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Prashant V. Kamat

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.


Papers
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TL;DR: In this paper, photoinduced halide ion segregation in mixed halide perovskites can introduce a detrimental effect on the photovoltaic performance of solar cells over extended light exposure.
Abstract: Photoinduced halide ion segregation in mixed halide perovskites can introduce a detrimental effect on the photovoltaic performance of perovskite solar cells over extended light exposure. The photoc...

77 citations

Journal ArticleDOI
TL;DR: In this paper, tetra(4-aminophenyl) porphyrin (TAPP) with Ag nanoparticles is confirmed by ground-state absorption and Raman spectroscopy.
Abstract: Highly photoactive porphyrin is shown to form charge-transfer complex with silver nanoparticles. Complexation of tetra(4-aminophenyl) porphyrin (TAPP) with Ag nanoparticles is confirmed by ground-state absorption and Raman spectroscopy. Strong Raman enhancement indicates both electromagnetic and chemical enhancement. Evidence of chemical enhancement includes a selective enhancement of porphyrin Raman bands. Fast charge separation in the complex is indicated by ultrafast transient absorption and fluorescence upconversion measurements. The charge-separated state is shown to have a lifetime of 116 ± 6 ps. Porphyrin substituents are shown to play a role in the formation of charge-transfer complex.

77 citations

Journal ArticleDOI
TL;DR: The photovoltaic performance was evaluated over a period of a few weeks to demonstrate the stability of AgInS2-ZnS when utilized as sensitizers in solar cells and a power conversion efficiency of 2.25% of the champion cell 1 month after its fabrication is reported.
Abstract: Multinary quantum dots such as AgInS2 and alloyed AgInS2–ZnS are an emerging class of semiconductor materials for applications in photovoltaic and display devices. The nanocrystals of (AgInS2)x–(ZnS)1–x (for x = 0.67) exhibit a broad emission with a maximum at 623 nm and interact strongly with TiO2 nanostructures by injecting electrons from the excited state. The electron transfer rate constant as determined from transient absorption spectroscopy was 1.8 × 1010 s–1. The photovoltaic performance was evaluated over a period of a few weeks to demonstrate the stability of AgInS2–ZnS when utilized as sensitizers in solar cells. We report a power conversion efficiency of 2.25% of our champion cell 1 month after its fabrication. The limitations of AgInS2–ZnS nanocrystals in achieving greater solar cell efficiency are discussed.

76 citations

Journal ArticleDOI
TL;DR: In this paper, the photoinduced charge transfer between CdSe/CdS core/shell semiconductor nanorods and methyl viologen (MV2+) was investigated.
Abstract: CdSe/CdS core/shell semiconductor nanorods (NR) with rod-in-rod morphology offer new strategies for designing highly emissive nanostructures. The interplay between energetically matched semiconductors results in enhanced emission from the CdSe core. In order to further evaluate the cooperative role of these two semiconductors in a core/shell geometry, we have probed the photoinduced charge transfer between CdSe/CdS core/shell semiconductor NR and methyl viologen (MV2+). The quenching of the emission by the electron acceptor, MV2+, as well as the production of electron transfer product MV•+ depends on the aspect ratio (l/w) of the NR thus pointing out the role of CdS shell in determining the overall photocatalytic efficiency. Transient absorption measurements show that the presence of MV2+ influences only the bleaching recovery of the CdS shell and not of the CdSe core recovery. Thus, optimization of shell aspect ratio plays a crucial role in maximizing the efficiency of this photocatalytic system.

76 citations

Journal ArticleDOI
21 Apr 2020
TL;DR: Two-dimensional (2D) lead halide perovskites represent an emerging class of materials given their tunable optoelectronic properties and long-term stability in solar cells.
Abstract: Two-dimensional (2D) lead halide perovskites represent an emerging class of materials given their tunable optoelectronic properties and long-term stability in perovskite solar cells. In order to as...

76 citations


Cited by
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[...]

08 Dec 2001-BMJ
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

Journal ArticleDOI
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

Journal ArticleDOI
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

Journal ArticleDOI
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

Journal ArticleDOI
Ryoji Asahi1, Takeshi Morikawa1, T. Ohwaki1, Koyu Aoki1, Y. Taga1 
13 Jul 2001-Science
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