Silicon Surface Morphology and the Reaction of Silicon with Oxygen

1992 ◽  
Vol 259 ◽  
Author(s):  
Frances M. Ross ◽  
J. Murray Gibson

ABSTRACTWe discuss the measurement of the morphology of exposed surfaces and buried interfaces using plan view transmission electron microscopy techniques. We have observed the evolution of the silicon/oxide interface during both oxidation and oxygen etching of the Si (111) surface. We describe the interface morphology, the mechanisms of these oxidation reactions and the implications of these results for the processing of silicon surfaces.

1995 ◽  
Vol 378 ◽  
Author(s):  
M Benamara ◽  
A Rocher ◽  
A Laporte ◽  
G Sarrabayrouse ◽  
L Lescouzères ◽  
...  

AbstractThe so-called Direct Wafer Bonding (DWB) technique opens new possibilities for the electronic industry but still suffers from the poor knowledge we have of the microstructure of these interfaces and hence of their electrical activity. In this work, we have extensively used Transmission Electron Microscopy techniques in plan-view and cross-section to identify the structure of the interfaces found between two bonded silicon wafers. The general structure of these interfaces is that of a perfect grain boundary and evidently depends on the misorientation between the two bonded wafers. A twist component in the range 0>θ>13˚ creates a square network of pure screw dislocation whereas an unavoidable tilt component (<0.5˚) is compensated by a periodic array of 60˚ dislocation lines perpendicular to the tilt direction. Therefore, the regularity of these networks can be disrupted by the presence of steps (of up to several nanometers) in the interface plane. Silicon oxide precipitates are seen heterogeneously distributed on the interface with preferential nucleation sites on the dislocations.


2004 ◽  
Vol 10 (1) ◽  
pp. 134-138 ◽  
Author(s):  
Masaki Takeguchi ◽  
Kazutaka Mitsuishi ◽  
Miyoko Tanaka ◽  
Kazuo Furuya

About 1 monolayer of palladium was deposited onto a silicon (111) 7 × 7 surface at a temperature of about 550 K inside an ultrahigh vacuum transmission electron microscope, resulting in formation of Pd2Si nanoislands and a 1 × 1 surface layer. Pd clusters created from an excess of Pd atoms on the 1 × 1 surface layer were directly observed byin situplan view high-resolution transmission electron microscopy. When an objective aperture was introduced so that electron diffractions less than 0.20 nm were filtered out, the lattice structure of the 1 × 1 surface with 0.33 nm spacing and the Pd clusters with a trimer shape were visualized. It was found that image contrast of the 1 × 1 lattice on the specific height terraces disappeared, and thereby an atomic structure of the Pd clusters was clearly observed. The appearance and disappearance of the 1 × 1 lattice was explained by the effect of the kinematical diffraction. It was identified that a Pd cluster was composed of three Pd atoms without a centered Si atom, which is consistent with the model proposed previously. The feature of the Pd clusters stuck at the surface step was also described.


1997 ◽  
Vol 477 ◽  
Author(s):  
Steven Verhaverbeke ◽  
Jennifer W. Parker ◽  
Chris F. McConnell

The RCA Standard Clean, developed by W. Kern and D. Puotinen in 1965 and disclosed in 1970 [1] is extremely effective at removing contamination from silicon surfaces and is the defacto industry standard.[2]. The RCA clean consists of two sequential steps: the Standard Clean 1 (SC-1) followed by the Standard Clean 2 (SC-2). The SC-1 solution, consisting of a mixture of ammonium-hydroxide, hydrogen-peroxide, and water, is the most efficient particle removing agent found to date. This mixture is also referred to as the Ammonium- Hydroxide/Hydrogen-Peroxide Mixture (APM). In the past, SC-1 solutions had the tendency to deposit metals on the surface of the wafers, and consequently treatment with the SC-2 mixture was necessary to remove metals. Ultra-clean chemicals minimize the need for SC-2 processing. SC-I solutions facilitate particle removal by etching the wafer underneath the particles; thereby loosening the particles, so that mechanical forces can readily remove the particles from the wafer surface. The ammonium hydroxide in the solution steadily etches silicon dioxide at the boundary between the oxide and the aqueous solution (i.e., the wafer surface). The hydrogen peroxide in SC-I serves to protect the surface from attack by OH" by re-growing a protective oxide directly on the silicon surface (i.e., at the silicon/oxide interface). If sufficient hydrogen peroxide is not present in the solution, the silicon will be aniostropically etched and surface roughening will quickly occur. On the other hand, hydrogen peroxide readily dissociates and forms water and oxygen. If the concentration of the resulting oxygen is too high, bubbles will appear in the solution. The gas liquid interfaces that result from the bubble formation act as a “getter” for particles that can re-deposit on the wafer surface if a bubble comes in contact with the wafer.


1996 ◽  
Vol 451 ◽  
Author(s):  
Christopher P. Wade ◽  
Huihong Luo ◽  
William L. Dunbar ◽  
Matthew R. Linford ◽  
Christopher E.D. Chidsey

ABSTRACTWe have assembled a scanning tunneling microscope with an inverted sample that allows the sample surface to be contacted by fluid electrolytes in a controlled atmosphere. A hanging meniscus is formed between the sample and a small cup surrounding the tunneling tip. In-situ imaging of the electrode/electrolyte interface is conveniently achieved with clean samples under potentiostatic control. The functioning of the microscope is illustrated by the imaging of the electrodeposition of copper on gold. This microscope has been used to image hydrogen-terminated silicon surfaces and to demonstrate that islands, tentatively assigned as silicon oxide, are formed on rinsing in water but can be avoided if the surface is not rinsed on withdrawal from the ammonium fluoride etching solution. Finally, STM shows that the convenient, gas-phase photochlorination of H-Si(111) produces the simple Cl-Si(111)(1×1) structure with little or no etching of the silicon surface.


1990 ◽  
Vol 204 ◽  
Author(s):  
A.C. Dillon ◽  
P. Gupta ◽  
M.B. Robinson ◽  
A.S. Bracker ◽  
S.M. George

ABSTRACTFourier transform infrared (FTIR) transmission spectroscopy. was used to monitor the decomposition of H2O (D2O) and NH3(ND3) on silicon surfaces. Experiments were performed in-situ in an ultra-high vacuum (UHV) chamber using high surface area poroussilicon samples. The FTIR spectra revealed that H2O dissociates upon adsorption at 300K to form SiH and SiNH2 surface species. NH3 also issociates upon adsorption at 300 K to form SiH and SiOH2 species. Silicon samples with saturation exposures of H2O and NH3 were progressively annealed from 300 K to 860 K. The FTIR spectra of an H2O-saturated silicon surface revealed that the SiOH species decomposed to form a silicon oxide species and additional surface hydrogen between 460 K and 580 K. Likewise, the SiNH2 species decomposed between 540 K and 660 K to produce silicon nitride and additional surface hydrogen. In both cases, the Sill surface species decreased as H2 desorption from the silicon surface was observed above 700 K.


1992 ◽  
Vol 259 ◽  
Author(s):  
Kun—Chih Wang ◽  
Huey—Liang Hwang ◽  
Chung—Yuan Kung ◽  
Tri—Rung Yew

ABSTRACTThis paper presents the results of surface cleaning and passivation of Si and oxide surfaces for the growth of Si/oxide/Si structures. Silicon surfaces are cleaned by the spin—etch process prior to the growth of silicon oxide. A silicon layer is then deposited after subsequent surface cleaning and chemical treatment on the surface of oxide/Si. Both the oxide and the silicon layers are grown in a plasma enhanced chemical vapor deposition system. The interface structure between layers of deposited Si/oxide/Si are observed by cross—section transmission electron microscopy (XTEM).


1986 ◽  
Vol 10-12 ◽  
pp. 217-222 ◽  
Author(s):  
A. Ourmazd ◽  
D.W. Taylor ◽  
J. Bevk ◽  
B.A. Davidson ◽  
Leonard C. Feldman ◽  
...  

1986 ◽  
Vol 74 ◽  
Author(s):  
M. K. El-Ghor ◽  
S. J. Pennycook ◽  
T. P. Sjoreen ◽  
J. Narayan

AbstractHigh doses of oxygen were implanted in silicon to produce stoichiometric buried oxide structures. Microstructural analysis was performed using transmission electron microscopy, electron energy loss spectroscopy, and Rutherford backscattering/channeling techniques. Cavities were observed in the top silicon layers of the as-implanted samples in two forms: spherical cavities (30–300 Å in diameter) in the first 1000 Å below the surface, followed by a 500 Å wide lamellar array of elongated cavities. A post implantation annealing was carried out at temperatures between 1150°C and 1250°C for 3 h during which the cavities became faceted and a denuded zone of 400 Å was formed. However, with a 1300°C anneal the cavities disappeared and the density of the two prominent types of defects, namely precipitates (mostly amorphous, but occasionally crystalline) and dislocations, decreased significantly. The silicon-oxide interface became increasingly planar. Possible mechanisms of annealing of the cavities, the precipitates, and the associated planarization of the interface are proposed.


1989 ◽  
Vol 148 ◽  
Author(s):  
J. M. Gibson ◽  
M. Y. Lanzerotti

ABSTRACTInterfacial roughness can be measured at buried interfaces using plan view transmission electron diffraction. The method relies on surface termination Bragg reflections and is applied to the Si/SiO2 system. In contrast to other methods, this does not require stripping of the SiO2 overlayer or projection assumptions. We find that thermal oxide interfaces are significantly flatter than previously supposed.The Si/SiO2 interface has been extensively examined by a wide variety of techniques. A subset of these studies have focussed on the interfacial roughness and it has been shown that increased step density reduces electron mobility.[1, 2 ] Although supporting the correlation of mobility with step density, the data presented here shows thermally oxidized Si/SiO2 interfaces to be significantly flatter than previously assumed.


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