4 research outputs found
Alkali-Templated Surface Nanopatterning of Chalcogenide Thin Films: A Novel Approach Toward Solar Cells with Enhanced Efficiency
Concepts of localized contacts and
junctions through surface passivation layers are already advantageously
applied in Si wafer-based photovoltaic technologies. For Cu(In,Ga)Se<sub>2</sub> thin film solar cells, such concepts are generally not applied,
especially at the heterojunction, because of the lack of a simple
method yielding features with the required size and distribution.
Here, we show a novel, innovative surface nanopatterning approach
to form homogeneously distributed nanostructures (<30 nm) on the
faceted, rough surface of polycrystalline chalcogenide thin films.
The method, based on selective dissolution of self-assembled and well-defined
alkali condensates in water, opens up new research opportunities toward
development of thin film solar cells with enhanced efficiency
Sodium Assisted Sintering of Chalcogenides and Its Application to Solution Processed Cu<sub>2</sub>ZnSn(S,Se)<sub>4</sub> Thin Film Solar Cells
Cu<sub>2</sub>ZnSn(S,Se)<sub>4</sub> thin layers processed from
solution-deposited earth-abundant precursors emerge as absorber materials
for low-cost thin film solar cells. A frequently observed drawback
of the chemical solution processingpoor crystallinity of the
chalcogenide absorbercan be overcome by employing a sodium-containing
reactive agent. We demonstrate a massive improvement in grain growth
in the presence of sodium. It enhances the surface chemisorption of
selenium molecules and can promote the formation of liquid Na<sub>2</sub>Se<sub><i>x</i></sub> phases during reactive annealing
of the precursor. The sodium is also incorporated into the semiconductor
absorber and significantly modifies its electronic properties. By
adjusting the sodium precursor quantity, it is possible to tune doping
levels and gradients to maximize the collection of photogenerated
carriers in thin film Cu<sub>2</sub>ZnSn(S,Se)<sub>4</sub> solar cells.
The presented approach can be extended to other solution-processed
metal chalcogenides to enhance their structural and electronic properties,
which are critical for applications such as thin film solar cells
and transistors
Refractive indices of layers and optical simulations of Cu(In,Ga)Se<sub>2</sub> solar cells
<p>Cu(In,Ga)Se<sub>2</sub>
-based solar cells have reached efficiencies close to 23%. Further knowledge-driven improvements require accurate determination of the material properties. Here, we present refractive indices for all layers in Cu(In,Ga)Se<sub>2</sub> solar cells with high efficiency. The optical bandgap of Cu(In,Ga)Se<sub>2</sub> does not depend on the Cu content in the explored composition range, while the absorption coefficient value is primarily determined by the Cu content. An expression for the absorption spectrum is proposed, with Ga and Cu compositions as parameters. This set of parameters allows accurate device simulations to understand remaining absorption and carrier collection losses and develop strategies to improve performances.</p
Formation of a KInSe Surface Species by NaF/KF Postdeposition Treatment of Cu(In,Ga)Se<sub>2</sub> Thin-Film Solar Cell Absorbers
A NaF/KF
postdeposition treatment (PDT) has recently been employed to achieve
new record efficiencies of Cu(In,Ga)Se<sub>2</sub> (CIGSe) thin film
solar cells. We have used a combination of depth-dependent soft and
hard X-ray photoelectron spectroscopy as well as soft X-ray absorption
and emission spectroscopy to gain detailed insight into the chemical
structure of the CIGSe surface and how it is changed by different
PDTs. Alkali-free CIGSe, NaF-PDT CIGSe, and NaF/KF-PDT CIGSe absorbers
grown by low-temperature coevaporation have been interrogated. We
find that the alkali-free and NaF-PDT CIGSe surfaces both display
the well-known Cu-poor CIGSe chemical surface structure. The NaF/KF-PDT,
however, leads to the formation of bilayer structure in which a KInSe
species covers the CIGSe compound that in composition is identical
to the chalcopyrite structure of the alkali-free and NaF-PDT absorber