Demonstration of a Gel-Polymer Electrolyte-Based Electrochromic Device Outperforming Its Solution-Type Counterpart in All Merits: Architectural Benefits of CeO₂ Quantum Dot and Nanorods

For years, solution-type electrochromic devices (ECDs) have intrigued researchers’ interest and eventually rendered themselves into commercialization. Regrettably, challenges such as electrolyte leakage, high flammability, and complicated edge-encapsulation processes limit their practical utilization, hence necessitating an efficient alternate. In this quest, although the concept of solid/gel-polymer electrolyte (SPE/GPE)-based ECDs settled some issues of solution-type ECDs, an array of problems like high operating voltage, sluggish response time, and poor cycling stability have paralyzed their commercial applicability. Herein, we demonstrate a choreographed-CeO2-nanofiller-doped GPE-based ECD outperforming its solution-type counterpart in all merits. The filler-incorporated polymer electrolyte assembly was meticulously weaved through the electrospinning method, and the resultant host was employed for immobilizing electrochromic viologen species. The filler engineering benefits conceived through the tuned shape of CeO2 nanorod and quantum dots, along with the excellent redox shuttling effect of Ce3+/Ce4+, synchronously yielded an outstanding class of GPE, which upon utilization in ECDs delivered impressive electrochromic properties. A combination of features possessed by a particular device (QD-NR/PVDF-HFP/IL/BzV-Fc ECD) such as exceptionally low driving voltage (0.9 V), high transmittance change (ΔT, ∼69%), fast response time (∼1.8 s), high coloration efficiency (∼339 cm2/C), and remarkable cycling stability (∼90% ΔT-retention after 25,000 cycles) showcased a striking potential in the yet-to-realize market of GPE-based ECDs. This study unveils the untapped potential of choreographed nanofillers that can promisingly drive GPE-based ECDs to the doorstep of commercialization

Demonstration of a Gel-Polymer Electrolyte-Based Electrochromic Device Outperforming Its Solution-Type Counterpart in All Merits: Architectural Benefits of CeO₂ Quantum Dot and Nanorods

For years, solution-type electrochromic devices (ECDs) have intrigued researchers’ interest and eventually rendered themselves into commercialization. Regrettably, challenges such as electrolyte leakage, high flammability, and complicated edge-encapsulation processes limit their practical utilization, hence necessitating an efficient alternate. In this quest, although the concept of solid/gel-polymer electrolyte (SPE/GPE)-based ECDs settled some issues of solution-type ECDs, an array of problems like high operating voltage, sluggish response time, and poor cycling stability have paralyzed their commercial applicability. Herein, we demonstrate a choreographed-CeO2-nanofiller-doped GPE-based ECD outperforming its solution-type counterpart in all merits. The filler-incorporated polymer electrolyte assembly was meticulously weaved through the electrospinning method, and the resultant host was employed for immobilizing electrochromic viologen species. The filler engineering benefits conceived through the tuned shape of CeO2 nanorod and quantum dots, along with the excellent redox shuttling effect of Ce3+/Ce4+, synchronously yielded an outstanding class of GPE, which upon utilization in ECDs delivered impressive electrochromic properties. A combination of features possessed by a particular device (QD-NR/PVDF-HFP/IL/BzV-Fc ECD) such as exceptionally low driving voltage (0.9 V), high transmittance change (ΔT, ∼69%), fast response time (∼1.8 s), high coloration efficiency (∼339 cm2/C), and remarkable cycling stability (∼90% ΔT-retention after 25,000 cycles) showcased a striking potential in the yet-to-realize market of GPE-based ECDs. This study unveils the untapped potential of choreographed nanofillers that can promisingly drive GPE-based ECDs to the doorstep of commercialization

Tracing the Surfactant-Mediated Nucleation, Growth, and Superpacking of Gold Supercrystals Using Time and Spatially Resolved X‑ray Scattering

The nucleation and growth process of gold supercrystals in a surfactant diffusion approach is followed by simultaneous small- and wide-angle X-ray scattering (SAXS/WAXS), supplemented with scanning electron microscopy. The results indicate that supercrystal nucleation can be activated efficiently upon placing a concentrated surfactant solution of a nematic phase on top of a gold nanocrystal solution droplet trapped in the middle of a vertically oriented capillary tube. Supercrystal nuclei comprised of tens of gold nanocubes are observed nearly instantaneously in the broadened liquid–liquid interface zone of a steep gradient of surfactant concentration, revealing a diffusion-kinetics-controlled nucleation process. Once formed, the nuclei can sediment into the naoncrystal zone below, and grow efficiently into cubic or tetragonal supercrystals of ∼1 μm size within ∼100 min. Supercrystals matured during sedimentation in the capillary can accumulate and face-to-face align at the bottom liquid–air interface of the nanocrystal droplet. This is followed by superpacking of the supercrystals into highly oriented hierarchical sheets, with a huge number of gold nanocubes aligned for largely coherent crystallographic orientations