In recent years,renewable energy sources,which aim to replace rapidly depleting fossil fuels,face challenges due to limited energy storage and conversion technologies.To enhance energy storage and conversion efficienc...In recent years,renewable energy sources,which aim to replace rapidly depleting fossil fuels,face challenges due to limited energy storage and conversion technologies.To enhance energy storage and conversion efficiency,extensive research has been conducted in the academic community on numerous potential materials.Among these materials,metal fluorides have attracted significant attention due to their ionic metal-fluorine bonds and tunable electronic structures,attributed to the highest electronegativity of fluorine in their chemical composition.This makes them promising candidates for future electrochemical applications in various fields.However,metal fluorides encounter various challenges in different application directions.Therefore,we comprehensively review the applications of metal fluorides in the field of energy storage and conversion,aiming to deepen our understanding of their exhibited characteristics in different electrochemical processes.In this paper,we summarize the difficulties and improvement methods encountered in different types of battery applications and several typical electrode optimization strategies in the field of supercapacitors.In the field of water electrolysis,we focus on surface reconstruction and the critical role of fluorine,demonstrating the catalytic performance of metal fluorides from the perspectives of reconstruction mechanism and process analysis.Finally,we provide a summary and outlook for this field,aiming to offer guidance for future breakthroughs in the energy storage and conversion applications of metal fluorides.展开更多
Developing electrocatalysts to inhibit polysulfide shuttling and expedite sulfur species conversion is vital for the evolution of Lithium-sulfur(Li-S)batteries.This work provides a facile strategy to design an intimat...Developing electrocatalysts to inhibit polysulfide shuttling and expedite sulfur species conversion is vital for the evolution of Lithium-sulfur(Li-S)batteries.This work provides a facile strategy to design an intimate heterostructure of MIL-88A@CdS as a sulfur electrocatalyst combining high sulfur adsorption and accelerated polysulfide conversion.The MIL-88A can give a region of high-ordered polysulfide adsorption,whereas the CdS is an effective nanoreactor for the sulfur reduction reaction(SRR).Notedly,the significant size difference between MIL-88A and CdS enables the unique heterostructure interactions.The largesize MIL-88A ensures a uniform distribution of CdS nanoparticles as a substrate.This configuration facilitates control of the initial polysulfide adsorption position relative to its final deposition site as lithium sulfide.The heterostructure also demonstrates rapid transport and efficient conversion of lithium polysulfides.Consequently,the Li-S battery with MIL-88A@CdS heterostructure modified separator delivers exceptional performance,achieving an areal capacity exceeding 6 mAh cm^(−2),an excellent rate capability of 980 mAh g^(−1) at 5 C,and notable cycling stability in a 2 Ah pouch cell over 100 cycles.This work is significant for elucidating the relationship between heterostructure and electrocatalytic performance,providing great insights for material design aimed at highly efficient future electrocatalysts in practical applications.展开更多
Lithium metal is regarded as the ultimate negative electrode material for secondary batteries due to its high energy density.However,it suffers from poor cycling stability because of its high reactivity with liquid el...Lithium metal is regarded as the ultimate negative electrode material for secondary batteries due to its high energy density.However,it suffers from poor cycling stability because of its high reactivity with liquid electrolytes.Therefore,continuous efforts have been put into improving the cycling Coulombic efficiency(CE)to extend the lifespan of the lithium metal negative electrode.Herein,we report that using dual-salt additives of LiPF_(6) and LiNO_(3) in an ether solvent-based electrolyte can significantly improve the cycling stability and rate capability of a Li-carbon(Li-CNT)composite.As a result,an average cycling CE as high as 99.30% was obtained for the Li-CNT at a current density of 2.5 mA cm^(-2) and an negative electrode to positive electrode capacity(N/P)ratio of 2.The cycling stability and rate capability enhancement of the Li-CNT negative electrode could be attributed to the formation of a better solid electrolyte interphase layer that contains both inorganic components and organic polyether.The former component mainly originates from the decomposition of the LiNO_(3) additive,while the latter comes from the LiPF_(6)-induced ring-opening polymerization of the ether solvent.This novel surface chemistry significantly improves the CE of Li negative electrode,revealing its importance for the practical application of lithium metal batteries.展开更多
High quality gallium oxide(Ga_2O_3) thin films are deposited by remote plasma-enhanced atomic layer deposition(RPEALD) with trimethylgallium(TMG) and oxygen plasma as precursors. By introducing in-situ NH3 plasma pret...High quality gallium oxide(Ga_2O_3) thin films are deposited by remote plasma-enhanced atomic layer deposition(RPEALD) with trimethylgallium(TMG) and oxygen plasma as precursors. By introducing in-situ NH3 plasma pretreatment on the substrates, the deposition rate of Ga_2O_3 films on Si and GaN are remarkably enhanced, reached to 0.53 and 0.46 ?/cycle at 250 °C,respectively. The increasing of deposition rate is attributed to more hydroxyls(–OH) generated on the substrate surfaces after NH3 pretreatment, which has no effect on the stoichiometry and surface morphology of the oxide films, but only modifies the surface states of substrates by enhancing reactive site density. Ga_2O_3 film deposited on GaN wafer is crystallized at 250 °C, with an epitaxial interface between Ga_2O_3 and GaN clearly observed. This is potentially very important for reducing the interface state density through high quality passivation.展开更多
As a special order of electronic correlation induced by spatial modulation, the charge density wave(CDW) phenomena in condensed matters attract enormous research interests. Here, using scanning-tunneling microscopy in...As a special order of electronic correlation induced by spatial modulation, the charge density wave(CDW) phenomena in condensed matters attract enormous research interests. Here, using scanning-tunneling microscopy in various temperatures, we discover a hidden incommensurate stripe-like CDW order besides the(■) CDW phase at low-temperature of 4 K in the epitaxial monolayer 1T-VSe_(2) film. Combining the variable-temperature angle-resolved photoemission spectroscopic(ARPES) measurements, we discover a two-step transition of an anisotropic CDW gap structure that consists of two parts △_(1) and△_(2). The gap part ?1 that closes around ~ 150 K is accompanied with the vanish of the(√7×√3) CDW phase. While another momentum-dependent gap part △_(2) can survive up to ~ 340 K, and is suggested to the result of the incommensurate CDW phase. This two-step transition with anisotropic gap opening and the resulted evolution in ARPES spectra are corroborated by our theoretical calculation based on a phenomenological form for the self-energy containing a two-gap structure △_(1) +△_(2), which suggests different forming mechanisms between the(√7×√3) and the incommensurate CDW phases. Our findings provide significant information and deep understandings on the CDW phases in monolayer 1T-VSe_(2) film as a two-dimensional(2D) material.展开更多
The atomic structure and surface chemistry of GaP/Si(100)heterostructure with different pre-layers grown by molecu-lar beam epitaxy are studied.It is found that GaP epilayer with Ga-riched pre-layers on Si(100)substra...The atomic structure and surface chemistry of GaP/Si(100)heterostructure with different pre-layers grown by molecu-lar beam epitaxy are studied.It is found that GaP epilayer with Ga-riched pre-layers on Si(100)substrate has regular surface mor-phology and stoichiometric abrupt heterointerfaces from atomic force microscopes(AFMs)and spherical aberration-corrected transmission electron microscopes(ACTEMs).The interfacial dynamics of GaP/Si(100)heterostructure is investigated by X-ray photoelectron spectroscopy(XPS)equipped with an Ar gas cluster ion beam,indicating that Ga pre-layers can lower the inter-face formation energy and the bond that is formed is more stable.These results suggest that Ga-riched pre-layers are more con-ducive to the GaP nucleation as well as the epitaxial growth of GaP material on Si(100)substrate.展开更多
Ni-Fe-based catalysts are considered to be among the most active catalysts for the oxygen evolution reaction(OER)under alkaline conditions,with Fe playing a crucial role.However,Fe leaching occurs during the reaction ...Ni-Fe-based catalysts are considered to be among the most active catalysts for the oxygen evolution reaction(OER)under alkaline conditions,with Fe playing a crucial role.However,Fe leaching occurs during the reaction due to thermodynamic instability,which has resulted in conflicting reports within the literature regarding its role.To clarify this point,we propose a strategy consisting of modulating the electronic orbital occupancy to suppress the extensive loss of Fe atoms during the OER process.Theoretical calculations,in-situ X-ray photoelectron spectroscopy,molecular dynamics simulations,and a series of characterization showed that the stable presence of Fe not only accelerates the electron transfer process but also optimizes the reaction barriers of the oxygen evolution intermediates,promoting the phase transition of Fe_(5)Ni_(4)S_(8)to highly active catalytic species.The modulated Fe_(5)Ni_(4)S_(8)-based pre-catalysts exhibit improved OER activity and long-term durability.This study provides a novel perspective for understanding the role of Fe in the OER process.展开更多
Two-dimensional honeycomb crystals have inspired intense research interest for their novel properties and great potential in electronics and optoelectronics. Here, through molecular beam epitaxy on SrTiO_3(001), we re...Two-dimensional honeycomb crystals have inspired intense research interest for their novel properties and great potential in electronics and optoelectronics. Here, through molecular beam epitaxy on SrTiO_3(001), we report successful epitaxial growth of metal-rich chalcogenide Fe_(2)Te, a honeycomb-structured film that has no direct bulk analogue, under Te-limited growth conditions. The structural morphology and electronic properties of Fe_(2)Te are explored with scanning tunneling microscopy and angle resolved photoemission spectroscopy, which reveal electronic bands cross the Fermi level and nearly flat bands. Moreover, we find a weak interfacial interaction between Fe_(2)Te and the underlying substrates, paving a newly developed alternative avenue for honeycomb-based electronic devices.展开更多
Monolayer MnTe_(2)stabilized as 1 T structure has been theoretically predicted to be a two-dimensional(2 D)ferromagnetic metal and can be tuned via strain engineering.There is no naturally van der Waals(vdW)layered Mn...Monolayer MnTe_(2)stabilized as 1 T structure has been theoretically predicted to be a two-dimensional(2 D)ferromagnetic metal and can be tuned via strain engineering.There is no naturally van der Waals(vdW)layered MnTe_(2)bulk,leaving mechanical exfoliation impossible to prepare monolayer MnTe_(2).Herein,by means of molecular beam epitaxy(MBE),we successfully prepared monolayer hexagonal MnTe_(2)on Si(111)under Te rich condition.Sharp reflection high-energy electron diffraction(RHEED)and low-energy electron diffraction(LEED)patterns suggest the monolayer is atomically flat without surface reconstruction.The valence state of Mn^(4+)and the atom ratio of([Te]:[Mn])further confirm the MnTe_(2)compound.Scanning tunneling spectroscopy(STS)shows the hexagonal MnTe_(2)monolayer is a semiconductor with a large bandgap of~2.78 eV.The valence-band maximum(VBM)locates at theΓpoint,as illustrated by angle-resolved photoemission spectroscopy(ARPES),below which three hole-type bands with parabolic dispersion can be identified.The successful synthesis of monolayer MnTe_(2)film provides a new platform to investigate the 2D magnetism.展开更多
Hydrogen energy carrier produced by water electrolysis in alkaline electrolytes is rather meaningful and significant for global sustainability imperatives,while the highpH condition usually leads to a poor reversibili...Hydrogen energy carrier produced by water electrolysis in alkaline electrolytes is rather meaningful and significant for global sustainability imperatives,while the highpH condition usually leads to a poor reversibility of proton adsorption and desorption that significantly determines the hydrogen-generation activity in hydrogen evolution reaction(HER)process.Herein,we demonstrate a remarkable Ru-Mo solid-solution nanocrystal catalyst in alkaline HER process by a very simple but feasible pyrolysis and alkali leaching strategy.Benefiting from the pinning effect and local chemical-and electronic-structure regulations of Mo solute atoms,an ultra-low overpotential(17.3 mV)and an exceptional stability(>100 h)at the typical current density of 10 mA·cm^(−2)are achieved on the ultrasmall Ru-Mo solid-solution nanocrystal catalyst in 1.0 M KOH electrolyte.Density function theory(DFT)calculations gain an insight into the synergistic effect of neighboring Ru and Mo sites in alkaline HER process,where Mo solute atoms are beneficial for the adsorption and activation of water molecules for proton generation and accumulation due to their rich outermost 4d vacant orbitals,while the energy-favorable Ru sites are responsible for the fast deprotonation kinetics of hydrogen intermediates.Our work may provide an interesting route for the development of efficient and stable solid-solution alloy nanocrystals towards alkaline water electrolysis and beyond.展开更多
Ga_(2)O_(3)has been regarded as a promising material for solar-blind detection due to its ultrawide bandgap and low growth cost.Although semiconductor microwires(MWs)possess unique optical and electronic characteristi...Ga_(2)O_(3)has been regarded as a promising material for solar-blind detection due to its ultrawide bandgap and low growth cost.Although semiconductor microwires(MWs)possess unique optical and electronic characteristics,the performances of photodetectors developed from Ga_(2)O_(3)MWs are still less than satisfactory.Herein,we demonstrate high-performance solar-blind photodetectors based on Sn-doped Ga_(2)O_(3)MWs,possessing a light/dark current ratio of 107 and a responsivity of 2,409 A/W at 40 V.Moreover,a 1×10 solar-blind photodetector linear array is developed based on the Sn-doped Ga_(2)O_(3)MWs via a patternedelectrodes method.And clear solar-blind images are obtained by using the photodetector array as the imaging unit of a solarblind imaging system.The results provide a convenient way to construct high-performance solar-blind photodetector arrays based on Ga_(2)O_(3)MWs,and thus may push forward their future applications.展开更多
In this work,we have successfully grown high quality epitaxialβ-Ga_(2)O_(3)thin films onβ-Ga_(2)O_(3)(100)and Al_(2)O_(3)(0001)substrates using pulsed laser deposition(PLD).By optimizing temperature and oxygen press...In this work,we have successfully grown high quality epitaxialβ-Ga_(2)O_(3)thin films onβ-Ga_(2)O_(3)(100)and Al_(2)O_(3)(0001)substrates using pulsed laser deposition(PLD).By optimizing temperature and oxygen pressure,the best conditions were found to be 650-700℃and 0.5 Pa.To further improve the quality of hetero-epitaxialβ-Ga_(2)O_(3),the sapphire substrates were pretreated for atomic terraced surface by chemical cleaning and high temperature annealing.From the optical transmittance measurements,the films grown at 600-750℃exhibit a clear absorption edge at deep ultraviolet region around 250-275 nm wavelength.High resolution transmission electron microscope(HRTEM)images and X-ray diffraction(XRD)patterns demonstrate thatβ-Ga_(2)O_(3)(-201)//Al_(2)O_(3)(0001)epitaxial texture dominated the epitaxial oxide films on sapphire substrate,which opens up the possibilities of high power electric devices.展开更多
Li has been considered as the ultimate anode material for high energy density secondary Li batteries.However,its practical application has been limited due to its low Coulombic efficiency(CE)and the formation of lithi...Li has been considered as the ultimate anode material for high energy density secondary Li batteries.However,its practical application has been limited due to its low Coulombic efficiency(CE)and the formation of lithium dendrites.Recently,we have developed a microspherical Li-carbon nanotube(Li-CNT)composite material passivated with octadecylphosphonic acid(OPA)self-assembled monolayer(SAM)exhibiting suppressed lithium dendrite formation and improved environmental/electrochemical stability.In this work,we demonstrated the significantly enhanced passivation effects of a SAM using dihexadecanoalkyl phosphate(DHP),a molecule that is comprised of double hydrophobic alkyl chains and forms a denser SAM on surfaces with large curvature.As a result,the DHP SAM delivers superior environmental and electrochemical stability to the OPA passivated Li-CNT material.In specific,the DHP passivated Li-CNT composite(DHP-Li-CNT)delivers a high CE of 99.25%under a 33.3%depth of discharge(DOD)at 1 C,when it is paired with a LiFePO4 cathode.The evolution of the SAM during cycling and the effects of DOD and current density on the CE of the DHP-Li-CNT anode have also been investigated.The improved SAM passivation constitutes an important step in achieving the goal of practically applicable Li anodes.展开更多
卷对卷(R2R)凹版印刷具有高的边缘分辨率、可图案化、高加工速度等优势,是制备大面积柔性有机太阳能电池(FOSCs)的一种可行技术.有机光活性层的薄膜质量是决定有机太阳能电池器件性能的关键.对于凹版印刷过程而言,墨水的转移是影响印刷...卷对卷(R2R)凹版印刷具有高的边缘分辨率、可图案化、高加工速度等优势,是制备大面积柔性有机太阳能电池(FOSCs)的一种可行技术.有机光活性层的薄膜质量是决定有机太阳能电池器件性能的关键.对于凹版印刷过程而言,墨水的转移是影响印刷薄膜厚度和质量的关键.本文深入研究了有机光活性层的墨水粘度对墨水转移率和薄膜缺陷的影响.我们开发了紫外可见光谱法,量化凹版印刷过程中墨水的转移率.通过对墨水的流变行为分析、流体动力学模拟和实验验证,深入研究了油墨粘度与油墨转移率、膜厚和膜均匀性之间的关系.结果表明,油墨粘度约为25 m Pa·s是R2R凹版印刷有机光活性层薄膜的适合粘度.通过对油墨配方的优化,我们制备了全R2R印刷FOSCs,其中1 cm^(2);电池的效率超过12%.展开更多
Li metal has become a strong candidate for anode due to its high theoretical specific capacity and lowest electrochemical potential.However,the poor reversibility caused by continuous chemical and electrochemical degr...Li metal has become a strong candidate for anode due to its high theoretical specific capacity and lowest electrochemical potential.However,the poor reversibility caused by continuous chemical and electrochemical degradation hinders the practical application of Li metal.Solid-solution-based metal alloy phases have been proposed as hosts for regulating the non-dendrite electrodeposition,but the fundamental understanding remains unclear due to the drastically different deposition behaviors of Li on them.Here we found the difference in the diffusion coefficient of Li atoms on solid-solution-based metal alloy phases(Li-Mg and Li-Ag alloys)was a major contributor to the different deposition behaviors.The low Li atom diffusion coefficient of Li-Mg alloy showed a preferential Li accumulation on the upper surface rather than the inward-growth plating of Li atoms into alloy foil in Li-Ag alloy.By the process of secondary recrystallization,we improved the diffusion coefficient of Li atoms in Li-Mg alloy that facilitates the inward transfer rather than surface plating of Li atoms.In this case,the recrystallized Li-Mg alloy underwent a solidsolution phase change in the delithiation-lithiation cycles which yielded a high Coulombic efficiency of 99.3%with a reversible gravimetric capacity of 2,874 mAh·g−1 and superior cycling stability over 5,000 h without dendrite growth.展开更多
Heterostructured sulfur electrocatalysts have long been heralded as an effective approach to settle the issues of the shuttle effect and sluggish reaction kinetics of lithium polysulfides(LiPSs)in lithium-sulfur(Li-S)...Heterostructured sulfur electrocatalysts have long been heralded as an effective approach to settle the issues of the shuttle effect and sluggish reaction kinetics of lithium polysulfides(LiPSs)in lithium-sulfur(Li-S)batteries.However,the limited active sites on the interface of the heterostructure offer unsatisfactory LiPSs conversion capability,rendering sluggish reaction kinetics.Herein,we have designed abnormal step-scheme nano-heterointerfaces,containing P-N,N-semimetal,and P-semimetal heterostructures as sulfur electrocatalysts to regulate the LiPSs catalytic conversion behavior,which demonstrates efficient catalytic activity and robust structural stability.The excellent electron-confinement contributed by the step-scheme barrier endows the electron gathering at the nano-heterointerfaces,conferring high selectivity and durability of electrocatalyst for an accelerated sulfur reduction reaction.The unique robust structure design further bestows the sulfur composite with favored ion/mass transportation within the electrode.Attributed to these structural features,the Li-S cell delivers excellent performance under high areal capacity over 7 mAh cm^(−2) and lean electrolyte/sulfur ratio below 2.5μL mg^(−1),decent rate capability up to 8 C,remarkable cyclic stability over 500 cycles,and satisfactory energy density of 386.3 Wh kg^(−1) in a 7.5 Ah pouch cell.This nano-heterointerface structure design strategy endows a sulfur cathode with superior LiPSs catalytic activity,opening new insights into high-performance Li-S batteries.展开更多
ZnO nanoparticles(nps)among metal oxide(MOs)are proven to be essential electron transporting layers(ETLs)applied in organic solar cells(OSCs).However,intrinsic defects,interfacial charge recombination,and catalytic be...ZnO nanoparticles(nps)among metal oxide(MOs)are proven to be essential electron transporting layers(ETLs)applied in organic solar cells(OSCs).However,intrinsic defects,interfacial charge recombination,and catalytic behavior towards the active layer restrict the applications of ZnO nps for efficient and long-term stable OSCs.The commonly available biomolecule cytidine 5'-monophosphate(CMP-OH)with phosphonic acid,its salt cytidine 5'-monophosphate disodium salt(CMP-ONa)with a phosphate group as an anchoring group and conjugated terminal functional in both analogous molecules provide carrier transfer bridge at bottom interface of the active layer.Systematized theoretical investigations and characterizations have discovered the multi-site coordination of CMP-OH towards acceptor molecules and ZnO nps.The dual-side alignment of CMP analogous molecules hinders interfacial charge recombination and enhances charge transfer potential at once.Inevitably,PM6:L8-BO-based OSCs with modified ETL obtain 18.13%efficiency,12%higher than that of unmodified nps.Besides higher efficiency,CMP-OH-based OSC devices illustrate remarkably improved thermal stability for 500 h at 85℃with 72%of initial PCE and operation stability for 2000 h with 90.1%of initial PCE.This work reveals the passivation mechanism of multi-anchoring groups towards MOs and single-functional groups towards the active layer to optimize the interface for efficient and highly stable OSCs.展开更多
Intercalation is an effective method to modify physical properties and induce novel electronic states of transition metal dichalcogenide(TMD)materials.However,it is difficult to reveal the microscopic electronic state...Intercalation is an effective method to modify physical properties and induce novel electronic states of transition metal dichalcogenide(TMD)materials.However,it is difficult to reveal the microscopic electronic state evolution in the intercalated TMDs.Here we successfully synthesize the copper-intercalated 1T-TaS_(2) and characterize the structural and electronic modification combining resistivity measurements,atomic-resolution scanning transmission electron microscopy(ADF-STEM),and scanning tunneling microscopy(STM).The intercalated Cu atom is determined to be directly below the Ta atom and suppresses the commensurate charge density wave(CCDW)phase.Two specific electronic modulations are discovered in the near-commensurate(NC)CDW phase:the electron doping state near the defective star of Davids(SDs)in metallic domains and the spatial evolution of the Mott gap in insulating domains.Both modulations reveal that intercalated Cu atoms act as a medium to enhance the interaction between intralayer SDs,in addition to the general charge transfer effect.It also solidifies the Mott foundation of the insulating gap in pristine samples.The intriguing electronic evolution in Cu-intercalated 1T-TaS_(2) will motivate further exploration of novel electronic states in the intercalated TMD materials.展开更多
基金National Natural Science Foundation of China,Grant/Award Number:51073067Scientific and Technological Development Program of Jilin Province,Grant/Award Number:20220201138GX.
文摘In recent years,renewable energy sources,which aim to replace rapidly depleting fossil fuels,face challenges due to limited energy storage and conversion technologies.To enhance energy storage and conversion efficiency,extensive research has been conducted in the academic community on numerous potential materials.Among these materials,metal fluorides have attracted significant attention due to their ionic metal-fluorine bonds and tunable electronic structures,attributed to the highest electronegativity of fluorine in their chemical composition.This makes them promising candidates for future electrochemical applications in various fields.However,metal fluorides encounter various challenges in different application directions.Therefore,we comprehensively review the applications of metal fluorides in the field of energy storage and conversion,aiming to deepen our understanding of their exhibited characteristics in different electrochemical processes.In this paper,we summarize the difficulties and improvement methods encountered in different types of battery applications and several typical electrode optimization strategies in the field of supercapacitors.In the field of water electrolysis,we focus on surface reconstruction and the critical role of fluorine,demonstrating the catalytic performance of metal fluorides from the perspectives of reconstruction mechanism and process analysis.Finally,we provide a summary and outlook for this field,aiming to offer guidance for future breakthroughs in the energy storage and conversion applications of metal fluorides.
基金supported by the Natural Science Foundation of China(22309179)the Natural Science Foundation of China(12404049)+4 种基金Natural Science Foundation of Ningxia(2023AAC01003)Guangdong Basic and Applied Basic Research Foundation(2021A1515110156,2022A1515010724,2023A1515110521,2023B1515120095,2024A1515011260)Science and Technology Program of Guangzhou(No.2019050001)the Outstanding Youth Project of Guangdong Natural Science Foundation(2021B1515020051)Dalian Revitalization Talents Program(No.2022RG01).
文摘Developing electrocatalysts to inhibit polysulfide shuttling and expedite sulfur species conversion is vital for the evolution of Lithium-sulfur(Li-S)batteries.This work provides a facile strategy to design an intimate heterostructure of MIL-88A@CdS as a sulfur electrocatalyst combining high sulfur adsorption and accelerated polysulfide conversion.The MIL-88A can give a region of high-ordered polysulfide adsorption,whereas the CdS is an effective nanoreactor for the sulfur reduction reaction(SRR).Notedly,the significant size difference between MIL-88A and CdS enables the unique heterostructure interactions.The largesize MIL-88A ensures a uniform distribution of CdS nanoparticles as a substrate.This configuration facilitates control of the initial polysulfide adsorption position relative to its final deposition site as lithium sulfide.The heterostructure also demonstrates rapid transport and efficient conversion of lithium polysulfides.Consequently,the Li-S battery with MIL-88A@CdS heterostructure modified separator delivers exceptional performance,achieving an areal capacity exceeding 6 mAh cm^(−2),an excellent rate capability of 980 mAh g^(−1) at 5 C,and notable cycling stability in a 2 Ah pouch cell over 100 cycles.This work is significant for elucidating the relationship between heterostructure and electrocatalytic performance,providing great insights for material design aimed at highly efficient future electrocatalysts in practical applications.
基金the National Natural Science Foundation of China(Grant nos.21625304 and 21733012)the Ministry of Science and Technology(Grant No.2016YFA0200703).
文摘Lithium metal is regarded as the ultimate negative electrode material for secondary batteries due to its high energy density.However,it suffers from poor cycling stability because of its high reactivity with liquid electrolytes.Therefore,continuous efforts have been put into improving the cycling Coulombic efficiency(CE)to extend the lifespan of the lithium metal negative electrode.Herein,we report that using dual-salt additives of LiPF_(6) and LiNO_(3) in an ether solvent-based electrolyte can significantly improve the cycling stability and rate capability of a Li-carbon(Li-CNT)composite.As a result,an average cycling CE as high as 99.30% was obtained for the Li-CNT at a current density of 2.5 mA cm^(-2) and an negative electrode to positive electrode capacity(N/P)ratio of 2.The cycling stability and rate capability enhancement of the Li-CNT negative electrode could be attributed to the formation of a better solid electrolyte interphase layer that contains both inorganic components and organic polyether.The former component mainly originates from the decomposition of the LiNO_(3) additive,while the latter comes from the LiPF_(6)-induced ring-opening polymerization of the ether solvent.This novel surface chemistry significantly improves the CE of Li negative electrode,revealing its importance for the practical application of lithium metal batteries.
基金supported jointly by the National Natural Science Foundation of China(Nos.61674165,61604167,61574160,61704183,61404159,11604366)the Natural Science Foundation of Jiangsu Province(Nos.BK20170432,BK20160397,BK20140394)+2 种基金the National Key R&D Program of China(No.2016YFB0401803)the Strategic Priority Re-search Program of the Chinese Academy of Science(No.XDA09020401)the support at the Platform for Characterization&Test,Suzhou Institute of Nano-Tech and Nano-Bionics(SINANO),Chinese Academy of Sciences
文摘High quality gallium oxide(Ga_2O_3) thin films are deposited by remote plasma-enhanced atomic layer deposition(RPEALD) with trimethylgallium(TMG) and oxygen plasma as precursors. By introducing in-situ NH3 plasma pretreatment on the substrates, the deposition rate of Ga_2O_3 films on Si and GaN are remarkably enhanced, reached to 0.53 and 0.46 ?/cycle at 250 °C,respectively. The increasing of deposition rate is attributed to more hydroxyls(–OH) generated on the substrate surfaces after NH3 pretreatment, which has no effect on the stoichiometry and surface morphology of the oxide films, but only modifies the surface states of substrates by enhancing reactive site density. Ga_2O_3 film deposited on GaN wafer is crystallized at 250 °C, with an epitaxial interface between Ga_2O_3 and GaN clearly observed. This is potentially very important for reducing the interface state density through high quality passivation.
基金Project supported by the National Natural Science Foundation of China (Grant Nos. 92165205, 11790311, 12004172, 11774152, 11604366, and 11634007)the National Key Research and Development Program of China (Grant Nos. 2018YFA0306800 and 2016YFA0300401)+1 种基金the Program of High-Level Entrepreneurial and Innovative Talents Introduction of Jiangsu Province, the Jiangsu Planned Projects for Postdoctoral Research Funds (Grant No. 2020Z172)the Natural Science Foundation of Jiangsu Province, China (Grant No. BK 20160397)。
文摘As a special order of electronic correlation induced by spatial modulation, the charge density wave(CDW) phenomena in condensed matters attract enormous research interests. Here, using scanning-tunneling microscopy in various temperatures, we discover a hidden incommensurate stripe-like CDW order besides the(■) CDW phase at low-temperature of 4 K in the epitaxial monolayer 1T-VSe_(2) film. Combining the variable-temperature angle-resolved photoemission spectroscopic(ARPES) measurements, we discover a two-step transition of an anisotropic CDW gap structure that consists of two parts △_(1) and△_(2). The gap part ?1 that closes around ~ 150 K is accompanied with the vanish of the(√7×√3) CDW phase. While another momentum-dependent gap part △_(2) can survive up to ~ 340 K, and is suggested to the result of the incommensurate CDW phase. This two-step transition with anisotropic gap opening and the resulted evolution in ARPES spectra are corroborated by our theoretical calculation based on a phenomenological form for the self-energy containing a two-gap structure △_(1) +△_(2), which suggests different forming mechanisms between the(√7×√3) and the incommensurate CDW phases. Our findings provide significant information and deep understandings on the CDW phases in monolayer 1T-VSe_(2) film as a two-dimensional(2D) material.
基金supported in part by the National Key R&D Program(Grant No.2018YFB2003305)the National Natural Science Foundation of China(Grant Nos.61774165,61704186,and 61827823)the program from SINANO(Y8AAQ11003 and Y4JAQ21005)。
文摘The atomic structure and surface chemistry of GaP/Si(100)heterostructure with different pre-layers grown by molecu-lar beam epitaxy are studied.It is found that GaP epilayer with Ga-riched pre-layers on Si(100)substrate has regular surface mor-phology and stoichiometric abrupt heterointerfaces from atomic force microscopes(AFMs)and spherical aberration-corrected transmission electron microscopes(ACTEMs).The interfacial dynamics of GaP/Si(100)heterostructure is investigated by X-ray photoelectron spectroscopy(XPS)equipped with an Ar gas cluster ion beam,indicating that Ga pre-layers can lower the inter-face formation energy and the bond that is formed is more stable.These results suggest that Ga-riched pre-layers are more con-ducive to the GaP nucleation as well as the epitaxial growth of GaP material on Si(100)substrate.
基金financially supported by the Scientific and Technological Development Program of Jilin Province(20220201138GX)the support of the National Key R&D Program of China(No.2022YFA1503801)+1 种基金CAS Project for Young Scientists in Basic Research(No.YSBR-022)the Young Cross Team Project of CAS(No.JCTD-2021-14)。
文摘Ni-Fe-based catalysts are considered to be among the most active catalysts for the oxygen evolution reaction(OER)under alkaline conditions,with Fe playing a crucial role.However,Fe leaching occurs during the reaction due to thermodynamic instability,which has resulted in conflicting reports within the literature regarding its role.To clarify this point,we propose a strategy consisting of modulating the electronic orbital occupancy to suppress the extensive loss of Fe atoms during the OER process.Theoretical calculations,in-situ X-ray photoelectron spectroscopy,molecular dynamics simulations,and a series of characterization showed that the stable presence of Fe not only accelerates the electron transfer process but also optimizes the reaction barriers of the oxygen evolution intermediates,promoting the phase transition of Fe_(5)Ni_(4)S_(8)to highly active catalytic species.The modulated Fe_(5)Ni_(4)S_(8)-based pre-catalysts exhibit improved OER activity and long-term durability.This study provides a novel perspective for understanding the role of Fe in the OER process.
基金Supported by the National Natural Science Foundation of China (Grant Nos. 51788104, 11604366, 11774192, and 11634007)the National Key R&D Program of China (Grant Nos. 2017YFA0304600 and 2018YFA0305603)。
文摘Two-dimensional honeycomb crystals have inspired intense research interest for their novel properties and great potential in electronics and optoelectronics. Here, through molecular beam epitaxy on SrTiO_3(001), we report successful epitaxial growth of metal-rich chalcogenide Fe_(2)Te, a honeycomb-structured film that has no direct bulk analogue, under Te-limited growth conditions. The structural morphology and electronic properties of Fe_(2)Te are explored with scanning tunneling microscopy and angle resolved photoemission spectroscopy, which reveal electronic bands cross the Fermi level and nearly flat bands. Moreover, we find a weak interfacial interaction between Fe_(2)Te and the underlying substrates, paving a newly developed alternative avenue for honeycomb-based electronic devices.
基金Project supported by the National Natural Science Foundation of China(Grant Nos.11604366,11634007,21872099,and 22072102)the National Natural Science Foundation of Jiangsu Province,China(Grant No.BK 20160397)support from the Youth Innovation Promotion Association of Chinese Academy of Sciences(Grant No.2017370)。
文摘Monolayer MnTe_(2)stabilized as 1 T structure has been theoretically predicted to be a two-dimensional(2 D)ferromagnetic metal and can be tuned via strain engineering.There is no naturally van der Waals(vdW)layered MnTe_(2)bulk,leaving mechanical exfoliation impossible to prepare monolayer MnTe_(2).Herein,by means of molecular beam epitaxy(MBE),we successfully prepared monolayer hexagonal MnTe_(2)on Si(111)under Te rich condition.Sharp reflection high-energy electron diffraction(RHEED)and low-energy electron diffraction(LEED)patterns suggest the monolayer is atomically flat without surface reconstruction.The valence state of Mn^(4+)and the atom ratio of([Te]:[Mn])further confirm the MnTe_(2)compound.Scanning tunneling spectroscopy(STS)shows the hexagonal MnTe_(2)monolayer is a semiconductor with a large bandgap of~2.78 eV.The valence-band maximum(VBM)locates at theΓpoint,as illustrated by angle-resolved photoemission spectroscopy(ARPES),below which three hole-type bands with parabolic dispersion can be identified.The successful synthesis of monolayer MnTe_(2)film provides a new platform to investigate the 2D magnetism.
基金supports from the National Natural Science Foundation of China(No.22109171)the Chongqing Talent Program(No.cstc2024ycjh-bgzxm0068))+1 种基金the Science and Technology Research Program of Chongqing Municipal Education Commission(No.KJZD-K202301101)the Natural Science Foundation of Chongqing(No.CSTB2023NSCQ-MSX0315).
文摘Hydrogen energy carrier produced by water electrolysis in alkaline electrolytes is rather meaningful and significant for global sustainability imperatives,while the highpH condition usually leads to a poor reversibility of proton adsorption and desorption that significantly determines the hydrogen-generation activity in hydrogen evolution reaction(HER)process.Herein,we demonstrate a remarkable Ru-Mo solid-solution nanocrystal catalyst in alkaline HER process by a very simple but feasible pyrolysis and alkali leaching strategy.Benefiting from the pinning effect and local chemical-and electronic-structure regulations of Mo solute atoms,an ultra-low overpotential(17.3 mV)and an exceptional stability(>100 h)at the typical current density of 10 mA·cm^(−2)are achieved on the ultrasmall Ru-Mo solid-solution nanocrystal catalyst in 1.0 M KOH electrolyte.Density function theory(DFT)calculations gain an insight into the synergistic effect of neighboring Ru and Mo sites in alkaline HER process,where Mo solute atoms are beneficial for the adsorption and activation of water molecules for proton generation and accumulation due to their rich outermost 4d vacant orbitals,while the energy-favorable Ru sites are responsible for the fast deprotonation kinetics of hydrogen intermediates.Our work may provide an interesting route for the development of efficient and stable solid-solution alloy nanocrystals towards alkaline water electrolysis and beyond.
基金the National Natural Science Foundation of China(Nos.61804136,U1804155,and 62027816).
文摘Ga_(2)O_(3)has been regarded as a promising material for solar-blind detection due to its ultrawide bandgap and low growth cost.Although semiconductor microwires(MWs)possess unique optical and electronic characteristics,the performances of photodetectors developed from Ga_(2)O_(3)MWs are still less than satisfactory.Herein,we demonstrate high-performance solar-blind photodetectors based on Sn-doped Ga_(2)O_(3)MWs,possessing a light/dark current ratio of 107 and a responsivity of 2,409 A/W at 40 V.Moreover,a 1×10 solar-blind photodetector linear array is developed based on the Sn-doped Ga_(2)O_(3)MWs via a patternedelectrodes method.And clear solar-blind images are obtained by using the photodetector array as the imaging unit of a solarblind imaging system.The results provide a convenient way to construct high-performance solar-blind photodetector arrays based on Ga_(2)O_(3)MWs,and thus may push forward their future applications.
基金the National Natural Science Foundation of China(61674165,61604167,61574160,61704183,61404159,11604366)the Natural Science Foundation of Jiangsu Province(BK20170432,BK20160397,BK20140394)+2 种基金the National Key R&D Program of China(2016YFB0401803)the Strategic Priority Research Program of the Chinese Academy of Science(XDA09020401)XRD,AFM and TEM experiments were performed at the Platform for Characterization&Test,Suzhou Institute of Nano-Tech and Nano-Bionics(SINANO),Chinese Academy of Sciences.
文摘In this work,we have successfully grown high quality epitaxialβ-Ga_(2)O_(3)thin films onβ-Ga_(2)O_(3)(100)and Al_(2)O_(3)(0001)substrates using pulsed laser deposition(PLD).By optimizing temperature and oxygen pressure,the best conditions were found to be 650-700℃and 0.5 Pa.To further improve the quality of hetero-epitaxialβ-Ga_(2)O_(3),the sapphire substrates were pretreated for atomic terraced surface by chemical cleaning and high temperature annealing.From the optical transmittance measurements,the films grown at 600-750℃exhibit a clear absorption edge at deep ultraviolet region around 250-275 nm wavelength.High resolution transmission electron microscope(HRTEM)images and X-ray diffraction(XRD)patterns demonstrate thatβ-Ga_(2)O_(3)(-201)//Al_(2)O_(3)(0001)epitaxial texture dominated the epitaxial oxide films on sapphire substrate,which opens up the possibilities of high power electric devices.
基金supported by the National Natural Science Foundation of China(Nos.21625304,21733012)the"Strategic Priority Research Program”of Chinese Academy of Sciences(No.XDA09010600)the Ministry of Science and Technology(No.2016YFA0200703).
文摘Li has been considered as the ultimate anode material for high energy density secondary Li batteries.However,its practical application has been limited due to its low Coulombic efficiency(CE)and the formation of lithium dendrites.Recently,we have developed a microspherical Li-carbon nanotube(Li-CNT)composite material passivated with octadecylphosphonic acid(OPA)self-assembled monolayer(SAM)exhibiting suppressed lithium dendrite formation and improved environmental/electrochemical stability.In this work,we demonstrated the significantly enhanced passivation effects of a SAM using dihexadecanoalkyl phosphate(DHP),a molecule that is comprised of double hydrophobic alkyl chains and forms a denser SAM on surfaces with large curvature.As a result,the DHP SAM delivers superior environmental and electrochemical stability to the OPA passivated Li-CNT material.In specific,the DHP passivated Li-CNT composite(DHP-Li-CNT)delivers a high CE of 99.25%under a 33.3%depth of discharge(DOD)at 1 C,when it is paired with a LiFePO4 cathode.The evolution of the SAM during cycling and the effects of DOD and current density on the CE of the DHP-Li-CNT anode have also been investigated.The improved SAM passivation constitutes an important step in achieving the goal of practically applicable Li anodes.
基金supported by the National Natural Science Foundation of China(22135001)Young Cross Team Project of CAS(JCTD-2021-14)+1 种基金“Dual Carbon”Science and Technology Innovation of Jiangsu Province(Industrial Prospect and Key Technology Research Program)(BE2022021)Vacuum Interconnected Nanotech Workstation,Suzhou Institute of Nano-Tech and Nano-Bionics,and Chinese Academy of Sciences(CAS)。
文摘卷对卷(R2R)凹版印刷具有高的边缘分辨率、可图案化、高加工速度等优势,是制备大面积柔性有机太阳能电池(FOSCs)的一种可行技术.有机光活性层的薄膜质量是决定有机太阳能电池器件性能的关键.对于凹版印刷过程而言,墨水的转移是影响印刷薄膜厚度和质量的关键.本文深入研究了有机光活性层的墨水粘度对墨水转移率和薄膜缺陷的影响.我们开发了紫外可见光谱法,量化凹版印刷过程中墨水的转移率.通过对墨水的流变行为分析、流体动力学模拟和实验验证,深入研究了油墨粘度与油墨转移率、膜厚和膜均匀性之间的关系.结果表明,油墨粘度约为25 m Pa·s是R2R凹版印刷有机光活性层薄膜的适合粘度.通过对油墨配方的优化,我们制备了全R2R印刷FOSCs,其中1 cm^(2);电池的效率超过12%.
基金funding support from the National Natural Science Foundation of China(Nos.22125902,U2032202,and 21975243)the National Program for Support of Topnotch Young Professionals,the Fundamental Research Funds for the Central Universities(No.WK2030020032)+1 种基金the DNL cooperation Fund,CAS(No.DNL202020)the Anhui Science Fund for Distinguished Young Scholars(No.2208085J15).
文摘Li metal has become a strong candidate for anode due to its high theoretical specific capacity and lowest electrochemical potential.However,the poor reversibility caused by continuous chemical and electrochemical degradation hinders the practical application of Li metal.Solid-solution-based metal alloy phases have been proposed as hosts for regulating the non-dendrite electrodeposition,but the fundamental understanding remains unclear due to the drastically different deposition behaviors of Li on them.Here we found the difference in the diffusion coefficient of Li atoms on solid-solution-based metal alloy phases(Li-Mg and Li-Ag alloys)was a major contributor to the different deposition behaviors.The low Li atom diffusion coefficient of Li-Mg alloy showed a preferential Li accumulation on the upper surface rather than the inward-growth plating of Li atoms into alloy foil in Li-Ag alloy.By the process of secondary recrystallization,we improved the diffusion coefficient of Li atoms in Li-Mg alloy that facilitates the inward transfer rather than surface plating of Li atoms.In this case,the recrystallized Li-Mg alloy underwent a solidsolution phase change in the delithiation-lithiation cycles which yielded a high Coulombic efficiency of 99.3%with a reversible gravimetric capacity of 2,874 mAh·g−1 and superior cycling stability over 5,000 h without dendrite growth.
基金supported by the Natural Science Foundation of China(grant no.22309179)Natural Science Foundation of Ningxia(grant no.2023AAC01003)Chinese Academy of Sciences,and the Foundation of State Key Laboratory of High Efficiency Utilization of Coal and Green Chemical Engineering(grant no.2022-K79)。
文摘Heterostructured sulfur electrocatalysts have long been heralded as an effective approach to settle the issues of the shuttle effect and sluggish reaction kinetics of lithium polysulfides(LiPSs)in lithium-sulfur(Li-S)batteries.However,the limited active sites on the interface of the heterostructure offer unsatisfactory LiPSs conversion capability,rendering sluggish reaction kinetics.Herein,we have designed abnormal step-scheme nano-heterointerfaces,containing P-N,N-semimetal,and P-semimetal heterostructures as sulfur electrocatalysts to regulate the LiPSs catalytic conversion behavior,which demonstrates efficient catalytic activity and robust structural stability.The excellent electron-confinement contributed by the step-scheme barrier endows the electron gathering at the nano-heterointerfaces,conferring high selectivity and durability of electrocatalyst for an accelerated sulfur reduction reaction.The unique robust structure design further bestows the sulfur composite with favored ion/mass transportation within the electrode.Attributed to these structural features,the Li-S cell delivers excellent performance under high areal capacity over 7 mAh cm^(−2) and lean electrolyte/sulfur ratio below 2.5μL mg^(−1),decent rate capability up to 8 C,remarkable cyclic stability over 500 cycles,and satisfactory energy density of 386.3 Wh kg^(−1) in a 7.5 Ah pouch cell.This nano-heterointerface structure design strategy endows a sulfur cathode with superior LiPSs catalytic activity,opening new insights into high-performance Li-S batteries.
基金supported by the National Key Research and Development Program of China(2018YFA0306800,2021YFA1400400,2018YFA0306200,and 2021YFA1202901)the National Natural Science Foundation of China(92165205,11790311,12004172,51861145201,52072168,21733001,and 91750101)+2 种基金the Innovation Program for Quantum Science and Technology for China(2021ZD0302803)the Jiangsu Planned Projects for Postdoctoral Research Funds(2020Z172)the Program of High-Level Entrepreneurial and Innovative Talents Introduction of Jiangsu Province,China。
基金supported by the National Natural Science Foundation of China(22135001)Young Cross Team Project of CAS(No.JCTD-2021-14)+2 种基金Suzhou Science and Technology Program(ST202219)"Dual Carbon"Science and Technology Innovation of Jiangsu Province(Industrial Prospect and Key Technology Research Program)(BE2022021)Vacuum Interconnected Nanotech Workstation,and Suzhou Institute of Nano-Tech and Nano-Bionics,Chinese Academy of Sciences(CAS).
文摘ZnO nanoparticles(nps)among metal oxide(MOs)are proven to be essential electron transporting layers(ETLs)applied in organic solar cells(OSCs).However,intrinsic defects,interfacial charge recombination,and catalytic behavior towards the active layer restrict the applications of ZnO nps for efficient and long-term stable OSCs.The commonly available biomolecule cytidine 5'-monophosphate(CMP-OH)with phosphonic acid,its salt cytidine 5'-monophosphate disodium salt(CMP-ONa)with a phosphate group as an anchoring group and conjugated terminal functional in both analogous molecules provide carrier transfer bridge at bottom interface of the active layer.Systematized theoretical investigations and characterizations have discovered the multi-site coordination of CMP-OH towards acceptor molecules and ZnO nps.The dual-side alignment of CMP analogous molecules hinders interfacial charge recombination and enhances charge transfer potential at once.Inevitably,PM6:L8-BO-based OSCs with modified ETL obtain 18.13%efficiency,12%higher than that of unmodified nps.Besides higher efficiency,CMP-OH-based OSC devices illustrate remarkably improved thermal stability for 500 h at 85℃with 72%of initial PCE and operation stability for 2000 h with 90.1%of initial PCE.This work reveals the passivation mechanism of multi-anchoring groups towards MOs and single-functional groups towards the active layer to optimize the interface for efficient and highly stable OSCs.
基金This work was supported by the National Key Research and Development Program(No.2019YFA0308602)the Key Research and Development Program of Zhejiang Province,China(No.2021C01002)+6 种基金Vacuum Interconnected Nanotech Workstation(Nano-X)(B2004)the Fundamental Research Funds for the Central Universities in ChinaD.D.and C.J.thank the National Natural Science Foundation of China(Nos.NSFC-51772265 and NSFC-61721005)J.G.,W.W.,X.L.,W.L.,and Y.S.thank the support of the National Key Research and Development Program(No.2016YFA0300404)the National Natural Science Foundation of China(Nos.NSFC-11674326 and NSFC-11874357)the Joint Funds of the National Natural Science Foundation of Chinathe Chinese Academy of Sciences’Large-scale Scientific Facility(Nos.U1832141,U1932217,and U2032215).
文摘Intercalation is an effective method to modify physical properties and induce novel electronic states of transition metal dichalcogenide(TMD)materials.However,it is difficult to reveal the microscopic electronic state evolution in the intercalated TMDs.Here we successfully synthesize the copper-intercalated 1T-TaS_(2) and characterize the structural and electronic modification combining resistivity measurements,atomic-resolution scanning transmission electron microscopy(ADF-STEM),and scanning tunneling microscopy(STM).The intercalated Cu atom is determined to be directly below the Ta atom and suppresses the commensurate charge density wave(CCDW)phase.Two specific electronic modulations are discovered in the near-commensurate(NC)CDW phase:the electron doping state near the defective star of Davids(SDs)in metallic domains and the spatial evolution of the Mott gap in insulating domains.Both modulations reveal that intercalated Cu atoms act as a medium to enhance the interaction between intralayer SDs,in addition to the general charge transfer effect.It also solidifies the Mott foundation of the insulating gap in pristine samples.The intriguing electronic evolution in Cu-intercalated 1T-TaS_(2) will motivate further exploration of novel electronic states in the intercalated TMD materials.
基金supported by the National Natural Science Foundation of China(U1832202,11888101,11920101005,12141402,and 12274459)the Chinese Academy of Sciences(QYZDB-SSW-SLH043,XDB33020100,and XDB28000000)+4 种基金the Beijing Municipal Science and Technology Commission(Z171100002017018,and Z200005)the National Key R&D Program of China(2018YFE0202600,2022YFA1403100,and 2022YFA1403800)the Fundamental Research Funds for the Central Universities and Research Funds of Renmin University of China(RUC)(18XNLG14,19XNLG13,19XNLG17,and 20XNH062)the Synergic Extreme Condition User Facility,Beijing,ChinaBeijing National Laboratory for Condensed Matter Physics。
