Journal of Photochemistry and Photobiology C Photochemistry Reviews (J PHOTOCH PHOTOBIO C)

Publisher: Nihon Shashinka Kyōkai, Elsevier

Journal description

The international journal, Photochemistry Reviews, as the official journal of the Japanese Photochemistry Association, provides a forum for mutual communication among scientists in various fields of photochemistry and aims to promote new interdisciplinary fields. The scope includes fundamental molecular photochemistry in gas, liquid, and solid phases, organic photochemistry, inorganic photochemistry, supramolecular photochemistry, photochemical aspects of photosynthesis and photobiology, photoelectrochemistry, photocatalysis, solar energy conversion, photochemical devices, photofabrication, photofunctionalization, new chemistry for photonics, and other related areas.

Current impact factor: 16.09

Impact Factor Rankings

2015 Impact Factor Available summer 2016
2014 Impact Factor 16.091
2013 Impact Factor 11.625
2012 Impact Factor 8.069
2011 Impact Factor 10.36
2010 Impact Factor 10.81
2009 Impact Factor 7.952
2008 Impact Factor 5.36
2007 Impact Factor 5.731
2006 Impact Factor 7.32
2005 Impact Factor 8.167

Impact factor over time

Impact factor

Additional details

5-year impact 14.82
Cited half-life 6.90
Immediacy index 2.20
Eigenfactor 0.00
Article influence 3.63
Website Journal of Photochemistry and Photobiology C: Photochemistry Reviews website
Other titles Journal of photochemistry and photobiology., Photochemistry reviews
ISSN 1389-5567
OCLC 44806989
Material type Document, Periodical, Internet resource
Document type Internet Resource, Computer File, Journal / Magazine / Newspaper

Publisher details


  • Pre-print
    • Author can archive a pre-print version
  • Post-print
    • Author can archive a post-print version
  • Conditions
    • Authors pre-print on any website, including arXiv and RePEC
    • Author's post-print on author's personal website immediately
    • Author's post-print on open access repository after an embargo period of between 12 months and 48 months
    • Permitted deposit due to Funding Body, Institutional and Governmental policy or mandate, may be required to comply with embargo periods of 12 months to 48 months
    • Author's post-print may be used to update arXiv and RepEC
    • Publisher's version/PDF cannot be used
    • Must link to publisher version with DOI
    • Author's post-print must be released with a Creative Commons Attribution Non-Commercial No Derivatives License
    • Publisher last reviewed on 03/06/2015
  • Classification

Publications in this journal

  • Journal of Photochemistry and Photobiology C Photochemistry Reviews 10/2015; DOI:10.1016/j.jphotochemrev.2015.10.001

  • Journal of Photochemistry and Photobiology C Photochemistry Reviews 10/2015; DOI:10.1016/j.jphotochemrev.2015.09.001
  • [Show abstract] [Hide abstract]
    ABSTRACT: Widespread implementation of renewable energy technologies, while preventing significant increases in greenhouse gas emissions, appears to be the only viable solution to meeting the world's energy demands for a sustainable energy future. The final energy mix will include conservation and energy efficiency, wind, geothermal, biomass, and others, but none more ubiquitous or abundant than the sun. Over several decades of development, the cost of photovoltaic cells has decreased significantly with lifetimes that exceed 25 years and there is promise for widespread implementation in the future. However, the solar input is intermittent and, to be practical at a truly large scale, will require an equally large capability for energy storage. One approach involves artificial photosynthesis and the use of the sun to drive solar fuel reactions for water splitting into hydrogen and oxygen or to reduce CO2 to reduced carbon fuels. An early breakthrough in this area came from an initial report by Honda and Fujishima on photoelectrochemical water splitting at TiO2 with UV excitation. Significant progress has been made since in exploiting semiconductor devices in water splitting with impressive gains in spectral coverage and solar efficiencies. An alternate, hybrid approach, which integrates molecular light absorption and catalysis with the band gap properties of oxide semiconductors, the dye-sensitized photoelectrosynthesis cell (DSPEC), has been pioneered by the University of North Carolina Energy Frontier Research Center (UNC EFRC) on Solar Fuels. By utilizing chromophore-catalyst assemblies, core/shell oxide structures, and surface stabilization, the EFRC recently demonstrated a viable DSPEC for solar water splitting.
    Journal of Photochemistry and Photobiology C Photochemistry Reviews 08/2015; DOI:10.1016/j.jphotochemrev.2015.08.002

  • Journal of Photochemistry and Photobiology C Photochemistry Reviews 07/2015; DOI:10.1016/j.jphotochemrev.2015.07.003
  • [Show abstract] [Hide abstract]
    ABSTRACT: ‘Supramolecular Photochemistry’ (SP) deals with a study of the properties of molecules in their excited states where the medium plays a significant role. While ‘Molecular Photochemistry’ (MP) deals with studies in isotropic solution, the SP deals with reactant molecules that interact weakly with their surroundings. The surroundings in general are highly organized assemblies such as crystals, liquid crystals, micelles, host-guest structures etc. The behavior of exited molecules in SP unlike in isotropic solution is controlled not only by their inherent electronic and steric properties but also by the immediate surroundings. The weak interactions that control the chemistry include van der Walls, hydrophobic, C-H---π, π---π and several types of hydrogen bonds. In this review the uniqueness of SP compared to MP is highlighted with examples chosen from reactions in crystals, micelles and host-guest assemblies. In spite of distinctly different structures (crystals, micelles etc.) the influence of the medium could be understood on the basis of a model developed by G. M. J. Schmidt for photoreactions in crystals. The principles of reaction cavity model are briefly outlined in this review. There are a few important features that are specific to SP. For example, highly reactive molecules and intermediates could be stabilized in a confined environment; they enable phosphorescence to be observed at room temperature and favor chiral induction in photochemical reactions. Using such examples the uniqueness of SP is highlighted. The future of SP depends on developing efficient and unique catalytic photoreactions using easily available reaction ‘containers’. In addition, their value in artificial photosynthesis should be established for SP to occupy a center stage in the future.
    Journal of Photochemistry and Photobiology C Photochemistry Reviews 05/2015; 23. DOI:10.1016/j.jphotochemrev.2015.04.002
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    ABSTRACT: Photonic crystals are periodic dielectric nanostructures that can affect the propagation of light. Polymer-based photonic crystals have attracted great attentions for their potential application as sensors or optical switches due to their stimuli-responsive properties. This review summarizes the recent developments in one-dimensional (1-D) polymer-based photonic crystals, including the inspiration of the material from nature, principles for design and fabrication, mechanism of color tuning, and their tunable structural color in responsive to various stimuli. A number of fabrication methods, either by bottom-up or top-down approaches for 1-D polymeric photonic crystals have been overviewed.
    Journal of Photochemistry and Photobiology C Photochemistry Reviews 05/2015; 23. DOI:10.1016/j.jphotochemrev.2015.05.001
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    ABSTRACT: The development of biologically templated artificial light harvesting antennae and energy transfer devices is a highly active research area with exceptional challenges. Natural energy harvesting complexes have exquisite spectrally- and spatially-tuned systems with high redundancy to maximize their ability to gather, channel, and distribute electromagnetic radiation. Attempting to mimic these highly efficient systems requires at the very least (sub)nanoscale precision in the positioning of light sensitive molecules, the latter of which must also possess carefully selected photophysical properties; in essence, these two fundamental properties must be exploited in a synergistic manner. First, the scaffold must be highly organized, ideally with multiple symmetrical components that are spatially arranged with nanoscale accuracy. Second, the structure must be amenable to chemical modification in order to be (bio)functionalized with the desired light sensitive moieties which have expanded greatly to now include organic dyes, metal chelates, fluorescent proteins, dye-doped and noble metal nanoparticles, photoactive polymers, along with semiconductor quantum dots amongst others. Several families of biological scaffolding molecules offer strong potential to meet these stringent requirements. Recent advances in bionanotechnology have provided the ability to assemble diverse naturally-derived scaffolds along with manipulating their properties and this is allowing us to understand the capabilities and limitations of such artificial light-harvesting antennae and devices. The range of scaffold or template materials that have been used varies from highly symmetrical virus capsids to self-assembled biomaterials including nucleic acids and small peptides as well as a range of hybrid inorganic-biological systems. This review surveys the burgeoning field of artificial light-harvesting and energy transfer complexes that utilize biological scaffolds from the perspective of what each has to offer for optimized energy transfer. We highlight each biological scaffold with prominent examples from the literature and discuss some of the benefits and liabilities of each approach. Cumulatively, the available data suggest that DNA is the most versatile biological material currently available, though it has challenges including precise dye placement and subsequent dye performance. We conclude by providing a perspective on how this field will progress in both the short and long term, with a focus on the transition to applications and devices.
    Journal of Photochemistry and Photobiology C Photochemistry Reviews 01/2015; 23. DOI:10.1016/j.jphotochemrev.2014.12.002
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    ABSTRACT: The cryptochrome/photolyase superfamily is a class of flavoproteins that can regulate the growth and development in plants, as well as the circadian clock and the potential magnetic navigation in animals, primarily by absorbing UV-A and blue light. It is generally agreed that these functions depend on the photochemical reaction of the flavin adenine dinucleotide (FAD) chromophore, non-covalently binding to cryptochromes or photolyases. Irradiation can initiate either photoreduction between FAD and certain electron donors or electron jumping in FAD, thereby leading to the generation of intermediates that activate the protein. This signaling process is known as photoactivation. Subsequently, the activated protein will interact with downstream receptors to transfer the photo and magnetic signals. Based on in-depth research on photoactivation, two photo-cycle mechanisms for the photoreception/photosignaling of the cryptochrome/photolyase superfamily, i.e., the photolyase model and the phototropin model, have been proposed. There is no apparent alternative to the photo-cycle of cyclobutane pyrimidine dimer (CPD) or (6-4) photolyase following the photolyase model. However, the mechanism is not clear for the photoactivation of cryptochromes and CRY-DASH, a new subcategory of photolyase. Since the photoactivation process is the first step for the physiological function of proteins, more and improved research efforts in this field have been widely developed. This review first briefly presents the structure, the photoactivation, and the repair mechanism of CPD and (6-4) photolyase. Next, we review in detail the photoactivation of cryptochromes and CRY-DASH by analyzing the current status of research, as well as the contradictions in the resting redox states of FAD, intermediates in photoreactions, the photo-cycle of FAD, the singnaling state of proteins, and the necessity of given tryptophans for protein activity. Based on these studies, the correlations of photoactivation and photo-cycle mechanisms, as well as the correlations of photoactivation and megnetoreception of proteins, are discussed. Finally the crucial open questions regarding the photoactivation mechanisms of the cyrptochrome/photolyase superfamily are outlined, considering the hypothesis for a cryptochrome-based model of avian magnetoreception.
    Journal of Photochemistry and Photobiology C Photochemistry Reviews 12/2014; 22. DOI:10.1016/j.jphotochemrev.2014.12.001
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    ABSTRACT: Surface enhanced Raman scattering (SERS) spectroscopy is a powerful technique that provides molecular information through greatly enhanced Raman scattering from minute amounts of substance near nanostructured metallic surfaces. SERS is thus a promising technique for ultrasensitive sensing applications. Plasmonic nanostructures including metal nanoparticles and lithographically prepared nanostructures are ideal substrates to produce enhanced Raman signals. Numerous studies have been published on the production of SERS-active substrates for SERS measurements including solution phase methods and solid supports. In SERS applications, hot spots where the electromagnetic field is particularly intense, play a key role. In this review, we provide an overview of techniques designed for the creation of SERS hot spots both in solution and on solid supports. We first introduce the self-assembly of spherical and anisotropic nanoparticles in solution, to then focus on a wide variety of techniques to assemble nanoparticles onto solid supports. We also describe top-down approaches typically based on lithography techniques. Finally, we provide our own view on the current state of the field and the aspects where further development is expected.
    Journal of Photochemistry and Photobiology C Photochemistry Reviews 12/2014; 21. DOI:10.1016/j.jphotochemrev.2014.09.001