4.7 Article

Ultralow noble metals doping enables metal-organic framework derived Ni (OH)2 nanocages as efficient water oxidation electrocatalysts

期刊

CHEMICAL ENGINEERING JOURNAL
卷 429, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.132478

关键词

Noble metal doping; Ni(OH)(2) nanocages; Oxygen evolution reaction; Electrocatalysis

资金

  1. China Scholarship Council [201908430138]
  2. Natural Science Foundation of Hunan Province [2021JJ40430, 2019JJ50473, 2021JJ40431]
  3. Young Backbone Teachers Plan of Hunan Province (2018)
  4. Research Foundation of Education Bureau of Hunan Province [20A389, 20B459, 19C1332]
  5. Science and Technology Plan Project of Huaihua [2021R3108, 2020R2203]
  6. Scientific Research Project of Huaihua University [HHUY2020-02]

向作者/读者索取更多资源

This study successfully designed a novel type of ultralow noble metals doped hollow Ni (OH) (2) nanocage electrocatalysts, showing remarkable OER activity and outstanding performance. The catalyst modifies the electronic structure of Ni (OH) (2) and provides more exposed active sites, contributing to its remarkable OER performance.
Rational design of highly efficient electrocatalysts with favorable electronic and geometric structure toward sluggish oxygen evolution reaction (OER) grasps the key in unlocking the wide application of hydrogen energy through water electrolysis. Herein, an innovative type of ultralow noble metals (Ir and Ru) doped hollow Ni (OH)(2) nanocage electrocatalysts are successfully constructed through an ion-assisted etching protocol. Interestingly, a remarkable OER activity is achieved for Ir-Ni(OH)(2) nanocage, delivering a current density of 10 mA cm(-2) with an ultralow overpotential of 248 mV in 1 M KOH electrolyte. More importantly, this synthetic method can also be extended to the synthesis of Ru-Ni(OH)(2) nanocages with outstanding OER performance. Mechanism study reveals that the superior OER performance is attributed to the ultralow noble metal doping, which not only effectively modifies the electronic structure of Ni(OH)(2), but also functions as the active sites toward OER. Moreover, the highly open hollow nanocage structure enables the catalyst to provide more exposed active sites available for reaction intermediates, contributing to the outstanding OER performance.

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