首页> 外文会议>PRiME Joint International Meeting of the Electrochemical Society, the Electrochemical Society of Japan, and the Korean Electrochemical Society >Cobalt Phosphide Based Nanostructures as Bifunctional Electrocatalysts for Low Temperature Alkaline Water Splitting
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Cobalt Phosphide Based Nanostructures as Bifunctional Electrocatalysts for Low Temperature Alkaline Water Splitting

机译:基于磷化钴的纳米结构作为低温碱性水分裂的双官能电催化剂

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Cobalt phosphide based thin films and nanoparticles were prepared by the thermal phosphidation of spinel Co_3O_4 precursor films and nanoparticles, respectively. CoP films were prepared with overall retention of the Co_3O_4 nanoplatelet morphology while the spherical/cubic Co_3O_4 and Ni_(0.15)Co_(2.85)O_4 nanoparticles were converted to nanorods or nanoparticles, respectively. The inclusion of nickel in the nanoparticles resulted in a 2.5 fold higher surface area leading to higher gravimetric performance. In each case high surface area structures were obtained with CoP as the primary phase. All materials were found to act as effective bifunctional electrocatalysts for both the HER and the OER and compared well to commercial precious metal benchmark materials in alkaline electrolyte. A symmetrical water electrolysis cell prepared from the CoP-based film operated at a low overpotential of 0.41-0.51 V.
机译:通过分别通过尖晶石CO_3O_4前体膜和纳米颗粒的热磷酸化制备钴基磷化薄膜和纳米颗粒。制备COP膜,通过总体保留CO_3O_4纳米片形态,同时球形/立方CO_3O_4和Ni_(0.15)CO_(2.85)O_4纳米颗粒分别转化为纳米棒或纳米颗粒。在纳米颗粒中包含镍导致2.5倍的表面积,导致更高的重量性能。在每种情况下,用COP作为初级相获得高表面积结构。发现所有材料都是用作她和伊尔的有效双官能电催化剂,并与碱性电解质中的商业贵金属基准材料进行比较。由基于COP的薄膜制备的对称水电解槽,在0.41-0.51V的低过电位下操作。

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