Zeng Yifan, Wang Yanyong, Huang Gen, Chen Chen, Huang Liangliang, Chen Ru, Wang Shuangyin
State Key Laboratory of Chem/Bio-Sensing and Chemometrics, Provincial Hunan Key Laboratory for Graphene Materials and Devices, College of Chemistry and Chemical Engineering, Hunan University, Changsha, 410082, P. R. China.
Chem Commun (Camb). 2018 Feb 6;54(12):1465-1468. doi: 10.1039/c7cc08838h.
Porous materials are widely studied in many applications due to their high surface area and rich edge sites. Here, for the first time, we reported a simple and convenient method to synthesize porous nanosheets of metal hydroxides by selectively etching amphoteric Al in CoAl layered double hydroxides on carbon paper (CoAl-LDH/CP), and then convert them into porous cobalt phosphide nanosheets on carbon paper (p-CoP/CP) via low temperature phosphidation. In contrast to pristine cobalt phosphide nanosheets on carbon paper (CoP/CP), p-CoP/CP has lower overpotential, Tafel slope and charge transfer resistance as well as higher electrochemically active surface area. The excellent electrochemical characteristics make it have outstanding catalytic activity and stability over the whole pH range. In 1.0 M KOH, the p-CoP/CP only requires an overpotential of 57 mV to drive 10 mA cm. To achieve the same current density, it only needs overpotentials of 39 and 60 mV in 1.0 M HSO and 1.0 M PBS, respectively. To our knowledge, it is the best among those nonprecious electrocatalysts used for hydrogen evolution in neutral solution. Moreover, this catalyst offers good durability over the whole pH range.
多孔材料因其高比表面积和丰富的边缘位点而在许多应用中得到广泛研究。在此,我们首次报道了一种简单便捷的方法,通过选择性蚀刻碳纸上钴铝层状双氢氧化物(CoAl-LDH/CP)中的两性Al来合成金属氢氧化物多孔纳米片,然后通过低温磷化将其转化为碳纸上的多孔磷化钴纳米片(p-CoP/CP)。与碳纸上的原始磷化钴纳米片(CoP/CP)相比,p-CoP/CP具有更低的过电位、塔菲尔斜率和电荷转移电阻以及更高的电化学活性表面积。优异的电化学特性使其在整个pH范围内具有出色的催化活性和稳定性。在1.0 M KOH中,p-CoP/CP仅需57 mV的过电位即可驱动10 mA cm。为达到相同的电流密度,在1.0 M HSO和1.0 M PBS中分别仅需39和60 mV的过电位。据我们所知,它是用于中性溶液中析氢的非贵金属电催化剂中性能最佳的。此外,该催化剂在整个pH范围内具有良好的耐久性。