Wang Ling, Huang Xiaolei, Xue Junmin
Department of Materials Science and Engineering, Faculty of Engineering, National University of Singapore, 9 Engineering Drive 1, Singapore, 117576, Singapore.
ChemSusChem. 2016 Jul 21;9(14):1835-42. doi: 10.1002/cssc.201600323. Epub 2016 Jun 17.
Earth-abundant transition metal oxides and hydroxides have been intensively investigated as promising catalysts for the oxygen evolution reaction (OER). However, the overall OER performance of the transition metal oxides/hydroxides is largely jeopardized by their inherent low electrical conductivity. Mesoporous carbon has been a commonly used as a carrier material for these oxides/hydroxides to promote the electrical conductivity and provide a large specific surface area. However, most of the available mesoporous carbon carriers are amorphous. It has been very challenging to synthesize graphitic mesoporous carbon owing to the extremely high graphitization temperature. In this work, we report a new strategy used to prepare graphitic mesoporous carbon (GMC) by employing Fe metal as the graphitization catalyst. The graphitic carbon was obtained at 1000 °C, at which it retained its mesoporous structure. The conductivity of the obtained GMC was approximately 550 S m(-1) , which was almost ten times higher than that of amorphous carbon. The GMC was further loaded with Fe-Ni hydroxide to fabricate the OER catalyst. The obtained catalyst showed good OER activity with an overpotential of 320 mV at a current density of 10 mA cm(-2) and a low Tafel slope of 57 mV dec(-1) . The synthesized catalyst also possessed excellent stability, with almost no current drop even after 2000 cycles and at a constant voltage for 2 h.
储量丰富的地球过渡金属氧化物和氢氧化物作为析氧反应(OER)的潜在催化剂受到了广泛研究。然而,过渡金属氧化物/氢氧化物的整体OER性能在很大程度上受到其固有低电导率的影响。介孔碳已被普遍用作这些氧化物/氢氧化物的载体材料,以提高电导率并提供大的比表面积。然而,现有的大多数介孔碳载体都是无定形的。由于极高的石墨化温度,合成石墨化介孔碳一直极具挑战性。在这项工作中,我们报道了一种以铁金属作为石墨化催化剂制备石墨化介孔碳(GMC)的新策略。在1000 °C下获得了石墨化碳,此时它保留了其介孔结构。所得GMC的电导率约为550 S m(-1) ,几乎是无定形碳的十倍。将GMC进一步负载氢氧化铁镍以制备OER催化剂。所得催化剂表现出良好的OER活性,在电流密度为10 mA cm(-2) 时过电位为320 mV,塔菲尔斜率低至57 mV dec(-1) 。合成的催化剂还具有出色的稳定性,即使在2000次循环后以及在恒定电压下持续2 h,电流几乎没有下降。