Low resistivity transparent conducting Al-doped ZnO films prepared by pulsed laser deposition

A series of AZO films were grown on glass substrates by a method of pulsed laser deposition using a split target divided into AZO (Al₂O₃: 1 wt.%) and AZO (Al₂O₃: 2 wt.%). The film deposition took place at a substrate temperature of 230 °C within a magnetic field applied perpendicularly to the plume. To suppress the droplet generation caused by the intense laser energy, the laser energy density was reduced to 0.75 J/cm² (15 mJ). For an approximately 280-nm thick-AZO film grown at a target-to-substrate distance of 25 mm, we obtained the lowest resistivity of 8.54×10⁻⁵ Ω·cm and an average transmittance of more than 88% in the visible range. In the cross-sectional TEM observation and XRD spectra, the regularity in the crystal growth was generated immediately from the interface between the substrate and the film.     

ZnO thin films prepared by pulsed laser deposition

Zinc oxide (ZnO) thin films were deposited on soda lime glass substrates by pulsed laser deposition (PLD) in an oxygen-reactive atmosphere. The structural, optical, and electrical properties of the as-prepared thin films were studied in dependence of substrate temperature and oxygen pressure. High quality polycrystalline ZnO films with hexagonal wurtzite structure were deposited at substrate temperatures of 100 and 300 °C. The RMS roughness of the deposited oxide films was found to be in the range 2-9 nm and was only slightly dependent on substrate temperature and oxygen pressure. Electrical measurements indicated a decrease of film resistivity with the increase of substrate temperature and the decrease of oxygen pressure. The ZnO films exhibited high transmittance of 90% and their energy band gap and thickness were in the range 3.26-3.30 eV and 256-627 nm, respectively.     

Metal-semiconductor transition in Nb-doped ZnO thin films prepared by pulsed laser deposition

The structural, electrical and optical properties of Nb-doped ZnO films were investigated with different Nb contents (0, 0.15, 0.31, 0.46, 0.62, and 0.94 at.%) in this article. The film with 0.46 at.% Nb content showed the lowest resistivity of 8.95 × 10^− 4 Ω cm and high transmittance about 80% with high c-axis orientation. The undoped ZnO film showed a semiconducting behavior. And Nb-doped ZnO films showed a metal-semiconductor transition (MST), which was connected with localization of degenerate electrons. The films showed metallic conductivity at temperatures closer to the ambient temperature and semiconducting behavior at lower temperatures. It was noted that the NZO films with much lower Nb concentration of 0.15 at.% presented MST compared with other transparent conducting oxides films.     

Reversible wettability of ZnO nanostructured thin films prepared by pulsed laser deposition

This work reports on the photoinduced wettability changes of high quality nanostructured ZnO films grown on Si by pulsed laser deposition (PLD) under different growth parameters. The wetting behavior of the resulting films can be reversibly switched from hydrophobic to hydrophilic, through alternation of UV illumination and dark storage. The kinetics of this wetting transition are studied by monitoring the time evolution of the corresponding contact angles. Finally, the influence of the film properties over the observed wetting response is discussed.     

Transparent conducting F-doped SnO2 thin films grown by pulsed laser deposition

Transparent conducting fluorine-doped tin oxide (SnO₂:F) films have been deposited on glass substrates by pulsed laser deposition. The structural, electrical and optical properties of the SnO₂:F films have been investigated as a function of F-doping level and substrate deposition temperature. The optimum target composition for high conductivity was found to be 10 wt.% SnF₂ + 90 wt.% SnO₂. Under optimized deposition conditions (T_s = 300 °C, and 7.33 Pa of O₂), electrical resistivity of 5 × 10^− 4 Ω-cm, sheet resistance of 12.5 Ω/□, average optical transmittance of 87% in the visible range, and optical band-gap of 4.25 eV were obtained for 400 nm thick SnO₂:F films. Atomic force microscopy measurements for these SnO₂:F films indicated that their root-mean-square surface roughness ( 6 Å) was superior to that of commercially available chemical vapor deposited SnO₂:F films ( 85 Å).     

Transparent p-type conducting K-doped NiO films deposited by pulsed plasma deposition

Transparent p-type conducting K-doped NiO thin films were prepared by pulsed plasma deposition. The structural, electrical and optical properties of the films were investigated using X-ray diffraction, atomic force microscope, X-ray photoelectron spectroscopy, Hall measurement, and ultraviolet-visible spectroscopy, respectively. The dependency of film properties on K doping content and substrate temperature was studied. The film with K doping content of 25 at.% deposited at room temperature exhibits the highest conductivity of 4.25 S cm^− 1 and an average transmittance of nearly 60% in visible light region.     

Electric properties and surface characterization of transparent Al-doped ZnO thin films prepared by pulsed laser deposition

We grew 2 wt.% Al-doped ZnO (AZO) films on 5.08 cm-diameter polymer substrates at room temperature by the pulsed laser deposition (PLD) technique added the beam-rastering function. The structural properties, surface morphology, resistivity, mobility and chemical bonding states of AZO/polymer films were measured. The structuring of polymer surface by atmospheric plasma can occur at nm scales and can influence adhesion, optical and wettability properties of the materials. With increasing plasma treatment power, surface hydrophilicity and roughness for PET and PES polymer increased, respectively.     

Al-doped ZnO films by pulsed laser deposition at room temperature

Polycrystalline Al-doped ZnO films with good photoluminescence property were successfully deposited on quartz glass substrates by pulsed laser deposition (PLD) at room temperature. The films were obtained by ablating a metallic target (Zn:Al 3 wt%) at various laser energy densities (1.0-2.1 J/cm²) in oxygen atmosphere (9 Pa). The structure of the films was characterized by XRD. Ultraviolet photoluminescence centered at 359-361 nm was observed in the room temperature PL spectra of the Al-doped ZnO films.     

Nano-polycrystalline vanadium oxide thin films prepared by pulsed laser deposition

Nano-polycrystalline vanadium oxide thin films have been successfully produced by pulsed laser deposition on Si(100) substrates using a pure vanadium target in an oxygen atmosphere. The vanadium oxide thin film is amorphous when deposited at relatively low substrate temperature (500 degrees C) and enhancing substrate temperature (600-800 degrees C) appears to be efficient in crystallizing VOx thin films. Nano-polycrystalline V3O7 thin film has been achieved when deposited at oxygen pressure of 8 Pa and substrate temperature of 600 degrees C. Nano-polycrystalline VO2 thin films with a preferred (011) orientation have been obtained when deposited at oxygen pressure of 0.8 Pa and substrate temperatures of 600-800 degrees C. The vanadium oxide thin films deposited at high oxygen pressure (8 Pa) reveal a mix-valence of V5+ and V4+, while the VOx thin films deposited at low oxygen pressure (0.8 Pa) display a valence of V4+. The nano-polycrystalline vanadium oxide thin films prepared by pulsed laser deposition have smooth surface with high qualities of mean crystallite size ranging from 30 to 230 nm and Ra ranging from 1.5 to 22.2 nm. Relative low substrate temperature and oxygen pressure are benifit to aquire nano-polycrystalline VOx thin films with small grain size and low surface roughness.     

脉冲激光沉积氮化铝薄膜的电学性能研究

采用脉冲激光沉积(PLD)技术在硅片上合成了AlN薄膜.X射线衍射(XRD)结果证实制备的AlN薄膜具有(002)择优取向的六方纤锌矿晶体结构,并且结晶质量随Si衬底温度的提高而改善.电流-电压(I-V)、电容-电压(C-V)、极化曲线结果表明室温生长的AlN薄膜的击穿场强约2.5MV/cm,同时呈现明显的极化现象(类铁电),对应矫顽场强为150kV/cm,剩余极化为0.002C/m2.晶态AlN存在较强的自发极化,薄膜中可动电荷密度高,据此提出了动态电荷模型,指出较大的AlN薄膜极化回线是由于可动电荷在电场中的再分布形成的,因而有别于铁电材料.     

Superhard tungsten tetraboride films prepared by pulsed laser deposition method

Attempts to synthesize and/or theoretically predict new superhard materials are the subject of an intense research activity. The trials to deposit them in the form of films have just began. WB(2) (77 wt % WB(2) and 23 wt % WB(4)) and WB(4) (65 wt % WB(4) and 35 wt % WB(2)) polycrystalline bulk samples were obtained in this work via electron beam synthesis technique and, subsequently, used as targets for films preparation by the pulsed laser deposition method. The targets were irradiated by a frequency-doubled Nd:glass laser with a pulse duration of 250 fs. The films grown on SiO(2) substrates at 600 °C were characterized by X-ray diffraction, scanning electron and atomic force microscopies, and Vickers microhardness technique. The deposited films are composed of WB(4). The intrinsic film hardness, calculated according to the "law-of-mixtures" model, lies in the superhardness region 42-50 GPa.     

ZnO(101) films by pulsed reactive crossed-beam laser ablation

We have employed pulsed reactive crossed-beam laser ablation (PRCLA) to deposit a (101) oriented ZnO film. In this method, a supersonic jet of oxygen pulse is made to cross the laser plume from a zinc metal target while being carried to the Si(111) substrate. The obtained deposit was nanocrystalline ZnO as confirmed by a host of characterization techniques. When the substrate was held at varying temperatures, from room temperature to 900°C, the crystallinity of the obtained films increased as expected, but importantly, the crystallographic orientation of the films was varied. High substrate temperatures produced the usual (001) oriented films, while lower substrate temperatures gave rise to increasingly (101) oriented films. The substrate held at room temperature contained only the (101) orientation. The film morphology also varied with the substrate temperature, from being nanoparticulate to rod-like deposits for higher deposition temperatures. Surprisingly, the (101) orientation showed reactivity with acetone forming carbonaceous nanostructures on the surface.     

Microstructural evolution in lubricious ZnO films grown by pulsed laser deposition

Zinc oxide (ZnO) is well known to the electronic industry as a piezoelectric material. Recent research from this laboratory also indicates the potential of ZnO as a tribological material. The current work describes the evolution of microstructure with deposition parameters in pulsed laser deposited ZnO thin films, specifically targeted for friction and wear applications. Films were characterized by high resolution scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD). Friction and wear measurements were made using a ball-on-disk tribometer. Films were grown in vacuum (V) as well as in 5 mTorr of oxygen (O₂), while the substrates were kept at room temperature (RT). The RT/V ZnO films have (002) columnar texture with an average column width of 20 nm. The RT/O₂ films also are nanoclumnar with (002) texture, but each column is a mosaic of low-angle boundaries. Deformation mechanisms associated with nanocrystalline grain structure were analyzed with particular reference to sliding contact. Mechanisms to provide the observed low friction of RT/O₂ films (μ=0.15–0.20) have been activated by its mosaic structure.     

Effect of GaN doping on ZnO films by pulsed laser deposition

The present study reveals the codoping of Ga and N into ZnO films on sapphire substrates by pulsed laser deposition (PLD) with GaN doped ZnO targets. The glow discharge mass spectroscopy (GDMS) spectra confirm the presence of Ga and N in the doped films. The XRD measurements show that for GaN concentration up to 0.8 mol%, the full width at half maximum (FWHM) is almost unchanged thereby maintaining the crystallinity of the films, while for 1 mol% the FWHM increases. The PL spectra only show the strong near band edge (NBE) emission, whereas the deep level emissions are almost undetectable, indicating that they have been considerably suppressed. Our Hall measurements indicate that all the GaN doped ZnO films are of n-type. However, as the GaN concentration is greater than 0.6 mol%, the film shows a decrease in the carrier concentration, suggesting that N acceptors are not sufficient to compensate the native donor defects.     

Structural analysis of Ti-Fe thin films prepared by pulsed laser deposition

Titanium iron oxide (Ti-Fe-O) thin films have been successfully deposited by pulsed laser deposition (PLD). Experiments were carried out by using some targets. One was a Ti-50 at.% Fe-sintered target, while the others were Ti and Fe plates with various surface area ratio [S_R=S_Fe/(S_Fe+S_Ti)] from 30 to 70%. The thin films were analyzed by X-ray diffractometry, Rutherford backscattering spectroscopy (RBS) and transmission electron microscopy (TEM). From XRD analysis, the main phase in the thin films deposited at S_R=30 and 50% was β-Ti (Fe). By increasing S_R to 70%, the main phase of the thin film changed to TiFe. By phase diagram, composition of TiFe must be between Ti-47.5-50.3 at.% Fe at a temperature of 1085 °C. However, the composition of the thin film deposited at S_R=70% was found to be Ti_0.15Fe_0.62O_0.23. Thus, the composition of Fe in the thin film was much greater than the solubility limit. This fact suggests two possibilities. One is that the thin films, which we have deposited, were in a metastable state. The other is that metal oxides of amorphous state could be contained in the thin film.     

Characterization of rhenium nitride films produced by reactive pulsed laser deposition

Rhenium nitride (ReN_x) films were grown on (100)-Si substrates by the reactive pulsed laser deposition (PLD) method using a high purity Re rod in an environment of molecular nitrogen. The resulting films are characterized by several techniques, which include in situ Auger electron spectroscopy, X-ray photoelectron spectroscopy and ex situ X-ray diffraction, scanning electron and atomic force microscopy. Additionally, the four-probe method is used to determine the sheet resistance of deposited layers. Results show that films with N/Re ratios (x) lower than 1.3 are very good conductors. In fact, the resistivity of ReN films for 0.2 < x < 1.3 is of the order of 5% of that of Re films, while at x = 1.3 there is an abrupt increment in resistivity, resulting in dielectric films for 1.3 < x < 1.35. These results differ from the prior understanding that in transition metals, resistivity should increase with nitrogen incorporation.     

Ultrathin Al-doped transparent conducting zinc oxide films fabricated by pulsed laser deposition

Al-doped transparent conducting zinc oxide (AZO) films, approximately 20-110 nm-thick, were deposited on glass substrates at substrate temperatures between 200 and 300 °C by pulsed laser deposition (PLD) using an ArF excimer laser (λ = 193 nm). When fabricated at a substrate temperature of 260 °C, a 40-nm-thick AZO film showed a low resistivity of 2.61 × 10^− 4 Ω·cm, carrier concentration of 8.64 × 10²⁰ cm^− 3, and Hall mobility of 27.7 cm²/V·s. Furthermore, for an ultrathin 20-nm-thick film, a resistivity of 3.91 × 10^− 4 Ω·cm, carrier concentration of 7.14 × 10²⁰ cm^− 3, and Hall mobility of 22.4 cm²/V·s were obtained. X-ray diffraction (XRD) spectra, obtained by the θ-2θ method, of the AZO films grown at a substrate temperature of 260 °C showed that the diffraction peak of the ZnO (0002) plane increased as the film thickness increased from 20 to 110 nm. The full-width-at-half-maximum (FWHM) values were 0.5500°, 0.3845°, and 0.2979° for film thicknesses of 20, 40, and 110 nm, respectively. For these films, the values of the average transmittance in visible light wavelengths (400-700 nm) were 95.1%, 94.2%, and 96.6%, respectively. Field emission scanning electron microscopy (FE-SEM) and atomic force microscopy (AFM) observations showed that even the 20-nm-thick films did not show island structures. In addition, exfoliated areas or vacant and void spaces were not observed for any of the films.     

Growth and characterization of non-polar ZnO thin films by pulsed laser deposition

Non-polar ZnO thin films were fabricated on r-plane sapphire substrates by pulsed laser deposition at various temperatures from 100 to 500 °C. The effects of the substrate temperature on structural, morphological and optical properties of the films were investigated. Based on the X-ray diffraction analysis, the ZnO thin films grown at 300, 400 and 500 °C exhibited the non-polar (a-plane) orientation and those deposited below 300 °C exhibited polar (c-plane) orientation. In the optical properties of non-polar ZnO films, there were two photoluminescence peaks detected. The peaks (near-band edge emission, blue emission) are due to electron transitions from band-to-band and shallow donor level to valence band, respectively.