Electrochemical dechlorination of dichloromethane (DCM)
to high-value
methane not only reduces carbon emission and environmental pollution
but also alleviates energy shortages. In this study, a series of carbon-confined
NiCo2O4−β/C
x
(NCO4−β/C
x
, x = 0, 0.5, 1, 2, 3) with hierarchical nano-microflower
structures were successfully constructed via combining the hydrothermal
method and dopamine in situ polymerization, which were utilized as
electrocatalysts for electrochemical dechlorination of DCM. The as-prepared
NCO4−β/C1 showed remarkable electrocatalytic
dechlorination performance of DCM with a high methane selectivity
of 87% and methane Faradaic efficiency of 17%, where the production
rate of methane is up to 3538.25 μmol g–1 h–1 at −2.98 V (vs Ag/AgCl/Me4NCl).
Notably, it could be experimentally proved that nickel cobaltite encapsulated
in the carbon layer may accelerate the charge transfer and then build
up the dechlorination activity. Additionally, two possible dichlorination
mechanisms of DCM to methane are theoretically confirmed at the Ni
active sites, which is proved by DFT calculations. This study presents
promising ideas for developing efficacious dechlorination electrocatalysts
and the efficient transformation of chlorinated volatile compounds
(Cl-VOCs) to value-added methane in an environmentally benign manner.