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| 1 | Electronically coupled layered double hydroxide/MXene quantum dot metallic hybrids for high-performance flexible zinc–air batteries显示文摘Precise control of the local electronic structure and properties of electrocatalysts is important for enhancing the multifunctionality and durability of electrocatalysts and for correlating the structure/chemistry with the catalytic properties.Herein,we report electronically coupled metallic hybrids of NiFe layered double hydroxide nanosheet/Ti3C2 MXene quantum dots deposited on a nitrogen-doped graphene surface(LDH/MQD/NG)for high-performance flexible Zn-air batteries(ZABs).As verified from the Mott-Schottky and Nyquist plots,as well as spectroscopic,electrochemical,and computational analyses,the electronic and chemical coupling of LDH/MQD/NG modulates the local electronic and surface structure of the active LDH to provide metallic conductivity and abundant active sites,leading to significantly improved bifunctional activity and electrocatalytic kinetics.The rechargeable ZABs with LDH/MQD/NG hybrids are superior to the previous LDH-based ZABs,demonstrating a high power density(113.8 mW cm^(-2))and excellent cycle stability(150 h at 5 mA cm^(-2)).Moreover,the corresponding quasi solid-state ZABs are completely flexible and practical,affording a high power density of 57.6 mW cm^(-2)even in the bent state,and in real-life operation of tandem cells for powering various electronic devices. | Xiaotong Han Nannan Li Peixun Xiong Min Gyu Jung Yingbo Kang Qingyun Dou Qing Liu Jin Yong Lee Ho Seok Park | 2021 | InfoMat2021，3，10： | 4 |
| 2 | A redox-active conjugated microporous polymer cathode for highperformance lithium/potassium-organic batteries显示文摘Organic redox-active materials have emerged as a class of electrode materials for rechargeable batteries due to their high redox activity,low cost,structure diversity and flexibility.However,the high solubility of organic small molecules in organic electrolytes commonly leads to the fast capacity decay with cycling.Herein,we report a redox-active conjugated microporous polymer of poly(pyrene-co-anthraquinone)(Py Aq)cathode material consisting of pyrene and anthraquinone units.Benefiting from the highly cross-linked polymer structure with insoluble nature in organic electrolytes,the high surface area and the plentiful redox-active carbonyl groups,the Py Aq cathode demonstrates outstanding electrochemical performances for both lithium-ion batteries(LIBs)and potassium-ion batteries(KIBs).Specifically,the Py Aq cathode for LIBs delivers a high reversible capacity of 169 m Ah g^-1 at the current density of 20 m A g^-1,a high rate capability(142 m Ah g^-1 at 1000 m A g^-1)and an excellent cycling stability for 4000 cycles.Additionally,the Py Aq cathode for KIBs also exhibits a high reversible capacity of143 m Ah g^-1 with a long cycling life over 800 cycles.The excellent electrochemical performance demonstrates that the newly developed Py Aq could be an attractive cathode material for the advanced energy storage technologies. | Lian-Wei Luo Chong Zhang Peixun Xiong Yongbo Zhao Wenyan Ma Yu Chen Jing Hui Zeng Yunhua Xu Jia-Xing Jiang | 2021 | Science China Chemistry2021，64，1： | 3 |
| 3 | Extraordinarily stable and wide-temperature range sodium/potassium-ion batteries based on 1D SnSe2-SePAN composite nanofibers显示文摘Developing electrodes with long lifespan and wide-temperature adaptability is crucial important to achieve high-performance sodium/potassium-ion batteries(SIBs/PIBs).Herein,the SnSe2-SePAN composite was fabricated for extraordinarily stable and wide-temperature range SIBs/PIBs through a coupling strategy between controllable electrospinning and selenylation,in which SnSe2 nanoparticles were uniformly encapsulated in the SePAN matrix.The unique structure of SnSe2-SePAN not only relieves drastic volume variation but also guarantees the structural integrity of the composite,endowing SnSe2-SePAN with excellent sodium/potassium storage properties.Consequently,SnSe2-SePAN displays a high sodium storage capacity and excellent feasibility in a wide working temperature range(-15 to 60℃:300 mAh g^(-1)/700 cycles/-15℃;352 mAh g^(-1)/100 cycles/60℃at 0.5 A g^(-1)).At room temperature,it delivers a record-ultralong cycling life of 192 mAh g^(-1)that exceeds 66000 cycles even at 15 A g^(-1).It exhibits extremely superb electrochemical performance in PIBs(157 mAh g^(-1)exceeding 15000 cycles at 5 A g^(-1)).The ex situ XRD and TEM results attest the conversion-alloy mechanism of SnSe2-SePAN.Also,computational calculations verify that SePAN takes an important role in intensifying the electrochemical performance of SnSe2-SePAN electrode.Therefore,this study breaks new ground on solving the polyselenide dissolution issue and improving the wide temperature workable performance of sodium/potassium storage. | Yiyi Wang Fuyu Xiao Xi Chen Peixun Xiong Chuyuan Lin Hong-En Wang Mingdeng Wei Qingrong Qian Qinghua Chen Lingxing Zeng | 2023 | InfoMat2023，5，9： | 1 |
| 4 | Two-Dimensional Pseudocapacitive Nanomaterials for High-Energy-and High-Power-Oriented Applications of Supercapacitors显示文摘CONSPECTUS:Supercapacitors(SCs)are electrochemical energy storage devices that can fill the gap between batteries and electrolytic capacitors.However,the widespread applications of commercialized carbon-based SCs are limited by their energy density,arising from their physical charge storage mechanism,which is by far lower than that of batteries.Moreover,the highpowered applications of SCs are also limited by their kinetics,which are slower than those of electrolytic capacitor due to the diffusion and distribution of ions onto the tortuous porous surface.Therefore,the energy and power performance of SCs need to be improved to open or further extend their practical applications.Since all atoms of two-dimensional(2D)nanomaterials are located on the surface,the design of surface structure is critical to determining the bulk electrochemical properties.Such a surface-oriented property of 2D nanomaterials is well fitted to control the surface charge storage mechanism of SCs,thereby discovering emerging capacitive materials through the rational design of surface chemistry and multiscale structures.This Account discusses our recent progress on 2D pseudocapacitive materials for high-energyand high-power-oriented SCs applications and provides our perspective into the rational design of the microstructure,multiscale architecture,and surface chemistry.Examples of 2D nanomaterials include heteroatom-doped graphene,black phosphorus,transition-metal dichalcogenides,and transition-metal carbide/nitrides(MXene).We also highlight the in-depth spectroelectrochemical and computational analyses that can correlate the structures and chemistries of 2D nanomaterials with their charge storage/transport/transfer behaviors.In this Account,our design concept of 2D nanomaterials is based on two aspects of charge storage capability and kinetics that can determine the thermodynamic(capacitance)and kinetic(rate)performances.First,chemical strategies,such as atomic incorporation,surface functionalization/coordination,and hybridization of 2D nanomaterials,will be provided and correlated with the population of redox storage sites and interaction between sites and ions.The charge storage capacitance can be improved by controlling these factors for high-energy-oriented applications.Second,we will address key factors such as charge-transfer kinetics,ion-transporting pathways,and percolated electron transport for high-power-oriented applications.Several approaches such as multiscale architecture,hybridization with electronically conductive materials,pore orientation,and an expanded interlayer space will be introduced to improve the kinetic performance of 2D nanomaterials.Finally,we will provide our perspective on technical impediments and future research directions of 2D nanomaterials for practical energy-and power-oriented applications of SCs. | Puritut Nakhanivej Qingyun Dou Peixun Xiong Ho Seok Park | 2021 | Accounts of Materials Research2021，2，2： | 0 |
| 5 | Single-Phase Ternary Compounds with a Disordered Lattice and Liquid Metal Phase for High-Performance Li-Ion Battery Anodes显示文摘Si is considered as the promising anode materials for lithium-ion batteries(LIBs)owing to their high capacities of 4200 mAh g-1and natural abundancy.However,severe electrode pulverization and poor electronic and Li-ionic conductivities hinder their practical applications.To resolve the afore-mentioned problems,we first demonstrate a cation-mixed disordered lattice and unique Li storage mechanism of single-phase ternary GaSiP_(2)compound,where the liquid metallic Ga and highly reactive P are incorporated into Si through a ball milling method.As confirmed by experimental and theoretical analyses,the introduced Ga and P enables to achieve the stronger resistance against volume variation and metallic conductivity,respectively,while the cation-mixed lattice provides the faster Li-ionic diffusion capability than those of the parent GaP and Si phases.The resulting GaSiP_(2)electrodes delivered the high specific capacity of 1615 mAh g-1and high initial Coulombic efficiency of 91%,while the graphite-modified GaSiP_(2)(GaSiP_(2)@C)achieved 83%of capacity retention after 900 cycles and high-rate capacity of 800 at 10,000 mA g-1.Furthermore,the LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)//Ga SiP_(2)@C full cells achieved the high specific capacity of 1049 mAh g-1after 100 cycles,paving a way for the rational design of high-performance LIB anode materials. | Yanhong Li Lei Zhang Hung-Yu Yen Yucun Zhou Gun Jang Songliu Yuan Jeng-Han Wang Peixun Xiong Meilin Liu Ho Seok Park Wenwu Li | 2023 | Nano-Micro Letters2023，15，5： | 0 |
| 6 | A class of Ga-Al-P-based compounds with disordered lattice as advanced anode materials for Li-ion batteries显示文摘Phosphides possess large reversible capacity, small voltage hysteresis, and high energy efficiency, thus promising to be new anode candidates to replace commercial graphite for Li-ion batteries(LIBs).Through a facile mechanochemistry method, we prepare a novel ternary phosphide of Ga0.5Al0.5P whose crystalline structure is determined to be a cation-disordered cubic zinc sulfide structure according to XRD refinement. As an anode for LIBs, the Ga0.5Al0.5P delivers a reversible capacity of 1,352 mA h g^(-1)at100 mA g^(-1)with an initial Coulombic efficiency(ICE) up to 90.0% based on a reversible Li-storage mechanism integrating intercalation and subsequent conversion processes as confirmed by various characterizations techniques including in-situ XRD, ex-situ Raman, and XPS and electrochemical characterizations.Graphite-modified Ga0.5Al0.5P exhibits a long-lasting cycling stability of retaining 1,182 mA h g^(-1)after300 cycles at 100 m A g^(-1), and 625 mA h g^(-1)after 800 cycles at 2,000 mA g^(-1), and a high-rate performance of remaining 342 m A h g^(-1)at 20,000 mA g^(-1). The outstanding electrochemical performances can be attributed to enhanced reaction kinetics enabled by the capacitive behaviors and the faster Liion diffusion enabled by the cation-mixing. Importantly, by tuning the cationic ratio, we develop a novel series of cation-mixed compounds of Ga_(1/3)Al_(2/3)P, Ga_(1/4)Al_(3/4)P, Ga_(1/5)Al_(4/5)P, Ga_(2/3)Al_(1/3)P, Ga_(3/4)Al_(1/4)P, and Ga_(4/5)Al_(1/5)P, which demonstrate large capacity, high ICE, and suitable anode potentials. Broadly, these compounds with disordered lattices probably present novel physicochemical properties, and high electrochemical performances, thus providing a new perspective for new materials design. | Yanhong Li Peixun Xiong Lei Zhang Songliu Yuan Wenwu Li | 2023 | Journal of Energy Chemistry2023，，4： | 0 |
| 7 | Progress in Electrolyte Engineering of Aqueous Batteries in a Wide Temperature Range显示文摘Aqueous rechargeable batteries are safe and environmentally friendly and can be made at a low cost;as such,they are attracting attention in the field of energy storage.However,the temperature sensitivity of aqueous batteries hinders their practical application.The solvent water freezes at low temperatures,and there is a reduction in ionic conductivity,whereas it evaporates rapidly at high temperatures,which causes increased side reactions.This review discusses recent progress in improving the performance of aqueous batteries,mainly with respect to electrolyte engineering and the associated strategies employed to achieve such improvements over a wide temperature domain.The review focuses on fi ve electrolyte engineer-ing(aqueous high-concentration electrolytes,organic electrolytes,quasi-solid/solid electrolytes,hybrid electrolytes,and eutectic electrolytes)and investigates the mechanisms involved in reducing the solidifi cation point and boiling point of the electrolyte and enhancing the extreme-temperature electrochemical performance.Finally,the prospect of further improving the wide temperature range performance of aqueous rechargeable batteries is presented. | Lingjun He Chuyuan Lin Peixun Xiong Hui Lin Wenbin Lai Jingran Zhang Fuyu Xiao Liren Xiao Qingrong Qian Qinghua Chen Lingxing Zeng | 2023 | Transactions of Tianjin University2023，29，5： | 0 |
| 8 | MXene ink hosting zinc anode for high performance aqueous zinc metal batteries显示文摘Despite the safety,low cost,and high theoretical capacity(820 mA h g^(-1))of Zn metal anodes,the practical application of aqueous Zn metal batteries remains a critical challenge due to the Zn dendrite growth,corrosion,and hydrogen evolution reaction.Herein,we demonstrate the MXene ink hosting Zn metal anodes(MX@Zn)for high-performance and patternable Zn metal full batteries.The as-designed MX@Zn electrode is more facile and reversible than bare Zn and CC@Zn,as verified by better cyclic stability and lower overpotentials of symmetric cells with the plating capacity of 0.05 mA h cm^(-2)at 0.1 m A cm^(-2)and of 1 m A h cm^(-2)at 1 m A cm^(-2).The MX@Zn|MnO_(2)full cells deliver a high specific capacity of 281.9 m A h g^(-1),91.5%of the theoretical capacity,achieving 50%capacity retention from 60 mA g^(-1)to 300 mA g^(-1)and 79.7%of initial capacity after 200 cycles.Moreover,the patterned devices based on the MX@Zn electrode achieve high energy and power densities of 348.57 Wh kg^(-1)and 1556 W kg^(-1),respectively,along with a capacity retention of 64%and Coulombic efficiency of 99%over 500 cycles.The high performance of MX@Zn is attributed to the high electrical conductivity and hydrophilicity of MXene and rapid ion diffusion through the 3D interconnected porous channels. | Jae Min Park Milan Jana Sang Ha Baek Taehun Kang Peixun Xiong Jeong Hee Park Jun Soo Kim Ali Shayesteh Zeraati Mikhail Shekhirev Paul V.Braun Yury Gogotsi Ho Seok Park | 2023 | Journal of Energy Chemistry2023，，1： | 0 |
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