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Pt掺杂的纳米Ni电催化氧化甲醇性能的研究 被引量:5

Performance of Nano-Ni Doped with Pt for Methanol Electro-catalytic Oxidation
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摘要 采用溶胶凝胶法制备了碳载纳米双金属Ni-Pt(5%,质量分数)/C电催化剂,用TEM、XRD和XPS表征金属粒子的形貌、晶相结构、表面元素及其价态,循环伏安法测试催化剂在碱性溶液中电催化氧化甲醇的活性。结果表明,Ni-Pt金属粒子在碳载体上分布均匀,粒径为3~6nm,少量Pt的掺杂对纳米Ni活性有明显提高,其中,合金型Ni-Pt(5%)/C在1.0mol/LNaOH+1.0mol/LCH3OH溶液中峰电流密度可达85.6mA/mg,是Ni/C峰电流密度的8.7倍,达到Pt/C峰电流密度的15.3%。单位质量铂的电流显著提高。 Carbon supported nano-nickel-platinum electrocatalyst samples of Ni-Pt(5wt%)/C were prepared by the colloidal-gelatin method.Transmission electron microscopy(TEM),X-ray diffraction(XRD) and X-ray photoelectron spectroscopy(XPS) were used to evaluate the metal particles' morphology,crystal configuration,superficial element constitution and value.Moreover,cyclic voltammeter was employed to measure the catalytic activity for the electro-catalytic oxidation of methanol in an alkaline medium.The results show that Ni-Pt particles are distributed homogeneously on the carbon,with the particle sizes of 3-6 nm;the Pt doping improves largely the activity of Ni nano-particles,and the peak current density of alloy Ni-Pt(5wt%)/C catalyst reaches 85.6 mA/mg in the solution of 1.0 mol/L NaOH + 1.0 mol/L CH3OH,which is 8.7 times of that of Ni/C,and 15.3% of that of Pt/C.The current of Pt per unit mass is increased obviously.
出处 《稀有金属材料与工程》 SCIE EI CAS CSCD 北大核心 2012年第1期58-63,共6页 Rare Metal Materials and Engineering
基金 国家自然科学基金(20676088 20776091) 高校博士点基金(200801120010) 太原科技局大学生创新创业专项(09122049)资助
关键词 Ni-Pt/C 电催化 甲醇电氧化 碱性介质 Ni-Pt/C electro-catalysis methanol electro-oxidation alkaline media
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参考文献16

  • 1Kumar K S, Prathap Haridoss, Seshadri S K. J Surf Coat Technol[J], 2008, 202(9): 1764.
  • 2Shobha T, Aravinda C L, Parthasarathi Bet al. J Mater Chem Phys[J], 2003, 80(3): 656.
  • 3Orozco G, Pe'rez M C, Rinco'n A et al. JElectroanal Chem[J], 2000, 495(1): 71.
  • 4Guo D J, Li H L. J Carbon[J], 2005, 43(6): 1259.
  • 5Khalil M W, Abdel Rahim M A, Zimmer A et al. J Power Sources[J], 2005, 144(1): 35.
  • 6Abdel Rahim M A, Abdel Hameed R M, Khalil M W. J Power Sources[J], 2004, 134(2): 160.
  • 7Abdel Rahim M A, Hanaa B, Hassan R M et al. J Power Sources[J], 2006, 154(1): 59.
  • 8Kowal A, Port S N, Nichols R J. J Catal Today[J], 1997, 38(4): 483.
  • 9Taraszewska J, Rosonel G. J Electroanal Chem[J], 1994, 364(1-2): 209.
  • 10El-shafei AA. JElectroanal Chem[J], 1999, 471(2): 89.

二级参考文献29

  • 1Schultz T, Zhou S, Sundmaeher K. Chem Eng & Tech[J], 2001, 24:1223.
  • 2Hamnet A. Catal Today[J], 1997, 38:445.
  • 3Tarasevich M R, Kariehev Z R, Bogdanovskaya V A. Russian Journal of Electrochemistry[J], 2005, 41: 736.
  • 4Shen P K, Xu C W. Electrochemistry Communications[J], 2006, 8:184.
  • 5Prabhram J, Manoharan R. J Applied Electrochemistry[J], 1998, 28:935.
  • 6Wang Y, Li L, Hu Let al. Electrochemistry Communications[J], 2003, 5(8): 662.
  • 7Grigoriev S A, Lyutikova E K, Martemianov S et al. Journal of Hydrogen Energy[J], 2007, 32:4438.
  • 8Luo J, Lou Y B, Mathew M Met al. Electrochemistry Communications[J], 2001, 3:172.
  • 9Zhang X, Zhang F, Chan K Y et al. Catalysis Communications [J], 2004, 5:749.
  • 10Choi J H, Park K W, Lee H K et al. Electrochimica Acta[J], 2003, 48:2781.

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  • 1许炜,陶占良,陈军.储氢研究进展[J].化学进展,2006,18(2):200-210. 被引量:92
  • 2Kim T. International Journal of Hydrogen Energy [J], 2012, 37 2440.
  • 3Orimo S, Nakamori Y, Eliseo J R et al. Chemical Reviews[J], 2007, 107: 4111.
  • 4Makowski P, Thomas A, Kuhn Pet al. Energy Environmental Science[J], 2009, (2): 480.
  • 5Zhao B, Song J, Ran R et al. International Journal of Hydrogen Energy[J], 2012, 37:1133.
  • 6Jiang H L, Singh S K, Yah J Metal. Chem Sus Chem[J], 2010, 35:41.
  • 7Umegaki T, Yan J M, Zhang X Bet al. International Journal of Hydrogen Energy [J], 2009, 34:2303.
  • 8Kojima Y, Haga T. International Journal of Hydrogen Energy [J], 2003, 28 (9): 989.
  • 9Cavaliere S, Hannauer J, Demirci U Bet al. Catalysis Today [J], 2011, 170:3.
  • 10Simona B, Yu H, Emil O et al. International Journal of Hydrogen Energy [J], 2011, 36:7431.

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