Department of Chemistry, Indiana University, 800 East Kirkwood Avenue, Bloomington, Indiana 47401, United States.
Department of Chemistry, North Carolina State University, 2620 Yarbrough Drive, Raleigh, North Carolina 27695, United States.
Inorg Chem. 2022 Aug 22;61(33):12998-13006. doi: 10.1021/acs.inorgchem.2c00909. Epub 2022 Aug 10.
This work reports a combined experimental and computational study of the activation of an otherwise catalytically inactive cobalt complex, [Co(TIM)Br], for aqueous nitrite reduction. The presence of phosphate buffer leads to efficient electrocatalysis, with rapid reduction to ammonium occurring close to the thermodynamic potential and with high Faradaic efficiency. At neutral pH, increasing buffer concentrations increase catalytic current while simultaneously decreasing overpotential, although high concentrations have an inhibitory effect. Controlled potential electrolysis and rotating ring-disk electrode experiments indicate that ammonium is directly produced from nitrite by [Co(TIM)Br], along with hydroxylamine. Mechanistic investigations implicate a vital role for the phosphate buffer, specifically as a proton shuttle, although high buffer concentrations inhibit catalysis. These results indicate a role for buffer in the design of electrocatalysts for nitrogen oxide conversion.
本工作报道了一种组合实验和计算研究,即激活一种原本无催化活性的钴配合物[Co(TIM)Br],用于水相亚硝酸根还原。存在磷酸盐缓冲液可实现有效的电催化,亚硝酸根快速还原为接近热力学电势的铵,且法拉第效率高。在中性 pH 值下,缓冲浓度增加会增加催化电流,同时降低过电势,但高浓度会产生抑制作用。恒电位电解和旋转环盘电极实验表明,[Co(TIM)Br]直接将亚硝酸根还原为铵,同时生成羟胺。机理研究表明,磷酸盐缓冲液起着至关重要的作用,特别是作为质子穿梭体,尽管高浓度的缓冲液会抑制催化作用。这些结果表明,缓冲液在设计用于氮氧化物转化的电催化剂方面发挥着作用。