在复合衬底γ-Al2O3/Si(001）上生长GaN

采用分子束外延（MBE）生长方法，使用γ-Al₂O₃材料作为新型过渡层，在Si(001）衬底上获得了没有裂纹的GaN外延层，实验结果表明使用γ-Al₂O₃过渡层有效地缓解了外延层中的应力. 通过生长并测试分析几种不同结构的外延材料，研究了复合衬底γ-Al₂O₃/Si (001）生长GaN情况，得到了六方相GaN单晶材料，实现了GaN c面生长. 预铺薄层Al及高温AlN层可以提高GaN晶体质量，低温AlN缓冲层可以改善GaN表面的粗糙度. 为解决Si(001）衬底上GaN的生长问题提供了有益的探索.     

H2对UHV/CVD低温选择性外延生长Si1-xGex的影响

利用超高真空化学气相沉积(UHV/CVD)成功实现了Si_1-xGe_x的低温选择性外延生长,并研究了H2对选择性外延生长的影响及其作用机理. 以SiH4和GeH4为反应气源,在开有6mm×6mm窗口氧化硅片上进行Si_1-xGe_x外延层的生长.首先分别以不含H2(纯GeH4)和含H2(90% H2稀释的GeH4)的两种Ge源进行选择性外延生长.通过SEM观察两种情况下氧化硅片表面,发现H2的存在对选择性外延生长有至关重要的作用.接着以90% H2稀释的GeH4为Ge源,变化Si源和Ge源的流量比改变H2分压,以获得SiH4和GeH4 (90% H2）的最佳流量比，使外延生长的选择性达到最好. 利用SEM观察在不同流量比时，经40min外延生长后各样品的表面形貌，并对其进行比较，分析了H2分压在Si_1-xGe_x选择性外延生长中的作用机理.     

基于再生长欧姆接触工艺的220 GHz InAlN/GaN 场效应晶体管

本文在蓝宝石衬底上研制了具有高电流增益截止频率(f_T)的InAlN/GaN异质结场效应晶体管 (HFETs)。基于MOCVD外延n -GaN欧姆接触工艺实现了器件尺寸的缩小,有效源漏间距(L_sd)缩小至600 nm。此外,采用自对准工艺制备了50 nm直栅。由于器件尺寸的缩小,V_gs= 1 V下器件最大饱和电流(I_ds)达到2.11 A/mm,峰值跨导达到609 mS/mm。小信号测试表明,器件f_T达到220 GHz、最大振荡频率(f_max)达到48 GHz。据我们所知,该f_T值是目前国内InAlN/GaN HFETs器件报道的最高结果。     

锗单晶在酸性SiO2抛光液条件下的抛光机理及加工工艺

该文研究了化学机械抛光(CMP)条件下,锗单晶在含HNO₃的SiO₂抛光液中的腐蚀过程。通过改变抛光时间,分析锗单晶表面状态的变化规律。结果表明,在SiO₂抛光液pH值为1~2时,SiO₂抛光液中存在 Si—OH和 Si—O^-形式;锗单晶先与HNO₃反应生成Ge(NO₃)₄,而后Ge⁴⁺的含氧酸盐会剧烈水解生成Ge—OH,Ge—OH 继续反应并以Ge—OH₂⁺形式存在。由于表面电荷的吸引,Si—O^-和Ge—OH₂⁺在锗单晶表面生成Si—O—Ge软化层,从动力学角度加快了腐蚀速率,促进了表面抛光的程度。抛光时间为15~20 min时,机械抛光和侵蚀的法向速度处于平衡状态,CMP抛光后锗单晶表面粗糙度S_a≤0.8 nm,10倍显微镜下无划痕、麻点。     

环形叉指电极型压电鼓膜驱动器的制备及其性能测试

制备了一种基于Pb(Zr52)O₃(P ZT52)材料的自适应光学用压电驱动器。驱动器采用鼓膜结构, 其工作区域由主动层—PZT52压电层和被动层—ZrO₂/Si复合层两部 分构成。PZT52压电层 采用环形叉值电极(IDT)驱动。采用Si(100)单晶作为衬底,并采用 溶胶-凝胶(Sol-gel) 法在其上制备ZrO₂阻挡层和PZT52压电层,其中引入PbTiO₃(PT) 种子层有利 于PZT52膜层的(110)择优取向。随后在其上热 蒸镀Al顶电极,并采用光刻方法制备图形,得到的IDT电极最大环形直径为 10.5mm,电极间距为0.05mm,中心非激活区 域直径为2mm。鼓膜结构则通过对Si衬底背部 进行各向异性湿法刻蚀(ODE)得到,保留的支持层厚度为5～10μm, 直径为 12mm。测试结果表明,压电驱动器阵列单元在100kV/cm驱动下,可产生6.5μm左右的形 变量。最后利用有限元分析方法(FEM)拟合了压电驱动器单元的面型,并分析了其形变模式 产生的内部原因。     

氮化对蓝宝石衬底上AlGaN/GaN异质结

研究了不同氮化条件对蓝宝石衬底上生长的AlGaN/GaN异质结材料特性的影响。研究表明,随着氮化过程NH₃流量的增大,GaN外延层的晶体质量得到了改善,GaN内应力释放,但是AlGaN/GaN异质结构中二维电子气的迁移率有所恶化。讨论了上述现象出现的原因。     

氧化镓生长模拟中的流场与反应参数优化研究

建立了用于生长直径为15.24cm(6inch)的Ga₂O₃材料的氢化物气相外延(HVPE)生长腔的二维几何模型,对Ga₂O₃材料的生长进行了数值模拟。依次优化了GaCl进气速度、O₂进气速度、喷口到衬底间的距离等关键参数,在较高生长速率下使衬底上的Ga₂O₃膜厚相对均匀度达到7.02%。此外,对仿真中不同的反应活化能设置进行了对比实验,发现活化能参数虽然对平均生长速率有明显影响,但是对样品的生长速率分布及均匀性影响不大。     

GaInAsP过渡层在808 nm GaAsP/(Al)GaInP半导体激光器中降电压的应用

利用金属有机化学气相沉积的方法在GaAs衬底上生长了GaInAsP外延层及GaAsP/(Al)GaInP激光器外延层。生长的GaInAsP外延层与GaAs晶格匹配,并且带隙处于Ga_0.5In_0.5P与GaAs中间。在GaInP/GaAs异质结界面插入此结构的GaInAsP过渡层,可以有效的降低异质结的带阶,尤其是价带带阶。相比于突变GaInP/GaAs异质结的808 nm GaAsP/(Al)GaInP半导体激光器,含有GaInAsP过渡层的半导体激光器具有更低的工作电压。因此,在350 mW输出功率下,半导体激光器的功率转换效率由52%提高至60%。并且在大电流注入下,含有GaInAsP过渡层的半导体激光器由于产生的焦耳热减少,具有更高的输出功率。     

石墨烯掺杂Cs2CO3作为高效电子注入层的OLEDs性能研究

研制了石墨烯掺杂Cs₂CO₃(Cs₂CO₃:Graphe ne )作为高效电子注入层、结构为ITO/N,N′-bis-(1-naphthyl) -N,N′-diphenyl-1,1′-biphenyl-4,4′-diamine (NPB)(50 nm)/tris-(8-hydroxy quinoline)-aluminum Alq₃(80 nm)/Cs₂CO₃:Gra phene (mss 20% 1nm)/Al(120 nm)的OLEDs。将其与标准器件ITO/NPB(50 nm)/Alq₃(80 n m)/LiF(0.5 nm)/Al(120 nm)作性能比较,研究石墨烯掺杂在Cs₂CO₃中作为电子注入层 对 OLEDs性能的影响。结果表明,基于Cs₂CO₃:Graphene结构作为电子注入层的器 件效率要高于LiF作为电子注入层的器件,其最大电流效率达到2.02 cd/A, 是标准器件的2.59倍;亮度也高于LiF作为电子注入层的器件,在10 V时达 到最大值7690cd/m²,是标准器件最大亮度 的2.07倍。性能得到提高的主要机理是由于Cs₂CO₃:Graphene的引入提高了电子注入效率。     

用溶胶-凝胶法制备的Cu2Bi2Cr2O8薄膜 及其光学和铁磁性能研究

以硝酸铜Cu(NO₃)₂·3H₂O、硝酸铬Cr(NO₃)₃·9H₂O、硝酸铋Bi(NO₃)₃·3H₂O和乙二醇为原料,利用溶胶-凝胶工艺在石英衬底上制备了纳米Cu₂Bi₂Cr₂O₈薄膜。通过X射线衍射(X-Ray Diffraction, XRD)和拉曼测试对样品进行了表征。结果表明,Cu₂Bi₂Cr₂O₈薄膜具有良好的光学特性,其禁带宽度为1.49 eV;在磁性测试方面,Cu₂Bi₂Cr₂O₈薄膜呈现出了良好的铁磁性。     

Nickel silicidation techniques for strained Si1?xGex, Si1?x?yGexCy, and Si1?yCy alloys material-device applications

A nickel silicide process for Si_1-xGe_x, Si_1-x-yGe_xC_y, and Si_1-yC_y alloy materials compatible with Si technology has been developed. Low-resistivity-phase (12–20 μΘ cm) nickel silicides have been obtained for these alloys with different low sheet-resistance temperature windows. The study shows that thin (15–18 nm) silicide layers with high crystalline quality, smooth silicide surface, and smooth interface between silicide and the underlying material are achievable. The technique could be used to combine the benefits of Ni silicide and Si_1-xGe_x, Si_1-x-yGe_xC_y, and Si_1-yC_y alloys. The technique is promising for Si or Si_1-xGe_x, Si_1-x-yGe_xC_y, and Si_1-yC_y alloy-based metal-oxide semiconductor, field-effect transistors (MOSFETs) or other device applications.     

YBa2Cu3-xZnxO7薄膜红外探测器的研究

在对红外探测器进行理论分析的基础上,设计并研制了液氮温度下的Yba2Cu3-xZnxO7薄膜红外探测器,系统地测试了器件的特征参数.最好的结果为:对于波长为10μm,调制频率为f=500Hz,带宽为Δf=1Hz的红外输入辐射Rv(500,10,1)=3587V/W,NEP(500,10,1)=6.5×10-12W/Hz1/2,D*(500,10,1)=7.2×1012cmHz1/2/W,τ(500,10,1)=1.2ms.     

SiNx/SiOxNy叠层结构防潮能力的研究

研究了等离子体增强化学气相沉积(PECVD)工艺参数对SiN_x及SiO_xN_y防潮能力的影响,并测试了SiN_x/SiO_xN_y叠层薄膜的水汽渗透速率(WVTR)。实验结果表明:单层SiN_x薄膜和SiO_xN_y薄膜都存在临界厚度,当膜厚大于临界值时,继续增大厚度不会明显改善薄膜的WVTR。当沉积温度从50℃提高到250℃,SiN_x薄膜的WVTR从0.031g/(m²·day)降至0.010g/(m²·day)。SiO_xN_y沉积时,增大N₂O通入量对薄膜的WVTR影响不明显,但可以有效改善薄膜的弯曲性能。最后,4个SiN_x/SiO_xN_y叠层膜的WVTR下降到了4.4×10-4g/(m²·day)。叠层膜防潮能力的显著提升归因于叠层结构可以有效解耦层与层之间的缺陷,延长水汽渗透路径。     

New TIT capacitor with ZrO2/Al2O3/ZrO2 dielectrics for 60 nm and below DRAMs

New ZrO₂/Al₂O₃/ZrO₂ (ZAZ) dielectric film was successfully developed for DRAM capacitor dielectrics of 60 nm and below technologies. ZAZ dielectric film grown by ALD has a mixture structure of crystalline phase ZrO₂ and amorphous phase Al₂O₃ in order to optimize dielectric properties. ZAZ TIT capacitor showed small Tox.eq of 8.5 Å and a low leakage current density of 0.35 fA/cell, which meet leakage current criteria of 0.5 fA/cell for mass production. ZAZ TIT capacitor showed a smaller cap leak fail bit than HAH capacitor and stable leakage current up to 550 °C anneal. TDDB (time dependent dielectric breakdown) behavior reliably satisfied the 10-year lifetime criteria within operation voltage range.     

Comparison between Pt/TiO2/Pt and Pt/TaOX/TaOY/Pt based bipolar resistive switching devices

Nonvolatile memories have emerged in recent years and have become a leading candidate towards replacing dynamic and static random-access memory devices. In this article, the performances of TiO₂ and TaO₂ nonvolatile memristive devices were compared and the factors that make TaO₂ memristive devices better than TiO₂ memristive devices were studied. TaO₂ memristive devices have shown better endurance performances (10⁸ times more switching cycles) and faster switching speed (5 times) than TiO₂ memristive devices. Electroforming of TaO₂ memristive devices requires~4.5 times less energy than TiO₂ memristive devices of a similar size. The retention period of TaO₂ memristive devices is expected to exceed 10 years with sufficient experimental evidence. In addition to comparing device performances, this article also explains the differences in physical device structure, switching mechanism, and resistance switching performances of TiO₂ and TaO₂ memristive devices. This article summarizes the reasons that give TaO₂ memristive devices the advantage over TiO₂ memristive devices, in terms of electroformation, switching speed, and endurance.     

Excellent performance of gas sensor based on In2O3-Fe2O3 nanotubes

In₂O₃-Fe₂O₃ nanotubes are synthesized by an electrospinning method. The as-synthesized materials are characterized by scanning electron microscope and X-ray powder diffraction. The gas sensing results show that In₂O₃-Fe₂O₃ nanotubes exhibit excellent sensing properties to acetone and formaldehyde at different operating temperatures. The responses of gas sensors based on In₂O₃-Fe₂O₃ nanotubes to 100 ppm acetone and 100 ppm formaldehyde are 25 (240℃) and 15 (260℃), and the response/recovery times are 3/7 s and 4/7 s, respectively. The responses of In₂O₃-Fe₂O₃ nanotubes to 1 ppm acetone (240℃) and formaldehyde (260℃) are 3.5 and 1.8, respectively. Moreover, the gas sensor based on In₂O₃-Fe₂O₃ nanotubes also possesses an excellent selectivity to acetone and formaldehyde.     

Electrodepositing ZnxMnyOz alloys from zinc oxide to manganese oxide

Electrodeposition has emerged as a practical and simple method to synthesise semiconductor materials under different forms, thin films or nanostructured layers. This work reports on the cathodic electrodeposition of ZnMnO thin layers using both zinc and manganese chlorides as precursors. The composition of thin films can be varied from binary zinc oxide to manganese oxide varying the Mn/(Mn+Zn) ratio between 0 and 1. The composition of Zn_xMn_yO_z films was obtained by energy dispersive spectroscopy. Zn_1−xMn_xO films with Mn/Zn ratio less than 10% exhibit a crystalline wurtzite structure typical of ZnO fully oriented in the (0 0 2) direction. Higher Mn content leads to deformation of the ZnO lattice and the wurtzite structure is no longer maintained. X-ray photoelectron spectroscopy points out that Mn₃O₄ tends to be deposited when a high Mn/Zn ratio is used in the starting solution. Magnetic measurements on films with Mn/(Zn+Mn) ratio near 1 reveal magnetic characteristics similar to Mn₃O₄ compounds. The transmission spectra of Zn_xMn_yO_z show the typical absorption edge of crystalline ZnO while the wurtzite structure is maintained and it shifts to higher wavelengths when Mn content increases.     

具有界面依赖光致发光的双层WS2/Ga2O3异质结的能带工程(英文)

利用垂直WS₂/Ga₂O₃异质结构中异质界面诱导了反常的光致发光(PL)发射。垂直堆栈的WS₂/Ga₂O₃异质界面使其形成了II型能带结构,导致与Ga₂O₃层接触的底层WS₂的PL强度下降。而异质界面的强耦合作用也影响了双层WS₂中的同质层间相互作用,使得上层WS₂出现反常的PL增强。这种堆栈新型二维异质结构为定制目标能带结构并控制其光子和电子行为提供一种新的手段。     

Investigation of Ta2O5/SiO2/4H-SiC MIS capacitors

Tantalum pentoxide (Ta₂O₅) deposited by pulsed DC magnetron sputtering technique as the gate dielectric for 4H-SiC based metal-insulator-semiconductor (MIS) structure has been investigated. A rectifying current-voltage characteristic was observed, with the injection of current occurred when a positive DC bias was applied to the gate electrode with respect to the n type 4H-SiC substrate. This undesirable behavior is attributed to the relatively small band gap of Ta₂O₅ of around 4.3 eV, resulting in a small band offset between the 4H-SiC and Ta₂O₅. To overcome this problem, a thin thermal silicon oxide layer was introduced between Ta₂O₅ and 4H-SiC. This has substantially reduced the leakage current through the MIS structure. Further improvement was obtained by annealing the Ta₂O₅ at 900 °C in oxygen. The annealing has also reduced the effective charge in the dielectric film, as deduced from high frequency C-V measurements of the Ta₂O₅/SiO₂/4H-SiC capacitors.     

共沉淀法制备Y2O2SO4:Eu3+荧光粉及其光致发光研究

采用商业Y(NO3)3·6H2O、Eu(NO3)3·6H2O、(NH4)2SO4和NaOH为实验原料,通过共沉淀法制备了Y2O2SO4:Eu3+荧光粉。利用热分析(DTA-TG-DTG)、傅里叶变换红外(FT-IR)光谱、X射线衍射(XRD)、扫描电子显微镜(SEM)和光致发光(PL)光谱等手段对合成的粉体进行了表征。结果表明,当(NH4)2SO4引入到反应体系中时,前驱体具有非晶态结构,且在空气气氛中800℃煅烧2h能转化为单相的Y2O2SO4粉体,该Y2O2SO4粉体呈准球形,粒径范围分布在0.5~1.0μm之间,团聚较严重。PL光谱分析表明,在270nm紫外光激发下,Y2O2SO4:Eu3+荧光粉呈红光发射,主发射峰位于620nm,归属于Eu3+的5D0→7F2跃迁。Eu3+的猝灭浓度是5 mol%,其对应的荧光寿命为1.22 ms。另外,当(NH4)2SO4未引入到反应体系中时,采用类似的方法合成了Y2O3:Eu3+荧光粉,并对Y2O2SO4:Eu3+和Y2O3:Eu3+荧光粉的PL性能进行了比较。