Zhang Juntao, Li Min, Liang Xin, Zhuang Zhongbin
ACS Appl Mater Interfaces. 2019 Jan 9;11(1):1267-1273. doi: 10.1021/acsami.8b17612. Epub 2018 Dec 28.
Active nonprecious metal-based hydrogen evolution reaction (HER) electrocatalysts are critical for the clean and sustainable generation of hydrogen. Here, we synthesized multishelled FeCo@FeCoP@C hollow spheres by the carbonization and phosphorization of the FeCo-MIL-88 metal-organic framework. Owing to both composition (FeCo mixed phosphide) and morphology (multishelled morphology) effects, the as-obtained FeCo@FeCoP@C exhibits excellent HER performance with a low overpotential of 65 mV to achieve an HER current density of 10 mA cm and high stability in acidic solution. Density functional theory calculations show that the FeCoP have the optimal hydrogen absorption energy than that of FeP and CoP. The carbon shell prevents the oxidation of the phosphides, and the FeCo core provides better conductivity. Our work provides a new method to synthesize multishelled structure catalysts, which has potential applications in the further hydrogen production.
基于活性非贵金属的析氢反应(HER)电催化剂对于清洁且可持续的氢气生成至关重要。在此,我们通过对FeCo-MIL-88金属有机框架进行碳化和磷化,合成了多壳层FeCo@FeCoP@C空心球。由于组成(FeCo混合磷化物)和形态(多壳层形态)的双重效应,所制备的FeCo@FeCoP@C在酸性溶液中表现出优异的HER性能,实现10 mA cm⁻²的HER电流密度时过电位低至65 mV,且具有高稳定性。密度泛函理论计算表明,FeCoP比FeP和CoP具有更优的氢吸附能。碳壳可防止磷化物氧化,FeCo核提供更好的导电性。我们的工作提供了一种合成多壳层结构催化剂的新方法,在进一步的制氢方面具有潜在应用。