Irshad Ahamed, Munichandraiah Nookala
Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore-560012, India.
ACS Appl Mater Interfaces. 2015 Jul 29;7(29):15765-76. doi: 10.1021/acsami.5b02601. Epub 2015 Jul 14.
Large-scale production of hydrogen gas by water electrolysis is hindered by the sluggish kinetics of oxygen evolution reaction (OER) at the anode. The development of a highly active and stable catalyst for OER is a challenging task. Electrochemically prepared amorphous metal-based catalysts have gained wide attention after the recent discovery of a cobalt-phosphate (Co-Pi) catalyst. Herein, an amorphous iridium-phosphate (Ir-Pi) is investigated as an oxygen evolution catalyst. The catalyst is prepared by the anodic polarization of carbon paper electrodes in neutral phosphate buffer solutions containing IrCl3. The Ir-Pi film deposited on the substrate has significant amounts of phosphate and Ir centers in an oxidation state higher than +4. Phosphate plays a significant role in the deposition of the catalyst and also in its activity toward OER. The onset potential of OER on the Ir-Pi is about 150 mV lower in comparison with the Co-Pi under identical experimental conditions. Thus, Ir-Pi is a promising catalyst for electrochemical oxidation of water.
水电解大规模制氢受到阳极析氧反应(OER)缓慢动力学的阻碍。开发一种用于OER的高活性和稳定催化剂是一项具有挑战性的任务。在最近发现钴磷酸盐(Co-Pi)催化剂之后,电化学制备的非晶态金属基催化剂受到了广泛关注。在此,研究了一种非晶态铱磷酸盐(Ir-Pi)作为析氧催化剂。该催化剂通过在含有IrCl3的中性磷酸盐缓冲溶液中对碳纸电极进行阳极极化来制备。沉积在基底上的Ir-Pi薄膜含有大量磷酸盐和氧化态高于+4的Ir中心。磷酸盐在催化剂的沉积及其对OER的活性中都起着重要作用。在相同实验条件下,Ir-Pi上OER的起始电位比Co-Pi低约150 mV。因此,Ir-Pi是一种有前景的水电化学氧化催化剂。