首页> 外文期刊>Journal of the American Chemical Society >Electrocatalytic Hydrogen Evolution with a Cobalt Complex Bearing Pendant Proton Relays: Acid Strength and Applied Potential Govern Mechanism and Stability
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Electrocatalytic Hydrogen Evolution with a Cobalt Complex Bearing Pendant Proton Relays: Acid Strength and Applied Potential Govern Mechanism and Stability

机译:带有钴配合物的侧链质子继电器的电催化氢逸出:酸强度及其应用的电势调控机理和稳定性

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摘要

[Co(bapbpy)Cl]~+ (bapbpy. 6,6'-bis(2-aminopyrid-yl)-2,2'-bipyridine) is a polypyridyl cobalt(II) complex bearing both a redox-active bipyridine ligand and pendant proton relays. This compound catalyzes electro-assisted H_2 evolution in DMF with distinct mechanisms depending on the strength of the acid used as the proton source (_pK_a values ranging from 3.4 to 13.5 in DMF) and the applied potential. Electrochemical studies combining cyclic voltammetry and bulk electrolysis measurements enabled one to bring out four distinct catalytic processes. Where applicable, relevant kinetic information were obtained using either foot-of-the-wave analysis (FOWA) or analytical treatment of bulk electrolysis experiments. Among the different catalytic pathways identified in this study, a clear relationship between the catalyst performances and stability was evidenced. These results draw attention to a number of interesting considerations and may help in the development of future adequately designed catalysts.
机译:[Co(bapbpy)Cl]〜+(bapbpy.6,6'-双(2-氨基吡啶基)-2,2'-联吡啶)是一种聚吡啶基钴(II)配合物,带有氧化还原活性联吡啶配体和吊坠质子继电器。根据用作质子源的酸的强度(DMF中_pK_a值在3.4至13.5之间)和所施加的电势,该化合物以不同的机理催化DMF中的电助H_2演化。结合循环伏安法和本体电解测量法进行的电化学研究使人们可以得出四个不同的催化过程。在适用的情况下,可以使用波峰分析(FOWA)或大量电解实验的分析处理来获得相关的动力学信息。在本研究中确定的不同催化途径中,催化剂性能与稳定性之间存在明确的关系。这些结果引起人们对许多有趣考虑的注意,并可能有助于开发未来适当设计的催化剂。

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