格式化
化学
催化作用
乙腈
无机化学
铱
甲酸脱氢酶
光化学
钳形配体
钳子运动
选择性
溶剂
氢化物
二氧化碳电化学还原
有机化学
氢
一氧化碳
作者
Peng Kang,Thomas J. Meyer,Maurice Brookhart
出处
期刊:Chemical Science
[The Royal Society of Chemistry]
日期:2013-01-01
卷期号:4 (9): 3497-3497
被引量:139
摘要
A water-soluble Ir PCP-type pincer catalyst was developed to reduce CO2 to formate electrocatalytically in water with high efficiency and selectivity. Formate is the only reduced carbon product, formed in 93% Faradaic yield with no formation of CO. A small fraction of “background” H2 (ca. 7%) is directly produced at the electrode by solvent reduction. Detailed kinetic information relevant to the catalysis was obtained. The high selectivity for formate production over H2 originates from the aqueous stability of Ir dihydride species, the active species for hydride reduction of CO2. Under neutral pH, the Ir pincer complex does not catalyze the reduction of protons to H2 making water a viable solvent for use with this catalyst system. Addition of small amounts (ca. 1%) of acetonitrile reduces the over-potential and renders the catalysis sustainable. Mechanistic studies suggest that acetonitrile is a key ancillary ligand that ionizes formate effectively preventing catalyst deactivation.
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