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Here we report on the visible luminescence of single gold nanospherical particles diffusing in water excited by a pulsed-laser at 488 nm. The signal studied by fluorescence correlation spectroscopy does not display the expected characteristics. The main deviation is obtained for the diffusion time that depends on the laser irradiance. Additional advanced methods of measurements have been implemented to further characterize the emission. These methods have allowed us to demonstrate that the luminescence does not blink even in the picosecond domain and that it does not photobleach either. The comparison between the signals obtained under pulsed and continuous excitations at the same wavelength suggests that the increase in the particle temperature plays a role in the non-linear increase in the luminescence intensity with the excitation power. As in the case of two-photon excited luminescence, it implies that a model describing the luminescence process for a single particle diffusing in liquid must take into account the whole system composed of the gold particle, the capping ligands and the surrounding water.
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http://dx.doi.org/10.1039/c2cp43294c | DOI Listing |
Luminescence
September 2025
Department of Physics, Saveetha Engineering College (Autonomous), Chennai, Tamilnadu, India.
The iron nickel magnesium tetra-oxide (FeNiMgO) nanocomposites (NCs) first reported in this article were synthesized using the sol-gel method. For investigation using powder X-ray diffraction (PXRD), the presence of a cubic structure is confirmed. In Raman spectroscopy, the vibrational modes are investigated.
View Article and Find Full Text PDFRegulating the electronic structure by doping can promote photoluminescence emission of low-dimensional metal halides for developing white-light-emitting devices. Here, 0D metal halides RbBiCl have achieved a transition from nonluminescence to effective self-trapped excitons (STEs) emission after Sb ion doping at room temperature. The femtosecond transient absorption spectrum reveals the nonradiative recombination was suppressed, whose lifetimes change from 93.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2025
School of Materials Science and Engineering, Changchun University of Science and Technology Changchun, 130022, Jilin, People's Republic of China.
The synergistic effect of various ions with optical properties is an important method to regulate the Er ion upconversion luminescence process. However, the energy processes between them are complicated and difficult to separate, and it is challenging to clarify the results of each process when multiple ions are co-doped. Herein, a series of NaYF:Er were synthesized by the low-temperature combustion method, and the luminescence color of Er ions was modulated by doping Yb ions and Tm ions.
View Article and Find Full Text PDFAnal Chim Acta
November 2025
Institute of Materials Science, Vietnam Academy of Science and Technology, Hanoi, 10000, Viet Nam. Electronic address:
Background: Recent advancements in cancer therapeutics have catalyzed the development of noninvasive treatment modalities, including the utilization of fluorescent chemotherapeutic agents. These agents offer dual functionality, enabling targeted drug delivery, real-time tumor imaging, and personalized therapy monitoring. Such capabilities are instrumental in the progression toward more precise and effective cancer interventions.
View Article and Find Full Text PDFJ Phys Chem Lett
September 2025
Department of Chemistry, Indian Institute of Science Education and Research Bhopal, Bhopal Bypass Road, Bhauri, Bhopal 462 066, Madhya Pradesh, India.
Reported herein are long-lived, red-luminescent silver nanoclusters (AgNCs) protected by the small-molecule ligand thiolactic acid, which exhibit exceptional stability (shelf life exceeding three years, photostability ∼100%), water-solubility, and high biocompatibility, making them suitable for diverse applications such as sensing and live-cell imaging. The AgNCs display extremely sensitive (>2% K) temperature-dependent luminescence, monitored by a dual approach of changes in photoluminescence intensity and excited-state lifetime, enabling precise local thermal environment monitoring with a very high-resolution temperature sensing down to subdegree levels (<0.5 K).
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