...
首页> 外文期刊>Comptes Rendus Chimie >Vanadium-substituted Dawson-type polyoxometalates as versatile electrocatalysts
【24h】

Vanadium-substituted Dawson-type polyoxometalates as versatile electrocatalysts

机译:钒取代的道森型多金属氧酸盐作为多功能电催化剂

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

A selected series of mono-and multi-V-substituted derivatives of Dawson type structure were synthesized and characterized with the aim of exploring their electrochemistry and their electrocatalytic abilities.The focus was placed on the electrochemistry of[P2V2W16O62]~(8-)as a representative example.The redox processes of its two V-centers were observed in a potential domain well positive of those of the W-centers.They are pH-dependent,the first redox process exhibiting only modest and progressively smaller potential shifts from pH 0 to 4,while the second wave was far more sensitive to acidity changes from pH 0 to 8.In contrast,mono-substituted derivatives display very small or no pH-dependence of the V-wave.Finally,combination of this diversity in the number of V atoms with the presence of As or P as the central heteroatom in these tungstic and molybdo-tungstic structures modulates substantially the apparent formal potentials that span the range from+569 mV to+122 mV vs SCE at pH 7.This leaves considerable flexibility in the choice of POMs for electrocatalytic purposes.The homogeneous oxidation and the electrocatalytic reduction of nitrite and the electrocatalytic oxidation of NAD(P)H by an appropriate selection of these V-substituted anions were studied.
机译:合成了一系列精选的Dawson型结构的单-和多-V-取代的衍生物,并进行了表征,以探讨其电化学性质和电催化能力。重点研究了[P2V2W16O62]〜(8-)一个典型的例子。在一个与W中心正相关的势域中观察到了它的两个V中心的氧化还原过程。它们是pH依赖的,第一个氧化还原过程从pH 0开始仅表现出适度的逐渐减小的电位漂移。到4,而第二个波对pH值从0到8的酸度变化更为敏感。相反,单取代衍生物对V波的显示很小或没有pH依赖性。最后,数量的这种多样性的组合在这些钨和钼-钨结构中,具有As或P作为中心杂原子的V原子的存在实质上调节了在pH 7时相对于SCE范围从+569 mV到+122 mV的表观形式电位。在为电催化目的选择POM时留下了很大的灵活性。研究了通过适当选择这些V取代的阴离子对亚硝酸盐进行均相氧化和电催化还原以及对NAD(P)H进行电催化氧化的方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号