Tuning oxygen impurities and microstructure of nanocrystalline silicon photovoltaic materials through hydrogen dilution
© Wen et al.; licensee Springer. 2014
Received: 22 May 2014
Accepted: 6 June 2014
Published: 14 June 2014
As a great promising material for third-generation thin-film photovoltaic cells, hydrogenated nanocrystalline silicon (nc-Si:H) thin films have a complex mixed-phase structure, which determines its defectful nature and easy residing of oxygen impurities. We have performed a detailed investigation on the microstructure properties and oxygen impurities in the nc-Si:H thin films prepared under different hydrogen dilution ratio treatment by the plasma-enhanced chemical vapor deposition (PECVD) process. X-ray diffraction, transmission electron microscopy, Raman spectroscopy, and optical transmission spectroscopy have been utilized to fully characterize the microstructure properties of the nc-Si:H films. The oxygen and hydrogen contents have been obtained from infrared absorption spectroscopy. And the configuration state of oxygen impurities on the surface of the films has been confirmed by X-ray photoelectron spectroscopy, indicating that the films were well oxidized in the form of SiO2. The correlation between the hydrogen content and the volume fraction of grain boundaries derived from the Raman measurements shows that the majority of the incorporated hydrogen is localized inside the grain boundaries. Furthermore, with the detailed information on the bonding configurations acquired from the infrared absorption spectroscopy, a full explanation has been provided for the mechanism of the varying microstructure evolution and oxygen impurities based on the two models of ion bombardment effect and hydrogen-induced annealing effect.
As a low-cost, high-efficiency thin-film material, hydrogenated nanocrystalline silicon (nc-Si:H) has emerged as a very attractive candidate for the application of next-generation solar cells. Extensive optical and electrical investigations have been carried out to reveal the favorable features of nc-Si:H thin films such as tunable bandgap, strong optical absorption, high carrier mobility, and great stability against light soaking[1–4]. High efficiency and good stability of single-junction and tandem[6, 7] third-generation nc-Si:H thin-film solar cells have been realized based on the good properties of this material. The initial active-area efficiency of a triple-junction structured cell has been demonstrated to be 16.3% by taking advantage of the nc-Si:H material.
However, the nc-Si:H film is in nature a mixed-phase structure consisting of nanometer-sized grains embedded in an amorphous matrix, which determines that the defect microstructures such as grain boundaries and voids exist in the films with a large volume fraction. And oxygen impurities from post-deposition oxidation can easily diffuse into the film because of the porous defect structure and induce additional defects within the nc-Si:H films as well. Furthermore, incorporation of oxygen into the nc-Si:H films can lower the optical absorption of amorphous Si (a-Si)-based solar cells when nc-Si:H films are used as a window layer or tunnel junction. It has also been found that nc-Si:H is more sensitive to oxygen impurities than a-Si:H because oxygen can form weak donors in nc-Si:H materials, which raises the Fermi level towards the conduction band. Therefore, it is of significant importance to regulate the defect structure and the oxygen impurities in the films in order to better the performance of nc-Si:H material-based solar cells.
In this work, we have performed a detailed structural and optical investigation on nc-Si:H thin films with hydrogen dilution profiling to analyze the structure evolution and oxygen incorporation under the influence of hydrogen. The bonding configuration of surface oxygen has been identified by the X-ray photoelectron spectroscopy (XPS) spectra. Moreover, a detailed analysis on the infrared Si-H stretching mode has been given to reveal the tuning mechanism of hydrogen on structure and oxygen impurities during the growth process based on the two models of ion bombardment effect and hydrogen-induced annealing effect.
Summary of physical parameters of the nc-Si:H thin films prepared under various hydrogen dilution ratios
The film thicknesses were directly measured by a Dektak 6 M profilometer (Veeco Instruments Inc., Plainview, NY, USA). The average grain size d was derived from the (111) X-ray diffraction (XRD) peak, measured with a Bruker D-8 XRD system (Cu Kα radiation, 40 kV and 60 mA, Madison, WI, USA) at room temperature, and the grain size was also directly observed by high-resolution transmission electron microscopy (HRTEM; CM200, Philips, Amsterdam, The Netherlands). The crystalline volume fraction XC was calculated from the Raman spectra, measured with a Jobin Yvon LabRam HR800 UV micro-Raman spectrometer (backscattering configuration and Ar ion laser of 514.5 nm, Kyoto, Japan). The laser power density is 1 mW/mm2 to avoid any beam-induced crystallization. The long-wavelength limit of the refractive index n∞ was deduced from optical transmission spectra, measured with the double-beam ultraviolet-visible-near-infrared spectrometer PerkinElmer UV Lambda 35 (300- to 1,000-nm spectral range with 0.5-nm resolution, Waltham, MA, USA).
The hydrogen (oxygen) content bonded to silicon CH (CO), and its bonding configurations were obtained from infrared (IR) absorption spectra, measured with a Nicolet Nexus 870 Fourier transform IR spectrometer (400 to 4,000 cm-1, Thermo Fisher Scientific Inc., Waltham, MA, USA). XPS was used to study the silicon core energy level of the nc-Si:H. All the spectra were obtained with an electron takeoff angle of 90° using an Al Kα source monochromatic X-ray radiation. The Kratos charge neutralizer system (Kratos Analytical, Chestnut Ridge, NY, USA) was used on all the samples to compensate the charging effect of the sample surface. The narrow scan of the spectra was collected at a high-resolution mode with a pass energy of 20 eV. The binding energy was calibrated to the C1s emission (284.8 eV) arising from surface contamination. The background from each spectrum was subtracted using a Shirley-type background to remove most of the extrinsic loss structure. All the comparative data and spectra presented below are normalized with thickness.
Results and discussion
Figure 1c shows the typical experimental result of Raman spectrum corresponding to the sample with RH = 98.2%. The spectrum was decomposed into three satellite spectra, namely a broad Gaussian distribution around 480 cm-1 resulting from the transverse optical (TO1) mode of amorphous silicon, a Lorentzian peak near 520 cm-1 coming from the asymmetric TO2 vibrational mode of crystalline silicon, and one peak around 506 cm-1 originating from the intermediate mode of crystal-like phase at grain boundaries. The crystalline volume fraction XC of the nc-Si:H films can be estimated from the relation XC = (IA + IGB)/(IC + IGB + IA), where IA, IGB, and IC are the integrated peak intensity at 480, 506, and 520 cm-1, respectively. And the obtained crystalline volume fraction XC vs. hydrogen dilution ratio RH was plotted in the inset of Figure 1c. According to both the surface model and the growth zone model, increasing RH will result in an increase of XC. However, our experimental results show that XC increases only when RH is higher than 98.8%, and hence, the decrease of XC in the RH range up to 98.6% cannot be fully explained by the mentioned growth models. Therefore, additional discussion involving the hydrogen ion bombardment effect is necessary to fully explain the film growth mechanism as well as to understand the structure characterization.
Optical transmission measurements were performed at room temperature to generate optical information on the nc-Si:H thin-film samples. Figure 1d displays the experimental (open circles) and fitted (solid curve) optical transmission spectrum for the sample with RH = 98.2%. From the fitting process conducted within the framework of a modified four-layer-medium transmission model based on the envelop method, both the film thickness (approximately 636.9 nm) and the long-wavelength limit of the refractive index (n∞ ~ 2.663) were obtained. The thicknesses of the films are in good agreement with the values directly measured by the step profilometer as listed in Table 1. And the long-wavelength limit of the refractive index n∞ is an important optical parameter associated with the mass density and atomic structure of nc-Si:H thin films, which together with the XC obtained from the Raman measurement can be used to calculate the respective volume fractions of the three components, namely c-Si, a-Si, and voids in the films. Table 1 summarizes the structural and optical properties of the nc-Si:H thin films under various RH.
As a mixed-phase material with nanocrystallites embedded in an amorphous matrix, nc-Si:H contains a certain volume fraction of nanometer-sized voids, which should not be neglected when characterizing the microstructure of the films. The volume fraction of voids PV in these nc-Si:H thin films was calculated based on Bruggeman's effective media approximation using the crystalline fraction XC from the Raman analysis and the refractive index n∞ from the transmission calculation. As shown in Figure 2b, PV increases monotonically with the increase of RH, which indicates that the presence of microvoids in these thin films is enhanced by hydrogen dilution and that the compactness of the samples decreases with the increase of RH.
As also shown in Figure 2b, the total oxygen content CO for the samples initially has an increase from 3.33% to 10.92% with the increase of RH up to 98.6%, and then a downshift of CO occurs when further increasing RH. Researchers have found that most of the oxygen atoms were incorporated into the films through post-oxidation. Concerning the material structure, cavities and voids in the material are probably crucial for accommodation of oxygen molecules. Hence, the variation of CO along RH is expected to be similar to that of PV. Nevertheless, our experimental data show an interesting nonmonotonic correlation that higher PV is associated with less oxygen impurities when RH is above 98.6%, which deviates from the above expectation. And the deviation indicates that there should be some other type of defect structure overwhelmingly affecting the incorporation of the oxygen inside the films rather than voids.
To fully understand the relation between the defect microstructure and the oxidation effects, it is quite necessary to investigate the structure evolution mechanism and to elucidate the hydrogen behavior in the growth process of the nc-Si:H thin film, which is a complex synergy between surface and bulk reactions of impinging SiH x .
Moreover, we can notice from peak 3 that the nc-Si:H surface was well passivated with SiO2. Surface oxygen content as a function of RH is presented in the inset of Figure 3. From the inset, we notice that the sample with RH = 99.2% has a very low value of surface oxygen content, demonstrating that high RH hydrogen effectively limits the intermediate oxide formation by passivation at the near surface. It can be clearly seen from the evolution of the surface oxygen content that the surface oxygen content first shifts towards the highest value of 24.32% upon increasing RH up to 98.2%. But when RH is further increased to 99.2%, the surface oxygen content downshifts towards the lowest value of 13.56%. Besides, RH = 98.2% gives rise to the highest peak intensity of surface oxygen content while the oxygen content CO in the bulk is not the highest. This may be related to the surface smoothness at the atomic level of the sample, i.e., a rough surface of the silicon material produces more intermediate oxidation states. The oxygen content CO in the bulk is mainly influenced by H and the H-related defect structure, which we will discuss in the following part.
We show in Figure 4b the variation of CGB and CH as a function of RH. It can be clearly observed that CGB and CH have the same variation behavior as a function of RH, demonstrating that as an important defect microstructure, the volume fraction of grain boundaries in the nc-Si:H films can be effectively regulated by the bonded H. This positive correlation of CGB and CH also demonstrates that most of the hydrogen atoms in the nc-Si:H films are located in the grain boundaries, rather than voids or other quasiordered phases, even though the amorphous part accounts for most of the thin films. Grain boundaries can probably offer location for most of the oxygen impurities out of post-oxidization, where the oxygen atoms can incorporate the dangling bonds along the grain boundaries. On the other hand, the incorporation of oxygen impurities in the films is effectively influenced by H radicals. The mechanism is that H radicals generated in the plasma during the growth process of the films are accelerated by the RF power and impinge onto the growing surface of the films with a certain kinetic energy. Those H radicals with enough kinetic energy can passivate the dangling bonds along the grain boundaries and effectively prevent the oxygen impurities from post-oxidization.
The bonded H located at grain boundaries can form hydrides with a certain type of bonding configuration, which can be identified from the deconvoluted peaks of the Si-H stretching mode of the peak at 2,090 cm-1 as mentioned in Figure 2a. These hydrides with different types of bonding configurations were then investigated in this part to help us accurately understand the spatial correlation between the hydrogen-related microstructures and oxygen impurities.
Among the eight bonding configurations of hydrides, the MSM corresponding to the bonding configuration of the hydrides in the grain boundaries is the major mode that determines the mechanism of hydrogen's influence on oxygen impurities. We show in Figure 5b the integrated intensity of the MSM and the bonded oxygen content CO for all the samples with RH = 97.5% to 99.2%. It is clear that the integrated intensity of the MSM decreases with RH increasing from 97.5% to 98.6% and then increases when further increasing RH from 98.6% to 99.2%. As also shown in Figure 5b, CO has an inverse evolution compared with the integrated intensity of the MSM, illustrating that the MSM is closely related to the oxygen impurities. H atoms and ions incorporate the silicon dangling bonds along the platelet-like configuration of the amorphous-crystalline interface, that is, grain boundaries, and form the hydride corresponding to the MSM. These hydrides located in grain boundaries can effectively passivate the nc-Si:H films by preventing the oxygen incursions from inducing the increase of dangling bonds (Pb center defects). And this inverse correlation between the integrated intensity of the MSM and CO further proves that the oxygen impurities mainly reside at the grain boundaries of the nc-Si:H films.
Based on the above results and analysis, we can hereby draw a clear physical picture of the structure evolution mechanism and the effect of the hydrogen behavior on the structure as well as the oxygen impurities in the growth process of the nc-Si:H thin film. The growth of the nc-Si:H thin film is the overall effect of two competing processes: the formation of radicals and the etching of deposition. These two processes are significantly influenced by the proportions of the impinging SiH x radicals and atomic hydrogen ions, which vary with different hydrogen dilutions. During the initial stage, increasing RH from 97.5% to 98.6% led to the decrease of the density of the SiH x radicals, which together with the H etching effect resulted in the decrease of the growth rate. Considering the high RF power density applied on the depositing substrate, the ion bombardment effect should be taken into account. The ion bombardment effect of the increasing H species on the SiH x radicals during the growth process reduced the surface diffusion length of film precursors, and these precursors could not reach their favorable growing sites, leading to the formation of more microvoids with amorphous components in the nc-Si:H film. These subsequently formed microvoids induced larger areas of internal surfaces with dangling bonds and weaker Si-Si bonds in the growing film. Therefore, through H ion implantation, atomic hydrogen diffusion, and relevant chemical reactions, more hydrogen would be bonded to silicon or trapped in these microvoids, resulting in not only an increase in the volume fraction of voids PV within the film as shown in Figure 2b but also a decrease in both the grain size d and the crystalline volume fraction XC, as observed in both the XRD and Raman measurements presented in Figure 1a,c. In the meanwhile, the enhanced H abstraction reaction[34, 35] of the increasing H atoms and ions took away a certain number of the bonded H from the hydrides at grain boundaries, and more oxygen impurities could incorporate the dangling bonds at grain boundaries, giving rise to the decrease of the integrated intensity of the MSM and the increase of CO as shown in Figure 5b.
Further increasing RH from 98.6% to 99.2% led to a declining growth rate due to the further decreasing density of the SiH x radicals. At the same time, the PV of the growing film was further enhanced (see Figure 2b) because of the ion bombardment effect of the excessive H species. However, in this RH range, 98.6% to 99.2%, the hydrogen-induced annealing effect gradually became dominant over the effect of the ion bombardment-induced amorphization. The excessive H species presenting on the growing surface of the film could penetrate into the subsurface and rearrange the Si-Si network structure. These H atoms and ions saturated the present dangling bonds at the interface between the amorphous and crystalline regions and formed molecular hydrogen through the reaction of adsorbed hydrogen with clustered hydrogen in the subsurface, which was less mobile than the atomic hydrogen. Further H insertion reaction with the a-Si:H matrix destructed and perturbed the strained Si-Si bonds, and the subsequent structural relaxation of the Si-Si bonds resulted in the transformation of the film's structure from amorphous to nanocrystalline. Therefore, as a general result, excessive hydrogen presenting in the plasma could lead to a greater probability of crystallization, supported by the observation of XC in Figure 1c. The slight enhancement of the grain size d from 5.5 to 6.1 nm as seen in Figure 1a without any remarkable change can be attributed to the suppression of the growth by the excessive H ion implantation on the nucleation site, as well as the depletion of the SiH x radical by the hydrogen flux. On the other hand, the results of the increasing integrated intensity of the MSM and the decreasing CO as shown in Figure 5b in this RH range illustrate that those H atoms and ions penetrating into the subsurface could saturate the dangling bonds along the grain boundaries, and more hydrides were formed to effectively avoid the post-oxidation effect by preventing the oxygen impurities from incorporating the dangling bonds in the grain boundaries. Hence, compact-structure and well-passivated grain boundaries are less susceptible to oxygen impurities. Our previous work of applying an extra negative bias on the substrate offers an effective way to lower the defect density and the oxygen impurities inside nc-Si:H films.
In summary, we have conducted a detailed investigation on the mechanism of hydrogen's influence on structure evolution and oxygen impurities from a series of nc-Si:H thin films prepared under different hydrogen dilution ratio treatment in PECVD. XRD, TEM, Raman, and optical transmission techniques have been utilized to understand the microstructure characterization of nc-Si:H thin films. XPS results have confirmed that oxygen impurities on the surface of the nc-Si:H films have the dominant formation state of SiO2. The good agreement between the bonded hydrogen content and the volume fraction of grain boundary illustrates that as an important defect structure, the volume fraction of grain boundary in nc-Si:H films can be effectively regulated through hydrogen dilution. The inverse relationship between the integrated intensity of MSM and the oxygen content presents that the oxygen incursions due to post-oxidation originate from the location of grain boundaries inside nc-Si:H films. The tuning mechanism of hydrogen on oxygen impurities is that the hydrides corresponding to the MSM with a certain kind of bonding configuration are formed by the incorporation of H atoms and ions with the silicon dangling bonds located at grain boundaries, which can effectively prevent the oxygen incursions from residing along grain boundaries and further forming the Si-O/Si defects. Therefore, applying an extra negative bias on the substrate during the growth process is proposed to reduce the probability of oxygen contamination, which can produce films with better light absorption properties in the solar cell application.
This work was supported by the National Major Basic Research Projects (2012CB934302) and Natural Science Foundation of China (11174202 and 61234005).
- Kitao J, Harada H, Yoshida NJ, Kitao H, Yoshidaa HN, Kasuya Y, Nishio M, Sakamoto T, Itoh T, Nonomura S, Nitta S: Absorption coefficient spectra of μc-Si in the low-energy region 0.4–1.2 eV. Sol Energy Mater Sol Cells 2001, 66: 245–251. 10.1016/S0927-0248(00)00180-XView ArticleGoogle Scholar
- Zhang R, Chen XY, Zhang K, Shen WZ: Photocurrent response of hydrogenated nanocrystalline silicon thin films. J Appl Phys 2006, 100: 104310–104315. 10.1063/1.2388042View ArticleGoogle Scholar
- Chen XY, Shen WZ, He YL: Enhancement of electron mobility in nanocrystalline silicon/crystalline silicon heterostructures. J Appl Phys 2005, 97: 024305–5. 10.1063/1.1832752View ArticleGoogle Scholar
- Keppner H, Meier J, Torres P, Fischer D, Shah A: Microcrystalline silicon and micromorph tandem solar cells. Appl Phys A 1999, 69: 169–177. 10.1007/s003390050987View ArticleGoogle Scholar
- Mai Y, Klein S, Geng X, Finger F: Structure adjustment during high-deposition-rate growth of microcrystalline silicon solar cells. Appl Phys Lett 2004, 85: 2839–2841. 10.1063/1.1801676View ArticleGoogle Scholar
- Yang J, Yan B, Guha S: Amorphous and nanocrystalline silicon-based multi-junction solar cells. Thin Solid Films 2005, 487: 162–169. 10.1016/j.tsf.2005.01.058View ArticleGoogle Scholar
- Yamamoto K, Nakajima A, Yoshimi M, Sawada T, Fukuda S, Suezaki T, Ichikawa M, Koi Y, Goto M, Meguro T, Matsuda T, Kondo M, Sasaki T, Tawada Y: A thin-film silicon solar cell and module. Prog Photovolt Res Appl 2005, 13: 489–494. 10.1002/pip.645View ArticleGoogle Scholar
- Yan B, Yue G, Sivec L, Yang J, Guha S, Jiang C-S: Innovative dual function nc-SiOx:H layer leading to a >16% efficient multi-junction thin-film silicon solar cell. Appl Phys Lett 2011, 99: 113512–113513. 10.1063/1.3638068View ArticleGoogle Scholar
- He Y, Yin C, Cheng G, Wang L, Liu X, Hu GY: The structure and properties of nanosize crystalline silicon films. J Appl Phys 1994, 75: 797–803. 10.1063/1.356432View ArticleGoogle Scholar
- Finger F, Carius R, Dylla T, Klein S, Okur S, Gunes M: Stability of microcrystalline silicon for thin film solar cell applications. Circuits Dev Syst IEE Proc 2003, 150: 300–308. 10.1049/ip-cds:20030636View ArticleGoogle Scholar
- Das D, Jana M, Barua AK: Characterization of undoped μc-SiO:H films prepared from (SiH4 + CO2 + H2)-plasma in RF glow discharge. Sol Energy Mater Sol Cells 2000, 63: 285–297. 10.1016/S0927-0248(00)00035-0View ArticleGoogle Scholar
- Xu GY, Liu M, Wu XS, He YL, Wang TM: Transport mechanism of nanocrystalline-silicon film tunnelling diodes. J Phys Condens Matter 1999, 11: 8495. 10.1088/0953-8984/11/43/312View ArticleGoogle Scholar
- Kilper T, Beyer W, Bräuer G, Bronger T, Carius R, van den Donker MN, Hrunski D, Lambertz A, Merdzhanova T, Mück A, Rech B, Reetz W, Schmitz R, Zastrow U, Gordijn A: Oxygen and nitrogen impurities in microcrystalline silicon deposited under optimized conditions: influence on material properties and solar cell performance. J Appl Phys 2009, 105: 074509. 10.1063/1.3104781View ArticleGoogle Scholar
- Fitzsimmons MR, Eastman JA, Müller-Stach M, Wallner G: Structural characterization of nanometer-sized crystalline Pd by x-ray-diffraction techniques. Phys Rev B 1991, 44: 2452–2460.View ArticleGoogle Scholar
- Achiq A, Rizk R, Gourbilleau F, Madelon R, Garrido B, Perez-Rodriguez A, Morante JR: Effects of prior hydrogenation on the structure and properties of thermally nanocrystallized silicon layers. J Appl Phys 1998, 83: 5797–5803. 10.1063/1.367435View ArticleGoogle Scholar
- Iqbal Z, Vepřek S, Webb AP, Capezzuto P: Raman scattering from small particle size polycrystalline silicon. Solid State Commun 1981, 37: 993–996. 10.1016/0038-1098(81)91202-3View ArticleGoogle Scholar
- Matsuda A: Formation kinetics and control of microcrystallite in μc-Si:H from glow discharge plasma. J Non-Cryst Solids 1983, Part 2: 59–60. 67–774 67–774Google Scholar
- Street RA: Model for growth of a-Si:H and its alloys. Phys Rev B 1991, 44: 10610–10616. 10.1103/PhysRevB.44.10610View ArticleGoogle Scholar
- Kalache B, Kosarev AI, Vanderhaghen RI, Cabarrocas PR: Ion bombardment effects on microcrystalline silicon growth mechanisms and on the film properties. J Appl Phys 2003, 93: 1262–1273. 10.1063/1.1524707View ArticleGoogle Scholar
- Chen H, Gullanar MH, Shen WZ: Effects of high hydrogen dilution on the optical and electrical properties in B-doped nc-Si:H thin films. J Cryst Growth 2004, 260: 91–101. 10.1016/j.jcrysgro.2003.08.048View ArticleGoogle Scholar
- Brodsky MH, Cardona M, Cuomo JJ: Infrared and Raman spectra of the silicon-hydrogen bonds in amorphous silicon prepared by glow discharge and sputtering. Phys Rev B 1977, 16: 3556–3571. 10.1103/PhysRevB.16.3556View ArticleGoogle Scholar
- Lucovsky G, Nemanich RJ, Knights JC: Structural interpretation of the vibrational spectra of a-Si: H alloys. Phys Rev B 1979, 19: 2064–2073. 10.1103/PhysRevB.19.2064View ArticleGoogle Scholar
- Freeman EC, Paul W: Infrared vibrational spectra of rf-sputtered hydrogenated amorphous silicon. Phys Rev B 1978, 18: 4288–4300. 10.1103/PhysRevB.18.4288View ArticleGoogle Scholar
- Tsu DV, Lucovsky G, Davidson BN: Effects of the nearest neighbors and the alloy matrix on SiH stretching vibrations in the amorphous SiOr:H (0 < r < 2) alloy system. Phys Rev B 1989, 40: 1795–1805.View ArticleGoogle Scholar
- Langford AA, Fleet ML, Nelson BP, Lanford WA, Maley N: Infrared absorption strength and hydrogen content of hydrogenated amorphous silicon. Phys Rev B 1992, 45: 13367–13377. 10.1103/PhysRevB.45.13367View ArticleGoogle Scholar
- Moss SC, Graczyk JF: Evidence of voids within the as-deposited structure of glassy silicon. Phys Rev Lett 1969, 23: 1167–1171. 10.1103/PhysRevLett.23.1167View ArticleGoogle Scholar
- Bruggeman DAG: Berechnung verschiedener physikalischer Konstanten von heterogenen Substanzen. I. Dielektrizitätskonstanten und Leitfähigkeiten der Mischkörper aus isotropen Substanzen. Ann Phys 1935, 416: 636–664. 10.1002/andp.19354160705View ArticleGoogle Scholar
- Hessel CM, Henderson EJ, Veinot JGC: An investigation of the formation and growth of oxide-embedded silicon nanocrystals in hydrogen silsesquioxane-derived nanocomposites. J Phys Chem C 2007, 111: 6956–6961. 10.1021/jp070908cView ArticleGoogle Scholar
- Himpsel FJ, McFeely FR, Taleb-Ibrahimi A, Yarmoff JA, Hollinger G: Microscopic structure of the SiO2/Si interface. Phys Rev B 1988, 38: 6084–6096. 10.1103/PhysRevB.38.6084View ArticleGoogle Scholar
- Niwano M, Katakura H, Takeda Y, Takakuwa Y, Miyamoto N, Hiraiwa A, Yagi K: Photoemission study of the SiO2/Si interface structure of thin oxide films on Si(100), (111), and (110) surfaces. J Vac Sci Technol A 1991, 9: 195–200. 10.1116/1.577520View ArticleGoogle Scholar
- Smets AHM, van de Sanden MCM: Relation of the Si-H stretching frequency to the nanostructural Si-H bulk environment. Phys Rev B 2007, 76: 073202.View ArticleGoogle Scholar
- Anutgan T, Uysal S: Low temperature plasma production of hydrogenated nanocrystalline silicon thin films. Curr Appl Phys 2013, 13: 181–188. 10.1016/j.cap.2012.07.001View ArticleGoogle Scholar
- Niwano M, Kageyama J-I, Kurita K, Kinashi K, Takahashi I, Miyamoto N: Infrared spectroscopy study of initial stages of oxidation of hydrogen-terminated Si surfaces stored in air. J Appl Phys 1994, 76: 2157–2163. 10.1063/1.357627View ArticleGoogle Scholar
- Mahan AH, Xu Y, Williamson DL, Beyer W, Perkins JD, Vanecek M, Gedvilas LM, Nelson BP: Structural properties of hot wire a-Si:H films deposited at rates in excess of 100 Å/s. J Appl Phys 2001, 90: 5038–5047. 10.1063/1.1407317View ArticleGoogle Scholar
- Robertson J: Deposition mechanism of hydrogenated amorphous silicon. J Appl Phys 2000, 87: 2608–2617. 10.1063/1.372226View ArticleGoogle Scholar
- Kroll U, Meier J, Shah A, Mikhailov S, Weber J: Hydrogen in amorphous and microcrystalline silicon films prepared by hydrogen dilution. J Appl Phys 1996, 80: 4971–4975. 10.1063/1.363541View ArticleGoogle Scholar
- Wen C, Xu H, Liu H, Li ZP, Shen WZ: Passivation of nanocrystalline silicon photovoltaic materials employing a negative substrate bias. Nanotechnology 2013, 24: 455602. 10.1088/0957-4484/24/45/455602View ArticleGoogle Scholar
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