Sparenberg M, Zykov A, Beyer P, Pithan L, Weber C, Garmshausen Y, Carlà F, Hecht S, Blumstengel S, Henneberger F, Kowarik S
Humboldt Universität zu Berlin, Department of Physics, Berlin, Germany.
Phys Chem Chem Phys. 2014 Dec 21;16(47):26084-93. doi: 10.1039/c4cp04048a. Epub 2014 Oct 31.
We report on the impact of partial fluorination of para-sexiphenyl (6P) on the growth mode when deposited on the non-polar ZnO(101̄0) surface. The evolution of the thin film structure and morphology is monitored by in situ atomic force microscopy and in situ real-time X-ray scattering. Both 6P and its symmetrical, terminally fluorinated derivative (6P-F4) grow in a highly crystalline mode, however, with a distinctly different morphology. While 6P films are characterised by the formation of two different phases with three-dimensional nanocrystallites and consequently a rather rough surface morphology, layer-by-layer growth and phase purity in case of 6P-F4 prevails leading to smooth terraced thin films. We relate the different growth behaviour to specifics of the thin film structure.
我们报告了对三联苯(6P)进行部分氟化处理后,其在非极性ZnO(101̄0)表面沉积时生长模式的影响。通过原位原子力显微镜和原位实时X射线散射监测薄膜结构和形态的演变。6P及其对称的末端氟化衍生物(6P-F4)均以高度结晶的模式生长,然而,它们的形态明显不同。6P薄膜的特征是形成了具有三维纳米微晶的两种不同相,因此表面形态相当粗糙,而6P-F4则以逐层生长且相纯度高为主,形成了光滑的梯田状薄膜。我们将不同的生长行为与薄膜结构的特性联系起来。