Na_(3)V_(2)(PO_(4))_(3)(NVP)has garnered great attentions as a prospective cathode material for sodium-ion batteries(SIBs)by virtue of its decent theoretical capacity,superior ion conductivity and high structural stab...Na_(3)V_(2)(PO_(4))_(3)(NVP)has garnered great attentions as a prospective cathode material for sodium-ion batteries(SIBs)by virtue of its decent theoretical capacity,superior ion conductivity and high structural stability.However,the inherently poor electronic conductivity and sluggish sodium-ion diffusion kinetics of NVP material give rise to inferior rate performance and unsatisfactory energy density,which strictly confine its further application in SIBs.Thus,it is of significance to boost the sodium storage performance of NVP cathode material.Up to now,many methods have been developed to optimize the electrochemical performance of NVP cathode material.In this review,the latest advances in optimization strategies for improving the electrochemical performance of NVP cathode material are well summarized and discussed,including carbon coating or modification,foreign-ion doping or substitution and nanostructure and morphology design.The foreign-ion doping or substitution is highlighted,involving Na,V,and PO_(4)^(3−)sites,which include single-site doping,multiple-site doping,single-ion doping,multiple-ion doping and so on.Furthermore,the challenges and prospects of high-performance NVP cathode material are also put forward.It is believed that this review can provide a useful reference for designing and developing high-performance NVP cathode material toward the large-scale application in SIBs.展开更多
Four-dimensional(4D)printing technology is a revolutionary development that produces structures that can adapt in response to external stimuli.However,the responsiveness and printability of smart materials with shape ...Four-dimensional(4D)printing technology is a revolutionary development that produces structures that can adapt in response to external stimuli.However,the responsiveness and printability of smart materials with shape memory properties,which are necessary for 4D printing,remain limited.Biomass materials derived from nature have offered an effective solution due to their various excellent and unique properties.Biomass materials have been abundant in resources and low in carbon content,contributing to the then-current global green energy-saving goals,including carbon peaking and carbon neutrality.This review focused on different sources of biomass materials used in 4D printing,including plant-based,animal-based,and microbial-based biomass materials.It systematically outlined the responsive deformation mechanisms of printed objects that contained biomass materials and delved into the roles and unique advantages of biomass materials in those printed objects.Leveraging these advantages,the review discussed the potential applications of biomass materials in biomedicine,food printing,and other fields to support ongoing development and application efforts.Additionally,it emphasized the crucial role played by bio-fabrication technologies utilizing biomass materials in the integration of biomass materials with 4D printing.Finally,this paper discussed the then-current challenges and potential future directions of biomass materials in 4D printing,aiming to promote the effective development of biomass materials in 4D printing applications.展开更多
To explore high value-added utilization pathways of fly ash,the mesoporous structure of silicon dioxide extracted from fly ash(FA-SiO_(2))was utilized to restrict the dicyandiamide(DCDA)thermal degradation process.Thi...To explore high value-added utilization pathways of fly ash,the mesoporous structure of silicon dioxide extracted from fly ash(FA-SiO_(2))was utilized to restrict the dicyandiamide(DCDA)thermal degradation process.This produced chemically bonded interacting composite photocatalysts of FA-SiO,and graphitic-phase carbon nitride(g-C_(3)N_(4)).Compared with the spherical silicon dioxide prepared using tetraethyl orthosilicate(TEOS-SiO_(2)),the mesoporous structure of FA-SiO_(2),allowed DCDA to react in a smaller space,which facilitated the transformation of DCDA to melamine by the thermal degradation kinetics of FA-C_(3)N_(4)/DCDA.This ultimately boosted the formation of an N-atom-removed triazine ring structure and a multistage structure combining lumps and rods in the composite photocatalysts of g-C_(3)N_(4),and FA-SiO_(2),which led to a higher visible-light utilization efficiency,a suitable valence-band position,and the photocatalytic activity for methylene blue reaching 3.56 times that of g-C_(3)N_(4).The findings indicate that mesoporous FA-SiO,has the potential to improve the structural and photocatalytic properties of g-C_(3)N_(4),-based materials.展开更多
Li_(3)PO_(4)@Li_(0.99)K_(0.01)Ni_(0.83)Co_(0.11)Mn_(O.06)O_(2)(NCM-KP) cathode powders are synthesized via K^(+)doping in calcination processes and H_3PO_4 coating in sol-gel processes.K^(+) precisely enters into the ...Li_(3)PO_(4)@Li_(0.99)K_(0.01)Ni_(0.83)Co_(0.11)Mn_(O.06)O_(2)(NCM-KP) cathode powders are synthesized via K^(+)doping in calcination processes and H_3PO_4 coating in sol-gel processes.K^(+) precisely enters into the lattice to widen the(003) plane to 0.4746 nm with a lower cationic disordered degree of 1.87%.Moreover,the surface residual lithium salts are treated by H_3PO_4 to generate a uniform Li_(3)PO_(4) coating layer of approximately 11.41 nm,which completely covers on the surface of secondary spherical particles to improve the interfacial stability.At 25℃,the NCM-KP electrode delivers a discharge specific capacity of 148.9 mAh·g^(-1) with a remarkable capacity retention ratio of 84.1% after 200 cycles at 1.0C and retains a high reversible specific capacity of 154.4 mAh·g^(-1) at 5.0C.Even at 1.0C and 60℃,it can maintain a reversible discharge specific capacity of 114.6 mAh·g^(-1) with 0.21% of capacity decay per cycle after 200 cycles,which is significantly lower than 0.40% for the pristine NCM powders.Importantly,the charge transfer resistance of 238.89 Ω for the NCM-KP electrode is significantly lower than 947.41 Ω for the pristine NCM one by restricting the interfacial side reactions.Therefore,combining K+doping and Li_(3)PO_(4) coating is an effective strategy to enable the significant improvement of the electrochemical property of high-nickel cathode materials,which may be mainly attributed to the widened diffusion pathway and the formed Li_(3)PO_(4) protective layer,thus promoting Li~+diffusion rate and preventing the erosion of HF.展开更多
Aqueous zinc(Zn)-ion batteries(AZIBs)have gained significant interest in energy storage due to several unique advantages.Utilizing waterbased electrolytes enhances environmental sustainability,while the abundance and ...Aqueous zinc(Zn)-ion batteries(AZIBs)have gained significant interest in energy storage due to several unique advantages.Utilizing waterbased electrolytes enhances environmental sustainability,while the abundance and affordability of Zn offer economic benefits.Manganese(Mn)-based materials,commonly used as cathodes in these batteries,provide high theoretical capacity,high electrical conductivity,and good structural stability.However,these materials suffer from capacity degradation over repeated cycles due to structural collapse and limited conductivity.To address this problem,we synthesized a magnesium(Mg)-and Mn-based composite,Mg^(2+)-Mn_(3)O_(4),using the hydrothermal method with an optimized amount of ammonium hydroxide(NH_(4)OH)solution.This approach effectively stabilizes the structure during cycling,enhancing both capacity retention and conductivity.The Zn^(2+)/H+intercalation/deintercalation process was confirmed by experimental results and ex-situ X-ray diffraction analysis,which demonstrates that Mg^(2+),along with optimized NH_(4)OH amount,prevents structural collapse and improves conductivity.Under optimal process conditions,the composite electrode(Mg^(2+)-Mn_(3)O_(4)–8 ml)achieved a capacity of 173.58 mA h g^(-1) at 0.5 A g^(-1),with excellent rate performance of 71.39 mA h g^(-1) at 10 A g^(-1).Remarkably,even at 5 A g^(-1),the electrode maintained a capacity of 86.87 mA h g^(-1) over 2100 cycles,underscoring the role of Mg^(2+)and NH_(4)OH in enhancing the reversible insertion/extraction stability of Zn^(2+)in Mn-based layered materials.This study presents a novel strategy for metal-ion incorporation in Mn-based AZIBs,offering insights into the optimization of cathode materials and advancing research on associated storage mechanisms.展开更多
The high-value utilization of manganese ore tailings is of great significance for saving mineral resources and achieving environmental protection.Herein,an olivine LiFe_(0.5)Mn_(0.5)PO_(4)/rGO composite is synthesized...The high-value utilization of manganese ore tailings is of great significance for saving mineral resources and achieving environmental protection.Herein,an olivine LiFe_(0.5)Mn_(0.5)PO_(4)/rGO composite is synthesized by a simple precipitation method and subsequent high-temperature calcination process using the manganese ore tailings as raw material.The prepared LiFe_(0.5)Mn_(0.5)PO_(4)/rGO composite exhibits superior cycling stability(with 113.5 mAh·g^(-1)after 300 cycles at1.0C(1.0C=170 mA·g^(-1)))and superior rate performance(with 65.6 mAh·g^(-1)at 10.0C).Ex-situ XRD and electrochemical impedance spectroscopy(EIS)analyses evidence that the LiFe_(0.5)Mn_(0.5)PO_(4)/rGO material has excellent structural stability and electrochemical reversibility during charge and discharge processes.Furthermore,the LiFe_(0.5)Mn_(0.5)PO_(4)/rGO//graphite full Li-ion battery also exhibits excellent cycling stability indicating its potential commercialization value.展开更多
B_(4)C/Al composites are widely utilized as neutron absorbing materials for the storage and transportation of spent nuclear fuel.In order to improve the high-temperature mechanical properties of B_(4)C/Al composites,i...B_(4)C/Al composites are widely utilized as neutron absorbing materials for the storage and transportation of spent nuclear fuel.In order to improve the high-temperature mechanical properties of B_(4)C/Al composites,in-situ nano-Al_(2)O_(3)was introduced utilizing oxide on Al powder surface.In this study,the Al_(2)O_(3)content was adjusted by utilizing spheroid Al powder with varying diameters,thereby investigating the impact of Al_(2)O_(3)content on the tensile properties of(B_(4)C+Al_(2)O_(3))/Al composites.It was found that the pinning effect of Al_(2)O_(3)on the grain boundaries could hinder the recovery of dislocations and lead to dislocation accumulation at high temperature.As the result,with the increase in Al_(2)O_(3)content and the decrease in grain size,the high-temperature strength of the composites increased significantly.The finest Al powder used in this investigation had a diameter of 1.4μm,whereas the resultant composite exhibited a maximum strength of 251 MPa at room temperature and 133 MPa at 350℃,surpassing that of traditional B_(4)C/Al composites.展开更多
In this work,porous hollow spherical NiCo_(2)S_(4) nanomaterials composed of loosely porous nanowires on the surface were prepared using nickel foam as the substrate through a secondary hydrother-mal reaction method.T...In this work,porous hollow spherical NiCo_(2)S_(4) nanomaterials composed of loosely porous nanowires on the surface were prepared using nickel foam as the substrate through a secondary hydrother-mal reaction method.The synthesized materials were then characterized using techniques such as X-ray powder diffraction,scanning electron microscopy and energy-dispersive X-ray spectroscopy.Finally,elec-trochemical performance tests were conducted on the synthesized cobalt-nickel bimetallic compound elec-trode materials,the specific capacitance of the synthesized NiCo_(2)S_(4) nanomaterial reached 3.20 F·cm-2,Moreover,the specific capacitance remained 95.8%of its initial value after 500 cycles.The electrochemical performance was superior to that of the prepared NiCo2O4 nanomaterial.The results suggest that the prepared NiCo_(2)S_(4) with special structure could be a great potential as a material for supercapacitor electrodes.展开更多
The Li3V2（PO4）3/C composite cathode material was synthesized via sol-gel method using three different chelating agents （citric acid, salicylic acid and polyacrylic acid） at pH value of 3 or 7. The crystal structur...The Li3V2（PO4）3/C composite cathode material was synthesized via sol-gel method using three different chelating agents （citric acid, salicylic acid and polyacrylic acid） at pH value of 3 or 7. The crystal structure, morphology, specific surface area and electrochemical performance of the prepared samples were investigated by X-ray diffraction （XRD）, scanning electron microscopy （SEM）, cyclic voltammetry （CV）, electrochemical impedance spectroscopy （EIS） and galvanostatic charge/discharge test. The results show that the effects of pH value on the performance of the prepared materials are greatly related to the chelating agents. With salicylic acid or polyacrylic acid as the chelating reagent, the structure, morphology and electrochemical performance of the samples are greatly influenced by the pH values. However, the structure of the materials with citric acid as the chelating agent does not change as pH value changes, and the materials own uniform particle size distribution and good electrochemical performance. It delivers an initial discharge capacity of 113.58 mA·h/g at 10C, remaining as high as 108.48 mA·h/g after 900 cycles, with a capacity retention of 95.51%.展开更多
Li3V2（PO4）3 precursor was obtained with V2Os.nH2O , LiOH＇H2O, NH4H2PO4 and sucrose as starting materials by grinding-sol-gel method, and then the monoclinic-typed Li3Vz（PO4）3 cathode material was prepared by sint...Li3V2（PO4）3 precursor was obtained with V2Os.nH2O , LiOH＇H2O, NH4H2PO4 and sucrose as starting materials by grinding-sol-gel method, and then the monoclinic-typed Li3Vz（PO4）3 cathode material was prepared by sintering the amorphous Li3V2（PO4）3. The as-sintered samples were investigated by X-ray diffraction （XRD）, transmission electron microscopy （TEM）, N2 adsorption-desorption and electrochemical measurement. It is found that Li3Vz（PO4）3 sintered at 700 ℃ possesses good wormhole-like mesoporous structure with the largest specific surface area of 188 cmZ/g, and the smallest pore size of 9.3 nm. Electrochemical test reveals that the initial discharge capacity of the 700 ℃ sintered sample is 155.9 mA.h/g at the rate of 0.2C, and the capacity retains 154 mA.h/g after 50 cycles, exhibiting a stable discharge capacity at room temperature.展开更多
LiFePO4-Li3V2（PO4）3 composites were synthesized by solid-hydrothermal method and by ball milling,respectively.The electrochemical performance of the solid-hydrothermally obtained materials（C-LFVP） was significantl...LiFePO4-Li3V2（PO4）3 composites were synthesized by solid-hydrothermal method and by ball milling,respectively.The electrochemical performance of the solid-hydrothermally obtained materials（C-LFVP） was significantly improved compared with LiFePO4（LFP） and Li3V2（PO4）3（LVP）,and it was also much better than that of the ball-milled LiFePO4-Li3V2（PO4）3（P-LFVP）.C-LFVP and P-LFVP both had four REDOX peaks（voltage plateaus）,which coincided with that of LFP and LVP.Some new trace substances were found in C-LFVP which had more perfect morphology,this was responsible for the better electrochemical performance of C-LFVP than P-LFVP.展开更多
Li3V2-2/3xMnx（PO4）3（0≤x≤0.12） powders were synthesized by sol-gel method. The effect of Mn2＋-doping on the structure and electrochemical performances of Li3V2（PO4）3/C was characterized by XRD, SEM, XPS, galva...Li3V2-2/3xMnx（PO4）3（0≤x≤0.12） powders were synthesized by sol-gel method. The effect of Mn2＋-doping on the structure and electrochemical performances of Li3V2（PO4）3/C was characterized by XRD, SEM, XPS, galvanostatic charge /discharge and electrochemical impedance spectroscopy（EIS）. The XRD study shows that a small amount of Mn2＋-doped does not alter the structure of Li3V2（PO4）3/C materials, and all Mn2＋-doped samples are of pure single phase with a monoclinic structure （space group P21/n）. The XPS analysis indicates that valences state of V and Mn are ＋3 and ＋2 in Li3V1.94Mn0.09（PO4）3/C, respectively, and the citric acid in raw materials was decomposed into carbon during calcination, and residual carbon exists in Li3V1.94Mn0.09（PO4）/C. The results of electrochemical measurements show that Mn2＋-doping can improve the cyclic stability and rate performance of these cathode materials. The Li3V1.94Mn0.09（PO4）3/C cathode material shows the best cyclic stability and rate performance. For example, at the discharge current density of 40 mA/g, after 100 cycles, the discharge capacity of Li3V1.94Mn0.09（PO4）3/C declines from initial 158.8 mA·h/g to 120.5 mA·h/g with a capacity retention of 75.9%; however, that of the Mn-undoed sample declines from 164.2 mA·h/g to 72.6 mA·h/g with a capacity retention of 44.2%. When the discharge current is increased up to 1C, the intial discharge capacity of Li3V1.94Mn0.09（PO4）3/C still reaches 146.4 mA·h/g, and the discharge capacity maintains at 107.5 mA·h/g after 100 cycles. The EIS measurement indicates that Mn2＋-doping with a appropriate amount of Mn2＋ decreases the charge transfer resistance, which is favorable for the insertion/extraction of Li＋.展开更多
The LiMnPO4/C composite material was synthesized via a sol-gel method based on the citric acid. The X-ray diffraction （XRD）, scanning electron microscopy （SEM） and electrochemical performance tests were adopted to...The LiMnPO4/C composite material was synthesized via a sol-gel method based on the citric acid. The X-ray diffraction （XRD）, scanning electron microscopy （SEM） and electrochemical performance tests were adopted to characterize the properties of LiMnPO4/C. The XRD studies show that the pure olivine phase LiMnPO4 can be obtained at a low temperature of 500 °C. The SEM analyses illustrate that the citric acid used as the chelating reagent and carbon source can restrain the particle size of LiMnPO4/C well. The LiMnPO4/C sample synthesized at 500 °C for 10 h performs the highest initial discharge capacity of 122.6 mA-h/g, retaining 112.4 mA-h/g over 30 cycles at 0.05C rate. The citric acid based sol-gel method is favor to obtain the high electrochemical performance of LiMnPO4/C.展开更多
In order to enhance electrochemical properties of LiFePO4 （LFP） cathode materials, spherical porous nano/micro structured LFP/C cathode materials were synthesized by spray drying, followed by calcination. The result...In order to enhance electrochemical properties of LiFePO4 （LFP） cathode materials, spherical porous nano/micro structured LFP/C cathode materials were synthesized by spray drying, followed by calcination. The results show that the spherical precursors with the sizes of 0.5-5 μm can be completely converted to LFP/C when the calcination temperature is higher than 500 ℃. The LFP/C microspheres obtained at calcination temperature of 700 ℃ are composed of numerous particles with sizes of -20 nm, and have well-developed interconnected pore structure and large specific surface area of 28.77 mE/g. The specific discharge capacities of the LFP/C obtained at 700 ℃ are 162.43, 154.35 and 144.03 mA.h/g at 0.5C, 1C and 2C, respectively. Meanwhile, the capacity retentions can reach up to 100% after 50 cycles. The improved electrochemical properties of the materials are ascribed to a small Li＋ diffusion resistance and special structure of LFP/C microspheres.展开更多
LiMnPO_4 /C composites were synthesized via solid-state reaction with different carbon sources: sucrose, citric acid and oxalic acid. The sam- ples were characterized by X-ray diffraction (XRD), scanning electron micr...LiMnPO_4 /C composites were synthesized via solid-state reaction with different carbon sources: sucrose, citric acid and oxalic acid. The sam- ples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and electrochemical performance test. The results of XRD reveal that carbon coating has no effect on the phase of LiMnPO_4 . The LiMnPO_4 /C synthesized at 600 °C with citric acid as carbon source shows an initial discharge capacity of 117.8 mA·hg^-1 at 0.05 C rate. After 30 cycles, the capacity remains 98.2 mAh·g^-1 . The improved electrochemical properties of LiMnPO_4 /C is attributed to the decomposition of organic acid during the sintering process.展开更多
LiNiCoAlO（NCA） with Zr（OH）coating is demonstrated as high performance cathode material for lithium ion batteries（LIBs）. The coated materials are synthesized via a simple dry coating method of NCA with Zr（OH）po...LiNiCoAlO（NCA） with Zr（OH）coating is demonstrated as high performance cathode material for lithium ion batteries（LIBs）. The coated materials are synthesized via a simple dry coating method of NCA with Zr（OH）powders, and then characterized with scanning electron microscopy（SEM）, transmission electron microscopy（TEM） and X-ray photoelectron spectroscopy（XPS）. Experimental results show that amorphous Zr（OH）powders have been successfully coated on the surface of spherical NCA particles, exhibiting improved electrochemical performance. 0.50 wt% Zr（OH）coated NCA delivers a capacity of 197.6 mAh/g at the first cycle and 154.3 mAh/g after 100 cycles with a capacity retention of 78.1% at 1 C rate. In comparison, the pure NCA shows a capacity of 194.6 mAh/g at the first cycle and 142.5 mAh/g after 100 cycles with a capacity retention of 73.2% at 1 C rate. Electrochemical impedance spectroscopy（EIS） results show that the coated material exhibits a lower resistance, indicating that the coating layer can efficiently suppress transition metals dissolution and decrease the side reactions at the surface between the electrode and electrolyte. Therefore, surface coating with amorphous Zr（OH）is a simple and useful method to enhance the electrochemical performance of NCA-based materials for the cathode of LIBs.展开更多
The rapid development of additive manufacturing and advances in shape memory materials have fueled the progress of four-dimensional （4D） printing. With the right external stimulus, the need for human interaction, se...The rapid development of additive manufacturing and advances in shape memory materials have fueled the progress of four-dimensional （4D） printing. With the right external stimulus, the need for human interaction, sensors, and batteries will be eliminated, and by using additive manufacturing, more complex devices and parts can be produced. With the current understanding of shape memory mechanisms and with improved design for additive manufacturing, reversibility in 4D printing has recently been proven to be feasible. Conventional one-way 4D printing requires human interaction in the programming （or shapesetting） phase, but reversible 4D printing, or two-way 4D printing, will fully eliminate the need for human interference, as the programming stage is replaced with another stimulus. This allows reversible 4D printed parts to be fully dependent on external stimuli; parts can also be potentially reused after every recovery, or even used in continuous cycles-an aspect that carries industrial appeal. This paper presents a review on the mechanisms of shape memory materials that have led to 4D printing, current findings regarding 4D printing in alloys and polymers, and their respective limitations. The reversibility of shape memory materials and their feasibility to be fabricated using three-dimensional （3D） printing are summarized and critically analyzed. For reversible 4D printing, the methods of 3D printing, mechanisms used for actuation, and strategies to achieve reversibility are also highlighted. Finally, prospective future research directions in reversible 4D printing are suggested.展开更多
基金partly supported by the National Natural Science Foundation of China(Grant No.52272225).
文摘Na_(3)V_(2)(PO_(4))_(3)(NVP)has garnered great attentions as a prospective cathode material for sodium-ion batteries(SIBs)by virtue of its decent theoretical capacity,superior ion conductivity and high structural stability.However,the inherently poor electronic conductivity and sluggish sodium-ion diffusion kinetics of NVP material give rise to inferior rate performance and unsatisfactory energy density,which strictly confine its further application in SIBs.Thus,it is of significance to boost the sodium storage performance of NVP cathode material.Up to now,many methods have been developed to optimize the electrochemical performance of NVP cathode material.In this review,the latest advances in optimization strategies for improving the electrochemical performance of NVP cathode material are well summarized and discussed,including carbon coating or modification,foreign-ion doping or substitution and nanostructure and morphology design.The foreign-ion doping or substitution is highlighted,involving Na,V,and PO_(4)^(3−)sites,which include single-site doping,multiple-site doping,single-ion doping,multiple-ion doping and so on.Furthermore,the challenges and prospects of high-performance NVP cathode material are also put forward.It is believed that this review can provide a useful reference for designing and developing high-performance NVP cathode material toward the large-scale application in SIBs.
基金the support by National Natural Science Foundation of China(No.52375314,12472147,U23A20412)the National Key R&D Program of China(No.2024YFB4710205,2024YFD2200700)Heilongjiang Provincial Natural Science Foundation of China(No.2022ZX02C25).
文摘Four-dimensional(4D)printing technology is a revolutionary development that produces structures that can adapt in response to external stimuli.However,the responsiveness and printability of smart materials with shape memory properties,which are necessary for 4D printing,remain limited.Biomass materials derived from nature have offered an effective solution due to their various excellent and unique properties.Biomass materials have been abundant in resources and low in carbon content,contributing to the then-current global green energy-saving goals,including carbon peaking and carbon neutrality.This review focused on different sources of biomass materials used in 4D printing,including plant-based,animal-based,and microbial-based biomass materials.It systematically outlined the responsive deformation mechanisms of printed objects that contained biomass materials and delved into the roles and unique advantages of biomass materials in those printed objects.Leveraging these advantages,the review discussed the potential applications of biomass materials in biomedicine,food printing,and other fields to support ongoing development and application efforts.Additionally,it emphasized the crucial role played by bio-fabrication technologies utilizing biomass materials in the integration of biomass materials with 4D printing.Finally,this paper discussed the then-current challenges and potential future directions of biomass materials in 4D printing,aiming to promote the effective development of biomass materials in 4D printing applications.
基金supported by the Medical Special Cultivation Project of Anhui University of Science and Technology(Nos.YZ2023H2B013 and YZ2023H2B012),China.
文摘To explore high value-added utilization pathways of fly ash,the mesoporous structure of silicon dioxide extracted from fly ash(FA-SiO_(2))was utilized to restrict the dicyandiamide(DCDA)thermal degradation process.This produced chemically bonded interacting composite photocatalysts of FA-SiO,and graphitic-phase carbon nitride(g-C_(3)N_(4)).Compared with the spherical silicon dioxide prepared using tetraethyl orthosilicate(TEOS-SiO_(2)),the mesoporous structure of FA-SiO_(2),allowed DCDA to react in a smaller space,which facilitated the transformation of DCDA to melamine by the thermal degradation kinetics of FA-C_(3)N_(4)/DCDA.This ultimately boosted the formation of an N-atom-removed triazine ring structure and a multistage structure combining lumps and rods in the composite photocatalysts of g-C_(3)N_(4),and FA-SiO_(2),which led to a higher visible-light utilization efficiency,a suitable valence-band position,and the photocatalytic activity for methylene blue reaching 3.56 times that of g-C_(3)N_(4).The findings indicate that mesoporous FA-SiO,has the potential to improve the structural and photocatalytic properties of g-C_(3)N_(4),-based materials.
基金financially supported by the National Natural Science Foundation of China (Nos.52274292 and 51874046)the Outstanding Youth Foundation of Hubei Province (No.2020CFA090)。
文摘Li_(3)PO_(4)@Li_(0.99)K_(0.01)Ni_(0.83)Co_(0.11)Mn_(O.06)O_(2)(NCM-KP) cathode powders are synthesized via K^(+)doping in calcination processes and H_3PO_4 coating in sol-gel processes.K^(+) precisely enters into the lattice to widen the(003) plane to 0.4746 nm with a lower cationic disordered degree of 1.87%.Moreover,the surface residual lithium salts are treated by H_3PO_4 to generate a uniform Li_(3)PO_(4) coating layer of approximately 11.41 nm,which completely covers on the surface of secondary spherical particles to improve the interfacial stability.At 25℃,the NCM-KP electrode delivers a discharge specific capacity of 148.9 mAh·g^(-1) with a remarkable capacity retention ratio of 84.1% after 200 cycles at 1.0C and retains a high reversible specific capacity of 154.4 mAh·g^(-1) at 5.0C.Even at 1.0C and 60℃,it can maintain a reversible discharge specific capacity of 114.6 mAh·g^(-1) with 0.21% of capacity decay per cycle after 200 cycles,which is significantly lower than 0.40% for the pristine NCM powders.Importantly,the charge transfer resistance of 238.89 Ω for the NCM-KP electrode is significantly lower than 947.41 Ω for the pristine NCM one by restricting the interfacial side reactions.Therefore,combining K+doping and Li_(3)PO_(4) coating is an effective strategy to enable the significant improvement of the electrochemical property of high-nickel cathode materials,which may be mainly attributed to the widened diffusion pathway and the formed Li_(3)PO_(4) protective layer,thus promoting Li~+diffusion rate and preventing the erosion of HF.
基金supported by a National Research Foundation of Korea(NRF)grant funded by the Korean government(MSIT)(No.2018R1A6A1A03025708).
文摘Aqueous zinc(Zn)-ion batteries(AZIBs)have gained significant interest in energy storage due to several unique advantages.Utilizing waterbased electrolytes enhances environmental sustainability,while the abundance and affordability of Zn offer economic benefits.Manganese(Mn)-based materials,commonly used as cathodes in these batteries,provide high theoretical capacity,high electrical conductivity,and good structural stability.However,these materials suffer from capacity degradation over repeated cycles due to structural collapse and limited conductivity.To address this problem,we synthesized a magnesium(Mg)-and Mn-based composite,Mg^(2+)-Mn_(3)O_(4),using the hydrothermal method with an optimized amount of ammonium hydroxide(NH_(4)OH)solution.This approach effectively stabilizes the structure during cycling,enhancing both capacity retention and conductivity.The Zn^(2+)/H+intercalation/deintercalation process was confirmed by experimental results and ex-situ X-ray diffraction analysis,which demonstrates that Mg^(2+),along with optimized NH_(4)OH amount,prevents structural collapse and improves conductivity.Under optimal process conditions,the composite electrode(Mg^(2+)-Mn_(3)O_(4)–8 ml)achieved a capacity of 173.58 mA h g^(-1) at 0.5 A g^(-1),with excellent rate performance of 71.39 mA h g^(-1) at 10 A g^(-1).Remarkably,even at 5 A g^(-1),the electrode maintained a capacity of 86.87 mA h g^(-1) over 2100 cycles,underscoring the role of Mg^(2+)and NH_(4)OH in enhancing the reversible insertion/extraction stability of Zn^(2+)in Mn-based layered materials.This study presents a novel strategy for metal-ion incorporation in Mn-based AZIBs,offering insights into the optimization of cathode materials and advancing research on associated storage mechanisms.
基金financially supported by the National Natural Science Foundation of China(No.51964012)。
文摘The high-value utilization of manganese ore tailings is of great significance for saving mineral resources and achieving environmental protection.Herein,an olivine LiFe_(0.5)Mn_(0.5)PO_(4)/rGO composite is synthesized by a simple precipitation method and subsequent high-temperature calcination process using the manganese ore tailings as raw material.The prepared LiFe_(0.5)Mn_(0.5)PO_(4)/rGO composite exhibits superior cycling stability(with 113.5 mAh·g^(-1)after 300 cycles at1.0C(1.0C=170 mA·g^(-1)))and superior rate performance(with 65.6 mAh·g^(-1)at 10.0C).Ex-situ XRD and electrochemical impedance spectroscopy(EIS)analyses evidence that the LiFe_(0.5)Mn_(0.5)PO_(4)/rGO material has excellent structural stability and electrochemical reversibility during charge and discharge processes.Furthermore,the LiFe_(0.5)Mn_(0.5)PO_(4)/rGO//graphite full Li-ion battery also exhibits excellent cycling stability indicating its potential commercialization value.
基金supported by the National Key R&D Program of China(Grant No.2023YFB3710601)the National Natural Science Foundation of China(Grant Nos.52203385 and 52171056)+2 种基金the CNNC Science Fund for Talented Young Scholars,the Institute of Metal Research(IMR)Innovation Fund(Grant No.2021-ZD02)the Natural Science Foundation of Liaoning Province(Grant No.2022-BS-009)Young Elite Scientists Sponsorship Program by CAST(Grant No.YESS20220225).
文摘B_(4)C/Al composites are widely utilized as neutron absorbing materials for the storage and transportation of spent nuclear fuel.In order to improve the high-temperature mechanical properties of B_(4)C/Al composites,in-situ nano-Al_(2)O_(3)was introduced utilizing oxide on Al powder surface.In this study,the Al_(2)O_(3)content was adjusted by utilizing spheroid Al powder with varying diameters,thereby investigating the impact of Al_(2)O_(3)content on the tensile properties of(B_(4)C+Al_(2)O_(3))/Al composites.It was found that the pinning effect of Al_(2)O_(3)on the grain boundaries could hinder the recovery of dislocations and lead to dislocation accumulation at high temperature.As the result,with the increase in Al_(2)O_(3)content and the decrease in grain size,the high-temperature strength of the composites increased significantly.The finest Al powder used in this investigation had a diameter of 1.4μm,whereas the resultant composite exhibited a maximum strength of 251 MPa at room temperature and 133 MPa at 350℃,surpassing that of traditional B_(4)C/Al composites.
基金supported by Department of Education of Jilin Province and Technology Research Projects(JJKH20220183KJ)Jilin Engineering Normal University PhD Startup Foundation(BSKJ201841)Jilin Engineering Normal University Undergraduate Innovation Training Program Project(202410204027,202410204057).
文摘In this work,porous hollow spherical NiCo_(2)S_(4) nanomaterials composed of loosely porous nanowires on the surface were prepared using nickel foam as the substrate through a secondary hydrother-mal reaction method.The synthesized materials were then characterized using techniques such as X-ray powder diffraction,scanning electron microscopy and energy-dispersive X-ray spectroscopy.Finally,elec-trochemical performance tests were conducted on the synthesized cobalt-nickel bimetallic compound elec-trode materials,the specific capacitance of the synthesized NiCo_(2)S_(4) nanomaterial reached 3.20 F·cm-2,Moreover,the specific capacitance remained 95.8%of its initial value after 500 cycles.The electrochemical performance was superior to that of the prepared NiCo2O4 nanomaterial.The results suggest that the prepared NiCo_(2)S_(4) with special structure could be a great potential as a material for supercapacitor electrodes.
基金Project(2007BAQ01055)supported by the National Key Technology R&D Program of ChinaProject(2011SCU11081)supported by the Sichuan University Funds for Young Scientists,ChinaProject(20120181120103)supported by Ph.D.Programs Foundation of the Ministry of Education of China
文摘The Li3V2（PO4）3/C composite cathode material was synthesized via sol-gel method using three different chelating agents （citric acid, salicylic acid and polyacrylic acid） at pH value of 3 or 7. The crystal structure, morphology, specific surface area and electrochemical performance of the prepared samples were investigated by X-ray diffraction （XRD）, scanning electron microscopy （SEM）, cyclic voltammetry （CV）, electrochemical impedance spectroscopy （EIS） and galvanostatic charge/discharge test. The results show that the effects of pH value on the performance of the prepared materials are greatly related to the chelating agents. With salicylic acid or polyacrylic acid as the chelating reagent, the structure, morphology and electrochemical performance of the samples are greatly influenced by the pH values. However, the structure of the materials with citric acid as the chelating agent does not change as pH value changes, and the materials own uniform particle size distribution and good electrochemical performance. It delivers an initial discharge capacity of 113.58 mA·h/g at 10C, remaining as high as 108.48 mA·h/g after 900 cycles, with a capacity retention of 95.51%.
基金Project (51162026) supported by the National Natural Science Foundation of ChinaProjects (20100480949, 201104509) supported by China Postdoctoral Science FoundationProject (133274341015501) supported by Postdoctoral Science Foundation of Central South University, China
文摘Li3V2（PO4）3 precursor was obtained with V2Os.nH2O , LiOH＇H2O, NH4H2PO4 and sucrose as starting materials by grinding-sol-gel method, and then the monoclinic-typed Li3Vz（PO4）3 cathode material was prepared by sintering the amorphous Li3V2（PO4）3. The as-sintered samples were investigated by X-ray diffraction （XRD）, transmission electron microscopy （TEM）, N2 adsorption-desorption and electrochemical measurement. It is found that Li3Vz（PO4）3 sintered at 700 ℃ possesses good wormhole-like mesoporous structure with the largest specific surface area of 188 cmZ/g, and the smallest pore size of 9.3 nm. Electrochemical test reveals that the initial discharge capacity of the 700 ℃ sintered sample is 155.9 mA.h/g at the rate of 0.2C, and the capacity retains 154 mA.h/g after 50 cycles, exhibiting a stable discharge capacity at room temperature.
基金Project (2007BAQ01055) supported by the National Key Technology R&D Programs of ChinaProject (50574063) supported by theNational Natural Science Foundation of China
文摘LiFePO4-Li3V2（PO4）3 composites were synthesized by solid-hydrothermal method and by ball milling,respectively.The electrochemical performance of the solid-hydrothermally obtained materials（C-LFVP） was significantly improved compared with LiFePO4（LFP） and Li3V2（PO4）3（LVP）,and it was also much better than that of the ball-milled LiFePO4-Li3V2（PO4）3（P-LFVP）.C-LFVP and P-LFVP both had four REDOX peaks（voltage plateaus）,which coincided with that of LFP and LVP.Some new trace substances were found in C-LFVP which had more perfect morphology,this was responsible for the better electrochemical performance of C-LFVP than P-LFVP.
基金Project (20771100) supported by the National Natural Science Foundation of China
文摘Li3V2-2/3xMnx（PO4）3（0≤x≤0.12） powders were synthesized by sol-gel method. The effect of Mn2＋-doping on the structure and electrochemical performances of Li3V2（PO4）3/C was characterized by XRD, SEM, XPS, galvanostatic charge /discharge and electrochemical impedance spectroscopy（EIS）. The XRD study shows that a small amount of Mn2＋-doped does not alter the structure of Li3V2（PO4）3/C materials, and all Mn2＋-doped samples are of pure single phase with a monoclinic structure （space group P21/n）. The XPS analysis indicates that valences state of V and Mn are ＋3 and ＋2 in Li3V1.94Mn0.09（PO4）3/C, respectively, and the citric acid in raw materials was decomposed into carbon during calcination, and residual carbon exists in Li3V1.94Mn0.09（PO4）/C. The results of electrochemical measurements show that Mn2＋-doping can improve the cyclic stability and rate performance of these cathode materials. The Li3V1.94Mn0.09（PO4）3/C cathode material shows the best cyclic stability and rate performance. For example, at the discharge current density of 40 mA/g, after 100 cycles, the discharge capacity of Li3V1.94Mn0.09（PO4）3/C declines from initial 158.8 mA·h/g to 120.5 mA·h/g with a capacity retention of 75.9%; however, that of the Mn-undoed sample declines from 164.2 mA·h/g to 72.6 mA·h/g with a capacity retention of 44.2%. When the discharge current is increased up to 1C, the intial discharge capacity of Li3V1.94Mn0.09（PO4）3/C still reaches 146.4 mA·h/g, and the discharge capacity maintains at 107.5 mA·h/g after 100 cycles. The EIS measurement indicates that Mn2＋-doping with a appropriate amount of Mn2＋ decreases the charge transfer resistance, which is favorable for the insertion/extraction of Li＋.
基金Project (0991025) supported by Natural Science Foundation of Guangxi, ChinaProject (51164007) supported by the National Natural Science Foundation of ChinaProject (201101ZD008) supported by Educational Commission of Guangxi, China
文摘The LiMnPO4/C composite material was synthesized via a sol-gel method based on the citric acid. The X-ray diffraction （XRD）, scanning electron microscopy （SEM） and electrochemical performance tests were adopted to characterize the properties of LiMnPO4/C. The XRD studies show that the pure olivine phase LiMnPO4 can be obtained at a low temperature of 500 °C. The SEM analyses illustrate that the citric acid used as the chelating reagent and carbon source can restrain the particle size of LiMnPO4/C well. The LiMnPO4/C sample synthesized at 500 °C for 10 h performs the highest initial discharge capacity of 122.6 mA-h/g, retaining 112.4 mA-h/g over 30 cycles at 0.05C rate. The citric acid based sol-gel method is favor to obtain the high electrochemical performance of LiMnPO4/C.
基金Project(2013AA050901)supported by the National High-tech Research and Development Program of China
文摘In order to enhance electrochemical properties of LiFePO4 （LFP） cathode materials, spherical porous nano/micro structured LFP/C cathode materials were synthesized by spray drying, followed by calcination. The results show that the spherical precursors with the sizes of 0.5-5 μm can be completely converted to LFP/C when the calcination temperature is higher than 500 ℃. The LFP/C microspheres obtained at calcination temperature of 700 ℃ are composed of numerous particles with sizes of -20 nm, and have well-developed interconnected pore structure and large specific surface area of 28.77 mE/g. The specific discharge capacities of the LFP/C obtained at 700 ℃ are 162.43, 154.35 and 144.03 mA.h/g at 0.5C, 1C and 2C, respectively. Meanwhile, the capacity retentions can reach up to 100% after 50 cycles. The improved electrochemical properties of the materials are ascribed to a small Li＋ diffusion resistance and special structure of LFP/C microspheres.
基金supported by Natural Science of Guangxi(No.0991025)Program for Excellent Talents in Guangxi Higher Education Institutions(GuiJiaoRen[No.2010]65)+5 种基金National Natural Science Foundation of China(No.51164007)Innovation Project of Guangxi Graduate EducationEducational Commission of Guangxi(No.201101ZD008)the Important National Science&Technology Specific(No.2008ZX07317-02-03E)the Key Science Research of Ministry of Education of the Pepople's Republic of China(GuiKeGong0092008)the Provincial Natural Science Foundation of Guangxi
文摘LiMnPO_4 /C composites were synthesized via solid-state reaction with different carbon sources: sucrose, citric acid and oxalic acid. The sam- ples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and electrochemical performance test. The results of XRD reveal that carbon coating has no effect on the phase of LiMnPO_4 . The LiMnPO_4 /C synthesized at 600 °C with citric acid as carbon source shows an initial discharge capacity of 117.8 mA·hg^-1 at 0.05 C rate. After 30 cycles, the capacity remains 98.2 mAh·g^-1 . The improved electrochemical properties of LiMnPO_4 /C is attributed to the decomposition of organic acid during the sintering process.
基金supported by the National Projects of NSFC(21322101 and 21231005)MOE(B12015 and IRT13R30)
文摘LiNiCoAlO（NCA） with Zr（OH）coating is demonstrated as high performance cathode material for lithium ion batteries（LIBs）. The coated materials are synthesized via a simple dry coating method of NCA with Zr（OH）powders, and then characterized with scanning electron microscopy（SEM）, transmission electron microscopy（TEM） and X-ray photoelectron spectroscopy（XPS）. Experimental results show that amorphous Zr（OH）powders have been successfully coated on the surface of spherical NCA particles, exhibiting improved electrochemical performance. 0.50 wt% Zr（OH）coated NCA delivers a capacity of 197.6 mAh/g at the first cycle and 154.3 mAh/g after 100 cycles with a capacity retention of 78.1% at 1 C rate. In comparison, the pure NCA shows a capacity of 194.6 mAh/g at the first cycle and 142.5 mAh/g after 100 cycles with a capacity retention of 73.2% at 1 C rate. Electrochemical impedance spectroscopy（EIS） results show that the coated material exhibits a lower resistance, indicating that the coating layer can efficiently suppress transition metals dissolution and decrease the side reactions at the surface between the electrode and electrolyte. Therefore, surface coating with amorphous Zr（OH）is a simple and useful method to enhance the electrochemical performance of NCA-based materials for the cathode of LIBs.
基金supported by the Singapore Centre for 3D Printing which is funded by the Singapore National Research Foundation.
文摘The rapid development of additive manufacturing and advances in shape memory materials have fueled the progress of four-dimensional （4D） printing. With the right external stimulus, the need for human interaction, sensors, and batteries will be eliminated, and by using additive manufacturing, more complex devices and parts can be produced. With the current understanding of shape memory mechanisms and with improved design for additive manufacturing, reversibility in 4D printing has recently been proven to be feasible. Conventional one-way 4D printing requires human interaction in the programming （or shapesetting） phase, but reversible 4D printing, or two-way 4D printing, will fully eliminate the need for human interference, as the programming stage is replaced with another stimulus. This allows reversible 4D printed parts to be fully dependent on external stimuli; parts can also be potentially reused after every recovery, or even used in continuous cycles-an aspect that carries industrial appeal. This paper presents a review on the mechanisms of shape memory materials that have led to 4D printing, current findings regarding 4D printing in alloys and polymers, and their respective limitations. The reversibility of shape memory materials and their feasibility to be fabricated using three-dimensional （3D） printing are summarized and critically analyzed. For reversible 4D printing, the methods of 3D printing, mechanisms used for actuation, and strategies to achieve reversibility are also highlighted. Finally, prospective future research directions in reversible 4D printing are suggested.
