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Enriching Surface-Accessible CO2 in the Zero-Gap Anion-Exchange-Membrane-Based CO2 Electrolyzer
被引:51
作者:

Xu, Qiucheng
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Tech Univ Denmark, Dept Phys, Surface Phys & Catalysis Surf Cat Sect, DK-2800 Lyngby, Denmark Tech Univ Denmark, Dept Phys, Surface Phys & Catalysis Surf Cat Sect, DK-2800 Lyngby, Denmark

Xu, Aoni
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Tech Univ Denmark, CatTheory Ctr, Dept Phys, DK-2800 Lyngby, Denmark Tech Univ Denmark, Dept Phys, Surface Phys & Catalysis Surf Cat Sect, DK-2800 Lyngby, Denmark

Garg, Sahil
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Tech Univ Denmark, Dept Phys, Surface Phys & Catalysis Surf Cat Sect, DK-2800 Lyngby, Denmark Tech Univ Denmark, Dept Phys, Surface Phys & Catalysis Surf Cat Sect, DK-2800 Lyngby, Denmark

Moss, Asger B.
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Tech Univ Denmark, Dept Phys, Surface Phys & Catalysis Surf Cat Sect, DK-2800 Lyngby, Denmark Tech Univ Denmark, Dept Phys, Surface Phys & Catalysis Surf Cat Sect, DK-2800 Lyngby, Denmark

Chorkendorff, Ib
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Tech Univ Denmark, Dept Phys, Surface Phys & Catalysis Surf Cat Sect, DK-2800 Lyngby, Denmark Tech Univ Denmark, Dept Phys, Surface Phys & Catalysis Surf Cat Sect, DK-2800 Lyngby, Denmark

Bligaard, Thomas
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Tech Univ Denmark, Dept Energy Convers & Storage, DK-2800 Lyngby, Denmark Tech Univ Denmark, Dept Phys, Surface Phys & Catalysis Surf Cat Sect, DK-2800 Lyngby, Denmark

Seger, Brian
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Tech Univ Denmark, Dept Phys, Surface Phys & Catalysis Surf Cat Sect, DK-2800 Lyngby, Denmark Tech Univ Denmark, Dept Phys, Surface Phys & Catalysis Surf Cat Sect, DK-2800 Lyngby, Denmark
机构:
[1] Tech Univ Denmark, Dept Phys, Surface Phys & Catalysis Surf Cat Sect, DK-2800 Lyngby, Denmark
[2] Tech Univ Denmark, CatTheory Ctr, Dept Phys, DK-2800 Lyngby, Denmark
[3] Tech Univ Denmark, Dept Energy Convers & Storage, DK-2800 Lyngby, Denmark
关键词:
Carbon Dioxide Reduction;
Electrocatalysis;
Membrane-Electrode Assemblies;
Pulse Methods;
CARBON-DIOXIDE;
REDUCTION;
ELECTROREDUCTION;
PRODUCTS;
SYSTEMS;
D O I:
10.1002/anie.202214383
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Zero-gap anion exchange membrane (AEM)-based CO2 electrolysis is a promising technology for CO production, however, their performance at elevated current densities still suffers from the low local CO2 concentration due to heavy CO2 neutralization. Herein, via modulating the CO2 feed mode and quantitative analyzing CO2 utilization with the aid of mass transport modeling, we develop a descriptor denoted as the surface-accessible CO2 concentration ([CO2](SA)), which enables us to indicate the transient state of the local [CO2]/[OH-] ratio and helps define the limits of CO2-to-CO conversion. To enrich the [CO2](SA), we developed three general strategies: (1) increasing catalyst layer thickness, (2) elevating CO2 pressure, and (3) applying a pulsed electrochemical (PE) method. Notably, an optimized PE method allows to keep the [CO2](SA) at a high level by utilizing the dynamic balance period of CO2 neutralization. A maximum j(CO) of 368 +/- 28 mA cm(geo)(-2) was achieved using a commercial silver catalyst.
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