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Prashant V. Kamat

Researcher at University of Notre Dame

Publications -  760
Citations -  86006

Prashant V. Kamat is an academic researcher from University of Notre Dame. The author has contributed to research in topics: Excited state & Racism. 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.

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Photosensitized charge injection into TiO2 particles as studied by microwave absorption

TL;DR: In this article, microwave measurements on suspensions of these dye-coated particles have shown large absorption signals when the suspension is irradiated with pulses of 532 nm light from a laser, attributed to mobile charge carriers injected into the TiO2 from the excited singlet state of the dye.
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Photoelectrochemistry in semiconductor particulate systems. 13. Surface modification of cadmium sulfide semiconductor colloids with diethyldithiocarbamate

TL;DR: Etude de l'interaction entre le diethyldithiocarbamate and une electrode constituee par une suspension de particules colloidales de CdS as discussed by the authors.
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Interactions of Single Wall Carbon Nanotubes with Methyl Viologen Radicals. Quantitative Estimation of Stored Electrons

TL;DR: In this paper, the electron storage and discharge properties of single wall carbon nanotubes (SWCNTs) are probed by their interaction with radiolytically and photolytic produced methyl viologen (MV+•) radicals.
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Radiation-induced catalysis on oxide surfaces : degradation of hexachlorobenzene on gamma -irradiated alumina nanoparticles

TL;DR: In this article, the radiolytic transformation of hexachlorobenzene (HCB) adsorbed to alumina and potassium bromide (KBr) was monitored by suite of analytical methods including diffuse reflectance, UV, and Fourier transform infrared spectroscopy (FTIR), as well as GC-ECD and GC-MS.
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Solvent dependence of the charge-transfer properties of a quaterthiophene-anthraquinone dyad

TL;DR: In this paper, the electron donor-acceptor dyad (quaterthiophene-anthraquinone) mediates ultrafast intramolecular photoinduced charge separation and consequent charge recombination when in polar or moderately polar solvents.