Heterogeneous Water Oxidizing Catalysts from Inert Transitio

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Heterogeneous Water Oxidizing Catalysts from Inert Transition Metal Oxide Spinels



Manganese oxides occur naturally as minerals in at least 30 different crystal structures, providing a rigorous test system to explore the significance of atomic positions on the catalytic efficiency of water oxidation. We chose to systematically compare eight synthetic oxide structures containing Mn(III) and Mn(IV) only, with particular emphasis on the five known structural polymorphs of MnO2. We have adapted literature synthesis methods to obtain pure polymorphs and validated their homogeneity and crystallinity by powder X-ray diffraction and both transmission and scanning electron microscopies. Measurement of water oxidation rate by oxygen evolution in aqueous solution was conducted with dispersed nanoparticulate manganese oxides and a standard ruthenium dye photo-oxidant system. No Ru was absorbed on the catalyst surface as observed by XPS and EDX. The post reaction atomic structure was completely preserved with no amorphization, as observed by HRTEM. Catalytic activities, normalized to surface area (BET), decrease in the series Mn2O3 > Mn3O4 λ-MnO2, where the latter is derived from spinel LiMn2O4 following partial Li+ removal. No catalytic activity is observed from LiMn2O4 and four of the MnO2 polymorphs, in contrast to some literature reports with polydispersed manganese oxides and electro-deposited films. Catalytic activity within the eight examined Mn oxides was found exclusively for (distorted) cubic phases, Mn2O3 (bixbyite), Mn3O4 (hausmannite), and λ-MnO2 (spinel), all containing Mn(III) possessing longer Mn–O bonds between edge-sharing MnO6 octahedra. Electronically degenerate Mn(III) has antibonding electronic configuration eg1 which imparts lattice distortions due to the Jahn–Teller effect that are hypothesized to contribute to structural flexibility important for catalytic turnover in water oxidation at the surface.Get more news about Molekularsieb 4a,you can vist our website!

2. Structure/Function Relations in Oxygen Evolution Catalysis by Cobalt Oxides

Two polymorphs of nanocrystalline cubic spinel and rhombohedral layered lithium cobalt oxides have been prepared and their application in the photocatalytic oxidation of water examined. The main factor that determines the catalytic activity of the different phases is the presence of a Co4O4 cubic core, which is present in the cubic form of the catalyst, but not in the layered structure
Transition metal oxides containing cubic B4O4 subcores are noted for their catalytic activity in water oxidation (OER). We synthesized a series of ternary spinel oxides, AB2O4, derived from LiMn2O4 by either replacement at the tetrahedral A site or Co substitution at the octahedral B site and measured their electrocatalytic OER activity. Atomic emission and powder X-ray diffraction confirmed spinel structure type and purity. Weak activation of the OER occurs upon A-site substitution: Zn2+ > Mg2+ > A-vacancy > Li+ = 0. Zn and Mg substitution is accompanied by (1) B-site conversion of Mn(IV) to Mn(III), resulting in expansion and higher symmetry of the [Mn4O4]4+ core relative to LiMn2O4 (inducing greater flexibility of the core and lower reorganization barrier to distortions), and (2) the electrochemical oxidation potential for Mn(III)/IV) increases by 0.15–0.2 V, producing a stronger driving force for water oxidation. Progressive replacement of Mn(III/IV) by Co(III) at the B site (LiMn2–xCoxO4, 0 ≤ x ≤ 1.5) both symmetrizes the [Mn4–xCoxO4] core and increases the oxidation potential for Co(III/IV), resulting in the highest OER activity within the spinel structure type. These observations point to two predictors of OER catalysis: (1) Among AMn2O4 spinels, those starting with Mn(III) in the resting lattice (prior to oxidation) result in longer, weaker Mn–O bonds for this eg1 antibonding electronic configuration, yielding greater core flexibility and a higher oxidation potential to Mn(IV), and (2) a linear free energy relationship exists between the electrocatalytic rate and the binding affinity of the substrate oxygen (*OH and *OOH) to the B site.

The two polymorphs of lithium cobalt oxide, LiCoO2, present an opportunity to contrast the structural requirements for reversible charge storage (battery function) vs. catalysis of water oxidation/oxygen evolution (OER; 2H2O → O2 + 4H+ + 4e−). Previously, we reported high OER electrocatalytic activity from nanocrystals of the cubic phase vs. poor activity from the layered phase – the archetypal lithium-ion battery cathode. Here we apply transmission electron microscopy, electron diffraction, voltammetry and elemental analysis under OER electrolysis conditions to show that labile Li+ ions partially deintercalate from layered LiCoO2, initiating structural reorganization to the cubic spinel LiCo2O4, in parallel with formation of a more active catalytic phase. Comparison of cubic LiCoO2 (50 nm) to iridium (5 nm) nanoparticles for OER catalysis (commercial benchmark for membrane-based systems) in basic and neutral electrolyte reveals excellent performance in terms of Tafel slope (48 mV dec−1), faradaic yield (100%) and OER stability (no loss in 14 hours). The inherent OER activity of cubic LiCoO2 and spinel LiCo2O4 is attributed to the presence of [Co4O4]n+ cubane structural units, which provide lower oxidation potential to Co4+ and lower inter-cubane hole mobility. By contrast, the layered phase, which lacks cubane units, exhibits extensive intra-planar hole delocalization which entropically hinders the four electron/hole concerted OER reaction. An essential distinguishing trait of a truly relevant catalyst is efficient continuous operation in a real electrolyzer stack. Initial trials of cubic LiCoO2 in a solid electrolyte alkaline membrane electrolyzer indicate continuous operation for 1000 hours (without failure) at current densities up to 400 mA cm−2 and overpotential lower than proven PGM (platinum group metal) catalysts.

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