Marika Edoff

A Detrimental Reaction at the Molybdenum Back Contact in Cu2ZnSn(S,Se)4 Thin-Film Solar Cells

Experimental proof is presented for a hitherto undetected solid-state reaction between the solar cell material Cu(2)ZnSn(S,Se)(4) (CZTS(e)) and the standard metallic back contact, molybdenum. Annealing experiments combined with Raman and transmission electron microscopy studies show that this aggressive reaction causes formation of MoS(2) and secondary phases at the CZTS|Mo interface during thermal processing. A reaction scheme is presented and discussed in the context of current state-of-the-art synthesis methods for CZTS(e). It is concluded that alternative back contacts will be important for future improvements in CZTS(e) quality.

A monolithic device for solar water splitting based on series interconnected thin film absorbers reaching over 10% solar-to-hydrogen efficiency

Efficient production of hydrogen from solar energy is anticipated to be an important component in a future sustainable post-carbon energy system. Here we demonstrate that series interconnected absorbers in a PV-electrolysis configuration based on the compound semiconductor CIGS, CuInxGa1−xSe2, are a highly interesting concept for solar water splitting applications. The band gap energy of CIGS can be adjusted to a value close to optimum for efficient absorption of the solar spectrum, but is too low to drive overall water splitting. Therefore we connect three cells in series, into a monolithic device, which provides sufficient driving force for the full reaction. Integrated with a catalyst this forms a stable PV/photo-electrochemical device, which when immersed in water reaches over 10% solar-to-hydrogen efficiency for unassisted water splitting. The results show that series interconnected device concepts, which enable use of a substantial part of the solar spectrum, provide a simple route towards highly efficient water splitting and could be used also for other solar absorbers with similar electro-optical properties. We discuss how the efficiency could be increased for this particular device, as well as the general applicability of the concepts used in this work. We also briefly discuss advantages and disadvantages of photo-electrochemical cells in relation to PV-electrolysis with respect to our results.

Diffusion of indium and gallium in Cu(In,Ga)Se2 thin film solar cells

The diffusion of indium and gallium in polycrystalline thin film Cu(In,Ga)Se2 layers has been investigated. Bilayer structures of CuInSe2 on top of CuGaSe2 and vice versa have been fabricated in both a Cu-rich and Cu-poor process (in relation to the ideal stoichiometry). In each process molybdenum coated soda-lime glass with and without a sodium barrier was used. These bilayers were analyzed with secondary ion mass spectrometry, X-ray diffraction, scanning electron microscope and transmission electron microscope equipped with energy dispersive X-ray spectroscopy. It was found that the grain boundary diffusion was not significantly higher than the diffusion inside the grains, also for Cu-rich layers. The diffusion is suggested to mainly proceed via vacant metal sites in the lattice structure. In sodium free films a higher diffusion into the bottom layers, compared to films with sodium, was seen in all cases. This observation was explained with a larger number of vacancies, that facilitates indium and gallium diffusion, in the sodium free films. The difference in diffusion between indium in CGS layers and gallium in CIS layers, in both Cu-rich and Cu-poor processes, was small for layers with sodium. q 2003 Elsevier Ltd. All rights reserved.

Direct evidence of current blocking by ZnSe in Cu2ZnSnSe4 solar cells

Thin films of polycrystalline Cu2ZnSnSe4 were made by selenization of co-sputtered metallic precursors and processed to solar cells. Electron beam induced current (EBIC) in combination with microsc ...

Sustainable solar hydrogen production: from photoelectrochemical cells to PV-electrolyzers and back again

Sustainable hydrogen production could, in principle, be accomplished along several different routes, where some of the most promising approaches involve utilization of solar energy. Photoelectroche ...

Employing Si solar cell technology to increase efficiency of ultra-thin Cu(In,Ga)Se2 solar cells

Reducing absorber layer thickness below 500 nm in regular Cu(In,Ga)Se2 (CIGS) solar cells decreases cell efficiency considerably, as both short-circuit current and open-circuit voltage are reduced because of incomplete absorption and high Mo/CIGS rear interface recombination. In this work, an innovative rear cell design is developed to avoid both effects: a highly reflective rear surface passivation layer with nano-sized local point contact openings is employed to enhance rear internal reflection and decrease the rear surface recombination velocity significantly, as compared with a standard Mo/CIGS rear interface. The formation of nano-sphere shaped precipitates in chemical bath deposition of CdS is used to generate nano-sized point contact openings. Evaporation of MgF2 coated with a thin atomic layer deposited Al2O3 layer, or direct current magnetron sputtering of Al2O3 are used as rear surface passivation layers. Rear internal reflection is enhanced substantially by the increased thickness of the passivation layer, and also the rear surface recombination velocity is reduced at the Al2O3/CIGS rear interface. (MgF2/)Al2O3 rear surface passivated ultra-thin CIGS solar cells are fabricated, showing an increase in short circuit current and open circuit voltage compared to unpassivated reference cells with equivalent CIGS thickness. Accordingly, average solar cell efficiencies of 13.5% are realized for 385 nm thick CIGS absorber layers, compared with 9.1% efficiency for the corresponding unpassivated reference cells.

Inline Cu(In,Ga)Se

In this paper, co-evaporation of Cu(In,Ga)Se2 (CIGS) in an inline single-stage process is used to fabricate solar cell devices with up to 18.6% conversion efficiency using a CdS buffer layer and 18.2% using a Zn1-xSnxOy Cd-free buffer layer. Furthermore, a 15.6-cm2 mini-module, with 16.8% conversion efficiency, has been made with the same layer structure as the CdS baseline cells, showing that the uniformity is excellent. The cell results have been externally verified. The CIGS process is described in detail, and material characterization methods show that the CIGS layer exhibits a linear grading in the [Ga]/([Ga]+[In]) ratio, with an average [Ga]/([Ga]+[In]) value of 0.45. Standard processes for CdS as well as Cd-free alternative buffer layers are evaluated, and descriptions of the baseline process for the preparation of all other steps in the Ångström Solar Center standard solar cell are given.

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An innovative rear contacting structure for copper indium gallium (di) selenide (CIGS) thin-film solar cells is developed in an industrially viable way and demonstrated in tangible devices. The idea stems from the silicon (Si) industry, where rear surface passivation layers are combined with micron-sized local point contacts to boost the open-circuit voltage (VOC) and, hence, cell efficiency. However, compared with Si solar cells, CIGS solar cell minority carrier diffusion lengths are several orders lower in magnitude. Therefore, the proposed CIGS cell design reduces rear surface recombination by combining a rear surface passivation layer and nanosized local point contacts. Atomic layer deposition of Al2O3 is used to passivate the CIGS surface and the formation of nanosphere-shaped precipitates in chemical bath deposition of CdS to generate nanosized point contact openings. The manufactured Al2O3 rear surface passivated CIGS solar cells with nanosized local rear point contacts show a significant improvement in VOC compared with unpassivated reference cells.

Co-evaporation for High-Efficiency Solar Cells and Modules

Recently, Cu(In,Ga)Se2 (CIGS) solar cells have achieved 21% world-record efficiency, partly due to the introduction of a postdeposition potassium treatment to improve the front interface of CIGS absorber layers. However, as high-efficiency CIGS solar cells essentially require long diffusion lengths, the highly recombinative rear of these devices also deserves attention. In this paper, an Al2O3 rear surface passivation layer with nanosized local point contacts is studied to reduce recombination at the standard Mo/CIGS rear interface. First, passivation layers with well-controlled grids of nanosized point openings are established by use of electron beam lithography. Next, rear-passivated CIGS solar cells with 240-nm-thick absorber layers are fabricated as study devices. These cells show an increase in open-circuit voltage (+57 mV), short-circuit current (+3.8 mA/cm2), and fill factor [9.5% (abs.)], compared with corresponding unpassivated reference cells, mainly due to improvements in rear surface passivation and rear internal reflection. Finally, solar cell capacitance simulator (SCAPS) modeling is used to calculate the effect of reduced back contact recombination on high-efficiency solar cells with standard absorber layer thickness. The modeling shows that up to 50-mV increase in open-circuit voltage is anticipated.

Improved Rear Surface Passivation of Cu(In,Ga)Se

Highly efficient Cu(In,Ga)(S,Se)2 photovoltaic thin film solar cells often have a compositional variation of Ga to In in the absorber layer, here described as a Ga-profile. In this work we have stu ...