Porous nanoMoC@graphite shell derived from a MOFs-directed strategy: an efficient electrocatalyst for the hydrogen evolution reaction
文献情報
Zhangping Shi, Yangxia Wang, Huanlei Lin, Hongbin Zhang, Meikun Shen, Songhai Xie, Yahong Zhang, Qingsheng Gao, Yi Tang
The hydrogen evolution reaction using noble-metal free electrocatalysts has captured increasing attention due to its importance in renewable hydrogen production. Herein, a highly active and stable electrocatalyst of MoC encapsulated by graphitized carbon shells (nanoMoC@GS) has been developed via an in situ carburization of a Mo-based metal–organic framework (Mo-MOF) with the atomic periodic structure. The ultrafine MoC nanoparticles (∼3 nm) confined by 1–3 layered graphite shells significantly favor the efficient HER in both acidic and basic media. In particular, a low overpotential (η10 = 124 and 77 mV at a current density of −10 mA cm−2), a small Tafel slope (43 and 50 mV dec−1) and a high exchange current density (j0 = 0.015 and 0.212 mA cm−2) are achieved on nanoMoC@GS in 0.5 M H2SO4 and 1.0 M KOH, respectively. Such remarkable activity, outperforming most current noble-metal-free electrocatalysts, stems from the cooperative/synergistic effects of ultrafine MoC nanostructure, ultrathin and conductive graphitized carbon shells, and enriched porosity. This work demonstrates a feasible way to design high-performance electrocatalysts via converting “atomic contact” hybrid structures (e.g., MOFs), illustrating a new perspective for developing nanocatalysts in the energy chemistry field.
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