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The preparation and performance of high activity Ni-Cr binary catalysts for direct borohydride fuel cells 被引量:1

The preparation and performance of high activity Ni-Cr binary catalysts for direct borohydride fuel cells
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摘要 Ni-Cr binary anode catalysts used in direct borohydride fuel cells (DBFCs) were prepared using a constant potential electrodepo- sition method. Compared with pure metal Ni catalysts, the electro-oxidation currents of borohydride ions (BH-4) more than doubled when using Ni-Cr binary catalysts under the same conditions. The enhanced activity of the Ni-Cr binary catalysts could be attributed to the change in distribution of BH-4ions on the surface of the Ni electrode. This is due to Cr electrodeposits, which allows a greater number of hydrogen atoms to catalyze from each tetrahedron BH-4 ion. The performance of Ni-Cr binary catalysts could also be improved by optimizing the electrodeposition conditions. The results show that Ni-Cr binary catalysts are optimally prepared using an electrodeposition method of 1s with a Cr3+ concentration of 0.2 mol L-1 and a potential of -0.100 V. Ni-Cr binary anode catalysts used in direct borohydride fuel cells (DBFCs) were prepared using a constant potential electrodeposition method. Compared with pure metal Ni catalysts, the electro-oxidation currents of borohydride ions (BH4) more than doubled when using Ni-Cr binary catalysts under the same conditions. The enhanced activity of the Ni-Cr binary catalysts could be attributed to the change in distribution of BH4 ions on the surface of the Ni electrode. This is due to Cr electrodeposits, which allows a greater number of hydrogen atoms to catalyze from each tetrahedron BI-E ion. The performance of Ni-Cr binary catalysts could also be improved by optimizing the electrodeposition conditions. The results show that Ni-Cr binary catalysts are optimally prepared using an electrodeposition method of 1 s with a Cr^3+ concentration of 0.2 mol L^-1 and a potential of-0.100 V.
出处 《Chinese Science Bulletin》 SCIE EI CAS 2013年第20期2435-2439,共5页
基金 supported by the Graduate Student Science and Technology Innovation Foundation of Chongqing University (CDJXS10220013)
关键词 二元催化剂 硼氢化物 燃料电池 制备 NI-CR合金 性能 高活性 电沉积方法 Ni-Cr binary catalysts borohydride ion electro-oxidation fuel cell
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  • 1刘洁,刘世斌,张忠林,郝晓刚,李一兵.DMFC用阴极抗甲醇催化剂[J].电池,2006,36(1):77-79. 被引量:3
  • 2王久亮.形变与热处理对Cu-Cr合金力学性能的影响[J].热加工工艺,2006,35(10):16-18. 被引量:5
  • 3Demirci U B. Direct borohydride fuel cell: main issues met by the membrane-electrodes-assembly and potential solutions[ J]. J Power Sources,2007,172(2) :676 - 687.
  • 4Cheng H,Scott K, Lovell K V, et al. Evaluation of new ion exchange membranes for direct borohydride fuel cells[J]. J Membrane ,Science, 2007,288 ( 1-2 ) : 168 - 174.
  • 5Wee J H. A comparison of sodium borohydride as a fuel for proton exchange membrane fuel cells and for direct borohydride fuel cells [J]. J Power Sources,2006,155(2) :329 - 339.
  • 6Amendola S C, Onnerud P, Kelly M T, et al. A novel high power density borohydfide-air cell[ J ]. J Power Sources, 1999, 84 ( 1 ) : 130- 133.
  • 7Li Z P, Liu B H, Araa K, et al. Development of the direct borohydride fuel cell[J]. J Alloys Compd, 2005,404 - 406: 648 - 652.
  • 8Gyenge E. Electrooxidation of borohydride on platinum and gold electrodes:implications for direct borohydride fuel cells[J]. Electrochim Acta, 2004,49(6) : 965 - 978.
  • 9Leona C P,Walsh F C, Pleteher D, et al. Direct borohydride fuel cells[J]. J Power Sources,2006,155(2) : 172 - 181.
  • 10Mirkin M V, Fan F R F, Bard A J. Direct electrochemical measurements inside a 2000-angstrom thick polymer film by scanning electrochemical microscopy[J]. Science, 1992,257(5 068) :364 - 366.

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