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Nov 2008

Volume 26, Issue 6, pp. 1369-1546

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Surface patterns from block copolymer self-assembly

Ho-Cheol Kim and William D. Hinsberg

J. Vac. Sci. Technol. A 26, 1369 (2008); http://dx.doi.org/10.1116/1.3000056 (14 pages) | Cited 12 times

Online Publication Date: 30 October 2008

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It is widely recognized that further extension of optical lithography to even smaller dimensions will be accompanied by rapid increasing cost and difficulty. There is growing interest in devising alternative patterning methods that will support the evolution of microelectronics to the 10 nm length scale. Block copolymer lithography, which uses self-assembled microdomains of block copolymers in thin films, can provide arrays of periodic patterns of 10–50 nm length scales with a simple process and low cost. While this capability is attractive, the periodic nature of the microdomain patterns places significant restrictions on how block copolymer lithography can be practically implemented. In this review, the authors survey materials and methods for carrying out the controlled assembly of block copolymers in thin films for surface patterning applications. After a brief introduction to block copolymers and their phase behavior, the authors discuss ordering of block copolymer in thin films based on four different thickness categories. Approaches to directed self-assembly are reviewed along with the limitations and challenges of block copolymer lithography. Finally the authors note the circumstances that make it an opportune time to resolve the remaining technological issues facing block copolymer lithography and to demonstrate its utility as an adjunct to traditional photolithography.
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68.47.Mn Polymer surfaces
68.35.bm Polymers, organics
42.82.Cr Fabrication techniques; lithography, pattern transfer
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Fabrication of surface plasmon waveguides and integrated components on ultrathin freestanding membranes

Pierre Berini, Nancy Lahoud, and Robert Charbonneau

J. Vac. Sci. Technol. A 26, 1383 (2008); http://dx.doi.org/10.1116/1.2975196 (9 pages) | Cited 8 times

Online Publication Date: 30 October 2008

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The fabrication and physical characterisation of waveguides and integrated components on freestanding membranes are described. The waveguides consist of a thin (20–25 nm) narrow ( ∼ 5 μm) Au/Cr stripe, on an ultrathin (20–30 nm) large-area ( ∼ 1 mm2) freestanding Si3N4 membrane clamped around its perimeter to an underlying Si substrate. The integrated components are implemented with this waveguide and consist of Mach-Zehnder interferometers and couplers. The waveguide and components are dimensioned such that they propagate long-range surface plasmon-polariton waves in a vacuum (air) or H2O background. The fabrication process flow adopted and some specific process steps are described. Physical characterisation was conducted on structures having undergone intermediate process steps and on finished structures, and characterisation results are given and discussed. The structures were found to be robust enough for careful use, and to routinely sustain ∼ 3 μN of point force without shattering.
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42.79.Gn Optical waveguides and couplers
73.20.Mf Collective excitations (including excitons, polarons, plasmons and other charge-density excitations)
78.68.+m Optical properties of surfaces
71.36.+c Polaritons (including photon-phonon and photon-magnon interactions)

Molecular-dynamics investigation of the surface characteristics of Fe–Cu magnetic thin-film layers

Soon-Gun Lee and Yong-Chae Chung

J. Vac. Sci. Technol. A 26, 1392 (2008); http://dx.doi.org/10.1116/1.2975197 (5 pages) | Cited 1 time

Online Publication Date: 30 October 2008

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Using molecular dynamics simulation, the structural characteristics of Fe and Cu thin films grown on Cu and Fe(001) substrates, respectively, were investigated with respect to the incident energy of adatoms and substrate temperature. In the case of Cu on Fe(001), no surface alloying at the interface was observed in the early stage of thin-film deposition, and growth generally followed the layer-by-layer growth mode. For Fe on a Cu(001) surface, a mixture confined to a single atomic layer at the Cu(001) surface was found to form at room temperature while films showed island growth. The steering effect due to atomic attraction was also observed at low incident energy, resulting in a rougher surface. Fe/Cu(001) growth changed to a layer-by-layer mode for an incident energy of 6 eV. The different aspects of surface morphology between Fe/Cu(001) and Cu/Fe(001) systems were explained in terms of surface free energy and impact cascade diffusion.
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75.70.Ak Magnetic properties of monolayers and thin films
68.35.Fx Diffusion; interface formation
68.35.bd Metals and alloys
68.55.at Other materials
68.35.Md Surface thermodynamics, surface energies
68.43.-h Chemisorption/physisorption: adsorbates on surfaces

Film continuity and interface bonding of thin boron carbonitride films on Ge(100) and Si(100)

P. R. Fitzpatrick and J. G. Ekerdt

J. Vac. Sci. Technol. A 26, 1397 (2008); http://dx.doi.org/10.1116/1.2976564 (10 pages) | Cited 2 times

Online Publication Date: 30 October 2008

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Motivated by the need for a passivation layer for Ge, thin (<10 nm) films of amorphous boron carbonitride (BCN) were deposited on Ge(100) surfaces to study film continuity and interface bonding. Chemical vapor deposition on Ge(100) and Si(100) (studied for comparison) produced BC0.75N0.07 and BCN0.07 stoichiometry films, respectively. When BCN is nominally 2.5–5 nm thick, the film’s coverage of Ge(100) is continuous. This range was determined by (i) 0.5 kV He+ ion scattering spectroscopy scans, in which the underlying Ge(100) substrate signal disappears upon continuous BCN coverage and (ii) the convergence to unity of the ratio of BCN thicknesses estimated by two angle resolved x-ray photoelectron spectroscopy (ARXPS) techniques. Only 1.5–2 nm BCN was required for continuous coverage of Si(100), possibly due to better nucleation on this surface. ARXPS analysis indicates that the BCN-Ge(100) interface is clean and abrupt, with no evidence of an interfacial layer due to elemental intermixing. Constituent bonding in the BCN bulk is maintained at the Ge(100) interface. Preservation of the Ge 3d and Ge 2p full width at half maximum values after BCN deposition suggests a lack of distortion of Ge surface bonds, a criterion necessary for passivation if low interface state densities are to be achieved. BCN-Si(100) interface characteristics were similar to BCN-Ge(100).
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68.55.A- Nucleation and growth
81.65.Rv Passivation
81.15.Gh Chemical vapor deposition (including plasma-enhanced CVD, MOCVD, ALD, etc.)
79.60.Dp Adsorbed layers and thin films

Ti surface alloying of an AISI 316L stainless steel by low energy high current pulsed electron beam treatment

K. M. Zhang, J. X. Zou, T. Grosdidier, C. Dong, and S. Weber

J. Vac. Sci. Technol. A 26, 1407 (2008); http://dx.doi.org/10.1116/1.2976566 (8 pages) | Cited 6 times

Online Publication Date: 30 October 2008

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Ti has been added into the surface layer of an AISI 316L stainless steel—by means of rapid surface alloying of Ti powder—using the low energy, high current pulsed electron beam (LEHCPEB) technique with the aim of enhancing its corrosion resistance. The alloyed layer contained a mixture of the α and γ phases and its depth increased with the number of pulses. Compared to the samples treated under the conventional LEHCPEB treatment (i.e., without surface alloying), Ti addition improved further the corrosion resistance. This can be attributed to the addition of Ti into the surface layer together with the removal of MnS inclusions. However, the homogeneity of the Ti distribution decreased when the number of pulses increased. Therefore, contrary to the conventional LEHCPEB treatment, as a result of this decreased homogeneity, the corrosion resistance decreased when the number of LEHCPEB was too high. Therefore, a good control of the processing parameters is required to take the full advantage of the surface Ti addition by LEHCPEB.
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81.65.Kn Corrosion protection
61.72.Qq Microscopic defects (voids, inclusions, etc.)

Test particle simulation of the role of ballistic electrons in hybrid dc/rf capacitively coupled plasmas in argon

K. Denpoh and P. L. G. Ventzek

J. Vac. Sci. Technol. A 26, 1415 (2008); http://dx.doi.org/10.1116/1.2981064 (10 pages) | Cited 13 times

Online Publication Date: 30 October 2008

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Hybrid dc/rf plasma sources are an emerging equipment technology in plasma etching for semiconductor manufacturing. In this work, test particle simulations are used to describe the nature and role of the ballistic electrons, which originate as secondary electrons on a dc/rf (i.e., VHF, 60 MHz) biased upper electrode and are then accelerated in the sheath toward the opposite non-dc biased lower electrode. This opposite electrode, on which a wafer is placed, may have rf bias power applied to it at low frequencies. 2 MHz is typical. While a hybrid dc/rf plasma source is sustained by the VHF power source, simulations reveal ballistic electrons assist in the production of a plasma characterized by a relatively high ionization rate constant, especially in the dc sheath. The dc source helps to provide a source of high energy electrons that may reach the wafer. However, when the rf bias is applied on the lower electrode, ballistic electrons are confined in the potential well formed between electrodes and easily thermalized in the bulk. The simulated electron density dependencies on the dc bias and lower electrode rf power describe a dual mode source and are consistent with measured data. When no rf power is applied on the electrode opposite to the dc power source, the bulk electron density drops with increasing dc power at constant VHF power; when rf power is applied to the electrode opposite to the dc power source, the bulk electron density increases with dc power at constant VHF power. The fraction of electrons significantly above thermal reaching the wafer is much higher when no rf power is applied at the lower electrode but the total flux lower. Depending on its level, rf power applied to the wafer may effectively suppress the number of ballistic electrons that reach the wafer. Finally, the ionization rate constant due to ballistic electrons can be fitted as a simple function of the electric field in the dc sheath.
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52.65.-y Plasma simulation
52.40.Kh Plasma sheaths
94.20.Fg Plasma temperature and density
52.80.-s Electric discharges

Properties of octadecanethiol self-assembled monolayers deposited on GaAs from liquid and vapor phases

H. A. Budz and R. R. LaPierre

J. Vac. Sci. Technol. A 26, 1425 (2008); http://dx.doi.org/10.1116/1.2981067 (7 pages) | Cited 6 times

Online Publication Date: 30 October 2008

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Octadecanethiol (ODT), CH3(CH2)17SH, self-assembled monolayers (SAMs) were deposited on GaAs (100) substrates from solution and from vapor phase. The monolayers assembled from solution were prepared by incubating the substrate in a dilute millimolar ODT/ethanol solution, while vapor-deposited monolayers were prepared from vapor phase transport of ODT in an ultrahigh vacuum environment. The structural and optical characteristics of the resulting SAMs were examined with contact angle (CA) analysis, photoluminescence (PL) spectroscopy, atomic force microscopy (AFM), and spectroscopic ellipsometry. Static CA measurements of the SAMs indicated the successful formation of highly organized monolayers by both preparation routes. In contrast, PL spectroscopy, AFM, and ellipsometry measurements showed differences in the optical and structural properties of SAMs prepared from liquid and vapor phases. The data obtained indicate that more densely packed monolayers exhibiting greater surface coverage and therefore, increased passivation characteristics are assembled from vapor phase.
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68.60.Wm Other nonelectronic physical properties
81.15.-z Methods of deposition of films and coatings; film growth and epitaxy
78.55.Kz Solid organic materials
78.66.Qn Polymers; organic compounds
81.15.Lm Liquid phase epitaxy; deposition from liquid phases (melts, solutions, and surface layers on liquids)

In situ monitoring of material processing by a pulsed laser beam coupled via a lensed fiber into a scanning electron microscope

David J. Hwang, Nipun Misra, Costas P. Grigoropoulos, Andrew M. Minor, and Samuel S. Mao

J. Vac. Sci. Technol. A 26, 1432 (2008); http://dx.doi.org/10.1116/1.2987946 (7 pages) | Cited 3 times

Online Publication Date: 30 October 2008

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In this study, a new method coupling laser irradiation into a dual-beam scanning electron microscope (SEM) and focused-ion-beam (FIB) system is developed. By using a lensed fiber, pulsed laser illumination could be successfully delivered onto the sample under SEM imaging, providing in situ monitoring for laser material processing applications including local modification of micro-/nanostructures and laser-assisted chemical vapor deposition. In situ characterization of the laser-induced features by high resolution SEM imaging and energy dispersive x-ray spectrometry was successfully carried out. Furthermore, in situ repair of a contaminated lensed fiber probe during laser-assisted chemical vapor deposition was demonstrated via FIB milling. The results demonstrate the full compatibility of the lensed fiber apparatus with the dual-beam apparatus without disturbing the original functions of the system. The combination of guided laser radiation with SEM and FIB instruments offers a powerful capability for in situ monitoring of multilevel laser-based micro- and nanoscale material processing.
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42.62.-b Laser applications
07.78.+s Electron, positron, and ion microscopes; electron diffractometers
81.15.Gh Chemical vapor deposition (including plasma-enhanced CVD, MOCVD, ALD, etc.)

Surface sealing of electron beam physical vapor deposited thermal barrier coatings by high-intensity pulsed ion beam

C. Liu, X. G. Han, Z. C. Xu, X. P. Zhu, and M. K. Lei

J. Vac. Sci. Technol. A 26, 1439 (2008); http://dx.doi.org/10.1116/1.2987948 (4 pages)

Online Publication Date: 30 October 2008

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A surface sealing technology by employing high-intensity pulsed ion beam (HIPIB) technique is developed for electron beam physical vapor deposited (EB-PVD) thermal barrier coatings (TBCs) to further improve the high temperature performance. The HIPIB irradiation can deliver a high-density energy up to 100 J/cm2 into the shallow ion range of about 0.1–10 μm within a short pulse width of less than 1 μs, by which a micrometer-thick bridging layer was achieved on the gap between columnar grains of EB-PVD TBCs under a single pulse of 4.5 J/cm2. The thin bridging layer provided atmosphere shielding for the TBCs along with matching strain tolerance of the columnar top coat during thermal cycling. Cyclic oxidation tests at 1050 °C demonstrated that weight gain of the sealed TBC samples is decreased by about 60% from 0.8 mg/cm2 of the as-deposited ones.
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81.15.Jj Ion and electron beam-assisted deposition; ion plating
81.65.Mq Oxidation
81.15.-z Methods of deposition of films and coatings; film growth and epitaxy

Optimization of electrostatic lens systems for low-energy scanning microcolumn applications

Tae-Sik Oh, Dae-Wook Kim, Seungjoon Ahn, Young Chul Kim, Ho-Seob Kim, and Seong Joon Ahn

J. Vac. Sci. Technol. A 26, 1443 (2008); http://dx.doi.org/10.1116/1.2987949 (7 pages) | Cited 1 time

Online Publication Date: 30 October 2008

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The optimization of a low-energy scanning microcolumn is proposed by adopting a modified Einzel lens sandwiched between an aligner and a deflector. The modified Einzel lens is composed of four electrodes, and the two center electrodes are specially designed quadrupole lenses having keyhole type rather than circular apertures. The outer electrodes of the Einzel lens having circular apertures are grounded, and the quadrupole lens is operated by applying the quadrupole voltages. The effects of the separated deflector system and the static quadrupole lens were investigated by analyzing the scanning electron beam spot at the target, and the results show that the proposed system can improve the performance of the scanning microcolumn.
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41.85.Ne Electrostatic lenses, septa

Optical properties of carbonaceous nanoparticles produced in sputtering discharges

A. Zeinert, C. Arnas, C. Dominique, and A. Mouberi

J. Vac. Sci. Technol. A 26, 1450 (2008); http://dx.doi.org/10.1116/1.2987950 (5 pages) | Cited 1 time

Online Publication Date: 30 October 2008

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In this work, the authors report on the optical properties of carbonaceous nanoparticles produced in argon sputtering dc discharges. These particles are the result of a nucleation-condensation mechanism in gas phase and form porous particulates with a mean diameter greater than 20 nm. The resulting powderlike deposit, which can be collected in the chamber, is analyzed in terms of an effective medium approximation that allows the determination of their optical constants. These parameters are then used in a simple application of the Lorenz-Mie theory, in combination with a laser-extinction experiment, to provide the particle density in the plasma.
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78.20.Ci Optical constants (including refractive index, complex dielectric constant, absorption, reflection and transmission coefficients, emissivity)
61.46.Df Structure of nanocrystals and nanoparticles ("colloidal" quantum dots but not gate-isolated embedded quantum dots)

Angular distribution of elemental composition of films deposited by laser ablation of a SrZrO3 target

I. Konomi, T. Motohiro, M. Horii, and M. Kawasumi

J. Vac. Sci. Technol. A 26, 1455 (2008); http://dx.doi.org/10.1116/1.2987952 (7 pages) | Cited 4 times

Online Publication Date: 30 October 2008

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The angular distributions of elemental composition of films prepared by laser ablation of perovskite oxide SrZrO3 have been investigated using electron probe microanalysis with wavelength-dispersive spectroscopy. Each constituent element showed two modal distribution composed of a broad cosmθ (m = 2–3) distribution and a sharp cosnθ (n = 8–23) distribution. Oxygen showed a broader distribution than that of Sr and Zr. At the polar angle close to surface normal direction (polar angle <12°), Zr concentration was higher than that of Sr in vacuum whereas in oxygen-containing atmosphere their concentrations were about the same. Below oxygen pressure of 1.3 Pa, Sr and Zr concentration increased and decreased with the increase in polar angle, respectively, whereas in oxygen partial pressure of 10 Pa, both elements showed no angular dependences. Broadening of angular distribution of all the elements was observed when deposition was performed under oxygen partial pressure of 10 Pa, which is considered to be caused by collisional scatterings of more than ten times with ambient gas molecules.
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68.55.Nq Composition and phase identification
82.80.-d Chemical analysis and related physical methods of analysis
81.15.Fg Pulsed laser ablation deposition

Effects of oxygen on low-temperature growth and band alignment of ZnO/GaN heterostructures

H. F. Liu, G. X. Hu, H. Gong, K. Y. Zang, and S. J. Chua

J. Vac. Sci. Technol. A 26, 1462 (2008); http://dx.doi.org/10.1116/1.2990853 (7 pages) | Cited 14 times

Online Publication Date: 30 October 2008

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Continuous ZnO thin films have been grown at low temperature (400 °C) on GaN/c-sapphire substrates in a radio-frequency magnetron-sputtering chamber employing a substoichiometric ZnO target with and without extra oxygen feeding. The effects of oxygen on the growth and band alignment of the ZnO/GaN heterostructures were investigated by using scanning-electron microscopy, x-ray diffraction, photoluminescence and transmittance/absorbance, ultraviolet-resonant Raman scattering, and x-ray photoelectron spectroscopy. Very remarkable changes of the structural and optical properties resulted from the introduction of oxygen: the surface hexahedral facets were diminished; the size of the surface islands and, hence, the compressive strains were reduced; ultraviolet transparency of the ZnO film was enhanced, together with an increased band gap due to the reduced intrinsic shallow-donor defects; and hence, the free-electron concentration. The offset in valence bands of the ZnO/GaN heterostructure was increased by ∼ 90 meV at certain conditions. This is likely due to the increased Ga–O bonds at the ZnO/GaN interface by the incorporation of extra oxygen at the initial growth of ZnO.
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81.05.Dz II-VI semiconductors
81.15.Cd Deposition by sputtering
78.40.Fy Semiconductors
78.55.Et II-VI semiconductors
78.66.Hf II-VI semiconductors
79.60.Jv Interfaces; heterostructures; nanostructures
71.20.Nr Semiconductor compounds
61.66.Fn Inorganic compounds

Room temperature ferromagnetism of Fe-implanted ZnO film

B. Zhang, Q. H. Li, L. Q. Shi, H. S. Cheng, and J. Z. Wang

J. Vac. Sci. Technol. A 26, 1469 (2008); http://dx.doi.org/10.1116/1.2990855 (5 pages) | Cited 2 times

Online Publication Date: 30 October 2008

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The ZnO-based diluted magnetic semiconductors (DMSs) with room temperature ferromagnetism were achieved by ion implantation. Fe+ ions at 80 keV with doses ranging from 1×1016 to 8×1016 cm−2 were implanted into n-type ZnO films at room temperature. Subsequently, the samples were annealed at 700 °C for 1 h in air ambient. The Fe-implanted content was determined by proton induced x-ray emission. The magnetic property was measured by the Quantum Design MPMS superconducting quantum interference device magnetometer. No trace of secondary phases or clusters was observed within the sensitivity of x-ray diffraction. Raman spectrum showed that the Fe ions replaced Zn atoms and incorporated into the crystal lattice positions of ZnO. Apparent ferromagnetic hysteresis loops measured at 300 K were observed, and the temperature-dependent magnetization showed that their Curie temperature exceeded room temperature.
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75.70.Ak Magnetic properties of monolayers and thin films
75.50.Pp Magnetic semiconductors
75.50.Dd Nonmetallic ferromagnetic materials
75.60.Ej Magnetization curves, hysteresis, Barkhausen and related effects
75.30.Kz Magnetic phase boundaries (including classical and quantum magnetic transitions, metamagnetism, etc.)
78.30.Hv Other nonmetallic inorganics

In situ ultrahigh vacuum residual gas analyzer “calibration”

O. B. Malyshev and K. J. Middleman

J. Vac. Sci. Technol. A 26, 1474 (2008); http://dx.doi.org/10.1116/1.2990856 (6 pages) | Cited 6 times

Online Publication Date: 30 October 2008

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Knowing the residual gas spectrum is essential for many applications and research in ultrahigh vacuum (UHV). Residual gas analyzers (RGAs) are used for both qualitative and quantitative gas analyses, where the quadrupole mass analyzers are now the most popular. It was found that RGAs supplied by different manufacturers are not necessarily well calibrated for quantitative gas analysis. A procedure applied for in situ RGA “calibration” against a calibrated UHV total pressure gauge is described in this article. It was found that special attention should be paid to H2 calibration, as RGAs are usually much more sensitive to H2 than ionization gauges. The calibration coefficients are quite reproducible in Faraday cup mode, however, using the secondary electron multiplier requires frequent checks of the calibration coefficients. The coefficients obtained for the RGA allow the use of the RGA as an accurate device for gas spectrum analysis.
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82.80.-d Chemical analysis and related physical methods of analysis
07.30.-t Vacuum apparatus
06.20.fb Standards and calibration

Effect of gas mixing ratio on etch behavior of ZrO2 thin films in Cl2-based inductively coupled plasmas

Alexander Efremov, Nam-Ki Min, Sun Jin Yun, and Kwang-Ho Kwon

J. Vac. Sci. Technol. A 26, 1480 (2008); http://dx.doi.org/10.1116/1.2998806 (7 pages) | Cited 3 times

Online Publication Date: 30 October 2008

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The analysis of the ZrO2 thin film etch mechanism in the Cl2/Ar, Cl2/He, and Cl2/N2 inductively coupled plasmas was carried out. It was found that an increase in additive gas fraction at fixed gas pressure and input power results in increasing ZrO2 etch rate, which changes from 1.2 nm/min for pure Cl2 plasma up to 3.15, 2.40, and 2.31 nm/min for 80% Ar, N2, and He, respectively. Langmuir probe diagnostics and zero-dimensional plasma modeling indicated that both plasma parameters and active species kinetics are noticeably influenced by the initial composition of the gas mixture. From the model-based analysis of etch kinetics, it was shown that, similarly to the case of BCl3-based plasmas, the behavior of the ZrO2 etch rate corresponds to the ion-flux-limited etch regime.
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81.65.Cf Surface cleaning, etching, patterning
52.77.Bn Etching and cleaning
52.70.Ds Electric and magnetic measurements

Effect of oxygen on growth and properties of diamond thin film deposited at low surface temperature

D. Das, Raj N. Singh, I. T. Barney, A. G. Jackson, and S. M. Mukhopadhyay

J. Vac. Sci. Technol. A 26, 1487 (2008); http://dx.doi.org/10.1116/1.2998807 (10 pages) | Cited 2 times

Online Publication Date: 30 October 2008

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Polycrystalline diamond thin films are grown on a p-type Si (100) single crystal substrate at a low surface deposition temperature of 455 °C using a microwave plasma enhanced chemical vapor deposition process in an Ar-rich Ar/H2/CH4 plasma containing different oxygen levels from 0% to 0.75%. The surface deposition temperatures are measured and monitored by an IR thermometer capable of working in a plasma environment without any interference from the plasma emissions. The lower surface deposition temperature at high microwave power of 1300 W and higher gas pressure of 95 torr is achieved by active cooling of the substrate from the backside using a specially designed cooling stage. An enhanced growth rate from 0.19 to 0.63 μm/h is observed with varying oxygen from 0% to 0.75% in the plasma. Diamond grain size also increased from 0.69 μm for the sample with no oxygen to 1.74 μm for the sample with 0.75% oxygen. The diamond films are characterized using x-ray diffraction, environmental scanning electron microscopy field emission gun, Raman spectroscopy, and x-ray photoelectron spectroscopy. The enhanced growth rate is correlated with the enhanced atomic hydrogen to C2 ratio with increasing oxygen concentration in the plasma, which is measured by an in situ optical emission spectroscopy.
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81.15.Gh Chemical vapor deposition (including plasma-enhanced CVD, MOCVD, ALD, etc.)
68.55.ag Semiconductors
73.61.Cw Elemental semiconductors
52.77.Dq Plasma-based ion implantation and deposition
79.60.Bm Clean metal, semiconductor, and insulator surfaces
78.30.Am Elemental semiconductors and insulators

Copper ion transport induced dielectric failure: Inclusion of elastic drift and consequences for reliability

Ravi S. Achanta, Joel L. Plawsky, and William N. Gill

J. Vac. Sci. Technol. A 26, 1497 (2008); http://dx.doi.org/10.1116/1.2998808 (4 pages) | Cited 3 times

Online Publication Date: 30 October 2008

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The authors have modeled the copper ion concentration and internal electric field profiles in a SiO2 dielectric by solving the transient nonlinear continuity/Poisson equations. The predicted time-to-failure of the dielectric correlates well with the theory that failure occurs once copper ions accumulate to the point where the induced electric field at the cathode exceeds a critical value. However, the copper ion concentration at the cathode required for failure was much higher than the reported ion solubility, raising doubts about the validity of the model. More realistic values for the required copper ion concentration were obtained by incorporating an “elastic” diffusion term in the continuity equation. Adding this new term and increasing solubility, Ce, to the maximum value reported in the literature reduces the concentration at the cathode to a logically consistent value but does not significantly alter the predicted time-to-failure. The new formulation predicts a higher minimum applied electric field required to induce breakdown. This minimum field is larger than current devices see during operation.
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77.22.Jp Dielectric breakdown and space-charge effects
66.30.H- Self-diffusion and ionic conduction in nonmetals

Reclamation of a molecular beam epitaxy system and conversion for oxide epitaxy

Alexander G. Carver, Walter Henderson, and W. Alan Doolittle

J. Vac. Sci. Technol. A 26, 1501 (2008); http://dx.doi.org/10.1116/1.2998810 (6 pages)

Online Publication Date: 30 October 2008

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An early 1980s vintage molecular beam epitaxy system, a Varian Gen II system, originally used for HgCdTe epitaxy, was converted into a system capable of growing thin-film complex metal oxides. The nature of some of the alternative oxides requires a thorough cleaning and, in some cases, complete replacement of system components. Details are provided regarding the chemistry of the etchants used, safety requirements for properly handling, and disposal of large quantities of etchants and etch by-products, and components that can be reused versus components that require replacement are given. Following the given procedures, an ultimate base pressure of 2×10−10 Torr was obtained. Films grown in the system after reclamation contained no evidence of previously present materials down to the detection limit of secondary ion mass spectrometry.
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81.15.Hi Molecular, atomic, ion, and chemical beam epitaxy
68.55.A- Nucleation and growth

Surface water reactivity of polycrystalline MgO and CaO films investigated using x-ray photoelectron spectroscopy

H. S. Craft, R. Collazo, M. D. Losego, Z. Sitar, and J.-P. Maria

J. Vac. Sci. Technol. A 26, 1507 (2008); http://dx.doi.org/10.1116/1.3000058 (4 pages) | Cited 2 times

Online Publication Date: 30 October 2008

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The authors report a study comparing the surface reactivities of the alkaline earth oxides MgO and CaO with respect to water vapor under ultrahigh and high vacuum conditions. Using x-ray photoelectron spectroscopy and a series of in vacuo exposures spanning ∼ 10−10 Torr vacuum, to 10−6 Torr flowing oxygen, the extent of surface hydroxylation was investigated by monitoring the O 1s photoelectron line. After the most aggressive exposures, the MgO surface reacted to form a maximum hydroxyl coverage of ∼ 1.3 ML (monolayer), while the CaO surface reached a maximum coverage of ∼ 3.0 ML. Both surface hydroxides could be removed by in vacuo thermal anneals; exposure to 250 and 500 °C were required for MgO and CaO, respectively. These results are framed in terms of the suitability of these oxides in complex oxide-compound semiconductor heteroepitaxial multifunctional devices and with respect to understanding the development of surface morphology in epitaxial 111-oriented CaO and MgO thin films.
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82.65.+r Surface and interface chemistry; heterogeneous catalysis at surfaces
79.60.Dp Adsorbed layers and thin films
68.35.bt Other materials
81.40.Gh Other heat and thermomechanical treatments
68.55.aj Insulators

Preparation and thermal desorption properties of dc sputtered zirconium-hydrogen-helium thin films

Y. C. Wei, L. Q. Shi, L. Zhang, Z. J. He, B. Zhang, and L. B. Wang

J. Vac. Sci. Technol. A 26, 1511 (2008); http://dx.doi.org/10.1116/1.2990852 (8 pages)

Online Publication Date: 3 November 2008

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We developed a new approach for preparing hydrogen and helium co-containing zirconium films (Zr–H–He) to simulate aging metal tritides. We also studied the effect of hydrogen on helium behavior, in which we applied direct current magnetron sputtering in a mixture of working gases (helium, argon, and hydrogen). The amount and depth profile of helium and hydrogen trapped in the films were determined using the elastic recoil detection analysis. The microstructure and surface morphology of the Zr–H–He films were studied by x-ray diffraction, transmission electron microscopy, and atomic force microscopy. To investigate the effect of hydrogen on the thermal release behavior of helium in the Zr film, thermal desorption spectrometry (TDS) was used, which revealed a similar desorption behavior to aged tritides. TDS experiments showed that the spectra were constituted by low-temperature peaks around 300 °C and high temperature peaks above 750 °C. Furthermore, the solid-phase α to δ transformation changed the shapes of the high-temperature peaks related to microstates of helium bubbles and caused the peak with a massive helium release shift toward lower temperature obviously.
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82.45.Mp Thin layers, films, monolayers, membranes
68.43.Nr Desorption kinetics
61.72.Dd Experimental determination of defects by diffraction and scattering
68.35.B- Structure of clean surfaces (and surface reconstruction)
68.37.Og High-resolution transmission electron microscopy (HRTEM)
81.15.Cd Deposition by sputtering

Optical second-harmonic generation in thin film systems

J. J. H. Gielis, P. M. Gevers, I. M. P. Aarts, M. C. M. van de Sanden, and W. M. M. Kessels

J. Vac. Sci. Technol. A 26, 1519 (2008); http://dx.doi.org/10.1116/1.2990854 (19 pages) | Cited 6 times

Online Publication Date: 3 November 2008

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The surface and interface sensitive nonlinear optical technique of second-harmonic generation (SHG) is a very useful diagnostic in studying surface and interface properties in thin film systems and can provide relevant information during thin film processing. An important aspect when applying SHG is the interpretation of the SHG response. In order to utilize the full potential of SHG during materials processing it is necessary to have a good understanding of both the macroscopic and the microscopic origin of the SHG response, particularly in thin film or multilayer systems where the propagation of radiation is another important aspect that should be considered carefully. A brief theoretical overview on the origin of the SHG response and a description of the propagation of radiation will be given. Furthermore, several methods will be discussed that might reveal the possible macroscopic and microscopic origins of the SHG response in thin film systems. The different approaches will be illustrated by examples of real-time and spectroscopic SHG experiments with thin film systems relevant in Si etching and deposition environments, such as (1) hydrogenated amorphous Si films deposited by hot-wire chemical vapor deposition on both Si(100) and fused silica substrates, (2) amorphous Si generated by low-energy Ar+-ion bombardment of H terminated Si(100), and (3) Al2O3 films deposited by plasma-assisted atomic layer deposition on H terminated Si(100).
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68.55.ag Semiconductors
81.65.Cf Surface cleaning, etching, patterning
82.33.Ya Chemistry of MOCVD and other vapor deposition methods
81.15.Gh Chemical vapor deposition (including plasma-enhanced CVD, MOCVD, ALD, etc.)
42.65.Ky Frequency conversion; harmonic generation, including higher-order harmonic generation
81.15.-z Methods of deposition of films and coatings; film growth and epitaxy

Structure and interdiffusion of epitaxial ZnO/ZnMgO nanolayered thin films

B. L. Stevens, D. J. Cohen, and S. A. Barnett

J. Vac. Sci. Technol. A 26, 1538 (2008); http://dx.doi.org/10.1116/1.2993257 (4 pages) | Cited 1 time

Online Publication Date: 3 November 2008

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Interdiffusion was studied in Zn1−xMgxO:Al/ZnO expitaxial superlattices with periods of 15 and 25 nm grown on basal-plane sapphire by dc reactive sputtering. Interdiffusion coefficients were determined by analyzing low angle x-ray reflectivity peak intensity decreases during isothermal annealing, using analytical interdiffusion expressions. The results were corroborated with diffusion data obtained from secondary ion mass spectrometry compositional depth profiles. An initial fast diffusion stage was observed for, e.g., the first few hours at 500 °C, followed by slower diffusion at longer times.
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81.05.Dz II-VI semiconductors
66.30.Ny Chemical interdiffusion; diffusion barriers
68.55.ag Semiconductors
68.65.Cd Superlattices
61.72.Cc Kinetics of defect formation and annealing
81.15.Cd Deposition by sputtering

Investigation of negative electron affinity in hydrogen complex deactivated surface of InP:Zn (100)

M. D. Williams

J. Vac. Sci. Technol. A 26, 1542 (2008); http://dx.doi.org/10.1116/1.2998809 (4 pages)

Online Publication Date: 3 November 2008

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Ultraviolet photoemission spectroscopy is used to investigate the development of negative electron affinity at the surface of hydrogenated Zn-doped InP (100). Hydrogen injected into the material electronically passivates the local carrier concentration. Reverse-biased anneals of the InP under ultrahigh vacuum show a dramatic change in the work function of the material within a set annealing temperature range suggesting the establishment of negative electron affinity at the surface. The strength of the negative electron affinity is 1.08 eV. This value is consistent with the deactivation energy of the H–Zn complex (1.14 eV) determined previously. Spectral features are also shown to be sensitive to sample temperature. Hydrogen retrapping at the surface limits the effect and it is dependent on whether the surface is smooth or roughened. The electron affinity of the material is thus controlled with defect density and annealing temperature.
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33.15.Ry Ionization potentials, electron affinities, molecular core binding energy
07.60.Rd Visible and ultraviolet spectrometers
61.72.Cc Kinetics of defect formation and annealing
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Erratum: Oxygen adsorption on well-defined gold particles on TiO2(110) [ J. Vac. Sci. Technol. A 17, 1717 (1999) ]

Charles T. Campbell

J. Vac. Sci. Technol. A 26, 1546 (2008); http://dx.doi.org/10.1116/1.2981066 (1 page) | Cited 1 time

Online Publication Date: 3 November 2008

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Abstract Unavailable
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99.10.Cd Errata
68.43.-h Chemisorption/physisorption: adsorbates on surfaces
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