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Metal phosphate compounds are considered promising candidates as positive electrode materials for Na-ion batteries because they offer higher cation-insertion potentials than analogous metal oxides. One such example is sodium iron fluorophosphate (Na2FePO4F), a compound that is typically synthesized by high-temperature solid-state routes. In this study, we prepare phase-pure Na2FePO4F using the polyol route, a low-temperature process that allows for the synthesis of nanoparticles (15–25 nm), a form that enhances Na-ion insertion kinetics and cycling stability. We then apply two methods to enhance the electronic conductivity of Na2FePO4F: (i) converting residual organic byproducts of the polyol synthesis to conductive carbon coatings; and (ii) preparing a nanocomposite with reduced graphene oxide. The resulting electrode materials are characterized in nonaqueous Na-ion electrolytes, assessing such metrics as specific capacity, rate capability, and cycling stability. A thorough electrochemical kinetics analysis is performed to deconvolve surface-vs.-bulk Na-ion insertion as a function of composite structure. Specific capacities between 60–110 mA h g−1 were achieved in galvanostatic charge–discharge tests when cycling in the range from 10C to C/10, respectively. [ABSTRACT FROM AUTHOR]

By applying differential pair distribution function (DPDF) analyses to the energy-storage relevant MnOx/carbon system―but in a 3D architectural rather than powder-composite configuration―we can remove contributions of the carbon nanofoam paper scaffold and quantify the multiphasic oxide speciation as the nanoscale, disordered MnOx grafted to the carbon walls (MnOx@CNF) structurally rearranges in situ from disordered birnessite AMnOx (A = Na+; Li+) to tetragonal Mn3O4 to spinel LiMn2O4. The first reaction step involves topotactic exchange of interlayer Na+ by Li+ in solution followed by thermal treatments to crystal engineer the ∼10 nm-thick 2D layered oxide throughout the macroscale nanofoam paper into a cubic phase. The oxide remains affixed to the walls of the nanofoam throughout the phase transformations. The DPDF fits are improved by retention of one plane of birnessite-like oxide after conversion to spinel. We support the DPDF-derived assignments by X-ray photoelectron spectroscopy and Raman spectroscopy, the latter of which tracks how crystal engineering the oxide affects the disorder of the carbon substrate. We further benchmark MnOx@CNF with nonaqueous electrochemical measurements versus lithium as the oxide converts from X-ray-amorphous birnessite to interlayer-registered LiMnOx to spinel. The lamellar AMnOx displays pseudocapacitive electrochemical behavior, with a doubling of specific capacitance for the interlayer-registered LiMnOx, while the spinel LiMn2O4@CNF displays a faradaic electrochemical response characteristic of Li-ion insertion. Our results highlight the need for holistic understanding when crystal engineering an (atomistic) charge-storing phase within the (architectural) structure of practical electrodes. [ABSTRACT FROM AUTHOR]

Vanadium-substituted iron oxide aerogels (2 : 1 Fe : V ratio; VFe2Ox) are synthesized using an epoxide-initiated sol–gel method to form high surface-area, mesoporous materials in which the degree of crystallinity and concentration of defects are tuned via thermal treatments under controlled atmospheres. Thermal processing of the X-ray amorphous, as-synthesized VFe2Ox aerogels at 300 °C under O2-rich conditions removes residual organic byproducts while maintaining a highly defective γ-Fe2O3-like local structure with minimal long-range order and vanadium in the +5 state. When as-synthesized VFe2Ox aerogels are heated under low partial pressure of O2 (e.g., flowing argon), a fraction of vanadium sites are reduced to the +4 state, driving crystallization to a Fe3O4-like cubic phase. Subsequent thermal oxidation of this nanocrystalline VFe2Ox aerogel re-oxidizes vanadium +4 to +5, creating additional cation vacancies and re-introducing disordered oxide domains. We correlate the electrochemical charge-storage properties of this series of VFe2Ox aerogels with their degree of order and chemical state, as verified by X-ray diffraction, X-ray photoelectron spectroscopy, and X-ray absorption spectroscopy. We find that the disordered O2-heated VFe2Ox aerogel yields the highest Li+- and Na+-insertion capacities among this series, approaching 130 mA h g−1 and 70 mA h g−1, respectively. Direct heat-treatment of the VFe2Ox aerogel in flowing argon to yield the partially reduced, nanocrystalline form results in significantly lower Li+-insertion capacity (77 mA h g−1), which improves to 105 mA h g−1 by thermal oxidation to create additional vacancies and structural disorder. [ABSTRACT FROM AUTHOR]