配对
电解
甲醛
材料科学
纵横比(航空)
图层(电子)
电压
纳米技术
Atom(片上系统)
喷嘴
光电子学
电极
物理
化学
电气工程
计算机科学
凝聚态物理
热力学
物理化学
工程类
有机化学
嵌入式系统
电解质
超导电性
作者
Min Zhang,Xinyu Wang,Junjie Ding,Chaogang Ban,Yajie Feng,Chaohe Xu,Xiaoyuan Zhou
出处
期刊:Nanoscale
[Royal Society of Chemistry]
日期:2024-01-01
卷期号:16 (14): 7076-7084
被引量:11
摘要
The development of advanced multi-functional electrocatalysts and their industrial operation on paired electrocatalysis systems presents a promising avenue for the gradual penetration of renewable energy into practical production. Herein, a self-supported conductive network of silverene nanobelts (Ag-ene NBs) was delicately assembled (Ag-NB-NWs), in which ultralong and few-atom-layer Ag-ene NBs with a high edge-to-facet ratio were interconnected, serving as "superreactors" for electron transfer and mass transport during the reaction. Such superstructures as electrocatalysts delivered an unparalleled performance toward the CO2-to-CO conversion with exclusively high faradaic efficiency (FE) and partial current densities of up to 1 A cm-2. Remarkably, the membrane electrode assembly (MEA) cell with Ag-NB-NWs as the cathode was capable of ultrastable and continuous operation for over 240 h at 0.4 A with ∼100% selectivity. More importantly, by further using Ag-NB-NWs as a bifunctional electrocatalyst, a record-low voltage overall CO2 electrolysis system coupling cathodic CO2 reduction with anodic formaldehyde oxidation in MEA cell was performed to achieve concurrent feed gas generation and formate production, substantially improving electrochemical techno-economic feasibility.
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