Yong Bok Go

Photochemical Water Oxidation by Crystalline Polymorphs of Manganese Oxides: Structural Requirements for Catalysis

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. In this study, 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 e(g)(1) 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.

Structural Requirements in Lithium Cobalt Oxides for the Catalytic Oxidation of Water

The development of water oxidation catalysts (WOCs) to replace costly noble metals in commercial electrolyzers and solar fuel cells is an unmet need that is preventing the global development of hydrogen fuel technologies. Two of the main challenges in realizing catalytic water splitting are lowering the substantial overpotential that is required to achieve practical operating current densities in the O2-evolving halfreaction at the anode, and the use of earth-abundant elements for the fabrication of inexpensive electrodes that are free from noble metals. To meet these challenges, molecular catalysts that are based upon the cubic CaMn4Ox core within photosystem II in photosynthetic organisms, which is the gold standard of catalytic efficiency, have begun to appear. Among solid-state materials, several noble-metal oxides, which include IrO2 and RuO2, are already in use in industrial electrolyzers, but are not globally scalable. Aqueous solutions of cobalt phosphate form water-oxidation catalysts under electrolysis and photolysis that are suitable for the fabrication of noncrystalline electrode materials. Nanocrystalline spinel-phase metal oxides (AM2O4, M= transition metals) that are comprised of M4O4 cubical subunits and are active water oxidation catalysts have been developed. The catalytic activity of the spinel Co3O4 has been reported for Co3O4 nanorods that are incorporated into SBA-15 silica, as well as Co3O4 nanoparticles that are adsorbed onto Ni electrodes. NiCo2O4 spinel also oxidizes water when the nanoparticles are electrophoretically deposited onto a Ni electrode. Reports that examined the effect of lithium doping on the surface of Co3O4 electrodes in solutions of KOH attributed the higher evolution rate of O2 to better electrical conductivity. However, the oxidation of water by Co3O4 was strongly dependent on crystallite size and surface area and frequently necessitates high overpotentials and alkaline conditions to accelerate the rate of reaction. In contrast, we recently reported that the catalytically inert spinel LiMn2O4 gives spinel l-MnO2, which is an active water oxidation catalyst, upon topotactic delithiation. Thus, the importance of removing the A-site lithium for catalysis by the cubic Mn4O4 core of spinels was revealed. [11]

Structural basis for differing electrocatalytic water oxidation by the cubic, layered and spinel forms of lithium cobalt oxides

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), overpotential (η = ∼420 mV@10 mA cm−2 at pH = 14), 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.

Synthesis, crystal structure, and properties of KSbO_{3} -type Bi_{3}Mn_{1.9}Te_{1.1}O_{11}

Single crystals of Bi3Mn1.9Te1.1O11 were prepared from NaCl þKCl flux. This compound adopts KSbO3type crystal structure as evidenced by electron and single crystal X-ray diffraction analysis. The threedimensional channel structure is formed by corner-sharing octahedral (Mn0.63Te0.37)2O10 dimers and two identical (Bi1)4(Bi2)2 interpenetrating lattices. The intra-dimer Mn/Te–Mn/Te distances in Bi3Mn1.9Te1.1O11 are short and are consistent with weak metal–metal interactions. The mixed oxidation state of manganese and the edge-sharing octahedral features are confirmed by X-ray near edge absorption spectroscopy measurements, which indicate Bi3(Mn IIIMn IV)Te VIO11 with 57.7% Mn 3 þ and 42.3% Mn 4 þ . The partial substitution of Te for Mn perturbs long-range magnetic interactions, thereby destroying the ferromagnetic ordering found in Bi3Mn3O11 (TC¼ 150 K).