期刊文献+

形貌可控的钯纳米粒子的电化学制备及电催化性质 被引量:9

Electrochemical Preparation of Shape-controlled Pd Nanoparticles and Their Electrocatalytic Properties
下载PDF
导出
摘要 以NaPdCl4为前驱体,以柠檬酸钠为包裹剂,通过两步恒电势法在氧化铟锡(ITO)导电玻璃基底上沉积得到不同形貌的钯纳米粒子(PdNPs).通过调节晶种沉积电势和粒子生长电势、柠檬酸根和溴离子的浓度及反应温度等因素,可以控制PdNPs的形貌、尺寸及在ITO基底上的生长密度;制备出了钯纳米锥阵列及球形、花状和多面体形的PdNPs.研究结果表明,钯纳米锥阵列与其它形状的PdNPs相比,在单位面积ITO基底上具有更大的表面积,表现出对甲醇更强的电化学氧化能力. The electrochemical preparation of shape-controlled palladium nanoparticles (PdNPs) and their catalytic activity toward methanol electrooxidation were reported. PdNPs were prepared on indium tin oxides (ITO) conductive substrates by a two-step constant potential deposition method, in which Na2PdCl4 and citrate were used as precursor and capping agent. The morphology, size, and growing density of PdNPs can be controlled by varying the electrodeposition parameters, such as nanoseeds generation potential, particle growth potential, the concentration of citrate and bromide, and the deposition temperature. The Pd nanohorn arrays, spherical, flower-like and polyhedronal PdNPs were prepared on ITO substrates. The electrocatalytic properties for methanol oxidation on PdNPs with different morphologies were investigated in alkaline solution. Compared with other PdNPs, the Pd nanohorns demonstrated a much larger surface area on an ITO substrate with a fixed area due to their larger height. As a result, the Pd nanohorn arrays exhibite a higher catalytic activity toward methanol electrooxidation, making them a potential candidate for alkaline direct fuel cell anode materials.
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2011年第11期2650-2656,共7页 Chemical Journal of Chinese Universities
基金 国家自然科学基金(批准号:20973020 20773007) 高等学校博士学科点基金(博导类)(批准号:20101102110002) 新世纪优秀人才支持计划(批准号:NCET-08-0034)资助
关键词 钯纳米粒子 电化学沉积 氧化铟锡导电玻璃 甲醇 电催化 Palladium nanoparticle Electrodeposition Indium tin oxides (ITO) conductive glass Methanol Electrocatalysis
  • 相关文献

参考文献34

  • 1Xiong Y. J. , Chen J. Y. , Wiley B. , Xia Y. N.. J. Am. Chem. Soc. [J] , 2005, 127(20) : 7332-7333.
  • 2Xiong Y. J., Cai H. G., Wiley B. J., WangJ. G., KimM. J., XiaY. N.. J. Am. Chem. Soc. [J], 20071 129(12):3665-3675.
  • 3Huang X. Q. , Tang S. H. , Zhang H. H. , Zhou Z. Y. , Zheng N. F.. J. Am. Chem. Soc. [J~ , 2009, 131(39) : 13916-13917.
  • 4XiongY. J., MclellanJ. M., ChenJ. Y., YinY. D., LiZ. Y., XiaY. N.. J. Am. Chem. Soc.[J~, 2005, 127(48): 17118- 17127.
  • 5Xiong Y. J. , Washio I. , Chen J. Y. , Cai H. G. , Li Z. Y. , Xia Y. N.. Langmuir[J] , 2006 22(20) : 8563-8570.
  • 6Berhauh G. , Bausach M. , Bisson L. , Becerra L. , Thomazeau C. , Uzio D.. J. Phys. Chem. C[J], 2007, 111(16) : 5915-5925.
  • 7Umar A. A. , Oyama M.. Cryst. Growth Des.[J] , 2008, 8(6): 1808-1811.
  • 8Chen Y. H., Hung H. H., Huang M. H.. J. Am. Chem. Soc. [J], 2009, 131(25): 9114--0121.
  • 9Bisson L. , Boissiere C. , Nicole L. , Grosso D. , Jolivet J. P. , Thomazeau C. , Uzio D. , Berhauh G. , Sanchez C.. Chem. Mat. [J] , 2009, 21(13) : 2668-2678.
  • 10Niu W. X. , Zhang L. , Xu G. B.. ACS Nano[J] , 2010, 4(4) : 1987-1996.

同被引文献152

引证文献9

二级引证文献9

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部