期刊文献+

直接甲醇燃料电池的Ir-Fe/C阴极催化剂性能 被引量:1

Electrocatalytic Performance of Cathodic Ir-Fe/C Catalyst in Direct Methanol Fuel Cell
下载PDF
导出
摘要 合成了直接甲醇燃料电池的Ir-Fe/C阴极催化剂,用X射线衍射(XRD)谱和X射线能量色散谱(EDS)等方法对该催化剂进行表征,研究了碳载Ir-Fe(Ir-Fe/C)催化剂对氧还原的电催化活性和抗甲醇能力.研究发现,氧在碳载Ir(Ir/C)和Ir-Fe/C催化剂电极上还原的起始氧还原电位分别为0.57和0.65 V.在0.2 V下的电流密度分别为4.6和5.8 mA/cm2,表明Ir-Fe/C催化剂对氧还原的电催化性能要优于Ir/C催化剂,而且Ir-Fe/C催化剂也有很好的抗甲醇能力. Ir-Fe/C catalyst was prepared. The electrocatalytic activity of the Ir-Fe/C catalyst for the oxygen reduction and its methanol tolerance ability were investigated,based on the characterization with X-ray diffractometer(XRD) and energy dispersive spectrometer(EDS). The results show that the onset potentials of the oxygen reduction at the Ir/C and Ir-Fe/C catalyst electrodes are 0.57 and 0.65 V,respectively,and the current densities at 0.2 V are 4.6 and 5.8 mA/cm2,respectively.It indicates that the electrocatalytic activity of the Ir-Fe/C catalyst for the oxygen reduction is better than that of the Ir/C catalyst.In addition,the Ir-Fe/C catalyst possesses the high methanol tolerance ability.These results lay a strong basis for the use of the Ir-Fe/C cathodic catalyst in direct methanol fuel cell(DMFC).
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2012年第5期1007-1010,共4页 Chemical Journal of Chinese Universities
基金 国家自然科学基金(批准号:21073094) 江苏高校优势学科建设工程资助项目资助
关键词 碳载Ir-Fe催化剂 甲醇氧化 抗甲醇能力 直接甲醇燃料电池 Carbon supported Ir-Fe catalyst Methanol oxidation Methanol tolerance ability Direct methanol fuel cell(DMFC)
  • 相关文献

参考文献19

  • 1IEXiao-Feng(谢晓峰),FANXing-He(范星河).燃料电池技术[M],Bei jing:Chemical Industry Press,2004.
  • 2GUOPan-Pan(郭盼盼) LIWei-Shan(李伟善) HUANGYou-Ju(黄幼菊).电池工业,2008,13(4):141-146.
  • 3Demirci U. B.. J. Power Sources[J]. 2007, 169(2) : 239-246.
  • 4Heinzel A. , Barrag6n V. M.. J. Power Sources[J]. 1999, 84(1) : 70-74.
  • 5Wang W. , Zheng D. , Du C. , Zou Z. , Zhang X. , Xia B. , Yang H. , Akins D. L.. J. Power Sources[J]. 2007, 167(2) : 243-249.
  • 6Fernandez L. L., Walsh D. A., Bard A. J.. J. Am. Chem. Soc. [J]. 2005, 127(1) : 357-365.
  • 7Fernandez L. L., Raghuveer V., Manthiram A., Bard A. J.. J. Am. Chem. Soc. [J]. 2005, 127(38): 13100-13101.
  • 8RaghuveerV., Manthiram A., Bard A. J.. J. Phys. Chem. B[J]. 2005, 109(48) : 22909-22912.
  • 9Raghuveer V., Ferreira P. J., Manthiram A.. Electrochem. Commun. [J]. 2006, 8(5) : 807-814.
  • 10Tarasevich M. R. , Zhutaeva G. V. , Bogdanovskaya V. A. , Radina M. V. , Ehrenburg M. R. , Chalykh A. E.. Electrochim. Acta [J]. 2007, 52(15): 5108-5118.

二级参考文献14

  • 1陈煜,唐亚文,吴伟,曹洁明,刘长鹏,邢巍,陆天虹.合金化程度对炭载Pt-Ru催化剂性能的影响[J].高等学校化学学报,2006,27(4):676-679. 被引量:10
  • 2唐亚文,曹爽,陈煜,包建春,陆天虹.碳纳米管结构对碳纳米管载Pt催化剂电催化性能的影响[J].高等学校化学学报,2007,28(5):936-939. 被引量:15
  • 3de Vooys A.C.A.,Koper M.T.M.,van Santen R.A.,van Veen J.A.R.J..Electroanal.Chem.[J] ,2001,506:127-137.
  • 4HANYi-Ping(韩益苹) LUOPeng(罗鹏) CAIChen-Xin(蔡称心) LUTian-Hong(陆天虹).应用化学学报,2008,25:361-365.
  • 5Valentini L.,Cantalini C.,Lozzi L.,Picozzi S.,Armentano I.,Kenny J.M.,Santucci S..Sensor.Actuat.Chem.B[J] ,2004,100:33-40.
  • 6Wang J.J.,Yin G.P.,Shao Y.Y.,Wang Z.B.,Gao Y.Z..J.Phys.Chem.C[J] ,2008,112:5784-5789.
  • 7Park K.W.,Sung Y.E.,Han S.J.,Yun Y.K.,Hyeon T.H..J.Phys.Chem.B[J] ,2004,108:939-944.
  • 8Jie C.,Xiang X.,Peng X..Mater.Chem.Phys.[J] ,2009,116:57-61.
  • 9XICai-Ming(奚彩明) CHENYu(陈煜) ZHOUYi-Ming(周益明) TANGYa-Wen(唐亚文) CHENFeng-Feng(陈凤凤) LUTian-Hong(陆天虹).高等学校化学学报,2010,31(1):1-4.
  • 10Liu J.,Rinzler A.G.,Smalley R.E..Science[J] ,1998,280:1253-1256.

共引文献1

同被引文献14

  • 1ZHANG J, TANG S H, LIAO Y Y, et al. Progress in non-platinum catalysts with applications in low temperature fuel cells [J]. Chin J Catal, 2013, 34(6) :1051-1065.
  • 2YIN J, QIU Y J, YU J. Onion-like graphitic nanoshell structured Fe-N/C nanofibers deriverd from electrospinning for oxy- gen reduction reaction in acid media[ J]. Electrochem Commun, 2013, 30:1-4.
  • 3YANG S B, FENG X L, WANG X C, et al. Graphene-based carbon nitride nanosheets as efficient metal-free electrocata- lysts for oxygen reduction reactions[ J ]. Angew Chem Int Ed, 2011, 50(23 ) :5339-5343.
  • 4YANG Z Y, ZHANG Y X, LIN J, et al. Beanpod-shaped Fe-C-N composites as promising ORR catalyst for fuel cells opera- ted in neutral media[J]. J Mater Chem A, 2014, 2(8) :2623-2627.
  • 5LIANG H W, WEI W, WU Z S, et al. Mesoporous metal-nitrogen-doped carbon electrocatalysts for highly efficient oxygen reductionreaction[J].JAmChemSoc,2013,135(43):16002-16005.
  • 6WANG Y R, OHNISHI R, YOO E, et al. Nano- and micro-sized TiN as the electrocatalysts for ORR in Li-air fuel cell with alkaline aqueous electrolyte[ J]. J Mater Chem, 2012, 22(31) : 15549-15555.
  • 7AVASARALA B, HALDAR P. On the stability of TiN-based electrocatalysts for fuel cell applications [ J ]. Int J Hydrogen Energy, 2011, 36(6) :3965-3974.
  • 8KIM H, MINK C, JEONG A K, et al. Highly efficient and durable TiN nanofiber electrocatalysts supports[ J]. Nanoscale, 2015, 7(44) : 18429-18434.
  • 9AVASARALA B, HALDAR P. Elcetrochemical oxidation behavior of titanium nitride based electi'ocatalyst under PEM fuel cell conditions [ J ]. Electrochim Acta, 2010, 55 (28) :9024-9034.
  • 10YANG D, BHATTACHARJYA D, INAMDAR S, et al. Phosphorus-doped ordered mesoporous carbons with different lengths as efficient metal-free electrocatalysts for oxygen reduction reaction in alkaline media[ J]. J Am Chem Soc, 2012, 134 (39) :16127-16130.

引证文献1

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