Immobilization of Air-Stable Copper Nanoparticles on Graphene Oxide Flexible Hybrid Films for Smart Clothes.

Through the use of organic/inorganic hybrid dispersants-which are composed of polymeric dispersant and two-dimension nanomaterial graphene oxide (GO)-copper nanoparticles (CuNPs) were found to exhibit nano stability, air-stable characteristics, as well as long-term conductive stability. The polymeric dispersant consists of branched poly(oxyethylene)-segmented esters of trimellitic anhydride adduct (polyethylene glycol-trimethylolpropane-trimellitic anhydride, designated as PTT). PTT acts as a stabilizer for CuNPs, which are synthesized via in situ polymerization and redox reaction of the precursor Cu(CH3COO)2 within an aqueous system, and use graphene oxide to avoid the reduction reaction of CuNPs. The results show that after 30 days of storage the CuNPs/PTT/GO composite film maintains a highly conductive network (9.06 × 10-1 Ω/sq). These results indicate that organic/inorganic PTT/GO hybrid dispersants can effectively maintain the conductivity stability of CuNPs and address the problem of CuNP oxidation. Finally, the new CuNPs/PTT/GO composite film was applied to the electrocardiogram (ECG) smart clothes. This way, a stable and antioxidant-sensing electrode can be produced, which is expected to serve as a long-term ECG monitoring device.

Facile Fabrication of Flexible Electrodes and Immobilization of Silver Nanoparticles on Nanoscale Silicate Platelets to Form Highly Conductive Nanohybrid Films for Wearable Electronic Devices.

This study investigated films with remarkably high electrical conductivity after they were easily prepared from organic/inorganic nanohybrid solutions containing an organic polymeric dispersant and two-dimensional nanoscale silicate platelets as the inorganic stabilizer dispersed with silver nanoparticles. Transmission electron microscopy shows that the production of silver nanoparticles synthesized by the in situ chemical reduction of AgNO3 in an aqueous solution by N,N-dimethylformamide results in an average silver nanoparticle diameter of circa 20 nm. Thin films of silver nanoparticles were prepared on a 1-µm-thick film with a low sheet resistance of 8.24 × 10-4 Ω/sq, achieved through the surface migration of silver nanoparticles and prepared by sintering at 300 °C to form an interconnected network. This was achieved with a silver nanoparticle content of 5 wt%, using nanoscale silicate platelets/polyoxyethylene-segmented polyimide/AgNO3 at a weight ratio of 1:10:35. During sintering, the color of the hybrid film changed from gold to milky white, suggesting the migration of silver nanoparticles and the formation of an interconnected network. The results show promise for the fabrication of novel silver-based electrocardiogram electrodes and a flexible wireless electrocardiogram measurement system for wearable electronics.

Designing Novel Poly(oxyalkylene)-Segmented Ester-Based Polymeric Dispersants for Efficient TiO2 Photoanodes of Dye-Sensitized Solar Cells.

A family of new polymeric dispersants, branched poly(oxyethylene)-segmented esters of trimellitic anhydride adduct (polyethylene glycol-trimethylolpropane-trimellitic anhydride, designated as PTT), were synthesized and utilized to homogeneously disperse TiO2 nanoparticles. The weight fraction of poly(oxyethylene)-segment in the dispersants and the molecular architecture in favoring the branched shape are two predominant factors for designing the effective dispersants. In particular, the poly(oxyethylene) block of 1000 g/mol from PEG1000 as the starting material and a total molecular weight of 12 000 g/mol have constituted the polymeric dispersants for the best performance for homogenizing TiO2 nanoparticles. The dispersant structures were characterized by using Fourier-transform infrared spectroscopy, acid value determination, and gel permeation chromatography. The TiO2 dispersibility was evaluated by dynamic light scattering and transmission electron microscopy. The synthesized dispersants were utilized to homogenize the as-prepared TiO2, further fabricated into films of photoanodes for dye-sensitized solar cells (DSSCs). The ultimate performance of DSSC was measured to be 8.17 ± 0.13% for the device efficiency (η) which was significantly higher than the conventional TiO2 photoanode at η = 7.14 ± 0.12%. The photoanode film was characterized by X-ray diffraction, Brunauer-Emmett-Teller surface area, and dye-loading amount measurements. The kinetics of photogenerated electron in the photoanode, including electron lifetime and electron transit time of the film, was studied via electrochemical impedance spectroscopy, intensity-modulated photocurrent spectroscopy, and intensity-modulated photovoltage spectroscopy.

Novel polymer gel electrolyte with organic solvents for quasi-solid-state dye-sensitized solar cells.

A cross-linked copolymer was previously synthesized from poly(oxyethylene) diamine (POE-amine) and an aromatic anhydride and cured to generate an amide-imide cross-linking structure. The copolymer containing several chemical groups such as POE, amido acids, and imide, enabled to absorb liquid electrolytes in methoxypropionitrile (MPN) for suitable uses in dye-sensitized solar cells. To establish the advantages of polymer gel electrolytes (PGE), the same copolymer was studied by using different electrolyte solvents including propylene carbonate (PC), dimethylformamide, and N-methyl-2-pyrrolidone, and shown their long-term stability. The morphology of the copolymer after absorbing liquid electrolytes in these solvents was proven the same as a 3D interconnected nanochannels, evidenced field emission-scanning electron microscopy. Among these solvents, PC was selected as the optimized PGE, which demostrated a higher power conversion efficiency (8.31%) than that of the liquid electrolyte (7.89%). In particular, the long-term stability of only a 5% decrease in the cell efficiency after 1000 h of testing was achieved. It was proven the developed copolymer as PGE was versatile for different solvents showing high efficiency and long-term durability.