Electrospinning is an inexpensive and versatile technique for fabricating micro- and nano- scaled fibers. There have been limited attempts to employ it for the fabrication of thermochromic (TC) fibers, and the fabrication of a three-component (dye, developer, and solvent) TC material has required the use of a more complicated coaxial electrospinning technique. Herein, a simple and novel method for creating thermochromic fibers by electrospinning single strands of poly (methyl methacrylate) (PMMA) with embedded thermochromic powder of a polymer encapsulated three-component system was employed. Unlike past leuco dye-based thermochromic fibers, an unmodified syringe tip can be used for the spinning process and only one flow rate needs to be determined. A solution of solvent (either N-dimethylformamide or chloroform), PMMA, and a commercially available black thermochromic powder was prepared and spun using a custom-made electrospinning apparatus. The spun fibers exhibited a clear color transition from grey to white and had average diameters of 2.53 µm and 1.96 µm for chloroform and N-dimethylformamide based fibers, respectively. The fibers were characterized by scanning electron and optical microscopy to determine their morphology, Fourier transform infrared spectroscopy to determine their chemical composition, and differential scanning calorimetry and thermogravimetric analysis to characterize their thermal properties.
A polyaniline (PANI)‐based gel material with a redox‐active nature has demonstrated unique charge storage, photovoltaic, and electrochromic properties in the bulk of the gel. The specific capacitance in the volume of the gel was measured to be 428.9 mF g−1. Also, a hybrid device for concurrent solar energy harvesting and charge storage was made simply by placing a layer of the gel between a TiO2 coated electrode and a carbon electrode. The hybrid device showed 137 mV open circuit voltage under the light condition with only 10 mV voltage drop in 600 s after cessation of light. The electrochromic property of the composite gel was also studied in a device made of two transparent electrodes. The results showed 64 % transmittance at 564 nm and zero transmittance when the cell was biased at 0.0 V and 2.0 V, respectively. The photoelectric property and the redox‐active nature of the gel suggest existence of both ionic and electronic conductions through the electrolytes. The results are encouraging to further customize the composite gel for various applications, including supercapacitors, solar cells, photoactive supercapacitors, and electrochromic windows.
This study is mainly focused on the fabrication of SiO2 as an inorganic shell material encapsulated an organic thermochromic (TC) core material comprises of either the (i) three-component as-synthesized blue dyes [BDTCM@SiO2] or (ii) off-the-shelf (commercial) black dyes [CDTCM@SiO2]. Both the SiO2 encapsulated thermochromic systems have successfully demonstrated the color transition at around 31 °C. For the three-component thermochromic microcapsules, we have used the crystal violet lactone (CVL) as a leuco dye, bisphenol-A (BPA) as a color developer, and 1-tetradecanol (TD) as a solvent. Different ratios of the thermochromic dye and the metal oxide were prepared to examine the effect of the core@shell ratio on the microstructural and thermal properties of the encapsulated microcapsules. The mean particles sizes of the BDTCM@SiO2 are below 100 nm, whereas, the CDTCM@SiO2 samples exhibited the mean particle sizes varied in a range of 100-1000 nm. The endothermic phase transition due to melting and in general, the thermal stabilities of these SiO2 encapsulated TCMs have been explored for the purpose of deploying these systems for thermal energy savings or storage applications.
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