Engineering Triboelectric Charge in Natural Rubber-Ag Nanocomposite for Enhancing Electrical Output of a Triboelectric Nanogenerator.

An environmentally friendly triboelectric nanogenerator (TENG) is fabricated from a natural rubber (NR)-Ag nanocomposite for harvesting mechanical energy from human motions. Ag nanoparticles (AgNPs) synthesized with two different capping agents are added to NR polymer for improving dielectric constant that contributes to the enhancement of TENG performance. Dielectric constant is modulated via interfacial polarization between AgNPs and NR matrix. The effects of AgNP concentration, particle size and dispersion in NR composite, and type of capping agents on dielectric properties and electrical output of the NR composite TENG are elucidated. It is found that, apart from AgNPs content in the NR-Ag nanocomposite, cations of CTAB capping agent play important roles not only on the dispersion of AgNPs in NR matrix but also on intensifying tribopositive charges in the NR composite. In addition, the application of the NR-Ag TENG as a shoe insole is also demonstrated to convert human footsteps into electricity to power small electronic devices. Furthermore, with the presence of Ag nanoparticles, the fabricated shoe insole also exhibits antibacterial property against Staphylococcus aureus that causes foot odor.

Natural Rubber-TiO2 Nanocomposite Film for Triboelectric Nanogenerator Application.

In this research, natural rubber (NR)-TiO2 nanocomposites were developed for triboelectric nanogenerator (TENG) application to harvest mechanical energy into electrical energy. Rutile TiO2 nanoparticles were used as fillers in NR material to improve dielectric properties so as to enhance the energy conversion performance of the NR composite TENG. The effect of filler concentration on TENG performance of the NR-TiO2 composites was investigated. In addition, ball-milling method was employed to reduce the agglomeration of TiO2 nanoparticles in order to improve their dispersion in the NR film. It was found that the TENG performance was significantly enhanced due to the increased dielectric constant of the NR-TiO2 composite films fabricated from the ball-milled TiO2. The TENG, fabricated from the NR-TiO2 composite using 24 h ball-milled TiO2 at 0.5%wt, delivered the highest power density of 237 mW/m2, which was almost four times higher than that of pristine NR TENG. Furthermore, the applications of the fabricated NR-TiO2 TENG as a power source to operate portable electronics devices were also demonstrated.

Ag Nanoparticle-Incorporated Natural Rubber for Mechanical Energy Harvesting Application.

The energy conversion performance of the triboelectric nanogenerator (TENG) is a function of triboelectric charges which depend on the intrinsic properties of materials to hold charges or the dielectric properties of triboelectric materials. In this work, Ag nanoparticles were synthesized and used to incorporate into natural rubber (NR) in order to enhance the dielectric constant for enhancing the electrical output of TENG. It was found that the size of Ag nanoparticles was reduced with the increasing CTAB concentration. Furthermore, the CTAB surfactant helped the dispersion of metallic Ag nanoparticles in the NR-insulating matrix, which promoted interfacial polarization that affected the dielectric properties of the NR composite. Ag nanoparticle-incorporated NR films exhibited an improved dielectric constant of up to almost 40% and an enhanced TENG performance that generated the highest power density of 262.4 mW/m2.

Preparation and electrochemical performance of nitrogen-enriched activated carbon derived from silkworm pupae waste.

In this study, nitrogen-enriched activated carbon from silkworm pupae waste (P-AC) was successfully prepared and its electrochemical performances in aqueous and organic electrolytes were investigated. Silkworm pupae waste is beneficial because it is a nitrogen-enriched, inexpensive, and locally available material. The preparation process includes hydrothermal treatment of the silkworm pupae waste at 200 °C, and chemical activation using zinc chloride at activation temperatures of 700, 800 and 900 °C (P700, P800, and P900, respectively). The nitrogen content in the P-ACs was approximately 3.8-6.4 at%, decreasing with activation temperature, while the surface area was approximately 1062-1267 m2 g-1, increasing with activation temperature. Compared to a commercial AC, the P-ACs show higher nitrogen content but lower surface area. Furthermore, the P800 exhibited superior specific capacitance (154.6 and 91.6 F g-1 in aqueous and organic electrolytes) compared to a commercial AC despite possessing smaller surface area. The high nitrogen content enhanced the pseudocapacitance and improved the electrical conductivity of the P-ACs. These properties were confirmed by relatively low series and charge transfer resistances, a capacity retention higher than 88% at a current density of 0.5 A g-1 and excellent cycling stability demonstrated by maintaining 97.6% of its capacitance after 3000 cycles. These results demonstrate that silkworm pupae waste is a viable source of nitrogen-enriched AC for application in supercapacitors.

Preparation of injectable hydrogels from temperature and pH responsive grafted chitosan with tuned gelation temperature suitable for tumor acidic environment.

In this present work, stimuli responsive polymers that can respond to the temperature and pH of the environment were prepared. A series of temperature responsive diblock copolymers based on poly(ethylene glycol) methyl ether (mPEG) and ε-caprolactone (CL) were synthesized. Subsequently, the diblock copolymers were grafted onto chitosan, a pH responsive biopolymer. These chitosan-graft-(mPEG-block-PCL) (chitosan-g-(mPEG-b-PCL)) graft copolymers were structurally characterized by 1H NMR and FTIR and their sol-gel phase transitions were analyzed by the test tube inversion method as well as dynamic rheological measurements. These chitosan-g-(mPEG-b-PCL) graft copolymers demonstrated tunable temperature and pH responsive sol-gel phase transitions that correspond well with body temperature and pH of acidic tumor microenvironments. Gelation temperature (Tgel) decreased with increasing pH of the system, increasing PCL composition in the diblock copolymers, increasing solution concentration and decreasing grafting content of the diblock copolymers on chitosan. The graft copolymer hydrogels successfully showed the sustained release of both doxorubicin and curcumin for up to 2 weeks. The designed system was based on chitosan-g-(mPEG-b-PCL) graft copolymers, of which chitosan showed pH responsive properties and mPEG-b-PCL acted as a temperature sensitive moiety. In addition, mPEG and PCL are recognized as biocompatible polymers and chitosan has been engaged in various pharmaceutical research. Thus, this system could be considered an alternative choice for drug delivery applications.

Epoxidized Natural Rubber/Chitosan Network Binder for Silicon Anode in Lithium-Ion Battery.

Polymeric binder is extremely important for Si-based anode in lithium-ion batteries due to large volume variation during charging/discharging process. Here, natural rubber-incorporated chitosan networks were designed as a binder material to obtain both adhesion and elasticity. Chitosan could strongly anchor Si particles through hydrogen bonding, while the natural rubber could stretch reversibly during the volume variation of Si particles, resulting in high cyclic performance. The prepared electrode exhibited the specific capacities of 1350 mAh/g after 1600 cycles at the current density of 8 A/g and 2310 mAh/g after 500 cycles at the current density of 1 A/g. Furthermore, the cycle test with limiting lithiation capacity was conducted to study the optimal binder properties at varying degree of the volume expansion of silicon, and it was found that the elastic property of binder material was strongly required when the large volume expansion of Si occurred.

Supercritical Carbon Dioxide-Assisted Process for Well-Dispersed Silicon/Graphene Composite as a Li ion Battery Anode.

The silicon (Si)/graphene composite has been touted as one of the most promising anode materials for lithium ion batteries. However, the optimal fabrication method for this composite remains a challenge. Here, we developed a novel method using supercritical carbon dioxide (scCO2) to intercalate Si nanoparticles into graphene nanosheets. Silicon was modified with a thin layer of polyaniline, which assisted the dispersion of graphene sheets by introducing π-π interaction. Using scCO2, well-dispersed Si/graphene composite was successfully obtained in a short time under mild temperature. The composite showed high cycle performance (1,789 mAh/g after 250 cycles) and rate capability (1,690 mAh/g at a current density of 4,000 mA/g). This study provides a new approach for cost-effective and scalable preparation of a Si/graphene composite using scCO2 for a highly stable lithium battery anode material.

Multiferroic polymer composites with greatly enhanced magnetoelectric effect under a low magnetic bias.

Multiferroic laminate composites consisting of chain-end cross-linked ferroelectric polymers and magnetostrictive Metglas are reported. The composites exhibit a greatly enhanced multiferroic voltage coefficient and sensitivity relative to analogous composites. These remarkable properties are attributed to high piezoelectric and electromechanical coupling coefficients, because of the formation of larger crystalline sizes and concurrent improvement in the polarization ordering in the cross-linked polymers.