TY - JOUR
T1 - Morphology and semiconducting properties of homoepitaxially grown phosphorus-doped (1 0 0) and (1 1 1) diamond films by microwave plasma-assisted chemical vapor deposition using triethylphosphine as a dopant source
AU - Saito, Takeyasu
AU - Kameta, Masanori
AU - Kusakabe, Katsuki
AU - Morooka, Shigeharu
AU - Maeda, Hideaki
AU - Hayashi, Yasunori
AU - Asano, Tanemasa
AU - Kawahara, Akihiko
N1 - Funding Information:
This study was partially supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Science, Sports and Culture, Japan, and the Research Project for Fundamental Engineering of CVD, organized by Professor Hiroshi Komiyama, The University of Tokyo. The advice of Dr. Satoshi Koizumi of NIRIM, Tsukuba, Japan is gratefully acknowledged.
PY - 1998/8/1
Y1 - 1998/8/1
N2 - Phosphorus-doped (1 0 0) and (1 1 1) diamond films were homoepitaxially formed on nondoped diamond films, which had been also formed homoepitaxially on type-Ib (1 0 0) and (1 1 1) diamond substrates, respectively, by microwave plasma-assisted chemical vapor deposition. Methane and triethylphosphine (TEP, P(C2H5)3) were used as the carbon and dopant sources, respectively. When the P/C ratio in the gas phase was in the range of 10-2-10-1 and the methane concentration was 0.5%, smooth homoepitaxial (1 0 0) diamond films with a thickness of approximately 800 nm were obtained at 1123 K. Raman spectroscopy showed that the P-doped (1 0 0) diamond films formed with gas phase P/C ratios higher than 4 × 10-2 contained sp2 carbon. Phosphorus was found to be uniformly incorporated in the films, as evidenced by secondary ion mass spectroscopy, and the phosphorus concentration in the doped (1 0 0) diamond films was estimated to be (2-8) × 1018 cm-3. All P-doped (1 0 0) diamond films showed insufficient ohmic contacts for a Hall-effect determination, and no n-type conduction was confirmed. However, a homoepitaxial (1 1 1) diamond film, which was formed at 1173 K using a gas-phase P/C ratio of 5 × 10-3 and a methane concentration of 0.1% on a nondoped homoepitaxial (1 1 1) diamond layer at 1123 K exhibited n-type conduction at temperatures higher than 485 K. The carrier concentration and Hall mobility at 500 K were 3.8 × 1016 cm-3 and 38 cm2/V s, respectively. Phosphorus was uniformly incorporated in the film at a concentration of 1 × 1020 cm-3.
AB - Phosphorus-doped (1 0 0) and (1 1 1) diamond films were homoepitaxially formed on nondoped diamond films, which had been also formed homoepitaxially on type-Ib (1 0 0) and (1 1 1) diamond substrates, respectively, by microwave plasma-assisted chemical vapor deposition. Methane and triethylphosphine (TEP, P(C2H5)3) were used as the carbon and dopant sources, respectively. When the P/C ratio in the gas phase was in the range of 10-2-10-1 and the methane concentration was 0.5%, smooth homoepitaxial (1 0 0) diamond films with a thickness of approximately 800 nm were obtained at 1123 K. Raman spectroscopy showed that the P-doped (1 0 0) diamond films formed with gas phase P/C ratios higher than 4 × 10-2 contained sp2 carbon. Phosphorus was found to be uniformly incorporated in the films, as evidenced by secondary ion mass spectroscopy, and the phosphorus concentration in the doped (1 0 0) diamond films was estimated to be (2-8) × 1018 cm-3. All P-doped (1 0 0) diamond films showed insufficient ohmic contacts for a Hall-effect determination, and no n-type conduction was confirmed. However, a homoepitaxial (1 1 1) diamond film, which was formed at 1173 K using a gas-phase P/C ratio of 5 × 10-3 and a methane concentration of 0.1% on a nondoped homoepitaxial (1 1 1) diamond layer at 1123 K exhibited n-type conduction at temperatures higher than 485 K. The carrier concentration and Hall mobility at 500 K were 3.8 × 1016 cm-3 and 38 cm2/V s, respectively. Phosphorus was uniformly incorporated in the film at a concentration of 1 × 1020 cm-3.
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U2 - 10.1016/S0022-0248(98)00360-1
DO - 10.1016/S0022-0248(98)00360-1
M3 - Article
AN - SCOPUS:0032142072
SN - 0022-0248
VL - 191
SP - 723
EP - 733
JO - Journal of Crystal Growth
JF - Journal of Crystal Growth
IS - 4
ER -