非晶态As2S8半导体薄膜波导的热处理效应

研究了非晶态As2S8半导体薄膜在热作用下的结构变化效应.采用棱镜耦合技术、喇曼光谱测试技术,确认了As2S8薄膜经热处理后,薄膜密度增高和折射率增大的现象.实验表明,淀积态非晶As2S8半导体薄膜经紫外光饱和照射后,再经退火处理,当光折变在退火温度不低于160℃时,出现不完全可逆现象,可逆程度跟退火温度有关.实验显示,退火态非晶As2S8半导体薄膜在玻璃转化温度130℃时退火处理,光折变存在完全可逆现象.光传输实验显示,热处理后的非晶态As2S8半导体薄膜波导,其传输损耗减小了约4dB/cm.     

非晶态As2S8半导体薄膜波导的热处理效应

研究了非晶态As2S8半导体薄膜在热作用下的结构变化效应.采用棱镜耦合技术、喇曼光谱测试技术,确认了As2S8薄膜经热处理后,薄膜密度增高和折射率增大的现象.实验表明,淀积态非晶As2S8半导体薄膜经紫外光饱和照射后,再经退火处理,当光折变在退火温度不低于160℃时,出现不完全可逆现象,可逆程度跟退火温度有关.实验显示,退火态非晶As2S8半导体薄膜在玻璃转化温度130℃时退火处理,光折变存在完全可逆现象.光传输实验显示,热处理后的非晶态As2S8半导体薄膜波导,其传输损耗减小了约4dB/cm.     

非晶As2S3半导体薄膜在激光作用下的性能及结构研究

在激光辐照或退火作用下 ,As2 S3非晶半导体薄膜的光学吸收边出现红移现象 ,并且随着激光功率的增大和辐照时间的延长 ,红移值增大 ,并最后达到饱和。这种红移在先经过退火处理再激光辐照的薄膜中是可逆的。从扫描电镜的形貌图中也可以看出 ,经激光辐照后 ,薄膜表面有晶相出现 ,且随着激光功率的增加 ,晶相出现增多。As2 S3非晶半导体薄膜中光致效应的产生是由于光致结构变化所致 ,对其产生原因 ,进行了机理分析     

退火对Ge掺杂SiO2薄膜的影响

用等离子体增强化学气相淀积制备了Ge掺杂SiO2薄膜,并对薄膜进行了不同温度的退火处理。采用棱镜耦合仪、原子力显微镜和傅里叶变换红外光谱分析技术研究了不同退火温度对Ge掺杂SiO2薄膜性质的影响。通过1 100℃退火处理后,正的折射率变化量和负的体积变化量随着GeH4流量增加而增大,Ge-O-Ge键增多;而通过900℃退火处理后,折射率没有随着GeH4流量增加而增大;薄膜的表面粗糙度随着退火温度升高而降低。研究结果表明,SiO2薄膜中Ge掺杂过量,其折射率反常下降;通过1 100℃退火处理后,折射率随着GeH4流量增加而增大,折射率的增大主要是由于薄膜密实化和Ge-O-Ge键的形成。     

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。     

快速退火温度对Ag/SrTiO_3/p~+-Si器件阻变特性的影响

采用溶胶-凝胶结合快速退火工艺在p~+-Si基片上制备了Sr Ti O_3薄膜,构建了Ag/Sr Ti O_3/p~+-Si结构的阻变器件,研究了退火温度对薄膜微观结构、阻变特性的影响。结果表明:不同退火温度下薄膜均呈结晶态,并且随退火温度升高,薄膜晶粒有增大的趋势,当退火温度为750℃时,薄膜的衍射峰不明显并且有杂峰出现。不同退火温度下Ag/Sr Ti O_3/p~+-Si器件都具有明显的双极性阻变特性,但退火温度为850℃与900℃的器件在扫描电压达到某一值时电流会出现一个极小值;经850℃退火处理的器件具有更高的高低电阻比(103～104)。当退火温度为800℃及更高时,器件在高阻态下的导电机制以肖特基势垒发射机制为主;低阻态的电荷传导机制则遵循空间电荷限制电流机制(SCLC)。器件在200次可逆循环测试下,退火温度为850℃时表现出较好的抗疲劳特性。     

真空退火对低频PECVD氮化硅薄膜性能的影响

研究了真空退火温度对不同流量比工艺参数下PECVD氮化硅薄膜性能的影响,测试了退火后氮化硅薄膜厚度、折射率以及在氢氟酸中的腐蚀速率。结果表明,退火后氮化硅薄膜厚度及折射率变化与薄膜沉积工艺条件有关,而薄膜在氢氟酸中的腐蚀速率在退火后大大降低。结合退火前后氮化硅薄膜的红外透射谱对以上测试结果进行了讨论。     

剥层椭偏法对As~ 注入Si热退火过程的进一步研究

本文用剥层椭偏光法对As离子注入硅的热退火过程作了较详细的研究.As 离子注入剂量为 5 ×10~(14)cm~(-2),能量为100keV.在300-800℃之间各种不同温度下退火,得到了在这几种温度下固相外延平均速率及复折射率分布的变化.我们发现在各种温度下非晶层的消光系数都变小,尾部的折射率变大.     

剥层椭偏法对As~+注入Si热退火过程的进一步研究

本文用剥层椭偏光法对As离子注入硅的热退火过程作了较详细的研究.As 离子注入剂量为 5 ×10~(14)cm~(-2),能量为100keV.在300-800℃之间各种不同温度下退火,得到了在这几种温度下固相外延平均速率及复折射率分布的变化.我们发现在各种温度下非晶层的消光系数都变小,尾部的折射率变大.     

退火温度和退火时间对不同衬底上Mg_(2)Si薄膜结构的影响北大核心CSCD

以Mg_(2)Si烧结靶为靶材,采用磁控溅射法在Si、石英和Al_(2)O_(3)衬底上先沉积一层Mg_(2)Si非晶薄膜,再进行退火处理,研究了衬底类型、退火温度及退火时间对Mg_(2)Si多晶薄膜结构的影响。结果表明:Si、石英、Al_(2)O_(3)三种衬底上Mg_(2)Si薄膜的最优退火温度和退火时间均为350◦C和1 h。Al_(2)O_(3)衬底上的Mg_(2)Si薄膜结晶质量最佳,Si衬底上的薄膜次之,石英衬底上的薄膜结晶质量最不理想,分析表明这种差异主要源于衬底与薄膜之间的热失配不同。     

Effects of annealing schedule on orientations of Bi3.2Nd0.8Ti3O12 ferroelectric films prepared by metalorganic solution deposition

Fatigue-free Bi_3.2Nd_0.8Ti₃O₁₂ ferroelectric thin films were successfully prepared on p-Si(1 1 1) substrate using metalorganic solution deposition process. The orientation and formation of thin film under different annealing schedules were studied using XRD and AFM. XRD analysis indicated that (2 0 0)-oriented films with degree of orientation of I₍₂₀₀₎/I₍₁₁₇₎ = 2.097 and 0.466 were obtained by preannealing the film at 400 °C for 10 min followed by rapid thermal annealing at 700 °C for 3 min, 10 min and 20 min, respectively, (0 0 8)-oriented film with degree of orientation of I₍₀₀₈₎/I₍₁₁₇₎ = 1.706 were obtained by rapid thermal annealing the film at 700 °C for 3 min without preannealing, and (0 0 8)-oriented film with degree of orientation of I₍₀₀₈₎/I₍₁₁₇₎ = 0.719 were obtained by preheating the film from room temperature to 700 °C at 20 °C/min followed by annealing for 10 min. The a-axis and c-axis orientation decreased as increase in annealing time due to effects of (1 1 1)-oriented substrate. AFM analysis further indicated that preannealing at 400 °C for 10 min followed by rapid thermal annealing at 700 °C for 3 min resulted in formation of platelike crystallite parallel to substrate surface, however rapid thermal annealing at 700 °C for 3 min without preannealing resulted in columnar crystallite perpendicular to substrate surface.     

MOS devices with tetragonal ZrO2 as gate dielectric formed by annealing ZrO2/Ge/ZrO2 laminate

A Ge-stabilized tetragonal ZrO₂ (t-ZrO₂) film with permittivity (κ) of 36.2 was formed by depositing a ZrO₂/Ge/ZrO₂ laminate and a subsequent annealing at 600 °C, which is a more reliable approach to control the incorporated amount of Ge in ZrO₂. On Si substrates, with thin SiON as an interfacial layer, the SiON/t-ZrO₂ gate stack with equivalent oxide thickness (EOT) of 1.75 nm shows tiny amount of hysteresis and negligible frequency dispersion in capacitance-voltage (C-V) characteristics. By passivating leaky channels derived from grain boundaries with NH₃ plasma, good leakage current of 4.8 × 10⁻⁸ A/cm² at V_g = V_fb − 1 V is achieved and desirable reliability confirmed by positive bias temperature instability (PBTI) test is also obtained.     

Influence of post deposition annealing on Y2O3-gated GaAs MOS capacitors and their reliability issues

The feasibility of employing yttrium oxide (Y₂O₃) as high-k gate dielectrics for GaAs metal-oxide-semiconductor (MOS) devices has been investigated. MOS capacitors were fabricated using RF-sputtered deposited Y₂O₃ films on NH₄OH treated n-GaAs substrate. Indeed high-k (Y₂O₃)/GaAs MOS capacitors exhibiting fairly good electrical characteristics, for instance, especially low leakage current density, low hysteresis and allowable density of interface states, have been achieved. The effects of several annealing treatments on Y₂O₃-gated GaAs MOS capacitors have been investigated in order to optimize the process conditions. A decrease in accumulation capacitance (C_acc) following PDA effectively increases the equivalent oxide thickness (EOT), which is predicted to be correlated with the growth and continuous increase in the physical thickness of a lower-k inter-layer sandwiched between Y₂O₃ and GaAs. However, leakage currents and interface trap densities are reduced with higher values of annealing temperature. The variation of current density with an equivalent oxide thickness (EOT) has also been investigated.     

Infrared spectroscopy and X-ray diffraction studies on the crystallographic evolution of La2O3 films upon annealing

Rare earth oxides (REOs) have lately received extensive attention in relation to the continuous scaling down of non-volatile memories (NVMs). In particular, La₂O₃ films are promising for integration into future NVMs because they are expected to crystallize above 400 °C in the hexagonal phase (h-La₂O₃) which has a higher κ value than the cubic phase (c-La₂O₃) in which most of REOs crystallize. In this work, La₂O₃ films are grown on Si by atomic layer deposition using La(C₅H₅)₃ and H₂O. Within the framework of the h-La₂O₃ formation, we systematically study the crystallographic evolution of La₂O₃ films versus annealing temperature (200-600 °C) by Fourier transform infrared spectroscopy (FTIR) and grazing incidence X-ray diffraction (GIXRD). As-grown films are chemically unstable in air since a rapid transformation into monoclinic LaO(OH) and hexagonal La(OH)₃ occurs. Vacuum annealing of sufficiently thick (>100 nm) La(OH)₃ layers induces clear changes in FTIR and GIXRD spectra: c-La₂O₃ gradually forms in the 300-500 °C range while annealing at 600 °C generates h-La₂O₃ which exhibits, as inferred from our electrical data, a desirable κ ∼ 27. A quick transformation from h-La₂O₃ into La(OH)₃ occurs due to H₂O absorption, indicating that the annealed films are chemically unstable. This study extends our recent work on the h-La₂O₃ formation.     

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.     

不同氧化退火工艺下SiO2/SiC界面特性研究

The effect of the different re-oxidation annealing （ROA） processes on the SiO2/SiC interface charac- teristics has been investigated. With different annealing processes, the flat band voltage, effective dielectric charge density and interface trap density are obtained from the capacitance-voltage curves. It is found that the lowest interface trap density is obtained by the wet-oxidation annealing process at 1050 ℃ for 30 min, while a large num- ber of effective dielectric charges are generated. The components at the SiO2/SiC interface are analyzed by X-ray photoelectron spectroscopy （XPS） testing. It is found that the effective dielectric charges are generated due to the existence of the C and H atoms in the wet-oxidation annealing process.     

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。     

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.     

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。     

In0.53Ga0.47As表面氮化和硫钝化对其Al/Al2O3/InGaAs MOS电容特性的影响

本文通过对比频散特性和滞回特性,计算界面态密度D_it和有效边界缺陷密度ΔN_bt,分析界面缺陷和漏电流等方法,系统的研究了In_0.53Ga_0.47As表面氮化和硫钝化对其Al/Al₂O₃/InGaAs结构MOS电容特性的影响。实验结果表明,这两种方法都能够在InGaAs表明形成一层界面钝化层。相比较于未处理的样品,经过氮气等离子体处理的样品表现出较好的界面特性,得到了最小的积累区频散、滞回电压,以及良好的I-V性能。经过(NH₄)₂S_x处理的样品则获得了最小的平带电压区频散以及最低的界面态密度Dit=2.6E11cm_-2eV_-1.