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Three-dimensional (3D) information of the optical response in the nanometre scale is important in the field of nanophotonics science. Using photoinduced force microscopy (PiFM), we can visualize the nano-scale optical field using the optical gradient force between the tip and sample. Here, we demonstrate 3D photoinduced force field visualization around a quantum dot in the single-nanometre spatial resolution with heterodyne frequency modulation technique, using which, the effect of the photothermal expansion of the tip and sample in the ultra-high vacuum condition can be avoided. The obtained 3D mapping shows the spatially localized photoinduced interaction potential and force field vectors in the single nano-scale for composite quantum dots with photocatalytic activity. Furthermore, the spatial resolution of PiFM imaging achieved is ~0.7 nm. The single-nanometer scale photoinduced field visualization is crucial for applications such as photo catalysts, optical functional devices, and optical manipulation.
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http://dx.doi.org/10.1038/s41467-021-24136-2 | DOI Listing |
Harnessing cooperative switching opens possibilities for engineering the responses of molecular films to external triggers and provides opportunities to control the directionality of switching/reactions and design novel nanostructures. Here, we demonstrate a one dimensional (1D) cascade effect in the thermal- and photo-induced switching of azobenzene derivatives deposited on a graphite surface. Upon thermal- and photo-induction, molecules switch between their geometric states ( and ) along a selected lattice within the assembly.
View Article and Find Full Text PDFJ Am Chem Soc
March 2025
J. Heyrovský Institute of Physical Chemistry, Czech Academy of Sciences, Dolejškova 3, CZ-182 23 Prague, Czech Republic.
We report real-time dynamics of photoinduced metal-metal bond formation acquired from ultrafast time-resolved stimulated emission and femtosecond stimulated Raman spectra (FSRS) of [Ir(2,5-dimethyl-2,5-diisocyanohexane)] (Ir(TMB)) in the region of low-frequency vibrations. Interpretation was supported by impulsive stimulated Raman experiments and time-dependent density-functional theory (TDDFT) calculations. The Ir-Ir stretching frequency doubled on going from ground to the lowest singlet excited state dσ*pσ, from 53 to 126 cm, demonstrating Ir-Ir bond formation.
View Article and Find Full Text PDFSoft Matter
February 2025
Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, 600 South Mathews Avenue, Urbana, Illinois 61801, USA.
Bottlebrush block copolymers (BBCPs), characterized by densely grafted side chains along their backbone, have emerged as promising materials for structural color applications. Their unique architecture prevents entanglement and facilitates rapid assembly kinetics, enabling the formation of various photonic crystals with high tunability of structural color from the visible to the infrared range. However, accessing non-1D structures has been largely limited to synthetic approaches.
View Article and Find Full Text PDFChem Sci
March 2025
Department of Chemistry, Graduate School of Advanced Science and Engineering, Hiroshima University 1-3-1 Kagamiyama Higashi-Hiroshima Hiroshima 739 8526 Japan
While the quantum yields of photosensitiser-derived one-electron-reduced species (OERSs) significantly impact the overall efficiencies of various redox-photosensitised photocatalytic reactions, the primary factors that influence them remain unclear. In this study, we systematically compared the photochemical formation quantum yields for OERSs associated with Ru(ii) and Os(ii) tris-diimine, , -[Re(diimine)(CO)(PR)], and cyclometalated Ir(iii) complexes in the presence of the same 1,3-dimethyl-2-phenyl-2,3-dihydro-1-benzo[]imidazole (BIH) reductant. The reduction potentials of the excited metal complexes, the heavy-atom effects of the central metal ions, and the oxidation potentials and charges of their OERSs were examined, which reveals that the driving force for photoinduced electron-transfer is the most important factor that determines the quantum yields associated with photochemical OERS formation.
View Article and Find Full Text PDFInorg Chem
February 2025
Yunnan Key Laboratory of Crystalline Porous Organic Functional Materials, College of Chemical and Materials Engineering, Qujing Normal University, Qujing 655011, China.
Designing and developing novel photochromic materials with additional functions such as photothermal conversion and photocatalysis are challenging but meaningful objectives. Crystalline naphthalenediimide (NDI)-based hybrids are an attractive class of multifunctional materials with fast-response photoinduced electron transfer and charge separation properties. They are promising photothermal conversion materials and photocatalysts.
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