NiFe co-doped TiO2 as a high-performance bifunctional photocatalyst for enhanced oxygen evolution and reduction reactions in efficient zinc-air battery systems

This study underscores the significant influence of Ni and Fe transition metal doping, as well as NiFe co-doping, on enhancing the properties of TiO 2 to address the critical challenges in developing high-performance photo-assisted Zn-air batteries, particularly the need for improved light absorption, charge carrier separation, and catalytic efficiency. The doping process notably enhances light absorption and charge carrier separation, while the reduction in TiO 2 crystallite size increases the surface area and shortens charge carrier diffusion paths, thereby minimizing recombination rates and improving photocatalytic efficiency. Moreover, the higher redox potentials of Ni and Fe oxidation states relative to TiO 2 's conduction band enable them to function as efficient electron acceptors, stabilizing charge carriers and accelerating reduction reactions. Electrochemical analysis reveals that NiFe-doped TiO 2 exhibits superior conductivity and reduced charge transfer resistance compared to its single-element-doped counterparts, facilitating faster reaction kinetics. For OER, the overpotential decreases from 307 mV to 221 mV, while for ORR, illumination improves the half-wave potential to 0.65 V and increases the diffusion-plateau current density from 3.96 mA/cm 2 to 4.6 mA/cm 2 . Battery performance testing demonstrates that under light irradiation, the charging potential is reduced to 1.63–1.66 V, and the discharge voltage is stabilized at 1.56–1.60 V, resulting in a round-trip efficiency of 96.34 %, compared to 77.59 % under dark conditions. These performance metrics approach the theoretical redox potential of 1.64 V, outperforming the capabilities of the state-of-the-art catalysts for photo-assisted Zn-air systems. Overall, this work establishes NiFe-doped TiO 2 as a highly effective bifunctional photocatalyst, highlighting its potential to optimize oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) processes, thereby contributing to advancements in sustainable energy storage technologies. • NiFe co-doping enhances TiO2 light absorption via band gap modification. • High-valence Ni and Fe ions boost OER and ORR kinetics. • NiFe-doped TiO2 achieves 96.34 % efficiency in Zn-air batteries under lights. • NiFe-doped TiO2 shows promise as a superior photocatalyst for Zn-air batteries.

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Publication Details

Journal
Electrochemistry Communications
Published
2025-04-22
DOI
https://doi.org/10.1016/j.elecom.2025.107942
Citations
10
Primary Topic
Advanced Photocatalysis Techniques
Type
article
Field-Weighted Citation Impact
3.63
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article

NiFe co-doped TiO2 as a high-performance bifunctional photocatalyst for enhanced oxygen evolution and reduction reactions in efficient zinc-air battery systems

Foysal Kabir Tareq, M. Zakir Hossain, Souman Rudra
10 citations
Electrochemistry Communications
Advanced Photocatalysis Techniques
3.63
article

NiFe co-doped TiO2 as a high-performance bifunctional photocatalyst for enhanced oxygen evolution and reduction reactions in efficient zinc-air battery systems

Foysal Kabir Tareq, M. Zakir Hossain, Souman Rudra
article en
10 citations

Abstract

This study underscores the significant influence of Ni and Fe transition metal doping, as well as NiFe co-doping, on enhancing the properties of TiO 2 to address the critical challenges in developing high-performance photo-assisted Zn-air batteries, particularly the need for improved light absorption, charge carrier separation, and catalytic efficiency. The doping process notably enhances light absorption and charge carrier separation, while the reduction in TiO 2 crystallite size increases the surface area and shortens charge carrier diffusion paths, thereby minimizing recombination rates and improving photocatalytic efficiency. Moreover, the higher redox potentials of Ni and Fe oxidation states relative to TiO 2 's conduction band enable them to function as efficient electron acceptors, stabilizing charge carriers and accelerating reduction reactions. Electrochemical analysis reveals that NiFe-doped TiO 2 exhibits superior conductivity and reduced charge transfer resistance compared to its single-element-doped counterparts, facilitating faster reaction kinetics. For OER, the overpotential decreases from 307 mV to 221 mV, while for ORR, illumination improves the half-wave potential to 0.65 V and increases the diffusion-plateau current density from 3.96 mA/cm 2 to 4.6 mA/cm 2 . Battery performance testing demonstrates that under light irradiation, the charging potential is reduced to 1.63–1.66 V, and the discharge voltage is stabilized at 1.56–1.60 V, resulting in a round-trip efficiency of 96.34 %, compared to 77.59 % under dark conditions. These performance metrics approach the theoretical redox potential of 1.64 V, outperforming the capabilities of the state-of-the-art catalysts for photo-assisted Zn-air systems. Overall, this work establishes NiFe-doped TiO 2 as a highly effective bifunctional photocatalyst, highlighting its potential to optimize oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) processes, thereby contributing to advancements in sustainable energy storage technologies. • NiFe co-doping enhances TiO2 light absorption via band gap modification. • High-valence Ni and Fe ions boost OER and ORR kinetics. • NiFe-doped TiO2 achieves 96.34 % efficiency in Zn-air batteries under lights. • NiFe-doped TiO2 shows promise as a superior photocatalyst for Zn-air batteries.

Electrochemistry CommunicationsVol. 176
University of Agder (NO)
Openalex Percentile: Top 7%
Advanced Photocatalysis Techniques
3.63
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