期刊文献+

磷钨酸修饰活性炭载Pd催化剂的制备及对甲酸氧化的电催化性能 被引量:4

Preparation of Phosphotungstic Acid-modified Carbon Supported Pd Catalyst and Its Electrocatalytic Performance for Formic Acid Oxidation
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摘要 通过水浴浸泡制备了磷钨酸(PWA)修饰的活性炭(PWA/C),再通过液相还原法将Pd沉积于PWA/C复合载体上制备了Pd-PWA/C催化剂.采用X射线能量色散(EDS)谱、X射线衍射(XRD)谱、透射电子显微镜(TEM)和X射线光电子能谱(XPS)对产物进行表征.结果表明,磷钨酸修饰活性炭不仅能有效降低Pd纳米粒子的粒径,而且与Pd纳米粒子间发生了强烈作用.电化学测试结果显示,Pd-PWA/C催化剂对甲酸氧化的电催化活性和稳定性均远优于Pd/C催化剂,这是由于Pd与PWA/C间的强烈作用既能有效降低CO在催化剂上的吸附强度和吸附量,又能降低甲酸分解的速率,从而减弱CO的毒化作用. Activated carbon was modified with phosphotungstic acid(PWA) at 80 ~C in a water bath, Pd was then loaded on the PWA/C hybrid support to prepare Pd-PWA/C catalyst by a simple impregnation-reduction method. The measurements of energy dispersive X-ray spectroscopy(EDS) , X-ray diffraction(XRD) pattern, transmission electron microscopy(TEM) and X-ray photoelectron spectroscopy (XPS) indicate that phospho- tungstie acid-modified carbon not only decreases the average size of Pd nanopartieles effectively but also interacts with Pd nanoparticles strongly. The electrochemical measurements demonstrate that the electrocataly- tic activity and stability of the Pd-PWA/C catalyst for formic acid oxidation are much better than that of the Pd/C catalyst. It is due to that the strong interaction between Pd and PWA/C not only decreases the adsorp- tion strength and amount of CO at the catalyst electrode but also decreases the decomposition rate of formic acid to decrease the CO poisoning.
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2014年第1期115-120,共6页 Chemical Journal of Chinese Universities
基金 国家自然科学基金(批准号:21073094,21273116,21201105,61171015) 江苏高校优势学科建设工程项目资助~~
关键词 钯催化剂 磷钨酸 甲酸氧化 甲酸分解 Pd catalyst Phosphotungstic acid Formic acid oxidation Decomposition of formic acid
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参考文献24

  • 1Yu X.,Pickup P.G.,J.Power Sources,2008,182(1),124-132.
  • 2Rhee Y.W.,Ha S.Y.,Masel R.I.,J.Power Sources,2003,117(1/2),35-38.
  • 3Lu L.,Li H.Z.,Hong Y.J.,Luo Y.F.,Tang Y.W.,Lu T.H.,J.Power Sources,2012,210(1),154-157.
  • 4Rice C.J.,Power Sources,2003,115(2),229-235.
  • 5Cheng T.T.,Gyenge E.L.,J.Appl.Electrochem.,2009,39(8),1925-1938.
  • 6李焕芝,沈娟章,杨改秀,唐亚文,陆天虹.直接甲酸燃料电池Pd阳极催化剂及其电催化稳定性[J].高等学校化学学报,2011,32(7):1445-1450. 被引量:19
  • 7Bulushev D.A.,Beloshapkin S.,Ross J.R.H.,Catal.Today,2010,154(1/2),7-12.
  • 8Ivanov E.A.,Popova G.Y.,Chesalov Y.A.,Andrushkevich T.V.,J.Mol.Catal.A: Chem.,2009,312(1/2),92-96.
  • 9Lu L.,Shen L.P.,Shi Y.,Chen T.T.,Jiang G.Q.,Ge C.W.,Tang Y.W.,Chen Y.,Lu T.H.,Electrochim.Acta,2012,85(1),187-194.
  • 10沈娟章,陈滢,杨改秀,唐亚文,陆天虹.直接甲酸燃料电池炭载Pd阳极催化剂的稳定性[J].高等学校化学学报,2011,32(11):2626-2629. 被引量:5

二级参考文献42

  • 1吕艳卓,韩飞,刘长鹏,李长志,邢巍,陆天虹,桑革.杂多酸修饰的电极对于甲醇电氧化的促进作用[J].高等学校化学学报,2004,25(10):1909-1911. 被引量:16
  • 2袁青云,唐亚文,周益明,刘长鹏,邢巍,陆天虹.甲酸作直接甲醇燃料电池替代燃料[J].应用化学,2005,22(9):929-932. 被引量:25
  • 3Rice C. , Ha S. , Masel R. I. , et al.. J. Power Sources[J] , 2003, 115:229-235
  • 4Ha S., Larsen R., Masel R I.. J. Power Sources[J], 2005, 144:28-34
  • 5Zhang L. L., Tang Y. W., Lu T. H., et al.. J. Power Sources[J], 2006, 162:177-179
  • 6Zhang L. L. , Lu T. H. , Li C. , et al.. Electrochem. Comm..[J] , 2006, 8:1625-1627
  • 7Llorca M. J. , Feliu J. M. , Aldaz A. , et al.. J. Electroanal. Chem. [J] , 1994, 376:151-160
  • 8Baldauf M. , Kolb D. M.. J. Phys. Chem. [J], 1996, 100:11375-11381
  • 9Thomas F. S. , Masel R. I.. Surface Science [J] , 2004, 573:169-175
  • 10Wang X. , Tang Y. W. , Lu T. H. , et al.. J. Power Sources[J] , 2008, 175:784-788

共引文献31

同被引文献89

  • 1袁青云,唐亚文,周益明,刘长鹏,邢巍,陆天虹.甲酸作直接甲醇燃料电池替代燃料[J].应用化学,2005,22(9):929-932. 被引量:25
  • 2Bartoli G., Marcantoni E., Sambri L., Synlett, 2003, (14), 2101—2116.
  • 3Bartoli G., Bosco M., Bellucci M. C., Marcantoni E., Sambri L., Torregiani E., Eur. J. Org. Chem., 1999, 617—620.
  • 4Bartoli G., Bartolacci M., Giuliani A., Marcantoni E., Massaccesi M., Torregiani E., J. Org. Chem., 2005, 70(1), 169—174.
  • 5Garg S. K., Kumar R., Chakraborti A. K., Synlett, 2005, (9), 1370—1374.
  • 6Garg S. K., Kumar R., Chakraborti A. K., Tetrahedron Lett., 2005, 46(10), 1721—1724.
  • 7Kawatsura M., Komatsu Y., Yamamoto M., Hayase S., Itoh T., Tetrahedron, 2008, 64(16), 3488—3493.
  • 8Yadav L. D. S., Rai V. K., Tetrahedron Lett., 2008, 49(38), 5553—5556.
  • 9Bartoli G., Bellucci M. C., Petrini M., Marcantoni E., Sambri L., Torregiani E., Org. Lett., 2000, 2(13), 1791—1793.
  • 10Bartoli G., Di Antonio G., Giovannini R., Giuli S., Lanari S., Paoletti M., Marcantoni E., J. Org. Chem., 2008, 73(5), 1919—1924.

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