Bimetal Oxides Anchored on Carbon Nanotubes/Nanosheets as High-Efficiency and Durable Bifunctional Oxygen Catalyst for Advanced Zn-Air Battery: Experiments and DFT Calculations.

To meet increasing requirement for innovative energy storage and conversion technology, it is urgent to prepare effective, affordable, and long-term stable oxygen electrocatalysts to replace precious metal-based counterparts. Herein, a two-step pyrolysis strategy is developed for controlled synthesis of Fe2O3 and Mn3O4 anchored on carbon nanotubes/nanosheets (Fe2O3-Mn3O4-CNTs/NSs). The typical catalyst has a high half-wave potential (E1/2 = 0.87 V) for oxygen reduction reaction (ORR), accompanied with a smaller overpotential (η10 = 290 mV) for oxygen evolution reaction (OER), showing substantial improvement in the ORR and OER performances. As well, density functional theory calculations are performed to illustrate the catalytic mechanism, where the in situ generated Fe2O3 directly correlates to the reduced energy barrier, rather than Mn3O4. The Fe2O3-Mn3O4-CNTs/NSs-based Zn-air battery exhibits a high-power density (153 mW cm-2) and satisfyingly long durability (1650 charge/discharge cycles/550 h). This work provides a new reference for preparation of highly reversible oxygen conversion catalysts.

Room temperature monitoring of SF6decomposition byproduct SO2F2based on TiO2/NiSO4composite nanofibers.

Sulfuryl fluoride (SO2F2) is one of the ideal decomposition components of sulfur hexafluoride (SF6), which is widely used as an insulating and arc extinguishing medium in gas-insulated switchgear. To detect the decomposition component of SF6at room temperature, the use of SO2F2is still a challenge. In this work, we have successfully fabricated TiO2nanofibers and nickel sulfate (NiSO4NPs) via simple electrospun and hydrothermal methods, followed by calcination process to improve the sensing performance. Metal oxide semiconductor materials (MOSs) are widely used in gas sensing applications due to their superior performance and fast recovery speed. Although the performance of our TiO2/NiSO4composite nanofiber sensor decreases at higher temperatures, it shows an excellent response to target gasses at room temperature. Ni-decoration on the outer surface of the nanofibers could maximize the sensing response of 100 ppm SO2F2by up to 189% at room temperature, showing that the TiO2/NiSO4composite nanofibers are 2.5 times superior to the pure TiO2nanofiber sensors. Thus, the approach for this novel composite nanofiber-based material is promising for the fabrication of superior gas sensors for decomposition of SF6.

Design of highly sensitive and selective ethanol sensor based on α-Fe2O3/Nb2O5 heterostructure.

The introduction of heterostructures is a new approach in gas sensing due to their easy and quick transport of charges. Herein, facile hydrothermal and solid-state techniques are employed to synthesize an α-Fe2O3/Nb2O5 heterostructure. The morphology, microstructure, crystallinity and surface composition of the synthesized heterostructures are investigated by scanning electron microscope, transmission electron microscope, x-ray diffraction, x-ray photoelectron spectroscopy and Brunauer-Emmett-Teller analyses. The successful fabrication of the heterostructures was achieved via the mutual incorporation of α-Fe2O3 nanorods with Nb2O5 interconnected nanoparticles (INPs). A sensor based on the α-Fe2O3(0.09)/Nb2O5 heterostructure with a high surface area exhibited enhanced gas-sensing features, maintaining high selectivity and sensitivity, and a considerable recovery percentage towards ethanol gas. The sensing response of the α-Fe2O3(0.09)/Nb2O5 heterostructure at lower operating temperature (160 °C) is around nine times higher than a pure Nb2O5 (INP) sensor at 180 °C with the flow of 100 ppm ethanol gas. The sensors also show excellent selectivity, good long-term stability and a rapid response/recovery time (8s/2s, respectively) to ethanol. The superior electronic conductivity and upgraded sensitivity performance of gas sensors based on the α-Fe2O3(0.09)/Nb2O5 heterostructure are attributed due to its unique structural features, high specific surface area and the synergic effect of the n-n heterojunction. The promising results demonstrate the potential application of the α-Fe2O3(0.09)/Nb2O5 heterostructure as a good sensing material for the fabrication of ethanol sensors.

Negative Index Metamaterial Lens for Subwavelength Microwave Detection.

Metamaterials are engineered periodic structures designed to have unique properties not encountered in naturally occurring materials. One such unusual property of metamaterials is the ability to exhibit negative refractive index over a prescribed range of frequencies. A lens made of negative refractive index metamaterials can achieve resolution beyond the diffraction limit. This paper presents the design of a metamaterial lens and its use in far-field microwave imaging for subwavelength defect detection in nondestructive evaluation (NDE). Theoretical formulation and numerical studies of the metamaterial lens design are presented followed by experimental demonstration and characterization of metamaterial behavior. Finally, a microwave homodyne receiver-based system is used in conjunction with the metamaterial lens to develop a far-field microwave NDE sensor system. A subwavelength focal spot of size 0.82λ was obtained. The system is shown to be sensitive to a defect of size 0.17λ × 0.06λ in a Teflon sample. Consecutive positions of the defect with a separation of 0.23λ was resolvable using the proposed system.

Development of high-performance sensor based on NiO/SnO2 heterostructures to study sensing properties towards various reducing gases.

In this work, we report the spontaneous formation of NiO nanoparticles-decorated onto smooth SnO2 nanofibers, which is an inexpensive and scalable method for yielding a high composite surface area via a simple two-step synthesis process based on electrospinning and the hydrothermal method. A Nickel Oxide proton-conducting electrolyte is deposited homogeneously over a large surface area in a transparent solution, mixed and decorated onto Tin dioxide nanofibers, as evidenced by cross sectional imaging of the electrospun nanofibers. The composite based on nanoparticle-decorated fibers enlarges the surface area of the exposed electrolyte, which fundamentally improves the overall gas sensing performance. The crystal structure, morphology, and physio-chemical surface state of the NiO/SnO2-based specimen are comprehensively examined using XRD, SEM, TEM, HRTEM, EDX, and photoelectron (XPS) spectroscopy. The composite based on NiO/SnO2 nanoparticle-decorated fibers exhibits an optimistic mesoporous nature with a huge specific area, which is key for superior gas sensors. The result reveals that NiO/SnO2 nanoparticle-decorated fibers with an average size of 180-260 nm in diameter, where the average length of fibers was about 1.5 µm. The composite-based heterojunction of NiO/SnO2 nanoparticle-decorated fibers enhances the adsorption of oxygen molecules, which show fast response, good selectivity and quick recovery speed against ethanol gas at an optimal temperature of about 160 °C. The maximum sensitivity response of the sensor-based composite NiO/SnO2 nanoparticle-decorated fibers was 23.87 in respect of 100 ppm ethanol gas at a low temperature of 160 °C; this is approximately about 7.2 times superior to that of pure SnO2 nanofibers. The superior gas sensing capabilities of a composite based on NiO/SnO2 nanoparticle-decorated fibers may be attributable to the enhanced catalytic effect of the small sized NiO nanoparticles on smooth SnO2 nanofibers, together with the p/n heterojunction effects between NiO and SnO2 heterostructures.

Noble metal-free FeCoNiMnV high entropy alloy anchored on N-doped carbon nanotubes with prominent activity and durability for oxygen reduction and zinc-air batteries.

Efficient and stable oxygen reduction reaction (ORR) catalysts are essential for constructing reliable energy conversion and storage devices. Herein, we prepared noble metal-free FeCoNiMnV high-entropy alloy supported on nitrogen-doped carbon nanotubes (FeCoNiMnV HEA/N-CNTs) by a one-step pyrolysis at 800 °C, as certificated by a set of characterizations. The graphitization degree of the N-CHTs was optimized by tuning the pyrolysis temperature in the control groups. The resultant catalyst greatly enhanced the ORR characteristics in the alkaline media, showing the positive onset potential (Eonset) of 0.99 V and half-wave potential (E1/2) of 0.85 V. More importantly, the above FeCoNiMnV HEA/N-CNTs assembled Zn-air battery exhibited a greater open-circuit voltage (1.482 V), larger power density (185.12 mW cm-2), and outstanding cycle stability (1698 cycles, 566 h). This study provides some valuable insights on developing sustainable ORR catalysts in Zn-air batteries.

Lignin-derived iron carbide/Mn, N, S-codoped carbon nanotubes as a high-efficiency catalyst for synergistically enhanced oxygen reduction reaction and rechargeable zinc-air battery.

Design of efficient and durable oxygen reduction reaction (ORR) electrocatalysts still remains challenge in sustainable energy storage and conversion devices. To achieve sustainable development, it is of importance to prepare high-quality carbon-derived ORR catalysts from biomass. Herein, Fe5C2 nanoparticles (NPs) were facilely entrapped in Mn, N, S-codoped carbon nanotubes (Fe5C2/Mn, N, S-CNTs) by a one-step pyrolysis of the mixed lignin, metal precursors and dicyandiamide. The resulting Fe5C2/Mn, N, S-CNTs had open and tubular structures, which exhibited positive shifts in the onset potential (Eonset = 1.04 V) and high half-wave potential (E1/2 = 0.85 V), showing excellent ORR characteristics. Further, the typical catalyst-assembled Zn-air battery showed a high power density (153.19 mW cm-2) and good cycling performance as well as obvious cost advantage. The research provides some valuable insights for rational construction of low-cost and environmentally sustainable ORR catalysts in clean energy field, coupled by offering some valuable insights for reusing biomass wastes.

Low-Temperature Detection of Sulfur-Hexafluoride Decomposition Products Using Octahedral Co3O4-Modified NiSnO3 Nanofibers.

Sulfur hexafluoride (SF6) is widely used in electrical equipment because of its excellent insulating properties. The type of internal fault in the power system can be identified by detecting SF6 decomposition products. In this manuscript, we report a novel sensing material based on octahedral Co3O4-modified NiSnO3 nanofibers synthesized via a two-step process based on electrospinning followed by a hydrothermal method for detecting the SF6 decomposition products. From the evaluation of various characterization techniques, it was determined that the Co3O4 octahedra adhered inflexibly to the surface of the NiSnO3 nanofibers, which consist of smaller particles and provide a huge surface area for the adsorption of an enormous amount of gas species. Planar-type chemical gas sensors were devised, and their gas detecting performance against SF6 decomposition products was systematically investigated. A comparison of the sensitivity properties of different amounts of charged Co3O4 octahedra in NiSnO3 nanofibers shows that the S-2-based Co3O4@NiSnO3 composite has a high selectivity for 100 ppm SO2F2 gas with a high sensing response of 22.5 at a relatively low temperature of 50 °C with a moderate response/recovery interval (∼200/∼268 s) and a low detection limit (5 ppm) over other interfering gases, such as SOF2, SO2, and H2S. Interestingly, the sensing properties of the fabricated sensors based on the Co3O4@NiSnO3 composites for the SO2F2 gas were improved in terms of lower operating temperatures, higher gas responses, and mild response/recovery intervals, which could be attributed to the unique microstructure effect, the catalytic influence of Co3O4 octahedra, and the creation of p/n junctions to increase the charge transfer and diffusion rate within the catalytic assembly of the sensor materials. This work highlights the importance of the heterostructure design in the construction of high-performance gas sensors for the real-time detection of SF6 decomposition products.

Recent advancement in conjugated polymers based photocatalytic technology for air pollutants abatement: Cases of CO2, NOx, and VOCs.

According to World Health Organization (WHO) survey, air pollution has become the major reason of several fatal diseases, which had led to the death of 7 million peoples around the globe. The 9 people out of 10 breathe air, which exceeds WHO recommendations. Several strategies are in practice to reduce the emission of pollutants into the air, and also strict industrial, scientific, and health recommendations to use sustainable green technologies to reduce the emission of contaminants into the air. Photocatalysis technology recently has been raised as a green technology to be in practice towards the removal of air pollutants. The scientific community has passed a long pathway to develop such technology from the material, and reactor points of view. Many classes of photoactive materials have been suggested to achieve such a target. In this context, the contribution of conjugated polymers (CPs), and their modification with some common inorganic semiconductors as novel photocatalysts, has never been addressed in literature till now for said application, and is critically evaluated in this review. As we know that CPs have unique characteristics compared to inorganic semiconductors, because of their conductivity, excellent light response, good sorption ability, better redox charge generation, and separation along with a delocalized π-electrons system. The advances in photocatalytic removal/reduction of three primary air-polluting compounds such as CO2, NOX, and VOCs using CPs based photocatalysts are discussed in detail. Furthermore, the synergetic effects, obtained in CPs after combining with inorganic semiconductors are also comprehensively summarized in this review. However, such a combined system, on to better charges generation and separation, may make the Adsorb & Shuttle process into action, wherein, CPs may play the sorbing area. And, we hope that, the critical discussion on the further enhancement of photoactivity and future recommendations will open the doors for up-to-date technology transfer in modern research.

A novel ethanol gas sensor based on α-Bi2Mo3O12/Co3O4 nanotube-decorated particles.

A novel composite based on α-Bi2Mo3O12/Co3O4 nanotube-decorated particles was successfully synthesized using a highly efficient and facile two step system using electrospinning and hydrothermal techniques. The small size Co3O4 nanoparticles were uniformly and hydrothermally developed on the electrospun α-Bi2Mo3O12 nanotubes. The pure α-Bi2Mo3O12 nanofibers and composite based on α-Bi2Mo3O12/Co3O4 were examined using X-ray powder diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS) and Brunauer-Emmett-Teller (BET) analyses. From the BET measurements, the composite based on α-Bi2Mo3O12/Co3O4 exhibits a large specific surface area of 54 m2 g-1 with mesopore diameter ranges of 2-10 nm, which is mainly attributed to the remarkable and dominant enhancement in gas sensing as compared to that of the pure α-Bi2Mo3O12 nanofibers (38 m2 g-1) and Co3O4 nanoparticles (32 m2 g-1), respectively. In this work, the novel composite based on α-Bi2Mo3O12/Co3O4 presented a high sensitivity of 30.25 with a quick response/recovery speed towards 100 ppm ethanol at an optimal working temperature of 170 °C, as compared to the pure α-Bi2Mo3O12 nanofibers and Co3O4 nanoparticles, which display a sensitivity of 13.10 and 2.99 at an optimal working temperature of 220 °C and 280 °C. The sensing performance of the composite based on the α-Bi2Mo3O12/Co3O4 sensor exhibits a superior sensing performance towards ethanol, which might be owed to the enormous number of superficial oxygen species, the small size catalytic effect of the Co3O4 nanoparticles and the interfacial effect formed between the n-type α-Bi2Mo3O12 and p-type Co3O4 leading to a high charge carrier concentration. This is a novel investigation of a composite based on an α-Bi2Mo3O12/Co3O4 sensor in the gas sensing era, which might be of vital importance in applications in the advanced gas sensing field.

A two-step synthesis of nanosheet-covered fibers based on α-Fe2O3/NiO composites towards enhanced acetone sensing.

A novel hierarchical heterostructures based on α-Fe2O3/NiO nanosheet-covered fibers were synthesized using a simple two-step process named the electrospinning and hydrothermal techniques. A high density of α-Fe2O3 nanosheets were uniformly and epitaxially deposited on a NiO nanofibers. The crystallinity, morphological structure and surface composition of nanostructured based on α-Fe2O3/NiO composites were investigated by XRD, SEM, TEM, EDX, XPS and BET analysis. The extremely branched α-Fe2O3/NiO nanosheet-covered fibers delivered an extremely porous atmosphere with huge specific surface area essential for superior gas sensors. Different nanostructured based on α-Fe2O3/NiO composites were also explored by adjusting the volume ratio of the precursors. The as-prepared samples based on α-Fe2O3/NiO nanocomposite sensors display apparently enhanced sensing characteristics, including higher sensing response, quick response with recovery speed and better selectivity towards acetone gas at lower operating temperature as compared to bare NiO nanofibers. The sensing response of S-2 based α-Fe2O3/NiO nanosheet-covered fibers were 18.24 to 100 ppm acetone gas at 169 °C, which was about 6.9 times higher than that of bare NiO nanofibers. The upgraded gas sensing performance of composites based on α-Fe2O3/NiO nanosheet-covered fibers might be ascribed to the exclusive morphologies with large surface area, p-n heterojunctions and the synergetic performance of α-Fe2O3 and NiO.

Marangoni effect induced macro porous surface films prepared through a facile sol-gel route.

Based on TiO2 as a model system, the sol-gel one step facile method is established to fabricate the macro-porous morphology films on the basis of Marangoni effect. In this proposed mechanism, the binary mixture of hydrophilic CuCl2 and lipophilic Ti-O network is used in sol to produce phase separation. A suitable evaporation rate in the gel film process leads to the macro-porous film due to Marangoni effect. It is observed that the macro-porous morphology of the film sustains during the annealing process, which suggests the creation of porous surface morphology in gel film stage rather than due to annealing. To analyze the preparation mechanism, the sol-gel process and microstructure of films are examined using TG-DTA, SEM, TEM, XRD, Raman, UV-Vis, XPS and FTIR. Furthermore, the optical-thermal properties are studied for the potential applications of such porous surface films as solar selective absorber.