Direct graphene growth on Co3O4(111) by molecular beam epitaxy

被引:26
作者
Zhou, Mi [1 ]
Pasquale, Frank L. [1 ]
Dowben, Peter A. [2 ,3 ]
Boosalis, Alex [4 ]
Schubert, Mathias [4 ]
Darakchieva, Vanya [5 ]
Yakimova, Rositza [5 ]
Kong, Lingmei [2 ,3 ]
Kelber, Jeffry A. [1 ]
机构
[1] Univ N Texas, Dept Chem, Denton, TX 76203 USA
[2] Univ Nebraska Lincoln, Nebraska Ctr Mat & Nanosci, Lincoln, NE 68588 USA
[3] Univ Nebraska Lincoln, Dept Phys & Astron, Lincoln, NE 68588 USA
[4] Univ Nebraska Lincoln, Dept Elect Engn, Walter Scott Engn Ctr 209N, Lincoln, NE 68588 USA
[5] Linkoping Univ, Dept Phys Chem & Biol IFM, SE-58183 Linkoping, Sweden
基金
美国国家科学基金会;
关键词
GRAPHITE; SINGLE; NIO(111); COPPER; LAYER; GAS;
D O I
10.1088/0953-8984/24/7/072201
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
Direct growth of graphene on Co3O4(111) at 1000 K was achieved by molecular beam epitaxy from a graphite source. Auger spectroscopy shows a characteristic sp(2) carbon lineshape, at average carbon coverages from 0.4 to 3 ML. Low energy electron diffraction (LEED) indicates (111) ordering of the sp2 carbon film with a lattice constant of 2.5(+/-0.1) angstrom characteristic of graphene. Sixfold symmetry of the graphene diffraction spots is observed at 0.4, 1 and 3 ML. The LEED data also indicate an average domain size of similar to 1800 angstrom, and show an incommensurate interface with the Co3O4(111) substrate, where the latter exhibits a lattice constant of 2.8(+/-0.1) angstrom. Core level photoemission shows a characteristically asymmetric C(1s) feature, with the expected pi to pi* satellite feature, but with a binding energy for the 3 ML film of 284.9(+/-0.1) eV, indicative of substantial graphene-to-oxide charge transfer. Spectroscopic ellipsometry data demonstrate broad similarity with graphene samples physically transferred to SiO2 or grown on SiC substrates, but with the pi to pi* absorption blue-shifted, consistent with charge transfer to the substrate. The ability to grow graphene directly on magnetically and electrically polarizable substrates opens new opportunities for industrial scale development of charge- and spin-based devices.
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页数:6
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