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Electrocatalytic CO2 Reduction with a Homogeneous Catalyst in Ionic Liquid: High Catalytic Activity at Low Overpotential

机译:离子液体中均相催化剂的电催化还原CO2:在低超电势下具有高催化活性

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We describe a new strategy for enhancing the efficiency of electrocatalytic CO2 reduction with a homogeneous catalyst, using a room-temperature ionic liquid as both the solvent and electrolyte. The electrochemical behavior of fac-ReCl(2,2′-bipyridine)- (CO)3 in neat 1-ethyl-3-methylimidazolium tetracyanoborate ([emim][TCB]) was compared with that in acetonitrile containing 0.1 M [Bu4N][PF6]. Two separate oneelectron reductions occur in acetonitrile (-1.74 and -2.11 V vs Fc~(+/0)), with a modest catalytic current appearing at the second reduction wave under CO2. However, in [emim][TCB], a two-electron reduction wave appears at -1.66 V, resulting in a ~0.45 V lower overpotential for catalytic reduction of CO2 to CO. Furthermore, the apparent CO2 reduction rate constant, kapp, in [emim][TCB] exceeds that in acetonitrile by over one order of magnitude (kapp = 4000 vs 100 M~(-1) s~(-1)) at 25 ± 3 °C. Supported by time-resolved infrared measurements, a mechanism is proposed in which an interaction between [emim]+ and the two-electron reduced catalyst results in rapid dissociation of chloride and a decrease in the activation energy for CO2 reduction.
机译:我们描述了一种新的策略,该策略可以提高均相催化剂的电催化CO2还原效率,同时使用室温离子液体作为溶剂和电解质。比较了fac-ReCl(2,2'-联吡啶)-(CO)3在纯净的1-乙基-3-甲基咪唑四氰基硼酸盐([emim] [TCB])中的电化学行为与在含有0.1 M [Bu4N]的乙腈中的电化学行为。 [PF6]。乙腈中发生两个单独的单电子还原(-1.74和-2.11 V vs Fc〜(+ / 0)),在CO2下的第二次还原波处出现适度的催化电流。但是,在[emim] [TCB]中,双电子还原波出现在-1.66 V,导致将CO2催化还原为CO的过电势降低了〜0.45V。此外,表观CO2还原速率常数kapp在[emim] [TCB]在25±3°C时比乙腈中的值超出一个数量级(kapp = 4000对100 M〜(-1)s〜(-1))。在时间分辨红外测量的支持下,提出了一种机制,其中[emim] +与两电子还原的催化剂之间的相互作用导致氯离子的快速离解和用于CO2还原的活化能的降低。

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