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https://www.selleckchem.com/products/ABT-263.html The structures of the ion-pairs formed in aqueous NaOH and LiOH solutions are elucidated by combining Raman multivariate curve resolution (Raman-MCR) experiments and ab initio molecular dynamics (AIMD) simulations. The results extend prior findings to reveal that the initially formed ion-pairs are predominantly water-shared, with the hydroxide ion retaining its full first hydration-shell, while direct contact ion-pairing only becomes significant at higher concentrations. Our results confirm previous experiments and simulations indicating greater ion-pairing in aqueous LiOH than NaOH as well as at high temperatures. Our results further imply that NaOH and LiOH ion-pairing free energies have an approximately linear (rather than square-root) dependence on ion concentration (in the molar range), with positive enthalpies and entropies that increase with concentration, thus implying that water-mediated interactions enthalpically disfavor and entropically favor ion-pair formation.A new hybrid nanomaterial based on the immobilization of cobalt-containing polyoxometalate (CoPOM) on the surface of reduced graphene oxide (rGO) was designed for an efficient electrocatalytic water splitting reaction. First, the surface of rGO was functionalized with aminopropylsilyl groups and protonated with hydrochloric acid to produce ammonium groups. Then, the electrostatic interaction of positively charged rGO-supported ammonium groups with anionic CoPOM produced a CoPOM-APTS-rGO hybrid nanomaterial. The achieved hybrid nanomaterial exhibited a low overpotential of 128 mV versus NHE at a current density of 10 mA cm-2 in the electrocatalytic water oxidation at pH 7. In addition, a fast reaction kinetic with a Tafel slope of 74 mV dec-1 was seen in the presence of the prepared hybrid nanomaterial. Linear sweep voltammetry analysis revealed the long-term stability and activity of CoPOM-APTS-rGO for water oxidation in neutral conditions.Herein,

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