4.7 Article

Fabrication of nanoporous Si electrocathode by high-energy argon ion irradiation for improved electrocatalytic hydrogen production

期刊

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 43, 期 1, 页码 64-71

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2017.08.034

关键词

Nanoporous Si; Hydrogen evolution reaction; Ions irradiation; Electrocatalysis

资金

  1. National Science Fund for Excellent Young Scholars [11522543]
  2. Natural Science Foundation of China [11475129, 51571153, 11375134]
  3. Natural Science Foundation of Hubei Province, China [2016CFA080]
  4. Natural Science Foundation of Jiangsu Province, China [BK20161247, BK20141212]
  5. Fundamental Research Funds for the Central Universities [2042017kf0194]

向作者/读者索取更多资源

Developing a cost-effective material to replace Pt catalysts for hydrogen evolution reaction (HER) holds great promising for clean energy technologies. In this work, we developed a simple way to prepare nanoporous Si by argon ion irradiation at 90 keV to fluences of 0.5, 1, 2 x 10(17) ions/cm(2). After post-irradiation annealing at 700 degrees C in vacuum (2 x 10(-4) pa) for 5 h, the nanoporous Si was formed which displays largely enhanced electrocatalytic water splitting compared with the unirradiated Si. We also investigated the influence of fluence on morphology and the HER performance of the electrocathodes. It was found that 1 x 10(17) Ar+ ions/cm(2) irradiated Si showed the highest HER performance. The largely enhanced HER activity comes from the unique morphology which results by Ar+ ions irradiation and post irradiation annealing. We further fabricated electrocathodes by coating Ni film on the nanoporous Si, significant improvement of the HER performance compared with Ni coated planar Si was found. Using the ion irradiation technology, we developed a new method to fabricate electrocathode with large specific surface area for largely enhanced hydrogen evolution reaction activities. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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