在嵌段共聚物基体中原位合成的尺寸控制的非晶态氮化镓纳米颗粒有序阵列的高分辨率电子显微镜和微观分析

V. Leppert, A. Murali, S. Risbud, M. Stender, P. Power, C. Nelson, P. Banerjee, A. Mayes
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引用次数: 3

摘要

摘要本研究的目的是制备一种有序排列的尺寸可控的氮化镓纳米颗粒。在聚苯乙烯(PS)-b-聚(4-乙烯基吡啶)(b-P4VP)嵌段共聚物基体中,通过原位配方和随后的分解合成了环三氮杂烷。基质作为模板介质来约束颗粒大小,并允许控制颗粒形态、间距和堆积排列。纳米颗粒的大小和间距受整个聚合物链的分子量(81 000g mol−1)控制,颗粒的形态和排列受隔离块与基质块的比例(元素分析结果为21 wt% P4VP: 79 wt% PS)控制。高分辨率和分析透射电子显微镜显示,非晶态纳米颗粒主要由镓和氮组成,直径约为10nm,颗粒间平均距离为60nm,呈规则的六角形排列。这种合成技术的影响是为系统地研究量子约束和量子耦合对小氮化镓粒子光学性质的影响提供了手段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-resolution electron microscopy and microanalysis of ordered arrays of size-controlled amorphous gallium nitride nanoparticles synthesized in situ in a block copolymer matrix
Abstract The objective of this work was to produce an ordered array of size-controlled gallium nitride (GaN) nanoparticles. The synthesis was performed by the in situ formulation and subsequent decomposition of cyclotrigallazane in a polystyrene (PS)-b-poly(4-vinylpyridine) (b-P4VP) block copolymer matrix. The matrix served as a templating medium to constrain the particle size and to allow the control of particle morphology, spacing and packing arrangement. The size and spacing of nanoparticles were controlled by the molecular weight of the entire polymer chain (81 000g mol−1), and the particle morphology and packing arrangement were controlled by the ratio of the sequestering block to the matrix block (21 wt% P4VP to 79 wt% PS by elemental analysis). High-resolution and analytical transmission electron microscopy revealed the amorphous nanoparticles to be composed mainly of gallium and nitrogen (with oxygen detected in some particles) about 10nm in diameter with an average interparticle distance of 60 nm and organized in a regular hexagonal packing arrangement. The impact of this synthesis technique is to afford the means to investigate systematically the effect of quantum confinement and quantum coupling on the optical properties of small GaN particles.
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