Photothermal utilization is an important approach for sustaining global ecological balance. Since the enhancement of light absorption through surface plasmon resonance, silver or gold nanostructures can be used as efficient...
Surface-enhanced spectroscopies, such as surface-enhanced Raman scattering (SERS), fluorescence (SEF), circular dichroism, etc., are powerful tools for investigating nano-entities with high sensitivities. Owing to the giant local electric field confined in a plasmonic nanogap, nanogap-enhanced spectroscopies could detect samples with ultralow concentrations, even down to the single-molecule level for SERS and SEF. This great ability to detect analytes with ultralow concentrations provides opportunities for early diagnosis and monitoring in modern biomedicine. However, local laser excitations would inevitably bring about unwanted disruptive background perturbations, local heating, and the consequent geometry reshaping and biological analyte damages. Remote spectroscopies avoiding direct laser exposure to the samples can be treated as remarkable solutions. Here, we combined the nanoparticle-on-mirror (NPoM) family with the philosophy of remote spectroscopy to construct so-called “NPoM pairs” structures. They consist of two identical NPoMs with matched resonances yet separate functions either as receiving or transmitting antennas. A figure of merit for evaluating the remote spectroscopies was put forward, which accounts for the efficiencies in three processes, i.e., receiving, transporting, and transmitting. In addition, we experimentally demonstrated the performances of these NPoM pairs by proof-of-principle applications on the remote SERS and SEF. The optical access of the spectral information in these NPoM pairs both locally and remotely manifests themselves as fundamental building blocks for remote spectroscopies.
Colloidal nanocrystals (NCs) play an important role in the field of optoelectronic devices such as photovoltaic cells, photodetectors, and light-emitting diodes (LEDs). The properties of NC films are strongly affected by ligands attached to them, which constitute a barrier for charge transport between adjacent NCs. Therefore, the method of surface modification by ligand exchange has been used to improve the electrical conductivity of NC films. However, surface modification to NCs in LEDs can also affect emission characteristics. Among NCs, nanorods have unique properties, such as suppression of nonradiative Auger recombination and linearly polarized light emission. In this work, CdSe/CdS nanorods (NRs) were prepared by the hot injection method. To increase the charge transport into CdSe/CdS NRs, we adopted ligand modification to CdSe/CdS NRs. Using this technique, we could shorten the injection barrier length between CdSe/CdS NRs and adjacent layers. It leads to a more balanced charge injection of electron/hole and a greatly increased current efficiency of CdSe/CdS NR-LEDs. In the NR-LEDs, the ligand exchange boosted the electroluminance, reaching a sixfold increase from 848 cd/m 2 of native surfactants to 5600 cd/m 2 of the exchanged n-octanoic acid ligands at 12 V. The improvement of CdSe/CdS NR-LED performance is closely correlated to the efficient control of charge balance via ligand modification strategy, which is expected to be indispensable to the future NR-LED-based optoelectronic system.
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