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二硫代亚氨基二膦酸酯配合物化学气相沉积法制备镍的硫化物、硒化物或磷化物的影响因素:沉积、光谱和计算研究。

Factors controlling material deposition in the CVD of nickel sulfides, selenides or phosphides from dichalcogenoimidodiphosphinato complexes: deposition, spectroscopic and computational studies.

机构信息

The School of Chemistry, The University of Manchester, Oxford Road, Manchester, UK M13 9PL.

出版信息

Dalton Trans. 2010 Jul 14;39(26):6080-91. doi: 10.1039/c002928a. Epub 2010 Jun 1.

Abstract

The series of nickel dichalcogenoimidodiphosphinates [Ni{(i)Pr(2)P(X1)NP(X2)(i)Pr(2)}(2)]: X1 = S, X2 = Se (1), X1 = X2 = S (2), and X1 = X2 = Se (3) have been successfully used as single-source precursors (SSPs) to deposit thin films of nickel sulfide, selenide or phosphide; the material deposited depended on both temperature and method used for the deposition. Aerosol-assisted (AA) chemical vapour deposition (CVD) and low-pressure (LP) CVD were used. The as-deposited films were characterised by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX) and X-ray photoelectron spectroscopy (XPS). A variety of phases including: Ni(2)P, Ni(0.85)Se and NiS(1.03) were deposited under different conditions. The mechanism of decomposition to the phosphide, selenide, or sulfide was studied by pyrolysis gas chromatography mass spectrometry (Py-GC-MS) and modelled by density functional theory (DFT).

摘要

该系列的镍二硫代亚膦酸亚胺二膦酸盐 [Ni{(i)Pr(2)P(X1)NP(X2)(i)Pr(2)}(2)]:X1 = S,X2 = Se(1),X1 = X2 = S(2),和 X1 = X2 = Se(3)已成功用作沉积硫化镍、硒化物或磷化物薄膜的单源前体(SSP);沉积的材料取决于沉积时使用的温度和方法。使用了气溶胶辅助(AA)化学气相沉积(CVD)和低压(LP)CVD。使用 X 射线衍射(XRD)、扫描电子显微镜(SEM)、能谱(EDX)和 X 射线光电子能谱(XPS)对沉积的薄膜进行了表征。在不同条件下沉积了包括:Ni(2)P、Ni(0.85)Se 和 NiS(1.03)等多种相。通过热重-气相色谱-质谱联用(Py-GC-MS)研究了分解为磷化物、硒化物或硫化物的机制,并通过密度泛函理论(DFT)进行了模拟。

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