Institut Lavoisier de Versailles, UMR 8180, Université de Versailles Saint-Quentin en Yvelines, 45 Avenue des Etats-Unis, 78035 Versailles cedex, France.
J Am Chem Soc. 2011 Aug 31;133(34):13363-74. doi: 10.1021/ja201165c. Epub 2011 Aug 5.
The grafting of the triangular 1,3,5-benzene tricarboxylate linkers (denoted trim) on tetrahedral ε-Keggin polyoxometalates (POMs) capped by Zn(II) ions, formed in situ under hydrothermal conditions, has generated three novel POM-based metal organic frameworks (POMOFs). (TBA)(3)[PMo(V)(8)Mo(VI)(4)O(36)(OH)(4)Zn(4)]C(6)H(3)(COO)(3)·6H(2)O (ε(trim)(4/3)) is a 3D open-framework built of molecular Keggin units connected by trim linkers, with channels occupied by tetrabutylammonium (TBA) counterions. ε(trim)(4/3) is a novel (3,4)-connected net, named ofp for open-framework polyoxometalate, and computer simulations have been used to evaluate its relative stability in comparison with ctn- and bor-like polymorphs, showing the stability of this novel phase directly related to its greatest density. A computational study was also undertaken with the aim of locating TBA molecules, the positions of which could not be deduced from single crystal X-ray diffraction, and further rationalizes their structure directing role. In (TBA)(3)[PMo(V)(8)Mo(VI)(4)O(37)(OH)(3)Zn(4)][C(6)H(3)(COO)(3)] (ε(2)(trim)(2)), the building unit is not the molecular Keggin but a dimerized form of this POM. Their connection via trim linkers generates a 3D framework with channels filled by TBA cations. In (TBA)(3)[PMo(V)(8)Mo(VI)(4)O(37)(OH)(3)Zn(4)][C(6)H(3)(COO)(3)]·8H(2)O (ε(trim)), zigzag chains are connected via the organic linkers, forming 2D grids. Modified electrodes were fabricated by direct adsorption of the POMOFs on glassy carbon or entrapment in carbon paste (CPE). A remarkable electrocatalytic hydrogen evolution reaction (HER) was detected with a yield greater than 95%, and a turnover number as high as 1.2 × 10(5) was obtained after 5 h. The reported POMOF-based electrodes are more active than platinum, with a roughly 260 mV anodic shift. Finally, the electrocatalytic activities of ε(trim)(4/3)/CPE electrodes in various XCl (X = Li, Na, K, Cs) media have been studied. This allowed us to detect a cation effect and propose an electrocatalytic mechanistic pathway for the HER.
三尖式 1,3,5-苯三甲酸配体(记为 trim)接枝到四面体 ε-Keggin 多金属氧酸盐(POM)上,这些 POM 由 Zn(II) 离子封端,在水热条件下原位形成,生成了三种新型的基于 POM 的金属有机骨架(POMOF)。(TBA)(3)[PMo(V)(8)Mo(VI)(4)O(36)(OH)(4)Zn(4)]C(6)H(3)(COO)(3)·6H(2)O (ε(trim)(4/3)) 是一种由分子 Keggin 单元通过 trim 连接体连接而成的 3D 开放式骨架,通道中填充有四丁基铵(TBA)抗衡离子。ε(trim)(4/3) 是一种新型的(3,4)连接网络,命名为 ofp 代表开放式骨架多金属氧酸盐,计算机模拟用于评估其与 ctn-和 bor-like 多晶型物相比的相对稳定性,表明这种新型相的稳定性与其最大密度直接相关。还进行了一项计算研究,旨在确定 TBA 分子的位置,这些位置无法从单晶 X 射线衍射中推断出来,并进一步合理化它们的结构导向作用。在 (TBA)(3)[PMo(V)(8)Mo(VI)(4)O(37)(OH)(3)Zn(4)][C(6)H(3)(COO)(3)] (ε(2)(trim)(2)) 中,构建单元不是分子 Keggin,而是这种 POM 的二聚体形式。它们通过 trim 连接体的连接生成了一个充满 TBA 阳离子的 3D 骨架。在 (TBA)(3)[PMo(V)(8)Mo(VI)(4)O(37)(OH)(3)Zn(4)][C(6)H(3)(COO)(3)]·8H(2)O (ε(trim)) 中,通过有机配体连接 zigzag 链,形成二维网格。通过将 POMOF 直接吸附在玻璃碳或包裹在碳糊(CPE)上来制备修饰电极。检测到显著的电催化析氢反应(HER),产率大于 95%,经过 5 小时后获得高达 1.2×10(5)的周转率。与铂相比,报道的基于 POMOF 的电极更具活性,约有 260 mV 的阳极位移。最后,研究了 ε(trim)(4/3)/CPE 电极在各种 XCl(X = Li、Na、K、Cs)介质中的电催化活性。这使得我们能够检测到阳离子效应,并提出了 HER 的电催化机理途径。