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Surface chemistry of group 11 atomic layer deposition precursors on silica using solid-state nuclear magnetic resonance spectroscopy

机译:第11族的表面化学原子层沉积前体使用固态核磁共振光谱法

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The use of chemical vapour deposition (CVD) and atomic layer deposition (ALD) as thin film deposition techniques has had a major impact on a number of fields. The deposition of pure, uniform, conformal thin films requires very specific vapour-solid reactivity that is largely unknown for the majority of ALD and CVD precursors. This work examines the initial chemisorption of several thin film vapour deposition precursors on high surface area silica (HSAS) using C-13, P-31, and quantitative Si-29 nuclear magnetic resonance spectroscopy (NMR). Two copper metal precursors, ylidene copper(I) hexamethyldisilazide (2), and one gold metal precursor, trimethylphosphine gold(III) trimethyl (3), are examined. Compounds 1 and 2 were found to chemisorb at the hydroxyl surface-reactive sites to form a parallel to-O-Cu-NHC surface species and fully methylated silicon (parallel to-SiMe3, due to reactivity of the hexamethyldisilazane (HMDS) ligand on the precursor) at 150 degrees C and 250 degrees C. From quantitative Si-29 solid-state NMR (SS-NMR) spectroscopy measurements, it was found that HMDS preferentially reacts at geminal disilanol surface sites while the copper surface species preferentially chemisorbed to lone silanol surface species. Additionally, the overall coverage was strongly dependent on temperature, with higher overall coverage of 1 at higher temperature but lower overall coverage of 2 at higher temperature. The chemisorption of 3 was found to produce a number of interesting surface species on HSAS. Gold(III) trimethylphosphine, reduced gold phosphine, methylated phosphoxides, and graphitic carbon were all observed as surface species. The overall coverage of 3 on HSAS was only about 10% at 100 degrees C and, like the copper compounds, had a preference for lone silanol surface reactive sites. The overall coverage and chemisorbed surface species have implications to the overall growth rate and purity of metal films grown with these precursors. Published by AIP Publish
机译:使用化学气相沉积(CVD)和原子层沉积(ALD)作为薄膜沉积技术对许多领域产生了重大影响。纯,均匀,保形薄膜的沉积需要非常特异性的蒸汽固体反应性,对于大多数Ald和CVD前体具有很大的蒸汽固体反应性。本作品使用C-13,P-31和定量Si-29核磁共振光谱(NMR)检查高表面积二氧化硅(HSA)上几种薄膜气相沉积前体的初始化学吸取。检查两种铜金属前体,赤肾(I)六甲基二硅基脲(2),以及一个金属前体,三甲基膦金(III)三甲基(3)。在羟基表面反应位点发现化合物1和2,以形成平行于O-Cu-NHC表面物质和完全甲基化硅(平行于SIME3,由于六甲基二硅氮烷(HMDS)配体上的反应性前体)在50℃和250℃下C.来自定量Si-29固态NMR(SS-NMR)光谱测量,发现HMD优先在初始二硅烷醇表面位点处反应,同时优先化学吸附到溶硅烷醇中的铜表面物种表面物种。另外,整体覆盖率强烈依赖于温度,在较高温度下,1的整体覆盖率较高,但在较高温度下较低的整体覆盖率。发现3的化学吸附在HSA上产生许多有趣的表面物种。金(III)三甲基膦,还原金膦,甲基化氧化膦和石墨碳全部观察到表面物质。 3对HSA的整体覆盖率在100摄氏度下仅为约10%,与铜化合物一样,偏好溶于硅烷醇表面活性位点。整体覆盖和化学表面物种对用这些前体生长的金属膜的总体生长速率和纯度有影响。由AIP发布发布

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