Development of solution processed, flexible, CuInSe₂ nanocrystal solar cells

Clean sources of energy, especially photovoltaics (PVs), are urgently needed to cope with global energy shortage and environmental pollution. For PVs to play a significant role in energy production, the current prices must be brought down. Thin film PVs made using layered Mo or Au/CuInGaSe₂(CIGS)/CdS/ZnO/ITO have already shown high efficiencies. Traditionally, most layers in CIGS solar cells are deposited using high-cost techniques requiring high temperatures and ultra-low pressures. By replacing the traditionally processed CIGS with a nanocrystal layer that can be deposited at mild processing conditions, the fabrication cost can be reduced. In this study, a high yielding synthesis method for CuInSe₂ nanocrystals has been developed which gives the best efficiency (3.1%), so far, for low-temperature processed CuInSe₂ nanocrystal PVs. An important challenge that nanocrystal solar cells currently face is low device efficiency, resulting in higher operating cost. CuInSe₂ nanocrystals can remain suspended in solution because of the long chain organic ligands attached to the surface. However, these ligands hinder charge transfer between nanocrystals causing low device efficiency. These ligands have been successfully replaced with smaller sulfide ions thereby improving the best efficiency of low-temperature processed CuInSe₂ nanocrystal solar cells from 3.1 % to 3.5%. Another approach to reducing the cost of CuInSe₂ PVs is by replacing the glass support medium with cheaper alternatives like paper. Flexible CuInSe₂ nanocrystal solar cells are successfully fabricated on paper with efficiencies reaching up to 2.25%. This is the first time a nanocrystal solar cell has been fabricated on paper. There is no significant loss in PV device performance after more than 100 flexes to 5 mm radius, and the devices continue to perform when folded into a crease. Apart from the absorber layer, the replacement of other high-temperature and vacuum processed device layers with ambient solution-processed layers lowers the manufacturing cost. This has been achieved by spin coating suitable nanomaterials as device layers. Lastly, for commercialization of CuInSe₂ nanocrystal solar cells, multiple devices need to be connected to achieve the desired current and voltage. A fabrication process has been developed for building multiple nanocrystal PVs on a single substrate using 3D printed masksChemical Engineerin

Uniform selenization of crack-free films of Cu(In,Ga)Se2 nanocrystals

Crack-free films of Cu(In,Ga)Se2 (CIGS) nanocrystals were deposited with uniform thickness (>1 μm) on Mo-coated glass substrates using an ink-based, automated ultrasonic spray process, then selenized and incorporated into photovoltaic devices (PVs). The device performance depended strongly on the homogeneity of the selenized films. Cracks in the spray-deposited films resulted in uneven selenization rates and sintering by creating paths for rapid, uncontrollable selenium (Se) vapor penetration. To make crack-free films, the nanocrystals had to be completely coated with capping ligands in the ink. The selenization rate of crack-free films then depended on the thickness of the nanocrystal layer, the temperature, and duration of Se vapor exposure. Either inadequate or excessive Se exposure leads to poor device performance, generating films that were either partially sintered or exhibited significant accumulation of carbon and selenium. The deposition of uniform nanocrystal films is expected to be important for a variety of electronic and optoelectronic device applications.Fil: Harvey, Taylor B.. Texas A&M University; Estados UnidosFil: Bonafé, Franco Paúl. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; ArgentinaFil: Updegrave, Ty. University of Texas at Austin; Estados UnidosFil: Voggu, Vikas Reddy. University of Texas at Austin; Estados UnidosFil: Thomas, Cherrelle. University of Texas at Austin; Estados UnidosFil: Kamarajugadda, Sirish C.. University of Texas at Austin; Estados UnidosFil: Stolle, C. Jackson. University of Texas at Austin; Estados UnidosFil: Pernik, Douglas. University of Texas at Austin; Estados UnidosFil: Du, Jiang. University of Texas at Austin; Estados UnidosFil: Korgel, Brian A.. University of Texas at Austin; Estados Unido

Orientationally ordered silicon nanocrystal cuboctahedra in superlattices

This is an open access article published under an ACS AuthorChoice License. See Standard ACS AuthorChoice/Editors' Choice Usage Agreement - https://pubs.acs.org/page/policy/authorchoice_termsofuse.htmlUniform silicon nanocrystals were synthesized with cuboctahedral shape and passivated with 1-dodecene capping ligands. Transmission electron microscopy, electron diffraction, and grazing incidence wide-angle and small-angle X-ray scattering show that these soft cuboctahedra assemble into face-centered cubic superlattices with orientational order. The preferred nanocrystal orientation was found to depend on the orientation of the superlattices on the substrate, indicating that the interactions with the substrate and assembly kinetics can influence the orientation of faceted nanocrystals in superlattices

Bubble Assemblies of Nanocrystals: Superlattices without a Substrate

A method was developed to create free-standing nanocrystal films in the form of solidified bubbles. Bubbles of octadecanethiol-capped gold nanocrystals were studied by in situ grazing incidence small-angle X-ray scattering (GISAXS) to determine how the absence of an underlying substrate influences a disorder–order transition of a nanocrystal superlattice. We find that the presence of the substrate does not significantly change the nature of the disorder–order transition but does lead to reduced interparticle separation and reduced thermal expansion. Bubble assemblies of silicon and copper selenide nanocrystals are also demonstrated

Orientationally ordered silicon nanocrystal cuboctahedra in superlattices

This is an open access article published under an ACS AuthorChoice License. See Standard ACS AuthorChoice/Editors' Choice Usage Agreement - https://pubs.acs.org/page/policy/authorchoice_termsofuse.htmlUniform silicon nanocrystals were synthesized with cuboctahedral shape and passivated with 1-dodecene capping ligands. Transmission electron microscopy, electron diffraction, and grazing incidence wide-angle and small-angle X-ray scattering show that these soft cuboctahedra assemble into face-centered cubic superlattices with orientational order. The preferred nanocrystal orientation was found to depend on the orientation of the superlattices on the substrate, indicating that the interactions with the substrate and assembly kinetics can influence the orientation of faceted nanocrystals in superlattices

Cooling Dodecanethiol-Capped 2 nm Diameter Gold Nanocrystal Superlattices below Room Temperature Induces a Reversible Order–Disorder Structure Transition

We recently observed that a disordered assembly of octadecanethiol-capped gold (Au) nanocrystals can order when heated from room temperature to 60 °C [Yu, Y.; Jain, A.; Guillaussier, A.; Voggu, V. R.; Truskett, T. M.; Smilgies, D.-M.; Korgel, B. A. <i>Faraday Discuss.</i> <b>2015</b>, <i>181</i>, 181–192]. This “inverse melting” structural transition was reversible and occurred near the melting-solidification temperature of the capping ligands. To determine the generality of this phenomenon, we studied by in situ grazing incidence small-angle X-ray scattering (GISAXS) the structure of assemblies of Au nanocrystals with shorter C₁₂ and C₅ alkanethiol capping ligands that form ordered superlattices at room temperature and have a ligand melting-solidification temperature below room temperature. Superlattices of dodecanethiol-capped Au nanocrystals disorder when cooled below 260 K, which is the melting-solidification temperature for dodecanethiol. Au nanocrystals capped with even shorter pentanethiol ligands that have a melting transition below 100 K (the lowest experimentally accessible temperature) do not undergo the disorder transition

Flexible CuInSe₂ Nanocrystal Solar Cells on Paper

Solar cells on paper have the potential to be inexpensive and portable due to several unique features of the substrate: paper is cheap, flexible, lightweight, biodegradable, and manufactured by roll-to-roll processing. Here, we report the first nanocrystal photovoltaic devices (PVs) made on paper. Using spray-deposited CuInSe₂ nanocrystals as the absorber material on substrates composed of bacterial cellulose nanofibers synthesized by the microorganism <i>Gluconacetobacter hansenii</i>, these devices demonstrate exceptional electrical and mechanical integrity. There is no significant loss in PV device performance after more than 100 flexes to 5 mm radius, and the devices continue to perform when folded into a crease. The practical use of these paper PVs is demonstrated with a prototype device powering liquid crystal displays (LCDs) mounted to various kinds of surfaces

Silicon Nanocrystal Superlattice Nucleation and Growth

Colloidal dodecene-passivated silicon (Si) nanocrystals were dispersed in hexane or chloroform and deposited onto substrates as face-centered cubic superlattices by slowly evaporating the solvent. The uniformity of the nanocrystals enables extended order; however, the solvent and the evaporation protocol significantly influence the self-assembly process, determining the morphology of the films, the extent of order, and the superlattice orientation on the substrate. Chloroform yielded superlattices with step-flow growth morphologies and (111)_SL, (100)_SL, and (110)_SL orientations. Hexane led to mostly island morphologies when evaporated at room temperature with exclusively (111)_SL orientations. Higher evaporation temperatures led to more extensive step-flow deposition. A model for the surface diffusion of nanocrystals adsorbed on the superlattice surface is developed

Orientationally Ordered Silicon Nanocrystal Cuboctahedra in Superlattices

Uniform silicon nanocrystals were synthesized with cuboctahedral shape and passivated with 1-dodecene capping ligands. Transmission electron microscopy, electron diffraction, and grazing incidence wide-angle and small-angle X-ray scattering show that these soft cuboctahedra assemble into face-centered cubic superlattices with orientational order. The preferred nanocrystal orientation was found to depend on the orientation of the superlattices on the substrate, indicating that the interactions with the substrate and assembly kinetics can influence the orientation of faceted nanocrystals in superlattices