首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Synthesis and characterization of novel zinc precursors for ZnO thin film deposition by atomic layer deposition
【24h】

Synthesis and characterization of novel zinc precursors for ZnO thin film deposition by atomic layer deposition

机译:用原子层沉积的ZnO薄膜沉积新型锌前体的合成与表征

获取原文
获取原文并翻译 | 示例
           

摘要

A novel series of zinc complexes, [EtZn(dab)](2) (1), [EtZn(damb)](2) (2), [EtZn(damp)](2) (3), and [EtZn(dadb)](2) (4), were prepared via single-step substitution. Further, these were analyzed by nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy (FT-IR), elemental analysis, single crystal X-ray diffraction analysis, and thermogravimetric analysis (TGA). The X-ray crystallography analysis revealed that all complexes exist as dimeric structures with distorted tetrahedral geometry having zinc centers that are interconnected via mu(2)-O bonding of the aminoalkoxy oxygen atom. TGA and thermal analysis of the complexes showed high volatilities and stabilities at sublimation temperatures of 70, 95, 90, and 105 degrees C at 0.5 Torr for the respective compounds. Precursor 3 was successfully used for ZnO thin film deposition by ALD. A growth rate per cycle (GPC) of 0.125 nm per cycle was obtained at 200 degrees C and XPS analysis confirmed the growth of highly pure ZnO films without carbon and nitrogen impurities, while XRD analysis revealed the deposition of reasonably crystalline films. Additionally, the high transmittance and wide bandgap of the films are suitable for optoelectronic applications.
机译:一种新型系列锌配合物,[EtzN(DAB)](2)(1),[EtZN(DAMB)](2)(2),[EtzN(潮湿)](2)(3),以及η( DADB)](2)(4)通过单步取代制备。此外,通过核磁共振(NMR),傅里叶变换红外光谱(FT-IR),元素分析,单晶X射线衍射分析和热重分析(TGA)分析这些。 X射线晶体术分析显示,所有复合物都存在于具有抗体的四面体几何形状的二聚体结构,其具有通过氨基烷氧基原子的μ-O键合互连的锌中心。复合物的TGA和热分析显示出70,95,90和105℃的升华温度下的高挥发性和稳定性,在0.5托的各自化合物的升温温度下。前体3已通过ALD成功用于ZnO薄膜沉积。在200摄氏度下获得每周期0.125nm的每循环(GPC)的生长速率,并且XPS分析证实了高纯ZnO膜的生长而不碳和氮杂质,而XRD分析显示合理结晶膜的沉积。另外,薄膜的高透射率和宽带隙适用于光电应用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号