A method of manufacturing improved thin-film solar cells entirely by sputtering includes a high efficiency back contact/reflecting multi-layer containing at least one barrier layer consisting of a transition metal nitride. A copper indium gallium diselenide (Cu(InxGal-X)Se2) absorber layer (X ranging from 1 to approximately 0.7) is co-sputtered from specially prepared electrically conductive targets using dual cylindrical rotary magnetron technology. The band gap of the absorber layer can be graded by varying the gallium content, and by replacing the gallium partially or totally with aluminum. Alternately the absorber layer is reactively sputtered from metal alloy targets in the presence of hydrogen selenide gas. RF sputtering is used to deposit a non-cadmium containing window layer of ZnS. The top transparent electrode is reactively sputtered aluminum doped ZnO. A unique modular vacuum roll-to-roll sputtering machine is described. The machine is adapted to incorporate dual cylindrical rotary magnetron technology to manufacture the improved solar cell material in a single pass.

Manufacturing apparatus and method for large-scale production of thin-film solar cells

Technological aspects of flexible CIGS solar cells and modules

A method of fabricating an organic film is provided. A non-reactive carrier gas is used to transport an organic vapor. The organic vapor is ejected through a nozzle block onto a cooled substrate, to form a patterned organic film. A device for carrying out the method is also provided. The device includes a source of organic vapors, a source of carrier gas and a vacuum chamber. A heated nozzle block attached to the source of organic vapors and the source of carrier gas has at least one nozzle adapted to eject carrier gas and organic vapors onto a cooled substrate disposed within the vacuum chamber.

Process and apparatus for organic vapor jet deposition

Among the armoury of photovoltaic materials, thin film heterojunction photovoltaics continue to be a promising candidate for solar energy conversion delivering a vast scope in terms of device design and fabrication. Their production does not require expensive semiconductor substrates and high temperature device processing, which allows reduced cost per unit area while maintaining reasonable efficiency. In this regard, superstrate CdTe/CdS solar cells are extensively investigated because of their suitable bandgap alignments, cost effective methods of production at large scales and stability against proton/electron irradiation. The conversion efficiencies in the range of 6–20% are achieved by structuring the device by varying the absorber/window layer thickness, junction activation/annealing steps, with more suitable front/back contacts, preparation techniques, doping with foreign ions, etc. This review focuses on fundamental and critical aspects like: (a) choice of CdS window layer and CdTe absorber layer; (b) drawbacks associated with the device including environmental problems, optical absorption losses and back contact barriers; (c) structural dynamics at CdS–CdTe interface; (d) influence of junction activation process by CdCl2 or HCF2Cl treatment; (e) interface and grain boundary passivation effects; (f) device degradation due to impurity diffusion and stress; (g) fabrication with suitable front and back contacts; (h) chemical processes occurring at various interfaces; (i) strategies and modifications developed to improve their efficiency. The complexity involved in understanding the multiple aspects of tuning the solar cell efficiency is reviewed in detail by considering the individual contribution from each component of the device. It is expected that this review article will enrich the materials aspects of CdTe/CdS devices for solar energy conversion and stimulate further innovative research interest on this intriguing topic.

Physics and chemistry of CdTe/CdS thin film heterojunction photovoltaic devices: fundamental and critical aspects

CIGS absorber layers fabricated using coated semiconducting nanoparticles and/or quantum dots are disclosed. Core nanoparticles and/or quantum dots containing one or more elements from group IB and/or IIIA and/or VIA may be coated with one or more layers containing elements group IB, IIIA or VIA. Using nanoparticles with a defined surface area, a layer thickness could be tuned to give the proper stoichiometric ratio, and/or crystal phase, and/or size, and/or shape. The coated nanoparticles could then be placed in a dispersant for use as an ink, paste, or paint. By appropriate coating of the core nanoparticles, the resulting coated nanoparticles can have the desired elements intermixed within the size scale of the nanoparticle, while the phase can be controlled by tuning the stochiometry, and the stoichiometry of the coated nanoparticle may be tuned by controlling the thickness of the coating(s).

Coated nanoparticles and quantum dots for solution-based fabrication of photovoltaic cells

A new, large-area, thin-film, flexible photovoltaic structure is disclosed, as well as a general fabrication procedure, including a preferably roll-to-roll-type, process-chamber-segregated, “continuous-motion”, method for producing such a structure. A special multi-material vapor-deposition environment is disclosed to implement an important co-evaporation, layer-deposition procedure performed in and as part of the fabrication procedure. A structural system adapted to create a vapor environment generally like that just referred to is disclosed, as is an organization of method steps involved in the generation of such a vapor environment. Also, a unique, vapor-creating, materials-distributing system, which includes specially designed heated crucibles with carefully arranged, spatially distributed, localized and generally point-like, heated-nozzle sources of different metallic vapors, and a special multi-fingered, comb-like, vapor-delivering manifold structure is shown.

Fabrication of thin-film, flexible photovoltaic module

Thin-film, flexible photovoltaic module

The reaction pathways to form Cu(InGa)Se2 or Cu(InGa)S2 films at 450°C from metallic precursors were evaluated by reacting Cu–In–Ga films in H2Se or H2S for 10, 30, or 90min and characterizing the phase composition of the resulting films. A starting composition comprising Cu9(In0.64Ga0.36)4 and In phases was detected by x-ray diffraction in Cu–Ga–In precursors annealed at 450°C in an Ar atmosphere. When the precursors were reacted in H2Se, a graded Cu(InGa)Se2 film was formed with a Ga-rich composition and residual Cu–Ga intermetallics at the interface with the Mo back contact. The intermetallic compounds were observed to evolve from Cu9(In0.64Ga0.36)4 to Cu9Ga4 with increasing selenization time. Reaction in H2S formed inhomogeneous Cu(InGa)S2 with Cu–In intermetallics. The results are consistent with thermochemical predictions of the preferential reaction of In with Se, and Ga with S. These reaction preferences can explain the formation of a graded Cu(InGa)Se2 film during reaction in H2Se and provide a r...

Incongruent reaction of Cu–(InGa) intermetallic precursors in H2Se and H2S

Control of the through-film composition and adhesion are critical issues for Cu(In,Ga)Se2 (CIGS) and/or Cu(In,Ga)(Se,S)2 (CIGSS) films formed by the reaction of Cu–In–Ga metal precursor films in H2Se or H2S. In this work, CIGSS films with homogenous Ga distribution and good adhesion were formed using a three-step reaction involving: (1) selenization in H2Se at 400 °C for 60 min, (2) temperature ramp-up to 550 °C and annealing in Ar for 20 min, and (3) sulfization in H2S at 550 °C for 10 min. The 1st selenization step led to fine grain microstructure with Ga accumulation near the Mo back contact, primarily in a Cu9(In1−xGax)4 phase. The 2nd Ar anneal step produces significant grain growth with homogenous through-film Ga distribution and the formation of an InSe binary compound near the Mo back contact. The 3rd sulfization step did not result in any additional change in Ga distribution or film microstructure but a small S incorporation near the CIGSS film surface and complete reaction of InSe to form CIGSS were observed. The three-step process facilitates good control of the film properties by separating different effects of the reaction process and a film growth model is proposed. Finally, CIGSS solar cells with the three-step reaction were fabricated and devices with efficiency = 14.2% and VOC = 599 mV were obtained.

Gregory M. Hanket

Papers

Fabrication of thin-film, flexible photovoltaic module

Thin-film, flexible photovoltaic module

Incongruent reaction of Cu–(InGa) intermetallic precursors in H2Se and H2S

Three-step H2Se/Ar/H2S reaction of Cu-In-Ga precursors for controlled composition and adhesion of Cu(In,Ga)(Se,S)2 thin films

The electronic structure of Cu(In1 − xGax)Se2 alloyed with silver