School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China.
Tianjin Key Laboratory of Advanced Functional Porous Materials, Institute for New Energy Materials and Low-Carbon Technologies, Tianjin University of Technology, Tianjin 300384, China.
Sci Rep. 2017 Apr 6;7:46154. doi: 10.1038/srep46154.
Nickel-based hydroxide hierarchical nanoarrays (NiM(OH) HNAs M = Fe or Zn) are doped with non-noble transition metals to create nanostructures and regulate their activities for the oxygen evolution reaction. Catalytic performance in these materials depends on their chemical composition and the presence of nanostructures. These novel hierarchical nanostructures contain small secondary nanosheets that are grown on the primary nanowire arrays, providing a higher surface area and more efficient mass transport for electrochemical reactions. The activities of the NiM(OH) HNAs for the oxygen evolution reaction (OER) followed the order of NiFe(OH) > Ni(OH) > NiZn(OH), and these trends are supported by density functional theory (DFT) calculations. The Fe-doped nickel hydroxide hierarchical nanoarrays (NiFe(OH) HNAs), which had an appropriate elemental composition and hierarchical nanostructures, achieve the lowest onset overpotential of 234 mV and the smallest Tafel slope of 64.3 mV dec. The specific activity, which is normalized to the Brunauer-Emmett-Teller (BET) surface area of the catalyst, of the NiFe(OH) HNAs is 1.15 mA cm at an overpotential of 350 mV. This is ~4-times higher than that of Ni(OH). These values are also superior to those of a commercial IrO electrocatalyst.
镍基氢氧化物分级纳米阵列(NiM(OH) HNAs,M=Fe 或 Zn)被掺杂非贵金属过渡金属以创造纳米结构并调节其氧析出反应的活性。这些材料的催化性能取决于其化学成分和纳米结构的存在。这些新型分级纳米结构包含在初级纳米线阵列上生长的小二级纳米片,为电化学反应提供了更高的表面积和更有效的质量传输。NiM(OH) HNAs 对氧析出反应(OER)的活性顺序为 NiFe(OH) > Ni(OH) > NiZn(OH),密度泛函理论(DFT)计算支持这些趋势。具有适当元素组成和分级纳米结构的 Fe 掺杂镍氢氧化物分级纳米阵列(NiFe(OH) HNAs)实现了最低的起始过电势 234 mV 和最小的 Tafel 斜率 64.3 mV dec。在 350 mV 的过电势下,NiFe(OH) HNAs 的比活性,即相对于催化剂的 Brunauer-Emmett-Teller(BET)表面积归一化的活性,为 1.15 mA cm。这比 Ni(OH) 高约 4 倍。这些值也优于商业 IrO 电催化剂的值。