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| 1 | Achieving high-capacity and long-life K^(+)storage enabled by constructing yolk-shell Sb_(2)S_(3)@N,S-doped carbon nanorod anodes显示文摘As promising anode candidates for potassium-ion batteries(PIBs),antimony sulfide(Sb_(2)S_(3))possesses high specific capacity but suffers from massive volume expansion and sluggish kinetics due to the large K^(+)insertion,resulting in inferior cycling and rate performance.To address these challenges,a yolk-shell structured Sb_(2)S_(3)confined in N,S co-doped hollow carbon nanorod(YS-Sb_(2)S_(3)@NSC)working as a viable anode for PIBs is proposed.As directly verified by in situ transmission electron microscopy(TEM),the buffer space between the Sb_(2)S_(3)core and thin carbon shell can effectively accommodate the large expansion stress of Sb_(2)S_(3)without cracking the shell and the carbon shell can accelerate electron transport and K^(+)diffusion,which plays a significant role in reinforcing the structural stability and facilitating charge transfer.As a result,the YS-Sb_(2)S_(3)@NSC electrode delivers a high reversible K^(+)storage capacity of 594.58 m A h g^(-1)at 0.1 A g^(-1)and a long cycle life with a slight capacity degradation(0.01%per cycle)for 2000 cycles at 1 A g^(-1)while maintaining outstanding rate capability.Importantly,utilizing in in situ/ex situ microscopic and spectroscopic characterizations,the origins of performance enhancement and K^(+)storage mechanism of Sb_(2)S_(3)were clearly elucidated.This work provides valuable insights into the rational design of high-performance and durable transition metal sulfides-based anodes for PIBs. | Bensheng Xiao Hehe Zhang Zhefei Sun Miao Li Yingzhu Fan Haichen Lin Haodong Liu Bing Jiang Yanbin Shen Ming-Sheng Wang Meicheng Li Qiaobao Zhang | 2023 | Journal of Energy Chemistry2023，，1： | 1 |
| 2 | Ultra-thick,dense dual-encapsulated Sb anode architecture with conductively elastic networks promises potassium-ion batteries with high areal and volumetric capacities显示文摘Ultra-thick,dense alloy-type anodes are promising for achieving large areal and volumetric performance in potassium-ion batteries(PIBs),but severe volume expansion as well as sluggish ion and electron diffusion kinetics heavily impede their widespread application.Herein,we design highly dense(3.1 g cm^(-3))Ti_(3)C_(2)T_(x) MXene and graphene dual-encapsulated nano-Sb monolith architectures(HD-Sb@Ti_(3)C_(2)T_(x)-G)with high-conductivity elastic networks(1560 S m^(-1))and compact dually encapsulated structures,which exhibit a large volumetric capacity of 1780.2 mAh cm^(-3)(gravimetric capacity:565.0 mAh g^(-1)),a long-term stable lifespan of 500 cycles with 82%retention,and a large areal capacity of 8.6 mAh cm^(-2)(loading:31 mg cm^(-2))in PIBs.Using ex-situ SEM,in-situ TEM,kinetic investigations,and theoretical calculations,we reveal that the excellent areal and volumetric performance mechanism stems from the three dimensional(3D)high-conductivity elastic networks and the dualencapsulated Sb architecture of Ti_(3)C_(2)T_(x) and graphene;these effectively mitigate against volume expansion and the pulverization of Sb,offering good electrolyte penetration and rapid ionic/electronic transmission.Ti_(3)C_(2)T_(x) also decreases the Kþdiffusion energy barrier,and the ultra-thick compact electrode ensures volumetric and areal performance.These findings provide a feasible strategy for fabricating ultra-thick,dense alloy-type electrodes to achieve high areal and volumetric capacity energy storage via highly-dense,dual-encapsulated architectures with conductive elastic networks. | Zhonggang Liu Xi Liu Bingchun Wang Xinying Wang Dongzhen Lu Dijun Shen Zhefei Sun Yongchang Liu Wenli Zhang Qiaobao Zhang Yunyong Li | 2023 | eScience2023，3，6： | 0 |
| 3 | Synergistic coupling of amorphous carbon and graphitic domains toward high-rate and long-life K^(+) storage显示文摘Amorphous carbon materials hold great potential for practical use in potassium-ion batteries(PIBs)due to their abundant resources,low cost and high structural stability.However,given the challenge of sluggish potassiation kinetics,the rate performance of amorphous carbon is severely hindered.Herein,amorphous carbon compounded with graphitic domains(HG-CNTs)was proposed as an advanced anode for PIBs.As directly verified by in situ transmission electron microscopy(TEM),the graphitic domains guarantee fast K-ions transport in the carbon composite at a high current density,while the amorphous carbon shells ensure the structural integrity during potassiation,thus boosting its fast and durable K^(+)storage.As a PlB anode,the HG-CNTs electrode exhibits not only a super-stable long-term cyclability(191.6 mAh g^(-1)at 1 A g^(-1)with almost no capacity decay over 3000 cycles),but also an outstanding rate performance(184.5 mAh g^(-1)at 2 A g^(-1)).Ex situ Raman and TEM results further suggest that the highly reversible structure of HG-CNTs is responsible for its superior electrochemical stability.This work provides helpful insights into the development of carbonaceous electrodes with both high rate capability and long cycle life for PIBs. | Hehe Zhang Wangqin Li Jianhai Pan Zhefei Sun Bensheng Xiao Weibin Ye Chengzhi Ke Haowen Gao Yong Cheng Qiaobao Zhang Ming-Sheng Wang | 2022 | Journal of Energy Chemistry2022，31，10： | 0 |
| 4 | Tuning the electron transport behavior at Li/LATP interface for enhanced cyclability of solid-state Li batteries显示文摘An interlayer is usually employed to tackle the interfacial instability issue between solid electrolytes(SEs)and Li metal caused by the side reaction.However,the failure mechanism of the ionic conductor interlayers,especially the influence from electron penetration,remains largely unknown.Herein,using Li1.3Al0.3Ti1.7(PO4)3(LATP)as the model SE and LiF as the interlayer,we use metal semiconductor contact barrier theory to reveal the failure origin of Li/LiF@LATP interface based on the calculation results of density functional theory(DFT),in which electrons can easily tunnel through the LiF grain boundary with F vacancies due to its narrow barrier width against electron injection,followed by the reduction of LATP.Remarkably,an Al-LiF bilayer between Li/LATP is found to dramatically promote the interfacial stability,due to the highly increased barrier width and homogenized electric field at the interface.Consequently,the Li symmetric cells with Al-LiF bilayer can exhibit excellent cyclability of more than 2,000 h superior to that interlayered by LiF monolayer(~860 h).Moreover,the Li/Al-LiF@LATP/LiFePO4 solid-state batteries deliver a capacity retention of 83.2%after 350 cycles at 0.5 C.Our findings emphasize the importance of tuning the electron transport behavior by optimizing the potential barrier for the interface design in high-performance solid-state batteries. | Linshan Luo Feng Zheng Haowen Gao Chaofei Lan Zhefei Sun Wei Huang Xiang Han Ziqi Zhang Pengfei Su Peng Wang Shengshi Guo Guangyang Lin Jianfang Xu Jianyuan Wang Jun Li Cheng Li Qiaobao Zhang Shunqing Wu Ming-Sheng Wang Songyan Chen | 2023 | Nano Research2023，16，1： | 0 |
| 5 | In situ atomic-scale observation of size-dependent (de) potassiation and reversible phase transformation in tetragonal FeSe anodes显示文摘Potassium-ion batteries(PIBs)are considered promising alternatives to lithium-ion batteries owing to cost-effective potassium resources and a suitable redox potential of-2.93 V(vs.-3.04 V for Li+/Li).However,the exploration of appro-priate electrode materials with the correct size for reversibly accommodating large K+ions presents a significant challenge.In addition,the reaction mecha-nisms and origins of enhanced performance remain elusive.Here,tetragonal FeSe nanoflakes of different sizes are designed to serve as an anode for PIBs,and their live and atomic-scale potassiation/depotassiation mechanisms are revealed for the first time through in situ high-resolution transmission electron micros-copy.We found that FeSe undergoes two distinct structural evolutions,sequen-tially characterized by intercalation and conversion reactions,and the initial intercalation behavior is size-dependent.Apparent expansion induced by the intercalation of K+ions is observed in small-sized FeSe nanoflakes,whereas unexpected cracks are formed along the direction of ionic diffusion in large-sized nanoflakes.The significant stress generation and crack extension originating from the combined effect of mechanical and electrochemical interactions are elucidated by geometric phase analysis and finite-element analysis.Despite the different intercalation behaviors,the formed products of Fe and K_(2)Se after full potassiation can be converted back into the original FeSe phase upon depotassiation.In particular,small-sized nanoflakes exhibit better cycling perfor-mance with well-maintained structural integrity.This article presents the first successful demonstration of atomic-scale visualization that can reveal size-dependent potassiation dynamics.Moreover,it provides valuable guidelines for optimizing the dimensions of electrode materials for advanced PIBs. | Ran Cai Lixia Bao Wenqi Zhang Weiwei Xia Chunhao Sun Weikang Dong Xiaoxue Chang Ze Hua Ruiwen Shao Toshio Fukuda Zhefei Sun Haodong Liu Qiaobao Zhang Feng Xu Lixin Dong | 2023 | InfoMat2023，5，1： | 0 |
| 6 | Ironing effect on surface integrity and fatigue behavior during ultrasonic peening drilling of Ti-6Al-4V显示文摘Imposing compressive residual stress field around a fastening hole serves as a universal method to enhance the hole fatigue strength in the aircraft assembly filed.Ultrasonic Peening Drilling(UPD)is a recently proposed hybrid hole making process,which can achieve an integration of strengthening and precision-machining with a one-shot-drilling operation.Due to the ironing effect of tool flank surface,UPD introduces large compressive residual stress filed in hole subsurface.In order to reveal the strengthening mechanism of UPD,the influence of ultrasonic vibration and tool dynamic relief angle on ironing coverage rate and its corresponding effect on surface integrity in UPD were analyzed.The experiments were conducted to verify the influence of ironing effect on surface integrity and fatigue behavior of Ti-6Al-4V hole in UPD.The results indicate that the specimen features smaller surface roughness,higher micro-hardness,plastic deformation degree and circumferential compress residual stress under higher ironing coverage rate.The fatigue life increases with the raise of ironing coverage rate,and the fatigue source site in UPD shifts from surface to subsurface comparing with that without vibration assistance.The results demonstrates that a better strengthening effect can be obtained by reasonably controlling the ironing coverage rate in UPD. | Yihang LIU Deyuan ZHANG Daxi GENG Zhenyu SHAO Zehua ZHOU Zhefei SUN Yonggang JIANG Xinggang JIANG | 2023 | Chinese Journal of Aeronautics2023，36，5： | 0 |
| 7 | Building better solid-state batteries with silicon-based anodes显示文摘Silicon(Si)-based solid-state batteries(Si-SSBs)are attracting tremendous attention because of their high energy density and unprecedented safety,making them become promising candidates for next-generation energy storage systems.Nevertheless,the commercialization of Si-SSBs is significantly impeded by enormous challenges including large volume variation,severe interfacial problems,elusive fundamental mechanisms,and unsatisfied electrochemical performance.Besides,some unknown electrochemical processes in Si-based anode,solid-state electrolytes(SSEs),and Si-based anode/SSE interfaces are still needed to be explored,while an in-depth understanding of solid–solid interfacial chemistry is insufficient in Si-SSBs.This review aims to summarize the current scientific and technological advances and insights into tackling challenges to promote the deployment of Si-SSBs.First,the differences between various conventional liquid electrolyte-dominated Si-based lithium-ion batteries(LIBs)with Si-SSBs are discussed.Subsequently,the interfacial mechanical contact model,chemical reaction properties,and charge transfer kinetics(mechanical–chemical kinetics)between Si-based anode and three different SSEs(inorganic(oxides)SSEs,organic–inorganic composite SSEs,and inorganic(sulfides)SSEs)are systemically reviewed,respectively.Moreover,the progress for promising inorganic(sulfides)SSE-based Si-SSBs on the aspects of electrode constitution,three-dimensional structured electrodes,and external stack pressure is highlighted,respectively.Finally,future research directions and prospects in the development of Si-SSBs are proposed. | Zhefei Sun Quanzhi Yin Haoyu Chen Miao Li Shenghui Zhou Sifan Wen Jianhai Pan Qizheng Zheng Bing Jiang Haodong Liu Kangwoon Kim Jie Li Xiang Han Yan-Bing He Li Zhang Meicheng Li Qiaobao Zhang | 2023 | Interdisciplinary Materials2023，2，4： | 0 |
| 8 | Shining light on transition metal tungstate-based nanomaterials for electrochemical applications:Structures,progress,and perspectives显示文摘Transition metal tungstate-based nanomaterials have become one of the research hotspots in electrochemistry due to their abundant natural resources,low costs,and environmental friendliness.Extensive studies have demonstrated their significant potentials for electrochemical applications,such as supercapacitors,Li-ion batteries,Na-ion batteries,electrochemical sensing,and electrocatalysis.Considering the rapidly growing research enthusiasm for this topic over the last several years,herein,a critical review of recent progress on the application of transition metal tungstates and their composites for electrochemical applications is summarized.The relationships between synthetic methods,nano/micro structures and electrochemical properties are systematically discussed.Finally,their promising prospects for future development are also proposed.It is anticipated that this review will inspire ongoing interest in rational designing and fabricating novel transition metal tungstate-based nanomaterials for high-performance electrochemical devices. | Kaijia Feng Zhefei Sun Yong Liu Feng Tao Junqing Ma Han Qian Renhong Yu Kunming Pan Guangxin Wang Shizhong Wei Qiaobao Zhang | 2022 | Nano Research2022，15，8： | 0 |
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