The quantum yield (QY) of semiconductor quantum dots (QDs) is severely hampered by the inherent fluorescence intermittency. The QY of QDs typically increases with an increase in the excitation wavelength. Here, we present a distinctive behavior, where the QY is found to decrease with an increase in the excitation wavelength in water-soluble CdTe QDs (CQDs). Single-particle level measurements highlight the increase in permanent single dark particles at longer wavelengths that comprehend the overall QY of the CQDs in bulk solution. Fluorescence correlation spectroscopy further revealed an increase in the number of dark particles at longer wavelengths. As confirmed by DO/HO exchange, the presence of H ions in water plays an important role in creating variable permanently dark states in the CQDs. This observation was further supported by the cell internalization study of the CQDs, where a much brighter image at a shorter wavelength than at a longer wavelength was observed. A study of the excitation wavelength-dependent QY in QDs may reveal new insights into the applicability of QDs in different device fabrication cases.
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http://dx.doi.org/10.1039/d4nr04344h | DOI Listing |
Nanoscale
January 2025
School of Chemical Sciences, Indian Institute of Technology Mandi, H.P. 175075, India.
The quantum yield (QY) of semiconductor quantum dots (QDs) is severely hampered by the inherent fluorescence intermittency. The QY of QDs typically increases with an increase in the excitation wavelength. Here, we present a distinctive behavior, where the QY is found to decrease with an increase in the excitation wavelength in water-soluble CdTe QDs (CQDs).
View Article and Find Full Text PDFPlant Cell Environ
December 2024
Copernicus Institute for Sustainable Development, Utrecht University, Utrecht, Netherlands.
Leaf photosynthesis models are used extensively in photosynthesis research and are embedded in many larger scale models. Typical photosynthesis models simplify light intensity as the integrated intensity over the 400-700 nm waveband (photosynthetic active radiation, PAR). However, far-red light (700-750 nm, FR) also drives photosynthesis when supplied in addition to light within the PAR spectrum.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Donghua University - Songjiang Campus: Donghua University, College of chemistry, chemical engineering and biotechnology, 2999 Renmin North Road, Shanghai, 201620, Shanghai, CHINA.
Developing new organic radical emission systems and regulating their luminescence properties presents a significant challenge. Herein, we build dynamic and multi-emission band radical luminescence systems by co-assembling inorganic metal salts with carbonyl compounds in ionic liquids. After the assembling, dual-band, and excitation wavelength-dependent emission was observed upon light irradiation, one emission band originates from carbonyl radical after light irradiation, the other band from the ligand-metal charge transfer (LMCT) state, which benefits from the charge transfer from the radicals to the metal salts.
View Article and Find Full Text PDFJ Mater Chem A Mater
December 2024
Department of Materials Engineering, Ben-Gurion University of the Negev Beer Sheva 8410500 Israel
Zinc ferrite (ZnFeO, ZFO) has gained attention as a candidate material for photoelectrochemical water oxidation. However, champion devices have achieved photocurrents far below that predicted by its bandgap energy. Herein, strong optical interference is employed in compact ultrathin film (8-14 nm) Ti-doped ZFO films deposited on specular back reflectors to boost photoanode performance through enhanced light trapping, resulting in a roughly fourfold improvement in absorption as compared to films deposited on transparent substrates.
View Article and Find Full Text PDFChemistry
December 2024
Indian Institute of Science, Framework Solids Laboratory, Sir C.V. Raman avenue, 560012, Bangalore, INDIA.
Herein, we report the high-temperature solid-state synthesis and intriguing optical features of Bi3+/Ln3+ doped Ca2YTi2Ga3O12 (CYT). The optical properties of CYT were fine-tuned by judiciously substituting Zr4+ ions at Ti4+ sites and Bi3+, Ln3+ ions at Y3+ sites. All these compounds are crystallized in a cubic crystal system with an Ia-3d (no.
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