GaAs(111) A and B surfaces in hydrazine sulfide solutions: Extreme polarity dependence of surface adsorption processes

被引:7
|
作者
Berkovits, V. L. [2 ]
Ulin, V. P. [2 ]
Tereshchenko, O. E. [3 ]
Paget, D. [1 ]
Rowe, A. C. H. [1 ]
Chiaradia, P. [4 ,5 ]
Doyle, B. P. [6 ]
Nannarone, S. [6 ,7 ,8 ]
机构
[1] Ecole Polytech, CNRS, F-91128 Palaiseau, France
[2] AF Ioffe Phys Tech Inst, St Petersburg 194021, Russia
[3] Novosibirsk State Univ, Inst Semicond Phys, Novosibirsk 630090, Russia
[4] Univ Roma Tor Vergata, Dipartimento Fis, CNISM Unit, I-00133 Rome, Italy
[5] Univ Roma Tor Vergata, NAST, I-00133 Rome, Italy
[6] CNR, INFM, Lab Nazl TASC, I-34012 Trieste, Italy
[7] Univ Modena & Reggio Emilia, Dipartimento Ingn Mat & Ambiente, I-41100 Modena, Italy
[8] CNISM, I-41100 Modena, Italy
关键词
adsorption; gallium arsenide; III-V semiconductors; photoelectron spectra; polaritons; GAAS-SURFACES; PHOTOEMISSION-SPECTROSCOPY; NITRIDATION; CHEMISTRY; PASSIVATION; NITROGEN; SULFUR; PLASMA; (111)A; GAN;
D O I
10.1103/PhysRevB.80.233303
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Chemical bonds formed by hydrazine-sulfide treatment of GaAs(111) were studied by synchrotron photoemission spectroscopy. At the B surface, the top arsenic atoms are replaced by nitrogen atoms, while GaAs(111)A is covered by sulfur, also bonded to underlying gallium, despite the sulfide molar concentration being 10(3) times smaller than that of the hydrazine. This extreme dependence on surface polarity is explained by competitive adsorption processes of HS- and OH- anions and of hydrazine molecules, on Ga-adsorption sites, which have distinct configurations on the A and B surfaces.
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页数:4
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