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Solvothermal preparation of nickel-iron phosphides hollow nanospheres derived from metal-organic frameworks for water oxidation reaction

机译:衍生自金属有机框架的镍铁磷酸磷化镍中空纳米球的溶剂热量制备用于水氧化反应的金属有机框架

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Developing active and stable water oxidation electrocatalysts is desired to increase the efficiency of water electrolyzers. Nickel phosphides have been reported as pre-catalysts for water oxidation reaction. However, their catalytic activities can further be improved through morphology engineering and tuning electronic structures. Here, nickel-iron phosphides hollow nanospheres ((Ni1-xFex)(2)P, x = 0-0.35) were synthesized through solvothermal treatment of Ni-Fe metal-organic framework precursors with white phosphorus. The hollow nano spheres have diameters around 20-50 nm, with the crystalized structure resembles Ni2P phase. When used to catalyze the water oxidation reaction in 1 M KOH, the (Ni0.73Fe0.27)(2)P/Ni foam electrode exhibits best catalytic performance, with only 243 mV overpotentials to reach 10 mA cm(-2) (loading 0.135 mg(Ni+Fe) cm(-2)), and with a Tafel slope similar to 30 mV dec(-1). The enhanced water oxidation activity is mainly owing to the electronic interaction between Ni and Fe. Ex-situ characterizations of the (Ni0.73Fe0.27)(2)P after water oxidation reaction reveal that surface phosphides are transformed into layered double hydroxides under anodic alkaline conditions. The solvothermal prepared (Ni1-xFex)2P hollow nanospheres can be a potential candidate as pre-catalysts for water oxidation reaction in water electrolyzers.
机译:期望开发活性和稳定的水氧化电催化剂来提高水电解槽的效率。已据报道磷化镍作为水氧化反应的前催化剂。然而,通过形态学工程和调整电子结构可以进一步改善它们的催化活性。这里,通过具有白色磷的镍铁金属 - 有机框架前体的溶剂热处理合成镍磷酸铁中空纳米球((Ni1-Xfex)(2)p,x = 0-0.35)。中空纳米球的直径约为20-50nm,结晶结构类似于Ni2P相。当用于在1M KOH中催化水氧化反应时,(Ni0.73Fe0.27)(2)P / Ni泡沫电极表现出最佳的催化性能,只有243mV过电势达10 mA cm(-2)(载入0.135mg(Ni + Fe)cm(-2)),以及类似于30 mV DEC(-1)的TAFEL斜率。增强的水氧化活性主要是由于Ni和Fe之间的电子相互作用。水氧化反应后(Ni0.73Fe0.27)(2)P的前风格表明,在阳极碱性条件下将表面磷酸转化为层状的双氢氧化物。制备的溶剂(Ni1-Xfex)2P中空纳米球可以是水电解槽中水氧化反应的潜在候选者。

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