2.3. Evaluation of Photocatalytic Water Splitting 6507 2.3.1. Photocatalytic Activity 6507 2.3.2. Photocatalytic Stability 6507 3. UV-Active Photocatalysts for Water Splitting 6507 3.1. d0 Metal Oxide Photocatalyts 6507 3.1.1. Ti-, Zr-Based Oxides 6507 3.1.2. Nb-, Ta-Based Oxides 6514 3.1.3. W-, Mo-Based Oxides 6517 3.1.4. Other d0 Metal Oxides 6518 3.2. d10 Metal Oxide Photocatalyts 6518 3.3. f0 Metal Oxide Photocatalysts 6518 3.4. Nonoxide Photocatalysts 6518 4. Approaches to Modifying the Electronic Band Structure for Visible-Light Harvesting 6519

Semiconductor-based Photocatalytic Hydrogen Generation

A review on g-C3N4-based photocatalysts

Photochemical splitting of water into H2 and O2 using solar energy is a process of great economic and environmental interest. Since the discovery of the first water splitting system based on TiO2 and Pt in 1972 by Fujishima and Honda, over 130 inorganic materials have been discovered as catalysts for this reaction. This review discusses the known inorganic catalysts with a focus on structure–activity relationships.

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Inorganic Materials as Catalysts for Photochemical Splitting of Water

Unique electronic and chemical properties of metal nanoparticles have drawn the attention of chemists, physicists, biologists, and engineers who wish to use them for the development of new generation nanodevices. Metal nanoparticles such as gold and silver show noticeable photoactivity under UV−visible irradiation as is evident from the photoinduced fusion and fragmentation processes. Binding a photoactive molecule (e.g., pyrene) to metal nanoparticle enhances the photochemical activity and renders the organic−inorganic hybrid nanoassemblies suitable for light-harvesting and optoelectronic applications. The nature of charge-transfer interaction of fluorophore with gold surface dictates the pathways with which the excited-state deactivates. Obtaining insight into energy and electron-transfer processes is important to improve the charge separation efficiencies in metal−fluorophore nanoassemblies and photocatalytic activity of metal−semiconductor composites.

https://pubs.acs.org/doi/pdf/10.1021/jp0209289

Photophysical, photochemical and photocatalytic aspects of metal nanoparticles

There is a growing interest in the conversion of water and solar energy into clean and renewable H2 fuels using earth-abundant materials due to the depletion of fossil fuel and its serious environmental impact. This critical review highlights some key factors influencing the efficiency of heterogeneous semiconductors for solar water splitting (i.e. improved charge separation and transfer, promoted optical absorption, optimized band gap position, lowered cost and toxicity, and enhanced stability and water splitting kinetics). Moreover, different engineering strategies, such as band structure engineering, micro/nano engineering, bionic engineering, co-catalyst engineering, surface/interface engineering of heterogeneous semiconductors are summarized and discussed thoroughly. The synergistic effects of the different engineering strategies, especially for the combination of co-catalyst loading and other strategies seem to be more promising for the development of highly efficient photocatalysts. A thorough understanding of electron and hole transfer thermodynamics and kinetics at the fundamental level is also important for elucidating the key efficiency-limiting step and designing highly efficient solar-to-fuel conversion systems. In this review, we provide not only a summary of the recent progress in the different engineering strategies of heterogeneous semiconductors for solar water splitting, but also some potential opportunities for designing and optimizing solar cells, photocatalysts for the reduction of CO2 and pollutant degradation, and electrocatalysts for water splitting.

Engineering heterogeneous semiconductors for solar water splitting

Neat glycerol was irradiated with beam of Ar atoms and ions produced by a Capillaritron gun operated at 5 KeV. The FAB spectrum produced changed markedly as the irradiation continued. Studies were made with irradiations lasting 12 minutes and 35 minutes. Both the absolute and relative intensities of the ions in the glycerol spectrum change, and new ions are formed. The glycerol sample after the irradiation contains clear crystals. The irradiated sample was subjected to negative chemical ionization analysis, which provided further evidence for the formation of radiation products from the glycerol and also evidence about the identities of the products. The major new products formed are

F. H. Field

Papers

Fast atom bombardment study of glycerol: mass spectra and radiation chemistry

Fast atom bombardment study of glycerol: mass spectra and radiation chemistry