Ga_(2)O_(3) is considered a potential anode material for next-generation lithium-ion batteries due to its high theoretical capacity and unique self-healing capability.To develop a novel preparation method and in-depth...Ga_(2)O_(3) is considered a potential anode material for next-generation lithium-ion batteries due to its high theoretical capacity and unique self-healing capability.To develop a novel preparation method and in-depth understanding of the electrochemical reaction mechanism of Ga_(2)O_(3),a brand-new liquid-liquid dealloying strategy was exploited to construct porous α-Ga_(2)O_(3) nanowire networks.Profiting from the well-designed porous structure,the material exhibits impressive cycling stability of a reversible capacity of 603.9 mA·h/g after 200 cycles at 1000 mA/g and a capacity retention of 125.2 mA·h/g after 100 cycles at 0.5C when assembling to Ga_(2)O_(3)//LiFePO_(4) full cells.The lithiation/delithiation reaction mechanism of the porous Ga_(2)O_(3) anodes is further revealed by ex-situ Raman,XRD,TEM measurements,and density functional theoretical(DFT)calculations,which establishes a correlation between the electrochemical performance and the phase transition fromα-Ga_(2)O_(3) to β-Ga_(2)O_(3) during cycling.展开更多
Electrochemical reduction of carbon dioxide(CO_(2)RR)is a promising approach to complete the carbon cycle and potentially convert CO_(2)into valuable chemicals and fuels.Cu is unique among transition metals in its abi...Electrochemical reduction of carbon dioxide(CO_(2)RR)is a promising approach to complete the carbon cycle and potentially convert CO_(2)into valuable chemicals and fuels.Cu is unique among transition metals in its ability to catalyze the CO_(2)RR and produce multi-carbon products.However,achieving high selectivity for C2+products is challenging for copper-based catalysts,as C–C coupling reactions proceed slowly.Herein,a surface modification strategy involving grafting long alkyl chains onto copper nanowires(Cu NWs)has been proposed to regulate the electronic structure of Cu surface,which facilitates*CO-*CO coupling in the CO_(2)RR.The hydrophobicity of the catalysts increases greatly after the introduction of long alkyl chains,therefore the hydrogen evolution reaction(HER)has been inhibited effectively.Such surface modification approach proves to be highly efficient and universal,with the Faradaic efficiency(FE)of C_(2)H_(4) up to 53%for the optimized Cu–SH catalyst,representing a significant enhancement compared to the pristine Cu NWs(30%).In-situ characterizations and theoretical calculations demonstrate that the different terminal groups of the grafted octadecyl chains can effectively regulate the charge density of Cu NWs interface and change the adsorption configuration of*CO intermediate.The top-adsorbed*CO intermediates(*COtop)on Cu–SH catalytic interface endow Cu–SH with the highest charge density,which effectively lowers the reaction energy barrier for*CO-*CO coupling,promoting the formation of the*OCCO intermediate,thereby enhancing the selectivity towards C_(2)H_(4).This study provides a promising method for designing efficient Cu-based catalysts with high catalytic activity and selectivity towards C2H4.展开更多
With high surface-to-volume ratio,the abundant surface states and high carrier concentration are challenging the nearinfrared photodetection behaviors of narrow band gap semiconductors nanowires.In this study,the narr...With high surface-to-volume ratio,the abundant surface states and high carrier concentration are challenging the nearinfrared photodetection behaviors of narrow band gap semiconductors nanowires.In this study,the narrow band gap semiconductor of Bi_(2)O_(2)Se nanosheets(NSs)is adopted to construct mixed-dimensional heterojunctions with GaSb nanowires(NWs)for demonstrating the impressive self-powered NIR photodetection.Benefiting from the built-in electric field of~140 meV,the as-constructed NW/NS mixeddimensional heterojunction self-powered photodetector shows the low dark current of 0.07 pA,high I_(light)/I_(dark)ratio of 82 and fast response times of<2/2 ms at room temperature.The self-powered photodetector performance can be further enhanced by fabricating the NW array/NS mixed-dimensional heterojunction by using a contact printing technique.The excellent photodetection performance promises the asconstructed NW/NS mixed-dimensional heterojunction self-powered photodetector in imaging and photocommunication.展开更多
Efficient removal of pollutant formaldehyde(HCHO) at room temperature using transition-metal oxides remains a huge challenge to date. Manganese oxide can oxidize formaldehyde, however, how to control the valence state...Efficient removal of pollutant formaldehyde(HCHO) at room temperature using transition-metal oxides remains a huge challenge to date. Manganese oxide can oxidize formaldehyde, however, how to control the valence states of manganese is the key to further improve the removal efficiency. We have successfully prepared porous manganese oxide nanowires(Mn OxNWs) with large surface area and multiple valence states of manganese using simple electrospinning followed by thermal calcination and potassium permanganate solution post-treatment(C/S process). The contents of trivalent and tetravalent manganese increased significantly after C/S process. Moreover, the composition of silver oxide coated silver nanowires(Ag@Ag_(2) O NWs) is realized by assistance with oxygen plasma, which further enhanced high valence manganese. The formaldehyde removal efficiency by Ag@Ag_(2) O–Mn Oxcomposite nanowires can reach 93.7%. The high-efficient catalytic activity is confirmed to attribute to the higher surface area of composite nanowires, the high-valence manganese and the silver oxide for oxidation of formaldehyde.展开更多
Assembling MnO_(2)nanowires into macroscopic membrane is a promising engineered technology for catalyst separation and enhancement of Fenton-like reaction activity,yet its development is limited by the deficiencies in...Assembling MnO_(2)nanowires into macroscopic membrane is a promising engineered technology for catalyst separation and enhancement of Fenton-like reaction activity,yet its development is limited by the deficiencies in preparation and property modulation of the MnO_(2)nanowires.In this work,we developed a facile method using C_(2)H_5OH and CH_(3)COOK as reductive and vital control reagents to react with KMnO_(4)by hydrothermal reaction at 140℃for 12 h,to prepare the ultralongα-MnO_(2)nanowires up to tens of micrometers with high purity and aspect ratio.Such strategy not only had the advantages of being mild,easily controlled and environmental pollution-free,but also endowedα-MnO_(2)nanowires with excellent ability as a Fenton catalyst when assembled into free-standing membrane for degrading phenolic compounds(k_(obs)=0.0738~0.1695 min^(-1))in a continuous flow reaction.The reactive oxygen species(i.e.,~·OH)from Fenton-like reaction were enriched within thisα-MnO_(2)nanowire membrane via nanoconfinement effect,which further enhanced the mass transportation of~·OH available for phenolic contaminants.MnO_(2)nanowire membrane using our method possessed the high practical potential for water purify due to its easy-preparation and enhanced catalytic performances.展开更多
Titania nanowires(TiO2-NW)with tunable aspect ratios and morphologies were directly synthesized using a simple alcohol-thermal technique.Specifically,ethanol and acetic acid were used as solvents and lithium ion was u...Titania nanowires(TiO2-NW)with tunable aspect ratios and morphologies were directly synthesized using a simple alcohol-thermal technique.Specifically,ethanol and acetic acid were used as solvents and lithium ion was used as the capping agent to promote the conversion of titanium butoxide into TiO2-NW.The morphologies and crystal phases of TiO2-NW were determined by the molar ratio of solvents and the content(mol%)of lithium ion.The band gap of TiO2-NW with pure anatase phase is slightly bigger than that of TiO2-NW with a mixture of anatase and rutile phases.All TiO2-NW could achieve effective decolorization of methyl blue(the decolorization rate is over 95%)after 35-min ultraviolet(UV)irradiation.展开更多
High-performance perovskite photodetectors with self-driven characteristic usually need electron/hole transport layers to extract carriers. However, these devices with transport layer structure are prone to result in ...High-performance perovskite photodetectors with self-driven characteristic usually need electron/hole transport layers to extract carriers. However, these devices with transport layer structure are prone to result in a poor perovskite/transport layer interface, which restricts the performance and stability of the device. To solve this problem, this work reports a novel device structure in which perovskite nanowires are in-situ prepared on PbI_(2), which serves as both a reaction raw material and efficient carrier extraction layer. By optimizing the thickness of PbI_(2), nanowire growth time, and ion exchange time, a selfdriven photodetector with an ITO/PbI_(2)/CsPbBr_(3)/carbon structure is constructed. The optimized device achieves excellent performance with the responsivity of 0.33 A/W, the detectivity of as high as 3.52 × 10^(13) Jones. Furthermore, the device can detect the light with its optical power lowered to 0.1 nW/cm^(2). This research provides a new method for preparing perovskite nano/micro devices with simple structure but excellent performance.展开更多
The commonly-employed material for thermal barrier coatings(TBCs)is 7 wt.%Y2O3 ZrO2(7YSZ),generally deposited by electron beam-physical vapor deposition(EB-PVD).Due to the increasing demand for higher operating temper...The commonly-employed material for thermal barrier coatings(TBCs)is 7 wt.%Y2O3 ZrO2(7YSZ),generally deposited by electron beam-physical vapor deposition(EB-PVD).Due to the increasing demand for higher operating temperature in aero-derivative gas turbines,a lot of effort has been made to prevent the premature failure of columnar 7YSZ TBCs,which is induced by the microstructure degradation,sintering and spallation after the deposition of infiltrated siliceous mineral(consisting of calcium magnesium aluminum silicate(CaO MgO Al2O3 SiO2,i.e.,CMAS)).A new method called Al-modification for columnar 7YSZ TBCs against CMAS corrosion was present.The Al film was magnetron-sputtered on the surface of the columnar 7YSZ TBCs,followed by performing vacuum heat treatment of the Al-deposited TBCs.During the heat treatment,the molten Al reacted with ZrO2 to formα-Al2O3 overlay that effectively hindered CMAS infiltration.Moreover,the Al film could evaporate and re-nucleate,leading to the generation of Al2O3 nanowires,which further restrained the moving of molten CMAS.展开更多
Although computational studies have demonstrated that metal ion doping can effectively narrow the bandgap of TiO_(2),the visible-light photoactivity of metal-doped TiO_(2) photoanodes is still far from satisfactory.He...Although computational studies have demonstrated that metal ion doping can effectively narrow the bandgap of TiO_(2),the visible-light photoactivity of metal-doped TiO_(2) photoanodes is still far from satisfactory.Herein,we report an effective strategy to activate the visible-light photoactivity of chromiumimplanted TiO_(2) via the incorporation of oxygen vacancies.The chromium-doped TiO_(2) activated by oxygen vacancies(Cr-TiO_(2)-vac)exhibited an incident photon-to-electron conversion efficiency(IPCE)of~6.8%at450 nm,which is one of the best values reported for metal-doped TiO_(2).Moreover,Cr-TiO_(2)-vac showed no obvious photocurrent decay after 100 h under visible-light illumination.展开更多
In this work, a fast(0.5 h), green microwave-assisted synthesis of single crystalline Sb_2Se_3 nanowires was developed. For the first time we demonstrated a facile solvent-mediated process, whereby intriguing nanostru...In this work, a fast(0.5 h), green microwave-assisted synthesis of single crystalline Sb_2Se_3 nanowires was developed. For the first time we demonstrated a facile solvent-mediated process, whereby intriguing nanostructures including antimony selenide(Sb_2Se_3) nanowires and selenium(Se) microrods can be achieved by merely varying the volume ratio of ethylene glycol(EG) and H_2O free from expensive chemical and additional surfactant. The achieved uniform Sb_2Se_3 nanowire is single crystalline along [001]growth direction with a diameter of 100 nm and a length up to tens of micrometers. When evaluated as an anode of lithium-ion battery, Sb_2Se_3 nanowire can deliver a high reversible capacity of 650.2 m Ah g^(-1) at 100 mA g^(-1) and a capacity retention of 63.8% after long-term 1000 cycles at 1000 mA g^(-1), as well as superior rate capability(389.5 m Ah g^(-1) at 2000 mA g^(-1)). This easy solvent-mediated microwave synthesis approach exhibits its great universe and importance towards the fabrication of high-performance metal chalcogenide electrode materials for future low-cost, large-scale energy storage systems.展开更多
Silicon nanowires(SiNWs)with diameter distributions ranging from 80 to 350 nm were prepared by electrochemical reduction of Ni/SiO2 in molten CaCl2.The effect of the content of nickel additives on the morphology of pr...Silicon nanowires(SiNWs)with diameter distributions ranging from 80 to 350 nm were prepared by electrochemical reduction of Ni/SiO2 in molten CaCl2.The effect of the content of nickel additives on the morphology of produced silicon was investigated.Large quantities of SiNWs are obtained by the electrochemical reduction of Ni/SiO2 blocks with SiO2 to Ni molar ratio of 20 and 10.Nickel additives repress the growth of irregular branches and promote longitudinal growth of SiNWs.Wire morphologies and surfaces are influenced by the electrolysis temperature.SiNWs become thicker with the increase of the electrolysis temperature.The optimum temperature to prepare single crystal SiNWs with high aspect ratio and extraordinary surface quality seems to be 1173 K.The amorphous layer of the silicon nanowire is thinner compared to the SiNWs obtained from the pure SiO2 pellets.The produced SiNWs show a photoluminescence emission peak at about 758 nm at room temperature.This work demonstrates the potentiality for the electrochemical reduction process to obtain large quantities of SiNWs with high quality.展开更多
TiO2 nanowire arrays were successfully fabricated by liquid-phase deposition method using porous alumina templates. The obtained TiO2 nanowires were characterized using Raman spectroscopy, X-ray diffraction （XRD）, s...TiO2 nanowire arrays were successfully fabricated by liquid-phase deposition method using porous alumina templates. The obtained TiO2 nanowires were characterized using Raman spectroscopy, X-ray diffraction （XRD）, scanning electron microscopy （SEM）, field emission scanning electron microscopy （FE- SEM）, transmission electron microscopy （TEM）, and selected area electron diffraction （SAED） analysis. Results of electron microscopic observations indicated that the nanowires were smooth and uniform with a diameter of about 50-80 nm and several micrometers in length. SAED, Raman, and XRD mea- surements showed that TiO2 nanowires were single-crystalline with a pure rutile structure after heating at 800 ~C for 10 h. In this situation, the nanowire constituents grew preferentially along the 〈001〉 direction. Furthermore, the formation process and mechanistic study of the Ti02 nanowire arrays were proposed and discussed in detail. The nanowires are clearly produced by the deposition of TiO2 particles on the inner wall of the template nanochannels.展开更多
Urea oxidation is a significant reaction for utilizing urea-rich wastewater or human urine as sustainable power sources which can ease the water eutrophication while generate electricity. A direct urea-hydrogen peroxi...Urea oxidation is a significant reaction for utilizing urea-rich wastewater or human urine as sustainable power sources which can ease the water eutrophication while generate electricity. A direct urea-hydrogen peroxide fuel cell is a new kind of fuel cell employing urea as fuel and hydrogen peroxide as oxidant which possesses a larger cell voltage. Herein, this work tries to promote the kinetics process of urea oxidation by preparing low-cost and high-efficient NiCo2S4 nanowires modified carbon sponge electrode. The carbon sponge used in this work with a similar three-dimensional multi-channel structure to Ni foam, is prepared by carbonizing recycled polyurethane sponge which is also a process of recycling waste. The performance of the prepared catalyst in an alkaline solution is investigated in a three-electrode system.With the introduction of Co element to the catalyst, a reduced initial urea oxidation potential and a high performance are obtained. Furthermore, a direct urea-hydrogen peroxide fuel cell is assembled using the NiCo2S4 nanowires modified carbon sponge anode. Results indicate that the prepared catalyst provides a chance to solve the current problems that hinder the development of urea electrooxidation(high initial urea oxidation potential, low performance, and high electrode costs).展开更多
The conversion of carbon dioxide into valuable organic compounds is a highly promising approach to address the energy issues and environmental problems(e.g., global warming). Herein, we presents a facile and efficient...The conversion of carbon dioxide into valuable organic compounds is a highly promising approach to address the energy issues and environmental problems(e.g., global warming). Herein, we presents a facile and efficient method to prepare highly dense and well-dispersed SnO2 nanocrystals on 1 D N-doped carbon nanowires as advanced catalysts for the efficient electroreduction of CO2 to formate. The ultrasmall SnO2 coated on the N-doped carbon nanowires(SnO2@N-CNW) has been synthesized via the simple hydrothermal treatment coupled with a pyrolysis process. The unique structure enables to expose the active tin oxide and also provides the facile pathways for rapid transfer of electron and electrolyte along with the highly porous carbon foam composed with interconnected carbon nanowires. Therefore, SnO2@NCNW electrocatalyst exhibits good durability and high selectivity for formate formation with a Faradaic efficiency of ca. 90%. This work demonstrates a simple method to rationally design high-dense tin oxide nanocrystals on the conductive carbon support as advanced catalysts for CO2 electroreduction.展开更多
Nanowire(NW) structures is an alternative candidate for constructing the next generation photoelectrochemical water splitting system, due to the outstanding optical and electrical properties. NW photoelectrodes compar...Nanowire(NW) structures is an alternative candidate for constructing the next generation photoelectrochemical water splitting system, due to the outstanding optical and electrical properties. NW photoelectrodes comparing to traditional semiconductor photoelectrodes shows the comparatively shorter transfer distance of photo-induced carriers and the increase amount of the surface reaction sites, which is beneficial for lowering the recombination probability of charge carriers and improving their photoelectrochemical(PEC) performances. Here, we demonstrate for the first time that super-long Cu_2O NWs, more than 4.5 μm,with highly efficient water splitting performance, were synthesized using a cost-effective anodic alumina oxide(AAO) template method. In comparison with the photocathode with planar Cu_2O films, the photocathode with Cu_2O NWs demonstrates a significant enhancement in photocurrent, from –1.00 to –2.75 mA/cm^2 at –0.8 V versus Ag/AgCl. After optimization of the photoelectrochemical electrode through depositing Pt NPs with atomic layer deposition(ALD) technology on the Cu_2O NWs, the plateau of photocurrent has been enlarged to –7 mA/cm^2 with the external quantum yield up to 34% at 410 nm. This study suggests that the photoelectrode based on Cu_2O NWs is a hopeful system for establishing high-efficiency water splitting system under visible light.展开更多
Mixed oxide photocatalysts, ZnO-Zn2SnO4 （ZnO-ZTO） nanowires with different sizes were prepared by a simple thermal evaporation method. The ZnO-ZTO nanowires were characterized with a scanning electron microscope, X-...Mixed oxide photocatalysts, ZnO-Zn2SnO4 （ZnO-ZTO） nanowires with different sizes were prepared by a simple thermal evaporation method. The ZnO-ZTO nanowires were characterized with a scanning electron microscope, X-ray diffraction, high-resolution transmission electron microscopy, energy-dispersive spectrom- eter, and X-ray photoelectron spectra. The photocatalytic activity of the ZnO-ZTO mixed nanowires were studied by observing the photodegradation behaviors of methyl orange aqueous solution. The results suggest that the ZnO-ZTO mixed oxide nanowires have a higher photocatalytic activity than pure ZnO and Zn2SnO4 nanowires. The photocatalyst concentration in the solution distinctly affects the degradation rate, and our results show that higher photodegradation efficiency can be achieved with a smaller amount of ZnO-ZTO nanowire catalyst, as compared to the pure ZnO and ZTO nanowires. Moreover, the photocatalytic activity can also be enhanced by reducing the average diameter of the nanowires. The activity of pure ZnO and ZTO nanowires are also enhanced by physically mixing them. These results can be explained by the synergism between the two semiconductors.展开更多
The recombination loss of photo-carriers in photocatalytic systems fatally determines the energy conversion efficiency of photocatalysts.In this work,an electrostatic field was used to inhibit the recombination of pho...The recombination loss of photo-carriers in photocatalytic systems fatally determines the energy conversion efficiency of photocatalysts.In this work,an electrostatic field was used to inhibit the recombination of photo-carriers in photocatalysts by separating photo-holes and photo-electrons in space.As a model structure,(010)facet-exposed BiVO_(4)nanowires were grown on PDMS-insulated piezo-substrate of piezoelectric transducer(PZT).The PZT substrate will generate an electrostatic field under a certain stress,and the photocatalytic behavior of BiVO_(4) nanowires is influenced by the electrostatic field.Our results showed that the photocatalytic performance of the BiVO_(4) nanowires in CO_(2)reduction in the negative electrostatic field is enhanced to 5.5-fold of that without electrostatic field.Moreover,the concentration of methane in the products was raised from 29% to 64%.The enhanced CO_(2) reduction efficiency is mainly attributed to the inhibited recombination loss of photo-carriers in the BiVO_(4) nanowires.The increased energy of photo-carriers and the enhanced surface absorption to polar molecules,which are CO in this case,were also play important roles in improving the photocatalytic activity of the photocatalyst and product selectivity.This work proposed an effective strategy to improve photo-carriers separation/transfer dynamics in the photocatalytic systems,which will also be a favorable reference for photovoltaic and photodetecting devices.展开更多
Low-cost and flexible solid polymer electrolytes are promising in all-solid-state Li-metal batteries with high energy density and safety.However,both the low room-temperature ionic conductivities and the small Li^(+)t...Low-cost and flexible solid polymer electrolytes are promising in all-solid-state Li-metal batteries with high energy density and safety.However,both the low room-temperature ionic conductivities and the small Li^(+)transference number of these electrolytes significantly increase the internal resistance and overpotential of the battery.Here,we introduce Gd-doped CeO_(2) nanowires with large surface area and rich surface oxygen vacancies to the polymer electrolyte to increase the interaction between Gd-doped CeO_(2) nanowires and polymer electrolytes,which promotes the Li-salt dissociation and increases the concentration of mobile Li ions in the composite polymer electrolytes.The optimized composite polymer electrolyte has a high Li-ion conductivity of 5×10^(-4)4 S cm^(-1) at 30℃ and a large Li+transference number of 0.47.Moreover,the composite polymer electrolytes have excellent compatibility with the metallic lithium anode and high-voltage LiNi_(0.8)Mn _(0.1)Co_(0.1)O_(2)(NMC)cathode,providing the stable cycling of all-solid-state batteries at high current densities.展开更多
Sodium-ion batteries(SIBs) and potassium-ion batteries(PIBs) have been attracting great attentions and widely been exploited due to the abundant sodium/potassium resources.Hence,the preparation of high-powered anode m...Sodium-ion batteries(SIBs) and potassium-ion batteries(PIBs) have been attracting great attentions and widely been exploited due to the abundant sodium/potassium resources.Hence,the preparation of high-powered anode materials for SIBs/PIBs plays a decisive role for the commercial applications of SIBs/PIBs in the future.Manganese selenides are a class of potential anode materials for SIBs/PIBs because of their small band gap and high electrical conductivity.In this work,MnSe and ReS_(2) core-shell nanowires connecting by polydopamine derived carbon nanotube(MnSe@NC@ReS_(2)) have been successfully synthesized from growing ReS_(2) nanosheets array on the surface of MnSe@NC nano wires,which present excellent Na^(+)/K^(+) storage performance.While applied as SIBs anode,the specific capacity of 300 mAh·g^(-1) was maintwined after 400 cycles at the current density of 1.0 A·g^(-1).Besides,it could also keep 120 mAh·g^(-1) specific capacity after 900 cycles at 1.0 A·g^(-1) for the anode of PIBs.These heterogeneous engineering and one-dimensional-two-dimensional(1D-2D) hybrid strategies could provide an ideal strategy for the synthesis of new hetero-structured anode materials with outstanding battery performance for SIBs and PIBs.展开更多
Superlattice nanowires are expected to show further enhanced thermoelectric performance compared with conventional nanowires or superlattice thin films. We report the epitaxial growth of high density Bi2Te3/Sb superla...Superlattice nanowires are expected to show further enhanced thermoelectric performance compared with conventional nanowires or superlattice thin films. We report the epitaxial growth of high density Bi2Te3/Sb superlattice nanowire arrays with a very small bilayer thickness by pulse electrodeposition. Transmission electron microscopy, selected area electron diffraction and high resolution transmission electron microscopy were used to characterize the superlattice nanowires, and Harman technique was employed to measure the figure of merit （ZT） of the superlattice nanowire array in high vacuum condition. The superlattice nanowire arrays exhibit a ZT of 0.15 at 330 K, and a temperature difference of about 6.6 K can be realized across the nanowire arrays.展开更多
基金the Natural Science Foundation of Hebei Province,China(No.E2023202253)Hebei Higher Education Teaching Reform Research and Practice Project,China(No.2021GJJG050).
文摘Ga_(2)O_(3) is considered a potential anode material for next-generation lithium-ion batteries due to its high theoretical capacity and unique self-healing capability.To develop a novel preparation method and in-depth understanding of the electrochemical reaction mechanism of Ga_(2)O_(3),a brand-new liquid-liquid dealloying strategy was exploited to construct porous α-Ga_(2)O_(3) nanowire networks.Profiting from the well-designed porous structure,the material exhibits impressive cycling stability of a reversible capacity of 603.9 mA·h/g after 200 cycles at 1000 mA/g and a capacity retention of 125.2 mA·h/g after 100 cycles at 0.5C when assembling to Ga_(2)O_(3)//LiFePO_(4) full cells.The lithiation/delithiation reaction mechanism of the porous Ga_(2)O_(3) anodes is further revealed by ex-situ Raman,XRD,TEM measurements,and density functional theoretical(DFT)calculations,which establishes a correlation between the electrochemical performance and the phase transition fromα-Ga_(2)O_(3) to β-Ga_(2)O_(3) during cycling.
文摘Electrochemical reduction of carbon dioxide(CO_(2)RR)is a promising approach to complete the carbon cycle and potentially convert CO_(2)into valuable chemicals and fuels.Cu is unique among transition metals in its ability to catalyze the CO_(2)RR and produce multi-carbon products.However,achieving high selectivity for C2+products is challenging for copper-based catalysts,as C–C coupling reactions proceed slowly.Herein,a surface modification strategy involving grafting long alkyl chains onto copper nanowires(Cu NWs)has been proposed to regulate the electronic structure of Cu surface,which facilitates*CO-*CO coupling in the CO_(2)RR.The hydrophobicity of the catalysts increases greatly after the introduction of long alkyl chains,therefore the hydrogen evolution reaction(HER)has been inhibited effectively.Such surface modification approach proves to be highly efficient and universal,with the Faradaic efficiency(FE)of C_(2)H_(4) up to 53%for the optimized Cu–SH catalyst,representing a significant enhancement compared to the pristine Cu NWs(30%).In-situ characterizations and theoretical calculations demonstrate that the different terminal groups of the grafted octadecyl chains can effectively regulate the charge density of Cu NWs interface and change the adsorption configuration of*CO intermediate.The top-adsorbed*CO intermediates(*COtop)on Cu–SH catalytic interface endow Cu–SH with the highest charge density,which effectively lowers the reaction energy barrier for*CO-*CO coupling,promoting the formation of the*OCCO intermediate,thereby enhancing the selectivity towards C_(2)H_(4).This study provides a promising method for designing efficient Cu-based catalysts with high catalytic activity and selectivity towards C2H4.
基金the Natural Science Foundation of Shandong Province(Nos.ZR2022JQ05 and ZR2024MF010).
文摘With high surface-to-volume ratio,the abundant surface states and high carrier concentration are challenging the nearinfrared photodetection behaviors of narrow band gap semiconductors nanowires.In this study,the narrow band gap semiconductor of Bi_(2)O_(2)Se nanosheets(NSs)is adopted to construct mixed-dimensional heterojunctions with GaSb nanowires(NWs)for demonstrating the impressive self-powered NIR photodetection.Benefiting from the built-in electric field of~140 meV,the as-constructed NW/NS mixeddimensional heterojunction self-powered photodetector shows the low dark current of 0.07 pA,high I_(light)/I_(dark)ratio of 82 and fast response times of<2/2 ms at room temperature.The self-powered photodetector performance can be further enhanced by fabricating the NW array/NS mixed-dimensional heterojunction by using a contact printing technique.The excellent photodetection performance promises the asconstructed NW/NS mixed-dimensional heterojunction self-powered photodetector in imaging and photocommunication.
基金financially supported by the National Natural Science Foundation of China (Grant No.51975151)the Heilongjiang Provincial Natural Science Foundation of China (Grant No.LH2019E041)Heilongjiang Touyan Team。
文摘Efficient removal of pollutant formaldehyde(HCHO) at room temperature using transition-metal oxides remains a huge challenge to date. Manganese oxide can oxidize formaldehyde, however, how to control the valence states of manganese is the key to further improve the removal efficiency. We have successfully prepared porous manganese oxide nanowires(Mn OxNWs) with large surface area and multiple valence states of manganese using simple electrospinning followed by thermal calcination and potassium permanganate solution post-treatment(C/S process). The contents of trivalent and tetravalent manganese increased significantly after C/S process. Moreover, the composition of silver oxide coated silver nanowires(Ag@Ag_(2) O NWs) is realized by assistance with oxygen plasma, which further enhanced high valence manganese. The formaldehyde removal efficiency by Ag@Ag_(2) O–Mn Oxcomposite nanowires can reach 93.7%. The high-efficient catalytic activity is confirmed to attribute to the higher surface area of composite nanowires, the high-valence manganese and the silver oxide for oxidation of formaldehyde.
基金The support from National Natural Science Foundation of China(Nos.52000050,52100024 and 42007115)Postdoctoral Science Foundation of China(Nos.2019M663245 and 2020M670913)+1 种基金Heilongjiang Postdoctoral Fund(No.LBH-Z20063)State Key Laboratory of Urban Water Resource and Environment(Harbin Institute of Technology)(Nos.2021TS22 and QAK202111)。
文摘Assembling MnO_(2)nanowires into macroscopic membrane is a promising engineered technology for catalyst separation and enhancement of Fenton-like reaction activity,yet its development is limited by the deficiencies in preparation and property modulation of the MnO_(2)nanowires.In this work,we developed a facile method using C_(2)H_5OH and CH_(3)COOK as reductive and vital control reagents to react with KMnO_(4)by hydrothermal reaction at 140℃for 12 h,to prepare the ultralongα-MnO_(2)nanowires up to tens of micrometers with high purity and aspect ratio.Such strategy not only had the advantages of being mild,easily controlled and environmental pollution-free,but also endowedα-MnO_(2)nanowires with excellent ability as a Fenton catalyst when assembled into free-standing membrane for degrading phenolic compounds(k_(obs)=0.0738~0.1695 min^(-1))in a continuous flow reaction.The reactive oxygen species(i.e.,~·OH)from Fenton-like reaction were enriched within thisα-MnO_(2)nanowire membrane via nanoconfinement effect,which further enhanced the mass transportation of~·OH available for phenolic contaminants.MnO_(2)nanowire membrane using our method possessed the high practical potential for water purify due to its easy-preparation and enhanced catalytic performances.
基金financially supported by the National Natural Science Foundation of China (No. 51408528)the Natural Science Foundation of Hebei Province, China (No. E2014203089)
文摘Titania nanowires(TiO2-NW)with tunable aspect ratios and morphologies were directly synthesized using a simple alcohol-thermal technique.Specifically,ethanol and acetic acid were used as solvents and lithium ion was used as the capping agent to promote the conversion of titanium butoxide into TiO2-NW.The morphologies and crystal phases of TiO2-NW were determined by the molar ratio of solvents and the content(mol%)of lithium ion.The band gap of TiO2-NW with pure anatase phase is slightly bigger than that of TiO2-NW with a mixture of anatase and rutile phases.All TiO2-NW could achieve effective decolorization of methyl blue(the decolorization rate is over 95%)after 35-min ultraviolet(UV)irradiation.
基金financially supported by the National Natural Science Foundation of China (51972101)the Research platforms and projects of Guangdong Universities in 2022 (2022ZDZX1028)Guangdong Provincial Key Laboratory Project (2023KSYS003)。
文摘High-performance perovskite photodetectors with self-driven characteristic usually need electron/hole transport layers to extract carriers. However, these devices with transport layer structure are prone to result in a poor perovskite/transport layer interface, which restricts the performance and stability of the device. To solve this problem, this work reports a novel device structure in which perovskite nanowires are in-situ prepared on PbI_(2), which serves as both a reaction raw material and efficient carrier extraction layer. By optimizing the thickness of PbI_(2), nanowire growth time, and ion exchange time, a selfdriven photodetector with an ITO/PbI_(2)/CsPbBr_(3)/carbon structure is constructed. The optimized device achieves excellent performance with the responsivity of 0.33 A/W, the detectivity of as high as 3.52 × 10^(13) Jones. Furthermore, the device can detect the light with its optical power lowered to 0.1 nW/cm^(2). This research provides a new method for preparing perovskite nano/micro devices with simple structure but excellent performance.
基金Project(2017YFB0306100) supported by the National Key Research&Development Plan of ChinaProjects(51801034,51771059) supported by the National Natural Science Foundation of China+3 种基金Projects(2018GDASCX-0949,2018GDASCX-0950,2017GDASCX-0111) supported by the Guangdong Academy of Sciences,ChinaProjects(2017B090916002,2017A070701027) supported by the Guangdong Technical Research Program,ChinaProjects(2016A030312015,2017A030310315) supported by the Natural Science Foundation of Guangdong Province,ChinaProjects(201605131008557,201707010385) supported by the Technical Research Program of Guangzhou City,China
文摘The commonly-employed material for thermal barrier coatings(TBCs)is 7 wt.%Y2O3 ZrO2(7YSZ),generally deposited by electron beam-physical vapor deposition(EB-PVD).Due to the increasing demand for higher operating temperature in aero-derivative gas turbines,a lot of effort has been made to prevent the premature failure of columnar 7YSZ TBCs,which is induced by the microstructure degradation,sintering and spallation after the deposition of infiltrated siliceous mineral(consisting of calcium magnesium aluminum silicate(CaO MgO Al2O3 SiO2,i.e.,CMAS)).A new method called Al-modification for columnar 7YSZ TBCs against CMAS corrosion was present.The Al film was magnetron-sputtered on the surface of the columnar 7YSZ TBCs,followed by performing vacuum heat treatment of the Al-deposited TBCs.During the heat treatment,the molten Al reacted with ZrO2 to formα-Al2O3 overlay that effectively hindered CMAS infiltration.Moreover,the Al film could evaporate and re-nucleate,leading to the generation of Al2O3 nanowires,which further restrained the moving of molten CMAS.
基金financially supported by the National Natural Science Foundation of China(U1867215,11722543,11875211,U1932134)the Suzhou Key Industrial Technology Innovation Project(SYG201828)+2 种基金the Hubei Provincial Natural Science Foundation(2019CFA036)the Fundamental Research Funds for the Central Universities(2042020kf0211)the financial support from the National Science Foundation(U.S.)under grant no.DMR-2003563。
文摘Although computational studies have demonstrated that metal ion doping can effectively narrow the bandgap of TiO_(2),the visible-light photoactivity of metal-doped TiO_(2) photoanodes is still far from satisfactory.Herein,we report an effective strategy to activate the visible-light photoactivity of chromiumimplanted TiO_(2) via the incorporation of oxygen vacancies.The chromium-doped TiO_(2) activated by oxygen vacancies(Cr-TiO_(2)-vac)exhibited an incident photon-to-electron conversion efficiency(IPCE)of~6.8%at450 nm,which is one of the best values reported for metal-doped TiO_(2).Moreover,Cr-TiO_(2)-vac showed no obvious photocurrent decay after 100 h under visible-light illumination.
基金supported by the National Key Research and Development Program of China(2016YFA0202603)the National Basic Research Program of China(2013CB934103)+5 种基金the National Natural Science Foundation of China(51521001,51602239)the National Natural Science Fund for Distinguished Young Scholars(51425204)Yellow Crane Talent(Science&Technology)Program of Wuhan Citythe Fundamental Research Funds for the Central Universities(WUT:2016III001,2016III003,2016IVA090)the Programme of Introducing Talents of Discipline to Universities(B17034)support from the Lorraine Region(nowpart of Grand Est Region)Cooperation Research Lorraine/Hubei Program 2015/2017
文摘In this work, a fast(0.5 h), green microwave-assisted synthesis of single crystalline Sb_2Se_3 nanowires was developed. For the first time we demonstrated a facile solvent-mediated process, whereby intriguing nanostructures including antimony selenide(Sb_2Se_3) nanowires and selenium(Se) microrods can be achieved by merely varying the volume ratio of ethylene glycol(EG) and H_2O free from expensive chemical and additional surfactant. The achieved uniform Sb_2Se_3 nanowire is single crystalline along [001]growth direction with a diameter of 100 nm and a length up to tens of micrometers. When evaluated as an anode of lithium-ion battery, Sb_2Se_3 nanowire can deliver a high reversible capacity of 650.2 m Ah g^(-1) at 100 mA g^(-1) and a capacity retention of 63.8% after long-term 1000 cycles at 1000 mA g^(-1), as well as superior rate capability(389.5 m Ah g^(-1) at 2000 mA g^(-1)). This easy solvent-mediated microwave synthesis approach exhibits its great universe and importance towards the fabrication of high-performance metal chalcogenide electrode materials for future low-cost, large-scale energy storage systems.
基金financially supported by the National Natural Science Foundation of China(No.51404032 and No.51504032)the National High Technology Research and Development Program of China(No.2013AA050904)
文摘Silicon nanowires(SiNWs)with diameter distributions ranging from 80 to 350 nm were prepared by electrochemical reduction of Ni/SiO2 in molten CaCl2.The effect of the content of nickel additives on the morphology of produced silicon was investigated.Large quantities of SiNWs are obtained by the electrochemical reduction of Ni/SiO2 blocks with SiO2 to Ni molar ratio of 20 and 10.Nickel additives repress the growth of irregular branches and promote longitudinal growth of SiNWs.Wire morphologies and surfaces are influenced by the electrolysis temperature.SiNWs become thicker with the increase of the electrolysis temperature.The optimum temperature to prepare single crystal SiNWs with high aspect ratio and extraordinary surface quality seems to be 1173 K.The amorphous layer of the silicon nanowire is thinner compared to the SiNWs obtained from the pure SiO2 pellets.The produced SiNWs show a photoluminescence emission peak at about 758 nm at room temperature.This work demonstrates the potentiality for the electrochemical reduction process to obtain large quantities of SiNWs with high quality.
基金supported by the Institute of Science and High Technology and Environmental Sciences(No.1/1859)
文摘TiO2 nanowire arrays were successfully fabricated by liquid-phase deposition method using porous alumina templates. The obtained TiO2 nanowires were characterized using Raman spectroscopy, X-ray diffraction （XRD）, scanning electron microscopy （SEM）, field emission scanning electron microscopy （FE- SEM）, transmission electron microscopy （TEM）, and selected area electron diffraction （SAED） analysis. Results of electron microscopic observations indicated that the nanowires were smooth and uniform with a diameter of about 50-80 nm and several micrometers in length. SAED, Raman, and XRD mea- surements showed that TiO2 nanowires were single-crystalline with a pure rutile structure after heating at 800 ~C for 10 h. In this situation, the nanowire constituents grew preferentially along the 〈001〉 direction. Furthermore, the formation process and mechanistic study of the Ti02 nanowire arrays were proposed and discussed in detail. The nanowires are clearly produced by the deposition of TiO2 particles on the inner wall of the template nanochannels.
基金the financial support of this study by the Ph.D.Student Research and Innovation Fund of the Fundamental Research Funds for the Central Universities(grant number GK6530260034)the National Natural Science Foundation of China(grant numbers:51572052)。
文摘Urea oxidation is a significant reaction for utilizing urea-rich wastewater or human urine as sustainable power sources which can ease the water eutrophication while generate electricity. A direct urea-hydrogen peroxide fuel cell is a new kind of fuel cell employing urea as fuel and hydrogen peroxide as oxidant which possesses a larger cell voltage. Herein, this work tries to promote the kinetics process of urea oxidation by preparing low-cost and high-efficient NiCo2S4 nanowires modified carbon sponge electrode. The carbon sponge used in this work with a similar three-dimensional multi-channel structure to Ni foam, is prepared by carbonizing recycled polyurethane sponge which is also a process of recycling waste. The performance of the prepared catalyst in an alkaline solution is investigated in a three-electrode system.With the introduction of Co element to the catalyst, a reduced initial urea oxidation potential and a high performance are obtained. Furthermore, a direct urea-hydrogen peroxide fuel cell is assembled using the NiCo2S4 nanowires modified carbon sponge anode. Results indicate that the prepared catalyst provides a chance to solve the current problems that hinder the development of urea electrooxidation(high initial urea oxidation potential, low performance, and high electrode costs).
基金financially supported by Guangdong Province Science and Technology Plan Project for Public Welfare Fund and Ability Construction Project(JCYJ20180301171324915)the National Natural Science Foundation of China(No.21503116)+1 种基金Taishan Scholars Program of Shandong Province(No.tsqn20161004)the Youth 1000 Talent Program of China。
文摘The conversion of carbon dioxide into valuable organic compounds is a highly promising approach to address the energy issues and environmental problems(e.g., global warming). Herein, we presents a facile and efficient method to prepare highly dense and well-dispersed SnO2 nanocrystals on 1 D N-doped carbon nanowires as advanced catalysts for the efficient electroreduction of CO2 to formate. The ultrasmall SnO2 coated on the N-doped carbon nanowires(SnO2@N-CNW) has been synthesized via the simple hydrothermal treatment coupled with a pyrolysis process. The unique structure enables to expose the active tin oxide and also provides the facile pathways for rapid transfer of electron and electrolyte along with the highly porous carbon foam composed with interconnected carbon nanowires. Therefore, SnO2@NCNW electrocatalyst exhibits good durability and high selectivity for formate formation with a Faradaic efficiency of ca. 90%. This work demonstrates a simple method to rationally design high-dense tin oxide nanocrystals on the conductive carbon support as advanced catalysts for CO2 electroreduction.
基金supported by European Research Council(HiNaPc:737616)European Research Council(ThreeDsurface:240144)+8 种基金BMBF(ZIK-3DNanoDevice:03Z1MN11)DFG(LE2249_4-1)BMBF(Meta-ZIK-BioLithoMorphie:03Z1M511)National Natural Science Foundation of China(Nos.21577086,51702130,21503209)Natural Science Foundation of Jiangsu Province(BK 20170550)Jiangsu Specially-Appointed Professor ProgramHundred-Talent Program(Chinese Academy of Sciences)Beijing Natural Science Foundation(No.2162042)Key Research Program of Frontier Science,CAS(No.QYZDBSSW-SLH006)
文摘Nanowire(NW) structures is an alternative candidate for constructing the next generation photoelectrochemical water splitting system, due to the outstanding optical and electrical properties. NW photoelectrodes comparing to traditional semiconductor photoelectrodes shows the comparatively shorter transfer distance of photo-induced carriers and the increase amount of the surface reaction sites, which is beneficial for lowering the recombination probability of charge carriers and improving their photoelectrochemical(PEC) performances. Here, we demonstrate for the first time that super-long Cu_2O NWs, more than 4.5 μm,with highly efficient water splitting performance, were synthesized using a cost-effective anodic alumina oxide(AAO) template method. In comparison with the photocathode with planar Cu_2O films, the photocathode with Cu_2O NWs demonstrates a significant enhancement in photocurrent, from –1.00 to –2.75 mA/cm^2 at –0.8 V versus Ag/AgCl. After optimization of the photoelectrochemical electrode through depositing Pt NPs with atomic layer deposition(ALD) technology on the Cu_2O NWs, the plateau of photocurrent has been enlarged to –7 mA/cm^2 with the external quantum yield up to 34% at 410 nm. This study suggests that the photoelectrode based on Cu_2O NWs is a hopeful system for establishing high-efficiency water splitting system under visible light.
基金ACKNOWLEDGMENTS This work was supported by the National Natu- ral Science Foundation of China （No.50121202 and No.90406009）, the National Research Foundation for the Doctoral Program of the Ministry of Education （No.20040358059） and the Natural Basic Program of China （No.2006CB922002）.
文摘Mixed oxide photocatalysts, ZnO-Zn2SnO4 （ZnO-ZTO） nanowires with different sizes were prepared by a simple thermal evaporation method. The ZnO-ZTO nanowires were characterized with a scanning electron microscope, X-ray diffraction, high-resolution transmission electron microscopy, energy-dispersive spectrom- eter, and X-ray photoelectron spectra. The photocatalytic activity of the ZnO-ZTO mixed nanowires were studied by observing the photodegradation behaviors of methyl orange aqueous solution. The results suggest that the ZnO-ZTO mixed oxide nanowires have a higher photocatalytic activity than pure ZnO and Zn2SnO4 nanowires. The photocatalyst concentration in the solution distinctly affects the degradation rate, and our results show that higher photodegradation efficiency can be achieved with a smaller amount of ZnO-ZTO nanowire catalyst, as compared to the pure ZnO and ZTO nanowires. Moreover, the photocatalytic activity can also be enhanced by reducing the average diameter of the nanowires. The activity of pure ZnO and ZTO nanowires are also enhanced by physically mixing them. These results can be explained by the synergism between the two semiconductors.
基金financially supported by the National Natural Science Foundation of China(21607066,51972153)Natural Science Foundation of Gansu Province of China(21JR7RA469)the Fundamental Research Funds for the Central Universities(lzujbky-2021-76).
文摘The recombination loss of photo-carriers in photocatalytic systems fatally determines the energy conversion efficiency of photocatalysts.In this work,an electrostatic field was used to inhibit the recombination of photo-carriers in photocatalysts by separating photo-holes and photo-electrons in space.As a model structure,(010)facet-exposed BiVO_(4)nanowires were grown on PDMS-insulated piezo-substrate of piezoelectric transducer(PZT).The PZT substrate will generate an electrostatic field under a certain stress,and the photocatalytic behavior of BiVO_(4) nanowires is influenced by the electrostatic field.Our results showed that the photocatalytic performance of the BiVO_(4) nanowires in CO_(2)reduction in the negative electrostatic field is enhanced to 5.5-fold of that without electrostatic field.Moreover,the concentration of methane in the products was raised from 29% to 64%.The enhanced CO_(2) reduction efficiency is mainly attributed to the inhibited recombination loss of photo-carriers in the BiVO_(4) nanowires.The increased energy of photo-carriers and the enhanced surface absorption to polar molecules,which are CO in this case,were also play important roles in improving the photocatalytic activity of the photocatalyst and product selectivity.This work proposed an effective strategy to improve photo-carriers separation/transfer dynamics in the photocatalytic systems,which will also be a favorable reference for photovoltaic and photodetecting devices.
基金This work was supported by the National Natural Science Foundation of China (51973157,61904123)the Tianjin Natural Science Foundation (18JCQNJC02900)+3 种基金the Special Grade of the Financial Support from the China Postdoctoral Science Foundation (2020T130469)the Sci-ence and Technology Plans of Tianjin (19PTSYJC00010)the Science&Technol-ogy Development Fund of Tianjin Education Commission for Higher Education (2018KJ196)State Key Laboratory of Membrane and Membrane Separation,Tiangong University.
文摘Low-cost and flexible solid polymer electrolytes are promising in all-solid-state Li-metal batteries with high energy density and safety.However,both the low room-temperature ionic conductivities and the small Li^(+)transference number of these electrolytes significantly increase the internal resistance and overpotential of the battery.Here,we introduce Gd-doped CeO_(2) nanowires with large surface area and rich surface oxygen vacancies to the polymer electrolyte to increase the interaction between Gd-doped CeO_(2) nanowires and polymer electrolytes,which promotes the Li-salt dissociation and increases the concentration of mobile Li ions in the composite polymer electrolytes.The optimized composite polymer electrolyte has a high Li-ion conductivity of 5×10^(-4)4 S cm^(-1) at 30℃ and a large Li+transference number of 0.47.Moreover,the composite polymer electrolytes have excellent compatibility with the metallic lithium anode and high-voltage LiNi_(0.8)Mn _(0.1)Co_(0.1)O_(2)(NMC)cathode,providing the stable cycling of all-solid-state batteries at high current densities.
基金financially supported by the National Natural Science Foundation of China (No.52101243)the Natural Science Foundation of Guangdong Province (No.2023A1515012619)the Science and Technology Planning Project of Guangzhou (No.202102010373)。
文摘Sodium-ion batteries(SIBs) and potassium-ion batteries(PIBs) have been attracting great attentions and widely been exploited due to the abundant sodium/potassium resources.Hence,the preparation of high-powered anode materials for SIBs/PIBs plays a decisive role for the commercial applications of SIBs/PIBs in the future.Manganese selenides are a class of potential anode materials for SIBs/PIBs because of their small band gap and high electrical conductivity.In this work,MnSe and ReS_(2) core-shell nanowires connecting by polydopamine derived carbon nanotube(MnSe@NC@ReS_(2)) have been successfully synthesized from growing ReS_(2) nanosheets array on the surface of MnSe@NC nano wires,which present excellent Na^(+)/K^(+) storage performance.While applied as SIBs anode,the specific capacity of 300 mAh·g^(-1) was maintwined after 400 cycles at the current density of 1.0 A·g^(-1).Besides,it could also keep 120 mAh·g^(-1) specific capacity after 900 cycles at 1.0 A·g^(-1) for the anode of PIBs.These heterogeneous engineering and one-dimensional-two-dimensional(1D-2D) hybrid strategies could provide an ideal strategy for the synthesis of new hetero-structured anode materials with outstanding battery performance for SIBs and PIBs.
文摘Superlattice nanowires are expected to show further enhanced thermoelectric performance compared with conventional nanowires or superlattice thin films. We report the epitaxial growth of high density Bi2Te3/Sb superlattice nanowire arrays with a very small bilayer thickness by pulse electrodeposition. Transmission electron microscopy, selected area electron diffraction and high resolution transmission electron microscopy were used to characterize the superlattice nanowires, and Harman technique was employed to measure the figure of merit （ZT） of the superlattice nanowire array in high vacuum condition. The superlattice nanowire arrays exhibit a ZT of 0.15 at 330 K, and a temperature difference of about 6.6 K can be realized across the nanowire arrays.
