Sol-gel processed high-k aluminum oxide dielectric films for fully solution-processed low-voltage thin-film transistors

High-k oxide dielectric films have attracted intense interest for thin-film transistors (TFTs). However, high-quality oxide dielectrics were traditionally prepared by vacuum routes. Here, amorphous high-k alumina (Al₂O₃) thin films were prepared by the simple sol-gel spin-coating and post-annealing process. The microstructure and dielectric properties of Al₂O₃ dielectric films were systematically investigated. All the Al₂O₃ thin films annealed at 300–600?°C are in amorphous state with ultrasmooth surface (RMS ~ 0.2?nm) and high transparency (above 95%) in the visible range. The leakage current of Al₂O₃ films gradually decreases with the increase of annealing temperature. Al₂O₃ thin films annealed at 600?°C showed the low leakage current density down to 3.9?×?10^?7 A/cm² at 3?MV/cm. With the increase of annealing temperature, the capacitance first decreases then increases to 101.1?nF/cm² (at 600?°C). The obtained k values of Al₂O₃ films are up to 8.2. The achieved dielectric properties of Al₂O₃ thin films are highly comparable with that by vapor and solution methods. Moreover, the fully solution-processed InZnO TFTs with Al₂O₃ dielectric layer exhibit high mobility of 7.23?cm² V^?1 s^?1 at the low operating voltage of 3?V, which is much superior to that on SiO₂ dielectrics with mobility of 1.22?cm²/V^?1 s^?1 at the operating voltage of 40?V. These results demonstrate that solution-processed Al₂O₃ thin films are promising for low-power and high-performance oxide devices.     

PREPARATION AND ELECTROCHEMICAL PROPERTIES OF NANOSCALE POROUS CARBON ELECTRODE MATERIALS BASED ON RICE PLANT SOOT

Supercapacitors are a kind of novel energy storage devices with long cycle stability and high power density. Electrode materials selection is one of the key factors that affect the properties of supercapacitors. Biomass-derived electrode materials – being low cost, renewable and environmentally friendly – are therefore attracting researchers’ attention. In this work, we adopted a simple process of carbonization and activation with rice plant soot, a common biomass material, as carbon source, and finally obtained the nanoscale porous carbon electrode (NPCE) materials. Then, the electrochemical properties of the as-prepared NPCE materials were tested in 6 M KOH, and the results indicated that the specific capacitance could reach 216?Fg^?1. Therefore, this low-cost, highly efficient technique is a significant milepost towards environmentally sustainable and commercially feasible fabrication of carbon electrode materials from biomass sources.     

In-situ preparation of cross-linked hybrid anion exchange membrane of quaternized poly (styrene-b-isobutylene-b-styrene) covalently bonded with graphene

Introducing graphene into polymer matrix is an effective way to enhance performances of anion exchange membrane (AEM). However, utilizing the advantages of graphene by physical approach is limited due to the weak interface interaction between graphene and polymer matrix. Herein, we report an effective strategy to covalently bond graphene with polymer matrix to improve the interface interaction and further to improve the properties of AEM. A series of cross-linked quaternized graphene-based hybrid AEM were fabricated by covalently bonding poly (vinylbenzyl chloride) grafted graphene (GN-g-PVBC) copolymer with chloromethyl functionalized poly (styrene-b-isobutylene-b-styrene) (SIBS) through the cross-linker (N,N,N′,N′-tetramethyl-1,6-hexanediamine) by in-situ synthetic approach. The interface interaction between graphene and QSIBS is greatly enhanced according to micromorphology characterization of the hybrid membrane. The cross-linked quaternized hybrid AEM containing 0.55 wt% of GN-g-PVBC exhibits obviously improved dynamical mechanical properties (storage modulus: 418 MPa), ion conductivity (1.81 × 10² S cm^?1), methanol barrier property (5.19 × 10^?7 cm² s^?1), selectivity (3.49 × 10⁴ S s cm^?3) at 60 °C and especially a comparably excellent chemical stability to that of Nafion 115 due to the enhanced interface interaction between graphene and the polymer matrix.     

熟料库清库门的几种设计方案

很多熟料库在设计时未注意清库门的设置，或者是设计的清库门不合理从而给施工和后期的实际使用造成很多麻烦。本文介绍了几种熟料清库门的几种设计方案，对比了其设计方式，设计要点及优缺点，为熟料库设计提供了有益的思路。     

CRM4622型立磨磨盘刮料架脱落的处理措施

我厂共有3台CRM4622型立式磨机生产矿渣粉，分别为#3，#4，#5立磨。其中#3，#4立磨（#3立磨投产于2010年，#4立磨投产于2012年）于2014年4月相继出现磨盘刮料架整体脱落情况。经过更换螺栓，情况得到暂时缓解。一段时间后，刮料架再次脱落。为了彻底解决刮料架脱落问题，决定对刮料架的固定方式进行改进，以提高刮料架的稳定性。     

抗冲ACR树脂的合成及其性能评价

采用种子乳液聚合法,以丙烯酸丁酯为核层单体、甲基丙烯酸甲酯为壳层单体、甲基丙烯酸烯丙酯为交联剂制备了抗冲ACR树脂。考察了不同加料方式对ACR乳液粒径及对PVC冲击性能的影响,结果表明:连续滴加方式可实现乳液粒径的稳定控制,并能得到性能优异的抗冲ACR树脂。     

Zr-4合金板材真空退火温度场的数值模拟

分析Zr-4合金板材真空退火过程中的传热方式,计算锆合金板材径向传热系数,利用ABAQUS对Zr-4合金板材退火温度场进行数值模拟,分析工装夹具对锆合金板材退火的影响,结果表明,工装夹具能改善锆合金板材温度场分布均匀性,使锆合金板材温度分布的最高温差由70 ℃降低至35 ℃,升温过程更加稳定,并且数值模拟结果与实测结果有较好的一致性。     

A Combined Ordered Macro‐Mesoporous Architecture Design and Surface Engineering Strategy for High‐Performance Sulfur Immobilizer in Lithium–Sulfur Batteries

The practical application of lithium–sulfur (Li–S) batteries is hindered by the “shuttle” of lithium polysulfides (LiPS) and sluggish Li–S kinetics issues. Herein, a synergistic strategy combining mesoporous architecture design and defect engineering is proposed to synthesize multifunctional defective 3D ordered mesoporous cobalt sulfide (3DOM N‐Co₉S_8?x) to address the shuttling and sluggish reaction kinetics of polysulfide in Li–S batteries. The unique 3DOM design provides abundant voids for sulfur storage and enlarged active interfaces that reduce electron/ion diffusion pathways. Meanwhile, X‐ray absorption spectroscopy shows that the surface defect engineering tunes the CoS₄ tetrahedra to CoS₆ octahedra on Co₉S₈, endowing abundance of S vacancies on the Co₉S₈ octahedral sites. The ever‐increasing S vacancies over the course of electrochemical process further promotes the chemical trapping of LiPS and its conversion kinetics, rendering fast and durable Li–S chemistry. Benefiting from these features, the as‐developed 3DOM N‐Co₉S_8?x/S cathode delivers high areal capacity, superb rate capability, and excellent cyclic stability with ultralow capacity fading rate under raised sulfur loading and low electrolyte content. This design strategy promotes the development of practically viable Li–S batteries and sheds lights on the material engineering in related energy storage application.