Coupling electrocatalytic CO2 reduction with glucose oxidation for concurrent production of formate with high efficiency

格式化 过电位 析氧 电解质 材料科学 催化作用 无机化学 法拉第效率 阳极 化学工程 限制电流 阴极 化学 电极 电化学 有机化学 物理化学 工程类
作者
Runyao Zhao,Yiding Wang,Guipeng Ji,Fengtao Zhang,Yuepeng Wang,Yanfei Zhao,Buxing Han,Zhimin Liu
出处
期刊:Chemical Engineering Journal [Elsevier]
卷期号:486: 150280-150280 被引量:11
标识
DOI:10.1016/j.cej.2024.150280
摘要

Electrocatalytic reduction of CO2 (CO2ER) coupled with the oxygen evolution reaction (OER) is an energy-intensive process that generates low-value oxygen, limiting its industrial application. To overcome this limitation, here we report a membrane electrode assembly (MEA) system that combines CO2ER with glucose electrooxidation (GEOR) to simultaneously produce formate using bismuth subcarbonate and carbon nanotube hybrid (BOC-CNT) and nickel cobalt oxide decorated on carbon fiber paper (NCO-CFP) as the cathode and anode catalysts, respectively. The BOC-CNT catalyst showed excellent electrocatalytic performance for CO2ER to formate, affording a high FEHCOO- of 97.9 % with current density of 360 mA cm−2 at −0.77 V vs. RHE (-580 mV overpotential), and the NCO-CFP catalyst achieved GEOR at 0.99 V (vs. RHE) with FEHCOO- >98 %. The coupled CO2ER//GEOR MEA exhibits a low onset cell voltage of 1.20 V and reaches ultrahigh apparent Faraday efficiency of formate (>190 %) in a wide range from 1.8 to 2.4 V, achieving ∼ 33.3 % energy savings compared to CO2ER//OER with a high formate yield of 0.92 mol g-1h−1 at 100 mA cm−2. Besides, all generated formate can be collected from the electrolyte on the anode side due to the spontaneous migration of formate under electric field, thus reducing cross-contamination from CO2 and alkaline electrolytes. In addition, the coupled CO2ER//GEOR system exhibited good electrocatalytic stability for at least 32 h. This strategy provides an innovative and promising approach for the co-electrolytic transformation of biomass derivatives and CO2 to formate.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
emuscle完成签到,获得积分10
刚刚
刚刚
1秒前
星辰大海应助Marybaby采纳,获得20
1秒前
可爱的函函应助Bigweenine采纳,获得10
1秒前
1秒前
日笙发布了新的文献求助10
2秒前
3秒前
东方元语发布了新的文献求助10
3秒前
BouncyTree发布了新的文献求助30
3秒前
科研通AI6应助科研通管家采纳,获得10
4秒前
深情安青应助科研通管家采纳,获得10
4秒前
bjbmtxy应助科研通管家采纳,获得10
4秒前
科研通AI6应助科研通管家采纳,获得10
4秒前
ding应助科研通管家采纳,获得10
4秒前
Lucas应助林小乌龟采纳,获得10
4秒前
丘比特应助科研通管家采纳,获得10
4秒前
4秒前
Jasper应助科研通管家采纳,获得10
4秒前
慕青应助科研通管家采纳,获得10
4秒前
NexusExplorer应助科研通管家采纳,获得10
4秒前
一叶知秋应助科研通管家采纳,获得10
4秒前
科研通AI6应助科研通管家采纳,获得10
4秒前
Hello应助科研通管家采纳,获得10
4秒前
科研通AI6应助科研通管家采纳,获得10
4秒前
5秒前
小青椒应助vivelejrlee采纳,获得40
5秒前
ghkjl应助科研通管家采纳,获得10
5秒前
思源应助科研通管家采纳,获得10
5秒前
Mic应助科研通管家采纳,获得10
5秒前
5秒前
上官若男应助科研通管家采纳,获得10
5秒前
天天快乐应助科研通管家采纳,获得10
5秒前
5秒前
Mic应助科研通管家采纳,获得10
5秒前
花卷花卷应助科研通管家采纳,获得10
5秒前
大模型应助科研通管家采纳,获得10
5秒前
英俊的铭应助科研通管家采纳,获得10
5秒前
科研通AI2S应助微光采纳,获得10
5秒前
共享精神应助科研通管家采纳,获得10
5秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
List of 1,091 Public Pension Profiles by Region 1581
Encyclopedia of Agriculture and Food Systems Third Edition 1500
Specialist Periodical Reports - Organometallic Chemistry Organometallic Chemistry: Volume 46 1000
Current Trends in Drug Discovery, Development and Delivery (CTD4-2022) 800
The Scope of Slavic Aspect 600
Foregrounding Marking Shift in Sundanese Written Narrative Segments 600
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 物理化学 基因 遗传学 催化作用 冶金 量子力学 光电子学
热门帖子
关注 科研通微信公众号,转发送积分 5531780
求助须知:如何正确求助?哪些是违规求助? 4620574
关于积分的说明 14573778
捐赠科研通 4560339
什么是DOI,文献DOI怎么找? 2498813
邀请新用户注册赠送积分活动 1478687
关于科研通互助平台的介绍 1450049