4.7 Article

The synergistic effect of nitrogen and fluorine co-doping in graphene quantum dot catalysts for full water splitting and supercapacitor

期刊

APPLIED SURFACE SCIENCE
卷 507, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.apsusc.2019.145157

关键词

Hydrogen evolution reaction; Tri-functional materials; Heteroatom doping; Electrocatalysts; Supercapacitor

资金

  1. Basic Science Research Program through the National Research Foundation of Korea - Ministry of Science and ICR [NRF-2017M3A7B4049176, 2018R1A5A1025224, 2018R1C1B6001267]
  2. Hyundai Moto Chung Mong-Koo Foundation
  3. National Research Foundation of Korea [2018R1C1B6001267, 2017M3A7B4049176] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Development of efficient electrochemical catalysts is crucial for clean energy technologies such as water splitting, and batteries, etc. Despite large amounts of electrocatalyst research, it remains a challenge to eco-friendly non-metal catalyst showing high performance as much as novel metal. To achieve high performance as much as noble-metal, carbon nanomaterials (CNMs) have been attracted as a candidate to the widespread application using electrochemical reaction. Herein, we report nitrogen, and fluorine co-doped graphene quantum dot (N,F-GQDs) synthesized by two-step functionalizing method for highly efficient overall water splitting. N,F-GQDs demonstrate electrocatalytic effect toward HER, and OER, and is fabricated as two-electrode full-water splitting showing good stability at various potential points. Furthermore, due to fluorine treatment, prepared N,F-GQDs exhibits enhanced electrochemical reaction property, which can induce capacitance due to the large difference of electronegativity between fluorine and carbon. N,F-GQDs is applied for the anode of super capacitance in the three-electrode system and reveal specific capacitance of 270 F g(-1) at 1 mV s(-1) from CV curves, and GCD capacitance of 244 F g(-1) at 3 mA cm(-2). This work provides a new avenue for enhancing both activities of the electrocatalytic and electrochemical reaction.

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