Efficient Hydrogen Production by In Situ Growth of sp‐C–P‐Cu Heterointerface

Abstract Herein, the construction of sp‐C–P‐Cu bridged graphdiyne (GDY)‐copper phosphides (Cu x P) heterointerface structure is described by controlled growth of GDY on the surface of Cu x P for efficient hydrogen evolution reaction (HER). The experimental results demonstrate that the newly formed sp‐C─P bonds at the interfaces between GDY and Cu x P have the dual roles of promoting faster charge transfer and producing large numbers of new intrinsic active sites, which facilitates the activation and dissociation of H 2 O to produce H 2 and greatly enhanced the intrinsic electrocatalytic activity. As expected, the as‐synthesized electrocatalyst exhibits excellent activity for hydrogen evolution reaction (HER) with overpotentials of 44 mV at 10 mA cm −2 , which is smaller than that of pure Cu x P and Cu foam electrocatalysts. These results correlate interface structure and HER activity and provide new insights into the design and synthesis of high‐performance electrocatalysts.

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Publication Details

Journal
Advanced Functional Materials
Published
2024-09-16
DOI
https://doi.org/10.1002/adfm.202413013
Citations
9
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.92

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article

Efficient Hydrogen Production by In Situ Growth of sp‐C–P‐Cu Heterointerface

Yurui Xue, Han Wu, Siao Chen, Jinze Li et al.
9 citations
Advanced Functional Materials
Electrocatalysts for Energy Conversion
0.92
article

Efficient Hydrogen Production by In Situ Growth of sp‐C–P‐Cu Heterointerface

Yurui Xue, Han Wu, Siao Chen, Jinze Li, Yuliang Li
article en
9 citations

Abstract

Abstract Herein, the construction of sp‐C–P‐Cu bridged graphdiyne (GDY)‐copper phosphides (Cu x P) heterointerface structure is described by controlled growth of GDY on the surface of Cu x P for efficient hydrogen evolution reaction (HER). The experimental results demonstrate that the newly formed sp‐C─P bonds at the interfaces between GDY and Cu x P have the dual roles of promoting faster charge transfer and producing large numbers of new intrinsic active sites, which facilitates the activation and dissociation of H 2 O to produce H 2 and greatly enhanced the intrinsic electrocatalytic activity. As expected, the as‐synthesized electrocatalyst exhibits excellent activity for hydrogen evolution reaction (HER) with overpotentials of 44 mV at 10 mA cm −2 , which is smaller than that of pure Cu x P and Cu foam electrocatalysts. These results correlate interface structure and HER activity and provide new insights into the design and synthesis of high‐performance electrocatalysts.

Advanced Functional MaterialsVol. 35(2)
Shandong University (CN), Chinese Academy of Sciences (CN), Institute of Chemistry (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China, Chinese Academy of Sciences
Openalex Percentile: Top 30%
Electrocatalysts for Energy Conversion
0.92
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