Author
Prashant V. Kamat
Other affiliations: Indian Institute of Technology Kanpur, Council of Scientific and Industrial Research, Université du Québec à Trois-Rivières ...read more
Bio: Prashant V. Kamat is an academic researcher from University of Notre Dame. The author has contributed to research in topics: Racism & Excited state. The author has an hindex of 140, co-authored 725 publications receiving 79259 citations. Previous affiliations of Prashant V. Kamat include Indian Institute of Technology Kanpur & Council of Scientific and Industrial Research.
Topics: Racism, Excited state, Electron transfer, Quantum dot, Flash photolysis
Papers published on a yearly basis
Papers
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TL;DR: Novel organic solar cells have been prepared using quaternary self-organization of porphyrin (donor) and fullerene (acceptor) units by clusterization with gold nanoparticles on nanostructured SnO2 electrodes by electrophoretic deposition method.
Abstract: Novel organic solar cells have been prepared using quaternary self-organization of porphyrin (donor) and fullerene (acceptor) units by clusterization with gold nanoparticles on nanostructured SnO2 electrodes. First, porphyrin-alkanethiolate monolayer-protected gold nanoparticles (H2PCnMPC: n is the number of methylene groups in the spacer) are prepared (secondary organization) starting from the primary component (porphyrin-alkanethiol). These porphyrin-modified gold nanoparticles form complexes with fullerene molecules (tertiary organization), and they are clusterized in acetonitrile/toluene mixed solvent (quaternary organization). The highly colored composite clusters can then be assembled as three-dimensional arrays onto nanostructured SnO2 films to afford the OTE/SnO2/(H2PCnMPC+C60)m electrode using an electrophoretic deposition method. The film of the composite clusters with gold nanoparticle exhibits an incident photon-to-photocurrent efficiency (IPCE) as high as 54% and broad photocurrent action spectra (up to 1000 nm). The power conversion efficiency of the OTE/SnO2/(H2PC15MPC+C60)m composite electrode reaches as high as 1.5%, which is 45 times higher than that of the reference system consisting of the both single components of porphyrin and fullerene.
437 citations
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TL;DR: In this paper, a new paradigm for tuning the optical properties of gold nanorods by organizing them longitudinally, using thioalkylcarboxylic acid based bifunctional molecules is reported.
Abstract: We report a new paradigm for tuning the optical properties of gold nanorods by organizing them longitudinally, using thioalkylcarboxylic acid based bifunctional molecules. The rationale behind the selection of the bifunctional molecule is based on the fact that the thiol group binds to the ends of the nanorods, which further assembles in a longitudinal fashion through cooperative hydrogen bonding between the carboxylic groups. A generalized procedure for uniaxial plasmon coupling through longitudinal self-assembly of Au nanorods, initially to dimers and further to linear assemblies, is presented. Uniaxial modulation of interplasmon coupling through stepwise self-assembly of Au nanorods will have application in nanoelectronics and plasmonics.
427 citations
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TL;DR: In this paper, the mechanistic and kinetic details of the charge injection from excited CdS into a large bandgap semiconductor such as AgI and TiO{sub 2} have been investigated by coupling the two semiconductor systems in the colloidal form.
Abstract: The mechanistic and kinetic details of the charge injection from excited CdS into a large bandgap semiconductor such as AgI and TiO{sub 2} have been investigated by coupling the two semiconductor systems in the colloidal form. The interaction between the two colloids led to the quenching of CdS emission. The rate constants for the charge injection from excited CdS into the conduction band of AgI and TiO{sub 2} colloids were determined to be 2.2 {times} 10{sup 7} and >5 {times} 10{sup 10} s{sup {minus}1}, respectively. Transmission electron microscopic analysis indicated the possibility of several CdS colloidal particles interacting with a single particle of TiO{sub 2} and participating in the charge injection process. Primary photochemical events in the CdS-TiO{sub 2} system were investigated by picosecond laser flash photolysis. The charge injected into the TiO{sub 2} colloid and trapped at the Ti{sup 4+} site was characterized from its broad absorption in the region of 500-760 nm. The extended lifetime of these trapped charge carriers indicated an improved charge separation in the coupled semiconductor system.
417 citations
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TL;DR: The results presented here provide a convenient way to tailor the photoelectrochemical properties of TiO(2)-SrTiO(3) nanotube array electrodes and employ them for dye- or quantum-dot-sensitized solar cells and/or photocatalytic hydrogen production.
Abstract: TiO2 nanotube arrays formed on Ti substrate by electrochemical anodization have been converted into TiO2−SrTiO3 heterostructures by controlled substitution of Sr under hydrothermal conditions. The growth of SrTiO3 crystallites on the nanotube array electrode was probed by electron microscopy and X-ray diffraction. As the degree of Sr substitution increases with the duration of hydrothermal treatment, an increase in the size of SrTiO3 crystallites was observed. Consequently, with increasing SrTiO3 fraction in the TiO2−SrTiO3 nanotube arrays, we observed a shift in the flat band potential to more negative potentials, thus confirming the influence of SrTiO3 in the modification of the photoelectrochemical properties. The TiO2−SrTiO3 composite heterostructures obtained with 1 h or less hydrothermal treatment exhibit the best photoelectrochemical performance with nearly 100% increase in external quantum efficiency at 360 nm. The results presented here provide a convenient way to tailor the photoelectrochemical ...
407 citations
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TL;DR: Graphene−TiO2 nanocomposites synthesized via a solution-based method involving photocatalytic reduction of graphene oxide have been employed as photoanodes as discussed by the authors.
Abstract: Graphene−TiO2 nanocomposites synthesized via a solution-based method involving photocatalytic reduction of graphene oxide have been employed as photoanodes. Nearly 90% enhancement in the photocurrent is seen as reduced graphene oxide serves as electron collector and transporter. Additionally, the graphene−TiO2 nanocomposite electrodes exhibit significant activity for the complete photocatalytic decomposition of 2,4-dichlorophenoxyacetic acid (2,4-D). Combined with safe, solution-based synthetic practices, the promising photocurrent and photocatalytic degradation rates provide the framework and motivation for the implementation of graphene−TiO2 nanocomposites on larger scales.
396 citations
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TL;DR: There is, I think, something ethereal about i —the square root of minus one, which seems an odd beast at that time—an intruder hovering on the edge of reality.
Abstract: There is, I think, something ethereal about i —the square root of minus one. I remember first hearing about it at school. It seemed an odd beast at that time—an intruder hovering on the edge of reality.
Usually familiarity dulls this sense of the bizarre, but in the case of i it was the reverse: over the years the sense of its surreal nature intensified. It seemed that it was impossible to write mathematics that described the real world in …
33,785 citations
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TL;DR: Two organolead halide perovskite nanocrystals were found to efficiently sensitize TiO(2) for visible-light conversion in photoelectrochemical cells, which exhibit strong band-gap absorptions as semiconductors.
Abstract: Two organolead halide perovskite nanocrystals, CH3NH3PbBr3 and CH3NH3PbI3, were found to efficiently sensitize TiO2 for visible-light conversion in photoelectrochemical cells. When self-assembled on mesoporous TiO2 films, the nanocrystalline perovskites exhibit strong band-gap absorptions as semiconductors. The CH3NH3PbI3-based photocell with spectral sensitivity of up to 800 nm yielded a solar energy conversion efficiency of 3.8%. The CH3NH3PbBr3-based cell showed a high photovoltage of 0.96 V with an external quantum conversion efficiency of 65%.
16,634 citations
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TL;DR: This work reviews the historical development of Transition metal dichalcogenides, methods for preparing atomically thin layers, their electronic and optical properties, and prospects for future advances in electronics and optoelectronics.
Abstract: Single-layer metal dichalcogenides are two-dimensional semiconductors that present strong potential for electronic and sensing applications complementary to that of graphene.
13,348 citations
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TL;DR: A review of gold nanoparticles can be found in this article, where the most stable metal nanoparticles, called gold colloids (AuNPs), have been used for catalysis and biology applications.
Abstract: Although gold is the subject of one of the most ancient themes of investigation in science, its renaissance now leads to an exponentially increasing number of publications, especially in the context of emerging nanoscience and nanotechnology with nanoparticles and self-assembled monolayers (SAMs). We will limit the present review to gold nanoparticles (AuNPs), also called gold colloids. AuNPs are the most stable metal nanoparticles, and they present fascinating aspects such as their assembly of multiple types involving materials science, the behavior of the individual particles, size-related electronic, magnetic and optical properties (quantum size effect), and their applications to catalysis and biology. Their promises are in these fields as well as in the bottom-up approach of nanotechnology, and they will be key materials and building block in the 21st century. Whereas the extraction of gold started in the 5th millennium B.C. near Varna (Bulgaria) and reached 10 tons per year in Egypt around 1200-1300 B.C. when the marvelous statue of Touthankamon was constructed, it is probable that “soluble” gold appeared around the 5th or 4th century B.C. in Egypt and China. In antiquity, materials were used in an ecological sense for both aesthetic and curative purposes. Colloidal gold was used to make ruby glass 293 Chem. Rev. 2004, 104, 293−346
11,752 citations
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TL;DR: Film and powders of TiO2-x Nx have revealed an improvement over titanium dioxide (TiO2) under visible light in optical absorption and photocatalytic activity such as photodegradations of methylene blue and gaseous acetaldehyde and hydrophilicity of the film surface.
Abstract: To use solar irradiation or interior lighting efficiently, we sought a photocatalyst with high reactivity under visible light. Films and powders of TiO 2- x N x have revealed an improvement over titanium dioxide (TiO 2 ) under visible light (wavelength 2 has proven to be indispensable for band-gap narrowing and photocatalytic activity, as assessed by first-principles calculations and x-ray photoemission spectroscopy.
11,402 citations