Electrocatalytic Hydrogen Precipitation Performances of B and Ce Codoped CoP/NiCoP over a Wide pH Range

Exploring efficient, low-cost, and pH-versatile electrocatalysts for hydrogen precipitation is vital for the development of practical hydrogen production via water electrolysis. However, most existing electrocatalysts suffer from limitations such as high overpotentials, a reliance on expensive noble metals, or poor stability under extreme pH conditions, hindering their practical application. Among the many electrocatalytic materials, transition metal phosphides (TMPs) are considered a promising class of hydrogen evolution reaction (HER) catalytic materials due to their abundant reserves and tunable electronic structures. Despite the demonstrated potential of TMPs in electrolytic water-to-hydrogen reactions in recent years, there are still several issues that must be addressed, including the insufficient exposure of active sites, high charge-transfer barriers under full pH conditions, and poor long-term stability. In this work, B and Ce codoped CoP/NiCoP heterostructured nanoarrays were grown on nickel foam. This codoped catalyst exhibits a larger electrochemically active surface area, which significantly improves its HER kinetics and charge-transfer ability. The B, Ce codoped CoP/NiCoP catalyst presents good catalytic performance over a wide pH range: at a current density of 10 mA cm<sup>-2</sup>, overpotentials of 89, 123, and 44 mV are achieved under acidic (0.5 M H<sub>2</sub>SO<sub>4</sub>), neutral (1 M PBS), and alkaline (1 M KOH) conditions, respectively. Moreover, the catalyst exhibits Tafel slopes of only 55 mV dec<sup>-1</sup> (0.5 M H<sub>2</sub>SO<sub>4</sub>), 105 mV dec<sup>-1</sup> (1 M PBS), and 51 mV dec<sup>-1</sup> (1 M KOH). After 20 h of stability testing at a current density of 100 mA cm<sup>-2</sup>, current density retention rates of 85, 60, and 92% are achieved under acidic, neutral, and alkaline conditions, respectively. This study provides new insights into the implementation of a cation-anion codoping strategy for the design and preparation of low-cost, high-efficiency electrocatalysts.

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Journal
ACS Applied Materials & Interfaces
Published
2025-08-11
DOI
https://doi.org/10.1021/acsami.5c09676
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
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article

Electrocatalytic Hydrogen Precipitation Performances of B and Ce Codoped CoP/NiCoP over a Wide pH Range

Jinyuan Zhou, Gang Zhao, Mengjing Jin, Xinhua Wang et al.
ACS Applied Materials & Interfaces
Electrocatalysts for Energy Conversion
article

Electrocatalytic Hydrogen Precipitation Performances of B and Ce Codoped CoP/NiCoP over a Wide pH Range

Jinyuan Zhou, Gang Zhao, Mengjing Jin, Xinhua Wang, Rui Wang, Ru Chen, Haixing Zhao, Shimin Wang, Xiao Jun Pan
article en

Abstract

Exploring efficient, low-cost, and pH-versatile electrocatalysts for hydrogen precipitation is vital for the development of practical hydrogen production via water electrolysis. However, most existing electrocatalysts suffer from limitations such as high overpotentials, a reliance on expensive noble metals, or poor stability under extreme pH conditions, hindering their practical application. Among the many electrocatalytic materials, transition metal phosphides (TMPs) are considered a promising class of hydrogen evolution reaction (HER) catalytic materials due to their abundant reserves and tunable electronic structures. Despite the demonstrated potential of TMPs in electrolytic water-to-hydrogen reactions in recent years, there are still several issues that must be addressed, including the insufficient exposure of active sites, high charge-transfer barriers under full pH conditions, and poor long-term stability. In this work, B and Ce codoped CoP/NiCoP heterostructured nanoarrays were grown on nickel foam. This codoped catalyst exhibits a larger electrochemically active surface area, which significantly improves its HER kinetics and charge-transfer ability. The B, Ce codoped CoP/NiCoP catalyst presents good catalytic performance over a wide pH range: at a current density of 10 mA cm<sup>-2</sup>, overpotentials of 89, 123, and 44 mV are achieved under acidic (0.5 M H<sub>2</sub>SO<sub>4</sub>), neutral (1 M PBS), and alkaline (1 M KOH) conditions, respectively. Moreover, the catalyst exhibits Tafel slopes of only 55 mV dec<sup>-1</sup> (0.5 M H<sub>2</sub>SO<sub>4</sub>), 105 mV dec<sup>-1</sup> (1 M PBS), and 51 mV dec<sup>-1</sup> (1 M KOH). After 20 h of stability testing at a current density of 100 mA cm<sup>-2</sup>, current density retention rates of 85, 60, and 92% are achieved under acidic, neutral, and alkaline conditions, respectively. This study provides new insights into the implementation of a cation-anion codoping strategy for the design and preparation of low-cost, high-efficiency electrocatalysts.

ACS Applied Materials & InterfacesVol. 17(33)
Lanzhou University (CN)
Natural Science Foundation of Gansu Province
Clean water and sanitation
Openalex Percentile: Top 87%
Electrocatalysts for Energy Conversion
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