中国环境科学, columnName=水污染与控制, runingTitle=null, highlight=null, articleAbstract=

本研究通过电化学测试、气相色谱测试(GC)和有机物氧化协同CO2原位还原实验评估了有机物氧化与阳极气还原的电化学性能,分析了各因素对协同系统的影响机理.电化学测试结果表明,Pt电极在0.1mol/L Na2SO4中对甘油(C3H8O3)催化活性最强,且其氧化产生的CO2可在阴极被还原.协同实验结果表明,Na2SO4浓度为0.1mol/L、阴极电位为-1.8V(vs.SCE)时,阳极氧化产生的CO2能最大程度被还原为甲酸,C利用率(Uc)高达79.24%,协同系统产甲酸电耗降低了45.6%,相较于C3H8O3电催化氧化与CO2还原单独处理系统整体可节省能耗65%.通过分析测试和实验结果发现,各因素通过影响电流密度及CO2和H+的供应进而影响阴阳极反应的选择性.

, authors=殷明明1, 陈冲2, 孙浩然1, 向俊威1, 王硕1, 王智敬2, 王立章1, *, authorsList=殷明明, 陈冲, 孙浩然, 向俊威, 王硕, 王智敬, 王立章, authorCompany=null, correspAuthors=王立章, authorNote=

殷明明(2001-),女,山东济宁人,硕士研究生,主要从事电化学水处理与CO2还原理论与技术研究..

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* 责任作者,教授,
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殷明明(2001-),女,山东济宁人,硕士研究生,主要从事电化学水处理与CO2还原理论与技术研究..

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殷明明(2001-),女,山东济宁人,硕士研究生,主要从事电化学水处理与CO2还原理论与技术研究..

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有机物电催化氧化协同CO2原位还原机理研究
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殷明明 1 , 陈冲 2 , 孙浩然 1 , 向俊威 1 , 王硕 1 , 王智敬 2 , 王立章 1, *
中国环境科学 | 水污染与控制 2025,45(12): 6649-6658
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中国环境科学 |水污染与控制 2025 , 45 (12) : 6649 -6658
有机物电催化氧化协同CO2原位还原机理研究
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殷明明1 , 陈冲2, 孙浩然1, 向俊威1, 王硕1, 王智敬2, 王立章1, *
作者信息
  • 1.中国矿业大学环境与测绘学院,江苏 徐州 221116
  • 2.济源霖林环保能源有限公司,河南 济源 454650
通讯作者:
* 责任作者,教授,
作者简介:

殷明明(2001-),女,山东济宁人,硕士研究生,主要从事电化学水处理与CO2还原理论与技术研究..

Mechanistic study on synergistic electrocatalytic oxidation of organic compounds and in-situ CO2 reduction
Ming-ming YIN1 , Chong CHEN2, Hao-ran SUN1, Jun-wei XIANG1, Shuo WANG1, Zhi-jing WANG2, Li-zhang WANG1, *
Affiliations
  • 1.School of Environment Science and Spatial Informatics, China University of Mining and Technology, Xuzhou 221116, China
  • 2.Jiyuan Linlin Environmental Energy Co, Ltd, Jiyuan 454650, China
出版时间: 2025-12-20
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本研究通过电化学测试、气相色谱测试(GC)和有机物氧化协同CO2原位还原实验评估了有机物氧化与阳极气还原的电化学性能,分析了各因素对协同系统的影响机理.电化学测试结果表明,Pt电极在0.1mol/L Na2SO4中对甘油(C3H8O3)催化活性最强,且其氧化产生的CO2可在阴极被还原.协同实验结果表明,Na2SO4浓度为0.1mol/L、阴极电位为-1.8V(vs.SCE)时,阳极氧化产生的CO2能最大程度被还原为甲酸,C利用率(Uc)高达79.24%,协同系统产甲酸电耗降低了45.6%,相较于C3H8O3电催化氧化与CO2还原单独处理系统整体可节省能耗65%.通过分析测试和实验结果发现,各因素通过影响电流密度及CO2和H+的供应进而影响阴阳极反应的选择性.

电催化氧化  /  有机污染物  /  原位CO2阴极还原  /  机理

This study evaluated the electrochemical performance of organic oxidation and anode-derived gas reduction through electrochemical measurements, gas chromatography (GC) tests, and experiments on in-situ CO2 reduction coupled with organic oxidation, and systematically analyzed the mechanisms by which key factors influenced the synergistic system. Electrochemical tests revealed that the Pt electrode exhibited optimal catalytic activity for glycerol (C3H8O3) in a 0.1mol/L Na2SO4 electrolyte, and anodically generated CO2 could be efficiently reduced at the cathode. Synergistic experimental results showed that at a Na2SO4 concentration of 0.1mol/L and a cathode potential of -1.8V (vs. SCE), the CO2 produced by anodic oxidation was converted to formic acid with maximum efficiency, achieving a carbon utilization efficiency (Uc) of 79.24%. The specific electrical energy consumption for formic acid production in the synergistic system decreased by 45.6%, and relative to the separate systems for electrocatalytic oxidation of C3H8O3 and CO2 reduction, the overall energy consumption was 65% lower. Analysis of the results indicated that operational parameters regulated the selectivity of anodic and cathodic reactions by modulating the current density and the supply of CO2 and H+.

electrocatalytic oxidation  /  organic pollutants  /  in-situ CO2 cathodic reduction  /  mechanism
殷明明, 陈冲, 孙浩然, 向俊威, 王硕, 王智敬, 王立章. 有机物电催化氧化协同CO2原位还原机理研究. 中国环境科学, 2025 , 45 (12) : 6649 -6658 .
Ming-ming YIN, Chong CHEN, Hao-ran SUN, Jun-wei XIANG, Shuo WANG, Zhi-jing WANG, Li-zhang WANG. Mechanistic study on synergistic electrocatalytic oxidation of organic compounds and in-situ CO2 reduction[J]. China Environmental Science, 2025 , 45 (12) : 6649 -6658 .
  • 国家自然科学基金资助项目(51978654)
  • 江苏省自然科学基金资助项目(BK20211248)
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  • 接收时间:2025-05-06
  • 首发时间:2026-10-08
  • 出版时间:2025-12-20
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  • 收稿日期:2025-05-06
基金
国家自然科学基金资助项目(51978654)
江苏省自然科学基金资助项目(BK20211248)
作者信息
    1.中国矿业大学环境与测绘学院,江苏 徐州 221116
    2.济源霖林环保能源有限公司,河南 济源 454650

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