O'Leary Leslie E, Strandwitz Nicholas C, Roske Christopher W, Pyo Suyeon, Brunschwig Bruce S, Lewis Nathan S
Beckman Institute and Kavli Nanoscience Institute, Division of Chemistry and Chemical Engineering, California Institute of Technology, 210 Noyes Laboratory, Pasadena, California 91125, United States.
J Phys Chem Lett. 2015 Feb 19;6(4):722-6. doi: 10.1021/jz502542a. Epub 2015 Feb 6.
Silicon surfaces terminated with a mixed monolayer containing both a propyl aldehyde functionality and methyl groups were prepared and used to control the interfacial chemical and electronic properties of Si(111) surfaces during atomic-layer deposition (ALD) of Al2O3 or MnO. Si(111) surfaces functionalized only with the aldehyde moiety exhibited surface recombination velocities, S, of 2500 ± 600 cm s(-1) whereas the mixed CH3-/HC(O)CH2CH2-Si(111) surfaces displayed S = 25 ± 7 cm s(-1). During the ALD growth of either Al2O3 or MnO, both the HC(O)CH2CH2-Si(111) and CH3-/HC(O)CH2CH2-Si(111) surfaces produced increased metal oxide deposition at low cycle number, relative to H-Si(111) or CH3-Si(111) surfaces. As detected by X-ray photoelectron spectroscopy after the ALD process, the CH3- and mixed CH3-/HC(O)CH2CH2- functionalized Si(111) surfaces exhibited less interfacial SiOx than was observed for ALD of metal oxides on H-Si(111) substrates.
制备了以含有丙醛官能团和甲基的混合单层封端的硅表面,并用于在氧化铝(Al2O3)或氧化锰(MnO)的原子层沉积(ALD)过程中控制Si(111)表面的界面化学和电子性质。仅用醛部分官能化的Si(111)表面的表面复合速度S为2500±600 cm s(-1),而混合的CH3-/HC(O)CH2CH2-Si(111)表面的S = 25±7 cm s(-1)。在Al2O3或MnO的ALD生长过程中,相对于H-Si(111)或CH3-Si(111)表面,HC(O)CH2CH2-Si(111)和CH3-/HC(O)CH2CH2-Si(111)表面在低循环数时都产生了增加的金属氧化物沉积。在ALD过程后通过X射线光电子能谱检测,CH3-官能化和混合CH3-/HC(O)CH2CH2-官能化的Si(111)表面比在H-Si(111)衬底上进行金属氧化物ALD时观察到的界面SiOx更少。