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Interface engineering of cobalt-sulfide-selenium core-shell nanostructures as bifunctional electrocatalysts toward overall water splitting
Ist Teil von
Nanoscale, 2021-04, Vol.13 (14), p.689-691
Ort / Verlag
England: Royal Society of Chemistry
Erscheinungsjahr
2021
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
The number of active sites and stability of the structure of electrocatalysts are the key factors in the process of overall water splitting. In this paper, cobalt-sulfide-selenium (Se:CoS
2−
x
) core-shell nanostructures are prepared by a simple two-step method, including hydrothermal reaction and chemical vapor deposition. The resulting product exhibits excellent electrochemical performance, owing to the synergistic effects between CoS
2
and CoSe
1−
x
, as well as the plentiful active sites in the electrode structure. The Se:CoS
2−
x
material shows a more improved hydrogen evolution reaction activity compared to CoS
2
and Co(OH)Cl precursor catalysts, with a low overpotential of only 240 mV achieved at 10 mA cm
−2
. Meanwhile, Se:CoS
2−
x
as a bifunctional water splitting catalyst also shows remarkably improved oxygen evolution reaction activity, with a low overpotential of only 1.32 V at 10 mA cm
−2
. The above results show that selenide/sulfide materials provide a new research direction for discovering high-performance and cheap electrode materials.
We report for the first time that core-shell selenium cobalt disulfide nanotubes are successfully synthesized
via
a simple two-step method. The Se:CoS
2−
x
electrode we obtained shows excellent electrocatalytic activity.