High-/medium-entropy alloys(H/MEAs)of face-centered-cubic-structured single phase usually suffer from a glaring drawback of low yield strength.Even worse,the trade-off emerges frustratingly between strength and ductil...High-/medium-entropy alloys(H/MEAs)of face-centered-cubic-structured single phase usually suffer from a glaring drawback of low yield strength.Even worse,the trade-off emerges frustratingly between strength and ductility as strength increases.Here,the lamellar heterostructure(HS)is designed in an equiatomic ternary CoNiFe ME A by means of cold rolling followed by an incomplete recrystallization annealing.The lamellar HS consists of the soft recrystallized grains as well as severely deformed structures which are partly reserved.By comparison to the coarse-grained counterpart,the lamellar HS,shows a well enhanced yield strength-ductility synergy,together with an increased yield strength.This is ascribed to the hetero-deformation-induced(HDI)stress in HS during tensile deformation.Accordingly,the HDI strain hardening is induced,serving as an important addition to the conventional forest hardening.The HDI hardening is evidenced experimentally to account for a large proportion of global strain hardening.Furthermore,a fully recrystallized microstructure is obtained to show a simultaneous increase in both yield strength and ductility.The microstructures are evaluated in detail prior to and after tensile deformation by using the electron backscattered diffraction and transmission electron microscope observations.The mechanism for HDI strain hardening in various microstructures is analyzed to correlate to the evolution of microstructures in terms of the kernel average misorientation values,Schmid factor,and dislocation behaviors in response to plastic deformation.展开更多
Photocatalysis is an important technology for using solar energy to produce hydrogen,convert CO_(2) to synthetic fuels,and decrease persistent pollutant.However,conventional photocatalysts have limitations,including p...Photocatalysis is an important technology for using solar energy to produce hydrogen,convert CO_(2) to synthetic fuels,and decrease persistent pollutant.However,conventional photocatalysts have limitations,including poor spectral absorption,inefficient charge separation,and structural instability under operational stress,which demand innovative durable materials with tailored electronic properties.Nanodiamond(ND)has recently been recognized as a suitable material because of its exceptional chemical stability,superior charge carrier mobility,and possible surface functionalization.While its intrinsic wide bandgap limits its response to visible-light,different methods have been demonstrated to activate its catalytic potential.Here,several emerging strategies for improving the catalytic performance of ND-based photocatalytic systems are summarized,including surface functionalization,plasmonic hybridization,heteroatom doping,and heterostructure design.And the structure-activity relationship and design principle are proposed to improve the light harvesting,charge transport,and redox kinetics for constructing high efficiency ND-based photocatalysts used in the renewable energy and environmental industries.展开更多
Despite their high theoretical capacity and energy density,lithiumsulfur(Li–S)batteries still face challenges such as soluble lithium polysulfides(LiPSs)shuttling and sluggish redox kinetics.In this work,we used a no...Despite their high theoretical capacity and energy density,lithiumsulfur(Li–S)batteries still face challenges such as soluble lithium polysulfides(LiPSs)shuttling and sluggish redox kinetics.In this work,we used a novel MoS_(2)-Mo_(2)C heterostructure anchored on a carbon sponge(CS)as a Li_(2)S host to solve these problems.A simple hydrothermal process following carbothermal reduction was used to construct the MoS_(2)-Mo_(2)C heterostructure,enabling control of the phases and integration of MoS_(2) and Mo_(2)C.Structural characterization confirmed the coherent interface of the heterostructure with a precise orientation relationship between the two phases and their uniform distribution.An evaluation of the adsorption and catalytic performance of the material showed that it has an exceptional LiPSs adsorption capacity with faster conversion from Li_(2)S_(4) to Li_(2)S_(2).Density functional theory calculations further confirmed these results.As a result,the cathode had a high initial discharge capacity of 693 mAh g^(−1) at 0.2 C and achieved stable cycling at 2 C for 500 cycles with a low decay rate of 0.107%per cycle.The heterostructure design,coupled with the macroporous CS framework,effectively prevented the shuttling and increased sulfur utilization,offering a promising way to produce practical high-energydensity Li–S batteries.展开更多
Interplay between topology and magnetism can give rise to exotic properties in topological materials.Two-dimensional bismuth has been extensively studied owing to its topological states with a strong spin-orbit coupli...Interplay between topology and magnetism can give rise to exotic properties in topological materials.Two-dimensional bismuth has been extensively studied owing to its topological states with a strong spin-orbit coupling,and 1T-VTe_(2)monolayer theoretically predicted to host an intrinsic magnetism as experimentally suggested.In this work,we successfully constructed a vertical heterostructure composed of the two-dimensional Bi(110)monolayer and 1T-VTe_(2)monolayer by using molecular beam epitaxy(MBE).Scanning tunneling microscopy(STM)measurements revealed that the growth of Bi preferably occurs along the step edges of the VTe_(2)monolayer,forming a Bi(110)monolayer on top of the VTe_(2)monolayer next to a peripheral Bi bilayer.The Bi(100)/VTe_(2)heterostructure exhibits a specific lattice registry with a well-defined moiréperiodicity.Scanning tunneling spectroscopy(STS)measurements further unveiled an universal suppression in the local density-of-states at the boundary of the Bi(110)/VTe_(2)bilayer.By examining the atomic structures of Bi(110)boundaries,we found this effect does not originate from the previously proposed atomic reconstruction at the step edge of Bi(110),but is likely related to the magnetic properties of the VTe_(2)monolayer.展开更多
Coulomb drag refers to the phenomenon in which a current driven through one conducting layer induces a voltage nearby,electrically isolated layer sorely through interlayer Coulomb interactions between charge carriers....Coulomb drag refers to the phenomenon in which a current driven through one conducting layer induces a voltage nearby,electrically isolated layer sorely through interlayer Coulomb interactions between charge carriers.It has been extensively studied in various systems,including parallel nanowires,double quantum wells,and double-layer graphene.Here,we report the observation of Coulomb drag in a novel system consisting of two graphene layers separated laterally by a 30 nm gap within the material plane,exhibiting behavior distinct from that in vertical graphene heterostructures.Our experiments reveal pronounced negative drag resistances under an out-of-plane magnetic field at the quantum Hall edges,reaching a maximum when the carrier densities in both graphene layers are tuned to the charge neutrality point via gate voltages.Our work establish two separate and spatially closed quantum Hall edge modes as a new platform to explore electronic interaction physics between one dimensional systems.展开更多
Interfacial superconductivity(IS)has been a topic of intense interest in condensed matter physics,due to its unique properties and exotic photoelectrical performance.However,there are few reports about IS systems cons...Interfacial superconductivity(IS)has been a topic of intense interest in condensed matter physics,due to its unique properties and exotic photoelectrical performance.However,there are few reports about IS systems consisting of two insulators.Here,motivated by the emergence of an insulator-metal transition in type-Ⅲ heterostructures and the superconductivity in some“special”two-dimensional(2D)semiconductors via electron doping,we predict that the 2D heterostructure SnSe_(2)/PtTe_(2) is a model system for realizing IS by using firstprinciples calculations.Our results show that due to slight but crucial interlayer charge transfer,SnSe_(2)/PtTe_(2) turns to be a type-Ⅲ heterostructure with metallic properties and shows a superconducting transition with the critical temperature(T_(c))of 3.73 K.Similar to the enhanced electron–phonon coupling(EPC)in the electrondoped SnSe_(2) monolayer,the IS in the SnSe_(2)/PtTe_(2) heterostructure mainly originates from the metallized SnSe_(2) layer.Furthermore,we find that its superconductivity is sensitive to tensile lattice strain,forming a domeshaped superconducting phase diagram.Remarkably,at 7%biaxial tensile strain,the superconducting T_(c) can increase more than twofold(8.80 K),resulting from softened acoustic phonons at the𝑀point and enhanced EPC strength.Our study provides a concrete example for realizing IS in type-Ⅲ heterostructures,which waits for future experimental verification.展开更多
Transition-metal dichalcogenides hosting multiple competing structural and electronic phases are thus ideal platforms for constructing polytype heterostructures with emergent quantum properties.However,controlling pha...Transition-metal dichalcogenides hosting multiple competing structural and electronic phases are thus ideal platforms for constructing polytype heterostructures with emergent quantum properties.However,controlling phase transitions to form diverse heterostructures inside a single crystal remains challenging.In this study,we realize vertical/lateral polytype heterostructures in a hole-doped Mott insulator via thermal annealing-induced structural transitions.Raman spectroscopy,atomic force microscopy and scanning Kelvin probe force microscopy confirm the coexistence of T-H polytype heterostructures.Atomic-scale scanning tunneling microscopy/spectroscopy measurements reveal the transparent effect in 1H/1T vertical heterostructures,where positive bias voltage induces in a pronounced superposition of the√13×√13 CDW of the 1T-layer on the 1H-layer.By systematically comparing the 1T/1H and 1T/1T interfaces,we demonstrate that the metallic 1H-layer induces a Coulomb screening effect on the 1T-layer,suppressing the formation of CDW domain walls and forming more ordered electronic states.These results clarify the interfacial coupling between distinct quantum many-body phases and establish a controllable pathway for constructing two-dimensional polytype heterostructures with tunable electronic properties.展开更多
Halide perovskites have emerged as promising materials for X-ray detection with exceptional properties and reasonable costs.Among them,heterostructures between 3D perovskites and low-dimensional perovskites attract in...Halide perovskites have emerged as promising materials for X-ray detection with exceptional properties and reasonable costs.Among them,heterostructures between 3D perovskites and low-dimensional perovskites attract intensive studies of their advantages due to low-level ion migration and decent stability.However,there is still a lack of methods to precisely construct heterostructures and a fundamental understanding of their structure-dependent optoelectronic properties.Herein,a gas-phase method was developed to grow 2D perovskites directly on 3D perovskites with nanoscale accuracy.In addition,the larger steric hindrance of organic layers of 2D perovskites was proved to enable slower ion migration,which resulted in reduced trap states and better stability.Based on MAPbBr_(3)single crystals with the(PA)_(2)PbBr_(4)capping layer,the X-ray detector achieved a sensitivity of 22,245μC Gy_(air)^(−1)cm^(−2),a response speed of 240μs,and a dark current drift of 1.17.10^(–4)nA cm^(−1)s^(−1)V^(−1),which were among the highest reported for state-of-the-art perovskite-based X-ray detectors.This study presents a precise synthesis method to construct perovskite-based heterostructures.It also brings an in-depth understanding of the relationship between lattice structures and properties,which are beneficial for advancing high-performance and cost-effective X-ray detectors.展开更多
Zinc telluride(ZnTe)with high density and low cost is considered as promising anode for sodium-ion batteries.However,ZnTe suffers from continuous capacity degradation owing to the low electronic conductivity,large vol...Zinc telluride(ZnTe)with high density and low cost is considered as promising anode for sodium-ion batteries.However,ZnTe suffers from continuous capacity degradation owing to the low electronic conductivity,large volume expansion,and high ion-diffusion energy barriers.Herein,the nitrogen-doped carbon confined ZnTe polyhedron heterostructure(ZnTe/NC)is proposed,exploiting its orbital rehybridization and the realignment of energy level to improve storage performance.Systematic ex situ/in situ characterizations and simulations demonstrated that the elaborate ZnTe/NC offers abundant electron/ion transport pathways,accelerates Na^(+)diffusion kinetics,and alleviates huge volume expansion.Notably,the nitrogen-doped carbon-support interaction induced via electron transfer between ZnTe sites and support elevates the energy level of Zn 3d orbital,greatly enhancing ion adsorption capability and reducing the ion diffusion barrier.As a result,the ZnTe/NC anode delivers a high discharge capacity of 470.5 mAh g^(−1)and long cycling durability over 1000 cycles.This work uncovers that optimizing sodium ion adsorption and diffusion via d-orbital energy level modulation enabled by nitrogen-doped support interaction is an effective method for developing high-performance transition metal telluride anodes for alkali ion storage.展开更多
High-voltage Li-rich Mn-based oxide(LRMO)cathodes are promising for breaking through the energy density limits of lithium-ion batteries,yet their practical application remains limited by electrochemical performance de...High-voltage Li-rich Mn-based oxide(LRMO)cathodes are promising for breaking through the energy density limits of lithium-ion batteries,yet their practical application remains limited by electrochemical performance degradation caused by unstable cathode-electrolyte interphase(CEI)evolution during longterm cycling.To address this issue,we propose a novel surface modification strategy using La_(0.7)Sr_(0.3)MnO_(3-σ)(LSMO)nanodots,which exhibit high electronic co nductivity and excellent corrosion resistance.These nanodots act as stable anchoring sites,facilitating the formation of a robust CEI on LRMO,The LSMOmodified cathode demonstrates significantly improved anionic redox reversibility,effectively mitigating transition metal migration and lattice oxygen loss.Furthermore,the optimized interfacial electrochemical kinetics ensure sustained rapid Li+diffusion throughout cycling,while the formation of a stable trilayer CEI structure suppresses electrolyte decomposition.Benefiting from these synergistic effects,the LSMO nanodot-engineered LRMO cathode delivers outstanding cycling stability,retaining 97.4%capacity after 300 cycles at 1 C.This work not only highlights the critical role of nanodot heterostructures in stabilizing CEI but also provides a new approach to designing high-voltage cathodes with superior interfacial compatibility and long-term durability.展开更多
Developing catalysts with excellent stability while significantly reducing the overpotential of the oxygen evolution reaction(OER) is crucial for advancing overall water splitting(OWS) systems.In this study,we synthes...Developing catalysts with excellent stability while significantly reducing the overpotential of the oxygen evolution reaction(OER) is crucial for advancing overall water splitting(OWS) systems.In this study,we synthesized the electrode material Ce-NiCo-LDHs@SnO_(2)/NF through a two-step hydrothermal reaction,where Ce-doped NiCo-LDHs are grown on nickel foam modified by a SnO_(2) layer.Ce doping adjusts the internal electronic distribution of Ni Co-LDHs,while the introduction of the SnO_(2) layer enhances electron transfer capability.Together,these factors contribute to the reduction of the OER energy barrier and experimental evidence confirms that the reaction proceeds via the lattice oxygen evolution mechanism(LOM).Consequently,Ce-NiCo-LDHs@SnO_(2)/NF exhibits high level electrochemical performance in OER,requiring only 234 m V overpotential to achieve a current density of 10 m A/cm^(2),with a Tafel slope of just 27.39 m V/dec.When paired with Pt/C/NF,an external potential of only 1.54 V is needed to drive OWS to attain a current density amounting to 10 m A/cm^(2).Furthermore,the catalyst demonstrates stability for 100 h during the OWS stability test.This study underscores the feasibility of enhancing the OER performance through Ce doping and the introduction of a conductive SnO_(2) layer.展开更多
The design and fabrication of ordered epitaxial MOF-on-MOF heterostructures as highly efficient electrocatalysts for water splitting is crucial but still challenging.In this study,a simple coordination-driven self-ass...The design and fabrication of ordered epitaxial MOF-on-MOF heterostructures as highly efficient electrocatalysts for water splitting is crucial but still challenging.In this study,a simple coordination-driven self-assembly method is used to fabricate controllable MOF-on-MOF multiscale heterostructures,where triangular host MOF(ZIF-67)nanosheets undergo in situ epitaxial growth to form uniform orthogonal vip MOF(CoFe PBA)nanosheets.Phosphorus(P)is further introduced in situ to fabricate CoP and Fe_(2)P heterostructured nanosheets(CoFe-P-NS),which exhibit excellent bifunctional electrocatalytic performance due to the enhancement of intrinsic electrocatalytic activity by p-d orbital hybridization.Specifically,the CoFe-P-NS requires low overpotential of 259 and 307 mV to reach 500 mA cm−2 for HER and OER,respectively.Remarkably,the assembled electrolysis cell maintained a large current density of 300 mA cm−2 for over 360 h with negligible voltage increase during alkaline seawater electrolysis.Experiments and theoretical calculations show that the synergistic catalytic activity of bimetallic phosphides arises from p-d orbital hybridization,where the CoP-P sites enhance HER by optimizing H*adsorption in the Volmer-Heyrovsky steps,while the Fe_(2)P-Fe sites accelerate OER by lowering the energy barrier of the rate-determining step from O*to OOH*.This study provides valuable insights into the design of a controllable MOF-on-MOF-based electrocatalyst toward alkaline seawater splitting.展开更多
Zinc-air batteries(ZABs)are promising candidates for flexible electronics due to their high energy density and low cost.However,their development is hindered by the sluggish kinetics of the oxygen evolution reaction(O...Zinc-air batteries(ZABs)are promising candidates for flexible electronics due to their high energy density and low cost.However,their development is hindered by the sluggish kinetics of the oxygen evolution reaction(OER)and oxygen reduction reaction(ORR).Herein,we present a novel heterostructured electrocatalyst composed of vertically aligned N-doped graphene(NVG)arrays anchored on Ru-doped ceria(RCO)nanofibers,synthesized via a one-step plasma-enhanced chemical vapor deposition process.Notably,during the plasma-enhanced driven NVG growth,Ru nanoparticles are spontaneously in-situ exsolved from the RCO lattice,forming a unique Ru@RCO-NVG heterostructure.Density functional theory calculations reveal that the Ru@RCO-NVG heterojunction induces interfacial electronic redistribution,thereby significantly lowering the energy barriers for both OER and ORR.Benefiting from the synergistic effects,the Ru@RCO-NVG catalyst exhibits exceptional intrinsic activity towards OER/ORR(an overpotential of 370 mV for OER at 10 mA cm^(−2)and a half-wave potential of 0.86 V for ORR),and higher all-solid-state flexible ZAB performance(peak power density of 286.1 mW cm^(−2)),surpassing commercial Pt/C-IrO_(2)catalysts.This work not only advances the integration of synergistic graphene/ceria composites but also offers a promising strategy for designing efficient electrocatalysts for next-generation energy conversion technologies.展开更多
Metal halide perovskites have emerged as highly promising candidates for the emissive layer in next-generation light-emitting diodes(LEDs)due to their narrow emission linewidths,high photoluminescence quantum yields,a...Metal halide perovskites have emerged as highly promising candidates for the emissive layer in next-generation light-emitting diodes(LEDs)due to their narrow emission linewidths,high photoluminescence quantum yields,and tunable emission wavelengths.Achieving high-performance perovskite LEDs(Pe LEDs)requires the emissive layer to possess efficient radiative recombination,low defect density,minimal ion mobility,and effective carrier confinement.Perovskite/perovskite heterostructure(PPHS)offers a compelling approach for engineering emissive layers with these desired attributes,owing to their ability to passivate surface defects,tailor bandgaps,and suppress ion migration.Pe LEDs based on PPHS have demonstrated superior performance compared to single-phase devices,particularly in terms of external quantum efficiency and operational stability.This review provides a comprehensive overview of the typical PPHS architectures applied in Pe LEDs,including vertical,lateral,and bulk configurations.We discuss representative fabrication strategies and the associated optoelectronic properties of these heterostructures,highlighting the mechanisms by which they enhance device efficiency and stability.Finally,we explore the remaining challenges and prospects for the application of PPHS in Pe LEDs and other luminescent technologies.展开更多
This study aims to synthesise,characterise and evaluate the performance characteristics of packaging films based on biodegradable natural resources incorporated with nanoparticles.Particularly,it is focused on the val...This study aims to synthesise,characterise and evaluate the performance characteristics of packaging films based on biodegradable natural resources incorporated with nanoparticles.Particularly,it is focused on the valorisation of the fibers from the underexploited Lonchocarpus cyanescens plant fromWest Africa as raw renewable lignocellulosebiomassmaterial source for the productionof carboxymethylcellulose(CMC).To this end,biodegradable films were prepared from CMC derived from the fibers of the Lonchocarpus cyanescens plant,and collagen.In order to improve the properties of these films,in particular their mechanical and humidity resistance and their ability to fight microbes,silver nanoparticles(Ag NPs),titanium dioxide nanoparticles(TiO2 NPs),as well as heterostructure Ag@TiO2 nanocomposite were incorporated.The different products obtained were characterised by differentmethods,including DLS,UV-VIS,SEM,contact angle,UTM,absorption and antimicrobial activity tests.The results show that the hybrid biocomposite films exhibit good mechanical properties,improved moisture resistance,and a significant antimicrobial effect against certain pathogenic bacteria.In particular,the synergy between Ag and TiO_(2) nanoparticles in the heterostructure Ag@TiO_(2) nanocomposite optimized the performance characteristics of the packaging films,particularly in terms of mechanical properties with a maximum stress of 38.77 MPa and a strain of 9%,low water absorption reaching 50% at 48 h,improved hydrophobic behaviorwith contact angle of 87°,and antimicrobial resistance compared with the control film without nanoparticles.This work highlights the valorisation of an underexploitedWest African local plant and contributes to the search for sustainable solutions for food packaging.展开更多
Conversion-type electrode materials hold significant promise for potassium-ion batteries(PIBs)due to their high theoretical capacities,yet their practical deployment is hindered by sluggish kinetics and irreversible s...Conversion-type electrode materials hold significant promise for potassium-ion batteries(PIBs)due to their high theoretical capacities,yet their practical deployment is hindered by sluggish kinetics and irreversible structural degradation.To overcome these limitations,we propose a rationally engineered nanoreactor architecture that stabilizes defect-rich MoS_(2)via interlayer incorporation of a carbon monolayer,followed by encapsulation within a nitrogen-doped carbon shell,forming a MoSSe@NC heterostructure.This tailored structure synergistically accelerates both K^(+)diffusion kinetics and electron transfer,enabling unprecedented rate performance(107 mAh g^(-1)at 10 Ag^(-1))and ultralong cyclability(86.5%capacity retention after 1200 cycles at 3 A g^(-1)).Mechanistic insights reveal a distinctive“adsorption-conversion”pathway,where sulfur vacancies on exposed S-Mo-S basal planes act as preferential K^(+)adsorption sites,effectively suppressing parasitic phase transitions during intercalation.In situ X-ray diffraction and transmission electron microscopy corroborate the structural reversibility of the conversion reaction,with the carbon matrix dynamically accommodating strain while preserving electrode integrity.This work not only advances the understanding of defect-driven interfacial chemistry in conversion-type materials but also provides a versatile strategy for designing high-performance anodes in next-generation PIBs through heterostructure engineering.展开更多
MnO_(2) emerges as a promising cathode material for aqueous zinc-ion batteries(AZIBs)due to its high theoretical capacity and ideal working voltage.However,inherent limitations in low electrical conductivity and struc...MnO_(2) emerges as a promising cathode material for aqueous zinc-ion batteries(AZIBs)due to its high theoretical capacity and ideal working voltage.However,inherent limitations in low electrical conductivity and structural instability restrict its widespread application.Herein,we fabricated layered δ-MnO_(2) and introduced Cu and Ce metal ions for structural regulation,thus constructing a δ/a-MnO_(2) heterostructure within the δ-MnO_(2) matrix,forming a heterointerface that simultaneously enhances the electrical conductivity and structural stability of the material.In this system,Cu^(2+)acts as a catalyst,promoting the reduction of high-valent Mn to Mn^(2+)and enabling local two-electron transfer,which significantly increases the discharge specific capacity of MnO_(2).For Ce^(3+),it functions as a structural regulator,inducing the partial transformation of δ-MnO_(2) to a-MnO_(2) and forming the δ/a-MnO_(2) heterostructure.Further supported by density functional theory(DFT)calculations and in-situ characterization results,the heterointerface between a-MnO_(2) andδ-MnO_(2) generates an internal electric field due to the difference in Fermi levels.This not only effectively enhances the electron transfer capability but also significantly improves structural stability.Benefiting from these advantages,the Cu,Ce co-incorporated MnO_(2)(CCMO)cathode delivers a high discharge capacity of 455.4 mAh g^(-1)at 0.2 A g^(-1)and maintains 191.2 mAh g^(-1)specific capacity after 1500 cycles with 95%capacity retention at 2 A g^(-1),which is significantly better than non-doped MnO_(2).This strategy of structural regulation and heterostructure construction using vip ions offers a new approach for developing high-performance Mn-based cathode materials for AZIBs.展开更多
Van der Waals(vdW)heterostructures have attracted much attention due to their distinctive optical,electrical,and thermal properties,demonstrating promising potential in areas such as photocatalysis,ultrafast photonics...Van der Waals(vdW)heterostructures have attracted much attention due to their distinctive optical,electrical,and thermal properties,demonstrating promising potential in areas such as photocatalysis,ultrafast photonics,and free electron radiation devices.Particularly,they are promising platforms for studying thermionic emission.It is illustrated that using vdW heterostructure-based thermionic emission can enhance heat transfer in vacuum devices.As a proof of concept,the approach is demonstrated to offer a promising solution for the long-standing overheating issue in X-ray tubes.Specifically,it is shown that the saturated target temperature of a 2000 W X-ray tube can be reduced from around 1200℃ to 490℃.Additionally,it is also demonstrated that by reducing the height of the Schottky barrier formed in the vdW heterostructures,the thermionic cooling performance can be enhanced.The findings pave the way for the development of high-power X-ray tubes.展开更多
Recurrence of solid tumors after surgical resection is a major barrier to tissue regeneration.As an emerging treatment strategy,photo-thermo-electric therapy ablates tumor cells via photothermal effects and generates ...Recurrence of solid tumors after surgical resection is a major barrier to tissue regeneration.As an emerging treatment strategy,photo-thermo-electric therapy ablates tumor cells via photothermal effects and generates reactive oxygen species(ROS)via thermoelectric effects to disrupt heat shock proteins,thereby suppressing their protective function in tumor cells.However,conventional materials suffer from low thermoelectric efficiency and weak tissue penetration ability.In this study,we fabricated iodine-doped bismuth sulfide(I-Bi_(2)S_(3))nanorods with bonding heterostructures to improve thermoelectric performance.The approach employed iodine doping to introduce additional electrons,thereby regulating the band structure of Bi_(2)S_(3)and exploiting the dual low-energy vibration effect of the heterostructures to reduce thermal conductivity.More importantly,controlling the type of heterostructure modulated the bandgap width,thereby expanding the light absorption range to the higher-penetration near-infrared(NIR)-Ⅱregion for deep tissue treatment.The I-Bi_(2)S_(3)nanorods were incorporated into poly-L-lactic acid(PLLA)scaffolds to confer antitumor functionality.According to the results,the bonding heterostructures enhanced the conductivity of Bi_(2)S_(3)and reduced its thermal conductivity,significantly enhancing thermoelectric efficacy.The heterostructures reduced the bandgap of Bi_(2)S_(3)from 1.23 to 0.88 eV,enabling optical absorption in the NIR-Ⅱregion.The ROS tests showed that the PLLA/I-Bi_(2)S_(3)scaffold exhibited good photothermal effects and ROS generation under 1064-nm laser irradiation.The antitumor efficacy of the PLLA/I-Bi_(2)S_(3)scaffold reached 84.6%against MG-63 cells,demonstrating its exceptional potential in cancer treatment.展开更多
The electrocatalytic oxidation of ethylene glycol(EG)into high-value chemicals like glycolic acid(GA)is a crucial step for upcycling waste plastics.However,catalyst deactivation and low selectivity pose significant ch...The electrocatalytic oxidation of ethylene glycol(EG)into high-value chemicals like glycolic acid(GA)is a crucial step for upcycling waste plastics.However,catalyst deactivation and low selectivity pose significant challenges.This work presents the low-coordination PtBi nanosheets(LC-PtBi NSs),featuring a unique amorphous-crystalline heterostructure with a low coordination number of 2.3-2.5.They can exhibit exceptional mass activity(8.3 A mg_(Pt)^(-1))and stability(maintaining 88.7%of initial activity after running for 3600 s)of the EG oxidation reaction(EGOR).They also achieve over 90%apparent selectivity for EG-to-GA conversion at low potentials(<0.7 V vs.RHE)and even more than 100-h continuous electrolysis.Density fu nctional theory(DFT)calculations reveal that the low-coordination PtBi heterogeneous interface is responsible for the high coverage of OH_(ad) species and weakened adsorption of carbonaceous intermediates on LC-PtBi NSs,thereby promoting the direct oxidation of C_(2) intermediates to GA.This work demonstrates a strategy of doping-mediated catalytic interface regulation and electron density rearrangement,offering insights for designing efficient Pt-based electrocatalysts toward selective oxidation of small molecules.展开更多
基金financially supported by the National Key R&D Program of China (Nos.2017YFA0204402 and 2019YFA0209900)the National Natural Science Foundation of China (Nos.11972350 and 11790293)the Strategic Priority Research Program of the Chinese Academy of Sciences (No. XDB22040503)
文摘High-/medium-entropy alloys(H/MEAs)of face-centered-cubic-structured single phase usually suffer from a glaring drawback of low yield strength.Even worse,the trade-off emerges frustratingly between strength and ductility as strength increases.Here,the lamellar heterostructure(HS)is designed in an equiatomic ternary CoNiFe ME A by means of cold rolling followed by an incomplete recrystallization annealing.The lamellar HS consists of the soft recrystallized grains as well as severely deformed structures which are partly reserved.By comparison to the coarse-grained counterpart,the lamellar HS,shows a well enhanced yield strength-ductility synergy,together with an increased yield strength.This is ascribed to the hetero-deformation-induced(HDI)stress in HS during tensile deformation.Accordingly,the HDI strain hardening is induced,serving as an important addition to the conventional forest hardening.The HDI hardening is evidenced experimentally to account for a large proportion of global strain hardening.Furthermore,a fully recrystallized microstructure is obtained to show a simultaneous increase in both yield strength and ductility.The microstructures are evaluated in detail prior to and after tensile deformation by using the electron backscattered diffraction and transmission electron microscope observations.The mechanism for HDI strain hardening in various microstructures is analyzed to correlate to the evolution of microstructures in terms of the kernel average misorientation values,Schmid factor,and dislocation behaviors in response to plastic deformation.
文摘Photocatalysis is an important technology for using solar energy to produce hydrogen,convert CO_(2) to synthetic fuels,and decrease persistent pollutant.However,conventional photocatalysts have limitations,including poor spectral absorption,inefficient charge separation,and structural instability under operational stress,which demand innovative durable materials with tailored electronic properties.Nanodiamond(ND)has recently been recognized as a suitable material because of its exceptional chemical stability,superior charge carrier mobility,and possible surface functionalization.While its intrinsic wide bandgap limits its response to visible-light,different methods have been demonstrated to activate its catalytic potential.Here,several emerging strategies for improving the catalytic performance of ND-based photocatalytic systems are summarized,including surface functionalization,plasmonic hybridization,heteroatom doping,and heterostructure design.And the structure-activity relationship and design principle are proposed to improve the light harvesting,charge transport,and redox kinetics for constructing high efficiency ND-based photocatalysts used in the renewable energy and environmental industries.
文摘Despite their high theoretical capacity and energy density,lithiumsulfur(Li–S)batteries still face challenges such as soluble lithium polysulfides(LiPSs)shuttling and sluggish redox kinetics.In this work,we used a novel MoS_(2)-Mo_(2)C heterostructure anchored on a carbon sponge(CS)as a Li_(2)S host to solve these problems.A simple hydrothermal process following carbothermal reduction was used to construct the MoS_(2)-Mo_(2)C heterostructure,enabling control of the phases and integration of MoS_(2) and Mo_(2)C.Structural characterization confirmed the coherent interface of the heterostructure with a precise orientation relationship between the two phases and their uniform distribution.An evaluation of the adsorption and catalytic performance of the material showed that it has an exceptional LiPSs adsorption capacity with faster conversion from Li_(2)S_(4) to Li_(2)S_(2).Density functional theory calculations further confirmed these results.As a result,the cathode had a high initial discharge capacity of 693 mAh g^(−1) at 0.2 C and achieved stable cycling at 2 C for 500 cycles with a low decay rate of 0.107%per cycle.The heterostructure design,coupled with the macroporous CS framework,effectively prevented the shuttling and increased sulfur utilization,offering a promising way to produce practical high-energydensity Li–S batteries.
基金financially supported by the National Key Research and Development Program of China(Grant No.2021YFA1400403)the National Natural Science Foundation of China(Grant Nos.12374183,92165205)+2 种基金the Natural Science Foundation of Jiangsu Province(Grant No.BK20233001)the Innovation Program for Quantum Science and Technology(Grant No.2021ZD0302800)the Fundamental Research Funds for the Central Universities(Grant No.020414380207).
文摘Interplay between topology and magnetism can give rise to exotic properties in topological materials.Two-dimensional bismuth has been extensively studied owing to its topological states with a strong spin-orbit coupling,and 1T-VTe_(2)monolayer theoretically predicted to host an intrinsic magnetism as experimentally suggested.In this work,we successfully constructed a vertical heterostructure composed of the two-dimensional Bi(110)monolayer and 1T-VTe_(2)monolayer by using molecular beam epitaxy(MBE).Scanning tunneling microscopy(STM)measurements revealed that the growth of Bi preferably occurs along the step edges of the VTe_(2)monolayer,forming a Bi(110)monolayer on top of the VTe_(2)monolayer next to a peripheral Bi bilayer.The Bi(100)/VTe_(2)heterostructure exhibits a specific lattice registry with a well-defined moiréperiodicity.Scanning tunneling spectroscopy(STS)measurements further unveiled an universal suppression in the local density-of-states at the boundary of the Bi(110)/VTe_(2)bilayer.By examining the atomic structures of Bi(110)boundaries,we found this effect does not originate from the previously proposed atomic reconstruction at the step edge of Bi(110),but is likely related to the magnetic properties of the VTe_(2)monolayer.
基金support from the National Key Projects for Research and Development of China(Grant Nos.2022YFA1204700,2021YFA1400400)National Natural Science Foundation of China(Grant No.12525403)+3 种基金Natural Science Foundation of Jiangsu Province(Grant Nos.BK20220066,BK20233001)Program for Innovative Talents and Entrepreneur in Jiangsu(Grant No.JSSCTD202101)support from the JSPS KAKENHI(Grant Numbers 21H05233 and 23H02052)World Premier International Research Center Initiative(WPI),MEXT,Japan.
文摘Coulomb drag refers to the phenomenon in which a current driven through one conducting layer induces a voltage nearby,electrically isolated layer sorely through interlayer Coulomb interactions between charge carriers.It has been extensively studied in various systems,including parallel nanowires,double quantum wells,and double-layer graphene.Here,we report the observation of Coulomb drag in a novel system consisting of two graphene layers separated laterally by a 30 nm gap within the material plane,exhibiting behavior distinct from that in vertical graphene heterostructures.Our experiments reveal pronounced negative drag resistances under an out-of-plane magnetic field at the quantum Hall edges,reaching a maximum when the carrier densities in both graphene layers are tuned to the charge neutrality point via gate voltages.Our work establish two separate and spatially closed quantum Hall edge modes as a new platform to explore electronic interaction physics between one dimensional systems.
基金supported by the National Key R&D Program of China (Grant Nos.2022YFA1403103 and 2019YFA0308603)the National Natural Science Foundation of China (Grant No.12304167)the Shandong Provincial Natural Science Foundation of China (Grant No.ZR2023QA020)。
文摘Interfacial superconductivity(IS)has been a topic of intense interest in condensed matter physics,due to its unique properties and exotic photoelectrical performance.However,there are few reports about IS systems consisting of two insulators.Here,motivated by the emergence of an insulator-metal transition in type-Ⅲ heterostructures and the superconductivity in some“special”two-dimensional(2D)semiconductors via electron doping,we predict that the 2D heterostructure SnSe_(2)/PtTe_(2) is a model system for realizing IS by using firstprinciples calculations.Our results show that due to slight but crucial interlayer charge transfer,SnSe_(2)/PtTe_(2) turns to be a type-Ⅲ heterostructure with metallic properties and shows a superconducting transition with the critical temperature(T_(c))of 3.73 K.Similar to the enhanced electron–phonon coupling(EPC)in the electrondoped SnSe_(2) monolayer,the IS in the SnSe_(2)/PtTe_(2) heterostructure mainly originates from the metallized SnSe_(2) layer.Furthermore,we find that its superconductivity is sensitive to tensile lattice strain,forming a domeshaped superconducting phase diagram.Remarkably,at 7%biaxial tensile strain,the superconducting T_(c) can increase more than twofold(8.80 K),resulting from softened acoustic phonons at the𝑀point and enhanced EPC strength.Our study provides a concrete example for realizing IS in type-Ⅲ heterostructures,which waits for future experimental verification.
基金supported by the National Natural Science Foundation of China (Grant Nos.92477128,92580137,92477205,12374200,11604063,11974422,and 12104504)the National Key R&D Program of China (MOST) (Grant No.2023YFA1406500)+3 种基金the Strategic Priority Research Program (Chinese Academy of Sciences,CAS) (Grant No.XDB30000000)the Fundamental Research Funds for the Central Universities and Research Funds of Renmin University of China (Grant No.21XNLG27)supported by the Outstanding Innovative Talents Cultivation Funded Programs 2023 of the Renmin University of Chinaan outcome of “Two-dimensional anisotropic series of materials FePd2+xTe2:a structural modulation study from the atomic scale to the mesoscopic scale” (RUC25QSDL128),funded by the “Qiushi Academic-Dongliang” Talent Cultivation Project at Renmin University of China in 2025。
文摘Transition-metal dichalcogenides hosting multiple competing structural and electronic phases are thus ideal platforms for constructing polytype heterostructures with emergent quantum properties.However,controlling phase transitions to form diverse heterostructures inside a single crystal remains challenging.In this study,we realize vertical/lateral polytype heterostructures in a hole-doped Mott insulator via thermal annealing-induced structural transitions.Raman spectroscopy,atomic force microscopy and scanning Kelvin probe force microscopy confirm the coexistence of T-H polytype heterostructures.Atomic-scale scanning tunneling microscopy/spectroscopy measurements reveal the transparent effect in 1H/1T vertical heterostructures,where positive bias voltage induces in a pronounced superposition of the√13×√13 CDW of the 1T-layer on the 1H-layer.By systematically comparing the 1T/1H and 1T/1T interfaces,we demonstrate that the metallic 1H-layer induces a Coulomb screening effect on the 1T-layer,suppressing the formation of CDW domain walls and forming more ordered electronic states.These results clarify the interfacial coupling between distinct quantum many-body phases and establish a controllable pathway for constructing two-dimensional polytype heterostructures with tunable electronic properties.
基金support from National Key Research and Development Program of China(2024YFE0217100)the National Natural Science Foundation of China(21905006,22261160370,and 62105075)+7 种基金the Guangdong Provincial Science and Technology Plan(2021A0505110003)the Natural Science Foundation of Hunan Province,China(2023JJ50132)Guangxi Department of Science and Technology(2020GXNSFBA159049 and AD19110030)the Shenzhen Science and Technology Program(SGDX20230116093205009,JCYJ20220818100211025 and 2022378670)the Natural Science Foundation of Top Talent of SZTU(GDRC202343)financial support of Innovation and Technology Fund(#GHP/245/22SZ)The University Grant Council of the University of Hong Kong(grant No.2302101786)General Research Fund(grant Nos.17200823 and 17310624)from the Research Grants Council.
文摘Halide perovskites have emerged as promising materials for X-ray detection with exceptional properties and reasonable costs.Among them,heterostructures between 3D perovskites and low-dimensional perovskites attract intensive studies of their advantages due to low-level ion migration and decent stability.However,there is still a lack of methods to precisely construct heterostructures and a fundamental understanding of their structure-dependent optoelectronic properties.Herein,a gas-phase method was developed to grow 2D perovskites directly on 3D perovskites with nanoscale accuracy.In addition,the larger steric hindrance of organic layers of 2D perovskites was proved to enable slower ion migration,which resulted in reduced trap states and better stability.Based on MAPbBr_(3)single crystals with the(PA)_(2)PbBr_(4)capping layer,the X-ray detector achieved a sensitivity of 22,245μC Gy_(air)^(−1)cm^(−2),a response speed of 240μs,and a dark current drift of 1.17.10^(–4)nA cm^(−1)s^(−1)V^(−1),which were among the highest reported for state-of-the-art perovskite-based X-ray detectors.This study presents a precise synthesis method to construct perovskite-based heterostructures.It also brings an in-depth understanding of the relationship between lattice structures and properties,which are beneficial for advancing high-performance and cost-effective X-ray detectors.
基金supported by the National Natural Science Foundation of China(52402298,52172224,52302240)Science and Technology Correspondent Project of Tianjin(24YDTPJC00240)+1 种基金the Macao Young Scholars Program(AM2023011)the Yuanguang Scholars Program,Hebei University of Technology(282022554).
文摘Zinc telluride(ZnTe)with high density and low cost is considered as promising anode for sodium-ion batteries.However,ZnTe suffers from continuous capacity degradation owing to the low electronic conductivity,large volume expansion,and high ion-diffusion energy barriers.Herein,the nitrogen-doped carbon confined ZnTe polyhedron heterostructure(ZnTe/NC)is proposed,exploiting its orbital rehybridization and the realignment of energy level to improve storage performance.Systematic ex situ/in situ characterizations and simulations demonstrated that the elaborate ZnTe/NC offers abundant electron/ion transport pathways,accelerates Na^(+)diffusion kinetics,and alleviates huge volume expansion.Notably,the nitrogen-doped carbon-support interaction induced via electron transfer between ZnTe sites and support elevates the energy level of Zn 3d orbital,greatly enhancing ion adsorption capability and reducing the ion diffusion barrier.As a result,the ZnTe/NC anode delivers a high discharge capacity of 470.5 mAh g^(−1)and long cycling durability over 1000 cycles.This work uncovers that optimizing sodium ion adsorption and diffusion via d-orbital energy level modulation enabled by nitrogen-doped support interaction is an effective method for developing high-performance transition metal telluride anodes for alkali ion storage.
基金the financial support from the National Key Research and Development Program of China(2023YFB2504000)。
文摘High-voltage Li-rich Mn-based oxide(LRMO)cathodes are promising for breaking through the energy density limits of lithium-ion batteries,yet their practical application remains limited by electrochemical performance degradation caused by unstable cathode-electrolyte interphase(CEI)evolution during longterm cycling.To address this issue,we propose a novel surface modification strategy using La_(0.7)Sr_(0.3)MnO_(3-σ)(LSMO)nanodots,which exhibit high electronic co nductivity and excellent corrosion resistance.These nanodots act as stable anchoring sites,facilitating the formation of a robust CEI on LRMO,The LSMOmodified cathode demonstrates significantly improved anionic redox reversibility,effectively mitigating transition metal migration and lattice oxygen loss.Furthermore,the optimized interfacial electrochemical kinetics ensure sustained rapid Li+diffusion throughout cycling,while the formation of a stable trilayer CEI structure suppresses electrolyte decomposition.Benefiting from these synergistic effects,the LSMO nanodot-engineered LRMO cathode delivers outstanding cycling stability,retaining 97.4%capacity after 300 cycles at 1 C.This work not only highlights the critical role of nanodot heterostructures in stabilizing CEI but also provides a new approach to designing high-voltage cathodes with superior interfacial compatibility and long-term durability.
基金supported by the National Natural Science Foundation of China (No.52274304)。
文摘Developing catalysts with excellent stability while significantly reducing the overpotential of the oxygen evolution reaction(OER) is crucial for advancing overall water splitting(OWS) systems.In this study,we synthesized the electrode material Ce-NiCo-LDHs@SnO_(2)/NF through a two-step hydrothermal reaction,where Ce-doped NiCo-LDHs are grown on nickel foam modified by a SnO_(2) layer.Ce doping adjusts the internal electronic distribution of Ni Co-LDHs,while the introduction of the SnO_(2) layer enhances electron transfer capability.Together,these factors contribute to the reduction of the OER energy barrier and experimental evidence confirms that the reaction proceeds via the lattice oxygen evolution mechanism(LOM).Consequently,Ce-NiCo-LDHs@SnO_(2)/NF exhibits high level electrochemical performance in OER,requiring only 234 m V overpotential to achieve a current density of 10 m A/cm^(2),with a Tafel slope of just 27.39 m V/dec.When paired with Pt/C/NF,an external potential of only 1.54 V is needed to drive OWS to attain a current density amounting to 10 m A/cm^(2).Furthermore,the catalyst demonstrates stability for 100 h during the OWS stability test.This study underscores the feasibility of enhancing the OER performance through Ce doping and the introduction of a conductive SnO_(2) layer.
基金financial support of the National Natural Science Foundation of China (21875247,21072221, 21172252)the Project of Talent Cultivation for Carbon Peak and Carbon Neutrality of the University of Chinese of Academy of Science
文摘The design and fabrication of ordered epitaxial MOF-on-MOF heterostructures as highly efficient electrocatalysts for water splitting is crucial but still challenging.In this study,a simple coordination-driven self-assembly method is used to fabricate controllable MOF-on-MOF multiscale heterostructures,where triangular host MOF(ZIF-67)nanosheets undergo in situ epitaxial growth to form uniform orthogonal vip MOF(CoFe PBA)nanosheets.Phosphorus(P)is further introduced in situ to fabricate CoP and Fe_(2)P heterostructured nanosheets(CoFe-P-NS),which exhibit excellent bifunctional electrocatalytic performance due to the enhancement of intrinsic electrocatalytic activity by p-d orbital hybridization.Specifically,the CoFe-P-NS requires low overpotential of 259 and 307 mV to reach 500 mA cm−2 for HER and OER,respectively.Remarkably,the assembled electrolysis cell maintained a large current density of 300 mA cm−2 for over 360 h with negligible voltage increase during alkaline seawater electrolysis.Experiments and theoretical calculations show that the synergistic catalytic activity of bimetallic phosphides arises from p-d orbital hybridization,where the CoP-P sites enhance HER by optimizing H*adsorption in the Volmer-Heyrovsky steps,while the Fe_(2)P-Fe sites accelerate OER by lowering the energy barrier of the rate-determining step from O*to OOH*.This study provides valuable insights into the design of a controllable MOF-on-MOF-based electrocatalyst toward alkaline seawater splitting.
基金supported by the National Natural Science Foundation of China(Grant No.22479133,and No.22469008)the Natural Science Foundation of Guangdong Province(Grant No.2024A1515012235).
文摘Zinc-air batteries(ZABs)are promising candidates for flexible electronics due to their high energy density and low cost.However,their development is hindered by the sluggish kinetics of the oxygen evolution reaction(OER)and oxygen reduction reaction(ORR).Herein,we present a novel heterostructured electrocatalyst composed of vertically aligned N-doped graphene(NVG)arrays anchored on Ru-doped ceria(RCO)nanofibers,synthesized via a one-step plasma-enhanced chemical vapor deposition process.Notably,during the plasma-enhanced driven NVG growth,Ru nanoparticles are spontaneously in-situ exsolved from the RCO lattice,forming a unique Ru@RCO-NVG heterostructure.Density functional theory calculations reveal that the Ru@RCO-NVG heterojunction induces interfacial electronic redistribution,thereby significantly lowering the energy barriers for both OER and ORR.Benefiting from the synergistic effects,the Ru@RCO-NVG catalyst exhibits exceptional intrinsic activity towards OER/ORR(an overpotential of 370 mV for OER at 10 mA cm^(−2)and a half-wave potential of 0.86 V for ORR),and higher all-solid-state flexible ZAB performance(peak power density of 286.1 mW cm^(−2)),surpassing commercial Pt/C-IrO_(2)catalysts.This work not only advances the integration of synergistic graphene/ceria composites but also offers a promising strategy for designing efficient electrocatalysts for next-generation energy conversion technologies.
基金supported by the Advanced Talents Incubation Program of Hebei University(No.521100224235)the National Natural Science Foundation of China(No.52503363)the Natural Science Foundation of Hebei Province(No.E2025201009)。
文摘Metal halide perovskites have emerged as highly promising candidates for the emissive layer in next-generation light-emitting diodes(LEDs)due to their narrow emission linewidths,high photoluminescence quantum yields,and tunable emission wavelengths.Achieving high-performance perovskite LEDs(Pe LEDs)requires the emissive layer to possess efficient radiative recombination,low defect density,minimal ion mobility,and effective carrier confinement.Perovskite/perovskite heterostructure(PPHS)offers a compelling approach for engineering emissive layers with these desired attributes,owing to their ability to passivate surface defects,tailor bandgaps,and suppress ion migration.Pe LEDs based on PPHS have demonstrated superior performance compared to single-phase devices,particularly in terms of external quantum efficiency and operational stability.This review provides a comprehensive overview of the typical PPHS architectures applied in Pe LEDs,including vertical,lateral,and bulk configurations.We discuss representative fabrication strategies and the associated optoelectronic properties of these heterostructures,highlighting the mechanisms by which they enhance device efficiency and stability.Finally,we explore the remaining challenges and prospects for the application of PPHS in Pe LEDs and other luminescent technologies.
基金funded by CSIR-TWAS Postdoctoral Fellowship grand number FR 3240316961.
文摘This study aims to synthesise,characterise and evaluate the performance characteristics of packaging films based on biodegradable natural resources incorporated with nanoparticles.Particularly,it is focused on the valorisation of the fibers from the underexploited Lonchocarpus cyanescens plant fromWest Africa as raw renewable lignocellulosebiomassmaterial source for the productionof carboxymethylcellulose(CMC).To this end,biodegradable films were prepared from CMC derived from the fibers of the Lonchocarpus cyanescens plant,and collagen.In order to improve the properties of these films,in particular their mechanical and humidity resistance and their ability to fight microbes,silver nanoparticles(Ag NPs),titanium dioxide nanoparticles(TiO2 NPs),as well as heterostructure Ag@TiO2 nanocomposite were incorporated.The different products obtained were characterised by differentmethods,including DLS,UV-VIS,SEM,contact angle,UTM,absorption and antimicrobial activity tests.The results show that the hybrid biocomposite films exhibit good mechanical properties,improved moisture resistance,and a significant antimicrobial effect against certain pathogenic bacteria.In particular,the synergy between Ag and TiO_(2) nanoparticles in the heterostructure Ag@TiO_(2) nanocomposite optimized the performance characteristics of the packaging films,particularly in terms of mechanical properties with a maximum stress of 38.77 MPa and a strain of 9%,low water absorption reaching 50% at 48 h,improved hydrophobic behaviorwith contact angle of 87°,and antimicrobial resistance compared with the control film without nanoparticles.This work highlights the valorisation of an underexploitedWest African local plant and contributes to the search for sustainable solutions for food packaging.
基金financially supported by the supported by Shandong Provincial Natural Science Foundation(ZR2024MB108)Taishan Young Scholar Program(tsqn202312312)Excellent Young Scholars of the Shandong Provincial Natural Science Foundation(Overseas)(2023HWYQ-112)。
文摘Conversion-type electrode materials hold significant promise for potassium-ion batteries(PIBs)due to their high theoretical capacities,yet their practical deployment is hindered by sluggish kinetics and irreversible structural degradation.To overcome these limitations,we propose a rationally engineered nanoreactor architecture that stabilizes defect-rich MoS_(2)via interlayer incorporation of a carbon monolayer,followed by encapsulation within a nitrogen-doped carbon shell,forming a MoSSe@NC heterostructure.This tailored structure synergistically accelerates both K^(+)diffusion kinetics and electron transfer,enabling unprecedented rate performance(107 mAh g^(-1)at 10 Ag^(-1))and ultralong cyclability(86.5%capacity retention after 1200 cycles at 3 A g^(-1)).Mechanistic insights reveal a distinctive“adsorption-conversion”pathway,where sulfur vacancies on exposed S-Mo-S basal planes act as preferential K^(+)adsorption sites,effectively suppressing parasitic phase transitions during intercalation.In situ X-ray diffraction and transmission electron microscopy corroborate the structural reversibility of the conversion reaction,with the carbon matrix dynamically accommodating strain while preserving electrode integrity.This work not only advances the understanding of defect-driven interfacial chemistry in conversion-type materials but also provides a versatile strategy for designing high-performance anodes in next-generation PIBs through heterostructure engineering.
基金supported by the National Natural Science Foundation of China(no.52574348)the Natural Science Foundation of Hebei Province(nos.E2024501010 and B2024501004)+3 种基金the Shijiazhuang Basic Research Project(no.241790667A)the Fundamental Research Funds for the Central Universities(no.N2423013)the National College Students Innovation and Entrepreneurship Training Program(no.202419145017)the Performance Subsidy Fund for Key Laboratory of Dielectric,Electrolyte Functional Material Hebei Province(no.22567627H)。
文摘MnO_(2) emerges as a promising cathode material for aqueous zinc-ion batteries(AZIBs)due to its high theoretical capacity and ideal working voltage.However,inherent limitations in low electrical conductivity and structural instability restrict its widespread application.Herein,we fabricated layered δ-MnO_(2) and introduced Cu and Ce metal ions for structural regulation,thus constructing a δ/a-MnO_(2) heterostructure within the δ-MnO_(2) matrix,forming a heterointerface that simultaneously enhances the electrical conductivity and structural stability of the material.In this system,Cu^(2+)acts as a catalyst,promoting the reduction of high-valent Mn to Mn^(2+)and enabling local two-electron transfer,which significantly increases the discharge specific capacity of MnO_(2).For Ce^(3+),it functions as a structural regulator,inducing the partial transformation of δ-MnO_(2) to a-MnO_(2) and forming the δ/a-MnO_(2) heterostructure.Further supported by density functional theory(DFT)calculations and in-situ characterization results,the heterointerface between a-MnO_(2) andδ-MnO_(2) generates an internal electric field due to the difference in Fermi levels.This not only effectively enhances the electron transfer capability but also significantly improves structural stability.Benefiting from these advantages,the Cu,Ce co-incorporated MnO_(2)(CCMO)cathode delivers a high discharge capacity of 455.4 mAh g^(-1)at 0.2 A g^(-1)and maintains 191.2 mAh g^(-1)specific capacity after 1500 cycles with 95%capacity retention at 2 A g^(-1),which is significantly better than non-doped MnO_(2).This strategy of structural regulation and heterostructure construction using vip ions offers a new approach for developing high-performance Mn-based cathode materials for AZIBs.
基金supported by National Natural Science Foundation of China(61921002 and 92163204)。
文摘Van der Waals(vdW)heterostructures have attracted much attention due to their distinctive optical,electrical,and thermal properties,demonstrating promising potential in areas such as photocatalysis,ultrafast photonics,and free electron radiation devices.Particularly,they are promising platforms for studying thermionic emission.It is illustrated that using vdW heterostructure-based thermionic emission can enhance heat transfer in vacuum devices.As a proof of concept,the approach is demonstrated to offer a promising solution for the long-standing overheating issue in X-ray tubes.Specifically,it is shown that the saturated target temperature of a 2000 W X-ray tube can be reduced from around 1200℃ to 490℃.Additionally,it is also demonstrated that by reducing the height of the Schottky barrier formed in the vdW heterostructures,the thermionic cooling performance can be enhanced.The findings pave the way for the development of high-power X-ray tubes.
基金National Key Research and Development Program of China(No.2023YFB4605800)The National Natural Science Foundation of China(Nos.52475362,52365046,and 52465041)+3 种基金Jiangxi Provincial Natural Science Foundation of China(No.20224ACB204013)Jiangxi Provincial Key Laboratory of Additive Manufacturing of Implantable Medical Device(No.2024SSY11161)Jiangxi Provincial Department of Education Science and Technology Project(No.GJJ2400708)Jiangxi Province Science and Technology Program(Nos.20252BAC200317 and 20252BEJ730195)。
文摘Recurrence of solid tumors after surgical resection is a major barrier to tissue regeneration.As an emerging treatment strategy,photo-thermo-electric therapy ablates tumor cells via photothermal effects and generates reactive oxygen species(ROS)via thermoelectric effects to disrupt heat shock proteins,thereby suppressing their protective function in tumor cells.However,conventional materials suffer from low thermoelectric efficiency and weak tissue penetration ability.In this study,we fabricated iodine-doped bismuth sulfide(I-Bi_(2)S_(3))nanorods with bonding heterostructures to improve thermoelectric performance.The approach employed iodine doping to introduce additional electrons,thereby regulating the band structure of Bi_(2)S_(3)and exploiting the dual low-energy vibration effect of the heterostructures to reduce thermal conductivity.More importantly,controlling the type of heterostructure modulated the bandgap width,thereby expanding the light absorption range to the higher-penetration near-infrared(NIR)-Ⅱregion for deep tissue treatment.The I-Bi_(2)S_(3)nanorods were incorporated into poly-L-lactic acid(PLLA)scaffolds to confer antitumor functionality.According to the results,the bonding heterostructures enhanced the conductivity of Bi_(2)S_(3)and reduced its thermal conductivity,significantly enhancing thermoelectric efficacy.The heterostructures reduced the bandgap of Bi_(2)S_(3)from 1.23 to 0.88 eV,enabling optical absorption in the NIR-Ⅱregion.The ROS tests showed that the PLLA/I-Bi_(2)S_(3)scaffold exhibited good photothermal effects and ROS generation under 1064-nm laser irradiation.The antitumor efficacy of the PLLA/I-Bi_(2)S_(3)scaffold reached 84.6%against MG-63 cells,demonstrating its exceptional potential in cancer treatment.
基金supported by the National Natural Science Foundation of China(NSFC,No.22172121)the Fundamental Research Funds for the Central Universities(No.ZYN2025267)Southwest Minzu University。
文摘The electrocatalytic oxidation of ethylene glycol(EG)into high-value chemicals like glycolic acid(GA)is a crucial step for upcycling waste plastics.However,catalyst deactivation and low selectivity pose significant challenges.This work presents the low-coordination PtBi nanosheets(LC-PtBi NSs),featuring a unique amorphous-crystalline heterostructure with a low coordination number of 2.3-2.5.They can exhibit exceptional mass activity(8.3 A mg_(Pt)^(-1))and stability(maintaining 88.7%of initial activity after running for 3600 s)of the EG oxidation reaction(EGOR).They also achieve over 90%apparent selectivity for EG-to-GA conversion at low potentials(<0.7 V vs.RHE)and even more than 100-h continuous electrolysis.Density fu nctional theory(DFT)calculations reveal that the low-coordination PtBi heterogeneous interface is responsible for the high coverage of OH_(ad) species and weakened adsorption of carbonaceous intermediates on LC-PtBi NSs,thereby promoting the direct oxidation of C_(2) intermediates to GA.This work demonstrates a strategy of doping-mediated catalytic interface regulation and electron density rearrangement,offering insights for designing efficient Pt-based electrocatalysts toward selective oxidation of small molecules.
