Department of Inorganic and Physical Chemistry Indian Institute of Science, Bangalore - 560012, India.
Phys Chem Chem Phys. 2014 Mar 21;16(11):5412-22. doi: 10.1039/c3cp54860k.
Formation of an amorphous cobalt based oxygen evolution catalyst called Co-Pi has been recently reported from a neutral phosphate buffer solution containing Co(2+). But the concentration of Co(2+) is as low as 0.5 mM due to poor solubility of a cobalt salt in phosphate medium. In the present study, a cobalt acetate based oxygen evolution catalyst (Co-Ac) is prepared from a neutral acetate buffer solution, where the solubility of Co(2+) is very high (>100 times in comparison with phosphate buffer solution). The Co-Ac possesses better catalytic activity than the Co-Pi with an additional advantage of easy bulk scale preparation. The comparative studies on the oxygen evolution reaction (OER) activity of Co-Ac and Co-Pi in phosphate and acetate buffer electrolytes reveal that the Co-Ac exhibits enhanced synergistic catalytic activity in phosphate solution, probably due to partial substitution of acetate in the catalyst layer by phosphate, resulting in the formation of a Co-Ac-Pi catalyst.
最近有报道称,在含有 Co(2+)的中性磷酸盐缓冲溶液中形成了一种称为 Co-Pi 的无定形钴基氧析出催化剂。但由于钴盐在磷酸盐介质中的溶解度较低,Co(2+)的浓度低至 0.5mM。在本研究中,一种基于醋酸钴的氧析出催化剂(Co-Ac)是从中性醋酸盐缓冲溶液中制备的,其中 Co(2+)的溶解度非常高(比磷酸盐缓冲溶液高 100 多倍)。与 Co-Pi 相比,Co-Ac 具有更好的催化活性,并且具有易于大规模制备的额外优势。在磷酸盐和醋酸盐缓冲电解液中对 Co-Ac 和 Co-Pi 的氧析出反应(OER)活性进行的比较研究表明,Co-Ac 在磷酸盐溶液中表现出增强的协同催化活性,这可能是由于催化剂层中部分醋酸盐被磷酸盐取代,从而形成了 Co-Ac-Pi 催化剂。