Citation: Ziqi Zhang, Yin Lei, Weimin Huang. Recent progress in carbon-based materials boosting electrochemical water splitting[J]. Chinese Chemical Letters, ;2022, 33(8): 3623-3631. doi: 10.1016/j.cclet.2021.11.041 shu

Recent progress in carbon-based materials boosting electrochemical water splitting

Ziqi Zhang ^a ,
Yin Lei ^a ,
Weimin Huang ^{a, b, c, *,}

a.
College of Chemistry, Jilin University, Changchun 130012, China
b.
Key Laboratory of Physics and Technology for Advanced Batteries of Ministry of Education, Jilin University, Changchun 130012, China
c.
School of Pharmaceutical Sciences, Jilin University, Changchun 130012, China

huangwm@jlu.edu.cn

Received Date: 13 September 2021
Revised Date: 12 October 2021
Accepted Date: 13 November 2021
Available Online: 18 November 2021

Figures(5)

As environmental crises such as global warming become more and more serious due to the large amount of carbon dioxide emitted by the burning of fossil fuels, much attention has been paid to carbon neutrality. Hydrogen, with zero carbon content, is a clean and renewable energy carrier having a large energy density. It is considered as one of the most desirable alternatives to fossil fuels. Electrochemical water splitting, unlike the steam reforming process accelerating fossil fuels depletion and CO₂ emissions, can produce H₂ powered by renewable energy such as solar or wind. As a promising way to promote carbon neutralization, hydrogen production by electrolysis of water is meaningful both in terms of scientific research and practical application. In order to drive electrochemical water splitting with low power consumption, efficient, durable and affordable electrocatalysts with low overpotentials are in urgent need. Therefore, this mini-review briefly introduces the current development status and mainstream obstacles of carbon-based materials used in electrochemical water splitting.
- Carbon-based materials,
- Water splitting,
- Electrocatalysis,
- Carbon neutrality,
- Hydrogen evolution reaction,
- Oxygen evolution reaction
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