Anode surface engineering of zinc-ion batteries using tellurium nanobelt as a protective layer for enhancing energy storage performance

Over the years,zinc-ion batteries(ZIBs)have attracted attention as a promising next-generation energy storage technology because of their excellent safety,long cycling performance,eco-friendliness,and high-power density.However,issues,such as the corrosion and dissolution of the Zn anode,limited wet-tability,and lack of sufficient nucleation sites for Zn plating,have limited their practical application.The introduction of a protective layer comprising of tellurium(Te)nanobelts onto the surface of Zn anode has emerged as a promising approach to overcome these limitations and improve the electrochemical behav-ior by enhancing the safety and wettability of ZIBs,as well as providing numerous nucleation sites for Zn plating.In the presence of a Te-based protective layer,the energy power density of the surface-engineered Zn anode improved significantly(ranging from 310 to 144 W h kg^(-1),over a power density range of 270 to 1,800 W kg^(-1)),and the lifespan capability was extended.These results demonstrate that the proposed strategy of employing Te nanobelts as a protective layer holds great promise for enhancing the energy storage performance of zIBs,making them even more attractive as a viable energy storage solution forthefuture.

Dual-Schottky-junctions coupling device based on ultra-longβ-Ga_(2)O_(3)single-crystal nanobelt and its photoelectric properties

High qualityβ-Ga_(2)O_(3)single crystal nanobelts with length of 2−3 mm and width from tens of microns to 132μm were synthesized by carbothermal reduction method.Based on the grown nanobelt with the length of 600μm,the dual-Schottky-junctions coupling device(DSCD)was fabricated.Due to the electrically floating Ga_(2)O_(3)nanobelt region coupling with the double Schottky-junctions,the current I_(S2)increases firstly and rapidly reaches into saturation as increase the voltage V_(S2).The saturation current is about 10 pA,which is two orders of magnitude lower than that of a single Schottky-junction.In the case of solar-blind ultraviolet(UV)light irradiation,the photogenerated electrons further aggravate the coupling physical mechanism in device.I_(S2)increases as the intensity of UV light increases.Under the UV light of 1820μW/cm^(2),I_(S2)quickly enters the saturation state.At V_(S2)=10 V,photo-to-dark current ratio(PDCR)of the device reaches more than 104,the external quantum efficiency(EQE)is 1.6×10^(3)%,and the detectivity(D*)is 7.5×10^(12)Jones.In addition,the device has a very short rise and decay times of 25−54 ms under different positive and negative bias.DSCD shows unique electrical and optical control characteristics,which will open a new way for the application of nanobelt-based devices.

Influence of Mn Doping on the Sensing Properties of SnO₂Nanobelt to Ethanol

Mn doped SnO2 nanobelts (Mn:SnO2 NBs) and pure SnO2 nanobelts (SnO2 NBs) were synthesized by thermal evaporation technique at 1355°C with Ar carrier gas (25 sccm, 150 Torr). The SEM, EDS, XRD, TEM, HRTEM, SAED, XPS, UV-Vis techniques were used to characterize the attained samples. The band gap of Mn doped SnO2 NBs by UV-Vis was measured to be 3.43 eV at room temperature, lower than that of the pure counterpart with ~3.66 eV. Mn:SnO2 NB and pure SnO2 NB sensors were developed. It is found that Mn:SnO2 NB device exhibits a higher sensitivity with 62.12% to 100 ppm of ethanol at 210°C, which is the highest sensitivity among the three tested VOC gases (ethanol, ethanediol, and acetone). The theoretical detection limit for ethanol of the sensor is 1.1 ppm. The higher response is related to the selective catalysis of the doped Mn ions.

Surface-effects-dominated thermal and mechanical responses of zinc oxide nanobelts

t Molecular dynamics （MD） simulations are carried out to characterize the mechanical and thermal responses of [011^-1]-oriented ZnO nanobelts with lateral dimensions of 21.22A × 18.95 A, 31.02A× 29.42 A, and40.81A ×39.89A over the temperature range of 300-1000 K. The Young＇s modulus and thermal conductivity of the nanobelts are evaluated. Significant surface effects on properties due to the highsurface-to-volume ratios of the nanobelts are observed. For the mechanical response, surface-stress-induced internal stress plays an important role. For the thermal response, surface scattering of phonons dominates. Calculations show that the Young＇s modulus is higher than the corresponding value for bulk ZnO and decreases by -33% as the lateral dimensions increase from 21.22 A × 18.95A to 40.81 A × 39.89A. The thermal conductivity is one order of magnitude lower than the corresponding value for bulk ZnO single crystal and decreases with wire size. Specifically, the conductivity of the 21.22 A × 18.95 A belt is approximately （31-18）% lower than that of the 40.81 A × 39.89 A belt over the temperature range analyzed. A significant dependence of properties on temperature is also observed, with the Young＇s modulus decreasing on average by 12% and the conductivity decreasing by 50% as temperature increases from 300 K to 1000 K.

Na2V6O16·2.14H2O nanobelts as a stable cathode for aqueous zinc-ion batteries with long-term cycling performance

Aqueous zinc-ion batteries(ZIBs) have been considered as one of the most promising electrochemical devices for large-scale energy storage system owing to their low cost and high safety. Herein, Na2V6O16·2.14H2O nanobelts are synthesized and applied as cathode material for ZIBs. The sample displays a high capacity of 466 m Ahg^-1 at 100 mAg^-1 and stable cycling performance with a capacity retention of 90% over 20 0 0 cycles at the 20 Ag^-1. Moreover, Na2V6O16·2.14H2O presents a capable rate ability and a high energy density of 312 Wh kg^-1 at a specific power of 70 Wkg^-1. The superior electrochemical performance is attributed to the large interlayer spacing and outstanding structure stability, which promise the highly reversible intercalation and extraction of zinc ion. The electrochemical kinetics and zinc ion storage mechanism are also investigated. This work demonstrates that nanoscale electrode materials with large interlayer spacing can effectively enhance the electrochemical performance of aqueous ZIBs, which can be extended to other metal ion batteries, such as magnesium ion batteries and aluminum ion batteries.

Tunable fabrication of single-crystalline CsPbI_(3) nanobelts and their application as photodetectors

Lead halide perovskites have received increasing attention recently as a candidate material in various optoelectronic areas because of their high performance as light absorbers.Herein,we report the growth of CsPbI_(3) nanobelts via a solution process.A single-crystalline CsPbI_(3) nanobelt with uniform morphology can be achieved by controlling the amount of PbI_(2).A single-crystalline CsPbI_(3) nanobelt possesses a mean width,length,and thickness of 100 nm,5μm,and 20 nm,respectively.In this work,photodetectors(PDs)based on individual CsPbI_(3) nanobelts are constructed and found to perform well with an external quantum efficiency and responsivity of 2.39×10^(5)% and 770 A/W,respectively.The PDs also show a high detectivity of up to 3.12×10^(12) Jones,which is at par with that of Si PDs.The PDs developed in this work exhibit great promise in various optoelectronic nanodevices.

Layered barium vanadate nanobelts for high-performance aqueous zinc-ion batteries

Aqueous zinc-ion batteries(ZIBs)are deemed as the idea option for large-scale energy storage systems owing to many alluring merits including low manufacture cost,environmental friendliness,and high operations safety.However,to develop high-performance cathode is still significant for practical application of ZIBs.Herein,Ba_(0.23)V_(2)O_(5)·1.1H_(2)O(BaVO)nanobelts were fabricated as cathode materials of ZIBs by a typical hydrothermal synthesis method.Benefiting from the increased interlayer distance of 1.31 nm by Ba2+ and H2O pre-intercalated,the obtained BaVO nanobelts showed an excellent initial discharge capacity of 378 mAh·g^(-1) at 0.1 A·g^(-1),a great rate performance(e.g.,172 mAh·g^(-1) at 5 A·g^(-1)),and a superior capacity retention(93% after 2000 cycles at 5 A·g^(-1)).

Controlled Growth and Cathodoluminescence Property of ZnS nanobelts with Large Aspect Ratio

ZnS nanobelts with large aspect ratio are successfully synthesized on a large scale through thermally evaporating of ZnS powder with a trace of SnO_2 powder using gold coated Si wafer as the substrate at 1100°C.The results indicate that the as-obtained ZnS nanobelts are about 10 nm in thickness and hundreds of micrometers in length,and the aspect ratio reaches more than 104.Substrate dependent experiments are conducted to better study the growth mechanism of the ZnS nanobelts.Subsequently,optical properties of the as-synthesized ZnS nanobelts are also investigated by using a cathodoluminescence(CL) system,which shows the existence of a strong ultraviolet emission at 342 nm and two poor emission peaks at 522 nm and 683 nm at room temperature,respectively.

Palladium Nanoparticles Loaded on Carbon Modified TiO_2 Nanobelts for Enhanced Methanol Electrooxidation

Carbon modified TiO_2 nanobelts(TiO_2-C) were synthesized using a hydrothermal growth method,as a support material for palladium(Pd) nanoparticles(Pd/TiO_2-C) to improve the electrocatalytic performance for methanol electrooxidation by comparison to Pd nanoparticles on bare TiO_2 nanobelts(Pd/TiO_2)and activated carbon(Pd/AC). Cyclic voltammetry characterization was conducted with respect to saturated calomel electrode(SCE) in an alkaline methanol solution, and the results indicate that the specific activity of Pd/TiO_2-C is 2.2 times that of Pd/AC and 1.5 times that of Pd/TiO_2. Chronoamperometry results revealed that the TiO_2-C support was comparable in stability to activated carbon, but possesses an enhanced current density for methanol oxidation at a potential of -0.2 V vs. SCE. The current study demonstrates the potential of Pd nanoparticle loaded on hierarchical TiO_2-C nanobelts for electrocatalytic applications such as fuel cells and batteries.

Intercalating Ultrathin MoO_3 Nanobelts into MXene Film with Ultrahigh Volumetric Capacitance and Excellent Deformation for High-Energy-Density Devices

The restacking hindrance of MXene films restricts their development for high volumetric energy density of flexible supercapacitors toward applications in miniature,portable,wearable or implantable electronic devices.A valid solution is construction of rational heterojunction to achieve a synergistic property enhancement.The introduction of spacers such as graphene,CNTs,cellulose and the like demonstrates limited enhancement in rate capability.The combination of currently reported pseudocapacitive materials and MXene tends to express the potential capacitance of pseudocapacitive materials rather than MXene,leading to low volumetric capacitance.Therefore,it is necessary to exploit more ideal candidate materials to couple with MXene for fully expressing both potentials.Herein,for the first time,high electrochemically active materials of ultrathin MoO3 nanobelts are intercalated into MXene films.In the composites,MoO3 nanobelts not only act as pillaring components to prevent restacking of MXene nanosheets for fully expressing the MXene pseudocapacitance in acidic environment but also provide considerable pseudocapacitive contribution.As a result,the optimal M/MoO3 electrode not only achieves a breakthrough in volumetric capacitance(1817 F cm-3 and 545 F g-1),but also maintains good rate capability and excellent flexibility.Moreover,the corresponding symmetric supercapacitor likewise shows a remarkable energy density of 44.6 Wh L-1(13.4 Wh kg-1),rendering the flexible electrode a promising candidate for application in high-energy-density energy storage devices.

Pampas grass-inspired FeOOH nanobelts as high performance anodes for sodium ion batteries

High-performance materials are the key to developing new alternative energy-storage systems[1-4].Sodium ion batteries(SIBs)are regarded as the promising large-scale electric energy storage owing to the high abundance and low cost of sodium resources[1,5-9].However,the sluggish kinetics of Na^(+)caused by the large-sized Na^(+)(1.02A)result in the lower energy density and unsatisfactory electrochemical properties[10-14].

Preparation and NO_2-gas sensing property of individual β-Ga_2O_3 nanobelt

Monoclinic gallium oxide （βGa2O3） nanobelts are synthesized from gallium and oxygen by thermal evaporation in an axgon atmosphere and their NO2 sensing properties are studied at room temperature. Electron microscopy studies show that the nanobelts have breadths ranging from 30 to 50 nm and lengths up to tens of micrometers. Both the x-ray diffraction （XRD） and the selected are electron diffraction （SAED） examinations indicate that β-Ga203 nanobelts have grown into single crystals. Room temperature NO2 sensing tests show that the current of individual β-Ga2O3 nanobelt decreases quickly, and then gently when the NO2 concentration increases from low to high. It is caused by the NO2 molecule chemisorption and desorption processes in the surface of β-Ga2O3 nanobelt.

Synthesis and Electrochemical Behaviors of a-MoO_3 Nanobelts/Carbon Nanotubes Composites for Lithium Ion Batteries

α-MoO3 nanobelts/carbon nanotubes（CNTs） composites were synthesized by simple hydrothermal method followed by CNTs incorporating, and characterized by X-ray diffraction（XRD） and scanning electron microscopy（SEM）. Cyclic voltammogram（CV）, electrochemical impedance spectroscopy（EIS）, and galvanostatic charge/discharge testing techniques were employed to evaluate the electrochemical behaviors of α-MoO3 nanobelts/CNTs composites. The results exhibited that compared to bare α-MoO3 nanobelts, the α-MoO3 nanobelts/CNTs composites have better electrochemical performances as cathode materials for lithium ion battery, maintaining a reversible specific capacity of 222.2 mAh/g at 0.3 C after 50 cycles, and 74.1% retention of the first reversible capacity. In addition, the Rct value of the α-MoO3 nanobelts/CNTs is 13 Ω, much lower than 66 Ω of the bare α-MoO3 nanobelts. The better electrochemical performances of the α-MoO3 nanobelts/CNTs composites can be attributed to the effects of the high conductive CNTs network.

Preparation of Manganese Oxide Nanobelts

Oriented nanobelts of manganese oxide have been firstly and successfully prepared by a microemulsion technique under controlled circumstances. The samples were characterized by X-ray diffraction (XRD), transmission electron microscope (TEM). Influences of sodium chloride and annealed temperature on the synthesis of Mn3O4 nanobelts were investigated. It was found that NaCI is the key factor to synthesize oriented Mn3O4 nanobelts and 827 K is optimum temperature to produce fine nanobelts. Oriented growth mechanism of Mn3O4 nanobelts was discussed.

Preparation and Characterization of Cu_3V_2O_7(OH)_2·2H_2O Hollow Spheres from Na_2V_6O_16·3H_2O Nanobelts

Monoclinic Cu3V2O7（OH）2·2H2O（copper polyvanadate） hollow spheres were prepared with Na2V6O16·3H2O nanobelts as V-precursor by hydrothermal method. The purity and structure of the products were characterized by X-ray powder diffraction（XRD）, Fourier transform infrared（FTIR） spectroscopy, Raman spectroscopy, thermogravimetric analysis（TGA） and X-ray photoelecton spectroscopy（XPS）. The morphology and size were observed by scanning electron microscopy（SEM）. We found that the Kagomé staircase-structural copper polyvanadate hollow spheres with an average diameter of 7 μm could be easily synthesized via the reaction of Na2V6O16·3H2O nanobelts with sufficient copper sulfate. The dielectric property of the copper polyvanadate demonstrates that dielectric loss hardly changes when the frequency of applied electric field is higher than 100 kHz. The formation process of the hollow spheres is discussed in detail by the observation of a series of products prepared for different reaction time.

Controllable synthesis of ultrathin vanadium oxide nanobelts via an EDTA-mediated hydrothermal process

Ultrathin VO_2 nanobelts with rough alignment features are prepared on the induction layer-coated substrates by an ethylenediaminetetraacetic acid（EDTA）-mediated hydrothermal process. EDTA acts as a chelating reagent and capping agent to facilitate the one-dimensional（1D） preferential growth of ultrathin VO_2 nanobelts with high crystallinities and good uniformities. The annealed induction layer and concentration of EDTA are found to play crucial roles in the formation of aligned and ultrathin nanobelts. Variation in EDTA concentration can change the VO_2 morphology of ultrathin nanobelts into that of thick nanoplates. Mild annealing of ultrathin VO_2 nanobelts at 350℃ in air results in the formation of V_2O_5 nanobelts with a nearly unchanged ultrathin structure. The nucleation and growth mechanism involved in the formations of nanobelts and nanoplates are proposed. The ethanol gas sensing properties of the V_2O_5 nanobelt networks-based sensor are investigated in a temperature range from 100℃ to 300℃ over ethanol concentrations ranging from 3 ppm to 500 ppm.The results indicate that the V_2O_5 nanobelt network sensor exhibits high sensitivity, good reversibility, and fast responserecovery characteristics with an optimal working temperature of 250℃.

Single crystalline boron carbide nanobelts:synthesis and characterization

This paper reports that the large-scale single crystalline boron carbide nanobelts have been fabricated through a simple carbothermal reduction method with B/B2O3/C/Fe powder as precursors at 1100℃. Transmission electron microscopy and selected area electron diffraction characterizations show that the boron carbide nanobelt has a B4C rhomb-centred hexagonal structure with good crystallization. Electron energy loss spectroscopy analysis indicates that the nanobelt contains only B and C, and the atomic ratio of B to C is close to 4：1. High resolution transmission electron microscopy results show that the preferential growth direction of the nanobelt is [101]. A possible growth mechanism is also discussed.

Facile Preparation and Visible-light Photocatalysis Enhancement of N-Doped β-TiO_2 Nanobelts

A facile preparation of nitrogen-doped β-TiO2（N-doped β-TiO2） nanobelts and their visible-light photocatalytic activity were reported.The preparation of N-doped β-TiO2 nanobelts consisted of cation-exchange between layered sodium titanate nanobelts and NH 4 ＋ in aqueous solution at room temperature and subsequent calcination in air.Such a calcination treatment is beneficial to the formation of monoclinic N-doped β-TiO2 nanobelts.Various measurement results indicate that not only were the nitrogen atoms doped into the lattice of β-TiO2 nanobelts resulting in a strong visible-light absorption,but also a large number of defects were caused by them in the lattice,increasing the stability of β-TiO2.The photocatalysis enhancement of N-doped β-TiO2 nanobelts for the photodegradation of Rhodamine B was demonstrated.

Self-assemble Mechanism of Nickel Nanobelts Prepared by Sol-precipitation and Thermal Decomposition Route

Using the idea of material design and the design of reaction system and conditions,quasi-one-dimensional nano-materials with ribbon-like structure were successfully prepared.Nickel tartrate nanobelts were prepared by a sol-precipitation route,using nickel chloride hexahydrate and tartaric acid as raw materials,and using ammonium hydroxide as pH value modifier.Nickel nanobelts with smooth surface were prepared by a thermal-decomposition route at about 355℃for about 30 minutes,in CO_(2) atmosphere,using nickel tartrate nanobelts as precursor.The analyses of atomic absorption spectrometry(AAS),organic elemental analyzer(OEA),infrared spectroscopy(IR)and ultraviolet-visible spectroscopy(UV-Vis)indicate that the products as-prepared is nickel tartrate,which has octahedral configuration of co-ordination of nickel atoms.The images of scanning electron microscopy(SEM)indicate that the morphology of nickel tartrate as-prepared is an obvious belt structure with clear and smooth surface.The images of SEM also indicate that the nickel nanobelts have clear and smooth surface.The nickel nanobelts are about tens of micrometers in length,tens of nanometers in thickness,and 100-200 nanometers in width.