Impact of Sb and Na Doping on the Surface Electronic Landscape of Cu2ZnSnS4 Thin Films

Open-circuit voltage deficiency is the key limiting factor in Cu2ZnSnS4 (CZTS) thin-film solar cells, which is commonly associated with band tails and deep gap states arising from elemental disorder. The introduction of dopants such as Na and Sb has led to improvement in device performance, yet their effects on the optoelectronic properties of CZTS are yet to be fully elucidated. In this Letter, we unraveled the effect of Sb and Na:Sb co-doping on the surface energy landscape of solution-processed CZTS films employing energy-filtered photoelectron emission microscopy. In the absence of the additives, 150 nm resolution photoemission maps reveal oscillations in the local effective work function as well as areas of low photoemission energy threshold. The introduction of dopants substantially reshapes the photoemission maps, which we rationalize in terms of Cu:Zn and Sn disorder. Finally, we establish unprecedented correlations between the photoemission landscape of thin films and the performance of over 200 devices

“Cross” Supermicelles via the Hierarchical Assembly of Amphiphilic Cylindrical Triblock Comicelles

Self-assembled “cross” architectures are well-known in biological systems (as illustrated by chromosomes, for example); however, comparable synthetic structures are extremely rare. Herein we report an in depth study of the hierarchical assembly of the amphiphilic cylindrical P–H–P triblock comicelles with polar (P) coronal ends and a hydrophobic (H) central periphery in a selective solvent for the terminal segments which allows access to “cross” supermicelles under certain conditions. Well-defined P–H–P triblock comicelles M­(PFS-<i>b</i>-PtBA)-<i>b</i>-M­(PFS-<i>b</i>-PDMS)-<i>b</i>-M­(PFS-<i>b</i>-PtBA) (M = micelle segment, PFS = polyferrocenyldimethylsilane, PtBA = poly­(<i>tert</i>-butyl acrylate), and PDMS = polydimethylsiloxane) were created by the living crystallization-driven self-assembly (CDSA) method. By manipulating two factors in the supermicelles, namely the H segment-solvent interfacial energy (through the central H segment length, <i>L</i>₁) and coronal steric effects (via the PtBA corona chain length in the P segment, <i>L</i>₂ related to the degree of polymerization DP₂) the aggregation of the triblock comicelles could be finely tuned. This allowed a phase-diagram to be constructed that can be extended to other triblock comicelles with different coronas on the central or end segment where “cross” supermicelles were exclusively formed under predicted conditions. Laser scanning confocal microscopy (LSCM) analysis of dye-labeled “cross” supermicelles, and block “cross” supermicelles formed by addition of a different unimer to the arm termini, provided complementary characterization to transmission electron microscopy (TEM) and dynamic light scattering (DLS) and confirmed the existence of these “cross” supermicelles as kinetically stable, micron-size colloidally stable structures in solution

Modifying the Morphology of Silicon Surfaces by Laser Induced Liquid Assisted Colloidal Lithography

Single, or isolated small arrays of, spherical silica colloidal particles (with refractive index ncolloid = 1.47 and radius R = 350 nm or 1.5 μm) were placed on a silicon substrate and immersed in carbon tetrachloride (nliquid = 1.48) or toluene (nliquid = 1.52). Areas of the sample were then exposed to a single laser pulse (8 ps duration, wavelength λ = 355 nm), and the spatial intensity modulation of the near field in the vicinity of the particles revealed via the resulting patterning of the substrate surface. In this regime, ncolloid &lt; nliquid and the near-field optical intensification is concentrated at and beyond the edge of the particle. Detailed experimental characterization of the irradiated Si surface using atomic force microscopy reveals contrasting topographies. The same optical behavior is observed with both liquids, i.e., the incident laser light diverges on interaction with the colloidal particle, but the resulting interaction with the substrate is liquid dependent. Topographic analysis indicates localized ablation and patterning of the Si substrate when using toluene, whereas the patterning induced under carbon tetrachloride is on a larger scale and extends well below the original substrate surface—hinting at a laser induced photochemical contribution to the surface patterning

Green and sustainable devulcanization of ground tire rubber using choline chloride–urea deep eutectic solvent †

This work describes the devulcanization of ground tire rubber (GTR) with particle sizes ranging from 0.6 to 0.122 mm using a non-toxic, biodegradable, and biocompatible deep eutectic solvent (DES) based on choline chloride and urea. In addition to reducing the environmental impact of the process, other goals of this study were to minimize time and energy consumption. To meet these targets, a new de-vulcanization method has been developed. The methodology consists of using probe and bath sonication. The de-vulcanized rubber samples were then characterized using attenuated total reflectance Fourier-transform infrared spectroscopy (ATR-FTIR), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), electron dispersive X-ray spectroscopy (EDX) and atomic force microscopy (AFM). Flory–Rehner and Horikx analyses were also carried out to calculate the devulcanization percentage and investigate the successful devulcanization of the samples through selective crosslink scission. The results showed that rubber samples of 120 mesh (0.122 mm) were devulcanized up to 58% by using 182 W power only during a 30 minutes process

High-speed AFM with a light touch

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