98%
921
2 minutes
20
Photobatteries, batteries with a light-sensitive electrode, have recently been proposed as a way of simultaneously capturing and storing solar energy in a single device. Despite reports of photocharging with multiple different electrode materials, the overall mechanism of operation remains poorly understood. Here, we use optical reflection microscopy to investigate light-induced charging in LiVO electrodes. We image the electrode, at the single-particle level, under three conditions: (a) with a closed circuit and light but no electronic power source (photocharging), (b) during galvanostatic cycling with light (photoenhanced), and (c) with heat but no light (thermal). We demonstrate that light can indeed drive lithiation changes in LiVO while maintaining charge neutrality, possibly via a combination of faradaic and nonfaradaic effects taking place in individual particles. Our results provide an addition to the photobattery mechanistic model highlighting that both intercalation-based charging and lithium concentration polarization effects contribute to the increased photocharging capacity.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10450808 | PMC |
http://dx.doi.org/10.1021/acs.nanolett.3c01148 | DOI Listing |
Environ Geochem Health
September 2025
Department of Chemistry, Government Arts College(A), Salem, Tamil Nadu, 636007, India.
A CoO/AgMoO/CeOternary nanocomposites photocatalyst was successfully synthesized through a straightforward ethanol-assisted chemical method. Comprehensive characterization of its structural and optical properties was conducted using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV-Vis diffuse reflectance spectroscopy (UV-DRS), and photoluminescence (PL) analysis. XRD analysis confirmed the presence of CoO, AgMoO and CeO in the ternary composite sample.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Institute of Chemistry of OrganoMetallic Compounds (ICCOM), National Research Council of Italy (CNR), Via G. Moruzzi 1, 56124 Pisa, Italy.
Mixed-halide perovskites of formula MAPb(BrI), where MA is methylammonium, are of great interest for optoelectronic applications (particularly high-efficiency solar cells) due to their finely tunable bandgap, which enables precise control over light absorption. However, their stability remains a critical challenge, notably due to reversible photoinduced halide segregation. Under continuous illumination, this process leads to the formation of Br- and I-rich domains, which lower device performance by introducing low-bandgap regions that trap charge carriers.
View Article and Find Full Text PDFJ Biophotonics
September 2025
Institute for Physical Research of National Academy of Sciences of Armenia, Ashtarak, Armenia.
We report the results of an experimental study of the movement and trapping of Gram-negative Escherichia coli (E. coli) bacteria in broth suspensions, under photovoltaic fields generated by an optical Bessel beam illumination of the surface of a lithium niobate crystal (photovoltaic tweezers). The study was performed using a phase-sensitive transmission microscope.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
State Key Laboratory of Photocatalysis on Energy and Environment, Fuzhou University, Fuzhou, Fujian 350116, China.
Constructing dual single-atom catalysts with distinct electronic structures holds significance for the design of catalytic active centers, yet it remains highly challenging. Here, a novel light-induced approach was created to construct Ni and Ni dual single-atom sites on ZnIn₂S₄ nanosheets (Ni-Ni/ZIS) for the photocatalytic reduction of CO₂. Characterizations and density functional theory (DFT) calculations results indicate that Ni and Ni single-atom sites can be selectively anchored in the Zn vacancies and lattice interstitials on the surface of ZIS, respectively.
View Article and Find Full Text PDFChem Commun (Camb)
September 2025
Department of Chemistry and Biological Science, College of Science and Engineering, Aoyama Gakuin University, 5-10-1 Fuchinobe, Chuo-ku, Sagamihara, Kanagawa 252-5258, Japan.
We report a binaphthyl-bridged imidazole dimer bearing alkylpyridinium groups that exhibit fast and visible-light-induced negative photochromism even in aqueous media. The introduction of ionic groups not only enhances water solubility but also induces charge-transfer absorption, enabling efficient blue-light activation.
View Article and Find Full Text PDF