Xiaojun Pan

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.

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.

Highly Flexible Freestanding Porous Carbon Nanofibers for Electrodes Materials of High-Performance All-Carbon Supercapacitors

Highly flexible porous carbon nanofibers (P-CNFs) were fabricated by electrospining technique combining with metal ion-assistant acid corrosion process. The resultant fibers display high conductivity and outstanding mechanical flexibility, whereas little change in their resistance can be observed under repeatedly bending, even to 180°. Further results indicate that the improved flexibility of P-CNFs can be due to the high graphitization degree caused by Co ions. In view of electrode materials for high-performance supercapacitors, this type of porous nanostructure and high graphitization degree could synergistically facilitate the electrolyte ion diffusion and electron transportation. In the three electrodes testing system, the resultant P-CNFs electrodes can exhibit a specific capacitance of 104.5 F g(-1) (0.2 A g(-1)), high rate capability (remain 56.5% at 10 A g(-1)), and capacitance retention of ∼94% after 2000 cycles. Furthermore, the assembled symmetric supercapacitors showed a high flexibility and can deliver an energy density of 3.22 Wh kg(-1) at power density of 600 W kg(-1). This work might open a way to improve the mechanical properties of carbon fibers and suggests that this type of freestanding P-CNFs be used as effective electrode materials for flexible all-carbon supercapacitors.

An overview on emerging photoelectrochemical self-powered ultraviolet photodetectors

In recent years, as a new member of ultraviolet photodetectors (UV-PDs), photoelectrochemical UV-PDs (PEC UV-PDs) have received great attention. Compared to conventional photoconductors, PEC UV-PDs exhibit a number of merits, including low cost, environmentally friendly nature, being self-powered, and fast response. This tutorial review provides a comprehensive introduction to this research field, covering from the basics of performance evaluation of PEC UV-PDs, the state-of-the-art advances in structural design, electrolyte matching, and electrode fabrication of PEC UV-PDs, to the integration of multiple functions into a PEC UV-PD. In the end, we present our perspectives on the future development of PEC UV-PDs and highlight the key technical challenges in aiming to stimulate further developments in this research field.

Wire-in-tube structure fabricated by single capillary electrospinning via nanoscale Kirkendall effect: the case of nickel–zinc ferrite

Wire-in-tube structures have previously been prepared using an electrospinning method by means of tuning hydrolysis/alcoholysis of a precursor solution. Nickel-zinc ferrite (Ni0.5Zn0.5Fe2O4) nanowire-in-nanotubes have been prepared as a demonstration. The detailed nanoscale characterization, formation process and magnetic properties of Ni0.5Zn0.5Fe2O4 nanowire-in-nanotubes has been studied comprehensively. The average diameters of the outer tubes and inner wires of Ni0.5Zn0.5Fe2O4 nanowire-in-nanotubes are around 120 nm and 42 nm, respectively. Each fully calcined individual nanowire-in-nanotube, either the outer-tube or the inner-wire, is composed of Ni0.5Zn0.5Fe2O4 monocrystallites stacked along the longitudinal direction with random orientation. The process of calcining electrospun polymer composite nanofibres can be viewed as a morphologically template nucleation and precursor diffusion process. This allows the nitrates precursor to diffuse toward the surface of the nanofibres while the oxides (decomposed from hydroxides and nitrates) products diffuse to the core region of the nanofibres; the amorphous nanofibres transforming thereby into crystalline nanowire-in-nanotubes. In addition, the magnetic properties of the Ni0.5Zn0.5Fe2O4 nanowire-in-nanotubes were also examined. It is believed that this nanowire-in-nanotube (sometimes called core-shell) structure, with its uniform size and well-controlled orientation of the long nanowire-in-nanotubes, is particularly attractive for use in the field of nano-fluidic devices and nano-energy harvesting devices.

Synthesis on Winged Graphene Nanofibers and Their Electrochemical Capacitive Performance

Assembly techniques of graphene have attracted intense attention since their performance strongly depends on the manners in which graphene nanosheets are arranged. In this work, we demonstrate a viable process to synthesize winged graphene nanofibers (G-NFs) which could generate optimized pore size distribution by the fiber-like feature of graphene. The G-NF frameworks were achieved by processing the precursor graphene oxide nanosheets with the following procedures: microwave (MW) irradiation, salt addition, freeze-drying, and chemical reduction. The resultant framework composed of winged G-NFs with a diameter of 200-500 nm and a length of 5-20 μm. Moreover, the crimp degree of G-NFs can be rationally controlled by MW irradiation time. A formation mechanism of such winged G-NFs based on the synergistic effects from MW irradiation and solution ionic strength change has been proposed. With a practice in flexible electrode, after decorated with amorphous MnO2, the G-NF frameworks shows an enhanced specific capacitance compared to graphene nanosheets (G-NSs). This research has developed a controllable method to synthesis G-NFs, which can offer hierarchical pore structures, this kind of graphene nanostructure might enhance their performance in supercapacitor and related fields.

Ni(OH)2 nanosheets grown on a 3D graphene framework as an excellent cathode for flexible supercapacitors

Ni(OH)2 nanosheet/3D graphene (3DG) framework hybrid materials have been prepared by combining chemical vapor deposition (CVD) technology and a facile hydrothermal method. The free-standing Ni(OH)2 nanosheet/3DG composite was investigated as the cathode material for supercapacitors without the need for addition of either binder or metal-based current collector. Consequently, the obtained Ni(OH)2 nanosheet/3DG composite electrode exhibits superior specific capacitance and rate capability to the Ni(OH)2 nanosheet/Ni foam and Ni(OH)2 nanosheet/carbon fiber cloth composite electrodes. This novel structure brings the composite an electrochemical capacitance as high as 2860 F g−1 at a current density of 2 A g−1, and maintains 1791 F g−1 at 30 A g−1. Moreover, the composite electrode also exhibits a high specific capacitance of 2461 F g−1 at a scan rate of 5 mV s−1.

Tunable white light emission by variation of composition and defects of electrospun Al2O3–SiO2 nanofibers

Summary Composite nanofibers consisting of Al2O3–SiO2 were prepared by electrospinning in combination with post-calcination in air. X-ray diffraction, scanning electron microscopy, and transmission electron microscopy were used to investigate the crystalline phase and microstructure of the composite nanofibers. Photoluminescence experiments indicated that the resulting white light emission can be tuned by the relative intensity of the individual spectral components, which are related to the individual defects such as: violet-blue emission from O defects, green emission from ≡Si(Al)–O–C∙=O, and red emission from intersystem radiative crossing. White light emission was realized at a Al/(Al–Si) ratio of 40 and 60 mol %. This research may offer a deeper understanding of the preparation of efficient and environmentally friendly, white luminescence materials.

Preparation and optical properties of GaN nanocrystalline powders

Abstract GaN nanocrystalline powders were synthesised by decomposition of gallium nitrate, followed by nitrogenising with ammonia under different temperature. X-ray diffraction (XRD) and the transmission electron microscopy (TEM) indicated that the crystallinity of the powder is improved and the average size of the GaN nanocrystallites increases from 4·8 to 23·9 nm as the temperature increases from 850 to 1050°C. The Raman spectra displayed four broadened peaks corresponding to A1 (LO), A1 (TO), E1 (TO) and E2 (high) modes of würtzite GaN respectively. Two additional modes at 252 and 421 cm–1 attributed to boundary phonons activated by the finite size effects and octahedral Ga–N6 bonds were observed respectively. A strong blue photoluminescence (∼353 nm) was detected for room temperature measurement, indicating that the GaN nanocrystalline powders have few defects and high quality.

Construction of Hierarchical CNT/rGO-Supported MnMoO4 Nanosheets on Ni Foam for High-Performance Aqueous Hybrid Supercapacitors

Rationally designed conductive hierarchical nanostructures are highly desirable for supporting pseudocapacitive materials to achieve high-performance electrodes for supercapacitors. Herein, manganese molybdate nanosheets were hydrothermally grown with graphene oxide (GO) on three-dimensional nickel foam-supported carbon nanotube structures. Under the optimal graphene oxide concentration, the obtained carbon nanotubes/reduced graphene oxide/MnMoO4 composites (CNT/rGO/MnMoO4) as binder-free supercapacitor cathodes perform with a high specific capacitance of 2374.9 F g-1 at the scan rate of 2 mV s-1 and good long-term stability (97.1% of the initial specific capacitance can be maintained after 3000 charge/discharge cycles). The asymmetric device with CNT/rGO/MnMoO4 as the cathode electrode and the carbon nanotubes/activated carbon on nickel foam (CNT-AC) as the anode electrode can deliver an energy density of 59.4 Wh kg-1 at the power density of 1367.9 W kg-1. These superior performances can be attributed to the synergistic effects from each component of the composite electrodes: highly pseudocapacitive MnMoO4 nanosheets and three-dimensional conductive Ni foam/CNTs/rGO networks. These results suggest that the fabricated asymmetric supercapacitor can be a promising candidate for energy storage devices.