Retracted: Earth‐Abundant Iron Diboride (FeB<sub>2</sub>) Nanoparticles as Highly Active Bifunctional Electrocatalysts for Overall Water Splitting

  • Hui Li
    Department of Chemistry Wake Forest University Winston‐Salem NC 27106 USA
  • Peng Wen
    Institute of Functional Nano and Soft Materials (FUNSON) Soochow University Suzhou Jiangsu 215123 China
  • Qi Li
    Physical Science Department IBM TJ Watson Center Yorktown Heights NY 10598 USA
  • Chaochao Dun
    Center for Nanotechnology and Molecular Materials Department of Physics Wake Forest University Winston‐Salem NC 27109 USA
  • Junheng Xing
    Department of Chemical Engineering and Materials Science Wayne State University Detroit MI 48202 USA
  • Chang Lu
    Department of Chemistry Wake Forest University Winston‐Salem NC 27106 USA
  • Shiba Adhikari
    Department of Chemistry Wake Forest University Winston‐Salem NC 27106 USA
  • Lin Jiang
    Institute of Functional Nano and Soft Materials (FUNSON) Soochow University Suzhou Jiangsu 215123 China
  • David L. Carroll
    Center for Nanotechnology and Molecular Materials Department of Physics Wake Forest University Winston‐Salem NC 27109 USA
  • Scott M. Geyer
    Department of Chemistry Wake Forest University Winston‐Salem NC 27106 USA

書誌事項

公開日
2017-05-11
権利情報
  • http://onlinelibrary.wiley.com/termsAndConditions#vor
DOI
  • 10.1002/aenm.201700513
公開者
Wiley

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説明

<jats:p>Developing efficient, durable, and earth‐abundant electrocatalysts for both hydrogen and oxygen evolution reactions is important for realizing large‐scale water splitting. The authors report that FeB<jats:sub>2</jats:sub> nanoparticles, prepared by a facile chemical reduction of Fe<jats:sup>2+</jats:sup> using LiBH<jats:sub>4</jats:sub> in an organic solvent, are a superb bifunctional electrocatalyst for overall water splitting. The FeB<jats:sub>2</jats:sub> electrode delivers a current density of 10 mA cm<jats:sup>−2</jats:sup> at overpotentials of 61 mV for hydrogen evolution reaction (HER) and 296 mV for oxygen evolution reaction (OER) in alkaline electrolyte with Tafel slopes of 87.5 and 52.4 mV dec<jats:sup>−1</jats:sup>, respectively. The electrode can sustain the HER at an overpotential of 100 mV for 24 h and OER for 1000 cyclic voltammetry cycles with negligible degradation. Density function theory calculations demonstrate that the boron‐rich surface possesses appropriate binding energy for chemisorption and desorption of hydrogen‐containing intermediates, thus favoring the HER process. The excellent OER activity of FeB<jats:sub>2</jats:sub> is ascribed to the formation of a FeOOH/FeB<jats:sub>2</jats:sub> heterojunction during water oxidation. An alkaline electrolyzer is constructed using two identical FeB<jats:sub>2</jats:sub>‐NF electrodes as both anode and cathode, which can achieve a current density of 10 mA cm<jats:sup>−2</jats:sup> at 1.57 V for overall water splitting with a faradaic efficiency of nearly 100%, rivalling the integrated state‐of‐the‐art Pt/C and RuO<jats:sub>2</jats:sub>/C.</jats:p>

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