还原(数学)
流量(数学)
化学
纳米技术
材料科学
生物物理学
生物
物理
几何学
数学
机械
作者
Shaoxuan Ren,Dorian Joulié,Danielle A. Salvatore,Kristian Torbensen,Min Wang,Marc Robert,Curtis P. Berlinguette
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2019-07-25
卷期号:365 (6451): 367-369
被引量:692
标识
DOI:10.1126/science.aax4608
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/cm2), but maintaining high selectivities at high current densities and efficiencies remains a challenge. Molecular CO2RR 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/cm2 The revelation that molecular catalysts can work efficiently under these operating conditions illuminates a distinct approach for optimizing CO2RR catalysts and electrolyzers.
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