| 1. |
- Donzel-Gargand, Olivier, et al.
(författare)
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Surface Modification And Secondary Phase Formation From a High Dose KF-Post Deposition Treatment of (Ag,Cu)(In,Ga)Se2 Solar Cell Absorbers
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Ingår i: Progress in Photovoltaics. - 1062-7995 .- 1099-159X.
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Tidskriftsartikel (refereegranskat)abstract
- In this study we assessed the potential of KF-Post Deposition Treatment (PDT) performed on a silver-alloyed Cu(Inx,Ga1-x)Se2 (ACIGS) solar absorber. ACIGS absorbers with Ag/Ag+Cu ratio (Ag/I) close to 20% were co-evaporated on a Mo-coated glass substrate and exposed to in-situ KF-PDT of various intensities. The current-voltage characteristics indicated that an optimized PDT can be beneficial, increasing in our study the median Voc and efficiency values by +48 mV and +0.9 %abs (from 728 mV and 16.1 % efficiency measured for the sample without PDT), respectively. However, an increased KF-flux during PDT resulted in a net deterioration of the performance leading to median Voc and efficiency values as low as 503 mV and 4.7 %. The chemical composition analysis showed that while the reference absorber without any PDT was homogeneous, the KF-PDT induced a clear change within the first 10 nm from the surface. Here, the surface layer composition was richer in K and In with an increased Ag/I ratio, and its thickness seemed to follow the KF exposure intensity. Additionally, high-dose KF-PDT resulted in substantial formation of secondary phases for the ACIGS. The secondary phase precipitates were also richer in Ag, K and In, and Electron and X-ray diffraction data match with the monoclinic C 1 2/c 1 space group adopted by the Ag-alloyed KInSe2 (AKIS) phase. It could not be concluded whether the performance loss for the solar cell devices originated from the thicker surface layer or the presence of secondary phases, or both for the high-dose KF-PDT sample.
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| 2. |
- Donzel-Gargand, Olivier, et al.
(författare)
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Cu-depleted patches induced by presence of K during growth of CIGS absorbers
- 2017
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Konferensbidrag (refereegranskat)abstract
- The conversion efficiency of the CIGS thin film solar cells has rapidly increased since introduction of the heavier alkali-doping (K, Rb, Cs). While the exclusive introduction of Na in the CIGS films has led to efficiencies up to 20,4% 1, the latest K, Rb or Cs post deposition treatments (PDT) have increased the efficiency to 22,6% 2. The exact role of this heavy-alkali PDT is still under discussion but three explanations have been discussed in the literature. First, that the heavy alkali PDT facilitates CdCu substitution, that results in an enhanced absorber type inversion, moving the p-n junction further into the CIGS bulk 3. Second, that the main effect from heavy alkali PDT is due to the formation of a K-In-Se2 layer, that passivates defects at the CIGS surface, reducing interface recombination 4. And third, that the heavy alkali PDT induces a Cu depletion at the surface of the CIGS which, by increasing the local Fermi level, increases the band bending; thus creating a higher potential barrier for holes to recombine 5.
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| 3. |
- Donzel-Gargand, Olivier, et al.
(författare)
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Deep surface Cu depletion induced by K in high-efficiency Cu(In,Ga)Se2 solar cell absorbers
- 2018
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Ingår i: Progress in Photovoltaics. - : Wiley. - 1062-7995 .- 1099-159X. ; 26:9, s. 730-739
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Tidskriftsartikel (refereegranskat)abstract
- In this work, we used K‐rich glass substrates to provide potassium during the coevaporation of Cu(In,Ga)Se2 (CIGS) absorber layers. Subsequently, we applied a postdeposition treatment (PDT) using KF or RbF to some of the grown absorbers. It was found that the presence of K during the growth of the CIGS layer led to cell effi- ciencies beyond 17%, and the addition of a PDT pushed it beyond 18%. The major finding of this work is the observation of discontinuous 100‐ to 200‐nm‐deep Cu‐ depleted patches in the vicinity of the CdS buffer layer, correlated with the presence of K during the growth of the absorber layer. The PDT had no influence on the forma- tion of these patches. A second finding concerns the composition of the Cu‐depleted areas, where an anticorrelation between Cu and both In and K was measured using scanning transmission electron microscopy. Furthermore, a steeper Ga/(In+Ga) ratio gradient was measured for the absorbers grown with the presence of K, suggesting that K hinders the group III element interdiffusion. Finally, no Cd in‐diffusion to the CIGS layer could be detected. This indicates that if CdCu substitution occurs, either their concentration is below our instrumental detection limit or its presence is contained within the first 6 nm from the CdS/CIGS interface.
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| 4. |
- Keller, Jan, et al.
(författare)
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Rubidium Fluoride Absorber Treatment for Wide-Gap (Ag,Cu)(In,Ga)Se-2 Solar Cells
- 2022
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Ingår i: Solar RRL. - : John Wiley & Sons. - 2367-198X. ; 6:6
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Tidskriftsartikel (refereegranskat)abstract
- This contribution studies the potential of an RbF postdeposition treatment (RbF-PDT) of wide-gap (Ag,Cu)(In,Ga)Se-2 (ACIGS) absorbers to improve the corresponding solar cell performance. While a higher open-circuit voltage (V-OC) and short-circuit current density are achieved, a lower fill factor (FF) is observed for most of the devices subjected to an RbF-PDT. However, the drop in FF can be avoided for some close-stoichiometric samples, leading to maximum efficiencies beyond 16% (without antireflection coating) at a bandgap energy (E-g) of 1.43 eV. For off-stoichiometric ACIGS, a record V-OC value of 926 mV at E-g = 1.44 eV is reached. Lower V-OC deficits likely require enhanced bulk quality of wide-gap chalcopyrite absorbers. Extensive material analysis shows that the heavy alkali PDT of ACIGS with high Ag and Ga contents leads to similar absorber modifications as commonly observed for low-gap Cu(In,Ga)Se-2 (CIGS). Rubidium is continuously distributed at "internal" (grain boundaries) and "external" (buffer and back contact) absorber interfaces. The results indicate that Rb diffusion into the absorber bulk (including 1:1:2 and 1:3:5 compounds) is restricted. Furthermore, the formation of a very thin RbInSe2 surface layer is suggested. It remains open, which effects alter the device characteristics after RbF-PDT.
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| 5. |
- Edoff, Marika, 1965-, et al.
(författare)
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High Voc in (Cu,Ag)(In,Ga)Se2 Solar Cells
- 2017
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Ingår i: IEEE Journal of Photovoltaics. - 2156-3381 .- 2156-3403. ; 7:6, s. 1789-1794
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Tidskriftsartikel (refereegranskat)abstract
- In this contribution, we show that silver substitution for copper in Cu(In,Ga)Se-2 (CIGS) to form (Ag,Cu)(In, Ga)Se-2 (ACIGS) leads to a reduction of the voltage loss expressed as E-g/q-V-oc. This, in turn, leads to higher device efficiencies as compared to similar CIGS devices without Ag. We report V-oc at 814 mV at a conversion efficiency of 21% for our best ACIGS device with 20% of the group I element consisting of silver. Comparing ACIGS and CIGS devices with the same Ga/(Ga+ In) ratio, the ACIGS devices exhibit about 0.05 eV higher bandgap. Alkali postdeposition treatment with KF leads to improvements in efficiency both for CIGS and ACIGS, but we find that the dose of KF needed for optimum device for ACIGS is 10-20% of the dose used for CIGS.
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| 6. |
- Keller, Jan, et al.
(författare)
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Direct comparison of atomic layer deposition and sputtering of In2O3:H used as transparent conductive oxide layer in CuIn1-xGaxSe2 thin film solar cells
- 2016
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Ingår i: Solar Energy Materials and Solar Cells. - : Elsevier BV. - 0927-0248 .- 1879-3398. ; 157, s. 757-764
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Tidskriftsartikel (refereegranskat)abstract
- In this study thin films of hydrogenated In2O3 (IOH) were fabricated by physical vapor deposition (PVD) with and without a post-annealing step, and by atomic layer deposition (ALD). The electro-optical properties on glass as well as the performance as a transparent conductive oxide (TCO) layer in CuIn1-xGaxSe2 (CIGSe)-based solar cells are compared and related to a ZnO:Al (AZO) baseline TCO. Corresponding TCO film thicknesses were adjusted to a resulting sheet resistance of about R-sh = 20 Omega/sq for all samples. Structural investigations were conducted by X-ray diffraction (XRD) and transmission electron microscopy (TEM), while Hall and optical absorption measurements were performed to analyze the electrical and optical quality of the window layers. It is shown that the fully crystallized IOH layers processed by ALD and PVD show similar microstructural and electro-optical properties, which are superior to the AZO baseline. The finalized solar cells were characterized by current-voltage and reflectance-corrected quantum efficiency measurements. While there is no significant gain in short circuit current density (J(sc)) for as-deposited PVD In2O3 layers, the application of crystalline In2O3 TCOs leads to an improvement of more than 2 mA/cm(2) due to an increase in "optical" band gap energy and less free charge carrier absorption (FCA). The open circuit voltage (V-oc) of the best cells is 10-15 mV higher as compared to the AZO reference, independent of the crystallinity and process of the In2O3 films. The results indicate that the gain in V-oc is due to inherent material properties of the IOH films and does not originate from less sputter damage or an affected i-ZnO/TCO interface. Device simulations show that the higher electron affinity chi of the IOH can explain an increased V-oc if the Fermi level (E-F) is pinned at the CIGSe/CdS interface and why it might not be possible to see the gain when alternative buffer layers are applied.
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| 7. |
- Keller, Jan, et al.
(författare)
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On the Paramount Role of Absorber Stoichiometry in (Ag,Cu)(In,Ga)Se2 Wide‐Gap Solar Cells
- 2020
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Ingår i: Solar RRL. - : Wiley. - 2367-198X. ; 4:12
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Tidskriftsartikel (refereegranskat)abstract
- This contribution evaluates the effect of absorber off‐stoichiometry in wide‐gap (Ag,Cu)(In,Ga)Se2 (ACIGS) solar cells. It is found that ACIGS films show an increased tendency to form ordered vacancy compounds (OVCs) with increasing Ga and Ag contents. Very little tolerance to off‐stoichiometry is detected for absorber compositions giving the desired properties of 1) an optimum bandgap (EG) for a top cell in tandem devices (EG = 1.6–1.7 eV) and at the same time 2) a favorable band alignment with a CdS buffer layer. Herein, massive formation of either In‐ or Ga‐enriched OVC patches is found for group I‐poor ACIGS. As a consequence, carrier transport and charge collection are significantly impeded in corresponding solar cells. The transport barrier appears to be increasing with storage time, questioning the long‐term stability of wide‐gap ACIGS solar cells. Furthermore, the efficiency of samples with very high Ga and Ag contents depends on the voltage sweep direction. It is proposed that the hysteresis behavior is caused by a redistribution of mobile Na ions in the 1:1:2 absorber lattice upon voltage bias. Finally, a broader perspective on OVC formation in the ACIGS system is provided and fundamental limitations for wide‐gap ACIGS solar cells are discussed.
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| 8. |
- Bayrak Pehlivan, Ilknur, et al.
(författare)
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NiMoV and NiO-based catalysts for efficient solar-driven water splitting using thermally integrated photovoltaics in a scalable approach
- 2021
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Ingår i: iScience. - : Cell Press. - 2589-0042. ; 24:1
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Tidskriftsartikel (refereegranskat)abstract
- In this work, a trimetallic NiMoV catalyst is developed for the hydrogen evolution reaction and characterized with respect to structure, valence, and elemental distribution. The overpotential to drive a 10 mA cm−2 current density is lowered from 94 to 78 mV versus reversible hydrogen electrode by introducing V into NiMo. A scalable stand-alone system for solar-driven water splitting was examined for a laboratory-scale device with 1.6 cm2 photovoltaic (PV) module area to an up-scaled device with 100 cm2 area. The NiMoV cathodic catalyst is combined with a NiO anode in alkaline electrolyzer unit thermally connected to synthesized (Ag,Cu) (In,Ga)Se2 ((A)CIGS) PV modules. Performance of 3- and 4-cell interconnected PV modules, electrolyzer, and hydrogen production of the PV electrolyzer are examined between 25°C and 50°C. The PV-electrolysis device having a 4-cell (A)CIGS under 100 mW cm−2 illumination and NiMoV-NiO electrolyzer shows 9.1% maximum and 8.5% averaged efficiency for 100 h operation.
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| 9. |
- Bodegard, Marika, et al.
(författare)
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The behaviour of Na implanted into Mo thin films during annealing
- 1999
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Ingår i: SOLAR ENERGY MATERIALS AND SOLAR CELLS. - 0927-0248. ; 58:2, s. 199-208
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Tidskriftsartikel (refereegranskat)abstract
- Na implants have been used to study diffusion of Na in rf diode sputtered Mo thin films used as back contacts for Cu(In,Ga)Se, solar cells. The samples were analysed with secondary ion mass spectrometry before and after vacuum anneals at 420 degrees C and
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| 10. |
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