Recent studies have shown the presence of an amorphous surface layer in nominally crystalline silicon nanocrystals (SiNCs) produced by some of the most common synthetic techniques. The amorphous surface layer can serve as a source of deep charge traps, which can dramatically affect the electronic and photophysical properties of SiNCs. We present results of a scanning tunneling microscopy/scanning tunneling spectroscopy (STM/STS) study of individual intragap states observed on the surfaces of hydrogen-passivated SiNCs deposited on the Au(111) surface. STS measurements show that intragap states can be formed reversibly when appropriate voltage-current pulses are applied to individual SiNCs. Analysis of STS spectra suggests that the observed intragap states are formed via self-trapping of charge carriers injected into SiNCs from the STM tip. Our results provide a direct visualization of the charge trap formation in individual SiNCs, a level of detail which until now had been achieved only in theoretical studies.
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http://dx.doi.org/10.1021/acs.jpclett.7b03299 | DOI Listing |
We propose a physical mechanism allowing topological excitations with the same Bloch momentum belonging to distinct gaps to be resonant switched. This offers an opportunity to observe both intra-gap and inter-gap resonant edge-state switching. Increasing modulation depth significantly accelerates the resonant switching, while frequency de-tuning inhibits the switching.
View Article and Find Full Text PDFNano Res
September 2024
Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio, 43210, USA.
Hot spot engineering in plasmonic nanostructures plays a significant role in surface enhanced Raman scattering for bioanalysis and cell imaging. However, creating stable, reproducible, and strong SERS signals remains challenging due to the potential interference from surrounding chemicals and locating SERS-active analytes into hot-spot regions. Herein, we developed a straightforward approach to synthesize intra-gap nanoparticles encapsulating 4-nitrobenzenethiol (4-NBT) as a reporter molecule within these gaps to avoid outside interference.
View Article and Find Full Text PDFBiosensors (Basel)
September 2024
State Key Laboratory for Organic Electronics and Information Displays & Jiangsu Key Laboratory for Biosensors, Institute of Advanced Materials (IAM), Jiangsu National Synergetic Innovation Center for Advanced Materials (SICAM), Nanjing University of Posts and Telecommunications, Nanjing 210023, China.
Plasmonic intragap nanostructures (PINs) have garnered intensive attention in Raman-related analysis due to their exceptional ability to enhance light-matter interactions. Although diverse synthetic strategies have been employed to create these nanostructures, the emphasis has largely been on PINs with simple configurations, which often fall short in achieving effective near-field focusing. Three-dimensional (3D) complex PINs, distinguished by their intricate networks of internal gaps and voids, are emerging as superior structures for effective light trapping.
View Article and Find Full Text PDFNanoscale
June 2024
Department of Physics "E. Pancini", University of Naples Federico II, Complesso Universitario di Monte S. Angelo, Via Cintia 21, 80126 Napoli, Italy.
The study of titanium dioxide (TiO) in the brookite phase is gaining popularity as evidence has shown the efficient photocatalytic performance of this less investigated polymorph. It has been recently reported that defective anisotropic brookite TiO nanorods display remarkable substrate-specific reactivity towards alcohol photoreforming, with rates of hydrogen production significantly (18-fold) higher than those exhibited by anatase TiO nanoparticles. To elucidate the basic photo-physical mechanisms and peculiarities leading to such an improvement in the photoactive efficiency, we investigated the recombination processes of photoexcited charge carriers in both stoichiometric and reduced brookite nanorods photoluminescence excitation spectroscopy in controlled environment.
View Article and Find Full Text PDFSolution-processed colloidal cadmium chalcogenide nanoplatelets (NPLs)-based photodetectors (PD) are promising materials for next-generation optoelectronic devices due to their excellent optical properties. Here, we report on ultrafast carrier relaxation dynamics of four monolayer (4 ML) Ag-doped CdSe (Ag: CdSe) NPLs using ultrafast transient absorption spectroscopy and their photodetectors applications. A broad dopant emission is observed at around 650 nm with a large FWHM of ~431 meV and band edge emission at 515 nm.
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