摘要
Proper control of a 3dtransition metal-based catalyst with advanced structures toward oxygen evolution reaction (OER) with a more feasible synthesis strategy is of great significance for sustainable energy-related devices. Herein, carbon nanotube interconnected NiCo layered double hydroxide rhombic dodecahedral nanocages (NiCo-LDH[email protected]) were developed here with the assistance of a feasible zeolitic imidazolate framework (ZIF) self-sacrificing template strategy as a highly efficient OER electrocatalyst. Profited by the well-fined rhombic dodecahedral nanocage architecture, CNTs’ interconnected characteristic and structural feature of the vertically aligned nanosheets, the as-synthesized NiCo-LDH[email protected]integrated large exposed active surface areas, enhanced electron transfer capacity and multidimensional mass diffusion channels, and thereby collaboratively afforded the remarkable electrocatalytic performance of the OER. Specifically, the designed NiCo-LDH[email protected]exhibited a distinguished OER activity, which only required a low overpotential of 255 mV to reach a current density of 10 mA cm−2for the OER. For the stability, no obvious current attenuation was detected, even after continuous operation for more than 27 h. We certainly believe that the current extraordinary OER activity combined with the robust stability of NiCo-LDH[email protected]enables it to be a great candidate electrocatalyst for economical and sustainable energy-related devices.Keywords:NiCo layered double hydroxides;carbon nanotubes;self-sacrificing template;hollow structure;oxygen evolution reaction
危险品化学品经营许可证(带存储)