Alkaline Water Splitting Using Hafnium‐Based Stable and Efficient Bifunctional Electrocatalyst
Abstract The desire to achieve sustainable development goals inspired exploring green energy as a favorable alternative to hazardous fossil fuel‐based energy. Alkaline water electrolysis is a promising candidate for producing low‐cost pure green hydrogen; however, the efficiency of non‐precious tran...
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Published in | ChemCatChem Vol. 15; no. 15 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
Wiley Subscription Services, Inc
07.08.2023
|
Subjects | |
Online Access | Get full text |
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Summary: | Abstract
The desire to achieve sustainable development goals inspired exploring green energy as a favorable alternative to hazardous fossil fuel‐based energy. Alkaline water electrolysis is a promising candidate for producing low‐cost pure green hydrogen; however, the efficiency of non‐precious transitional metal‐based catalysts is still behind noble electrocatalysts (like Pt and IrO
2
). To make hydrogen a next‐generation fuel, the replacement of high‐cost scarce noble metal is required. An attempt has been made to use a non‐precious transitional bimetallic combination of hafnium nickel diselenide/ reduced graphene oxide (HfNiSe
2
/rGO) for HER, OER, and overall water splitting. HfNiSe
2
/rGO demonstrated good electrocatalytic performance; for achieving 10 mA/cm
2
of current density, the overpotential requirement is 162 mV for hydrogen evolution reaction (HER) and 320 mV for oxygen evolution reaction (OER) at 20 mA/cm
2
of current density. Similarly, a low Tafel slope is required, 49 mV dec
−1
for HER and 66 mV dec
−1
for OER in 1 M KOH with high stability. HfNiSe
2
/rGO also showed highly stable activity for overall water splitting, requiring only 1.56 V to attain 10 mA/cm
2
of current density. The result indicates HfNiSe
2
/rGO is a suitable electrocatalyst for green hydrogen generation because of its ease of production, economical, good activity, and stability towards water splitting. |
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ISSN: | 1867-3880 1867-3899 |
DOI: | 10.1002/cctc.202300562 |