首页|Defined organic-octamolybdate crystalline superstructures derived Mo2C@C as efficient hydrogen evolution electrocatalysts

Defined organic-octamolybdate crystalline superstructures derived Mo2C@C as efficient hydrogen evolution electrocatalysts

扫码查看
Hydrogen evolution electrocatalysts derived from metal-organic crystalline frameworks can inherit the merits of ordered and adjustable structures with high surface area.In this paper,organic-octamolybdate crystalline superstructures(OOCS)with a fixed stoichiometric ratio of Mo8(L)2 and high Mo content(>40 wt%)were synthesized using flexible ligands with controllable lengths(named as OOCS-1-3).Then,molybdenum carbides coated with carbon layers as electrocatalysts(Mo2C@C-1-3)can be obtained di-rectly from a one-step high-temperature carbonization process using OOCS-1-3 as precursors.As a typical example,Mo2C@C-3 exhibits satisfactory hydrogen evolution activity with a low overpotential of 151 mV(1.0mol/L KOH)at 10mA/cm2 and stability for 24h.The electrocatalytic activity is mainly from the syn-ergistic interactions between the carbon layers and molybdenum carbide species.Furthermore,compared with the initial content of C,N,Mo in OOCS and Mo2C@C,the catalytic activity increases with the N amount.This work makes organic-octamolybdate crystalline superstructures used as general precursors to product high Mo content electrocatalysts applied in energy storage and conversion fields.

Molybdenum carbidesElectrocatalystsOrganic-octamolybdate crystallinesuperstructuresSynergistic interactionsHydrogen evolution reaction(HER)

Jiao Li、Chenyang Zhang、Chuhan Wu、Yan Liu、Xuejian Zhang、Xiao Li、Yongtao Li、Jing Sun、Zhongmin Su

展开 >

School of Materials Science and Engineering,Jilin Jianzhu University,Changchun 130018,China

School of Chemical and Environmental Engineering,Changchun University of Science and Technology,Changchun 130022,China

Joint Fund Project of the Natural Science Foundation of Jilin Province

YDZJ202301ZYTS290

2024

中国化学快报(英文版)
中国化学会

中国化学快报(英文版)

CSTPCD
影响因子:0.771
ISSN:1001-8417
年,卷(期):2024.35(6)