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Controlled Anisotropic Growth of Co-Fe-P from Co-Fe-O Nanoparticles.
Mendoza-Garcia, Adriana; Zhu, Huiyuan; Yu, Yongsheng; Li, Qing; Zhou, Lin; Su, Dong; Kramer, Matthew J; Sun, Shouheng.
Afiliación
  • Mendoza-Garcia A; Department of Chemistry, Brown University, Providence, RI 02912 (USA).
  • Zhu H; Department of Chemistry, Brown University, Providence, RI 02912 (USA).
  • Yu Y; Present address: Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831 (USA).
  • Li Q; Department of Chemistry, Brown University, Providence, RI 02912 (USA).
  • Zhou L; Present address: School of Chemical Engineering and Technology, Harbin Institute of Technology, Harbin, Heilongjiang 150001 (China).
  • Su D; Department of Chemistry, Brown University, Providence, RI 02912 (USA).
  • Kramer MJ; The Ames Laboratory, US Department of Energy, Iowa State University, Ames, IA 50011 (USA).
  • Sun S; Center for Functional Nanomaterials, Brookhaven National Laboratory, Upton, NY 11973 (USA).
Angew Chem Int Ed Engl ; 54(33): 9642-5, 2015 Aug 10.
Article en En | MEDLINE | ID: mdl-26118355
ABSTRACT
A facile approach to bimetallic phosphides, Co-Fe-P, by a high-temperature (300 °C) reaction between Co-Fe-O nanoparticles and trioctylphosphine is presented. The growth of Co-Fe-P from the Co-Fe-O is anisotropic. As a result, Co-Fe-P nanorods (from the polyhedral Co-Fe-O nanoparticles) and sea-urchin-like Co-Fe-P (from the cubic Co-Fe-O nanoparticles) are synthesized with both the nanorod and the sea-urchin-arm dimensions controlled by Co/Fe ratios. The Co-Fe-P structure, especially the sea-urchin-like (Co(0.54)Fe(0.46))2P, shows enhanced catalysis for the oxygen evolution reaction in KOH with its catalytic efficiency surpassing the commercial Ir catalyst. Our synthesis is simple and may be readily extended to the preparation of other multimetallic phosphides for important catalysis and energy storage applications.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2015 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2015 Tipo del documento: Article
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