Eugene Iwaniczko
National Renewable Energy Laboratory
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Featured researches published by Eugene Iwaniczko.
Applied Physics Letters | 2010
Qi Wang; M.R. Page; Eugene Iwaniczko; Yueqin Xu; Lorenzo Roybal; Russell Bauer; Bobby To; Hao-Chih Yuan; A. Duda; Falah S. Hasoon; Y. Yan; Dean H. Levi; Daniel L. Meier; Howard M. Branz; Tihu Wang
Efficient crystalline silicon heterojunction solar cells are fabricated on p-type wafers using amorphous silicon emitter and back contact layers. The independently confirmed AM1.5 conversion efficiencies are 19.3% on a float-zone wafer and 18.8% on a Czochralski wafer; conversion efficiencies show no significant light-induced degradation. The best open-circuit voltage is above 700 mV. Surface cleaning and passivation play important roles in heterojunction solar cell performance.
Applied Physics Letters | 1999
J. Thiesen; Eugene Iwaniczko; Kim M. Jones; A. H. Mahan; Richard S. Crandall
We demonstrate epitaxial silicon growth of 8 A/s at temperatures as low as 195 °C, using hot-wire chemical vapor deposition. Characterization by transmission electron microscopy shows epitaxial layers of Si. We briefly discuss various aspects of the process parameter space. Finally, we consider differences in the chemical kinetics of this process when compared to other epitaxial deposition techniques.
Applied Physics Letters | 2010
Kirstin Alberi; Ina T. Martin; Maxim Shub; Charles W. Teplin; Manuel J. Romero; Robert C. Reedy; Eugene Iwaniczko; A. Duda; Paul Stradins; Howard M. Branz; David L. Young
The performance of 2-μm-thick crystal silicon (c-Si) solar cells grown epitaxially on heavily doped wafer substrates is quantitatively linked to absorber dislocation density. We find that such thin devices have a high tolerance to bulk impurities compared to wafer-based cells. The minority carrier diffusion length is about half the dislocation spacing and must be roughly three times the absorber thickness for efficient carrier extraction. Together, modeling and experimental results provide design guidelines for film c-Si photovoltaic cells.
Thin Solid Films | 2001
Brent P. Nelson; Eugene Iwaniczko; A. Harv Mahan; Qi Wang; Yueqin Xu; Richard S. Crandall; Howard M. Branz
Abstract We grow hydrogenated amorphous silicon (a-Si:H) solar cells in a device structure denoted as SS/n–i–p/ITO. We grow all the a-Si:H layers by hot-wire chemical vapor deposition (HWCVD) and the indium-tin-oxide (ITO) by reactive evaporation. We are able to grow HWCVD i-layer materials that maintain an AM1.5 photoconductivity-to-dark-conductivity ratio of 105 at deposition rates up to 130 A/s. We have put these high-deposition rate i-layer materials into SS/n–i–p/ITO devices and light-soaked them for ≥1000 h under AM1.5 conditions. We obtain stabilized solar cell efficiencies of 5.5% at 18 A/s, 4.8% at 35 A/s, 4.1% at 83 A/s and 3.8% at 127 A/s.
Journal of Applied Physics | 2005
Charles W. Teplin; Dean H. Levi; Eugene Iwaniczko; Kim M. Jones; John D. Perkins; Howard M. Branz
Real-time spectroscopic ellipsometry (RTSE) is used to monitor the breakdown of low-temperature homoepitaxial growth of silicon on silicon wafers in a hot-wire chemical-vapor deposition reactor. We develop and evaluate two optical models to interpret the RTSE data, revealing the progression of epitaxy and its eventual breakdown into amorphous silicon growth. Comparison of the RTSE analysis with cross-sectional transmission electron microscopy, ex situ variable-angle spectroscopic ellipsometry, and Raman spectroscopy measurements shows that RTSE provides accurate and fast quantitative feedback about the progression of epitaxy.
Energy and Environmental Science | 2011
Charles W. Teplin; M. Parans Paranthaman; Thomas R. Fanning; Kirstin Alberi; L. Heatherly; Sung-Hun Wee; Kyunghoon Kim; F.A. List; Jerry Pineau; Jon Bornstein; Karen Bowers; D.F. Lee; Claudia Cantoni; Steve Hane; Paul Schroeter; David L. Young; Eugene Iwaniczko; Kim M. Jones; Howard M. Branz
Crystal silicon (c-Si) film photovoltaics (PV) fabricated on inexpensive substrates could retain the desirable qualities of silicon wafer PV—including high efficiency and abundant environmentally-benign raw materials—at a fraction of the cost. We report two related advances toward film c-Si PV on inexpensive metal foils. First, we grow heteroepitaxial silicon solar cells on 2 kinds of single-crystal Al2O3 layers from silane gas, using the rapid and scalable hot-wire chemical vapor deposition technique. Second, we fabricate heteroepitaxial c-Si layers on large-grained, cube-textured NiW metal foils coated with Al2O3. In both experiments, the deposition temperature is held below 840 °C, compatible with low fabrication costs. The film c-Si solar cells are fabricated on both single-crystal sapphire wafer substrates and single-crystal γ-Al2O3-buffered SrTiO3 wafer substrates. We achieve ∼400 mV of open-circuit voltage despite crystallographic defects caused by lattice mismatch between the silicon and underlying substrate. With improved epitaxy and defect passivation, it is likely that the voltages can be improved further. On the inexpensive NiW metal foils, we grow MgO and γ-Al2O3 buffer layers before depositing silicon. Transmission electron microscopy (TEM) and X-ray diffraction (XRD) confirm that the silicon layers are epitaxial and retain the ∼50 μm grain size and biaxial orientation of the foil substrate. With the addition of light-trapping, >15% film c-Si PV on metal foils is achievable.
photovoltaic specialists conference | 2005
Tihu Wang; Eugene Iwaniczko; Matthew R. Page; Dean H. Levi; Y. Yan; Vijay Yelundur; Howard M. Branz; Ajeet Rohatgi; Q. Wang
Thin hydrogenated amorphous silicon (a-Si:H) layers deposited by hot-wire chemical vapor deposition (HWCVD) are investigated for use in silicon heterojunction (SHJ) solar cells on p-type crystalline silicon wafers. A requirement for excellent emitter quality is minimization of interface recombination. Best results necessitate immediate a-Si:H deposition and an abrupt and flat interface to the c-Si substrate. We obtain a record planar HJ efficiency of 16.9% with a high V/sub oc/ of 652 mV on p-type float-zone (FZ) silicon substrates with HWCVD a-Si:H(n) emitters and screen-printed Al-BSF contacts. H pretreatment by HWCVD is beneficial when limited to a very short period prior to emitter deposition.
Journal of Non-crystalline Solids | 2002
A. H. Mahan; Yueqin Xu; Eugene Iwaniczko; D. L. Williamson; Brent P. Nelson; Q. Wang
Abstract The deposition conditions for hydrogenated amorphous silicon, deposited by hot wire chemical vapor deposition, are linked to the film structure as we increase deposition rates (Rd) to >100 A/s. At low Rd ( 100 A/s), optimum films are deposited under silane depletion conditions as high as 75–80%, and all structural properties except for the SAXS results once again indicate a compact material. We relate changes in the film electronic structure (Urbach edge) with increasing Rd to the increase in the SAXS signals, and note the invariance of the saturated defect density versus Rd, discussing reasons why these microvoids do not play a role in the Staebler–Wronski effect for these films. Finally, we present device results over the whole range of Rd that we have studied and suggest why, at high Rd, device quality films can be deposited at such high silane depletions.
Thin Solid Films | 2003
Qi Wang; M.R. Page; Yueqin Xu; Eugene Iwaniczko; Evan L. Williams; Tihu Wang
Abstract We have developed a p-type, crystalline Si-based solar cell using hot-wire chemical vapor deposition (HWCVD) n-type microcrystalline Si to form an n-p junction (emitter). The CVD process was rapid and a low substrate temperature was used. The p-type Czochralski (CZ) c-Si wafer has a thickness of 400 μm and has a thermally diffused Al back-field contact. Before forming the n-p junction, the front surface of the p-type c-Si was cleaned using a diluted HF solution to remove the native oxides. The n-type emitter was formed at 220 °C by depositing 50 A a-Si:H and then a 100 A μc-Si n-layer. The total deposition time to form the emitter was less than 1 min. The top contact of the device is a lithograph defined and isolated 1×1 cm 2 and 780 A indium tin oxides (ITO) with metal fingers on top. Our best solar cell conversion efficiency is 13.3% with V oc of 0.58 V, FF of 0.773, and J sc of 29.86 mA cm −2 under one-sun condition. Quantum efficiency (QE) measurement on this solar cell shows over 90% in the region between 540 and 780 nm, but poor response in the blue and deep red. We find that the ITO top contact that acts as an antireflection layer increases the QE in the middle region. To improve the device efficiency further, J sc needs to be increased. Better emitter and light trapping will be developed in future work. The cell shows no degradation after 1000 h of standard light soaking.
ieee world conference on photovoltaic energy conference | 2006
Matthew R. Page; Eugene Iwaniczko; Yueqin Xu; Qi Wang; Yanfa Yan; Lorenzo Roybal; Howard M. Branz; Tihu Wang
We have developed hydrogenated amorphous silicon (a-Si:H) back contacts to both p-and n-type silicon wafers, and employed them in double-heterojunction solar cells. These contacts are deposited entirely at low temperature (<250degC) and replace the standard diffused or alloyed back-surface-field contacts used in single-heterojunction (front-emitter only) cells. High-quality back contacts require excellent surface passivation, indicated by a low surface recombination velocity of minority-carriers (S) or a high open-circuit voltage (Voc). The back contact must also provide good conduction for majority carriers to the external circuit, as indicated by a high light I-V fill factor. We use hot-wire chemical vapor deposition (HWCVD) to grow a-Si:H layers for both the front emitters and back contacts. Our improved a-Si:H back contacts contribute to our recent achievement of a confirmed 18.2% efficiency in double-heterojunction silicon solar cells on p-type textured silicon wafers [1]