Lithium sulfur(Li-S)batteries are the promising power sources,but their commercialization is significantly impeded by poor energy-storage functions at high sulfur loading.Here we report that such an issue can be effec...Lithium sulfur(Li-S)batteries are the promising power sources,but their commercialization is significantly impeded by poor energy-storage functions at high sulfur loading.Here we report that such an issue can be effectively addressed by using a mussel-inspired binder comprised of chitosan grafted with catecholic moiety for sulfur cathodes.The resulting sulfur cathodes possess a high loading up to 12.2 mg cm-2 but also exhibit one of the best electrochemical properties among their counterparts.The excellent performances are attributed to the strong adhesion of the binder to sulfur particles,conducting agent,current collector,and polysulfide.The versatile adhesion effectively increases the sulfur loading,depresses the shuttle effect,and alleviates mechanical pulverization during cycling processes.The present investigation offers a new insight into high performance sulfur cathodes through a bio-adhesion viewpoint.展开更多
Three-dimensionally（3D） ordered mesoporous carbon sphere arrays（OMCS） are explored to support high loading（60 wt%） Pt nanoparticles as electrocatalysts for the methanol oxidation reaction（MOR）.The OMCS has a u...Three-dimensionally（3D） ordered mesoporous carbon sphere arrays（OMCS） are explored to support high loading（60 wt%） Pt nanoparticles as electrocatalysts for the methanol oxidation reaction（MOR）.The OMCS has a unique hierarchical nanostructure with ordered large mesopores and macropores that can facilitate high dispersion of the Pt nanoparticles and fast mass transport during the reactions. The prepared Pt/OMCS exhibits uniformly dispersed Pt nanoparticles with an average size of- 2.0 nm on the mesoporous walls of the carbon spheres. The Pt/OMCS catalyst shows significantly enhanced specific electrochemically active surface area（ECSA）（73.5 m^2g^-1） and electrocatalytic activity（0.69 mA cm^-2）for the MOR compared with the commercial 60 wt% Pt/C catalyst.展开更多
Mesoporous LiFePO4/C composites containing 80 wt% of highly dispersed LiFePO4 nanoparticles(4-6 nm) were fabricated using bimodal mesoporous carbon(BMC) as continuous conductive networks. The unique pore structure of ...Mesoporous LiFePO4/C composites containing 80 wt% of highly dispersed LiFePO4 nanoparticles(4-6 nm) were fabricated using bimodal mesoporous carbon(BMC) as continuous conductive networks. The unique pore structure of BMC not only promises good particle connectivity for LiFePO4, but also acts as a rigid nano-confinement support that controls the particle size. Furthermore, the capacities were investigated respectively based on the weight of LiFePO4 and the whole composite. When calculated based on the weight of the whole composite, it is 120 mAh·g-1at 0.1 C of the high loading electrode and 42 mAh·g-1at 10 C of the low loading electrode. The electrochemical performance shows that high LiFePO4 loading benefits large tap density and contributes to the energy storage at low rates, while the electrode with low content of LiFePO4 displays superior high rate performance, which can mainly be due to the small particle size, good dispersion and high utilization of the active material, thus leading to a fast ion and electron diffusion.展开更多
The pursuit of high energy density has promoted the development of high-performance lithium metal batteries(LMBs).However,the underestimated but non-negligible dendrites of Li anode have been observed to shorten batte...The pursuit of high energy density has promoted the development of high-performance lithium metal batteries(LMBs).However,the underestimated but non-negligible dendrites of Li anode have been observed to shorten battery lifespan.Herein,a composite separator(TiO_(2-x)@PP),in which TiO_(2)with electron-localized oxygen vacancies(TiO_(2-x))is coated on a commercial PP separator,is fabricated to homogenize lithium ion transport and stabilize the lithium anode interface.With the utilization of TiO_(2-x)@PP separators,the symmetric lithium metal battery displays enhanced cycle stability over 800 h under a high current density of 8 m A cm^(-2).Moreover,the LMBs assembled with high-loading LiFePO_(4)(9.24 mg cm^(-2))deliver a stable cycling performance over 900 cycles at a rate of 0.5 C.Comprehensive theoretical studies based on density functional theory(DFT)further unveil the mechanism.The favorable TiO_(2-x)is beneficial for facilitating fast Li+migration and impeding anions transfer.In addressing the Li dendrite issues,the use of TiO_(2-x)@PP separator potentially provides a facile and attractive strategy for designing well-performing LMBs,which are expected to meet the application requirements of rechargeable batteries.展开更多
High loading cathode with high active material proportion is a practical demand but far below the desirable value to achieve high energy density lithium-ion batteries(LIBs).Normally,the Li^(+)/electron transport betwe...High loading cathode with high active material proportion is a practical demand but far below the desirable value to achieve high energy density lithium-ion batteries(LIBs).Normally,the Li^(+)/electron transport between active materials and electrolyte/c arbon,however,it is poor and areal resistance is extremely high for a high loading/thick cathode.In this manuscript,taking high-voltage lithium cobalt oxide LiCoO_(2)(LCO)as an example,we design a facile liquid metal welding method enabled by a low melting-point indium-tin oxide In_(2)O_(3)/SnO_(2)(ITO)during a thermal treatment process,the strongly adhesion active particles show robust mechanical property for the free-standing LCO cathode with a pellet architecture.We also demonstrate that the O_(2)atmosphere plays a critical role on the interfacial property,that is preventing the layered structure to rock-salt Co_(3)O_(4)as well as further enhancing the interfacial mechanical integration.As expected,the LCO-ITO free-standing cathode not only shows robust mechanical property with densely packed configuration but also provides a fast Li^(+)/electron pathway at the interface.Consequently,the LCO-ITO composite cathode exhibits excellent electrochemical cycling performance in both liquid and solid-state cells.For example,even at a high active material mass of 56 mg·cm^(-2),the LCO cathode still delivers a specific capacity of 151 mAh·g^(-1)and maintains132.5 mAh·g^(-1)(corresponding to 7.4 mAh·cm^(-2))after 80cycles.The LCO-ITO-O_(2)cathode is also applicable to a solidstate cell,which exhibits a high capacity of 100.4 mAh·g^(-1)after 200 cycles of long-term cycling.The excellent electrochemical of the LCO-ITO-O_(2)reveals the successful engineering mechanical architecture and interfacial carriers transport,which may be expected as an alternative approach to achieve high energy density LIBs.展开更多
On the base of controllable variable stiffness property,variable stiffness composites were the main components of functional materials in aerospace.However,the relatively low mechanical strength,stiffness range,and re...On the base of controllable variable stiffness property,variable stiffness composites were the main components of functional materials in aerospace.However,the relatively low mechanical strength,stiffness range,and response rate restricted the application of variable stiffness composite.In this work,the novel variable stiffness composite system with characteristics of repeatable high load bearing and response rate was successfully prepared via the double-layer anisotropic structure to solve the bottlenecks of variable stiffness composites.The novel variable stiffness composite systems were composed of variable stiffness layer of polycaprolactone(PCL)and the driven layer of silicone elastomer with alcohol,which continuously changed Young’s modulus from 0.1 to 7.263 MPa(72.63 times variation)in 200 s and maintained maximum weight of 11.52 times its own weight(8.5 g).Attributed to the relatively high variable stiffness range and load bearing value of variable stiffness composite system,the repeatable response process led to the efficient high load driven as“muscle”and diversified precise grab of objects with different shapes as“gripper”,owning widespread application prospects in the field of bionics.展开更多
Lithium-sulfur(Li-S) batteries are one of the most promising rechargeable storage devices due to the high theoretical energy density.However,the low areal sulfur loading impedes their commercial development.Herein,a 3...Lithium-sulfur(Li-S) batteries are one of the most promising rechargeable storage devices due to the high theoretical energy density.However,the low areal sulfur loading impedes their commercial development.Herein,a 3 D free-standing sulfur cathode scaffold is rationally designed and fabricated by coaxially coating polar Ti_3 C_2 T_x flakes on sulfur-impregnated carbon cloth(Ti_3 C_2 T_x@S/CC) to achieve high loading and high energy density Li-S batteries,in which,the flexible CC substrate with highly porous structure can accommodate large amounts of sulfur and ensure fast electron transfer,while the outer-coated Ti_3 C_2 T_x can serve as a polar and conductive protective layer to further promote the conductivity of the whole electrode,achieve physical blocking and chemical anchoring of lithium-polysulfides as well as catalyze their conversion.Due to these advantages,at a sulfur loading of 4 mg cm^(-2),Li-S cells with Ti_3 C_2 T_x@S/CC cathodes can deliver outstanding cycling stability(746.1 mAh g^(-1) after 200 cycles at1 C),superb rate performance(866.8 mAh g^(-1) up to 2 C) and a high specific energy density(564.2 Wh kg^(-1) after 100 cycles at 0.5 C).More significantly,they also show the commercial potential that can compete with current lithium-ion batteries due to the high areal capacity of 6.7 mAh cm^(-2) at the increased loading of 8 mg cm^(-2).展开更多
The research on metal dimer clusters is of great importance,owing to the potential in modulating the adsorption behavior towards reaction intermediates.Here,we develop a loading heightening strategy to obtain a 32.5wt...The research on metal dimer clusters is of great importance,owing to the potential in modulating the adsorption behavior towards reaction intermediates.Here,we develop a loading heightening strategy to obtain a 32.5wt%Fe-dimer catalyst(Fe-32.5).The co-anchoring of two Fe atoms in a single triazine ring of carbon nitride with an atomic spacing of∼0.23nm is proved.Fe atoms occupy the pores of the triazine ring in the lower iron content sample(Fe-12.9 and Fe-17.1).However,with the increase of iron content to 32.5wt%,two Fe atoms simultaneously occupy one triazine ring.For Fe-32.5,besides the main peak located at∼1.5Åcorresponding to the Fe–N interaction,a peak attributed to Fe–Fe bonding is observed at∼2.2Åin Fourier-transformed k3-weithted extended X-ray absorption fine structure.Density functional theoretical calculations reveal that Fe-dimer in Fe-32.5 induces a charge redistribution compared with that in Fe-12.9 and Fe-17.1.H_(2)O^(∗)is adsorbed on O^(∗)via hydrogen bonding in Fe-12.9 and Fe-17.1.However,H_(2)O^(∗)and O^(∗)in Fe-32.5 are adsorbed on Fe–Fe dimer,resulting in a decrease in the total energy of the reaction process.For the two former,O_(2)^(-)∗adsorbs on individual Fe atoms.Fe-dimer in Fe-32.5 adsorbs O_(2)^(-)∗in the form of bridge bonds,which facilitates the·O_(2)^(-)release.Furthermore,an enhanced affinity for the substrate 3,3′,5,5′-tetramethylbenzidine and higher peroxidase-like activity were displayed.This work provides an effective mean to synthesize metal dimer clusters through high loading.展开更多
To address the inherent trade-off between mechanical strength and repair efficiency in conventional microcapsule-based self-healing technologies,this study presents an eggshell-inspired approach for fabricating high-l...To address the inherent trade-off between mechanical strength and repair efficiency in conventional microcapsule-based self-healing technologies,this study presents an eggshell-inspired approach for fabricating high-load rigid porous microcapsules(HLRPMs)through subcritical water etching.By optimizing the subcritical water treatment parameters(OH−concentration:0.031 mol/L,tem-perature:240°C,duration:1.5 h),nanoscale through-holes were generated on hollow glass microspheres(shell thickness≈700 nm).The subsequent gradient pressure infiltration of flaxseed oil enabled a record-high core content of 88.2%.Systematic investigations demonstrated that incorporating 3 wt%HLRPMs into epoxy resin composites preserved excellent dielectric properties(breakdown strength≥30 kV/mm)and enhanced tensile strength by 7.52%.In addressing multimodal damage,the system achieved a 95.5%filling efficiency for mechanical scratches,a 97.0%reduction in frictional damage depth,and a 96.2%recovery of insulation following electrical treeing.This biomimetic microcapsule system concurrently improved self-healing capability and matrix performance,offering a promising strategy for the development of next-generation smart insulating materials.展开更多
Rechargeable aqueous aluminum ion batteries(AIBs)are inspiring researchers’enthusiasm due to the low cost and high theoretical capacity of aluminum.Polyaniline(PANI)materials have the potential for aluminum ion stora...Rechargeable aqueous aluminum ion batteries(AIBs)are inspiring researchers’enthusiasm due to the low cost and high theoretical capacity of aluminum.Polyaniline(PANI)materials have the potential for aluminum ion storage due to the properties of its excellent conductivity and inherent theoretical capacity.However,the poor cycling stability and low loadings of PANI limit its application in energy storage.In this study,PANI-x electrodes with high mass loadings are successfully prepared by the electrodeposition method for reversible AlCl_(2)^(+)storage.Among them,the PANI-2 electrode possesses the highest areal capacity(0.59 and 0.51 mAh cm^(−2)at the current density of 0.5 and 10 mA cm^(−2))and excellent cycling stability in saturated AlCl3.Ex situ N 1s fitting spectra of PANI-2 and molecular dynamics simulations of 1 M,3 M,and saturated AlCl_(3)electrolytes demonstrate that PANI can achieve reversible redox reactions in saturated AlCl3,thereby achieving its excellent stability.Density functional theory calculations and ex situ spectra characterizations of PANI-2 demonstrate the insertion/de-insertion mechanism in the form of AlCl_(2)^(+)ions.In conclusion,PANI-2|Saturated AlCl_(3)|EG(exfoliated graphite foil)full cell is assembled successfully.This work provides promising guidance for the preparation of high-loading electrodes for AIBs.展开更多
The current single-atom catalysts(SACs)for medicine still suffer from the limited active site density.Here,we develop a synthetic method capable of increasing both the metal loading and mass-specific activity of SACs ...The current single-atom catalysts(SACs)for medicine still suffer from the limited active site density.Here,we develop a synthetic method capable of increasing both the metal loading and mass-specific activity of SACs by exchanging zinc with iron.The constructed iron SACs(h^(3)-FNC)with a high metal loading of 6.27 wt%and an optimized adjacent Fe distance of~4 A exhibit excellent oxidase-like catalytic performance without significant activity decay after being stored for six months and promising antibacterial effects.Attractively,a“density effect”has been found at a high-enough metal doping amount,at which individual active sites become close enough to interact with each other and alter the electronic structure,resulting in significantly boosted intrinsic activity of single-atomic iron sites in h^(3)-FNCs by 2.3 times compared to low-and medium-loading SACs.Consequently,the overall catalytic activity of h^(3)-FNC is highly improved,with mass activity and metal mass-specific activity that are,respectively,66 and 315 times higher than those of commercial Pt/C.In addition,h^(3)-FNCs demonstrate efficiently enhanced capability in catalyzing oxygen reduction into superoxide anion(O_(2)·^(−))and glutathione(GSH)depletion.Both in vitro and in vivo assays demonstrate the superior antibacterial efficacy of h^(3)-FNCs in promoting wound healing.This work presents an intriguing activity-enhancement effect in catalysts and exhibits impressive therapeutic efficacy in combating bacterial infections.展开更多
Tensile cracking is a predominant mode of failure in rocks within underground resource excavation and engineering structures,where rocks are frequently subjected to dynamic disturbances while simultaneously experienci...Tensile cracking is a predominant mode of failure in rocks within underground resource excavation and engineering structures,where rocks are frequently subjected to dynamic disturbances while simultaneously experiencing in-situ stresses.This paper proposes a new dynamic split tension setup utilising a cubic specimen to investigate the dynamic behaviour of rocks across various tensile strain rates and confining pressures.The objective is to extend the applicability of the triaxial Hopkinson bar in studying dynamic behaviour of geomaterials.For comparison,the dynamic Brazilian disc(BD)tests were performed using three rock types(e.g.,sandstone,granite and marble)under different strain rates ranging from 10^(−3)∼10^(2) s^(−1).Besides,the Digital Image Correlation(DIC)technique was adopted to measure full-field real-time tensile strain of rocks and demonstrated that tensile crack initiated at the middle part and split the specimen into two similar halves.Effects of specimen size,geometry,loading rate as well as the confining pressure are investigated in detail.The dynamic fracture behaviours,including dynamic tensile strength,tensile strain,time to fracture and dynamic increase factor(DIF),were characterised for the rocks.It is found that dynamic tensile strength of rock minimal dependence on size and geometry but is significantly influenced by loading rate and confinement.It exhibited a linear increase with strain rate(10^(0)∼10^(2) s^(−1))and demonstrated a nonlinear growth with lateral confinement from 0 to 15 MPa.The nonlinear dependency on confinement can be attributed to the restriction imposed on the opening and propagation of tensile cracks due to the presence of confinement.These findings enhance our understanding of the safety aspects associated with underground rock excavations,particularly in situations where considering in-situ stress is crucial for evaluating the dynamic tensile failure of rocks.展开更多
This article is aimed to experimentally validate the beneficial effects of boundary layer suction on improving the aerodynamic performance of a compressor cascade with a large camber angle. The flow field of the casca...This article is aimed to experimentally validate the beneficial effects of boundary layer suction on improving the aerodynamic performance of a compressor cascade with a large camber angle. The flow field of the cascade is measured and the ink-trace flow visualization is also presented. The experimental results show that the boundary layer suction reduces losses near the area of rnidspan in the cascade most effectively for all suction cases under test. Losses of the endwall could remarkably decrease only when the suction is at the position where the boundary layer has separated but still not departed far away from the blade surface. It is evidenced that the higher suction flow rate and the suction position closer to the trailing edge result in greater reduction in losses and the maximum reduction in the total pressure loss accounts to 16.5% for all cases. The suction position plays a greater role in affecting the total pressure loss than the suction flow rate does.展开更多
Controlled integration of ultrafine metal nanoparticles （MNPs） and metal- organic frameworks （MOFs） has drawn much attention due to their unique physical and chemical properties. However, the development of a one-...Controlled integration of ultrafine metal nanoparticles （MNPs） and metal- organic frameworks （MOFs） has drawn much attention due to their unique physical and chemical properties. However, the development of a one-step strategy for preparing ultrafine MNPs within MOFs still remains a great challenge. Herein, a facile synthetic approach toward the abovementioned composites was developed. In contrast to the conventional approach, these hybrids were prepared by the direct mixing of metal and MOF precursors in the reaction solution assisted by microwave irradiation. Impressively, the Au/MOF-199 composite with uniformly distributed ultrafine Au nanoparticles could be fabricated in only two minutes, and the Au loading could be increased up to a level of 5.13%. The multifunctional Au/MOF-199 catalysts exhibited high turnover numbers （TONs） and turnover frequencies （TOFs） in the three-component coupling reaction of formaldehyde, phenylacetylene, and piperidine （AB-coupling）. Owing to the confinement effect of MOF-199, the 5.13%Au/MOF-199 catalyst could be recycled for five runs without serious loss of activity, with no obvious aggregation of Au NPs detected.展开更多
This article experimentally studies the effects of air injection near the blade trailing edge on flow separation and losses in a highly loaded linear compressor cascade. Aerodynamic parameters of eight cascades with d...This article experimentally studies the effects of air injection near the blade trailing edge on flow separation and losses in a highly loaded linear compressor cascade. Aerodynamic parameters of eight cascades with different air injection slot configura- tions are measured by using a five-hole probe at the cascade outlets. Ink-trace flow visualization is performed to obtain the flow details around the air injection slots. The static pressure distribution is clarified with pressure taps on the endwalls. The...展开更多
Realizing a lithium sulfide(Li_(2)S)cathode with both high energy density and a long lifespan requires an innovative cathode design that maximizes electrochemical performance and resists electrode deterioration.Herein...Realizing a lithium sulfide(Li_(2)S)cathode with both high energy density and a long lifespan requires an innovative cathode design that maximizes electrochemical performance and resists electrode deterioration.Herein,a high-loading Li_(2)S-based cathode with micrometric Li_(2)S particles composed of two-dimensional graphene(Gr)and one-dimensional carbon nanotubes(CNTs)in a compact geometry is developed,and the role of CNTs in stable cycling of high-capacity Li–S batteries is emphasized.In a dimensionally combined carbon matrix,CNTs embedded within the Gr sheets create robust and sustainable electron diffusion pathways while suppressing the passivation of the active carbon surface.As a unique point,during the first charging process,the proposed cathode is fully activated through the direct conversion of Li_(2)S into S_(8) without inducing lithium polysulfide formation.The direct conversion of Li_(2)S into S_(8) in the composite cathode is ubiquitously investigated using the combined study of in situ Raman spectroscopy,in situ optical microscopy,and cryogenic transmission electron microscopy.The composite cathode demonstrates unprecedented electrochemical properties even with a high Li_(2)S loading of 10 mg cm^(–2);in particular,the practical and safe Li–S full cell coupled with a graphite anode shows ultra-long-term cycling stability over 800 cycles.展开更多
A high sulfur content sulfur–carbon composite was synthesized via in situ generation method in aqueous solution.When the sulfur loading is up to 90%,the electrode still exhibits good cycling performance with a revers...A high sulfur content sulfur–carbon composite was synthesized via in situ generation method in aqueous solution.When the sulfur loading is up to 90%,the electrode still exhibits good cycling performance with a reversible capacity of about 623 mAh·g^(-1)after 100 cycles.To further commercialize the Li–S battery,understanding the capacity degradation mechanism is very essential,especially with a high sulfur loading electrode.To achieve this goal,the electrochemical performance of the high sulfur loading electrode was studied,and the structure change of the electrode after cycling was also examined by ex situ scanning electron microscopy(SEM)and other techniques.The result shows that the Li_(2)S_(2)and Li_(2)S inhomogeneous precipitation contributes to the majority capacity fading of the high sulfur loading Li–S cells.展开更多
Electrochemical carbon dioxide reduction reaction(CO_(2)RR)provides an attractive approach to carbon capture and utilization for the production high-value-added products.However,CO_(2)RR still suffers from poor select...Electrochemical carbon dioxide reduction reaction(CO_(2)RR)provides an attractive approach to carbon capture and utilization for the production high-value-added products.However,CO_(2)RR still suffers from poor selectivity and low current density due to its sluggish kinetics and multitudinous reaction pathways.Single-atom catalysts(SACs)demonstrate outstanding activity,excellent selectivity,and remarkable atom utilization efficiency,which give impetus to the search for electrocatalytic processes aiming at high selectivity.There appears significant activity in the development of efficient SACs for CO_(2)RR,while the density of the atomic sites remains a considerable barrier to be overcome.To construct high-metal-loading SACs,aggregation must be prevented,and thus novel strategies are required.The key to creating high-density atomically dispersed sites is designing enough anchoring sites,normally defects,to stabilize the highly mobile separated metal atoms.In this review,we summarized the advances in developing high-loading SACs through defect engineering,with a focus on the synthesis strategies to achieve high atomic site loading.Finally,the future opportunities and challenges for CO_(2)RR in the area of high-loading single-atom electrocatalysts are also discussed.展开更多
July 25, 2014 / Accepted： August 18, 2014 / Published： November 25, 2014 Abstract： This paper presents the measurement results of a l1/2 stage LPT （low pressure turbine） test rig at Graz University of Technology ...July 25, 2014 / Accepted： August 18, 2014 / Published： November 25, 2014 Abstract： This paper presents the measurement results of a l1/2 stage LPT （low pressure turbine） test rig at Graz University of Technology incorporating two different rotor geometries： one with a regular blade loading and the other with a highly loaded blade geometry. The test rig was designed in cooperation with MTU Aero Engines and represented the last 1.5 stages of a commercial aero engine. Considerable efforts were put on the adjustment of all relevant model parameters （Mach number, blade count ratio, airfoil aspect ratio, blade loading, etc.） to reproduce the full scale LPT situation. The rig diameter is approximately half of that of a commercial aero engine LPT. The number of blades and vanes for the two investigated stages as well as the pressure ratio and power output are identical, resulting in a decrease in rotational speed of the HSL （high stage loading） rotor. Measurement data from a FRAPP （fast response pressure probe） is used to compare the flow fields of the two different stages. The effect of the different stage designs can be seen when comparing the exit flow fields. The highly loaded stage shows a more pronounced tip leakage vortex compared to the datum stage. The highly loaded stage shows wider wakes with a lower total pressure deficit. The fluctuations of total pressure within the flow field are directly related to the upstream wake. If the measurement position is located within a stator wake, the fluctuations are significantly smaller than that out of the wake.展开更多
Organic materials for aqueous zinc ion batteries have been attracted the attention of researchers because of their high safety,environmental friendliness,and structural designability.However,the limited specific capac...Organic materials for aqueous zinc ion batteries have been attracted the attention of researchers because of their high safety,environmental friendliness,and structural designability.However,the limited specific capacity,unsatisfactory cycling durability,and unclear charge storage mechanism limit their development and applications.Herein,NTCDA-2,3-DNQ,an organic compound with a benzimidazole ring structure,was designed through the number and distribution of active sites as well as the adjustment of molecular weight,and applied as the cathode for aqueous zinc-ion batteries.NTNQ exhibits high specific capacity of 290.5 mAh·g^(-1) at 0.05 A·g^(-1),excellent rate performance of 133.3 mAh·g^(-1) at 15 A·g^(-1),and relatively stable cycle life with 81.7%capacity retention over 10,000 superlong cycles at 10 A·g^(-1).Furthermore,the synergistic effect of neighboring active sites and multi-electron Zn^(2+)storage reactions are further explored by density functional theory(DFT)calculations,and the results show that NTNQ could stores 4Zn^(2+)while transferring 8e–in the N-Zn-O pathway during the storage of Zn^(2+).Interestingly,NTNQ still exhibits high specific capacity and favorable cycling stability at multiple ultra-high loadings.This work provides important chances including the design concepts of the organic molecules and the investigation of the Zn^(2+)storage mechanism for high performance aqueous zinc ion batteries.展开更多
基金supported by the National Natural Science Foundation of China(51473041)the Foundation for Innovative Research Groups of the National Natural Science Foundation of China(51521003)+2 种基金China Postdoctoral Science Foundation(no.2017M621262)Fundamental Research Funds for the Central Universities(No.HIT.NSRIF.201831)Postdoctoral Foundation of Hei long Jiang Province(LBH-Z17065)。
文摘Lithium sulfur(Li-S)batteries are the promising power sources,but their commercialization is significantly impeded by poor energy-storage functions at high sulfur loading.Here we report that such an issue can be effectively addressed by using a mussel-inspired binder comprised of chitosan grafted with catecholic moiety for sulfur cathodes.The resulting sulfur cathodes possess a high loading up to 12.2 mg cm-2 but also exhibit one of the best electrochemical properties among their counterparts.The excellent performances are attributed to the strong adhesion of the binder to sulfur particles,conducting agent,current collector,and polysulfide.The versatile adhesion effectively increases the sulfur loading,depresses the shuttle effect,and alleviates mechanical pulverization during cycling processes.The present investigation offers a new insight into high performance sulfur cathodes through a bio-adhesion viewpoint.
基金financial support from the National Natural Science Foundation of China (No. 51172014)the National 973 Program of China (No. 2009CB219903)the Scientific Innovation Grant for Excellent Young Scientists of Hebei University of Technology (No. 2015001)
文摘Three-dimensionally（3D） ordered mesoporous carbon sphere arrays（OMCS） are explored to support high loading（60 wt%） Pt nanoparticles as electrocatalysts for the methanol oxidation reaction（MOR）.The OMCS has a unique hierarchical nanostructure with ordered large mesopores and macropores that can facilitate high dispersion of the Pt nanoparticles and fast mass transport during the reactions. The prepared Pt/OMCS exhibits uniformly dispersed Pt nanoparticles with an average size of- 2.0 nm on the mesoporous walls of the carbon spheres. The Pt/OMCS catalyst shows significantly enhanced specific electrochemically active surface area（ECSA）（73.5 m^2g^-1） and electrocatalytic activity（0.69 mA cm^-2）for the MOR compared with the commercial 60 wt% Pt/C catalyst.
基金supported by the National Natural Science Foundation of China (NSFC 21103184)the Ph.D.Programs Foundation (20100041110017) of Ministry of Education of Chinathe Fundamental Research Funds for the Central Universities
文摘Mesoporous LiFePO4/C composites containing 80 wt% of highly dispersed LiFePO4 nanoparticles(4-6 nm) were fabricated using bimodal mesoporous carbon(BMC) as continuous conductive networks. The unique pore structure of BMC not only promises good particle connectivity for LiFePO4, but also acts as a rigid nano-confinement support that controls the particle size. Furthermore, the capacities were investigated respectively based on the weight of LiFePO4 and the whole composite. When calculated based on the weight of the whole composite, it is 120 mAh·g-1at 0.1 C of the high loading electrode and 42 mAh·g-1at 10 C of the low loading electrode. The electrochemical performance shows that high LiFePO4 loading benefits large tap density and contributes to the energy storage at low rates, while the electrode with low content of LiFePO4 displays superior high rate performance, which can mainly be due to the small particle size, good dispersion and high utilization of the active material, thus leading to a fast ion and electron diffusion.
基金financial support provided by the National Natural Science Foundation of China(52064049)the Key National Natural Science Foundation of Yunnan Province(2018FA028 and 2019FY003023)+1 种基金the International Joint Research Center for Advanced Energy Materials of Yunnan Province(202003AE140001)the Key Laboratory of Solid State Ions for Green Energy of Yunnan University(2019),the Analysis and Measurements Center of Yunnan University for the sample testing service,and the Postgraduate Research and Innovation Foundation of Yunnan University(2021Y348)。
文摘The pursuit of high energy density has promoted the development of high-performance lithium metal batteries(LMBs).However,the underestimated but non-negligible dendrites of Li anode have been observed to shorten battery lifespan.Herein,a composite separator(TiO_(2-x)@PP),in which TiO_(2)with electron-localized oxygen vacancies(TiO_(2-x))is coated on a commercial PP separator,is fabricated to homogenize lithium ion transport and stabilize the lithium anode interface.With the utilization of TiO_(2-x)@PP separators,the symmetric lithium metal battery displays enhanced cycle stability over 800 h under a high current density of 8 m A cm^(-2).Moreover,the LMBs assembled with high-loading LiFePO_(4)(9.24 mg cm^(-2))deliver a stable cycling performance over 900 cycles at a rate of 0.5 C.Comprehensive theoretical studies based on density functional theory(DFT)further unveil the mechanism.The favorable TiO_(2-x)is beneficial for facilitating fast Li+migration and impeding anions transfer.In addressing the Li dendrite issues,the use of TiO_(2-x)@PP separator potentially provides a facile and attractive strategy for designing well-performing LMBs,which are expected to meet the application requirements of rechargeable batteries.
基金financially supported by the National Natural Science Foundation of China(Nos.22209075,51902165)the Natural Science Foundation of Jiangsu Province(No.BK20200800)。
文摘High loading cathode with high active material proportion is a practical demand but far below the desirable value to achieve high energy density lithium-ion batteries(LIBs).Normally,the Li^(+)/electron transport between active materials and electrolyte/c arbon,however,it is poor and areal resistance is extremely high for a high loading/thick cathode.In this manuscript,taking high-voltage lithium cobalt oxide LiCoO_(2)(LCO)as an example,we design a facile liquid metal welding method enabled by a low melting-point indium-tin oxide In_(2)O_(3)/SnO_(2)(ITO)during a thermal treatment process,the strongly adhesion active particles show robust mechanical property for the free-standing LCO cathode with a pellet architecture.We also demonstrate that the O_(2)atmosphere plays a critical role on the interfacial property,that is preventing the layered structure to rock-salt Co_(3)O_(4)as well as further enhancing the interfacial mechanical integration.As expected,the LCO-ITO free-standing cathode not only shows robust mechanical property with densely packed configuration but also provides a fast Li^(+)/electron pathway at the interface.Consequently,the LCO-ITO composite cathode exhibits excellent electrochemical cycling performance in both liquid and solid-state cells.For example,even at a high active material mass of 56 mg·cm^(-2),the LCO cathode still delivers a specific capacity of 151 mAh·g^(-1)and maintains132.5 mAh·g^(-1)(corresponding to 7.4 mAh·cm^(-2))after 80cycles.The LCO-ITO-O_(2)cathode is also applicable to a solidstate cell,which exhibits a high capacity of 100.4 mAh·g^(-1)after 200 cycles of long-term cycling.The excellent electrochemical of the LCO-ITO-O_(2)reveals the successful engineering mechanical architecture and interfacial carriers transport,which may be expected as an alternative approach to achieve high energy density LIBs.
基金the project of the National Key Research and Development Program of China(2018YFA0703300)the National Natural Science Foundation of China(52105302,52175271,52021003,and 91848204)+1 种基金the team of Innovation and entrepreneurship of Jilin Province(20210509047RQ,20210508057RQ)the Program for JLU Science and Technology Innovative Research Team(2017TD-04).
文摘On the base of controllable variable stiffness property,variable stiffness composites were the main components of functional materials in aerospace.However,the relatively low mechanical strength,stiffness range,and response rate restricted the application of variable stiffness composite.In this work,the novel variable stiffness composite system with characteristics of repeatable high load bearing and response rate was successfully prepared via the double-layer anisotropic structure to solve the bottlenecks of variable stiffness composites.The novel variable stiffness composite systems were composed of variable stiffness layer of polycaprolactone(PCL)and the driven layer of silicone elastomer with alcohol,which continuously changed Young’s modulus from 0.1 to 7.263 MPa(72.63 times variation)in 200 s and maintained maximum weight of 11.52 times its own weight(8.5 g).Attributed to the relatively high variable stiffness range and load bearing value of variable stiffness composite system,the repeatable response process led to the efficient high load driven as“muscle”and diversified precise grab of objects with different shapes as“gripper”,owning widespread application prospects in the field of bionics.
基金supported by the National Natural Science Foundation of China (51772069)。
文摘Lithium-sulfur(Li-S) batteries are one of the most promising rechargeable storage devices due to the high theoretical energy density.However,the low areal sulfur loading impedes their commercial development.Herein,a 3 D free-standing sulfur cathode scaffold is rationally designed and fabricated by coaxially coating polar Ti_3 C_2 T_x flakes on sulfur-impregnated carbon cloth(Ti_3 C_2 T_x@S/CC) to achieve high loading and high energy density Li-S batteries,in which,the flexible CC substrate with highly porous structure can accommodate large amounts of sulfur and ensure fast electron transfer,while the outer-coated Ti_3 C_2 T_x can serve as a polar and conductive protective layer to further promote the conductivity of the whole electrode,achieve physical blocking and chemical anchoring of lithium-polysulfides as well as catalyze their conversion.Due to these advantages,at a sulfur loading of 4 mg cm^(-2),Li-S cells with Ti_3 C_2 T_x@S/CC cathodes can deliver outstanding cycling stability(746.1 mAh g^(-1) after 200 cycles at1 C),superb rate performance(866.8 mAh g^(-1) up to 2 C) and a high specific energy density(564.2 Wh kg^(-1) after 100 cycles at 0.5 C).More significantly,they also show the commercial potential that can compete with current lithium-ion batteries due to the high areal capacity of 6.7 mAh cm^(-2) at the increased loading of 8 mg cm^(-2).
基金financially supported by National Natural Science Foundation of China(No.52301011)Hainan Provincial Natural Science Foundation of China(No.524QN226)the Opening Project of Key Laboratory of Optoelectronic Chemical Materials and Devices,Ministry of Education,Jianghan University(No.JDGD-202315).
文摘The research on metal dimer clusters is of great importance,owing to the potential in modulating the adsorption behavior towards reaction intermediates.Here,we develop a loading heightening strategy to obtain a 32.5wt%Fe-dimer catalyst(Fe-32.5).The co-anchoring of two Fe atoms in a single triazine ring of carbon nitride with an atomic spacing of∼0.23nm is proved.Fe atoms occupy the pores of the triazine ring in the lower iron content sample(Fe-12.9 and Fe-17.1).However,with the increase of iron content to 32.5wt%,two Fe atoms simultaneously occupy one triazine ring.For Fe-32.5,besides the main peak located at∼1.5Åcorresponding to the Fe–N interaction,a peak attributed to Fe–Fe bonding is observed at∼2.2Åin Fourier-transformed k3-weithted extended X-ray absorption fine structure.Density functional theoretical calculations reveal that Fe-dimer in Fe-32.5 induces a charge redistribution compared with that in Fe-12.9 and Fe-17.1.H_(2)O^(∗)is adsorbed on O^(∗)via hydrogen bonding in Fe-12.9 and Fe-17.1.However,H_(2)O^(∗)and O^(∗)in Fe-32.5 are adsorbed on Fe–Fe dimer,resulting in a decrease in the total energy of the reaction process.For the two former,O_(2)^(-)∗adsorbs on individual Fe atoms.Fe-dimer in Fe-32.5 adsorbs O_(2)^(-)∗in the form of bridge bonds,which facilitates the·O_(2)^(-)release.Furthermore,an enhanced affinity for the substrate 3,3′,5,5′-tetramethylbenzidine and higher peroxidase-like activity were displayed.This work provides an effective mean to synthesize metal dimer clusters through high loading.
基金supported by the National Natural Science Foundation of China(Nos.52377133 and 52077014)the Youth Talent Support Program of Chongqing(CQYC2021058945)the General Program of the Natural Science Foundation of Chongqing Municipality(CSTB2022NSCQ-MSX0444).
文摘To address the inherent trade-off between mechanical strength and repair efficiency in conventional microcapsule-based self-healing technologies,this study presents an eggshell-inspired approach for fabricating high-load rigid porous microcapsules(HLRPMs)through subcritical water etching.By optimizing the subcritical water treatment parameters(OH−concentration:0.031 mol/L,tem-perature:240°C,duration:1.5 h),nanoscale through-holes were generated on hollow glass microspheres(shell thickness≈700 nm).The subsequent gradient pressure infiltration of flaxseed oil enabled a record-high core content of 88.2%.Systematic investigations demonstrated that incorporating 3 wt%HLRPMs into epoxy resin composites preserved excellent dielectric properties(breakdown strength≥30 kV/mm)and enhanced tensile strength by 7.52%.In addressing multimodal damage,the system achieved a 95.5%filling efficiency for mechanical scratches,a 97.0%reduction in frictional damage depth,and a 96.2%recovery of insulation following electrical treeing.This biomimetic microcapsule system concurrently improved self-healing capability and matrix performance,offering a promising strategy for the development of next-generation smart insulating materials.
基金supported by the National Natural Science Foundation of China(Grant No.21906015)the Fundamental Research Funds for the Central Universities(Grant No.N2205006 and N2225013).
文摘Rechargeable aqueous aluminum ion batteries(AIBs)are inspiring researchers’enthusiasm due to the low cost and high theoretical capacity of aluminum.Polyaniline(PANI)materials have the potential for aluminum ion storage due to the properties of its excellent conductivity and inherent theoretical capacity.However,the poor cycling stability and low loadings of PANI limit its application in energy storage.In this study,PANI-x electrodes with high mass loadings are successfully prepared by the electrodeposition method for reversible AlCl_(2)^(+)storage.Among them,the PANI-2 electrode possesses the highest areal capacity(0.59 and 0.51 mAh cm^(−2)at the current density of 0.5 and 10 mA cm^(−2))and excellent cycling stability in saturated AlCl3.Ex situ N 1s fitting spectra of PANI-2 and molecular dynamics simulations of 1 M,3 M,and saturated AlCl_(3)electrolytes demonstrate that PANI can achieve reversible redox reactions in saturated AlCl3,thereby achieving its excellent stability.Density functional theory calculations and ex situ spectra characterizations of PANI-2 demonstrate the insertion/de-insertion mechanism in the form of AlCl_(2)^(+)ions.In conclusion,PANI-2|Saturated AlCl_(3)|EG(exfoliated graphite foil)full cell is assembled successfully.This work provides promising guidance for the preparation of high-loading electrodes for AIBs.
基金supported by the National Key Research and Development Program of China(Grant No.2022YFB3804500)the National Natural Science Foundation of China(Grant No.52202352,22335006)+4 种基金the Shanghai Municipal Health Commission(Grant No.20224Y0010)the CAMS Innovation Fund for Medical Sciences(Grant No.2021-I2M-5-012)the Basic Research Program of Shanghai Municipal Government(Grant No.21JC1406000)the Fundamental Research Funds for the Central Universities(Grant No.22120230237,2023-3-YB-11,22120220618)the Basic Research Program of Shanghai Municipal Government(23DX1900200).
文摘The current single-atom catalysts(SACs)for medicine still suffer from the limited active site density.Here,we develop a synthetic method capable of increasing both the metal loading and mass-specific activity of SACs by exchanging zinc with iron.The constructed iron SACs(h^(3)-FNC)with a high metal loading of 6.27 wt%and an optimized adjacent Fe distance of~4 A exhibit excellent oxidase-like catalytic performance without significant activity decay after being stored for six months and promising antibacterial effects.Attractively,a“density effect”has been found at a high-enough metal doping amount,at which individual active sites become close enough to interact with each other and alter the electronic structure,resulting in significantly boosted intrinsic activity of single-atomic iron sites in h^(3)-FNCs by 2.3 times compared to low-and medium-loading SACs.Consequently,the overall catalytic activity of h^(3)-FNC is highly improved,with mass activity and metal mass-specific activity that are,respectively,66 and 315 times higher than those of commercial Pt/C.In addition,h^(3)-FNCs demonstrate efficiently enhanced capability in catalyzing oxygen reduction into superoxide anion(O_(2)·^(−))and glutathione(GSH)depletion.Both in vitro and in vivo assays demonstrate the superior antibacterial efficacy of h^(3)-FNCs in promoting wound healing.This work presents an intriguing activity-enhancement effect in catalysts and exhibits impressive therapeutic efficacy in combating bacterial infections.
基金supported by the Australian Research Council(LE150100058)the Open Research Fund of State Key Laboratory of Geomechanics and Geotechnical Engineering(Z020002)State Key Laboratory of Coal Mine Disaster Dynamics and Control.The specimens were scanned at the Imaging and Medical beamline(IMBL)under the Australian Synchrotron projects(NO:M15862 and M14428).
文摘Tensile cracking is a predominant mode of failure in rocks within underground resource excavation and engineering structures,where rocks are frequently subjected to dynamic disturbances while simultaneously experiencing in-situ stresses.This paper proposes a new dynamic split tension setup utilising a cubic specimen to investigate the dynamic behaviour of rocks across various tensile strain rates and confining pressures.The objective is to extend the applicability of the triaxial Hopkinson bar in studying dynamic behaviour of geomaterials.For comparison,the dynamic Brazilian disc(BD)tests were performed using three rock types(e.g.,sandstone,granite and marble)under different strain rates ranging from 10^(−3)∼10^(2) s^(−1).Besides,the Digital Image Correlation(DIC)technique was adopted to measure full-field real-time tensile strain of rocks and demonstrated that tensile crack initiated at the middle part and split the specimen into two similar halves.Effects of specimen size,geometry,loading rate as well as the confining pressure are investigated in detail.The dynamic fracture behaviours,including dynamic tensile strength,tensile strain,time to fracture and dynamic increase factor(DIF),were characterised for the rocks.It is found that dynamic tensile strength of rock minimal dependence on size and geometry but is significantly influenced by loading rate and confinement.It exhibited a linear increase with strain rate(10^(0)∼10^(2) s^(−1))and demonstrated a nonlinear growth with lateral confinement from 0 to 15 MPa.The nonlinear dependency on confinement can be attributed to the restriction imposed on the opening and propagation of tensile cracks due to the presence of confinement.These findings enhance our understanding of the safety aspects associated with underground rock excavations,particularly in situations where considering in-situ stress is crucial for evaluating the dynamic tensile failure of rocks.
基金National Basic Research Program of China (2007CB210100)National Natural Science Foundation of China (50876023)Chinese Specialized Research Fund for the Doctoral Program of Higher Education (20060213007)
文摘This article is aimed to experimentally validate the beneficial effects of boundary layer suction on improving the aerodynamic performance of a compressor cascade with a large camber angle. The flow field of the cascade is measured and the ink-trace flow visualization is also presented. The experimental results show that the boundary layer suction reduces losses near the area of rnidspan in the cascade most effectively for all suction cases under test. Losses of the endwall could remarkably decrease only when the suction is at the position where the boundary layer has separated but still not departed far away from the blade surface. It is evidenced that the higher suction flow rate and the suction position closer to the trailing edge result in greater reduction in losses and the maximum reduction in the total pressure loss accounts to 16.5% for all cases. The suction position plays a greater role in affecting the total pressure loss than the suction flow rate does.
基金The authors acknowledge the financial support from the National Natural Science Foundation of China （Nos. 21573286, 21173269, and 21572688）, Ministry ofScience and Technology of China （Nos. 2011BAK15B05 and 2015AA034603）, Specialized Research Fund for the Doctoral Program of Higher Education （No. 20130007110003）, and Science Foundation of China University of Petroleum, Beijing （No. 2462015YQ0304）.
文摘Controlled integration of ultrafine metal nanoparticles （MNPs） and metal- organic frameworks （MOFs） has drawn much attention due to their unique physical and chemical properties. However, the development of a one-step strategy for preparing ultrafine MNPs within MOFs still remains a great challenge. Herein, a facile synthetic approach toward the abovementioned composites was developed. In contrast to the conventional approach, these hybrids were prepared by the direct mixing of metal and MOF precursors in the reaction solution assisted by microwave irradiation. Impressively, the Au/MOF-199 composite with uniformly distributed ultrafine Au nanoparticles could be fabricated in only two minutes, and the Au loading could be increased up to a level of 5.13%. The multifunctional Au/MOF-199 catalysts exhibited high turnover numbers （TONs） and turnover frequencies （TOFs） in the three-component coupling reaction of formaldehyde, phenylacetylene, and piperidine （AB-coupling）. Owing to the confinement effect of MOF-199, the 5.13%Au/MOF-199 catalyst could be recycled for five runs without serious loss of activity, with no obvious aggregation of Au NPs detected.
基金National Natural Science Foundation of China (50876023)Chinese Specialized Research Fund for the Doctoral Pro-gram of Higher Education (20060213007)National Basic Research Program of China (2007CB210100)
文摘This article experimentally studies the effects of air injection near the blade trailing edge on flow separation and losses in a highly loaded linear compressor cascade. Aerodynamic parameters of eight cascades with different air injection slot configura- tions are measured by using a five-hole probe at the cascade outlets. Ink-trace flow visualization is performed to obtain the flow details around the air injection slots. The static pressure distribution is clarified with pressure taps on the endwalls. The...
基金Korea Institute of Energy Technology Evaluation and Planning,Grant/Award Number:20214000000320Samsung Research Funding&Incubation Center of Samsung Electronics,Grant/Award Number:SRFC-MA1901-06。
文摘Realizing a lithium sulfide(Li_(2)S)cathode with both high energy density and a long lifespan requires an innovative cathode design that maximizes electrochemical performance and resists electrode deterioration.Herein,a high-loading Li_(2)S-based cathode with micrometric Li_(2)S particles composed of two-dimensional graphene(Gr)and one-dimensional carbon nanotubes(CNTs)in a compact geometry is developed,and the role of CNTs in stable cycling of high-capacity Li–S batteries is emphasized.In a dimensionally combined carbon matrix,CNTs embedded within the Gr sheets create robust and sustainable electron diffusion pathways while suppressing the passivation of the active carbon surface.As a unique point,during the first charging process,the proposed cathode is fully activated through the direct conversion of Li_(2)S into S_(8) without inducing lithium polysulfide formation.The direct conversion of Li_(2)S into S_(8) in the composite cathode is ubiquitously investigated using the combined study of in situ Raman spectroscopy,in situ optical microscopy,and cryogenic transmission electron microscopy.The composite cathode demonstrates unprecedented electrochemical properties even with a high Li_(2)S loading of 10 mg cm^(–2);in particular,the practical and safe Li–S full cell coupled with a graphite anode shows ultra-long-term cycling stability over 800 cycles.
基金financially supported by the Beijing Municipal Science and Technology Project (No.Z171100000917021)。
文摘A high sulfur content sulfur–carbon composite was synthesized via in situ generation method in aqueous solution.When the sulfur loading is up to 90%,the electrode still exhibits good cycling performance with a reversible capacity of about 623 mAh·g^(-1)after 100 cycles.To further commercialize the Li–S battery,understanding the capacity degradation mechanism is very essential,especially with a high sulfur loading electrode.To achieve this goal,the electrochemical performance of the high sulfur loading electrode was studied,and the structure change of the electrode after cycling was also examined by ex situ scanning electron microscopy(SEM)and other techniques.The result shows that the Li_(2)S_(2)and Li_(2)S inhomogeneous precipitation contributes to the majority capacity fading of the high sulfur loading Li–S cells.
基金This project was supported by the National Natural Science Foundation of China(U19A2017,22272206,51976143)Natural Science Foundation of Hunan Province(S2021JJMSXM3153).
文摘Electrochemical carbon dioxide reduction reaction(CO_(2)RR)provides an attractive approach to carbon capture and utilization for the production high-value-added products.However,CO_(2)RR still suffers from poor selectivity and low current density due to its sluggish kinetics and multitudinous reaction pathways.Single-atom catalysts(SACs)demonstrate outstanding activity,excellent selectivity,and remarkable atom utilization efficiency,which give impetus to the search for electrocatalytic processes aiming at high selectivity.There appears significant activity in the development of efficient SACs for CO_(2)RR,while the density of the atomic sites remains a considerable barrier to be overcome.To construct high-metal-loading SACs,aggregation must be prevented,and thus novel strategies are required.The key to creating high-density atomically dispersed sites is designing enough anchoring sites,normally defects,to stabilize the highly mobile separated metal atoms.In this review,we summarized the advances in developing high-loading SACs through defect engineering,with a focus on the synthesis strategies to achieve high atomic site loading.Finally,the future opportunities and challenges for CO_(2)RR in the area of high-loading single-atom electrocatalysts are also discussed.
文摘July 25, 2014 / Accepted： August 18, 2014 / Published： November 25, 2014 Abstract： This paper presents the measurement results of a l1/2 stage LPT （low pressure turbine） test rig at Graz University of Technology incorporating two different rotor geometries： one with a regular blade loading and the other with a highly loaded blade geometry. The test rig was designed in cooperation with MTU Aero Engines and represented the last 1.5 stages of a commercial aero engine. Considerable efforts were put on the adjustment of all relevant model parameters （Mach number, blade count ratio, airfoil aspect ratio, blade loading, etc.） to reproduce the full scale LPT situation. The rig diameter is approximately half of that of a commercial aero engine LPT. The number of blades and vanes for the two investigated stages as well as the pressure ratio and power output are identical, resulting in a decrease in rotational speed of the HSL （high stage loading） rotor. Measurement data from a FRAPP （fast response pressure probe） is used to compare the flow fields of the two different stages. The effect of the different stage designs can be seen when comparing the exit flow fields. The highly loaded stage shows a more pronounced tip leakage vortex compared to the datum stage. The highly loaded stage shows wider wakes with a lower total pressure deficit. The fluctuations of total pressure within the flow field are directly related to the upstream wake. If the measurement position is located within a stator wake, the fluctuations are significantly smaller than that out of the wake.
基金National Natural Science Foundation of China(Nos.22109106 and 21865025)Foundation for High-Level Talents in Shihezi University(RCZK202002)+1 种基金Young Innovative Talent Program in Shihezi University(CXBJ202305)。
文摘Organic materials for aqueous zinc ion batteries have been attracted the attention of researchers because of their high safety,environmental friendliness,and structural designability.However,the limited specific capacity,unsatisfactory cycling durability,and unclear charge storage mechanism limit their development and applications.Herein,NTCDA-2,3-DNQ,an organic compound with a benzimidazole ring structure,was designed through the number and distribution of active sites as well as the adjustment of molecular weight,and applied as the cathode for aqueous zinc-ion batteries.NTNQ exhibits high specific capacity of 290.5 mAh·g^(-1) at 0.05 A·g^(-1),excellent rate performance of 133.3 mAh·g^(-1) at 15 A·g^(-1),and relatively stable cycle life with 81.7%capacity retention over 10,000 superlong cycles at 10 A·g^(-1).Furthermore,the synergistic effect of neighboring active sites and multi-electron Zn^(2+)storage reactions are further explored by density functional theory(DFT)calculations,and the results show that NTNQ could stores 4Zn^(2+)while transferring 8e–in the N-Zn-O pathway during the storage of Zn^(2+).Interestingly,NTNQ still exhibits high specific capacity and favorable cycling stability at multiple ultra-high loadings.This work provides important chances including the design concepts of the organic molecules and the investigation of the Zn^(2+)storage mechanism for high performance aqueous zinc ion batteries.
