The development of a water oxidation catalyst has been a demanding challenge in realizing water splitting systems. The asymmetric geometry and flexible ligation of the biological Mn4CaO5 cluster are important properties for the function of photosystem II, and these properties can be applied to the design of new inorganic water oxidation catalysts. We identified a new crystal structure, Mn3(PO4)2·3H2O, that precipitates spontaneously in aqueous solution at room temperature and demonstrated its high catalytic performance under neutral conditions. The bulky phosphate polyhedron induces a less-ordered Mn geometry in Mn3(PO4)2·3H2O. Computational analysis indicated that the structural flexibility in Mn3(PO4)2·3H2O could stabilize the Jahn-Teller-distorted Mn(III) and thus facilitate Mn(II) oxidation. This study provides valuable insights into the interplay between atomic structure and catalytic activity.

We report herein the fabrication of a hematite nanorod-graphene composite (α-Fe2O3 nanorod/RGO) via a facile template-free hydrothermal route with an aim to improve the photocatalytic efficiency of the α-Fe2O3 nanorod. The structural and morphological characterizations of the as-prepared composites were carried out using X-ray diffraction, Raman spectra, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy, N2 adsorption-desorption, etc. The α-Fe2O3 nanorods were well-decorated on the surface of the graphene sheets, which helps in electron transfer from α-Fe2O3 to graphene and hence can delay the recombination process, leading to the improvement in photocatalytic activity. The composite containing 5 wt % RGO and α-Fe2O3 nanorods shows a 4-fold enhancement in the photocatalytic activity. The performance of photocatalytic activity was discussed in light of surface area, interaction between nanorods and graphene nanosheets, synergism between α-Fe2O3 nanorods and RGO sheets, light-harvesting properties of the composites, photoluminescence spectra, photocurrent measurement, and hydroxyl radical formation.

This work reports the facile synthesis of α-Fe(2)O(3) nanorods and nano-hexagons and its application as sunlight-driven photocatalysis. The obtained products were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), selected area electron diffraction (SAED), scanning electron microscopy (SEM), diffused reflectance spectroscopy (DRUV-vis), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). The phase and crystallinity were confirmed from the XRD study. Electron microscopy study clearly indicates the formation of different morphologies of nanocrystals. These hematite nanostructures were used as a model system for studying the shape-dependent photocatalytic degradation of phenol, methylene blue, and congo red. Amongst all the nanostructured semiconductors, Pt-doped hematite nanorod showed 55% efficiency towards the decolonization of methylene blue and 63% toward congo red under sun light illumination. The difference in photocatalytic activity is discussed in terms of their crystallize size and morphological ordering.

The oxygen evolution reaction (OER) is considered a major bottleneck in the overall water electrolysis process. In this work, highly active manganese oxide nano-catalysts were synthesized via hot injection. Facile surface treatment generated Mn(III) species on monodisperse 10 nm MnO nanocrystals (NCs). Size dependency of MnO NCs on OER activity was also investigated. Surprisingly, the partially oxidized MnO NCs only required 530 mV @ 5 mA cm−2 under near neutral conditions.

A series of nanostructure zinc-iron mixed oxide photocatalysts have been fabricated by solution-combustion method using urea as the fuel, and nitrate salts of both iron and zinc as the metal source. Different characterization tools, such as X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), diffuse reflectance UV-visible spectra (DRUV-vis), electron microscopy, and photoelectrochemical measurement were employed to establish the structural, electronic, and optical properties of the material. Electron microscopy confirmed the nanostructure of the photocatalyst. The synthesized photocatalysts were examined towards photodegradation of 4-chloro-2-nitro phenol (CNP), rhodamine 6G (R6G), and photocatalytic hydrogen production under visible light (λ ≥ 400 nm). The photocatalyst having zinc to iron ratio of 50:50 showed best photocatalytic activity among all the synthesized photocatalysts.