介孔材料
电解质
电极
铜
甲醇
催化作用
金属有机骨架
金属
材料科学
电催化剂
化学工程
无机化学
比表面积
电化学
法拉第效率
多孔性
化学
吸附
冶金
有机化学
复合材料
物理化学
工程类
作者
Jonathan Albo,Daniel Vallejo,Garikoitz Beobide,Óscar Castillo,Pedro Castaño,Ángel Irabien
出处
期刊:Chemsuschem
[Wiley]
日期:2016-08-25
卷期号:10 (6): 1100-1109
被引量:403
标识
DOI:10.1002/cssc.201600693
摘要
Abstract The electrocatalytic reduction of CO 2 has been investigated using four Cu‐based metal–organic porous materials supported on gas diffusion electrodes, namely, (1) HKUST‐1 metal–organic framework (MOF), [Cu 3 (μ 6 ‐C 9 H 3 O 6 ) 2 ] n ; (2) CuAdeAce MOF, [Cu 3 (μ 3 ‐C 5 H 4 N 5 ) 2 ] n ; (3) CuDTA mesoporous metal–organic aerogel (MOA), [Cu(μ‐C 2 H 2 N 2 S 2 )] n ; and (4) CuZnDTA MOA, [Cu 0.6 Zn 0.4 (μ‐C 2 H 2 N 2 S 2 )] n . The electrodes show relatively high surface areas, accessibilities, and exposure of the Cu catalytic centers as well as favorable electrocatalytic CO 2 reduction performance, that is, they have a high efficiency for the production of methanol and ethanol in the liquid phase. The maximum cumulative Faradaic efficiencies for CO 2 conversion at HKUST‐1‐, CuAdeAce‐, CuDTA‐, and CuZnDTA‐based electrodes are 15.9, 1.2, 6, and 9.9 %, respectively, at a current density of 10 mA cm −2 , an electrolyte‐flow/area ratio of 3 mL min cm −2 , and a gas‐flow/area ratio of 20 mL min cm −2 . We can correlate these observations with the structural features of the electrodes. Furthermore, HKUST‐1‐ and CuZnDTA‐based electrodes show stable electrocatalytic performance for 17 and 12 h, respectively.
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