Absorption and scattering of infrared radiation by vanadium dioxide nanoparticles with a metallic shell

The numerical simulation of the absorption and scattering cross sections of vanadium dioxide nanoparticles with silver and gold shells are presented. The cross sections are evaluated for the spectral intervals 1–1.2, 1.3–1.7, and 9–12 µm both before and after the semiconductor-metal phase transition in VO₂. It is demonstrated that the transition of VO₂ to the metallic state near (or away from) plasmon resonances leads to a decrease (or increase) in the absorption and scattering cross sections for a given wavelength. The decrease is related to the shift of the plasmon resonance band, whereas the increase is directly related to the growth of the VO₂ absorption upon the phase transition.     

10.6 μm Infrared light photoinduced insulator-to-metal transition in vanadium dioxide

Vanadium dioxide has excellent phase transition characteristic. Before or after phase transition, its optical, electrical, magnetic characteristic hangs hugely. It has a wide application prospect in many areas. Now, the light which can make vanadium dioxide come to pass photoinduced phase transition range from soft X-ray to medium infrared light (6.9 μm, 180 meV). However, whether 10.6 μm (117 meV) long wave infrared light can make vanadium dioxide generate photoinduced phase transition has been not studied. In this paper, we researched the response characteristic of vanadium dioxide excited by 10.6 μm infrared light. We prepared the vanadium dioxide and test the changes of vanadium dioxide thin film’s transmittance to 632.8 nm infrared light when the thin film is irradiate by CO₂ laser. We also test the resistivity of vanadium dioxide. Excluding the effect of thermal induced phase transition, we find that the transmittance of vanadium dioxide thin film to 632.8 nm light and resistivity both changes when irradiating by 10.6 μm laser. This indicates that 10.6 μm infrared light can make the vanadium dioxide come to pass photoinduced phase transition. The finding makes vanadium has a potential application in recording the long-wave infrared hologram and making infrared detector with high resolution.     

Temperature-controlled surface plasmon resonance in VO (2) nanorods

The optical properties of VO(2) nanoparticles formed in an amorphous SiO(2) host by stoichiometric ion implantation of vanadium and oxygen and thermal annealing have been determined and correlated with the particle size and morphology. The results show that that the temperature-controlled semiconductor-to-metal phase transition of the VO(2) nanophase precipitates turns on the classical surface plasmon resonance, with specific features that depend on the size and aspect ratio of the VO(2) particles. This effect improves the optical contrast between the metallic and semiconducting states in the near-IR region of the spectrum as a result of dielectric confinement that is due to the SiO(2) host. A fiber-optic application is demonstrated, as is the ability to control the characteristics of the phase transition by using ion implantation to dope the VO(2) nanoparticles with tungsten or titanium ions.     

连续激光辐照下二氧化钒薄膜热致相变实验研究

 介绍了VO₂薄膜的相变原理，用磁控离子溅射法制备了VO₂薄膜，并进行了X射线衍射和不同温度下的光谱透过率测量。在1.319 μm 连续波激光辐照下，实时测量了VO₂薄膜的温度变化，以及由于温度变化引起相变后对激光透过率的变化。结果表明，入射到薄膜表面的平均功率为8.9 W、光斑直径2 mm时，激光出光480 ms后，VO₂的温度从室温上升到约100 ℃，薄膜发生了相变，其对1.319 μm激光的透过率从相变前的48％降为相变后的28％。     

Influence of hydrogenation on electrical conductivity of vanadium dioxide thin films

The influence of hydrogenation on electrical conductivity of vanadium dioxide thin films has been investigated. It has been shown using measurements of the electrical conductivity that the hydrogenation of vanadium dioxide thin films leads to a decrease in the temperature of the phase transition from the tetragonal phase (with “metallic” conductivity) to the semiconducting monoclinic phase. It has been found that, upon doping of vanadium dioxide with hydrogen, the electrical conductivity of the monoclinic phase can increase by several orders of magnitude. Nonetheless, the temperature dependence of the electrical conductivity of hydrogenated films exhibits a typical semiconducting behavior in the temperature range where the monoclinic phase is stable.     

Synthesis and the properties of vanadium dioxide nanocrystals in porous silicate glasses

Vanadium dioxide nanoparticles were synthesized in nanoporous silicate glasses with pore sizes of 7 and 17 nm. The temperature dependences of the optical and electrical properties of the composite obtained were studied near the temperature of the semiconductor-metal phase transition in vanadium dioxide. The non-linear optical response of the nanoparticles to picosecond laser pulses was studied in the visible and near-infrared ranges.     

金-二氧化钛（Au-TiO_2）复合薄膜的制备及局域表面等离子体共振（LSPR）效应

利用溶胶凝胶法在玻璃衬底上制备了金-二氧化钛（Au-TiO2）复合纳米薄膜,研究了热处理温度对复合薄膜表面纳米颗粒沉积的影响。利用原子力显微镜对样品进行了形貌表征,结果显示：复合薄膜是由纳米微晶组成的致密膜,温度越高越有利于Au粒子的形成。在550℃的热处理温度下,薄膜表面沉积的纳米微晶的粒径约为100nm。利用紫外-可见分光光度计测量了反射谱线,结果表明：由于局域表面等离子体共振（LSPR）的产生,在不同的热处理温度下,第一个反射峰（短波长处）不发生变化,第二个反射峰（长波长处）发生漂移（红移）。     

Terahertz spectroscopy studies on epitaxial vanadium dioxide thin films across the metal-insulator transition

We present results on terahertz (THz) spectroscopy on epitaxial vanadium dioxide (VO(2)) films grown on sapphire across the metal-insulator transition. X-ray diffraction indicates the VO(2) film is highly oriented with the crystallographic relationship: (002)(film)//(0006)(sub) and [010](film)//[2 ?1 ?10](sub). THz studies measuring the change in transmission as a function of temperature demonstrate an 85% reduction in transmission as the thin film completes its phase transition to the conducting phase, which is much greater than the previous observation on polycrystalline films. This indicates the crucial role of microstructure and phase homogeneity in influencing THz properties.     

Photoinduced heterostructure in a vanadium dioxide film

Physics of the Solid State - A photoinduced semiconductor–metal phase transition that occurs in a surface layer of vanadium dioxide film on an aluminum substrate within the time Δt...     

The characteristics of Au:VO2 nanocomposite thin film for photo-electricity applications

Au nanoparticles have been fabricated on normal glass substrates using nanosphere lithography (NSL) method. Vanadium dioxide has been deposited on Au/glass by reactive radio frequency (rf) magnetron sputtering. The structure and composition were determined by X-ray diffraction and X-ray photoelectron spectroscope. Electrical and optical properties of bare VO₂ and Au:VO₂ nanocomposite thin films were measured. Typical hysteresis behavior and sharp phase transition were observed. Nanopartical Au could effectively reduce the transition temperature to 40 °C. The transmittance spectrum for both Au:VO₂ nanocomposite thin film shows high transmittance under transition temperature and low transmittance above transition temperature. The characteristics present the Au:VO₂ nanocomposite thin film can be used for applications, such as “smart window” or “laser protector”.     

掺钨VO_2薄膜的电致相变特性

采用直流磁控溅射与后退火工艺相结合的方法,在掺氟SnO_2(FTO)导电玻璃基底上制备了高质量的掺钨VO_2薄膜,对薄膜的结构、表面形貌和光电特性进行测试,分析了钨掺杂对其相变性能的影响.结果表明,室温下掺钨VO_2薄膜的阈值电压为4.2 V,观察到阈值电压下约有两个数量级的电流突变.随着温度升高,相变的阈值电压降低,且电流突变幅度减小.当施加8 V电压时,分别在不同温度下测试了掺钨VO_2薄膜的透过率.温度为20和50℃时,掺钨VO_2薄膜相变前后的红外透过率差量分别为23%和27%.与未掺杂的VO_2薄膜相比,掺钨VO_2薄膜具有相变温度低、阈值电压低和电阻率小的特点,在高速光电器件中有广阔的应用前景.     

二氧化钒纳米点阵红外光学特性研究

针对二氧化钒纳米点阵从半导体到金属的可逆相变,考虑到点阵中各个点之间散射光的交互作用,基于VO2在不同温度和波长下的折射率和消光系数,以及小颗粒的吸收和散射特性,建立了VO2纳米颗粒的数学模型,研究了VO2纳米颗粒的相变光学特性.结果表明,随着波长变化,吸收截面相对散射截面占主导,金属相在980 nm附近出现吸收峰值|随着温度变化,可见光区域的消光系数变化较小,而红外区域较大,其中在近红外区域的消光系数变化最大.在纳米点阵中,消光截面随着颗粒间距变化,当颗粒间距增大时,消光峰值出现红移,且峰值大小也会随之增大|当间距超过一定数值后,峰值反而会逐渐减小.采用多孔氧化铝掩模的方法,通过磁控反应溅射制备VO2纳米点阵,测试结果表明其透过率比薄膜的透过率高.     

On a Photoinduced Heterostructure in a Vanadium Dioxide Film

Physics of the Solid State - An athermal photo-induced semiconductor-metal phase transition that occurs in a vanadium dioxide film on an aluminum substrate for time Δt < 1 ps is studied...     

Size-dependent optical properties of VO2 nanoparticle arrays

The size effects on the optical properties of vanadium dioxide nanoparticles in ordered arrays have been studied. Contrary to previous VO2 studies, we observe that the optical contrast between the semiconducting and metallic phases is dramatically enhanced in the visible region, presenting size-dependent optical resonances and size-dependent transition temperatures. The collective optical response as a function of temperature presents an enhanced scattering state during the evolving phase transition. The effects appear to arise because of the underlying VO2 mesoscale optical properties, the heterogeneous nucleation behind the phase transition, and the incoherent coupling between the nanoparticles undergoing an order-disorder-order transition. Calculations that support these interpretations are presented.     

Fabrication and optical study of Ag@SnO<Subscript>2</Subscript> core-shell structure nanoparticle thin films

Ag@SnO₂ core-shell nanoparticles dispersed in poly-(vinyl) alcohol films were fabricated on glass substrate by employing a dip-coating technique. Synthesis of Ag@SnO₂ nanoparticles with core-shell morphology is carried out by a soft-chemical technique in aqueous phase at 60°C. Formation of core-shell structure is monitored by the red-shift of the surface plasmon band of Ag nanoparticles (from 390 to 410 nm) in the UV-visible spectrum. These nanoparticles are deposited on the glass substrate. The structure and morphology of these films were investigated by X-ray diffraction technique and field-emission transmission electron microscopy, respectively. Optical properties of these pseudo-solids were studied by UV-visible spectroscopy. Surface plasmon spectrum of the core-shell nanoparticles film remained unaltered with increase in the number of layers. However, silver nanoparticles films have shown peak broadening and development of additional peaks with increase in the number of layers. Our investigations showed that the surface plasmon band of the silver nanoparticles could be preserved by controlled deposition of the tin dioxide shell.     

Plasmonic enhancement of the vanadium dioxide phase transition induced by low-power laser irradiation

Nanocomposites consisting of gold nanoparticle (NP) arrays and vanadium dioxide (VO₂) thin films are noteworthy for the tunability of both their thermal and optical properties. The localized surface plasmon resonance (LSPR) of the Au can be tuned when its dielectric environment is modulated by the semiconducting-to-metal phase transition (SMT) of the VO₂; the LSPR itself can be altered by changing the shape of the NPs and the pitch of the NP array. In principle, then it should be possible to choose a combination of VO₂ film and Au LSPR properties that maximizes the overall optical response of the nanocomposite. To demonstrate this effect, transient transmission measurements were conducted on lithographically fabricated arrays of Au NPs of diameter 140?nm, array spacing 350 nm, and covered with a 60?nm thick films of VO₂ via pulsed laser deposition. Both Au::VO₂ nanocomposites and bare VO₂ film were irradiated with a shuttered 785?nm pump laser, and their optical response was probed at 1550?nm by a fixed-frequency diode laser. The Au::VO₂ nanocomposite exhibited an increased effective absorption coefficient 1.5 times that of the plain film and required 37?% less laser power to induce the SMT. The time-dependent temperature rise in the film as a function of laser intensity was calculated from these measurements and compared with both analytic and finite-element models. Our results suggest that Au::VO₂ nanocomposites may be useful in applications such as thermal-management coatings for energy efficient ??smart?? windows.     

Ultrafast semiconductor-metal phase transition in vanadium dioxide induced by a femtosecond laser pulse

A model is proposed for a photoinduced Peierls-type semiconductor-metal phase transition that makes it possible to determine the time dependence of the bandgap width in the electronic spectrum of vanadium dioxide subjected to a light field and the dependence of the time at which a photoinduced semiconductor-metal phase transition occurs on the laser pulse duration. The theoretical results obtained are consistent with experimental data on the illumination of a VO₂ film with an intense laser pulse.     

Effect of grain sizes on the metal-semiconductor phase transition in vanadium dioxide polycrystalline thin films

Experimental data on the effect of grain sizes on the shape and width of the hysteresis loop characterizing a metal-semiconductor phase transition in vanadium dioxide films are analyzed in terms of the classical theory of nucleation. It is shown that the factors responsible for the changes in the shape and width of the hysteresis loop with variations in the size of the grains making up a film are associated with the heterogeneous character of nucleation of a new phase, on the one hand, and with the elastic stresses arising in the phase transition, on the other.     

Enhanced photosusceptibility near Tc for the light-induced insulator-to-metal phase transition in vanadium dioxide

We use optical-pump terahertz-probe spectroscopy to investigate the near-threshold behavior of the photoinduced insulator-to-metal (IM) transition in vanadium dioxide thin films. Upon approaching Tc a reduction in the fluence required to drive the IM transition is observed, consistent with a softening of the insulating state due to an increasing metallic volume fraction (below the percolation limit). This phase coexistence facilitates the growth of a homogeneous metallic conducting phase following superheating via photoexcitation. A simple dynamic model using Bruggeman effective medium theory describes the observed initial condition sensitivity.     

Magnetically tunable surface plasmon resonance based on a composite consisting of noble metal nanoparticles and a ferromagnetic thin film

We demonstrate magnetically tunable surface plasmon resonance based on a composite consisting of noble metal nanoparticles and ferromagnetic thin film. We found that both the frequency and linewidth of the localized surface plasmon resonance can be manipulated by applying an external magnetic field. The underlying mechanism is attributed to the variation of the dielectric constant in the ferromagnetic thin film resulting from the change of magnetization. Our result shown here paves an alternative route for manipulation of the characteristics of the surface plasmon resonance, which may serve as a new design concept for the development of magneto-optical devices.