Caitian Gao

An overview of carbon materials for flexible electrochemical capacitors

Under the background of the quick development of lightweight, flexible, and wearable electronic devices in our society, a flexible and highly efficient energy management strategy is needed for their counterpart energy-storage systems. Among them, flexible electrochemical capacitors (ECs) have been considered as one of the most promising candidates because of their significant advantages in power and energy densities, and unique properties of being flexible, lightweight, low-cost, and environmentally friendly compared with current energy storage devices. In a common EC, carbon materials play an irreplaceable and principal role in its energy-storage performance. Up till now, most progress towards flexible ECs technologies has mostly benefited from the continuous development of carbon materials. As a result, in view of the dual remarkable highlights of ECs and carbon materials, a summary of recent research progress on carbon-based flexible EC electrode materials is presented in this review, including carbon fiber (CF, consisting of carbon microfiber-CMF and carbon nanofiber-CNF) networks, carbon nanotube (CNT) and graphene coatings, CNT and/or graphene papers (or films), and freestanding three-dimensional (3D) flexible carbon-based macroscopic architectures. Furthermore, some promising carbon materials for great potential applications in flexible ECs are introduced. Finally, the trends and challenges in the development of carbon-based electrode materials for flexible ECs and their smart applications are analyzed.

A facile method to prepare SnO2 nanotubes for use in efficient SnO2–TiO2 core–shell dye-sensitized solar cells

A high-efficiency photoelectrode for dye-sensitized solar cells (DSSCs) should combine the advantageous features of fast electron transport, slow interfacial electron recombination and large specific surface area. However, these three requirements usually cannot be achieved simultaneously in the present state-of-the-art research. Here we report a simple procedure to combine the three conflicting requirements by using porous SnO(2) nanotube-TiO(2) (SnO(2) NT-TiO(2)) core-shell structured photoanodes for DSSCs. The SnO(2) nanotubes are prepared by electrospinning of polyvinyl pyrrolidone (PVP)/tin dichloride dihydrate (SnCl(2)·2H(2)O) solution followed by direct sintering of the as-spun nanofibers. A possible evolution mechanism is proposed. The power conversion efficiency (PCE) value of the SnO(2) NT-TiO(2) core-shell structured DSSCs (∼5.11%) is above five times higher than that of SnO(2) nanotube (SnO(2) NT) DSSCs (∼0.99%). This PCE value is also higher than that of TiO(2) nanoparticles (P25) DSSCs (∼4.82%), even though the amount of dye molecules adsorbed to the SnO(2) NT-TiO(2) photoanode is less than half of that in the P25 film. This simple procedure provides a new approach to achieve the three conflicting requirements simultaneously, which has been demonstrated as a promising strategy to obtain high-efficiency DSSCs.

Graphene-based composite materials beneficial to wound healing

We use electrospinning to prepare chitosan-PVA nanofibers containing graphene. The nanofibers can be directly used in wound healing: graphene, as an antibacterial material, can be beneficial for this. A possible antibacterial mechanism for graphene is presented.

High‐Performance Photoelectrochemical‐Type Self‐Powered UV Photodetector Using Epitaxial TiO2/SnO2 Branched Heterojunction Nanostructure

TiO₂/SnO₂ branched heterojunction nanostructure with TiO₂ branches on electrospun SnO2 nanofiber (B-SnO₂ NF) networks serves as a model architecture for efficient self-powered UV photodetector based on a photoelectrochemical cell (PECC). The nanostructure simultaneously offers a low degree of charge recombination and a direct pathway for electron transport. Without correcting 64.5% loss of incident photons through light absorption and scattering by the F-doped tin oxide (FTO) glass, the incident power conversion efficiency reaches 14.7% at 330 nm, more than twice as large as the nanocrystalline TiO₂ (TiO₂ NC, 6.4%)-film based PECC. By connecting a PECC to an ammeter, the intensity of UV light is quantified using the output short-circuit photocurrent density (J(sc)) without a power source. Under UV irradiation, the self-powered UV photodetector exhibits a high responsivity of 0.6 A/W, a high on/off ratio of 4550, a rise time of 0.03 s and a decay time of 0.01 s for J(sc) signal. The excellent performance of the B-SnO₂ NF-based PECC type self-powered photodetector will enable significant advancements for next-generation photodetection and photosensing applications.

Synthesis of cadmium sulfide quantum dot-decorated barium stannate nanowires for photoelectrochemical water splitting

We report the fabrication of cadmium sulfide (CdS) quantum dot-decorated barium stannate (BaSnO3) nanowires and their application as photoanodes for photoelectrochemical water splitting. First, polycrystalline BaSnO3 nanowires, which have a perovskite structure, were prepared by electrospinning their polyvinylpyrrolidone polymer precursors and calcining the resultant polymer fibres. Then, CdS quantum dots were decorated onto the BaSnO3 nanowires by a wet-chemical method. Our results show that the hybrid photoanode made of the CdS quantum dot-decorated BaSnO3 nanowires exhibits a high photocurrent density up to 4.8 mA cm−2 at 0 V (vs. saturated calomel electrode), which corresponds to a hydrogen generation rate of 71.8 μmol (h cm2)−1 with a faradaic efficiency of around 80%. Its favourable performance was attributed to the effective charge separation at the type II staggered gap heterojunction formed at the BaSnO3/CdS interface, and the low charge recombination in BaSnO3 nanowires during transport. Our findings indicate that the water splitting performance of photoelectrochemical cells can be highly improved by rationally building a type II band alignment heterojunction with sensitizing quantum dots and wide band gap semiconductor nanowires which have a low charge recombination rate during transport.

Photocatalytic properties of titania/porous carbon fibers composites prepared by self-template method

Photocatalytic degradation is one of the most popular routes applied in the wastewater treatments. But the most used nanoparticle photocatalysts have a serious drawback that the particles are not easy to precipitate and recover from water, which seriously hinder its applications. In this study, titania/porous carbon fibers composite prepared by a simple self-template method with micro-meter long carbon fibers and titania nanoparticles as precursors was investigated to solve these issues. The obtained composite can precipitate from the solution easily, which is the major reason that it can be used in actual applications. We found that the titania particles, as catalysts, could enhance the reaction between carbon fibers and oxygen during the calcinations process, and as a template, would determine the size and position of the pores on the fibers surface simultaneously. Due to the unique porous structure, the titania/porous carbon fibers composite shows considerable adsorption and high photocatalytic activity. Combining the advantages of titania and carbon fibers, the composite can be also applied in many other fields, such as water splitting for hydrogen and lithium ion batteries.