原子层沉积
钒
化学
石英晶体微天平
拉曼光谱
相(物质)
薄膜
化学工程
无机化学
分析化学(期刊)
结晶学
图层(电子)
材料科学
物理化学
纳米技术
有机化学
吸附
工程类
物理
光学
作者
Matthew S. Weimer,Robert McCarthy,Jonathan D. Emery,Michael J. Bedzyk,Fatih G. Sen,Alper Kınacı,Maria K. Y. Chan,Adam S. Hock,Alex B. F. Martinson
标识
DOI:10.1021/acs.chemmater.6b05084
摘要
Despite challenges to control stoichiometry in the vanadium–sulfur system, template-free growth of patrónite, VS4, thin films is demonstrated for the first time. A novel atomic layer deposition (ALD) process enables the growth of phase pure films and the study of electrical and vibrational properties of the quasi-one-dimensional (1D) transition metal sulfide. Self-limiting surface chemistry during ALD of VS4 is established via in situ quartz crystal microbalance and quadrupole mass spectrometry between 150 and 200 °C. The V precursor, unconventionally, sheds all organic components in the first half-cycle, while the H2S half-cycle generates the disulfide dimer moiety, S2–2, and oxidizes V3+ to V4+. X-ray analysis establishes VS4 crystallinity and phase purity, as well as a self-limiting growth rate of 0.33 Å/cy, modest roughness of 2.4 nm, and expected density of 2.7 g/cm3. Phase pure films enable a new assignment of vibrational modes and corresponding Raman activity of VS4 that is corroborated by density functional theory (DFT) calculations. Finally, at elevated growth temperatures, a change in the surface mechanism provides a synthetic route to a second vanadium–sulfur phase, V2S3.
科研通智能强力驱动
Strongly Powered by AbleSci AI