Two new inorganic-organic hybrid single pendant hexadecavanadate derivatives with bifunctional electrocatalytic activities

被引:36
作者
Dong, Baoxia [1 ]
Peng, Jun [1 ]
Tian, Aixiang [1 ]
Sha, Jingquan [1 ]
Li, Li [1 ]
Liu, Hongsheng [1 ]
机构
[1] NE Normal Univ, Fac Chem, Minist Educ, Keu Lab Polyoxometalate Sci, Changchun 130024, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
bifunctional electrocatalyst; electrochemistry; carbon paste electrode; hexadecavanadate; supramolecular architecture;
D O I
10.1016/j.electacta.2006.10.065
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Two new supramolecular assembly hexadecavanadate derivatives of H-2[Cd(phen)(3)](2){[Cd(H2O)(phen)(2)](V16O38Cl)}.2.5H(2)O 1 (phen = 1,10'-phenanthroline) and H-2[Cd(bipy)(3)][Cd(H2O)(bipy)(2)]{[Cd(H2O)(bipy)(2)](V16O38Cl)} center dot 1.5H(2)O(2) (bipy = 2,2'-bipyridine), have been prepared under mild hydrothermal conditions and structurally characterized by IR, XPS spectra, TG analyses and single-crystal X-ray diffraction. Compounds 1 and 2 are constructed from single pendant [CdL2] (L = phen, 1 and L = bipy, 2) modified hexadecavanadates. The hybrids 1 and 2 were used as solid bulkmodifier to fabricate bulk-modified carbon paste electrodes (CPEs) (1-CPE and 2-CPE) by direct mixing. The electrochemical behaviors and electrocatalysis of 1-CPE and 2-CPE indicate bifunctional electrocatalytic activities toward both the oxidation and reduction of nitrite. Furthermore, their electrocatalytic activities toward the reduction of bromate and oxidation of ascorbic acid are also studied in 1 M H2SO4 aqueous solutions. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3804 / 3812
页数:9
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