Cd饱和气氛退火对碲锌镉晶体导电类型转变界面的影响

在富Te生长条件下,通过垂直布里奇曼法制备的部分碲锌镉晶体内存在导电类型转变界面。采用富Te液相外延技术在含有导电类型转变界面的碲锌镉衬底上生长碲镉汞薄膜,制成的红外焦平面探测器响应图上存在明显的响应不均匀分界面。碲锌镉晶体的导电类型转变由缺陷类型的不同引起,为消除碲锌镉衬底的导电类型转变界面,提升碲镉汞红外焦平面的成像质量,对含有导电类型转变界面的碲锌镉晶体进行了Cd饱和气氛退火实验,研究了时间和温度等退火条件对晶体导电类型转变界面的影响,探讨了Cd间隙和Cd空位缺陷的形成机制,为晶体生长过程中的Cd空位缺陷抑制提出了解决思路。     

原位退火对碲锌镉晶体第二相夹杂缺陷的影响

采用传统布里奇曼法生长碲锌镉晶体,在配料过程中添加适当过量的Cd,并在晶体生长结束阶段的降温过程中加入晶锭原位退火工艺,晶体的第二相夹杂缺陷得到了有效抑制。根据晶体第二相夹杂缺陷的形成机理,结合热扩散理论和碲锌镉晶体的P-T相图,研究了退火温度对晶体第二相夹杂缺陷密度和粒度（尺寸）的影响,获得了抑制碲锌镉晶体第二相夹杂缺陷的退火条件。利用优化的退火条件制备碲锌镉晶体,晶体第二相夹杂缺陷的尺寸小于10 μm,密度小于250 cm－2。     

碲锌镉缓冲层液相外延技术的研究

文章报道了采用液相外延方法,在碲锌镉衬底上进行碲锌镉薄膜缓冲层生长的情况,并且采用X光双晶衍射仪、X光形貌仪、红外傅里叶光谱仪、二次离子质谱仪等手段对碲锌镉薄膜进行了表征,碲锌镉薄膜具有较好地组分及均匀性,晶体结构质量也较好.采用碲锌镉缓冲结构生长了碲镉汞液相外延片,其碲锌镉与碲镉汞薄膜界面附近的杂质得到了有效的控制.     

碲锌镉衬底重复利用技术研究

芯片制备工艺完成后,给芯片留有一定厚度的衬底,同时利用丝切割技术将多余的碲锌镉衬底取下,并对其进行重复抛光处理。碲锌镉衬底的锌值分布及半高宽(Full Width at Half Maximum, FWHM)测试结果表明,碲锌镉衬底质量较好,可以再次用来制备液相外延碲镉汞薄膜。该薄膜经过标准探测器芯片工艺后,性能合格。该研究使原本要完全去除的衬底得以重复利用,提高了碲锌镉衬底的利用率,降低了探测器的制造成本。     

中国电科11所碲镉汞薄膜材料制备技术进展

碲镉汞材料具有响应速度快、量子效率高、带隙连续可调等优点,广泛应用于红外探测领域,本文报道了近年来中国电科11所在碲镉汞薄膜材料制备方面的技术进展。在碲锌镉衬底材料制备方面,已突破135mm碲锌镉晶体生长技术,碲锌镉衬底平均位错腐蚀坑密度(EPD) <1×104cm-2,具备了80mm×80mm规格碲锌镉衬底的批量生产能力。在液相外延碲镉汞薄膜制备方面,富碲水平液相外延碲镉汞薄膜平均位错腐蚀坑密度EPD<4×104cm-2,具备80mm×80mm规格碲镉汞薄膜的制备能力;富汞垂直液相外延实现高质量双层异质结碲镉汞薄膜材料批量化制备,该种材料的半峰宽(FWHM)控制在(20～40)arcsec范围内,碲镉汞薄膜厚度极差≤±06μm。在分子束外延碲镉汞薄膜方面,实现了6 in硅基碲镉汞材料制备,组分标准偏差≤00015,表面宏观缺陷密度≤100cm-2;碲锌镉基碲镉汞材料已具备50mm×50mm制备能力,组分标准偏差为0002,厚度标准偏差为0047μm。从探测器验证结果来看,基于富碲水平液相外延碲镉汞薄膜实现了1 k×1 k、2 k×2 k等规格红外焦平面探测器的工程化制备;采用双层异质结碲镉汞薄膜实现了高温工作、长波及甚长波探测器的制备;使用分子束外延制备的碲镉汞薄膜实现了27 k×27 k、54 k×54 k、8 k×8 k等规格红外焦平面探测器研制,在宇航领域有巨大的应用潜力。     

碲锌镉晶体定向研究

碲锌镉材料是制备高性能碲镉汞红外焦平面探测器不可或缺的衬底材料.液相外延工艺和分子束外延工艺分别需要使用(111)晶面和(211)晶面碲锌镉衬底制备碲镉汞薄膜材料.低偏角、高精度衬底的选取有利于高质量碲镉汞外延层的获得.介绍了孪晶线快速定向法、使用X射线衍射仪(X-Ray Diffractome-ter,XRD)定向法...     

非晶态碲镉汞的暗电导率和吸收边(英文)

研究了非晶态碲镉汞(x=0.2)薄膜的暗电导率随温度变化关系,发现非晶态结构的碲镉汞材料具有明显的半导体特性,其室温禁带宽度在0.88～0.91eV之间,与通过光学方法获得的结果相符。在80～240K的温度区间非晶态碲镉汞(x=0.2)的暗电导率从1×10—8Ω—1.cm—1缓慢增大到5×10-8Ω—1.cm—1,温度大于240K时,其电导率剧烈增大到1×10—5Ω—1.cm—1,说明在240K附近非晶态碲镉汞材料的导电机制发生了变化,这对非晶态碲镉汞材料的应用研究具有重要意义。还研究了退火过程对非晶态碲镉汞薄膜电导率的影响,结果表明140℃退火后非晶态碲镉汞薄膜发生了部分晶化。     

退火对非晶态碲镉汞薄膜稳定态光电导的影响

利用射频磁控溅射方法,在宝石衬底上制备了非晶态碲镉汞(a-HgCdTe)薄膜。对原生a-HgCdTe薄膜进行了不同退火时间和不同退火温度的热退火,在80～300K温度范围内,分别测量了原生和退火处理后的a-HgCdTe薄膜样品的稳定态光电导,研究了退火时间和退火温度对非晶态HgCdTe薄膜的稳定态光电导和激活能的影响。结果表明,原生和退火a-HgCdTe薄膜的稳定态光电导具有热激活特性;随着退火时间增加或退火温度升高,a-HgCdTe薄膜的晶化程度提高,导致光电导增大,光电导激活能降低。利用非晶-多晶转变机制讨论了实验结果。     

碲锌镉缓冲层液相外延技术的研究

文章报道了采用液相外延方法，在碲锌镉衬底上进行碲锌镉薄膜缓冲层生长的情况，并且采用X光双晶衍射仪、X光形貌仪、红外傅里叶光谱仪、二次离子质谱仪等手段对碲锌镉薄膜进行了表征，碲锌镉薄膜具有较好地组分及均匀性，晶体结构质量也较好。采用碲锌镉缓冲结构生长了碲镉汞液相外延片，其碲锌镉与碲镉汞薄膜界面附近的杂质得到了有效的控制。     

碲锌镉缓冲层液相外延技术的研究

文章报道了采用液相外延方法，在碲锌镉衬底上进行碲锌镉薄膜缓冲层生长的情况，并且采用X光双晶衍射仪、X光形貌仪、红外傅里叶光谱仪、二次离子质谱仪等手段对碲锌镉薄膜进行了表征，碲锌镉薄膜具有较好地组分及均匀性，晶体结构质量也较好。采用碲锌镉缓冲结构生长了碲镉汞液相外延片，其碲锌镉与碲镉汞薄膜界面附近的杂质得到了有效的控制。     

Dark conductivity and photoconductivity of amorphous Hg0.78Cd0.22Te thin films

This paper reports the dark conductivity and photoconductivity of amorphous Hg0.78Cd0.22 Te thin films deposited on an Al2O3 substrate by RF magnetron sputtering.It is determined that dark conduction activation energy is 0.417 eV for the as-grown sample.Thermal quenching is absent for the as-grown sample during the testing temperature zone,but the reverse is true for the polycrystalline sample.Photosensitivity shows the maximum at 240 K for amorphous thin films,while it is higher for the as-grown sample than for polycrystalline thin films in the range from 170 to 300 K.The recombination mechanism is the monomolecular recombination process at room temperature,which is different from the low temperature range.Theμτ-product is low in the range of 10-11-10-9 cm2/V,which indicates that some defect states exist in the amorphous thin films.     

The impact of MOCVD growth ambient on carrier transport,defects, and performance of CdTe/CdS heterojunction solar cells

CdTe solar cells were fabricated by depositing CdTe films on CdS/SnO₂/glass substrates in various metalorganic chemical vapor deposition growth ambient with varying Te/Cd mole ratio in the range of 0.02 to 15. The short-circuit current density (J_sc) showed a minimum at a Te/Cd ratio of 0.1 and increased on both sides of this minimum. The open-circuit voltage (V_oc) was found to be the highest for the Te-rich growth ambient (Te/Cd∼6)and was appreciably lower (600 mV as opposed to 720 mV) for the stoichiometric and the Cd-rich growth conditions. This pattern resulted in highest cell efficiency (12%) on Te-rich CdTe films. Auger electron spectroscopy revealed a high degree of atomic interdiffusion at the CdS/CdTe interface when the CdTe films were grown in the Te-rich conditions. It was found that the current transport in the cells grown in the Cd-rich ambient was controlled by the tunneling/interface recombination mechanism, but the depletion region recombination became dominant in the Te-rich cells. These observations suggest that the enhanced interdiffusion reduces interface states due to stress reduction or to the gradual transition from CdS to CdTe. The hypothesis of reduced defect density in the CdTe cells grown in the Te-rich conditions is further supported by the high effective lifetime, measured by time-resolved photoluminescence, and the reduced sensitivity of quantum efficiency to forward/light bias.     

Effects of Heat Treatment on Thermoelectric and Infrared Properties of Bi2Te3 Films

In this work, Bi2Te3 films (250 nm) are fabricated on SiO2/Si substrates by radio frequency (RF) magnetron sputtering at room temperature, and the prepared films are annealed over the temperature range of 200 ℃ to 400 ℃. Crystallinity and electrical properties of the films can be tuned correspondingly. The power factors of Bi2Te3 films of 0.85 W/K2cm to 11.43 W/K2cm were achieved after annealing. The infrared reflectance measurements from 2.5 m to 5.0 m demonstrate that there is also a slight red-shift of the plasma oscillation frequency in the Bi2Te3 films. By means of plasmonic calculations, we attribute the red-shift of absorption peaks to the reduction of carrier concentration and the change of effective mass of Bi2Te3 films with the increased annealing temperature.     

非晶态碲镉汞薄膜晶化过程的椭圆偏振光谱研究(英文)

采用椭圆偏振光谱技术研究了非晶态碲镉汞薄膜在不同退火条件下的结构性能。结果表明非晶态碲镉汞薄膜在退火过程中的成核晶化是在薄膜内部均匀发生的,对于不同晶化程度的薄膜,其光学常数谱具有明显的特征,通过对光学常数谱的分析研究可以对非晶态碲镉汞薄膜的晶化程度进行量化表征,从而控制退火条件,优化材料质量。     

Effect of post deposition heat treatment on microstructure parameters,optical constants and composition of thermally evaporated CdTe thin films

Thin film microstructure and its properties can be effectively altered with post deposition heat treatments. In this respect, CdTe thin films were deposited on glass substrates at a substrate temperature of 200 °C using thermal evaporation technique, followed by air annealing at different temperatures from 200 to 500 °C. Structural analysis reveals that CdTe thin films have a cubic zincblend structure with two oxide phases related to CdTe₂O₅ and CdTeO₃ at annealing temperature of 400 and 500 °C respectively. Regardless of the annealing temperature, the plane (111) was found to be the preferred orientation for all films. The crystallite size was observed to increase with annealing temperature. All films were found to display higher lattice parameters than the standard, and hence found to carry a compressive stress. Optical measurements suggest high uniformity of films both before and after post deposition heat treatment. Films annealed at 400 °C displayed superior optical properties due to its high refractive index, optical conductivity, relative density and low disorder. Furthermore, according to the compositional measurements, CdTe thin films were found to exhibit Te rich and Cd rich nature at regions near the substrate and center of the film respectively, for all annealing temperatures. However, composition of the regions near the substrate was found to become more Te rich with increasing annealing temperature. The study suggests that changing the annealing temperature as a post deposition treatment affects structural and optical properties of CdTe thin film as well as its composition. According to the observations, films annealed at 400 °C can be concluded to be the best films for photovoltaic applications due to its superior optical and structural properties.     

Investigation on the atomic layer deposition of the Se doped Sb–Te phase change films using an alkyl-silyl precursor

We used TDMASb, Te(t-Bu)₂, and Se(SiMe₃)₂ as precursors to investigate the behavior of atomic vapor deposition (AVD) during formation of Se doped Sb–Te phase change films. The deposition was prepared by a sequential recipe for the atomic layer deposition (ALD) reaction with consideration of the electrostatic interactions between the Se alkyl-silyl precursor and the Sb and Te precursors. The Sb–Te–Se ternary films could be deposited by AVD at temperatures of 80–300 °C with fine controllability and high surface quality. The elemental composition of the films was controlled by varying the deposition temperature. The Se doping effect on the crystallization temperature and set resistance in the crystalline state was evaluated via electrical measurements and theoretical analyses by applying the glass transition temperature model and resonance bonding model. The results indicated that the incorporation of Se into Sb–Te films may provide for improved thermal stability and power consumption efficiency in phase-change random access memory (PCRAM) devices.     

CdTe钝化介质膜的溅射沉积及其X射线光电子能谱研究

用Ar^ 束溅射沉积技术实现了CdTe薄膜的低浊沉积生长。用X射线光电子能谱（XPS）分析技术对溅射沉积C dTe薄膜以及CdTe体晶中的Cd元素、Te元素化学环境进行了对比实验研究。实验表明：溅射沉积CdT e薄膜具有很好的组份均匀性,未探测到有元素（Cd、Te)沉积存在。     

Annealing experiments in heavily arsenic-doped (Hg,Cd)Te

Arsenic doped molecular beam epitaxy (MBE) (Hg,Cd)Te films were grown on (Cd,Zn)Te substrates. The concentration of arsenic was varied from 5 x 10¹⁸ cm^-3 to 1 x 10²⁰ cm^-3. After the growth, the epitaxial layers were annealed at various partial pressures of Hg within the existence region of (Hg,Cd)Te at temperatures ranging from 400 to 500°C. Hall effect and resistivity measurements were carried out subsequent to the anneals. 77K hole concentration measurements indicate that for concentrations of arsenic <10¹⁹ cm⁻³, most of the arsenic is electrically active acting as acceptors interstitially and/or occupying Te lattice sites at the highest Hg pressures. At lower Hg pressures, particularly at annealing temperatures of 450°C and higher, compensation by arsenic centers acting as donors appears to set in and the hole concentration decreases with decrease in Hg pressure. These results indicate the amphoteric behavior of arsenic and its similarity to the behavior of phosphorus in (Hg,Cd)Te previously inferred by us. A qualitative model which requires the presence of arsenic occupying both interstitial and Te lattice sites along with formation of pairs of arsenic centers is conjectured.     

氧化铁镍薄膜的制备与表征

首先提出射频反应磁控溅射中薄膜沉积速率同O2流量和溅射功率关系的理论计算模型;其次根据这一理论计算模型,在O2/Ar气氛中,利用射频反应磁控溅射制备氧化铁镍薄膜;最后分别采用台阶仪、X射线衍射(XRD)、X射线光电子能谱(XPS)、电子扫描镜(SEM)和电化学工作站对薄膜进行了表征,并分析了在制备过程中O2含量、工作压强和溅射功率对薄膜的沉积速率、结构、组分和表面形貌的影响.实验验证了所提出的理论计算模型以及Ni3 的存在;得到了膜厚与晶型以及工作压强与形貌的关系;电化学测试结果为:在电流密度为8 mA/cm2时的过电势为284 mV.