催化作用
电化学
电解质
水溶液
钴
质子
化学工程
化学
材料科学
纳米技术
化学物理
电极
无机化学
物理
物理化学
有机化学
工程类
量子力学
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2019-07-25
卷期号:365 (6451): 337.3-337
标识
DOI:10.1126/science.365.6451.337-c
摘要
Electrochemistry
Molecular electrocatalysts for CO2 reduction have often appeared to lack sufficient activity or stability for practical application. Ren et al. now show that design of the surrounding electrochemical cell can substantially boost both features. They directly exposed a known molecular catalyst, cobalt phthalocyanine, to gaseous CO2 in a flow cell architecture, rather than an aqueous electrolyte. The configuration accommodated current densities exceeding 150 milliamperes per square centimeter, with longevity limited by local proton concentration rather than catalyst stability.
Science , this issue p. [367][1]
[1]: /lookup/doi/10.1126/science.aax4608
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