ABSTRACT
Second-harmonic generation (SHG) has rapidly advanced with the miniaturization of on-chip devices and has found many applications, including optical frequency conversion, nonlinear imaging, and quantum technology. However, owing to the obvious phase-matching constraints involved in nonlinear optical interactions in bulk crystals and the decrease in the length and strength of nonlinear interactions in nanophotonic and surface/interface systems, improving the SHG efficiency and manipulating its optical properties at the nanoscale are challenging tasks. Herein, a monocrystalline silver microplate and nanocube-coupled nanocavity with double-resonance plasmonic modes and an ultrasmall gap were constructed, resulting in efficiently enhanced SHG. In particular, the SHG from the silver microplate (111) is polarization-dependent, and the anisotropy of the SHG in the plasmonic nanocavity can be further controlled via the superposition of symmetries at the interface and plasmonic waveguide-cavity modes. The interfacial SHG provides technology for developing lattice surface atomic arrangement and nanostructure rapid characterization, nonlinear light sources, and on-chip nonlinear nanophotonic devices.
ABSTRACT
Plasmonic metal nanostructures with the intrinsic property of localized surface plasmon resonance can effectively promote energy conversion in many applications such as photocatalysis, photothermal therapy, seawater desalinization, etc. It is known that not only are plasmonically excited hot electrons generated from metal nanostructures under light irradiation, which can effectively trigger chemical reactions, but also plasmonically induced heating simultaneously occurs. Although plasmonic catalysis has been widely explored in recent years, the underlying mechanisms for distinguishing the contribution of hot electrons from thermal effects are not fully understood. Here, a simple and efficient self-assembly system using silver nanoislands as plasmonic substrates is designed to investigate the photo-induced azo coupling reaction of nitro- and amino-groups at various temperatures. In the experiments, surface-enhanced Raman spectroscopy is employed to monitor the time and temperature dependence of plasmon-induced catalytic reactions. It was found that a combination of hot electrons and thermal effects contribute to the reactivity. The thermal effects play the dominant role in the plasmon-induced azo coupling reaction of nitro-groups, which suggests that the localized temperature must be considered in the development of photonic applications based on plasmonic nanomaterials.
ABSTRACT
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/m2 of native surfactants to 5600 cd/m2 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.
ABSTRACT
Plasmonic nanostructures with sharp tips are widely used for optical signal enhancement because of their strong light-confining abilities. These structures have a wide range of potential applications, for example, in sensing, bioimaging, and surface-enhanced Raman scattering. Au nanoparticles, which are important plasmonic materials with high photothermal conversion efficiencies in the visible to near-infrared region, have contributed greatly to the development of photothermal catalysis. However, the existing methods for synthesizing nanostructures with tips need the assistance of poly(vinylpyrrolidone), thiols, or biomolecules. This greatly hinders signal detection because of stubborn residues. Here, we propose an efficient binary surfactant-mediated method for controlling nanotip growth on Au nanoparticle surfaces. This avoids the effects of surfactants and can be used with other Au nanostructures. The Au architecture tip growth process can be controlled well by adjusting the ratio of hexadecyltrimethylammonium bromide to hexadecyltrimethylammonium chloride. This is due to the different levels of attraction between Br-/Cl- and Au3+ ions. The surface-enhanced Raman scattering and catalytic abilities of the synthesized nanoparticles with tips were evaluated by electromagnetic simulation and photothermal catalysis experiments (with 4-nitrothiophenol). The results show good potential for use in surface-enhanced Raman scattering applications. This method provides a new strategy for designing plasmonic photothermal nanostructures for chemical and biological applications.
ABSTRACT
Photothermal utilization is an important approach for sustaining global ecological balance. Due to the enhancement of light absorption through surface plasmon resonance, silver or gold nanostructures can be used as efficient photothermal heat sources in visible and near-infrared regions. Herein, a heat-trapping system of self-assembled gold nanoislands with a thin Al2O3 layer is designed to significantly enhance the photothermal effect, which can contribute to a fast crystal transformation. Compared with pure gold nanoislands, an approximately 10-fold enhancement of the photothermal conversion efficiency is observed by using the heat-trapping layer, which results from enhanced light absorption and efficient heat utilization. With the heat-trapping layer, a relatively high and stable photothermal conversion efficiency is realized even at low temperature, and the thermal stability of the plasmonic nanostructure is also observed to improve, especially for silver nanoislands used in air. These results provide a strong additional support for the further development of photothermal applications and offer an efficient pathway for the thermal manipulation of plasmons at the nanoscale.
ABSTRACT
With soil carbon cycle compartment model,this paper studied the carbon storage and flux of each carbon compartment of soil under Pinus tabulaeformis, a main forest type in the Huoditang forest region of Qinling Mountain. The results showed that the storage of soil organic carbon was 146.071 t x hm(-2), with 130.366 t x hm(-2) in mineral soil layer and 12.626 t x hm(-2) in litter layer. The storage was lower than the average value of forest soils in China and of oak Sharptooth forest soil in Huoditang, but higher than that of the soils under temperate coniferous forest and tropical forest. The annual carbon input into litter layer was 5.939 t x hm(-2), with 56.9% from above-ground litter and 43.1% from underground dead roots, while that into mineral soil layer via humic acid was 2. 034 t x hm(-2). The annual amount of carbon released from the respiration of P. zabulaeformis forest-soil system was 14. 012 t x hm(-2), with litter layer, mineral soil layer, dead root system, and live root system occupied 15.7%, 14.5%, 11.7% and 58.1%, respectively.
