AVS 64th International Symposium & Exhibition
    Electronic Materials and Photonics Division Tuesday Sessions
       Session EM+SS-TuA

Paper EM+SS-TuA7
Controlling GaAs and Si Oxide Surface Energies

Tuesday, October 31, 2017, 4:20 pm, Room 14

Session: Surface and Interface Challenges in Semiconductor Materials and Devices
Presenter: Karen L Kavanagh, Simon Fraser University, Canada
Authors: K. Kavanagh, Simon Fraser University, Canada
N. Herbots, Arizona State University
A. Brimhall, Arizona State University
R. Van Haren, Arizona State University
Y.W. Pershad, Arizona State University
S. Suhartono, Arizona State University
E. Landeros, Arizona State University
R.J. Culbertson, Arizona State University
R. Islam, Cactus Materials
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Bonding two different semiconductors into a single integrated device can yield economic, medical, and human benefits by increasing performance. Si and GaAs bonding can increase solar cell efficiency and, if the bonding is hermetic, the lifetime of bonded sensors and optoelectronic circuits is extended by reducing percolation. Bonding occurs when the electronic properties of the two surfaces complement each other, to enhance efficient electron transfer.[1] Complementary surfaces can be identified through measurement of their total surface energy, γT, since this property can be modeled by Van Oss theory, to consist of three component interaction energies: molecular dipoles (Lifschitz-Van der Waals), γLW, electron donors, γ-, and electron acceptors, γ+. Measurements of the total and individual components of the surface energy of Si and GaAs (100) surfaces has been carried out using contact angle measurements of liquid drops with known surface energies, ranging from polar (18 MW water), apolar (α-bromo-naphthalene) to non-polar (glycerin). Accurate reproducible results are obtained using class 100 clean-room environments and analysis of multiple drops of each type of surface energy. This three liquid contact angle analysis (3LCAA) brings a much greater level of sophistication to this well-known and apparently-simple method. When carried out with semiconductor-level control of cleanliness, the contribution of each component to the total surface energy of Si (100) native and non-native oxides has been found to depend linearly on γLW. In hydrophobic oxide surfaces, γT is due almost entirely to molecular interactions, γLW, to within a few % error. Thus, the highly-passivated, thermally-grown SiO2 surface with few defects or impurities, has a surface energy of 35.7 ± 3 mJ/m2 that is entirely explained by γLW. However, γT can be raised to 57.3 ± 2 mJ/m2. by generating defects, and unsaturated or dangling bonds that interact with electron acceptors and or donors. This situation applies to heavily-etched, oxide surfaces, or chemically-oxidized surfaces. The contributions from γ-and γ+, raises the total surface energy γT up to 40% above that of γLW, which is found to remain nearly constant. Similar experiments with GaAs (100) surfaces as a function of surface preparation find that the Si-doped GaAs native oxide to be hydrophobic with a γTof 35 ± 3 mJ/m2, with γLWcontributing 98 ± 2%, thus close to the entirety of γT. This indicates a well-reacted native oxide. [1] Herbots N. et al. US Patent 9,018,077 (2015); 9,589,801 (2017).