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MoSe_(2)/TiO_(2)heterostructure integrated in N-doped carbon nanosheets assembled porous core-shell microspheres for enhanced sodium storage

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Nano Research 2023年第7期16卷 9398-9406页

作者： Nianxiang Shi Guangzeng Liu Baojuan Xi Xuguang An Changhui Sun xinzheng Liu Shenglin xiong School of Chemistry and Chemistry Engineering Qilu Normal UniversityJinan 250200China School of Chemistry and Chemical Engineering and State Key Laboratory of Crystal MaterialsShandong UniversityJinan 250100China School of Mechanical Engineering Chengdu UniversityChengdu 610106China

Engineering the structure and composition of electrode materials is one of the essential means for achieving excellent electrochemical performance.The rational design of Na+host materials is still a massive challenge for sodium ion batteries(SIBs).Herein,MoSe_(2)/TiO_(2)heterostructure is integrated with N-doped carbon nanosheets to assemble into hierarchical flowerlike porous core-shell microspheres(MoSe_(2)/TiO_(2)@N-C),which is firstly reported by room-temperature stirring coupled with vulcanization treatment.The cavity of the core-shell structure could provide enough storage space for Na+and alleviate the volume expansion during charge/discharge processes.The apertures between nanosheets provide a guarantee for the rapid penetration of electrolyte to enhance the utilization rate of electrode materials.Furthermore,building heterostructures by combining different phase structures can facilitate electron transfer and accelerate reaction kinetics.Benefiting from the synergistic contributions of structure and composition,MoSe_(2)/TiO_(2)@N-C as SIBs anode material shows better reversible capacities of 302.5 mAh·g^(-1)at 1 A·g^(-1)for 400 cycles and 217.4 mAh·g^(-1)at 4 A·g^(-1)for 900 cycles.Strikingly,the reversible capacities can be restored entirely to the initial level after a high current density cycle.

关键词： MoSe_(2)/TiO_(2) flower-like hierarchical porous core-shell microspheres heterostructure sodium ion batteries

Introducing Ce ions and oxygen defects into V_(2)O_(5)nanoribbons for efficient aqueous zinc ion storage

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Nano Research 2023年第2期16卷 2445-2453页

作者： Mingying Bao Zhengchunyu Zhang Xuguang An Jie Liu Jinkui Feng Baojuan Xi Shenglin xiong Key Laboratory of Colloid and Interface Chemistry Ministry of EducationSchool of Chemistry and Chemical EngineeringState Key Laboratory of Crystal MaterialsShandong UniversityJinan 250100China Key Laboratory of Mechanical Engineering of Education School of Mechanical EngineeringChengdu UniversityChengdu 610106China Key Laboratory of High Performance Ceramics and Superfine Microstructure Shanghai Institute of CeramicsChinese Academy of SciencesShanghai 200050China School of Materials Science and Engineering Shandong UniversityJinan 250061China

Cost-effectively,eco-friendly rechargeable aqueous zinc-ion batteries(AZIBs)have reserved widespread concerns and become outstanding candidate in energy storage systems.However,the progress pace of AZIBs suffers from limitation of suitable and affordable cathode materials.Herein,a double-effect strategy is realized in a one-step hydrothermal treatment to prepare V_(2)O_(5)nanoribbons with intercalation of Ce and introduction of abundant oxygen defects(Od-Ce@V_(2)O_(5))to enhance electrochemical performance synergistically.Coupled with the theoretical calculation results,the introduction of Ce ions intercalation and oxygen vacancies in V2O5 structure enhances the electrical conductivity,reduces the adsorption energy of zinc ions,enlarges the interlayer distance,renders the structure more stable,and facilitates rapid diffusion kinetics.As expected,the desirable cathode delivers the reversible capacity of 444 mAh·g^(−1)at 0.5 A·g^(−1)and shows excellent Coulombic efficiency,as well as an extraordinary energy density of 304.9 Wh·kg^(−1).The strategy proposed here may aid in the further development of cathode materials with stable performance for AZIBs.

关键词： double-effect Ce element doping oxygen defects Od-Ce@V_(2)O_(5) aqueous zinc-ion batteries

Synthesis of carbon nanotubes-supported porous silicon microparticles in low-temperature molten salt for highperformance Li-ion battery anodes

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Nano Research 2022年第7期15卷 6184-6191页

作者： Qianliang Zhang Baojuan Xi Weihua Chen Jinkui Feng Yitai Qian Shenglin xiong Key Laboratory of Colloid and Interface Chemistry Ministry of EducationSchool of Chemistry and Chemical EngineeringState Key Laboratory of Crystal MaterialsShandong UniversityJinan 250100China Key Laboratory of Material Processing and Mold of Ministry of Education Zhengzhou UniversityZhengzhou 450001China Key Laboratory for Liquid-Solid Structural Evolution&Processing of Materials Ministry of EducationSchool of Materials Science and EngineeringShandong UniversityJinan 250061China

Silicon-based materials has attracted attention as a promising candidate for lithium-ion batteries(LIBs)with high energy density.However,severe volume variation,pulverization,and poor conductivity hindered the development of Si based materials.In this study,porous Si microparticles supported by carbon nanotubes(p-Si/CNT)are fabricated through simple molten salt assisted dealloying process at low temperature followed by acid treatment.The ZnCl2 molten salt not only provides the liquid environment to enhance the reaction,but also participates the dealloying process and works as template for porous structure when removes by acid treatment.Additionally,distribution of defect sites in CNTs also increases after molten salt process.Density function theory(DFT)calculations further prove the defects could improve the adsorption of Li+.The participation of CNTs can also contribute to the reaction kinetics and retain the integrity of the electrode.As expected,the p-Si/CNT anode manifests enhanced lithium-storage performance in terms of superior cycling stability and good rate capability.The p-Si/CNT//LiCoO_(2) full cell assembly further demonstrates its potential as a prospective anode for high-performance LIBs.

关键词： porous Si microparticles carbon nanotubes molten salt lithium-ion batteries

Rational design of F,N-rich artificial interphase via chemical prelithiation initiation strategy enabling high coulombic efficiency and stable micro-sized SiO anodes

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Journal of Energy Chemistry 2024年第5期92卷 224-232页

作者： Quanyan Man Hengtao Shen Chuanliang Wei Baojuan Xi Shenglin xiong Jinkui Feng Key Laboratory for Liquid-Solid Structural Evolution and Processing of Materials(Ministry of Education) School of Materials Science and EngineeringShandong UniversityJinan 250061ShandongChina School of Chemistry and Chemical Engineering Shandong UniversityJinan 250100ShandongChina

Silicon monoxide(SiO)is regarded as a potential candidate for anode materials of lithium-ion batteries(LIBs).Unfortunately,the application of SiO is limited by poor initial Coulombic efficiency(ICE)and unsteady solid electrolyte interface(SEI),which induce low energy,short cycling life,and poor rate properties.To address these drawbacks of SiO,we achieve in-situ construction of robust and fast-ion conducting F,N-rich SEI layer on prelithiated micro-sized SiO(P-μSiO)via the simple and continuous treatment ofμSiO in mild lithium 4,4′-dimethylbiphenyl solution and nonflammable hexafluorocyclotriphosphazene solution.Chemical prelithiation eliminates irreversible capacity through pre-forming inactive lithium silicates.Meanwhile,the symbiotic F,N-rich SEI with good mechanical stability and fast Li^(+)permeability is conductive to relieve volume expansion ofμSiO and boost the Li+diffusion kinetics.Consequently,the P-μSiO realizes an impressive electrochemical performance with an elevated ICE of 99.57%and a capacity retention of 90.67%after 350 cycles.Additionally,the full cell with P-μSiO anode and commercial LiFePO_(4) cathode displays an ICE of 92.03%and a high reversible capacity of 144.97 mA h g^(-1).This work offers a general construction strategy of robust and ionically conductive SEI for advanced LIBs.

关键词： Chemical prelithiation Silicon monoxide SEI Lithium-ion batteries Interphase engineering

Molybdenum Oxynitride Atomic Nanoclusters Bonded in Nanosheets of N-Doped Carbon Hierarchical Microspheres for Efficient Sodium Storage

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Nano-Micro Letters 2022年第10期14卷 148-163页

作者： xiaona Pan Baojuan Xi Huibing Lu Zhengchunyu Zhang Xuguang An Jie Liu Jinkui Feng Shenglin xiong School of Chemistry and Chemical Engineering State Key Laboratory of Crystal MaterialsShandong UniversityJinan 250100People’s Republic of China School of Mechanical Engineering Chengdu UniversityChengdu 610106People’s Republic of China The State Key Laboratory of High Performance Ceramics and Superfine Microstructure Shanghai Institute of CeramicsChinese Academy of SciencesShanghai 200050People’s Republic of China School of Materials Science and Engineering Shandong UniversityJinan 250100People’s Republic of China

Transition metal nitrides have attracted considerable attention as great potential anode materials due to their excellent metallic conductivity and high theoretical specific capacity.However,their cycling performance is impeded by their instability caused by the reaction mechanism.Herein,we report the engineering and synthesis of a novel hybrid architecture composed of MoO2.0N0.5 atomic nanoclusters bonded in nanosheets of N-doped carbon hierarchical hollow microspheres(MoO2.0N0.5/NC)as an anode material for sodium-ion batteries.The facile self-templating strategy for the synthesis of MoO2.0N0.5/NC involves chemical polymerization and subsequent one-step calcination treatments.The design is benefi-cial to improve the electrochemical kinetics,buffer the volume variation of electrodes during cycling,and provide more interfacial active sites for sodium uptake.Due to these unique structural and compositional merits,these MoO2.0N0.5/NC exhibits excellent sodium storage performance in terms of superior rate capability and stable long cycle life.The work shows a feasible and effective way to design novel host candidates and solve the long-term cycling stability issues for sodium-ion batteries.

关键词： Molybdenum oxynitride Atomic nanocluster Hollow microspheres Sodium-ion batteries

Rational cathode configuration with bilayer membranes to engineer current-collector-free high-areal-sulfur lithium-sulfur batteries

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Nano Research 2024年第6期17卷 5224-5232页

作者： Jianmei Han Hua Zhang Peng Wang Ning Song Xuguang An Baojuan Xi Shenglin xiong College of Chemistry and Chemical Engineering Taishan UniversityTai’an 271021China Key Laboratory of the Colloid and Interface Chemistry Ministry of Educationand School of Chemistry and Chemical EngineeringShandong UniversityJinan 250100China School of Mechanical Engineering Chengdu UniversityChengdu 610106China

The application of light-weight current collectors is preferred because of the increased energy density of the batteries.Bearing it in mind,the cathode is designed with self-made paperlike memberane as current collector coupled with another interlayer to enable the high-energy-density lithium-sulfur batteries.Via a facile and green step-by-step methodology,the hybrid membrane is finalized successfully,consisting of reduced graphene oxide sheets covering paper-derived carbon(GPC)bearing Fe@Fe2O3 and Fe1−xS@Fe2O3 core-shell nanoparticles(FeFeO/FeSFeO@GPC).The film works as the current collector and interlayer simultaneously considering the porous and conductive features.As demonstrated by the electrochemical testing,the FeFeO/FeSFeO@GPC hybrid cell exhibits attractive cycling stability and superior rate capability.The cell configuration and structural/composition merits of FeFeO/FeSFeO@GPC film facilitate the faster reaction kinetics,conducive to the improvement of capacity retention.In view of the effective cathode design,the areal sulfur loading is increased to 10.46 mg·cm^(−2)and a reversible capacity of 6.67 mAh·cm^(−2)can be retained after 60 cycles at 0.1 C.

关键词： light-weight self-made current collector core-shell high-areal-sulfur lithium-sulfur batteries

Recent progress,mechanisms,and perspectives for crystal and interface chemistry applying to the Zn metal anodes in aqueous zinc-ion batteries

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SusMat 2022年第2期2卷 114-141页

作者： Zhengchunyu Zhang Baojuan Xi xiaojian Ma Weihua Chen Jinkui Feng Shenglin xiong School of Chemistry and Chemical Engineering State Key Laboratory of Crystal MaterialsShandong UniversityJinanP.R.China Key Laboratory of Material Processing and Mold of Ministry of Education Zhengzhou UniversityZhengzhouP.R.China Key Laboratory for Liquid−Solid Structural Evolution&Processing of Materials Ministry of EducationSchool of Materials Science and EngineeringShandong UniversityJinanP.R.China

The need for large-scale electrochemical energy storage devices in the future has spawned several new breeds of batteries in which aqueous zinc ion batteries(AZIBs)have attracted great attention due to their high safety,low cost,and excellent electrochemical performance.In the current research,the dendrite and corrosion caused by aqueous electrolytes are the main problems being studied.However,the research on the zinc metal anode is still in its infancy.We think it really needs to provide clear guidelines about how to reasonably configure the system of AZIBs to realize high-energy density and long cycle life.Therefore,it is worth analyzing the works on the zinc anode,and several strategies are proposed to improve the stability and cycle life of the battery in recent years.Based on the crystal chemistry and interface chemistry,this review reveals the key factors and essential causes that inhibit dendrite growth and side reactions and puts forward the potential prospects for future work in this direction.It is foreseeable that guiding the construction of AZIBs with high-energy density and long cycle life in various systems would be quite possible by following this overview as a roadmap.

关键词： crystal chemistry interface chemistry side reaction Zn dendrites Zn metal anode

In-situ embedding CoTe catalyst into 1D-2D nitrogen-doped carbon to didirectionally regulate lithium-sulfur batteries

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Nano Research 2022年第10期15卷 8972-8982页

作者： Bin Li Peng Wang Baojuan Xi Ning Song Xuguang An Weihua Chen Jinkui Feng Shenglin xiong Key Laboratory of Colloid and Interface Chemistry Ministry of EducationSchool of Chemistry and Chemical EngineeringState Key Laboratory of Crystal MaterialsShandong UniversityJinan 250100China Key Laboratory of Mechanical Engineering of Education School of Mechanical EngineeringChengdu UniversityChengdu 610106China Key Laboratory of Material Processing and Mold of Ministry of Education Zhengzhou UniversityZhengzhou 450001China School of Materials Science and Engineering Shandong UniversityJinan 250061China

Lithium-sulfur(Li-S)batteries have been widely investigated attributed to their advantages of high energy density and cost effectiveness.However,it is still limited by the uncontrolled shuttle effect of the sulfur cathode and the promiscuous dendrite growth over the lithium anode.To handle the above issues,the highly conductive CoTe catalyst is precisely loaded onto nitrogendoped nanotube and graphene-like carbon(CoTe NCGs),which is employed as a bi-functionally integrated host.On the lithium anode,the CoTe NCGs with excellent lithiophilic property effectively regulate the uniform deposition of lithium and achieve the effect of suppressing the disorderly growth of lithium dendrites.On the sulfur cathode,the electrochemical conversion of lithium polysulfides(LiPSs)is catalyzed to mitigate the notorious shuttle effect.In view of the bifunctionality of CoTe NCGs,the assembled full cell can be steadily stable even for 800 cycles at a high rate of 2 C,and the capacity decay rate is only 0.05%per cycle.The areal capacity of 6.0 mAh·cm^(−2) is well retained after 50 cycles under the conditions of high sulfur loading,poor electrolyte(a low electrolyte-to-sulfur ratio,E/S=4.2),and low negative to positive capacity ratio(N/P=1.6:1).

关键词： CoTe nanocrystals dual-functional shuttling effect lithium dendrite Li-S batteries

Room-temperature liquid metal engineered iron current collector enables stable and dendrite-free sodium metal batteries in carbonate electrolytes

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Journal of Materials Science & Technology 2022年第20期115卷 156-165页

作者： Chuanliang Wei Liwen Tan Yuchan Zhang Huiyu Jiang Baojuan Xi Shenglin xiong Jinkui Feng Key Laboratory for Liquid-Solid Structural Evolution&Processing of Materials(Ministry of Education) Research Center for Carbon NanomaterialsSchool of Materials Science and EngineeringShandong UniversityJinan 250061China School of Chemistry and Chemical Engineering Shandong UniversityJinan 250100China

Metallic sodium(Na)is believed to be a promising anode material for sodium-ion batteries(SIBs)due to its low electrochemical potential,high theoretical specific capacity,superior electrical conductivity,and so on.However,issues such as high chemical activity,the growth of Na dendrites,large volume change,and unstable interface impede its practical application.We design a cheap iron(Fe)-based substrate decorated by a thin liquid metal Ga layer for stable and dendrite-free Na metal anodes in low-cost carbonate electrolytes.The inherent mechanism of Ga-based liquid metal in inhibiting the growth of Na dendrites was revealed for the first time.Liquid metal Ga with sodiophilic property can act as nucleation seeds to decrease the nucleation barrier and induce homogeneous Na+flux,resulting in uniform and dendrite-free Na deposition.Full cells with Na_(3)V_(2)(PO_(4))_(3) cathode were also assembled to verify the practical application ability of the modified Na metal anode.Under the regulation of the liquid metal layer,the Coulombic efficiency,cycling life,and capacity of batteries are obviously enhanced.The strategy proposed here cannot only reduce the cost of batteries but also improve their electrochemical and safety performance.

关键词： Stainless steel Current collector Sodium metal anode Liquid metal Carbonate electrolyte