Efficient CO2 Electrochemical Reduction by a Robust Electrocatalyst Fabricated by Electrodeposition of Indium and Zinc over Copper Foam

电催化剂 电化学 析氧 化学工程 材料科学 法拉第效率 氧化还原 电极 化学 无机化学 纳米技术 冶金 工程类 物理化学
作者
Suchada Sirisomboonchai,Hiroshi Machida,Khuyen Viet Bao Tran,Masaya Kawasumi,Koyo Norinaga
出处
期刊:ACS applied energy materials [American Chemical Society]
卷期号:5 (8): 9846-9857 被引量:19
标识
DOI:10.1021/acsaem.2c01564
摘要

Electrochemical reduction of CO2 comprising the CO2 reduction reactuib (CO2RR) and oxygen evolution reaction (OER) is one of the most promising technologies for electrification of the chemical process industry. Here, the performance of a electrocatalyst with a three-dimensional structure of InZnCu on Cu foam (CF) is presented. This electrocatalyst was fabricated by electrodeposition of In and Zn over Cu and exhibited a superior reduction of CO2 to CO at a Faradaic efficiency of 93.7% at −0.7 V and an excellently long duration of 100 h. Due to the synergy of the thin In layer, the Zn nanosheets provided a high surface-active area and strong mechanical robustness during the reaction. Additionally, a two-electrode system was constructed based on the CF-modified surface, which provided valuable guidelines on the overall CO2RR–OER system for further evolution. Furthermore, due to the facile synthesis, the bimetal-layer double hydroxide (LDH) exhibited high conductivity and high OER performance. Hence, the two-electrode system assembled excellent electrocatalysts for the CO2RR–OER (InZnCu/CF||Cu(OH)2 NWs@NiCo-LDH/CF) with high conversions of CO2 to CO of 67% and 88% at 2 and 50 mA cm–2, respectively. Notably, the CO2RR–OER system exhibited excellent stability in a 40 h CO2 conversion with a constant current density of 2 mA cm–2 at an ultralow voltage of 1.59 V. Moreover, the calculation of the energy input converting CO per ton of CO2 resulted in a low energy input range for further development in scalability. This overall CO2RR–OER proposes development in electrochemical CO2 reduction for industrial applications.
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
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
kingyuan完成签到,获得积分10
4秒前
南风完成签到,获得积分10
5秒前
5433完成签到 ,获得积分10
6秒前
9秒前
超男完成签到 ,获得积分10
11秒前
去码头整点薯条完成签到 ,获得积分10
12秒前
14秒前
zzz发布了新的文献求助10
14秒前
15秒前
风中可仁完成签到 ,获得积分10
15秒前
zhangxiaoqing完成签到,获得积分10
15秒前
Kinspact发布了新的文献求助10
17秒前
kitty完成签到,获得积分10
18秒前
Tysonqu完成签到,获得积分10
19秒前
摘星012发布了新的文献求助10
20秒前
苗苗043完成签到 ,获得积分10
20秒前
励志发SCI完成签到 ,获得积分10
22秒前
赘婿应助辰砂采纳,获得200
25秒前
蒋皓天完成签到,获得积分10
25秒前
28秒前
May完成签到 ,获得积分10
29秒前
摘星012完成签到,获得积分10
29秒前
吸吸灵光气完成签到,获得积分10
29秒前
佳期如梦完成签到 ,获得积分10
29秒前
Kinspact发布了新的文献求助10
34秒前
34秒前
Patience完成签到,获得积分10
35秒前
怡然的怀绿完成签到,获得积分10
35秒前
隐形荟完成签到 ,获得积分10
39秒前
39秒前
海中有月完成签到 ,获得积分10
40秒前
Monroe完成签到 ,获得积分10
41秒前
43秒前
深情安青应助贺鹏霖采纳,获得10
43秒前
老程完成签到,获得积分10
44秒前
细心水绿发布了新的文献求助10
49秒前
tigger完成签到,获得积分10
49秒前
Su完成签到 ,获得积分10
52秒前
panpanliumin完成签到,获得积分0
53秒前
隐形曼青应助xiaowang采纳,获得10
54秒前
高分求助中
Adhesion Science: Principles & Practice 1234
Signals, Systems, and Signal Processing 610
Burger's Medicinal Chemistry and Drug Discovery 400
A Step-by-Step Guide to Qualitative Data Coding 2nd Edition 400
Impact of Storage Orientation and Duration on Prefilled Syringe Performance: Break-Loose and Glide Forces, and Injection Time Across Multiple Time Points 360
Programming for Chemical Engineers Using C, C++, and MATLAB 300
Upland Kenya wild flowers and ferns: a flora of the flowers, ferns, grasses, and sedges of highland Kenya 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6663338
求助须知:如何正确求助?哪些是违规求助? 8413298
关于积分的说明 17984576
捐赠科研通 5867505
什么是DOI,文献DOI怎么找? 2975063
邀请新用户注册赠送积分活动 1950952
关于科研通互助平台的介绍 1876840