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Facile Synthesis of Nanoporous Transition Metal-Based Phosphates for Oxygen Evolution Reaction

机译:纳米多孔过渡金属基磷酸磷酸盐的构成

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Due to unique structural porosity, low-cost, and good catalytic activity, oxygen evolution reactions over 3d transition elements have gained immense attention in recent years. Herein, we report the fabrication of three different metal phosphates, e. g. Co-phosphate (CoPO), Ni-phosphate (NiPO), and Ni-Co-phosphate (NiCoPO) using the corresponding metal sources and phosphoric acid as a phosphorus source under hydrothermal conditions without using any structure-directing agent. Since the as-prepared metal-based phosphates exhibit high surface area with good interparticle porosity and contain transition metals in the material frameworks, these materials have been investigated for electrocatalytic oxygen evolution reaction (OER). Among the three metal phosphates, the as-synthesized CoPO catalyst shows efficient electrocatalytic activity toward OER, with an overpotential of 350 mV at 10 mA cm(-2) in 1.0 M KOH solution and a relatively low Tafel slope of 60.7 mV dec(-1). The good electrocatalytic performance of CoPO is attributed to its higher specific surface area and pore volume compared to other two catalysts. The CoPO-modified electrode also shows a high stability up to 15 h at a constant potential of 1.58 V, suggesting its promising future for OER catalysis.
机译:由于结构孔隙率独特,低成本和良好的催化活性,近年来,3D过渡元件的氧气演化反应越来越富有关注。在此,我们报告了三种不同金属磷酸盐的制造,例如, G。使用相应的金属源和磷酸作为在水热条件下的磷源,在不使用任何结构引导剂的情况下,共磷酸酯(Copo),Ni-磷酸酯(NiCOPO)和Ni-磷酸酯(NicoPo),其在水热条件下。由于原制的金属基磷酸盐具有良好的颗粒孔隙率的高表面积,并且含有材料框架中的过渡金属,因此已经研究了这些材料用于电催化氧气进化反应(Oer)。在三种金属磷酸盐中,AS合成的CoPO催化剂表现出对oer的有效电催化活性,其在1.0m KOH溶液中为10 mA cm(-2)的过电位,相对低的Tafel斜率为60.7 mV DEC( - 1)。与其他两种催化剂相比,Copo的良好电催化性能归因于其较高的比表面积和孔体积。 Copo-Demified电极还在1.58 V的恒定电位下显示出高达15小时的高稳定性,这表明其未来为OER催化的未来。

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