Journal
ACS NANO
Volume 16, Issue 11, Pages 18038-18047Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsnano.2c04090
Keywords
Electrocatalyst; Hydrogen evolution reaction; Leaf-like morphology; Pt-Co; Co4N
Categories
Funding
- National Natural Science Foundation of China [22002068, 52272222, 52072197]
- China Postdoctoral Science Foundation [2021M691700]
- Youth Innovation and Technology Foundation of Shandong Higher Education Institutions, China [2019KJC004]
- Outstanding Youth Foundation of Shandong Province, China [ZR2019JQ14]
- Taishan Scholar Young Talent Program [tsqn201909114]
- Major Scientific and Technological Innovation Project [2019JZZY020405]
- Major Basic Research Program of Natural Science Foundation of Shandong Province [ZR2020ZD09]
- Natural Science Foundation of Shandong Province of China [ZR2019BB002, ZR2018BB031]
- Australian Research Council (ARC) through Future Fellowship [FT210100298, FT210100806, DP220100603, LP210100467, LP210200504, LP210200345, IC180100005]
- CSIRO Energy Centre and Kick-Start Project
- Victorian Government through Study Melbourne
- Australian Research Council [LP210200345] Funding Source: Australian Research Council
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This study presents the development of a catalyst, T-Pt-Co4N, based on ginkgo leaf-like Co4N coupled with trace Pt through a metallic bond Pt-Co, for hydrogen evolution reaction (HER) in water electrolysis. The T-Pt-Co4N catalyst exhibits low overpotentials and excellent long-term stability in alkaline and neutral electrolytes, surpassing benchmark values. It also shows the ability to drive overall water splitting with the assistance of sustainable energies. The unique nanostructure of the catalyst accelerates the electrocatalytic process by providing abundant active sites and mass transport channels. Experimental and theoretical calculations confirm that the metallic bond Pt-Co plays a crucial role in optimizing the reaction kinetics for HER, leading to enhanced electrocatalytic performance.
Exploiting highly efficient electrocatalysts toward hydrogen evolution reaction (HER) has a significant role in the mass production of hydrogen energy through water electrolysis. Herein, ginkgo leaf-like Co4N coupled with trace Pt with metallic bond Pt-Co on nickel foam via solvothermal, tannic acid treated, and nitridation procedures for HER (T-Pt-Co4N) is developed. It only requires low overpotentials of 31 mV and 27 mV to achieve 10 mA cm-2 in alkaline and neutral electrolytes, respectively, surpassing the benchmark Pt/C and previously reported values. Moreover, it presents excellent long-term stability in the studied media and also can drive overall water splitting under the assistance of sustainable energies. The specific nanostructure favors the acceleration of the electrocatalytic process by exposing abundant active sites and providing numerous mass transport channels during the catalytic process. Moreover, experimental and theoretical calculation demonstrate that the atomic Pt coordinates with Co to form metallic bond Pt-Co also act as crucial role to boost the electrocatalytic performance by optimizing the reaction kinetics for HER.
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