Integration of Anodic and Cathodic Catalysts of Earth-Abundant Materials for Efficient, Scalable CO2 Reduction

被引:19
|
作者
Parajuli, Rishi [1 ]
Gerken, James B. [2 ]
Keyshar, Kunttal [1 ]
Sullivan, Ian [1 ]
Sivasankar, Narayanappa [1 ]
Teamey, Kyle [1 ]
Stahl, Shannon S. [2 ]
Cole, Emily Barton [1 ]
机构
[1] Liquid Light Inc, Monmouth Jct, NJ 08852 USA
[2] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
关键词
Water oxidation; CO2; electroreduction; Electrocatalyst; Formic acid; Cobalt oxide; Tin; WATER-OXIDATION CATALYSTS; CARBON-DIOXIDE; ELECTROCHEMICAL REDUCTION; METAL-ELECTRODES; CONTINUOUS REACTOR; IN-SITU; PHOTOELECTROCHEMICAL REDUCTION; FORMIC-ACID; KHCO3; MEDIA; COBALT;
D O I
10.1007/s11244-014-0345-x
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A fully integrated electrochemical cell for co-production of formate (HCOO-) and oxygen (O-2) from carbon dioxide (CO2) and water using only earth-abundant elements has been developed. The process converts CO2 to formate using electrons derived from anodic water oxidation. A novel cathodic catalyst system, consisting of a tin (Sn) cathode in combination with the soluble heterocycle 2-picoline, was identified for CO2 reduction. Water oxidation takes place at a fluorine-doped tin oxide electrode coated with an electrodeposited cobalt oxide (CoOx) electrocatalyst. Use of 2-picoline as a soluble cathodic co-catalyst lowered the overpotential and enhanced the stability of the Sn-mediated CO2 reduction process. Fluorophosphate served as a redox-stable electrolyte to buffer the anode compartment at mildly acidic pH (similar to 5 to 5.5), thereby stabilizing the CoOx electrocatalyst and supporting efficient water oxidation. The complete electrochemical cell maintained a stable cell voltage of less than 3 V over 5 days, with an average formate faradaic yield of 34 %. These results are presented together with an economical analysis of large-scale solar-driven production of formate/formic acid from CO2 and water.
引用
收藏
页码:57 / 66
页数:10
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