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Triplet Photosensitizers Showing Strong Absorption of Visible Light and Long-Lived Triplet Excited States and Application in Photocatalysis: A Mini Review

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This article is published in Energy & Fuels.The article was published on 2021-08-19. It has received 19 citations till now. The article focuses on the topics: Absorption (electromagnetic radiation).

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Research Progress on CO2 Photocatalytic Reduction with Full Solar Spectral Responses

TL;DR: In this article, the discovery of photocatalysts that can convert CO2 into hydrocarbons is discussed. But, the authors do not consider the effects of CO2 emissions on the environment.
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A cobalt mimochrome for photochemical hydrogen evolution from neutral water.

TL;DR: In this paper , a system for visible light-driven hydrogen production from water is reported, which makes use of a synthetic mini-enzyme known as a mimochrome (CoMC6*a) consisting of a cobalt deuteroporphyrin and two attached peptides as a catalyst, [Ru(bpy)3]2+ (bpy = 2,2′-bipyridine) as a photosensitizer, and ascorbic acid as a sacrificial electron donor.
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Long-lived excited states of platinum(II)-porphyrins for co-catalyst-free solar-driven hydrogen evolution

TL;DR: In this article , two Pt(II)-porphyrins conjugated with naphthalimide (NI) chromophore, PtT(p-NI)PP and PtD(p)-NIPP, are synthesized in excellent yields and characterized by photophysical, electrochemical, and density functional theory studies.
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Origins of Molecular-Twist-Triggered Intersystem Crossing in Functional Perylenediimides: Singlet-Triplet Gap versus Spin-Orbit Coupling.

TL;DR: In this article , the impact of molecular-twist on these energetics governing ISC is unveiled in a series of highly fluorescent prototype perylenediimides (PDIs) in dichloromethane implementing reliable quantum-chemical calculations.
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Tailoring intersystem crossing of perylenediimide through chalcogen-substitution at bay-position: A theoretical perspective.

TL;DR: In this article , a few chalcogen (X = O, S, Se) bay-substituted PDIs (PDI-X2) are computationally modeled aiming at introducing geometrical-strain at the PDI core and also mixing nπ* orbital character to ππ* in the lowest singlet and triplet excited states, which altogether may reduce ΔES-T and also improve the SOC.
References
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Journal ArticleDOI

Light-harvesting fullerene dyads as organic triplet photosensitizers for triplet-triplet annihilation upconversions.

TL;DR: It is proposed that C(60)-organic chromophore dyads can be used as a general molecular structural motif for organic triplet photosensitizers, which can be use for photocatalysis, photodynamic therapy, and TTA upconversions.
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Bodipy Derivatives as Organic Triplet Photosensitizers for Aerobic Photoorganocatalytic Oxidative Coupling of Amines and Photooxidation of Dihydroxylnaphthalenes

TL;DR: iodo-Bodipy derivatives that show strong absorption of visible light and long-lived triplet excited states as organic catalysts for photoredox catalytic organic reactions are used for two photocatalyzed reactions mediated by singlet oxygen.
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Efficiency Enhancement of Organic and Thin-Film Silicon Solar Cells with Photochemical Upconversion

TL;DR: In this article, a triplet-triplet annihilation (TTA-UC) based upconverter was proposed to boost thin-film solar cells by absorbing sub-bandgap photons and coupling the upconverted light back into the solar cell in a spectral region that can efficiently convert into electrical current.
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Visible-light initiated aerobic oxidations: a critical review

TL;DR: In the past ten years, visible light promoted aerobic oxidations have been emerging as one of the fastest growing fields in organic chemistry because of their low cost, easy availability and environmental friendliness as discussed by the authors.
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Styryl Bodipy-C60 dyads as efficient heavy-atom-free organic triplet photosensitizers.

TL;DR: C60-styryl Bodipy dyads that show strong absorption of visible light and a long-lived triplet excited state were used as heavy-atom-free organic triplet photosensitizers for photooxidation of 1,5-dihydroxynaphthalene via the photosensitizing of singlet oxygen ((1)O2).
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