镁合金表面铬掺杂类金刚石薄膜的制备与性能研究

本文利用阳极层离子束混合磁控溅射技术在AZ31镁合金表面制备了类金刚石涂层（DLC）和Cr掺杂DLC膜（Cr-DLC）,并利用Raman光谱、残余应力仪、划痕仪、摩擦磨损仪和电化学工作站等,对薄膜的碳结构、残余应力、结合力、摩擦学性能和耐腐蚀性进行了研究。结果表明：相比纯DLC膜,Cr-DLC膜具有较低的残余应力,较高的膜/基结合力。Cr-DLC膜能显著提高镁合金的抗摩擦磨损性能,但对改善镁合金耐腐蚀性能影响不大。     

大直径重掺硅单晶工艺研究

重掺单晶一些独有的特性,能有效解决目前集成电路面临的一些难题。对大直径重掺硅单晶生长过程中的一些工艺进行了研究,主要包括掺杂方式和拉速设定两个方面,通过实验分析,选取了适宜的掺杂方式与拉速,最终生长出外形良好,符合电阻率目标要求的单晶。     

水解工艺Yb3＋/Al3＋共掺石英玻璃的研制及特性表征

利用四氯化硅(SiCl₄)水解掺杂法结合高 频等离子体粉末熔融技术制备了Yb3＋/Al3＋共掺石英玻璃,并利用 X射 线衍射(XRD)、傅里叶变换红外(FTIR)光谱分析和热膨胀分析等对所制备玻璃样品的结 构特性、物理特性和光谱特 性进行了表征。结果表明,制备的Yb3＋/Al3＋共掺石英玻璃的密度和折 射率值与纯石英玻璃相接近,并且呈现出 较好的玻璃态,其热膨胀系数为2.87×10－6,具有较好的Yb3＋和Al 3＋掺杂均匀性,以及Yb3＋典型的吸 收特性和发射特性,表明采用本文方法制备的Yb3＋/Al3＋共掺石英玻璃 已具备成为大功率激光材料的潜质。     

Mg单原子替位掺杂β-Ga2O3的电子结构和光学性质计算研究

宽禁带半导体β-Ga2O3因其出色的物理化学性能而备受关注,通过掺杂改善β-Ga2O3性能一直是研究的热点.采用基于密度泛函理论的第一性原理方法,利用广义梯度近似加U对Mg单原子掺杂β-Ga2O3体系的晶体结构、电子结构和光学性质等进行了研究和分析.总能量和结合能的对比显示:单原子替位掺杂β-Ga2O3时,Mg优先替代八面体位的Ga原子形成Mg-Gao体系.电子结构显示,Mg-Gao体系变为间接半导体,带隙变窄为4.672eV;其自旋极化率为100％,呈现半金属特性.作为光学材料,Mg-Gao体系可在紫外、深紫外区域工作,并且折射率、反射率和吸收率有所降低,透射率明显提高.     

氟碳树脂基导电涂料的制备及其性能研究

以氟碳树脂为基体,掺铝氧化锌粉体为导电填料,制备导电性能优良的单组份导电涂料。借助热重-差热、X射线衍射、电镜等分析手段,探讨了掺铝氧化锌粉体的添加量和导电粉体的改性对导电涂料电性能、热稳定性和力学性能的影响。结果表明,当用乙烯基三乙氧基硅烷和硅烷偶联剂改性的导电填料掺量为35%时,制备的导电涂料性能最优,其体积电阻率为8.89×108Ω·cm、拉伸强度和断裂伸长率分别为19.36 MPa和200.45%。     

Well‐Combined Magnetically Separable Hybrid Cobalt Ferrite/Nitrogen‐Doped Graphene as Efficient Catalyst with Superior Performance for Oxygen Reduction Reaction

Catalysts with low‐cost, high activity and stability toward oxygen reduction reaction (ORR) are extremely desirable, but its development still remains a great challenge. Here, a novel magnetically separable hybrid of multimetal oxide, cobalt ferrite (CoFe₂O₄), anchored on nitrogen‐doped reduced graphene oxide (CoFe₂O₄/NG) is prepared via a facile solvothermal method followed by calcination at 500 °C. The structure of CoFe₂O₄/NG and the interaction of both components are analyzed by several techniques. The possible formation of Co/Fe N interaction in the CoFe₂O₄/NG catalyst is found. As a result, the well‐combination of CoFe₂O₄ nanoparticles with NG and its improved crystallinity lead to a synergistic and efficient catalyst with high performance to ORR through a four‐electron‐transfer process in alkaline medium. The CoFe₂O₄/NG exhibits particularly comparable catalytic activity as commercial Pt/C catalyst, and superior stability against methanol oxidation and CO poisoning. Meanwhile, it has been proved that both nitrogen doping and the spinel structure of CoFe₂O₄ can have a significant contribution to the catalytic activity by contrast experiments. Multimetal oxide hybrid demonstrates better catalysis to ORR than a single metal oxide hybrid. All results make the low‐cost and magnetically separable CoFe₂O₄/NG a promising alternative for costly platinum‐based ORR catalyst in fuel cells and metal‐air batteries.     

固相合成锂离子电池正极材料LiMn_(1-x)Fe_xPO_4/C的结构与电化学性能

以葡萄糖为碳源,对LiH2PO4、MnCO3、FeC2O4与葡萄糖等反应物进行湿法球磨,随后在750℃温度下煅烧,通过固相反应实现对LiMnPO4的铁离子掺杂和碳包覆改性,得到锂离子电池正极材料LiMn1-xFexPO4/C(x=0、0.05、0.10、0.15、0.20)。利用X射线衍射(XRD),扫描电镜(SEM)及电化学测试等手段研究铁离子掺杂量对磷酸锰锂的晶体结构、微观形貌与电性能的影响。结果表明,LiMn0.9Fe0.1PO4/C结晶度良好,颗粒较均匀细小,具有较好的电化学性能,0.05C倍率下的首次放电比容量达到110(mA·h)/g,经过30次循环后,放电比容量约80(mA·h)/g。     

Wettability and biomineralisation of laser cladded Si doped TiCN biocoating

Surface textured Si doped TiCN coatings were synthesised on Ti–6Al–4V alloy by laser cladding technique. Phase constituent examination by X-ray diffraction revealed the formation of similar phases of TiC_0.2N_0.8 and Ti₅Si₄ within all coated samples. Laser coated samples presented much higher surface free energy compared to Ti–6Al–4V control due to the textured structure, which in turn demonstrated a better wettability and improved biomineralisation. Variation of silica content presented no significant influence on surface free energy, indicating that the silica content can be varied in a large range. The mineralised samples obtained after immersion in simulated body fluid were characterised to understand the mechanism and kinetics of Ca–P precipitation. The results confirmed that the precipitation kinetics of Ca–P was influenced by the substitution of silica.     

Influence of Au Photodeposition and Doping in CdS Nanorods: Optical and Photocatalytic Study

Au-modified CdS nanorods (100–200 nm × 5–10 nm) are synthesized via two different techniques, namely photodeposition and doping. The prepared samples are characterized by x-ray powder diffraction, transmission electron microscopy (TEM), and UV–vis and fluorescence spectroscopy. X-ray diffraction study confirmed the hexagonal phase of bare and Au-CdS samples, whereas, 5 wt% Au³⁺ doping into CdS resulted in a slight distortion in the crystal structure toward higher degree side. TEM images revealed the fine distribution of Au nanodeposits of size in the range of 2.5–4.5 nm on to the CdS surface in the photodeposited sample. The optical spectrum shows a significant red-shift in absorption onset (485 nm → 515 nm) and band-edge emission (505 nm → 512 nm) of CdS nanorods with the replacement of certain Cd²⁺ ions with Au³⁺. The influence of Au photodeposition and doping in CdS nanorods was comparatively tested by photooxidation of RhB (50 ppm) dye aqueous solution under direct sunlight irradiation (35–40 mWcm^?2). Our results point out that 5 wt% Au³⁺ doping into CdS nanorods remarkably improved its activity and stability due to homogeneous dispersion of charge throughout the crystal, quick Fermi level equilibration, and an improvement in ionic bond formation.