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Synthesis of a highly active carbon-supported Ir-V/C catalyst for the hydrogen oxidation reaction in PEMFC

期刊

ELECTROCHIMICA ACTA
卷 54, 期 24, 页码 5614-5620

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2009.04.065

关键词

Anode; Ir-based catalyst; Ethylene glycol method; Hydrogen oxidation; PEMFC

资金

  1. Ministry of Science and Technology of China [2007DFC61690]
  2. National Research Council of Canada (MOST-NRC)
  3. Tongji University
  4. Program of Introducing Talents of Discipline (111 project)

向作者/读者索取更多资源

The active, carbon-supported It and Ir-V nanoclusters with well-controlled particle size, dispersity, and composition uniformity, have been synthesized via an ethylene glycol method using IrCl3 and NH4VO3 as the It and V precursors. The nanostructured catalysts were characterized by X-ray diffraction and high-resolution transmission electron microscopy. The catalytic activities of these carbon-supported nanoclusters were screened by applying on-line cyclic voltammetry and electrochemical impedance spectroscopy techniques, which were used to characterize the electrochemical properties of fuel cells using several anode Ir/C and Ir-V/C catalysts. It was found that Ir/C and Ir-V/C catalysts affect the performance of electrocatalysts significantly based on the discharge characteristics of the fuel cell. The catalyst Ir-V/C at 40 wt.% displayed the highest catalytic activity to hydrogen oxidation reaction and, therefore, high cell performance is achieved which results in a maximum power density of 563 mW cm(-2) at 0.512 V and 70 degrees C in a real H-2/air fuel cell. This performance is 20% higher as compared to the commercial available Pt/C catalyst. Fuel cell life test at a constant current density of 1000 mA cm(-2) in a H-2/O-2 condition shows good stability of anode Ir-V/C after 100 h of continuous operation. (C) 2009 Elsevier Ltd. All rights reserved.

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