synthesis of morphology-controlled MoO/FeS bifunctional catalysts for high-efficiency and stable alkaline water splitting
The advancement of a bifunctional electrocatalyst consisting of Earth's rich elements and exhibiting high efficiency is the key to obtain hydrogen fuel by overall water splitting (OWS). Here, a facile and extensible hydrothermal synthesis of an electrocatalyst on iron foam (MoO x /Fe 1− x S/IF)...
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Published in | Dalton transactions : an international journal of inorganic chemistry Vol. 51; no. 24; pp. 9486 - 9494 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Published |
21.06.2022
|
Online Access | Get full text |
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Summary: | The advancement of a bifunctional electrocatalyst consisting of Earth's rich elements and exhibiting high efficiency is the key to obtain hydrogen fuel by overall water splitting (OWS). Here, a facile and extensible hydrothermal synthesis of an electrocatalyst on iron foam (MoO
x
/Fe
1−
x
S/IF) as a robust bifunctional catalyst with excellent catalytic activity is designed for the hydrogen evolution reaction (HER) with an overpotential of 142 mV at 100 mA cm
−2
, and for the OER with lower overpotentials of 300 and 500 mV at 100 and 1000 mA cm
−2
. The good activity is ascribed to the controllable morphology, stronger bonding of the catalyst to a substrate and optimized electronic configuration. When used as bifunctional electrocatalysts toward alkaline overall water splitting, MoO
x
/Fe
1−
x
S/IF delivers a current density of 10 mA cm
−2
at a low cell voltage of 1.56 V for 110 h. Such high performance coupled with low-cost iron-based materials suggests that the present strategy may open new avenues for the rational design of electrocatalysts and for use in practical water splitting.
MoO
x
/Fe
1−
x
S/IF hollow microspheres were successfully synthesized with excellent HER, OER and overall water splitting properties and long-term stability. |
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Bibliography: | https://doi.org/10.1039/d2dt01098d Electronic supplementary information (ESI) available. See DOI |
ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/d2dt01098d |