4.7 Article

Ion modification of transition cobalt oxide by soaking strategy for enhanced water splitting

期刊

CHEMICAL ENGINEERING JOURNAL
卷 423, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.130218

关键词

Cobalt oxides; Nanoarray; Ion modification; Hydrogen; oxygen evolution reaction; Energy-free strategy

资金

  1. National Natural Science Foundation of China [51776094, 91963129]
  2. Foundation of Shenzhen Science and Technology Innovation Committee [JCYJ20180302174021198]
  3. Basic Research Project of Science and Technology Plan of Shenzhen [JCYJ20180504165655180]
  4. Special Funds for the Cultivation of Guangdong College Students' Scientific and Technological Innovation [pdjh2020c0]
  5. Fundamental Research Funds for the Central Universities [2020-YB-030, 2020IVA094]

向作者/读者索取更多资源

A smart soaking strategy of sulfur/iron ion modification was developed to activate Co3O4, forming a heterogeneous structure with excellent HER/OER performance. This study offers a facile approach for the development of transition metal oxides as splendid bifunctional catalysts, contributing to cost and energy savings for industrial applications and the design of advanced functional materials for energy chemistry.
Heterostructure engineering carries prime importance to enhance the catalytic activity of electrocatalysts for water splitting. However, developing nonprecious metal oxides as splendid bifunctional electrocatalysts in alkaline conditions remains a great challenge. Herein, we developed a smart soaking strategy of sulfur/iron ion modification, by which we could activate Co3O4 to spontaneously form heterogeneous structure with excellent hydrogen/oxygen evolution reaction (HER/OER) performance. The nickel foam supported Co3O4 nanoarrays embellished with NiCoSx (NiCoSx@Co3O4 NAs/NF) was easily obtained via sulfur ion modification, which has rich oxygen vacancies and active sites, leading to an outstanding HER performance (eta 10 = 59 mV, eta 400 = 264.0 mV). Furthermore, Fe(II) ion modified NiCoSx@Co3O4 NAs/NF (FeNiCoS@Co3O4 NAs/NF) achieved superior OER performance (eta 10 = 226 mV, eta 400 = 302 mV) than other recently reported cobalt-based catalysts due to the synergistic activity of Ni-Fe-S-Co. More importantly, this work offered a facile and energy-free strategy for developing transition metal oxides as splendid bifunctional catalysts and contributed to the cost and energy savings and mass production for industrial applications as well as the design of advanced functional materials for energy chemistry.

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