Synergistic Effects of Interlayer Anions in NiFe-LDH and Nickel Cobaltite Heterointerface for Energy-Efficient Alkaline Water Electrolysis

An energy-efficient, economically viable, and catalytically active bifunctional electrocatalyst with long-term stability could be a promising alternative to existing noble-metal-based electrocatalysts for producing carbon-neutral green hydrogen via alkaline water electrolysis (AWE). Here, we designed a nanostructured electrocatalyst, i.e., NiFe-LDH electrodeposited on hydrothermally grown Nickel Cobaltite (NCO) over a carbon cloth (CC) substrate, specified as NiFe-LDH/NCO@CC. A phase-pure synthesis is verified by an X-ray diffraction study, and field emission scanning electron microscopy suggests a core-shell (NiFe-LDH/NCO@CC) heterointerface composed of a core of NCO nanowires decorated with a shell of NiFe-LDH nanosheets for sulfate-anion intercalation and NiFe-LDH nanoparticles for nitrate-anion intercalation. The electrochemical analysis performed in 1 M KOH suggests that the optimized sulfate-intercalated NiFe-LDH/NCO@CC electrocatalyst shows superior electrochemical activity compared to pristine NiFe-LDH, NCO, and bare CC, with an overpotential η<sub>10</sub> of ∼141 and 226 mV for HER and OER, respectively. This superior performance is attributed to the heterointerface of anion-intercalated NiFe-LDH and NCO, which synergistically regulate the electronic structure, facilitating efficient charge transfer at the electrode-electrolyte interface. It can act as a bifunctional catalyst with an overall cell potential of ∼1.66 V, delivering a current density of 10 mA cm<sup>-2</sup>. It shows a high turnover frequency (TOF) of 5.64 × 10<sup>-2</sup> H<sub>2</sub> s<sup>-1</sup> and 3.75 × 10<sup>-2</sup> O<sub>2</sub> s<sup>-1</sup> at an overpotential of 260 mV. An anion-exchange membrane-based alkaline water electrolyzer is also tested with the synthesized electrocatalyst, showing prolonged stability of ∼50 h in an alkaline medium. The estimation of H<sub>2</sub> production cost reveals that NFS/NCO24@CC requires $1.28/gasoline-gallon equivalent of H<sub>2</sub>, which is less than the targeted cost set by the US Department of Energy for 2026. Thus, the present findings reveal that this heterostructure can be a feasible and cost-effective bifunctional electrocatalyst for energy-efficient overall water splitting.

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Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2025-10-20
DOI
https://doi.org/10.1021/acsami.5c17778
Citations
2
Primary Topic
Layered Double Hydroxides Synthesis and Applications
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article
Field-Weighted Citation Impact
1.04
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article

Synergistic Effects of Interlayer Anions in NiFe-LDH and Nickel Cobaltite Heterointerface for Energy-Efficient Alkaline Water Electrolysis

Ambesh Dixit, Chandra Prakash, Minakshi Sharma, Vijay Kumar Singh
2 citations
ACS Applied Materials & Interfaces
Layered Double Hydroxides Synthesis and Applications
1.04
article

Synergistic Effects of Interlayer Anions in NiFe-LDH and Nickel Cobaltite Heterointerface for Energy-Efficient Alkaline Water Electrolysis

Ambesh Dixit, Chandra Prakash, Minakshi Sharma, Vijay Kumar Singh
article en
2 citations

Abstract

An energy-efficient, economically viable, and catalytically active bifunctional electrocatalyst with long-term stability could be a promising alternative to existing noble-metal-based electrocatalysts for producing carbon-neutral green hydrogen via alkaline water electrolysis (AWE). Here, we designed a nanostructured electrocatalyst, i.e., NiFe-LDH electrodeposited on hydrothermally grown Nickel Cobaltite (NCO) over a carbon cloth (CC) substrate, specified as NiFe-LDH/NCO@CC. A phase-pure synthesis is verified by an X-ray diffraction study, and field emission scanning electron microscopy suggests a core-shell (NiFe-LDH/NCO@CC) heterointerface composed of a core of NCO nanowires decorated with a shell of NiFe-LDH nanosheets for sulfate-anion intercalation and NiFe-LDH nanoparticles for nitrate-anion intercalation. The electrochemical analysis performed in 1 M KOH suggests that the optimized sulfate-intercalated NiFe-LDH/NCO@CC electrocatalyst shows superior electrochemical activity compared to pristine NiFe-LDH, NCO, and bare CC, with an overpotential η<sub>10</sub> of ∼141 and 226 mV for HER and OER, respectively. This superior performance is attributed to the heterointerface of anion-intercalated NiFe-LDH and NCO, which synergistically regulate the electronic structure, facilitating efficient charge transfer at the electrode-electrolyte interface. It can act as a bifunctional catalyst with an overall cell potential of ∼1.66 V, delivering a current density of 10 mA cm<sup>-2</sup>. It shows a high turnover frequency (TOF) of 5.64 × 10<sup>-2</sup> H<sub>2</sub> s<sup>-1</sup> and 3.75 × 10<sup>-2</sup> O<sub>2</sub> s<sup>-1</sup> at an overpotential of 260 mV. An anion-exchange membrane-based alkaline water electrolyzer is also tested with the synthesized electrocatalyst, showing prolonged stability of ∼50 h in an alkaline medium. The estimation of H<sub>2</sub> production cost reveals that NFS/NCO24@CC requires $1.28/gasoline-gallon equivalent of H<sub>2</sub>, which is less than the targeted cost set by the US Department of Energy for 2026. Thus, the present findings reveal that this heterostructure can be a feasible and cost-effective bifunctional electrocatalyst for energy-efficient overall water splitting.

ACS Applied Materials & InterfacesVol. 17(43)
Indian Institute of Technology Ropar (IN), Indian Institute of Technology Jodhpur (IN), Advanced Materials and Devices (United States) (US), Clean Energy (United States) (US)
Openalex Percentile: Top 21%
Layered Double Hydroxides Synthesis and Applications
1.04
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