4.8 Article

Pine needle-derived microporous nitrogen-doped carbon frameworks exhibit high performances in electrocatalytic hydrogen evolution reaction and supercapacitors

期刊

NANOSCALE
卷 9, 期 3, 页码 1237-1243

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c6nr08139h

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资金

  1. National Materials Genome Project [2016YFB0700600]
  2. National 973 Basic Research Program [2015CB659300]
  3. National Natural Science Foundation of China [21403105, 21573108]
  4. China Postdoctoral Science Foundation [2015M580408, 2015M580413, 2015M581768]
  5. Natural Science Foundation for Young Scholars of Jiangsu Province [BK20150583, BK20150571, BK20160647]
  6. Fundamental Research Funds for the Central Universities
  7. Priority Academic Program Development (PAPD) of Jiangsu Higher Education Institutions

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The design of electrochemically active materials with appropriate structures and compositions is very important for applications in energy conversion and storage devices. Herein, we demonstrate an effective strategy to prepare microporous heteroatom-doped carbon frameworks derived from naturally-abundant pine needles. The preparation procedure is based on the carbonization of pine needles, followed by KOH activation at a temperature range of 700-1000 degrees C. The resultant nitrogen-doped carbon consists of abundant micropores and an ultrahigh specific surface area (up to 2433 m(2) g(-1)), leading to high performances in electrocatalytic hydrogen evolution reaction (HER) and supercapacitors. Specifically, when the pine needle-derived carbon (activated at 800 degrees C) serves as a HER electrocatalyst, it exhibits a low onset potential (4 mV), a small Tafel slope (similar to 45.9 mV dec(-1)) and a remarkable stability over long-term cycling. When evaluated as an electrode material for supercapacitors, the pine needle-derived carbon (activated at 900 degrees C) demonstrates high specific capacitance (236 F g(-1) at 0.1 A g(-1)), remarkable rate capability (183 F g(-1) at even 20 A g(-1)) and good long-term stability. Notably, the specific capacitance at 2.0 A g(-1) increased from similar to 205 to similar to 227 F g(-1) after cycling for 5000 times, owing to the further activation and wetting of the electrodes. This novel and low-cost biomass-derived carbon material is very promising for many applications, especially in electrocatalytic water splitting and supercapacitors.

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