Cu-doped nanocrystal carbon dots for integrated fabrication of ultrabright luminescent solar concentrators
Year: 2025
Type: article
Abstract: Carbon dots (CDs) are promising fluorophores for optoelectronic devices. Yet, achieving CDs with high solid-state photoluminescence quantum yields (PLQYs) remains a significant challenge. The development of metal-doped carbon dots (CDs) to effectively modulate their electronic properties and surface chemical reactivities is still in its early stages. This work introduces copper-doping to CDs (Cu-CDs) luminescent material to modify the optoelectronic properties of CDs. The as-synthesized CDs show a Stokes shift of ≈0.67 eV and high PLQYs of 62 %. The Cu-CDs show the highest power conversion efficiency of 2.36 % compared to CDs (2.04 %) with a Stokes shift of 0.71 eV. These findings demonstrate the possibility of tuning optical properties into CDs via metal doping, obtaining eco-friendly, high-efficiency LSCs through scalable production techniques, paving the way to the lab-to-fab transition of this kind of device. Our results demonstrate that dual-emission Cu-CDs with strong solid-state fluorescence are promising candidates as luminophores in efficient photovoltaic devices.
Source: Materials Today Sustainability
Institutions: Ca' Foscari University of Venice, Luleå University of Technology, Istituto di Fotonica e Nanotecnologie, Politecnico di Milano, Institute of Structure of Matter, University of Trieste, AREA Science Park, Centre National de la Recherche Scientifique, Institut Jean Lamour, Université de Lorraine
Language: English
Subfield: Materials Chemistry
Field: Materials Science
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $2,530
Awards: G3231043934, G3415601974, G3911295268, G4903191691, G598502428, G7007144497, G7407763450, CONFINED CATALYSIS IN LAYERED MATERIALS – A TRANSFORMATIONAL APPROACH FOR EFFICIENT WATER SPLITTING, CONFINED CATALYSIS IN LAYERED MATERIALS – A TRANSFORMATIONAL APPROACH FOR EFFICIENT WATER SPLITTING, G8572347110, G912668888, G972786147
OpenAlex ID: W7084091155
