Photon upconversion with indium phosphide quantum dots enables high-energy photoreactions using visible light

Photochemical reactions that rely on high-energy photons are limited by low solar abundance in the UV region and undesired photodecomposition. Photon upconversion processes, particularly triplet-triplet annihilation-based upconversion (TTA-UC), provide an alternate pathway to enable the use of low-energy, abundant visible and near-infrared (NIR) light for chemical transformations that typically require high-energy UV light. In this context, quantum dot (QD)-sensitized TTA-UC systems offer distinct advantages with respect to a larger anti-Stokes shift, enhanced upconversion quantum yield, and superior photostability. However, the successful application of QD-sensitized upconversion energy in photocatalysis remains limited, especially for high-energy reactions requiring UV-active catalysts. Here, we report the use of upconversion energy from a QD-sensitized TTA-UC system in performing a high-energy-driven dehalogenation reaction with visible light. Indium phosphide (InP) QDs are used as the sensitizer and diphenylanthracene (DPA) as the annihilator molecule, which gave a green-to-blue TTA-UC with a normalized upconversion quantum yield of ∼8.2% and an apparent anti-Stokes shift of 0.55 eV. The upconversion energy from the InP QD-sensitized TTA-UC system is effectively used to drive a photoredox C-C coupling reaction <i>via</i> the dehalogenation of substituted aryl halides in excellent yields. TTA-UC is the sole driving force for this photoredox reaction, as the required potential is beyond the maximum achievable redox potential of InP-QDs. Further, the scope of the QD-sensitized TTA-UC system is extended towards the radical polymerization of methyl methacrylate (MMA), resulting in the production of industrially important polymethyl methacrylate (PMMA). Our work overcomes key limitations of traditional UV-based photochemistry and introduces a sustainable, low-energy pathway for enabling high-energy transformations.

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Journal
Chemical Science
Published
2025-11-03
DOI
https://doi.org/10.1039/d5sc07232h
Primary Topic
Luminescence and Fluorescent Materials
Type
article
Field-Weighted Citation Impact
0.00

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article

Photon upconversion with indium phosphide quantum dots enables high-energy photoreactions using visible light

Ankit Dhankhar, Adhra S. Sury, Aman Chaturvedi, Pankaj Mandal et al.
Chemical Science
Luminescence and Fluorescent Materials
article

Photon upconversion with indium phosphide quantum dots enables high-energy photoreactions using visible light

Ankit Dhankhar, Adhra S. Sury, Aman Chaturvedi, Pankaj Mandal, Kaixing Wang, Indra Narayan Chakraborty, Pramod P. Pillai, Benjamin Dietzek‐Ivanšić
article en

Abstract

Photochemical reactions that rely on high-energy photons are limited by low solar abundance in the UV region and undesired photodecomposition. Photon upconversion processes, particularly triplet-triplet annihilation-based upconversion (TTA-UC), provide an alternate pathway to enable the use of low-energy, abundant visible and near-infrared (NIR) light for chemical transformations that typically require high-energy UV light. In this context, quantum dot (QD)-sensitized TTA-UC systems offer distinct advantages with respect to a larger anti-Stokes shift, enhanced upconversion quantum yield, and superior photostability. However, the successful application of QD-sensitized upconversion energy in photocatalysis remains limited, especially for high-energy reactions requiring UV-active catalysts. Here, we report the use of upconversion energy from a QD-sensitized TTA-UC system in performing a high-energy-driven dehalogenation reaction with visible light. Indium phosphide (InP) QDs are used as the sensitizer and diphenylanthracene (DPA) as the annihilator molecule, which gave a green-to-blue TTA-UC with a normalized upconversion quantum yield of ∼8.2% and an apparent anti-Stokes shift of 0.55 eV. The upconversion energy from the InP QD-sensitized TTA-UC system is effectively used to drive a photoredox C-C coupling reaction <i>via</i> the dehalogenation of substituted aryl halides in excellent yields. TTA-UC is the sole driving force for this photoredox reaction, as the required potential is beyond the maximum achievable redox potential of InP-QDs. Further, the scope of the QD-sensitized TTA-UC system is extended towards the radical polymerization of methyl methacrylate (MMA), resulting in the production of industrially important polymethyl methacrylate (PMMA). Our work overcomes key limitations of traditional UV-based photochemistry and introduces a sustainable, low-energy pathway for enabling high-energy transformations.

Chemical ScienceVol. 17(1)
Indian Institute of Science Education and Research Pune (IN), Leibniz Institute of Photonic Technology (DE), Leibniz Institute of Surface Engineering (DE)
Department of Science and Technology, Ministry of Science and Technology, India, Ministry of Education, India, Indian Institute of Science Education and Research Pune, Indian Institute of Science Education and Research Mohali, Science and Engineering Research Board
Openalex Percentile: Top 71%
Luminescence and Fluorescent Materials
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