Molecular electrocatalysts can mediate fast, selective CO2 reduction in a flow cell

被引:622
|
作者
Ren, Shaoxuan [1 ]
Joulie, Dorian [1 ,2 ]
Salvatore, Danielle [3 ]
Torbensen, Kristian [2 ]
Wang, Min [2 ]
Robert, Marc [2 ]
Berlinguette, Curtis P. [1 ,3 ,4 ,5 ]
机构
[1] Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
[2] Univ Paris, CNRS, Lab Electrochim Mol, F-75013 Paris, France
[3] Univ British Columbia, Dept Chem & Biol Engn, Vancouver, BC V6T 1Z3, Canada
[4] Univ British Columbia, Stewart Blusson Quantum Matter Inst, Vancouver, BC V6T 1Z4, Canada
[5] CIFAR, Toronto, ON M5G 1M1, Canada
关键词
ELECTROCHEMICAL REDUCTION; CARBON-DIOXIDE; CATALYST; ELECTROREDUCTION; CONVERSION; EFFICIENT; MONOXIDE; ELECTROLYSIS; ELECTRODES; MANGANESE;
D O I
10.1126/science.aax4608
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Practical electrochemical carbon dioxide (CO2) conversion requires a catalyst capable of mediating the efficient formation of a single product with high selectivity at high current densities. Solid-state electrocatalysts achieve the CO2 reduction reaction (CO2RR) at current densities >= 150 milliamperes per square centimeter (mA/cm(2)), but maintaining high selectivities at high current densities and efficiencies remains a challenge. Molecular CO2 RR catalysts can be designed to achieve high selectivities and low overpotentials but only at current densities irrelevant to commercial operation. We show here that cobalt phthalocyanine, a widely available molecular catalyst, can mediate CO2 to CO formation in a zero-gap membrane flow reactor with selectivities > 95% at 150 mA/cm(2). The revelation that molecular catalysts can work efficiently under these operating conditions illuminates a distinct approach for optimizing CO2RR catalysts and electrolyzers.
引用
收藏
页码:367 / +
页数:23
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