Preparation and gas-sensing properties of α-Fe2O3 thin films

Haematite (α-Fe₂O₃) thin films are prepared by two different chemical vapor deposition (CVD) processes: the atmospheric pressure CVD (APCVD) and the plasma enhanced CVD (PECVD). The films are analyzed by x-ray diffraction and scanning electron microscopy; their gas-sensing properties are also investigated. Experimental results show that APCVD α-Fe₂O₃ films are highly sensitive and selective to smoke while PECVD films are highly sensitive and selective to alcohol. A certain amount of quadrivalent metal in the films has an effect on their sensitivity and selectivity to gases. It is found that the films will “break down” under certain conditions.     

原子层沉积氧化铝薄膜对多晶太阳能电池表面钝化的影响

A stack of Al2O3/SiNx dual layer was applied for the back side surface passivation of p-type multi-crystalline silicon solar cells, with laser-opened line metal contacts, forming a local aluminum back surface field （local Al-BSF） structure. A slight amount of Al2O3, wrapping around to the front side of the wafer during the thermal atomic layer deposition process, was found to have a negative influence on cell performance. The different process flow was found to lead to a different cell performance, because of the Al2O3 wrapping around the front surface. The best cell performance, with an absolute efficiency gain of about 0.6% compared with the normal full Al-BSF structure solar cell, was achieved when the Al2O3 layer was deposited after the front surface of the wafer had been covered by a SiNx layer. We discuss the possible reasons for this phenomenon, and propose three explanations as the Ag paste, being hindered from firing through the front passivation layer, degraded the SiNx passivation effect and the Al2O3 induced an inversion effect on the front surface. Characterization methods like internal quantum efficiency and contact resistance scanning were used to assist our understanding of the underlying mechanisms.     

Structural,chemical, and electrical properties of Y2O3 thin films grown by atomic layer deposition with an (iPrCp)2Y(iPr-amd) precursor

Y₂O₃ thin films were grown by atomic layer deposition (ALD) through a heteroleptic liquid (iPrCp)₂Y(iPr-amd) precursor at 350 °C. The structural and chemical properties of both as-deposited and annealed Y₂O₃ films at 500 °C and 700 °C are analyzed by atomic force microscopy for variation in surface roughness, X-ray diffraction for crystalline structure, and X-ray photoelectron spectroscopy for chemical states. The as-deposited Y₂O₃ film shows the same crystalline orientation along the plane (222), a stoichiometric state, and minimal hydroxylate formation up to 700 °C. Being the dielectric layer in the metal-oxide-semiconductor capacitor, the as-deposited ALD-Y₂O₃ films with liquid (iPrCp)₂Y(iPr-amd) precursor without any post-deposition annealing show the much lower leakage density than ALD-Y₂O₃ with solid Y(MeCp)₃.     

Optical and electrical properties of Al2O3 films containing silicon nanocrystals

Optical, electrical, and structural properties of Al₂O₃ films subjected to silicon-ion implantation and annealing were investigated by means of photoluminescence measurements, current-voltage measurements and transmission electron microscopy. Transmission electron microscopy revealed that silicon nanocrystals were epitaxially formed in ϑ-Al₂O₃. Visible photolum inescence was observed, for the first time, from Al₂O₃ films containing silicon nanocrystals. Observed visible photoluminescence seems to be related to quantum size effects in silicon nanocrystals as well as localized radiative recombination centers located at the interface between silicon nanocrystals and matrix, similar to porous Si and other Si nanostructures. The conduction mechanism in the samples was studied by using dc current-voltage measurements. The conduction properties depend on temperature and applied electric fields. The conduction behavior in low electric fields consists of thermally activated region dominated by the Schottky conduction and nonthermally activated region in which carrier transport is controlled by space-charge-limited currents. The conduction behavior under relatively high electric fields is almost independent of temperature and well fitted by space-charge-limited conduction.     

电子束辐照下的石墨烯上的原子层沉积Al2O3介质层

为了研究石墨烯与高k介质的结合,使用原子层沉积氧化铝在石墨衬底上。沉积前使用电子束辐照,观测到了氧化铝明显改善的形貌。归因于电子束辐照过程中的石墨层的无定形变化过程。     

Preparation and characterization of sphere-like Cu2SnS3 nanoparticles and their dropcasted thin films

Ternary sphere-like Cu₂SnS₃(CTS) semiconductor and 2D hexagonal sheets were synthesized via a simple solvothermal method using PVP as the surface ligand at two temperatures of 180 and 220℃. The structural, morphological, and chemical compositions as well as optical properties of as-synthesized CTS particles were characterized using X-ray diffraction (XRD), Raman spectroscopy, energy dispersive X-ray spectrometry (EDS), field emission scanning electron microscopy (FESEM), and UV-Vis spectroscopy. The size of sphere-like particles and the side length of hexagonal sheets were within the range of 120-140 nm and 500 nm-2 μm, respectively. FESEM, XRD, and EDS were analyzed to investigate the mechanism of the morphological evolution of CTS particles. CTS particles showed proliferation of Sn atomic ratio, which is strongly sensitive to reaction temperature and, highly affects the increase of band gap energy from 1.36 to 1.53 eV due to generation metal defects and formation SnS₂. The optical analysis via the transmittance and reflectance reveals that the band-gap energy of dropcasted CTS thin films decreases after annealing due to grain growth and change of chemical compositions. Photo-responses of CTS nanocrystal thin films indicated a considerable increase in the conductivity of the films under light illumination. All these results showed the potential of these films for solar cell applications.     

Semiconductor nanowires surrounded by cylindrical Al2O3 shells

The GaN, GaP, InP, Si₃N₄, SiO₂/Si, SiC, and ZnO semiconductor nanowires were synthesized by a variety of growth methods, and they were wrapped cylindrically with amorphous aluminum oxide (Al₂O₃) shells. The Al₂O₃ was deposited on these seven different semiconductor nanowires by atomic layer deposition (ALD) at a substrate temperature of 200°C using trimethylaluminum (TMA) and distilled water (H₂O). Transmission electron microscopy (TEM) images taken for the nanowires revealed that Al₂O₃ cylindrical shells surround uniformly all these semiconductor nanowires. Our TEM study illustrates that the ALD of Al₂O₃ has an excellent capability to coat any semiconductor nanowires conformally; its coating capability is independent of the chemical component, lattice structure, and growth direction of the nanowires. This study suggests that the ALD of Al₂O₃ on nanowires is one of the promising methods to prepare cylindrical dielectric shells in coaxially gated, nanowire field-effect transistors (FETs).     

Effects of surface passivation during atomic layer deposition of Al2O3 on In0.53Ga0.47As substrates

In this work we investigate the effect of different III-V surface passivation strategies during atomic layer deposition of Al₂O₃. X-ray photoelectron spectroscopy indicates that bare As-decapped and sulfur passivated In_0.53Ga_0.47As present residual oxides on the surface just before the beginning of the Al₂O₃ deposition while the insertion of a Ge interface passivation layer results in an almost oxide free Ge/III-V interface. The study of the initial growth regimes, by means of in situ spectroscopic ellipsometry, shows that the growth of Al₂O₃ on Ge leads to an enhanced initial growth accompanied by the formation of Ge-O-Al species thus affecting the final electrical properties of the stack. Alternatively, deposition on decapped and S-passivated In_0.53Ga_0.47As results in a more controlled growth process. The sulfur passivation leads to a better electrical response of the capacitor that can be associated to a lower oxide/semiconductor interface trap density.     

Highly-impermeable Al2O3/HfO2 moisture barrier films grown by low-temperature plasma-enhanced atomic layer deposition

Polymer substrates are essential components of flexible electronic applications such as OTFTs, OPVs, and OLEDs. However, high water vapor permeability of polymer films can significantly reduce the lifetime of flexible electronic devices. In this study, we examined the water vapor permeation barrier properties of Al₂O₃/HfO₂ mixed oxide films on polymer substrates. Al₂O₃/HfO₂ films deposited by plasma-enhanced atomic layer deposition were transparent, chemically stable in water and densely amorphous. At 60 °C and 90% relative humidity (RH) accelerated condition, 50-nm-thick Al₂O₃/HfO₂ had water vapor transmission rate (WVTR) = 1.44 × 10⁻⁴ g m⁻² d⁻¹, whereas single layers of Al₂O₃ had WVTR = 3.26 × 10⁻⁴ g m⁻² d⁻¹ and of HfO₂ had WVTR = 6.75 × 10⁻² g m⁻² d⁻¹. At 25 °C and 40% RH, 50-nm-thick Al₂O₃/HfO₂ film had WVTR = 2.63 × 10⁻⁶ g m⁻² d⁻¹, which is comparable to WVTR of conventional glass encapsulation.     

Growth of CsLiB6O10 thin films on Si substrate by pulsed laser deposition using SiO2 and CaF2 as buffer layers

CsLiB₆O₁₀ (CLBO) thin films are grown on Si (100) and (111) substrates using lower index SiO₂ and CaF₂ as buffer layers by pulsed KrF (248 nm) excimer laser ablation of stoichiometric CLBO targets over a temperature range of 425 to 725°C. A CaF₂ buffer layer is grown on Si by laser ablation while SiO₂ is prepared by standard thermal oxidation. From extended x-ray analysis, it is determined that CaF₂ is growth with preferred orientation on Si (100) at temperatures lower than 525°C while on Si (111) substrate, CaF₂ is grown epitaxially over the temperature range; this agrees well with observed reflection high energy electron diffraction patterns. X-ray 2θ-scans indicate that crystalline CLBO are grown on SiO₂/Si and CaF₂/Si (100). Analysis of reflectance spectra from CLBO/SiO₂/Si yields the absorption edge at 182 nm. Surface roughness of the CaF₂ and CLBO/CaF₂/Si film are 19 and 15 nm, respectively. This relatively rough surface caused by the ablation of wide bandgap CaF₂ and CLBO limits the application of CLBO for waveguiding measurement.     

A comparison of liquid and gas phase surface preparation of III-V compound semiconductors for atomic layer deposition

Native oxide removal and surface termination of InAs(1 0 0) and InSb(1 0 0) using liquid and gas phase HF chemistries were studied using X-ray photoelectron spectroscopy. Aqueous HF etching removed the native oxides on InAs and produced elemental As, which reoxidized when exposed to air. On InSb the native oxides were not completely removed due to F-termination, which passivated the surface. Gas phase HF etching of InSb native oxide completely removed Sb₂O₅ producing a stoichiometric semiconductor surface terminated by F atoms on primarily In surface sites. On InAs gas phase HF completely removed As₂O₃ producing two surface stoichiometries. For the majority of HF to water molar ratios studied, a stoichiometric bulk metal and an As-rich overlayer were produced. For a lean HF composition, an As-rich bulk metal and In-rich overlayer were produced. Deposition of Al₂O₃ by atomic layer deposition (ALD) at 170 °C directly onto F-terminated InSb produced a chemically sharp Al₂O₃/InSb interface. ALD of Al₂O₃ on an In-rich overlayer on InAs resulted in an interfacial layer containing As-oxide.     

Sol-Gel processing of Nb-doped Pb(Zr,Ti)O3 thin films for ferroelectric memory applications

The ferroelectric properties of Nb-doped PZT thin films prepared by a sol-gel method were evaluated relative to memory device application requirements. Within the range of 0 to 4 mol %, Nb-doping of PZT compositions near the morphotropic phase boundary region (i.e. PZT 53/47) enhanced overall ferroelectric properties by reducing the te-tragonal distortion of the unit cell. A 4 mol % Nb-doped PZT 53/47 thin film (0.26 μm) had a coercivity of 8 V/ μm, a remanence ratio of 0.54, a switchable polarization of 45 μC/cm², and a specific resistivity of 3 x 10⁹ Ω-cm. Nb-doping levels in excess of 5 mol had a detrimental effect on the resulting thin film ferroelectric properties. X-ray diffraction (XRD) analysis of highly doped films showed development of a significant PbO phase accompanied by diffraction line broadening of the perovskite phase. As such, it was postulated that the creation of excessive lead vacancies in the PNZT lattice resulted in PbO accumulation at the grain boundaries which impeded grain growth, and hence, adversely affected ferroelectric switching performance. The fatigue performance of the sol-gel derived thin film capacitor system was a function of switching voltage. At switching fields sufficient to saturate the polarization, the endurance of the thin film capacitor was greater than 10⁹ cycles. Cycling with lower fields reduced endurance values, but in all cases, the switchable polarization decreased linearly with the logarithm of cycles. Nb-doping did not have a significant effect on the fatigue performance.     

ZnO缓冲层和退火处理对MgO薄膜结构的影响

采用直流反应磁控溅射法在Si衬底上引入ZnO缓冲层制备了沿(200)晶面择优取向生长的MgO薄膜,然后分别采用快速退火和常规退火两种不同的方式对MgO薄膜进行晶化处理。利用X射线衍射仪(XRD)以及原子力显微镜(AFM)研究了ZnO缓冲层以及两种不同的退火方式对MgO薄膜的结构和形貌的影响。结果表明:具有合适厚度的ZnO缓冲层可以显著地提高MgO薄膜的结晶质量。另外,与快速退火相比,常规退火处理后得到的MgO晶粒均匀圆润,有着较大的(200)衍射峰强度以及较小的表面粗糙度。     

原子层沉积薄膜之激光损伤性能分析

采用目前尚在国内鲜有报道的原子层沉积技术在熔石英和BK7玻璃基片上镀制了TiO2单层膜、AlO3单层膜以及TiO2/Al2O3增透膜,沉积温度在110℃和280℃.利用X射线粉末衍射仪对膜层微观结构进行了分析研究,并在激光损伤平台上进行了抗激光损伤阈值的测量.采用Nomarski微分干涉差显微镜和原子力显微镜对激光损伤...     

Ga2O3缓冲层厚度对柔性衬底沉积Cu/ITO薄膜性能的影响

Cu and Cu/ITO films were prepared on polyethylene terephthalate （PET） substrates with a Ga2O3 buffer layer using radio frequency （RF） and direct current （DC） magnetron sputtering. The effect of Cu layer thickness on the optical and electrical properties of the Cu film deposited on a PET substrate with a Ga2O3 buffer layer was studied, and an appropriate Cu layer thickness of 4.2 nm was obtained. Changes in the optoelectrical properties of Cu（4.2 nm）/ITO（30 nm） films were investigated with respect to the Ga2O3 buffer layer thickness. The optical and electrical properties of the Cu/ITO films were significantly influenced by the thickness of the Ga2O3 buffer layer. A maximum transmission of 86%, sheet resistance of 45 Ω/□ and figure of merit of 3.96 × 10^-3 Ω^ -1 were achieved for Cu（4.2 nm）/ITO（30 nm） films with a Ga2O3 layer thickness of 15 nm.     

Sub-nanometer atomic layer deposited Al2O3 barrier layer for improving stability of nonfullerene organic solar cells

Organic solar cells (OSCs) is a promising next-generation photovoltaic technology, however, the device stability remains to be the main barrier for its future commercialization. Herein, we reported the application of a sub-nanometer Al₂O₃ barrier layer in nonfullerene OSCs via atomic layer deposition (ALD), for the purpose of preventing metal ion diffusion from indium tin oxide (ITO) into the polymer layer caused by the corrosion of Poly(3,4-ethylenedioxythiophene): poly (styrenesulfonate) (PEDOT:PSS). The thickness of the ALD-Al₂O₃ barrier layer was precisely optimized by controlling the number of ALD cycles (n) to achieve simultaneously good photoelectric properties and conformal coverage. An average power conversion efficiency (PCE) of 15.02% was demonstrated for the optimal OSCs with ALD-Al₂O₃ barrier layer. The above mentioned suppression of metal ion diffusion was experimentally confirmed by the cross sectional observations of transmission electron microscopy (TEM) and chemical mapping from energy-dispersive X-ray spectroscopy (EDX), resulting in a significantly improved operational stability with a device lifetime 3-times longer than that without ALD-Al₂O₃ barrier layer. Such ALD-assisted interface modification provides an effective approach to realize high-performance and stable OSCs.     

A novel thermally-stable zirconium amidinate ALD precursor for ZrO2 thin films

ZrO₂ thin films were deposited by the atomic layer deposition process on Si substrates using tetrakis(N,N′-dimethylacetamidinate) zirconium (Zr-AMD) as a Zr precursor and H₂O as an oxidizing agent. Tetrakis (ethylmethylamino) zirconium (TEMA-Zr) was also evaluated for a comparative study. Physical properties of ALD-derived ZrO₂ thin films were studied using ellipsometry, grazing incidence XRD (GI-XRD), high resolution TEM (HRTEM), and atomic force microscopy (AFM). The ZrO₂ deposited using Zr-AMD showed a better thermal stability at high substrate temperature (>300 °C) compared to that using TEMA-Zr. GI-XRD analysis reveals that after 700 °C anneal both ZrO₂ films enter tetragonal phase. The electrical properties of N₂-annealed ZrO₂ film using Zr-AMD exhibit an EOT of 1.2 nm with leakage current density as low as 2 × 10⁻³ A/cm² (@V_fb−1 V). The new Zr amidinate is a promising ALD precursor for high-k dielectric applications.     

电子束沉积In2O3基W-Mo共掺薄膜的特性研究

利用电子束反应沉积技术制备了高迁移率I2O3基W-Mo共掺(IMWO,I<,2>O<,3>:WO<,3>/MoO<,3>)薄膜,研究了不同等量WO<,3>-MoO<,3>掺杂浓度对薄膜的微观结构、光学性能和电学性能的影响.IMWO薄膜的表面形貌呈现"类金字塔"型.随着WO<,3>-MoO<,3>共掺量的增加,IMWO薄...     

Chemical vapor deposition of B12As2 thin films on 6H-SiC

Icosahedral boron arsenide (B₁₂As₂) thin films were deposited on 6H-SiC substrates by chemical vapor deposition using B₂H₆ and AsH₃ sources. X-ray diffraction analysis of the thin films showed them to have the rhombohedral crystal structure and lattice parameters of B₁₂As₂. Transmission electron microscopy showed that the films were polycrystalline with oriented crystal grains. The preferential orientation of the film with respect to the SiC substrate was determined to be: [0001]_B12_{As 2}//[0001]_6H-SiC and [ ]_B12_{As 2}//[ ]_6H-SiC to within 3°. Electron diffraction also revealed the extremely small lattice mismatch (<0.5%) between the B₁₂As₂ basal-plane lattice parameter and twice the SiC basal-plane lattice parameter.     

Plasma enhanced chemical vapor deposition of SiO2 films at low temperatures using SiCl4 and O2

Silicon dioxide films have been deposited by Plasma-Enhanced Chemical Vapor Deposition (PECVD) technique using SiCl₄ and O₂ as reactive materials. Infra-red transmittance, Auger electron spectroscopy analysis, ellipsometry, electrical, and chemical etch measurements have been used to characterize these films. It is possible to obtain good quality oxides at a substrate temperature of 200° C using a low flow of reactant gases. High flow of reactant gases results in highly non-homogeneous porous films. The best oxide films obtained show destructive breakdown at electrical fields above 4 MV/cm and a fixed charge density of the order of 2.6 × 10¹¹ charges/cm².