Novel hollow α-Fe2O3 nanofibers with robust performance enabled multi-functional applications.

The synthetic strategies of achieving low-cost and high-performance nanofibers are of great significance in the field of catalysis and detection. In this work, a series of electrospun α-Fe2O3 nanofibers with hollow structure were prepared via combination technology of electrospinning, hydrothermal synthesis, and controlled calcination process. Especially, the influences of the crystal structure and morphology on the comprehensive properties of nanofibers have been explored in detail. The results indicated that α-Fe2O3 nanofibers could be obtained via the calcination at 600-800 °C. Rice-like α-Fe2O3 particles were observed to assemble a stable exoskeleton, supporting a robust tubular cavity. And this tubular structure turned gradually into groove-like structure as the calcination temperature increased, accompanied by tunable crystallization, specific surface area and magnetic property. Finally, combined with series of validation tests, including dye decolorization, electrochemical detection of trace cadmium ions and Fenton degradation of polyvinyl alcohol, the resultant α-Fe2O3 nanofibers have been demonstrated to show the potential application prospects.

Enabling Efficient Aerobic 5-Hydroxymethylfurfural Oxidation to 2,5-Furandicarboxylic Acid in Water by Interfacial Engineering Reinforced Cu-Mn Oxides Hollow Nanofiber.

Herein, a one-dimensional hollow nanofiber catalyst composed of tightly packed multiphase metal oxides of Mn2 O3 and Cu1.4 Mn1.6 O4 was constructed by electrospinning and tailored thermal treatment procedure. The characterization results comprehensively confirmed the special morphology and composition of various comparative catalysts. This strategy endowed the catalyst with abundant interfacial characteristics of components Mn2 O3 and Cu1.4 Mn1.6 O4 nanocrystal. Impressively, the tuning thermal treatment resulted in tailored CuI sites and surface oxygen species of the catalyst, thus affording optimized oxygen vacancies for reinforced oxygen adsorption, while the concomitant enhanced lattice oxygen activity in the constructed composite catalyst ensured the higher catalytic oxidation ability. More importantly, the regulated proportion of oxygen vacancy and lattice oxygen in the composite catalyst was obtained in the best catalyst, beneficial to accelerate the reaction cycle. Compared to other counterparts obtained by different temperatures, the CMO-500 sample exhibited superior selective aerobic 5-hydroxymethylfurfural (HMF) oxidation to 2,5-furandicarboxylic acid (FDCA, 96 % yield) in alkali-bearing aqueous solution using O2 at 120 °C, which resulted from the above-mentioned composition optimization and interfacial engineering reinforced surface oxygen consumption and regeneration cycle. The reaction mechanism was further proposed to uncover the lattice oxygen and oxygen vacancy participating HMF conversion process.

Interfacial engineering coupling with tailored oxygen vacancies in Co2Mn2O4 spinel hollow nanofiber for catalytic phenol removal.

Herein, one-dimensional Co2Mn2O4 (CMO) hollow nanofibers with a general spinel structure were constructed by electrospinning and tunning thermal-driven procedures. The resultant catalyst was endowed with appreciable active interfacial engineering effect, which revealed improved peroxymonosulfate (PMS) activation efficiency in catalytic phenol degradation with nearly 12.9 folds increment in reaction rate constant compared to the hydrothermally synthesized counterpart. Besides, tailored oxygen-vacancy sites including chemical environment and contents in the bimetallic spinel were rationally validated compared to the monometal spinel counterparts. The improved catalytic phenol degradation by reactive-oxidative-species (ROS) from PMS was well correlated with the more active Co(II) and Mn(II) species, reactive active oxygen-vacancy and the interfacial engineering effect in the CMO catalyst. These correlations were comprehensively demonstrated by various characterization techniques, catalytic results, and Density-Functional-Theoretical (DFT) calculations of the adsorption and activation of PMS. Besides, the results revealed that the specific content of cobalt species in the structural unit of the Co2Mn2O4 spinel resulting from the optimized thermal treatment could further improve the catalytic activity by the intermetallic synergy along with the beneficial electron transfer cycles. This work provides a practical understanding of the improvement of interfacial systems in catalysis efficiency and environmental remediation.

SO42-/SnO2 Solid Superacid Granular Stacked One-Dimensional Hollow Nanofiber for a Highly Conductive Proton-Exchange Membrane.

A novel sulfated tin oxide solid superacid granular stacked one-dimensional (1D) hollow nanofiber (SO42-/FSnO2) is proposed as a nanofiller in sulfonated poly(phthalazinone ether sulfone ketone) (SPPESK) to manipulate a highly conductive proton nanochannel. It has unique microstructures with an open-end hollow nanofibric morphology and grain-stacked single-layer mesoporous fiber wall, which greatly enlarge the specific surface area and aspect ratio. The diverse acid sites, that is, SO42-, Sn-OH Brönsted, and Sn4+ Lewis superacids, provide a high concentration of strong acidic proton carriers on the nanofiber surface and dynamically abundant hydrogen bonds for rapid proton transfer and interfacial interactions with -SO3H groups in the SPPESK along the 1D hollow nanofiber. As a result, long-range orientated ionic clusters are observed in the SO42-/FSnO2 incorporated membrane, leading to simultaneous enhancement of proton conductivity (226.7 mS/cm at 80 °C), mechanical stability (31.4 MPa for the hydrated membrane), fuel permeation resistance, and single-cell performance (936.5 and 147.3 mW/cm2 for H2/O2 and direct methanol fuel cells, respectively). The superior performance, as compared with that of the zero-dimensional nanoparticle-incorporated membrane, Nafion 115, and previously reported SPPESK-based membranes, suggests a great potential of elaborating superstructural 1D hollow nanofillers for highly conductive proton-exchange membranes.

Hollow WO3/SnO2 Hetero-Nanofibers: Controlled Synthesis and High Efficiency of Acetone Vapor Detection.

Metal oxide hetero-nanostructures have widely been used as the core part of chemical gas sensors. To improve the dispersion state of each constituent and the poor stability that exists in heterogeneous gas sensing materials, a uniaxial electro-spinning method combined with calcination was applied to synthesize pure SnO2 and three groups of WO3/SnO2 (WO3 of 0.1, 0.3, 0.9 wt%) hetero-nanofibers (HNFs) in our work. A series of characterizations prove that the products present hollow and fibrous structures composed of even nanoparticles while WO3 is uniformly distributed into the SnO2 matrix. Gas sensing tests display that the WO3/SnO2 (0.3 wt%) sensor not only exhibits the highest response (30.28) and excellent selectivity to acetone vapor at the lower detection temperature (170°C), 6 times higher than that of pure SnO2 (5.2), but still achieves a considerable response (4.7) when the acetone concentration is down to 100 ppb with the corresponding response/recovery times of 50/200 s, respectively. Such structure obviously enhances the gas sensing performance toward acetone which guides the construction of a highly sensitive acetone sensor. Meanwhile, the enhancement mechanism of such a special sensor is also discussed in detail.

Cu/CuO@ZnO Hollow Nanofiber Gas Sensor: Effect of Hollow Nanofiber Structure and P-N Junction on Operating Temperature and Sensitivity.

For the fast and easy detection of carbon monoxide (CO) gas, it was necessary to develop a CO gas sensor to operate in low temperatures. Herein, a novel Cu/CuO-decorated ZnO hollow nanofiber was prepared with the electrospinning, calcination, and photodeposition methods. In the presence of 100 ppm CO gas, the Cu/CuO-photodeposited ZnO hollow nanofiber (Cu/CuO@ZnO HNF) showed twice higher sensitivity than that of pure ZnO nanofiber at a relatively low working temperature of 300 °C. The hollow structure and p-n junction between Cu/CuO and ZnO would be considered to contribute to the enhancement of sensitivity to CO gas at 300 °C due to the improved specific surface area and efficient electron transfer.

Synthesis and Thermoelectric Characterization of Lead Telluride Hollow Nanofibers.

Lead telluride (PbTe) nanofibers were fabricated by galvanic displacement of electrospun cobalt nanofibers where their composition and morphology were altered by adjusting the electrolyte composition and diameter of sacrificial cobalt nanofibers. By employing Co instead of Ni as the sacrificial material, residue-free PbTe nanofibers were synthesized. The Pb content of the PbTe nanofibers was slightly affected by the Pb2+ concentration in the electrolyte, while the average outer diameter increased with Pb2+ concentration. The surface morphology of PbTe nanofibers was strongly dependent on the diameter of sacrificial nanofibers where it altered from smooth to rough surface as the Pb2+ concentration increased. Some of thermoelectric properties [i.e., thermopower (S) and electrical conductivity(σ)] were systematically measured as a function of temperature. Energy barrier height (Eb) was found to be one of the key factors affecting the thermoelectric properties-that is, higher energy barrier heights increased the Seebeck coefficient, but lowered the electrical conductivity.

One-Step Fabrication of Fe(OH)3@Cellulose Hollow Nanofibers with Superior Capability for Water Purification.

The conventional strategies employed for the synthesis of hollow nanofibers (HNFs) require either multistep treatments or special design of the equipment. An additional annealing process is always required, which inevitably consumes more energy and raises the manufacturing cost. In addition, the annealing process may also cause a waste of the matrix materials and the release of toxic gases. Herein, we report for the first time a novel one-step synthesis of hollow hybrid nanofibers via electrospinning. Cellulose was chosen as the polymer matrix, and Fe(OH)3 nanoparticles were grown in situ on the nanofibers during electrospinning. There was no need to remove cellulose to create the hollow nanofiber structure. This can significantly simplify the fabrication process without any negative influence to the air. The obtained Fe(OH)3@cellulose HNF membranes exhibited great mechanical properties and an extremely high water flux of 11 200 L m-2 h-1 bar-1. They could effectively remove various pollutants in water, including phosphate, heavy metal ions, and organic dyes, with excellent reusability. Importantly, this approach could also be applied for the fabrication of other hybrid HNFs, which may serve in a broad range of scientific and engineering applications, including water purification, energy conversion and storage, catalysts, sensors, and so on.

Hierarchically mesostructured porous TiO2 hollow nanofibers for high performance glucose biosensing.

Effective immobilization of enzymes on an electrode surface is of great importance for biosensor development, but it still remains challenging because enzymes tend to denaturation and/or form close-packed structures. In this work, a free-standing TiO2 hollow nanofibers (HNF-TiO2) was successfully prepared by a simple and scalable electrospun nanofiber film template-assisted sol-gel method, and was further explored for glucose oxidase (GOD) immobilization and biosensing. This porous and nanotubular HNF-TiO2 provides a well-defined hierarchical nanostructure for GOD loading, and the fine TiO2 nanocrystals facilitate direct electron transfer from GOD to the electrode, also the strong interaction between GOD and HNF-TiO2 greatly enhances the stability of the biosensor. The as-prepared glucose biosensors show good sensing performances both in O2-free and O2-containing conditions with good sensitivity, satisfactory selectivity, long-term stability and sound reliability. The novel textile formation, porous and hierarchically mesostructured nature of HNF-TiO2 with excellent analytical performances make it a superior platform for the construction of high-performance glucose biosensors.

Novel hollow α-Fe2O3 nanofibers via electrospinning for dye adsorption.

Nanomaterials such as iron oxides and ferrites have been intensively investigated for water treatment and environmental remediation applications. In this work, hollow α-Fe2O3 nanofibers made of rice-like nanorods were successfully synthesized via a simple hydrothermal reaction on polyvinyl alcohol (PVA) nanofiber template followed by calcination. The crystallographic structure and the morphology of the as-prepared α-Fe2O3 nanofibers were characterized by X-ray diffraction, energy dispersive X-ray spectrometer, and scanning electron microscope. Batch adsorption experiments were conducted, and ultraviolet-visible spectra were recorded before and after the adsorption to investigate the dye adsorption performance. The results showed that hollow α-Fe2O3 fiber assembles exhibited good magnetic responsive performance, as well as efficient adsorption for methyl orange in water. This work provided a versatile strategy for further design and development of functional nanofiber-nanoparticle composites towards various applications.