Institute of Environmental Science, Shanxi University, Taiyuan 030006, China.
Department of Chemistry and Chemical Engineering, Qingdao University, Qingdao, 266071, China.
Nanoscale. 2019 Nov 7;11(41):19579-19585. doi: 10.1039/c9nr06519a. Epub 2019 Oct 17.
Perovskite oxides have attracted great attention recently for their low cost and high intrinsic activity in the electrochemical oxygen evolution reaction (OER). In this work, we synthesized highly efficient OER electrocatalysts in alkaline solution by carbonization of polydopamine (PDA)-functionalized cobalt-doped lanthanum nickelate perovskite nanorod (LaNiCo) complexes. The calcination temperature and molar ratio for La, Ni, and Co were optimized. The as-prepared complex with a molar ratio of 5 : 3 : 2 (La : Ni : Co) and a calcination temperature of 500 °C displayed enhanced OER activity and excellent durability. In 1.0 M KOH, the overpotential of the as-prepared catalyst at a current density of 10 mA cm was 0.360 V, which is comparable to those of noble metal-based materials or perovskite-based materials. The Tafel slope is 48.1 mV dec, which is smaller than those of prepared composites. The satisfactory oxygen evolution activity could be attributed to the increased CoO, O/O, pyridine N, and quaternary N species after calcination treatment, and the improved amount of Ni during the OER process, as well as the high surface area and electrochemical surface area.
钙钛矿氧化物因其在电化学氧气析出反应(OER)中成本低和固有活性高而受到广泛关注。在这项工作中,我们通过碳化聚多巴胺(PDA)功能化的钴掺杂镧镍酸盐钙钛矿纳米棒(LaNiCo)复合物,在碱性溶液中合成了高效的 OER 电催化剂。优化了煅烧温度和 La、Ni 和 Co 的摩尔比。在 500°C 下煅烧摩尔比为 5:3:2(La:Ni:Co)的复合物显示出增强的 OER 活性和优异的耐久性。在 1.0 M KOH 中,制备的催化剂在电流密度为 10 mA cm时的过电势为 0.360 V,可与贵金属基材料或钙钛矿基材料相媲美。Tafel 斜率为 48.1 mV dec,小于制备的复合材料。令人满意的氧气析出活性可归因于煅烧处理后增加的 CoO、O/O、吡啶 N 和季铵 N 物种,以及 OER 过程中增加的 Ni 量,以及高表面积和电化学表面积。