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Bimetallic selenide heterostructure with directional built-in electricfield confined in N-doped carbon nanofibers for superior sodium storage with ultralong lifespan

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Journal of Energy Chemistry 2024年第4期91卷 407-416页

作者： Junying Weng Degui Zou Wenyong Yuan Pengfei Zhou Minghui Ding Jin Zhou Hailin Cong fangyi cheng School of Materials Science and Engineering Shandong University of TechnologyZibo 255000ShandongChina School of Chemistry and Chemical Engineering Shandong University of TechnologyZibo 255000ShandongChina Key Laboratory of Advanced Energy Materials Chemistry(Ministry of Education) College of ChemistryNankai UniversityTianjin 300071China

Constructing heterostructure is considered as an effective strategy to address the sluggish electronic and ionic kinetics of anode materials for sodium ion batteries(SIBs).However,realizing the orientated growth and uniform distribution of the heterostructure is still a great ***,the regulated novel CoSe_(2)/NiSe_(2)heterostructure confined in N-doped carbon nanofibers(CoSe_(2)/NiSe_(2)@N-C)are prepared by using Co/Ni-ZIF template,in which,the CoSe_(2)/NiSe_(2)heterostructures realize uniform distribution on a micro *** from the unique heterostructure and N-doped carbon nanofibers,the CoSe_(2)/NiSe_(2)@N-C deliveries superior rate capability and durable cycle lifespan with a reversible capacity of 400.5 mA h g^(-1)after 5000 cycles at 2 A g^(-1).The Na-ion full battery with CoSe_(2)/NiSe_(2)@N-C anode and layered oxide cathode displays a remarkable energy density of 563 W h kg^(-1)with 241.1 W kg^(-1)at 0.1 A g^(-1).The theoretical calculations disclose that the periodic and directional built-in electric-field along with the heterointerfaces of CoSe_(2)/NiSe_(2)@N-C can accelerate electrochemical reaction *** in(ex)situ experimental measurements reveal the reversible conversion reaction and stable structure of CoSe_(2)/NiSe_(2)@N-C during Na+insertion/*** study highlights the potential ability of precisely controlled heterostructure to stimulate the electrochemical performances of advanced anode for SIBs.

关键词： CoSe_(2)/NiSe_(2) heterostructure Built-in electric-field Rate capability Ultralong lifespan Sodium ion batteries

Homogenous coating of Li^(+)conductive Li_(5)AlO_(4)on single-crystalline nonstoichiometric Li_(1.04)Ni_(0.92)Al_(0.04)O_(2)for rechargeable lithium-ion batteries

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Journal of Energy Chemistry 2024年第8期95卷 651-659,I0014页

作者： Guoyu Ding Shizhou Wang Jinhan Li Ziyan Wu Jiayu Chen Jiayong Du Xinhui Huang Kuiming Liu Yudong Zhang Zhonghan Wu Yiyang Peng Qiancheng Zhao Meng Yu fangyi cheng Key Laboratory of Advanced Energy Materials Chemistry(Ministry of Education) Engineering Research Center of High-efficiency Energy Storage(Ministry of Education)College of ChemistryNankai UniversityTianjin 300071China State Key Laboratory of Advanced Chemical Power Sources Nankai UniversityTianjin 300071China Haihe Laboratory of Sustainable Chemical Transformations Tianjin 300192China

Cobalt-free,nickel-rich LiNi_(1-x)Al_(x)O_(2)(x≤0.1)is an attractive cathode material because of high energy density and low cost but suffers from severe structural degradation and poor rate *** this study,we propose a molten salt-assisted synthesis in combination with a Li-refeeding induced aluminum segregation strategy to prepare Li_(5)AlO_(4)-coated single-crystalline slightly Li-rich Li_(1.04)Ni_(0.92)Al_(0.04)O_(2).The symbiotic formation of Li_(5)AlO_(4)from reaction between molten lithium hydroxide and doped aluminum in the bulk ensures a high lattice matching between the Ni-rich oxide and the homogenous conductive Li_(5)AlO_(4)that permits high Li^(+)*** from mitigated undesirable side reactions and phase evolution,the Li_(5)AlO_(4)-coated single-crystalline Li_(1.04)Ni_(0.92)Al_(0.04)O_(2)delivers a high specific capacity of220.2 mA h g^(-1)at 0.1 C and considerable rate capability(182.5 mA h g^(-1)at 10 C).Besides,superior capacity retention of 90.8%is obtained at 1/3 C after 100 cycles in a 498.1 mA h pouch full ***,the particulate morphology of Li_(1.04)Ni_(0.92)Al_(0.04)O_(2)remains intact after cycling at a cutoff voltage of 4.3 V,whereas slightly Li-deficient Li_(0.98)Ni_(0.97)Al_(0.05)O_(2)features intragranular cracks and irreversible lattice *** results highlight the value of molten salt-assisted synthesis and Li-refeeding induced elemental segregation strategy to upgrade Ni-based layered oxide cathode materials for advanced Li-ion batteries.

关键词： Aluminum segregation Surface coating Nonstoichiometric oxides Molten synthesis Cathode materials

Fluorine-Doped High-Performance Li_6PS_5Cl Electrolyte by Lithium Fluoride Nanoparticles for All-Solid-State Lithium-Metal Batteries

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Transactions of Tianjin University 2024年第3期30卷 250-261页

作者： Xiaorou Cao Shijie Xu Yuzhe Zhang Xiaohu Hu Yifan Yan Yanru Wang Haoran Qian Jiakai Wang Haolong Chang fangyi cheng Yongan Yang Institute of Molecular Plus School of Chemical Engineering and TechnologyTianjin UniversityTianjin 300072China Haihe Laboratory of Sustainable Chemical Transformations Tianjin 300192China Key Laboratory of Advanced Energy Materials Chemistry(Ministry of Education) Nankai UniversityTianjin 300071China

All-solid-state lithium-metal batteries(ASSLMBs)are widely considered as the ultimately advanced lithium batteries owing to their improved energy density and enhanced safety *** various solid electrolytes,sulfide solid electrolyte(SSE)Li_(6)PS_(5)Cl has garnered significant ***,its application is limited by its poor cyclability and low critical current density(CCD).In this study,we introduce a novel approach to enhance the performance of Li_(6)PS_(5)Cl by doping it with fluorine,using lithium fluoride nanoparticles(LiFs)as the doping *** F-doped electrolyte Li_(6)PS_(5)Cl-0.2LiF(nano)shows a doubled CCD,from 0.5 to 1.0 mA/cm~2 without compromising the ionic conductivity;in fact,conductivity is enhanced from 2.82 to 3.30 mS/cm,contrary to the typical performance decline seen in conventionally doped Li_(6)PS_(5)Cl *** symmetric Li|SSE|Li cells,the lifetime of Li_(6)PS_(5)Cl-0.2LiF(nano)is 4 times longer than that of Li_(6)PS_(5)Cl,achieving 1500 h vs.371 h under a charging/discharging current density of 0.2 mA/cm~*** Li|SSE|LiNbO_3@NCM721 full cells,which are tested under a cycling rate of 0.1 C at 30℃,the lifetime of Li_(6)PS_(5)Cl-0.2LiF(nano)is four times that of Li_(6)PS_(5)Cl,reaching 100 cycles vs.26 ***,the doping of nano-LiF off ers a promising approach to developing high-performance Li_(6)PS_(5)Cl for ASSLMBs.

关键词： Sulfide solid electrolyte All-solid-state lithium batteries Li_6PS_5Cl Lithium fluoride F-doping

Cell-nucleus structured electrolyte for low-temperature aqueous zinc batteries

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能源化学:英文版 2023年第8期83卷 324-332,I0010页

作者： Yang Dong Ning Zhang Zhaodong Wang Jinhan Li Youxuan Ni Honglu Hu fangyi cheng Key Laboratory of Advanced Energy Materials Chemistry(Ministry of Education) Engineering Research Center of High-efficiency Energy Storage(Ministry of Education)College of ChemistryNankai UniversityTianjin 300071China Haihe Laboratory of Sustainable Chemical Transformations Tianjin 300192China College of Chemistry and Materials Science Analytical Science and Technology of Hebei ProvinceHebei UniversityBaoding 071002HebeiChina

Rechargeable aqueous zinc(Zn) batteries hold great promise for large-scale energy storage,but their implementation is plagued by poor Zn reversibility and unsatisfactory low-temperature ***,we design a cell-nucleus structured electrolyte by introducing low-polarity 1,2-dimethoxyethane(DME) into dilute 1 M zinc trifluoromethanesulfonate(Zn(OTf)_(2)) aqueous solution,which features an OTf--rich Zn2^(+)-primary solvation sheath(PSS,inner nucleus) and the DMEmodulated Zn^(2+)-outer solvation sheath(outer layer).We find that DME additives with a low dosage do not participate in the Zn2+-PSS but reinforce the Zn-OTf-coordination,which guarantees good reaction kinetics under ultralow ***,DME breaks the original H-bonding network of H2O,depressing the freezing point of electrolyte to-52.4℃.Such a cell-nucleus-solvation structure suppresses the H_(2)O-induced side reactions and forms an anion-derived solid electrolyte interphase on Zn and can be readily extended to 1,*** as-designed electrolyte enables the Zn electrode deep cycling stability over 3500 h with a high depth-of-discharge of 51.3% and endows the Zn‖V_(2)O_(5)full battery with stable cycling over 1000 cycles at 40℃.This work would inspire the solvation structure design for low-temperature aqueous batteries.

关键词： Aqueous zinc batteries Low temperature Cell-nucleus solvation structure Zn metal anode Solid electrolyte interphase

Biaxial strained dual-phase palladium-copper bimetal boosts formic acid electrooxidation

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Nano Research 2022年第1期15卷 280-284页

作者： Jiarun Geng Zhuo Zhu Youxuan Ni Haixia Li fangyi cheng Fujun Li Jun Chen Key Laboratory of Advanced Energy Materials Chemistry(Ministry of Education) Renewable Energy Conversion and Storage Center(RECAST)College of ChemistryNankai UniversityTianjin 300071China

Surface strain engineering is considered as an effective strategy to promote the electrocatalytic properties of noble metal ***,we construct a dual-phase palladium-copper(DP-PdCu)bimetallic electrocatalyst with remarkable biaxial strain via a one-pot wet-chemical approach for formic acid *** biaxial strain originates from the lattice mismatch between the disordered face-centered cubic(FCC)phase and ordered body-centered cubic(BCC)phase in each of DP-PdCu:*** proportion of FCC and BCC phases and size of PdCu nanoparticles are dependent on the addition amount of:capping agent,cetyltrimethylammonium bromide(CTAB).Density functional theory calculations reveal the downshift of d-band:center of Pd atoms due to the interfacial strain,which weakens the adsorption strength of undesired *** merit the,DP-PdCu catalyst with superior mass activity of 0.55 A·mg_(pd)^(-1) and specific activity of 1.91 mA·cm_(pd)^(-2) toward formic acid oxidation,outperforming the single FCC/EICC PdCu and commercial Pd/C *** will provide new insights into the structure design of high-performance electrocatalysts via strain engineering.

关键词： palladium-copper dual phase biaxial strain formic acid oxidation size-dependence

Vision-based docking system for an aromatic-hydrocarbon-inspired reconfigurable robot

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Science China(Technological Sciences) 2024年第6期67卷 1798-1816页

作者： XING fangyi XU cheng LIU JinGuo XUE ZhiHui State Key Laboratory of Robotics Shenyang Institute of AutomationChinese Academy of SciencesShenyang110016China School of Automation and Electrical Engineering Shenyang Ligong UniversityShenyang110158China Institutes for Robotics and Intelligent Manufacturing Chinese Academy of SciencesShenyang110169China University of Chinese Academy of Sciences Beijing100049China

Aromatic hydrocarbons generally refer to compounds containing benzene *** types of isomers can be formed by replacing hydrogen atoms on the benzene *** this paper,an aromatic-hydrocarbon-inspired modular robot(AHIMR)is *** robot can be reassembled into different configurations suitable for various task requirements.A vision-based docking system is designed for the *** system primarily consists of two stages:a remote guidance stage and a precise docking *** the remote guidance stage,an object module is identified using an illumination adaptive target recognition algorithm,and then the active module moves to the docking area through communication with *** the precise docking stage,the active module calculates the relative pose with the object module using a perspective-n-point method and dynamically adjusts its posture to *** this process,a Kalman filter is used to reduce target occlusion and jitter *** addition,the docking system feasibility is verified via several simulation *** module docking accuracy is controlled within 0.01 m,which meets the reconfiguration task requirements of the *** the AHIMR submodule docking experiment,the active module accurately moves to the expected position with a docking success rate of 95%.

关键词： modular robot reconfiguration aromatic hydrocarbon autonomous docking visual identification

Anionic formulation of electrolyte additive towards stable electrocatalytic oxygen evolution in seawater splitting

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Journal of Energy Chemistry 2022年第9期31卷 361-369,I0010页

作者： Meng Yu Jinhan Li Fangming Liu Jiuding Liu Wence Xu Honglu Hu Xijie Chen Weichao Wang fangyi cheng Key Laboratory of Advanced Energy Materials Chemistry(Ministry of Education) Engineering Research Center on High-Efficiency Energy Storage(Ministry of Education)Renewable Energy Conversion and Storage CenterCollege of ChemistryNankai UniversityTianjin 300071China Integrated Circuits and Smart System Lab.(Shenzhen) Renewable Energy Conversion and Storage CenterTianjin Key Laboratory of Photo-Electronic Thin Film Device and TechnologyCollege of Electronic Information and Optical EngineeringNankai UniversityTianjin 300071China

Hydrogen generation through seawater electrolysis provides a promising,attractive pathway towards the utilization of sustainable ***,the catalytic activity and stability of oxygen evolution anode are severely limited by the chloride-induced corrosion and competitive oxidation *** this work,we demonstrate an anion-assisted performance improvement strategy by quick and universal screening of electrolyte additive via correlating Cl-repellency with the anionic ***,the addition of phosphate ions is found to enable highly stable alkaline seawater splitting at industry-level current density(0.5 A cm^(-2))over 500 h using transition metal hydroxides as anodic *** situ experiments and theoretical simulations further reveal that the dynamic anti-corrosion behaviors of surface-adsorbed phosphate ions are attributed to three factors including repelling Cl-ions without significantly blocking OH-diffusion,preventing transition metal dissolution and acting as a local pH buffer to compensate the fast OH-consumption under high current electrolysis.

关键词： Alkaline seawater splitting Oxygen evolution reaction Stability enhancement Chloride corrosion Phosphate

Designing interstitial boron-doped tunnel-type vanadium dioxide cathode for enhancing zinc ion storage capability

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Carbon Energy 2023年第8期5卷 78-86页

作者： Shiwen Wang Hang Zhang Kang Zhao Wenqing Liu Nairui Luo Jianan Zhao Shide Wu Junwei Ding Shaoming Fang fangyi cheng Henan Provincial Key Laboratory of Surface&Interface Science College of Materials and Chemical EngineeringZhengzhou University of Light IndustryZhengzhouChina Key Laboratory of Advanced Energy Materials Chemistry(Ministry of Education) College of ChemistryNankai UniversityTianjinChina

Chemical doping is a powerful method to intrinsically tailor the electrochemical properties of electrode ***,an interstitial boron-doped tunnel-type VO_(2)(B)is constructed via a facile hydrothermal *** analysis techniques demonstrate that boron resides in the interstitial site of VO_(2)(B)and such interstitial doping can boost the zinc storage kinetics and structural stability of VO_(2)(B)cathode during ***,we found that the boron doping level has a saturation limit peculiarity as proved by the quantitative ***,the 2 at.%boron-doped VO_(2)(B)shows enhanced zinc ion storage performance with a high storage capacity of 281.7 mAh g^(-1) at 0.1 A g^(-1),excellent rate performance of 142.2 mAh g^(-1) at 20 A g^(-1),and long cycle stability up to 1000 cycles with the capacity retention of 133.3 mAh g^(-1) at 5 A g^(-1).Additionally,the successful preparation of the boron-doped tunneltype α-MnO_(2) further indicates that the interstitial boron doping approach is a general strategy,which supplies a new chance to design other types of functional electrode materials for multivalence batteries.

关键词： cathode interstitial boron doping tunnel-type VO_(2)(B) zinc ion battery

Porous V2O5 nanofibers as cathode materials for rechargeable aqueous zinc-ion batteries

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Journal of Energy Chemistry 2019年第11期28卷 20-25页

作者： Xuyong Chen Liubin Wang Hang Li fangyi cheng Jun Chen Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education) College of Chemistry Nankai University

Rechargeable aqueous zinc-ion batteries are recently gaining incremental attention because of low cost and material abundance, but their development is plagued by limited choice of cathode materials with satisfactory cycling performance. Here, we report a porous V2O5 nanofibers cathode with high Znstorage performance in an aqueous Zn(CF3SO3)2 electrolyte. We propose a reaction mechanism based on phase transition from orthorhombic V2O5 to zinc pyrovanadate on first discharging and reversible Zn^2+ (de)intercalation in the open-structured hosts during subsequent cycling. This open and stable architecture enables a high reversible capacity of 319 mAh g^-1 at 20 mAg^-1 and a capacity retention of 81% over 500 cycles. The remarkable electrochemical performance makes V2O5 a promising cathode for aqueous zinc-ion batteries.

关键词： Aqueous zinc-ion batteries Vanadium oxide Insertion reaction Phase transition