MgH_(2),albeit with slow desorption kinetics,has been extensively studied as one of the most ideal solid hydrogen storage materials.Adding such catalyst as Ni can improve the desorption kinetics of MgH_(2),whereas the...MgH_(2),albeit with slow desorption kinetics,has been extensively studied as one of the most ideal solid hydrogen storage materials.Adding such catalyst as Ni can improve the desorption kinetics of MgH_(2),whereas the catalytic role has been attributed to different substances such as Ni,Mg_(2)Ni,Mg_(2)NiH0.3,and Mg_(2)NiH4.In the present study,Ni nanoparticles(Ni-NPs)supported on mesoporous carbon(Ni@C)have been synthesized to improve the hydrogen desorption kinetics of MgH_(2).The utilization of Ni@C largely decreases the dehydrogenation activation energy from 176.9 to 79.3 kJ mol^(−1) and the peak temperature of dehydrogenation from 375.5 to 235℃.The mechanism of Ni catalyst is well examined by advanced aberration-corrected environmental transmission electron microscopy and/or x-ray diffraction.During the first dehydrogenation,detailed microstructural studies reveal that the decomposition of MgH_(2)is initially triggered by the Ni-NPs,which is the rate-limiting step.Subsequently,the generated Mg reacts rapidly with Ni-NPs to form Mg_(2)Ni,which further promotes the dehydrogenation of residual MgH_(2).In the following dehydrogenation cycle,Mg_(2)NiH4 can rapidly decompose into Mg_(2)Ni,which continuously promotes the decomposition of MgH_(2).Our study not only elucidates the mechanism of Ni catalyst but also helps design and assemble catalysts with improved dehydriding kinetics of MgH_(2).展开更多
High-frequency supercapacitors are being studied with the aim to replace the bulky electrolytic capacitors for current ripple filtering and other functions used in power systems. Here, 3 D edge-oriented graphene(EOG)w...High-frequency supercapacitors are being studied with the aim to replace the bulky electrolytic capacitors for current ripple filtering and other functions used in power systems. Here, 3 D edge-oriented graphene(EOG)was grown encircling carbon nanofiber(CNF) framework to form a highly conductive electrode with a large surface area. Such EOG/CNF electrodes were tested in aqueous and organic electrolytes for high-frequency supercapacitor development. For the aqueous and the organic cell, the characteristic frequency at-45° phase angle was found to be as high as 22 and 8.5 k Hz, respectively. At 120 Hz, the electrode capacitance density was 0.37 and 0.16 m F cm^(-2) for the two cells. In particular, the 3 V high-frequency organic cell was successfully tested as filtering capacitor used in AC/DC converter, suggesting the promisingpotential of this technology for compact power supply design and other applications.展开更多
The nanoparticles of the hydrophobic drug of danazol with narrow size distribution are facilely prepared by controlled high-gravity anti-solvent precipitation （HGAP） process. Intensified micromixing and uniform nucl...The nanoparticles of the hydrophobic drug of danazol with narrow size distribution are facilely prepared by controlled high-gravity anti-solvent precipitation （HGAP） process. Intensified micromixing and uniform nucleation environment are created by the high-gravity equipment （rotating packed bed） in carrying out the anti-solvent precipitation process to produce nanoparticles. The average particle size decreases from 55 μm of the raw danazol to 190 nm of the nanoparticles. The Brunauer-Emmett-Teller （BET） surface area sharply increases from 0.66 m^2·g^-1 to 15.08 m^2·g^-l. Accordingly, the dissolution rate is greatly improved. The molecular state, chemical composition, and crystal form of the danazol nanoparticles remains unchanged after processing according to Fourier transform infrared （FTIR） and X-ray diffraction （XRD）, The high recovery ratio and continuous production capacity are highly appreciated in industry. Therefore, the HGAP method might offer a general and facile platform for mass production of hydrophobic pharmaceutical danazol particles in nanometer range.展开更多
We discuss how recent advances in phase-recovery imaging techniques in combination with plasmonic UTSs （ultrathin condensers） with a semiconductor substrate have paved the way for the development of novel optical na...We discuss how recent advances in phase-recovery imaging techniques in combination with plasmonic UTSs （ultrathin condensers） with a semiconductor substrate have paved the way for the development of novel optical nanoscopes. These optical nanoscopes are capable of imaging the intensity and the phase of the electric field distribution at the sample＇s plane.展开更多
开发经济高效的析氧反应电催化剂对于推进可充电金属-空气电池和电解水技术的发展至关重要.一般来说,具有完整蜂窝结构的石墨碳基面是电化学惰性的,需要依赖缺陷或者掺杂结构诱导的电荷极化效应来提升催化活性.相比于基面,边缘位点具有...开发经济高效的析氧反应电催化剂对于推进可充电金属-空气电池和电解水技术的发展至关重要.一般来说,具有完整蜂窝结构的石墨碳基面是电化学惰性的,需要依赖缺陷或者掺杂结构诱导的电荷极化效应来提升催化活性.相比于基面,边缘位点具有特殊的局域电子态,为提升石墨碳电极的本征催化活性开辟了新的思路,然而其结构精准构筑目前仍面临极大挑战.本文以“人字形”多壁碳纳米管(H-MWCNTs)作为研究切入点,利用高温熔盐介质主导的插层剥离和截断效应,实现“边缘-平面位点”结构可控构筑,为实现高效电解水析氧反应(OER)提供了重要的结构基础.通过熔盐辅助热解方法可控制备了具有完全暴露的内外边缘平面的目标催化剂H-MWCNTs-MS,并研究其OER催化性能.在碱性介质中10 mA cm^(-2)电流密度所需过电位仅为236 mV,是目前报道的较好的非金属电催化剂.同时,H-MWCNTs-MS在10,50和100 mA cm^(-2)电流密度下均表现出较好的电化学稳定性.利用原位衰减全反射-表面增强红外吸收光谱(ATR-SEIRAS)技术研究了“边缘-平面位点”在OER过程中的结构重构过程,与理论计算分析的高能“边缘态”结果一致,并确定酮氧官能化位点为真实催化活性中心.理论计算结果表明,氧官能团修饰结构能够显著促进电荷的再分配,增强层间耦合作用,降低关键含氧中间体*OOH的形成能垒,加速OER反应动力学.此外,H-MWCNTs-MS的开放式结构极大程度提高了“边缘-平面位点”的利用率,减小的纳米管壁厚促进了层间电荷迁移,也是增强OER活性的关键要素.综上,精准构筑“边缘-平面位点”为开发高效石墨碳电极开辟了新的思路,通过原位谱学技术揭示边缘位点催化结构重构,能够进一步丰富研究者对于电催化协同效应的科学认识.展开更多
Fullerenes:The extensive development of nanoscience that has marked this century continues to evolve,producing new materials,structures,and devices for the treatments of diverse pathologies.Fullerenes are a family of ...Fullerenes:The extensive development of nanoscience that has marked this century continues to evolve,producing new materials,structures,and devices for the treatments of diverse pathologies.Fullerenes are a family of nanoparticles with great applicative promise due to their small size(approximately 1 nm in diameter),structure,and capacity to cross biological barriers.展开更多
The excessive demand for phosphorus-based fertilizers is contributing to the undesired byproduct of phosphogypsum(PG),typically found in large quantities in phosphoric acid industry.Without proper management,this indu...The excessive demand for phosphorus-based fertilizers is contributing to the undesired byproduct of phosphogypsum(PG),typically found in large quantities in phosphoric acid industry.Without proper management,this industrial waste poses a significant environmental pollution risk.Current technologies are struggle to effectively handle the volume of PG produced,but one promising solution is its conversion into hemihydrate gypsum(CaSO_(4)·0.5 H_(2)O,HH).HH can exist in two phases,α-HH andβ-HH,withα-hemihydrate gypsum(α-HH)being preferred for its complete crystal structure and lower water requirement for hydration.The morphology ofα-HH gypsum is crucial for its material applications,and controlling crystal morphology is possible through the use of suitable crystal modifiers.This review explores various aspects of crystal modifiers and highlights their role in the preparation ofα-HH from PG.It suggests that leveraging the interfacial properties of PG could lead to innovative applications.Additionally,the review outlines future directions for PG development and identifies challenges to be addressed in the next steps.展开更多
Li–CO_(2)/O_(2)batteries,a promising energy storage technology,not only provide ultrahigh discharge capacity but also capture CO_(2)and turn it into renewable energy.Their electrochemical reaction pathways'ambigu...Li–CO_(2)/O_(2)batteries,a promising energy storage technology,not only provide ultrahigh discharge capacity but also capture CO_(2)and turn it into renewable energy.Their electrochemical reaction pathways'ambiguity,however,creates a hurdle for their practical application.This study used copper selenide(CuSe)nanosheets as the air cathode medium in an environmental transmission electron microscope to in situ study Li–CO_(2)/O_(2)(mix CO_(2)as well as O_(2)at a volume ratio of 1:1)and Li–O_(2)batteries as well as Li–CO_(2)batteries.Primary discharge reactions take place successively in the Li–CO_(2)/O_(2)–CuSe nanobattery:(I)4Li^(+)+O_(2)+4e^(−)→2Li_(2)O;(II)Li_(2)O+CO_(2)→Li_(2)CO_(3).The charge reaction proceeded via(III)2Li_(2)CO_(3)→4Li^(+)+2CO_(2)+O_(2)+4e^(−).However,Li–O_(2)and Li–CO_(2)nanobatteries showed poor cycling stability,suggesting the difficulty in the direct decomposition of the discharge product.The fluctuations of the Li–CO_(2)/O_(2)battery's electrochemistry were also shown to depend heavily on O_(2).The CuSe‐based Li–CO_(2)/O_(2)battery showed exceptional electrochemical performance.The Li^–CO_(2)/O_(2)battery offered a discharge capacity apex of 15,492 mAh g^(−1) and stable cycling 60 times at 100 mA g^(−1).Our research offers crucial insight into the electrochemical behavior of Li–CO_(2)/O_(2),Li–O_(2),and Li–CO_(2)nanobatteries,which may help the creation of high‐performance Li–CO_(2)/O_(2)batteries for energy storage applications.展开更多
Mechanical strain can induce noteworthy structural and electronic changes in vanadium dioxide, imparting substantial scientific importance to both the exploration of phase transitions and the development of potential ...Mechanical strain can induce noteworthy structural and electronic changes in vanadium dioxide, imparting substantial scientific importance to both the exploration of phase transitions and the development of potential technological applications. Unlike the traditional rutile(R) phase, bronze-phase vanadium dioxide [VO_(2)(B)] exhibits an in-plane anisotropic structure. When subjected to stretching along distinct crystallographic axes, VO_(2)(B) may further manifest the axial dependence in lattice–electron interactions, which is beneficial for gaining insights into the anisotropy of electronic transport.Here, we report an anisotropic room-temperature metal–insulator transition in single-crystal VO_(2)(B) by applying in-situ uniaxial tensile strain. This material exhibits significantly different electromechanical responses along two anisotropic axes.We reveal that such an anisotropic electromechanical response mainly arises from the preferential arrangement of a straininduced unidirectional stripe state in the conductive channel. This insulating stripe state could be attributed to the in-plane dimerization within the distorted zigzag chains of vanadium atoms, evidenced by strain-modulated Raman spectra. Our work may open up a promising avenue for exploiting the anisotropy of metal–insulator transition in vanadium dioxide for potential technological applications.展开更多
Detecting tiny deformations or vibrations, particularly those associated with strains below 1%, is essential in various technological applications. Traditional intrinsic materials, including metals and semiconductors,...Detecting tiny deformations or vibrations, particularly those associated with strains below 1%, is essential in various technological applications. Traditional intrinsic materials, including metals and semiconductors, face challenges in simultaneously achieving initial metallic state and strain-induced insulating state, hindering the development of highly sensitive mechanical sensors. Here we report an ultrasensitive mechanical sensor based on a strain-induced tunable ordered array of metallic and insulating states in the single-crystal bronze-phase vanadium dioxide [VO_(2)(B)] quantum material. It is shown that the initial metallic state in the VO_(2)(B) flake can be tuned to the insulating state by applying a weak uniaxial tensile strain. Such a unique property gives rise to a record-high gauge factor of above 607970, surpassing previous values by an order of magnitude, with excellent linearity and mechanical resilience as well as durability. As a proof-of-concept application, we use our proposed mechanical sensor to demonstrate precise sensing of the micro piece, gentle airflows and water droplets. We attribute the superior performance of the sensor to the strain-induced continuous metal-insulator transition in the single-crystal VO_(2)(B) flake, evidenced by experimental and simulation results. Our findings highlight the potential of exploiting correlated quantum materials for next-generation ultrasensitive flexible mechanical sensors, addressing critical limitations in traditional materials.展开更多
染料污染是水污染中最严重的问题之一,吸引了很多科学家的关注.人们尝试了很多方法去解决该问题,如化学氧化法、物理吸附法、光催化降解法和生物降解法等.与其他几种方法相比,光催化法有着低能耗、环保以及高效等优势.三氧化钨是常见的...染料污染是水污染中最严重的问题之一,吸引了很多科学家的关注.人们尝试了很多方法去解决该问题,如化学氧化法、物理吸附法、光催化降解法和生物降解法等.与其他几种方法相比,光催化法有着低能耗、环保以及高效等优势.三氧化钨是常见的半导体材料,具有独特的光学性能,近年来受到了广泛的研究.本文以钨酸钠和硫脲为前驱体,通过水热法制备了三氧化钨/氧化银(WO_3/Ag_2O)复合材料,并用光催化降解亚甲基蓝来分析其光催化性能.通过X射线光电子能谱、X射线衍射、透射电子显微镜、扫描电子显微镜、紫外可见吸收光谱等表征手段对样品的形貌、晶格结构和光催化的性能进行表征.氧化银的带宽为1.2 e V,对可见光很敏感,三氧化钨和氧化银的复合使材料在可见光下的光催化活性显著增强,在可见光下对亚甲基蓝染料的光降解率可以达到98%.实验结果表明,复合材料中的三氧化钨纳米棒为六方相,其平均直径约为200 nm,平均长度约为4μm.而复合材料中的氧化银纳米颗粒为六方相,附着在氧化钨纳米棒的表面,平均晶粒尺寸为20 nm.氧化银的存在为复合材料提供了更多的反应活性位点.相较于单一组分,复合材料在可见光下的光吸收度更高,这说明三氧化钨和氧化银的复合改变了材料的能带结构.研究发现,三氧化钨和氧化银之间形成的异质结构是其优良光催化性能的来源.此外,三氧化钨和氧化银复合材料还具有良好的催化稳定性和化学稳定性.本文结果表明,可以通过给宽带隙的半导体材料复合一些带隙合适的金属氧化物以提升其光催化活性.展开更多
基金supported by the National Natural Science Foundation of China(Nos.22279111,51971195,and 11935004)the Natural Science Foundation of Hebei Province(No.B2020203037)Subsidy for Hebei Key Laboratory of Applied Chemistry after Operation Performance(No.22567616H).
文摘MgH_(2),albeit with slow desorption kinetics,has been extensively studied as one of the most ideal solid hydrogen storage materials.Adding such catalyst as Ni can improve the desorption kinetics of MgH_(2),whereas the catalytic role has been attributed to different substances such as Ni,Mg_(2)Ni,Mg_(2)NiH0.3,and Mg_(2)NiH4.In the present study,Ni nanoparticles(Ni-NPs)supported on mesoporous carbon(Ni@C)have been synthesized to improve the hydrogen desorption kinetics of MgH_(2).The utilization of Ni@C largely decreases the dehydrogenation activation energy from 176.9 to 79.3 kJ mol^(−1) and the peak temperature of dehydrogenation from 375.5 to 235℃.The mechanism of Ni catalyst is well examined by advanced aberration-corrected environmental transmission electron microscopy and/or x-ray diffraction.During the first dehydrogenation,detailed microstructural studies reveal that the decomposition of MgH_(2)is initially triggered by the Ni-NPs,which is the rate-limiting step.Subsequently,the generated Mg reacts rapidly with Ni-NPs to form Mg_(2)Ni,which further promotes the dehydrogenation of residual MgH_(2).In the following dehydrogenation cycle,Mg_(2)NiH4 can rapidly decompose into Mg_(2)Ni,which continuously promotes the decomposition of MgH_(2).Our study not only elucidates the mechanism of Ni catalyst but also helps design and assemble catalysts with improved dehydriding kinetics of MgH_(2).
基金supported by the National Science Foundation(1611060)
文摘High-frequency supercapacitors are being studied with the aim to replace the bulky electrolytic capacitors for current ripple filtering and other functions used in power systems. Here, 3 D edge-oriented graphene(EOG)was grown encircling carbon nanofiber(CNF) framework to form a highly conductive electrode with a large surface area. Such EOG/CNF electrodes were tested in aqueous and organic electrolytes for high-frequency supercapacitor development. For the aqueous and the organic cell, the characteristic frequency at-45° phase angle was found to be as high as 22 and 8.5 k Hz, respectively. At 120 Hz, the electrode capacitance density was 0.37 and 0.16 m F cm^(-2) for the two cells. In particular, the 3 V high-frequency organic cell was successfully tested as filtering capacitor used in AC/DC converter, suggesting the promisingpotential of this technology for compact power supply design and other applications.
基金Supported by the National High Technology Research and Development Program of China (2006AA030202)the Talent Training Program of Beijing (2007B022)
文摘The nanoparticles of the hydrophobic drug of danazol with narrow size distribution are facilely prepared by controlled high-gravity anti-solvent precipitation （HGAP） process. Intensified micromixing and uniform nucleation environment are created by the high-gravity equipment （rotating packed bed） in carrying out the anti-solvent precipitation process to produce nanoparticles. The average particle size decreases from 55 μm of the raw danazol to 190 nm of the nanoparticles. The Brunauer-Emmett-Teller （BET） surface area sharply increases from 0.66 m^2·g^-1 to 15.08 m^2·g^-l. Accordingly, the dissolution rate is greatly improved. The molecular state, chemical composition, and crystal form of the danazol nanoparticles remains unchanged after processing according to Fourier transform infrared （FTIR） and X-ray diffraction （XRD）, The high recovery ratio and continuous production capacity are highly appreciated in industry. Therefore, the HGAP method might offer a general and facile platform for mass production of hydrophobic pharmaceutical danazol particles in nanometer range.
文摘We discuss how recent advances in phase-recovery imaging techniques in combination with plasmonic UTSs （ultrathin condensers） with a semiconductor substrate have paved the way for the development of novel optical nanoscopes. These optical nanoscopes are capable of imaging the intensity and the phase of the electric field distribution at the sample＇s plane.
文摘开发经济高效的析氧反应电催化剂对于推进可充电金属-空气电池和电解水技术的发展至关重要.一般来说,具有完整蜂窝结构的石墨碳基面是电化学惰性的,需要依赖缺陷或者掺杂结构诱导的电荷极化效应来提升催化活性.相比于基面,边缘位点具有特殊的局域电子态,为提升石墨碳电极的本征催化活性开辟了新的思路,然而其结构精准构筑目前仍面临极大挑战.本文以“人字形”多壁碳纳米管(H-MWCNTs)作为研究切入点,利用高温熔盐介质主导的插层剥离和截断效应,实现“边缘-平面位点”结构可控构筑,为实现高效电解水析氧反应(OER)提供了重要的结构基础.通过熔盐辅助热解方法可控制备了具有完全暴露的内外边缘平面的目标催化剂H-MWCNTs-MS,并研究其OER催化性能.在碱性介质中10 mA cm^(-2)电流密度所需过电位仅为236 mV,是目前报道的较好的非金属电催化剂.同时,H-MWCNTs-MS在10,50和100 mA cm^(-2)电流密度下均表现出较好的电化学稳定性.利用原位衰减全反射-表面增强红外吸收光谱(ATR-SEIRAS)技术研究了“边缘-平面位点”在OER过程中的结构重构过程,与理论计算分析的高能“边缘态”结果一致,并确定酮氧官能化位点为真实催化活性中心.理论计算结果表明,氧官能团修饰结构能够显著促进电荷的再分配,增强层间耦合作用,降低关键含氧中间体*OOH的形成能垒,加速OER反应动力学.此外,H-MWCNTs-MS的开放式结构极大程度提高了“边缘-平面位点”的利用率,减小的纳米管壁厚促进了层间电荷迁移,也是增强OER活性的关键要素.综上,精准构筑“边缘-平面位点”为开发高效石墨碳电极开辟了新的思路,通过原位谱学技术揭示边缘位点催化结构重构,能够进一步丰富研究者对于电催化协同效应的科学认识.
基金supported by Ministarstvo Prosvete,Nauke i Tehnoloskog Razvoja,Grant/Award Number:451-03-9/2021-14/200007 and 451-03-9/2021-14/200017Zepter International Foundation,Grant/Award Number:5/2019(to Sl)。
文摘Fullerenes:The extensive development of nanoscience that has marked this century continues to evolve,producing new materials,structures,and devices for the treatments of diverse pathologies.Fullerenes are a family of nanoparticles with great applicative promise due to their small size(approximately 1 nm in diameter),structure,and capacity to cross biological barriers.
基金Project(2022YFC3902703)supported by the National Key R&D Program of ChinaProject(KF22028)supported by the Special Project for High Quality Development of the Ministry of Industry and Information Technology of China+1 种基金Project(62004143)supported by the National Natural Science Foundation of ChinaProject(2022BAA084)supported by the Key R&D Program of Hubei Province,China。
文摘The excessive demand for phosphorus-based fertilizers is contributing to the undesired byproduct of phosphogypsum(PG),typically found in large quantities in phosphoric acid industry.Without proper management,this industrial waste poses a significant environmental pollution risk.Current technologies are struggle to effectively handle the volume of PG produced,but one promising solution is its conversion into hemihydrate gypsum(CaSO_(4)·0.5 H_(2)O,HH).HH can exist in two phases,α-HH andβ-HH,withα-hemihydrate gypsum(α-HH)being preferred for its complete crystal structure and lower water requirement for hydration.The morphology ofα-HH gypsum is crucial for its material applications,and controlling crystal morphology is possible through the use of suitable crystal modifiers.This review explores various aspects of crystal modifiers and highlights their role in the preparation ofα-HH from PG.It suggests that leveraging the interfacial properties of PG could lead to innovative applications.Additionally,the review outlines future directions for PG development and identifies challenges to be addressed in the next steps.
基金Natural Science Foundation of Hebei Province,Grant/Award Number:F2021203097China Postdoctoral Science Foundation,Grant/Award Numbers:2021M702756,2023T160551National Natural Science Foundation of China,Grant/Award Numbers:51971245,52022088。
文摘Li–CO_(2)/O_(2)batteries,a promising energy storage technology,not only provide ultrahigh discharge capacity but also capture CO_(2)and turn it into renewable energy.Their electrochemical reaction pathways'ambiguity,however,creates a hurdle for their practical application.This study used copper selenide(CuSe)nanosheets as the air cathode medium in an environmental transmission electron microscope to in situ study Li–CO_(2)/O_(2)(mix CO_(2)as well as O_(2)at a volume ratio of 1:1)and Li–O_(2)batteries as well as Li–CO_(2)batteries.Primary discharge reactions take place successively in the Li–CO_(2)/O_(2)–CuSe nanobattery:(I)4Li^(+)+O_(2)+4e^(−)→2Li_(2)O;(II)Li_(2)O+CO_(2)→Li_(2)CO_(3).The charge reaction proceeded via(III)2Li_(2)CO_(3)→4Li^(+)+2CO_(2)+O_(2)+4e^(−).However,Li–O_(2)and Li–CO_(2)nanobatteries showed poor cycling stability,suggesting the difficulty in the direct decomposition of the discharge product.The fluctuations of the Li–CO_(2)/O_(2)battery's electrochemistry were also shown to depend heavily on O_(2).The CuSe‐based Li–CO_(2)/O_(2)battery showed exceptional electrochemical performance.The Li^–CO_(2)/O_(2)battery offered a discharge capacity apex of 15,492 mAh g^(−1) and stable cycling 60 times at 100 mA g^(−1).Our research offers crucial insight into the electrochemical behavior of Li–CO_(2)/O_(2),Li–O_(2),and Li–CO_(2)nanobatteries,which may help the creation of high‐performance Li–CO_(2)/O_(2)batteries for energy storage applications.
基金Project supported by the National Key R&D Program of China (Grant No. 2023YFF1203600)the National Natural Science Foundation of China (Grant Nos. 62122036, 62034004, 12322407, 61921005, and 12074176)+1 种基金the Strategic Priority Research Program of the Chinese Academy of Sciences (Grant No. XDB44000000)supported by the program for Outstanding Ph D Candidates of Nanjing University。
文摘Mechanical strain can induce noteworthy structural and electronic changes in vanadium dioxide, imparting substantial scientific importance to both the exploration of phase transitions and the development of potential technological applications. Unlike the traditional rutile(R) phase, bronze-phase vanadium dioxide [VO_(2)(B)] exhibits an in-plane anisotropic structure. When subjected to stretching along distinct crystallographic axes, VO_(2)(B) may further manifest the axial dependence in lattice–electron interactions, which is beneficial for gaining insights into the anisotropy of electronic transport.Here, we report an anisotropic room-temperature metal–insulator transition in single-crystal VO_(2)(B) by applying in-situ uniaxial tensile strain. This material exhibits significantly different electromechanical responses along two anisotropic axes.We reveal that such an anisotropic electromechanical response mainly arises from the preferential arrangement of a straininduced unidirectional stripe state in the conductive channel. This insulating stripe state could be attributed to the in-plane dimerization within the distorted zigzag chains of vanadium atoms, evidenced by strain-modulated Raman spectra. Our work may open up a promising avenue for exploiting the anisotropy of metal–insulator transition in vanadium dioxide for potential technological applications.
基金supported in part by the National Key R&D Program of China (Grant Nos.2023YFF1203600 and 2023YFF0718400)the National Natural Science Foundation of China (Grant Nos.62122036,12322407,62034004,61921005,and 12074176)+2 种基金the Leading-edge Technology Program of Jiangsu Natural Science Foundation (Grant No.BK20232004)the Strategic Priority Research Program of the Chinese Academy of Sciences (Grant No.XDB44000000)support from the AIQ Foundation and the eScience Center of Collaborative Innovation Center of Advanced Microstructures。
文摘Detecting tiny deformations or vibrations, particularly those associated with strains below 1%, is essential in various technological applications. Traditional intrinsic materials, including metals and semiconductors, face challenges in simultaneously achieving initial metallic state and strain-induced insulating state, hindering the development of highly sensitive mechanical sensors. Here we report an ultrasensitive mechanical sensor based on a strain-induced tunable ordered array of metallic and insulating states in the single-crystal bronze-phase vanadium dioxide [VO_(2)(B)] quantum material. It is shown that the initial metallic state in the VO_(2)(B) flake can be tuned to the insulating state by applying a weak uniaxial tensile strain. Such a unique property gives rise to a record-high gauge factor of above 607970, surpassing previous values by an order of magnitude, with excellent linearity and mechanical resilience as well as durability. As a proof-of-concept application, we use our proposed mechanical sensor to demonstrate precise sensing of the micro piece, gentle airflows and water droplets. We attribute the superior performance of the sensor to the strain-induced continuous metal-insulator transition in the single-crystal VO_(2)(B) flake, evidenced by experimental and simulation results. Our findings highlight the potential of exploiting correlated quantum materials for next-generation ultrasensitive flexible mechanical sensors, addressing critical limitations in traditional materials.
文摘染料污染是水污染中最严重的问题之一,吸引了很多科学家的关注.人们尝试了很多方法去解决该问题,如化学氧化法、物理吸附法、光催化降解法和生物降解法等.与其他几种方法相比,光催化法有着低能耗、环保以及高效等优势.三氧化钨是常见的半导体材料,具有独特的光学性能,近年来受到了广泛的研究.本文以钨酸钠和硫脲为前驱体,通过水热法制备了三氧化钨/氧化银(WO_3/Ag_2O)复合材料,并用光催化降解亚甲基蓝来分析其光催化性能.通过X射线光电子能谱、X射线衍射、透射电子显微镜、扫描电子显微镜、紫外可见吸收光谱等表征手段对样品的形貌、晶格结构和光催化的性能进行表征.氧化银的带宽为1.2 e V,对可见光很敏感,三氧化钨和氧化银的复合使材料在可见光下的光催化活性显著增强,在可见光下对亚甲基蓝染料的光降解率可以达到98%.实验结果表明,复合材料中的三氧化钨纳米棒为六方相,其平均直径约为200 nm,平均长度约为4μm.而复合材料中的氧化银纳米颗粒为六方相,附着在氧化钨纳米棒的表面,平均晶粒尺寸为20 nm.氧化银的存在为复合材料提供了更多的反应活性位点.相较于单一组分,复合材料在可见光下的光吸收度更高,这说明三氧化钨和氧化银的复合改变了材料的能带结构.研究发现,三氧化钨和氧化银之间形成的异质结构是其优良光催化性能的来源.此外,三氧化钨和氧化银复合材料还具有良好的催化稳定性和化学稳定性.本文结果表明,可以通过给宽带隙的半导体材料复合一些带隙合适的金属氧化物以提升其光催化活性.
