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一维亚微米多钼酸盐形貌可控合成及氧的电催化还原研究(英文) 被引量:1

Morphology-controlled Synthesis of 1D Submicro-structured Polyoxomolybdate Towards Electrocatalytic Oxygen Reduction
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摘要 通过调节反应pH值和反应物种实现了一维亚微米多钼酸盐的控制合成,以钼酸铵和十二烷基苯磺酸钠为原料,在pH=6时制备出亚微米线,在pH=2时制备出亚微米棒,而以钼酸铵和氯化钠为原料,在pH=6时制备出纳米带.在pH=6时,纳米材料在长胶束内生长成亚微米线,而pH值降低至2时,过多的H+不仅会形成大量的Mo3O102-,还会使得胶束变短,因此使得亚微米材料变短,成为亚微米棒.在没有模板剂十二烷基苯磺酸钠时,多钼酸铵就会长成结构更为稳定的纳米带.循环伏安测试结果表明在有机溶剂中,多钼酸盐的亚微米棒对氧电催化还原具有优异活性.研究表明,由于有机醇能与电解质溶液中的H+反应,因此有机醇能显著促进一维多钼酸盐亚微米材料的氧的电催化活性. 1D submicro-structured polyoxomolybdate submicro-wires,submicro-rods and nanobelts were synthesized by altering the pH value and reactants.Submicro-wires could be obtained by reacting(NH 4) 6 Mo 7 O 24.4H 2 O with sodium dodecyl benzene sulfonate(SDBS) at pH = 6,and that for submicro-rods at pH = 2.However,nanobelts could be synthesized by reacting(NH 4) 6 Mo 7 O 24.4H 2 O with NaCl at pH = 6.In solution of pH = 6,polyoxomolybdate should grow up submicro-wires in long micelles.At pH = 2,not only more Mo 3 O 10 2,but also short micelles formed by excessive H + cations,which leaded to the submicro-rods.Without template SDBS,polyoxomolybdate may exist in stable nanobelts.Cyclic voltammetry results indicated that polymolybdate submicro-rods exhibited excellent activity for oxygen electroreduction in organic solvent.Because alcohol could react with H + in the electrolyte,the activity of oxygen electroreduction over polymolybdate could be obviously promoted in the presence of alcohol.
出处 《分子催化》 EI CAS CSCD 北大核心 2012年第6期529-536,共8页 Journal of Molecular Catalysis(China)
基金 The National Basic Research Program of China(973 Program,No.2007CB613305,2009CB22003,and 2009AA05Z117) NSFC21173242 the 863 program(No.2009AA05Z117) Chinese Academy of Sciences Knowledge Innovation Program(KGCX2-YW-390-1)
关键词 多钼酸盐 一维亚微米结构 氧电催化还原 醇促进作用 Polyoxomolybdate 1D submicro-structured Oxygen electroreduction Alcohol promoted
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  • 1Golabi S M, Golikand A N. J Electroanal. Chem. [ J ]. 2002, 521(1/2) : 161-167.
  • 2Jarvi T D, Sriramulu S, Stuve E M. J. Phys. Chem. B [J]. 1997, 101(19): 3649-3652.
  • 3Lee K, Savadogo O, Ishihara A, et al. J. Electrochem. Soc. [J]. 2006, lS3(1): A20-A24.
  • 4Yang H, Alonso-Vante N, L6ger J M, et al. J. Phys. Chem. B [J]. 2004, 108(6): 1938-1947.
  • 5Song S Q, Wang Y, Tsiakaras P, et al. Appl. Catal. B [J]. 2008, 78(3/4): 381-387.
  • 6Tominaka S, Momma T, Osaka T. Electrochim. Acta [J]. 2008, 53(14):4679-4686.
  • 7Mustain W E, Kepler K, Prakash J. Electrochem. Com- mun. [J]. 2006, 8(3) : 406-410.
  • 8Jeyabharathi C, Venkateshkumar P, Mathiyarasu J, et al. Electrochim. Acta [J]. 2008, 54(2) : 448-454.
  • 9Wang W M, Huang Q H, Liu J Y, et al. Electrochem. Commun. [J]. 2008, 10(9): 1396-1399.
  • 10LiHQ, XinQ, LiWZ, etal. Chem. Commun. [J]. 2004 : 2776-2777.

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