纳米TiO_2光催化降解次甲基蓝的影响因素研究

以TiCl4为原料,采用水解沉淀法,并在空气气氛下于不同温度煅烧2h,制备得到纳米TiO2。采用XRD、TEM及UV-Vis对样品进行表征。在卤钨灯照射下,研究了不同煅烧温度、不同pH值以及H2O2的加入等因素对TiO2光催化降解次甲基蓝的影响。结果表明:以水解沉淀法制备的纳米TiO2,随煅烧温度的提高,在600℃开始向金红石相转变,1000℃时全部转变为金红石相,并且TiO2粒子长大,吸收带边向长波方向移动。锐钛矿相与金红石相共存的纳米TiO2比纯锐钛矿相和金红石相有更优异的光催化活性,在卤钨灯下照射90min,对次甲基蓝的降解率达到97%。     

Monodisperse Hollow Supraparticles via Selective Oxidation

A novel and general strategy to fabricate monodisperse hollow supraparticles (SPs) via selective chemical oxidation is developed. Core‐shell SPs made of semiconductor nanocrystals (NCs) are first obtained by an in situ assembly method. Subsequently, the cores can be selectively removed by preferential oxidation with dilute H₂O₂, resulting in formation of monodisperse hollow SPs. The structural parameters of the products, such as size, shell thickness, and composition, are tailored easily. The hollow structures achieved from CdSe/CdS core‐shell SPs possess high fluorescence quantum yields and a large Stokes shift, the latter is remarkably different from that of conventional organic dyes and quantum dots. In addition to simple hollow structures, rattle‐type nanostructures composed of semiconductor SPs or noble metal‐semiconductor hybrids are also prepared, exemplifying the versatility of the proposed strategy.     

The oxidation of titanium silicide

This paper investigates the morphology changes that occur with the oxidation of a ti-tanium silicide—polysilicon system. These changes were studied as a function of poly-silicon doping and silicide formation parameters. Emphasis was placed on transmission electron microscopy studies of the samples by planar and cross sectional techniques. Various surface analysis methods have also been used to characterize the films. This study helps to define the possible use and shortcomings of a self aligned titanium silicide insulator. The results show that varying quality insulators result, dependent largely on the initial conditions of the titanium silicide. After oxidation the Auger and TEM anal-ysis show that in all cases some form of silicon dioxide was created, but typically a considerable amount of titanium oxide was also present. For instance, it was apparent that more titanium oxide formed on the samples RTA’ed for 1 min at 700° C than the 5 min at 800° C and considerably more on the arsenic doped sample than the boron doped. The silicide also had morphology changes as the result of the oxidation. There was a phase change from the C49 to C54 phase for the 1 min at 700° C samples as would be expected at the time and temperature of the oxidation. There also was a sig-nificant amount of agglomeration and epitaxial growth observed. Further work is re-quired to completely characterize these phenomena.     

湿法氧化Al0.85Ga0.15As时SiO2层的保护作用

本文研究了有无氧化硅保护层时Al0.85Ga0.15As层的高温湿法氧化。实验结果表明：氧化硅层对Al0.85Ga0.15As层的高温侧向湿法氧化速率基本无影响;被氧化区域SEM图像的衬度和有氧化硅保护层样品As拉曼峰的缺乏归因于被氧化区域中不存在氧化反应产物As,这有利于提高氧化层的热稳定性;有SiO2保护层样品的发光强度比无SiO2保护层样品的发光强度强的多,且具有SiO2保护层样品的发光峰位和半高全宽与氧化前的样品基本一致,而无SiO2保护层样品的发光峰位红移,半高宽展宽,这是由于氧化硅层阻止了GaAs盖层的氧化。     

Janus‐Structured Co‐Ti3C2 MXene Quantum Dots as a Schottky Catalyst for High‐Performance Photoelectrochemical Water Oxidation

MXene materials have attracted increasing attention in electrochemical energy‐storage applications while MXene also becomes photo‐active at the quantum dot scale, making it an alternative for solar‐energy‐conversion devices. A Janus‐structured cobalt‐nanoparticle‐coupled Ti₃C₂ MXene quantum dot (Co‐MQD) Schottky catalyst with tunable cobalt‐loading content serving as a photoelectrochemical water oxidation photoanode is demonstrated. The introduction of cobalt triggers concomitant surface‐plasmon effects and acts as a water oxidation center, enabling visible‐light harvesting capability and improving surface reaction kinetics. Most importantly, due to the rectifying effects of Co‐MQD Schottky junctions, photogenerated carrier separation/injection efficiency can be fundamentally facilitated. Specifically, Co‐MQD‐48 exhibits both superior photoelectrocatalysis (2.99 mA cm^?2 at 1.23 V vs RHE) and charge migration performance (87.56%), which corresponds to 194% and 236% improvement compared with MQD. Furthermore, excellent photostability can be achieved with less than 6.6% loss for 10 h cycling reaction. This fills in gaps in MXene material research in photoelectrocatalysis and allows for the extension of MXene into optical‐related fields.     

N~+型重掺杂硅快速氧化新方法──氟化氢增强氧化之二

本文对重掺杂单晶硅和多晶硅薄膜的加HF增强氧化的行为进行了研究。氧气中HF含量为480ppm,温度为750至900℃。发现重掺磷或砷的硅的氧化反应速率很快,速率常数比轻掺杂硅的干氧氧化提高了几十倍至几百倍。而重掺硼的硅单晶对氧化速率并无明显影响。文中对重掺杂元素和HF增强硅氧化的机理作了分析,并提出了一个物理模型,可以较好地解释实验现象。     

C/C复合材料的氧化对激光防护的影响研究

研究了不同风速下激光辐照C/C复合材料的氧化速率,利用温度场计算结果,结合氧气在空气中的传质速率,计算了激光辐照下C/C复合材料的氧化烧蚀速率及氧化放热的影响。数值计算结果表明,激光辐照期间,较低风速下氧化对烧蚀的贡献很小。作为激光防护材料,C/C复合材料激光辐照期间的氧化烧蚀可以忽略。     

热氧化方法改善硅干法刻蚀波导的表面粗糙度

提出了一种热氧化的方法来改善干法刻蚀硅波导的表面质量.通过Suprem二维工艺模拟程序对氧化过程的物理模型进行了分析.用实验证实了该方法的可行性并与模拟结果进行了比较.实验中将硅波导的表面粗糙度由65.4nm降低到了8.8nm.另外讨论了分次氧化方法的利弊     

Rational Engineering of Multilayered Co3O4/ZnO Nanocatalysts through Chemical Transformations from Matryoshka‐Type ZIFs

Hybrid metal oxides with multilayered structures exhibit unique physical and chemical properties, particularly important to heterogeneous catalysis. However, regulations of morphology, spatial location, and shell numbers of the hybrid metal oxides still remain a challenge. Herein, binary Co₃O₄/ZnO nanocages with multilayered structures (up to eight layers) are prepared via chemical transformation from diverse Matryoshka‐type zeolitic imidazolate frameworks (ZIFs) via a straightforward and scalable calcination method. More importantly, the obtained ZIF‐derived metal oxides (ZDMOs) with versatile layer numbers exhibit remarkable catalytic activity for both gas‐phase CO oxidation and CO₂ hydrogenation reactions, which are directly related to the sophisticated shell numbers (i.e., Co₃O₄‐terminated layers or ZnO‐terminated layers). Particularly, in situ reflectance infrared Fourier transform spectroscopy (DRIFTS) results indicate that the promotional effects of the multilayered structures indeed exist in CO₂ hydrogenation, wherein the key reaction intermediates are quite different for five‐layer and six‐layer ZDMOs. For instance, *HCOO is the predominant intermediate over the six‐layer ZDMO; on the contrary, *H₃CO is the crucial species over the five‐layer ZDMO. The ZnO/Co₃O₄ interface should be the active sites for CO₂ hydrogenation to *HCOO and *H₃CO species, which are ultimately converted to the products (CH₄ or methanol). Accordingly, the work here provides a convenient way to facilely engineer multilayered Co₃O₄/ZnO nanocomposites with precisely controlled shell numbers for heterogeneous catalysis applications.     

用于甲醛检测的电化学生物传感器的设计

目前用于检测甲醛的传感器有电化学传感器、光学传感器和光生化传感器等。但是当用于实际检测的时候都会存在这样或者那样的问题,比如稳定性差、检出限低、所受干扰物多等等,针对这些问题,文章设计了一种简便、操作简单、适用于实时在线检测甲醛的电化学生物传感器,针对水溶液及混合溶液中甲醛的检测。