Surface species during ALD of platinum observed with in situ reflection IR spectroscopy

被引:26
作者
Van Daele, Michiel [1 ]
Detavernier, Christophe [1 ]
Dendooven, Jolien [1 ]
机构
[1] Univ Ghent, Dept Solid State Sci, CoCooN Res Grp, Krijgslaan 281-S1, B-9000 Ghent, Belgium
关键词
ATOMIC LAYER DEPOSITION; VIBRATIONAL-SPECTRA; PT(111); OXIDATION; HYDROGEN; DEHYDROGENATION; NANOPARTICLES; OXYGEN; ADSORPTION; DESORPTION;
D O I
10.1039/c8cp03585g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Thermal atomic layer deposition (ALD) and plasma-enhanced ALD (PE-ALD) of Pt, using MeCpPtMe3 as the precursor and O-2 gas or O-2 plasma as the reactant, are studied with in situ reflection Fourier transform infrared spectroscopy (FTIR) at different substrate temperatures. This is done to identify the functional groups present during Pt ALD and investigate the origin of the temperature dependent growth rate of the thermal process. Evidence is given that CH and C?C containing species are present on the surface after precursor exposure at low substrate temperatures (<150 degrees C), poisoning the surface during thermal ALD. Both species are removed by O-2 plasma enabling PE-ALD below 150 degrees C through combustion reactions. Above 150 degrees C, no CH stretching modes were detected and the C?C vibration diminished, indicating dehydrogenation reactions and ligand restructuring. In addition, the PE-ALD FTIR spectra revealed the presence of combustion reaction products on the surface after precursor exposure. These were removed during the reactant exposure and during this exposure the formation of surface OH groups was found for both high and low substrate temperatures. We conclude that the decrease in the growth rate for the thermal process is caused by the inability of the surface to properly dehydrogenate and restructure the poisoning precursor ligands.
引用
收藏
页码:25343 / 25356
页数:14
相关论文
共 51 条
[1]   Reaction mechanism studies on atomic layer deposition of ruthenium and platinum [J].
Aaltonen, T ;
Rahtu, A ;
Ritala, M ;
Leskelä, M .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2003, 6 (09) :C130-C133
[2]   Atomic layer deposition of platinum thin films [J].
Aaltonen, T ;
Ritala, M ;
Sajavaara, T ;
Keinonen, J ;
Leskelä, M .
CHEMISTRY OF MATERIALS, 2003, 15 (09) :1924-1928
[3]   BONDING AND REACTIVITY OF CYCLOPENTENE ON PT(111) [J].
AVERY, NR .
SURFACE SCIENCE, 1984, 146 (2-3) :363-381
[4]   VIBRATIONAL SPECTRUM OF DIMETHYLFERROCENE [J].
BAILEY, RT ;
LIPPINCOTT, ER .
SPECTROCHIMICA ACTA, 1965, 21 (03) :389-+
[5]   CARBON-MONOXIDE OXIDATION UNDER TRANSIENT CONDITIONS - A FOURIER-TRANSFORM INFRARED TRANSMISSION SPECTROSCOPY STUDY [J].
BARSHAD, Y ;
ZHOU, XC ;
GULARI, E .
JOURNAL OF CATALYSIS, 1985, 94 (01) :128-141
[6]   Enantioselective hydrogenation of alpha-ketoesters using cinchona modified platinum catalysts and related systems: A review [J].
Blaser, HU ;
Jalett, HP ;
Muller, M ;
Studer, M .
CATALYSIS TODAY, 1997, 37 (04) :441-463
[7]   Surface Infrared Spectroscopy during Low Temperature Growth of Supported Pt Nanoparticles by Atomic Layer Deposition [J].
Bosch, Roger H. E. C. ;
Bloksma, Frank L. ;
Huijs, Jochem M. M. ;
Verheijen, Marcel A. ;
Kessels, Wilhelmus M. M. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2016, 120 (01) :750-755
[8]   A review of the selective reduction of NOx, with hydrocarbons under lean-burn conditions with non-zeolitic oxide and platinum group metal catalysts [J].
Burch, R ;
Breen, JP ;
Meunier, FC .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2002, 39 (04) :283-303
[9]   A MOLECULAR-BEAM STUDY OF THE ADSORPTION AND DESORPTION OF OXYGEN FROM A PT(111)SURFACE [J].
CAMPBELL, CT ;
ERTL, G ;
KUIPERS, H ;
SEGNER, J .
SURFACE SCIENCE, 1981, 107 (01) :220-236
[10]   Dielectric constants of Ir, Ru, Pt, and IrO2:: Contributions from bound charges [J].
Choi, W. S. ;
Seo, S. S. A. ;
Kim, K. W. ;
Noh, T. W. ;
Kim, M. Y. ;
Shin, S. .
PHYSICAL REVIEW B, 2006, 74 (20)