Nitrogen doped carbon fibers derived from carbonization of electrospun polyacrylonitrile as efficient metal-free HER electrocatalyst
Development of durable and efficient electrocatalyst for hydrogen evolution reaction (HER) is significantly important for forwarding the commercialization of water splitting technology. In this work, we report a facile synthesis of nitrogen doped carbon fibers derived from the carbonization of the e...
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Published in | International journal of hydrogen energy Vol. 45; no. 7; pp. 4035 - 4042 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Ltd
07.02.2020
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Subjects | |
Online Access | Get full text |
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Summary: | Development of durable and efficient electrocatalyst for hydrogen evolution reaction (HER) is significantly important for forwarding the commercialization of water splitting technology. In this work, we report a facile synthesis of nitrogen doped carbon fibers derived from the carbonization of the electron-spun polyacrylonitrile (PAN) membrane at 800 °C (NCFs-800) as efficient and stable metal-free electrocatalyst for HER catalysis in both acidic and alkaline mediums. Ascribing to the homogenous nitrogen dopants in electrocatalyst, NCFs-800 requires only 114.3 mV and 198.6 mV vs. RHE to achieve current density of 10 mA cm−2 in 0.5 M H2SO4 and 1 M KOH electrolytes, respectively. Moreover, the HER activity is well maintained after 2000 potential cycles indicating that NCFs-800 possesses high durability in both acidic and alkaline conditions due to the fibrous structure with high corrosion resistance. Our study offers new strategy to synthesize stable and efficient metal-free electrocatalyst, which could be extended to other heteroatom doped carbon electrocatalyst.
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•Nitrogen doped carbon fibers are derived from the carbonization of polyacrylonitrile.•NCFs-800 requires 114.3 mV to achieve 10 mA cm−2 in 0.5 M H2SO4.•Overpotential for achieving 10 mA cm−2 in 1 M KOH is 198.6 mV for NCFs. |
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ISSN: | 0360-3199 1879-3487 |
DOI: | 10.1016/j.ijhydene.2019.11.204 |