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Polyoxometalate-Based Metal Organic Frameworks (POMOFs): Structural Trends, Energetics, and High Electrocatalytic Efficiency for Hydrogen Evolution Reaction

Nohra, Brigitte, El Moll, Hani, Rodriguez Albelo, L. Marleny, Mialane, Pierre, Marrot, Jérôme, Mellot-Draznieks, Caroline, O’Keeffe, Michael, Ngo Biboum, Rosa, Lemaire, Joël, Keita, Bineta, Nadjo, Louis, Dolbecq, Anne·2011·Journal of the American Chemical Society

Abstract

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)](4/3)·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.

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Metadata

Authors
Nohra, B., El Moll, H., Rodriguez Albelo, L. M., Mialane, P., Marrot, J., Mellot-Draznieks, C., O’Keeffe, M., Ngo Biboum, R., Lemaire, J., Keita, B., Nadjo, L., & Dolbecq, A.
Venue
Journal of the American Chemical Society
Published
2011-08-05
Volume
133
Issue
34
Pages
13363-13374
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2001970457
Cited by
545
References
0
FWCI
18.13
Type
journal article
Language
en
Open access
closed

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Nohra, B., El Moll, H., Rodriguez Albelo, L. M., Mialane, P., Marrot, J., Mellot-Draznieks, C., O’Keeffe, M., Ngo Biboum, R., Lemaire, J., Keita, B., Nadjo, L., & Dolbecq, A. (2011). Polyoxometalate-Based Metal Organic Frameworks (POMOFs): Structural Trends, Energetics, and High Electrocatalytic Efficiency for Hydrogen Evolution Reaction. Journal of the American Chemical Society. https://doi.org/10.1021/ja201165c

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