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Selective electrocatalytic reduction of carbon dioxide to formate by a water-soluble iridium pincer catalyst

机译:水溶性铱钳催化剂选择性电催化还原二氧化碳成甲酸酯

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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.
机译:开发了一种水溶性Ir PCP型钳形催化剂,可高效,高选择性地还原CO2以在水中电催化形成甲酸。甲酸酯是唯一还原的碳产物,以93%的法拉第产率形成,而没有形成CO。通过溶剂还原直接在电极上产生一小部分“背景” H2(约7%)。获得了与催化有关的详细动力学信息。在H2上生成甲酸的高选择性源于Ir二氢化物物质的水稳定性,Ir二氢化物物质是用于CO2的氢化物还原的活性物质。在中性pH值下,Ir夹钳络合物不会催化质子还原为H2,从而使水成为可用于此催化剂体系的可行溶剂。加入少量(约1%)的乙腈可减少过电位,并使催化可持续。机理研究表明,乙腈是离子化甲酸的关键辅助配体,可有效防止催化剂失活。

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