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Insights Into Ni2+-Dominated Phase Regulation of Accordion-Shaped CuNb2O6 Framework Toward Lithium-Ion Capacitors 认领 引用
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作者 Xu-Ting Li Chao Cheng +4 位作者 Hao Jiang Min-Yu Jia Zhen-Xiang Zhao Lin-Rui Hou Chang-Zhou Yuan 《Rare Metals》 SCIE EI CAS CSCD 2026年第1期392-404,共13页
The monoclinic CuNb2O6(M-CNO)with a columbite structure is a potential anode candidate for advanced lithium-ion capacitors(LICs).However,its practical application is plagued seriously by the irreversible phase t... The monoclinic CuNb2O6(M-CNO)with a columbite structure is a potential anode candidate for advanced lithium-ion capacitors(LICs).However,its practical application is plagued seriously by the irreversible phase transformation and sluggish kinetics.For this,herein,we develop an adjustable Cu-site Ni substituting strategy to regulate the phase transition(i.e.,NixCu1-xNb2O6)from M-CNO to orthorhombic NiNb2O6.With the fine optimization in Ni substitution,the stresshermal-induced phase transformation and the initial electrochemical conversion are effectively prevented in the optimal Ni0.5Cu0.5Nb2O6(55NCNO).Moreover,elaborate experimental observation and theoretical calculations synergistically authenticate that the orthorhombic 55NCNO phase is endowed intrinsically with both superb Li+and electronic conductivities,thanks to its large two-dimensional Li+diffusion channel and narrow band gap.Benefiting from such appealing merits,55NCNO with the solid-solution Li+-storage mechanism obtains attractive high-rate capacities and cycling stability,when evaluated as a competitive anode for LICs.Besides,the 55NCNO constructed LICs display a striking energy density of 49.5 Wh kg-1 at 10.8 kW kg-1 along with long-span cycle life(just 0.0065% capacitance decay per cycle).More significantly,the heteroatomic substitution methodology here will guide future design of advanced anodes for next-generation LICs,and propel their practical advancement. 展开更多
关键词 lithium-ion capacitors NixCu1-xNb2O6 Ni substitution phase-transition regulation solid-solution anode
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Hierarchically porous ZIF-67-based Au with enhanced electromagnetic,chemical,and mass-transfer properties for flexible gas-liquid SERS sensing 认领 引用
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作者 Jing Guo Zhi-Mei Mu +10 位作者 Jing Yu Guan-Liang Sun Lin-Rui Hou Xue-Zhi Qiao Shi-Kuan Yang Xing-Shuang Zhang Guan-Chen Xu Guo-An Liu Fan Yang Chang-Zhou Yuan Xiu Liang 《Rare Metals》 SCIE EI CAS CSCD 2025年第10期7672-7685,共14页
Metal-organic framework materials exhibit considerable potential as molecularly selective surfaceenhanced Raman spectroscopy(SERS)substrates because of their microporous structures,which enrich small molecules while e... Metal-organic framework materials exhibit considerable potential as molecularly selective surfaceenhanced Raman spectroscopy(SERS)substrates because of their microporous structures,which enrich small molecules while excluding larger ones.In this study,we develop a template-assisted chemical-etching strategy to prepare layered tuneable SERS substrates based on hierarchical porous zeolitic imidazolate framework-67(HP-ZIF-67)with a rhombic dodecahedral structure.The synergistic SERS enhancement mechanisms of HP-ZIF-67,which combine electromagnetic(EM)and chemical(CM)effects,were systematically studied through numerical simulations and experiments.Calculations revealed that under 633-nm laser excitation,the contributions of the EM and CM effects to the total SERS enhancement factor of HP-ZIF-67 were 60%and 40%,respectively.The hierarchical porous structure enhanced the fluid-flow flux over the microporous ZIF-67 because the increased pore radius reduced the viscous resistance and facilitated rapid molecular transport through the interconnected macro-meso-channels.Precise modulation of the CM and EM effects,combined with enhanced mass transfer,facilitated the development of HP-ZIF-67and HP-ZIF-67@Au as efficient SERS sensors.An investigation of the relationship between pore-size distribution and EM effects revealed the pivotal role of light confinement by whispering-gallery-mode microcavities in enhancing the SERS performance.The optimised HPZIF-67@Au composites functioned as flexible and highly sensitive in situ SERS sensors for gases and liquids,including volatile organic-compound gas and liquid-pesticide residues.This study introduces a novel design concept and provides a robust theoretical foundation for the future development of exhaled-breath point-of-care diagnostic devices and sweat-based wearable biomedical sensors. 展开更多
关键词 Surface-enhanced Raman scattering Hierarchical porous ZIF-67 Chemical enhancement Electromagnetic enhancement Fluid-mass transfer Gas-liquid sensing
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V2CTx MXene and its derivatives:synthesis and recent progress in electrochemical energy storage applications 认领 引用 被引量:18
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作者 Zhao-Lin Tan Jing-Xuan Wei +4 位作者 Yang Liu Fakhr uz Zaman Wajid Rehman Lin-Rui Hou Chang-Zhou Yuan 《Rare Metals》 SCIE EI CAS CSCD 2022年第3期775-797,共23页
With the continuous development of two-dimensional (2D) transition metal carbides and nitrides(collectively referred to as MXene).Nowadays,more than 70 MXene materials have been discovered,and the number is still incr... With the continuous development of two-dimensional (2D) transition metal carbides and nitrides(collectively referred to as MXene).Nowadays,more than 70 MXene materials have been discovered,and the number is still increasing.Among them,the V2CTx MXene has attracted considerable attentions due to its outstanding physical and chemical properties.In this review,we mainly discussed the emerging V2CTx MXene and its derivative systems in various energy storage devices.Firstly,an introduction of the V-based MXene and its derivatives along with their synthetic methodologies is provided,then we summarize their applications in specific energy storage devices,such as metal (Li,Na,K,Mg,Zn and Al) ion batteries,lithium-sulfur batteries,supercapacitors and metal-ion capacitors.Finally,the main challenges and future perspectives existing in V-based MXene and its derivatives are reasonably put forward. 展开更多
关键词 MXene V2CTx Two-dimensional material Derivatives Electrochemical energy storage applications
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Precipitant-free solvothermal construction of spindle-like CoCO3/reduced graphene oxide hybrid anode toward high-performance lithium-ion batteries 认领 引用 被引量:10
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作者 Yu-Yan Wang Zhi-Wei Zhao +2 位作者 Yang Liu Lin-Rui Hou Chang-Zhou Yuan 《Rare Metals》 SCIE EI CAS CSCD 2020年第9期1082-1091,共10页
Recently,CoCO3has attracted enormous attention as anodes for lithium-ion batteries(LIBs),benefiting from its high theoretical capacity and simple synthesis.However,the modest electronic conductivity and structural ... Recently,CoCO3has attracted enormous attention as anodes for lithium-ion batteries(LIBs),benefiting from its high theoretical capacity and simple synthesis.However,the modest electronic conductivity and structural instability over cycling hinder its wider applications.To well address the intrinsic issues,we explored a precipitantfree hydrothermal methodology for mass production of spindle-like CoCO3educed graphene oxide(S-CoCO3GO)toward advanced LIBs as a hybrid anode.The dimethylformamide plays a significant role of"two birds(i.e.,solvent and precipitant)with one stone"in the formation of the S-CoCO3GO,greatly improving its practical applicability.The purposeful introduction of rGO nanosheets as a two-dimensional flexible conductive network enhances the conductivity and stability of the S-CoCO3.It is the structural and compositional merits for LIBs that endow the S-CoCO3GO with remarkable lithium-storage performance in terms of enhanced interfacial storage capacity,high-rate reversible capacities(803 mAh·g-1at 2.0 A·g-1)and long-duration capacity retention of 82.1%over 2000 consecutive cycles at 2.0 A·g-1.More significantly,the simple yet efficient avenue here promises enormous commercial prospect of the S-CoCO3GO in next-generation LIBs. 展开更多
关键词 Spindle-like CoCO3 Reduced graphene oxide Precipitant-free synthesis Hybrid anodes Lithium-ion batteries
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Self-assemble construction of hetero-structured Co(OH)2/MXene aerogel toward Li-S batteries as a self-supported host and bifunctional catalyst 认领 引用 被引量:2
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作者 Yang Liu Ke Tan +6 位作者 Sen Liu Xu Zhang Mao-Qiang Shen Xue-Sen Liu Xin-Yue Gao Lin-Rui Hou Chang-Zhou Yuan 《Rare Metals》 SCIE EI CAS CSCD 2024年第11期5652-5663,共12页
The shuttling diffusion of polysulfides is a bottleneck that seriously limits the performance of Li-S batteries.Purposeful construction of sulfur cathodes with reliable trapping ability of polysulfides is the key to o... The shuttling diffusion of polysulfides is a bottleneck that seriously limits the performance of Li-S batteries.Purposeful construction of sulfur cathodes with reliable trapping ability of polysulfides is the key to overcome such limitation.Herein,a hierarchical porous architecture,i.e.,Co(OH)2sheets bonded Ti_3C2T_x MXene aerogel(Co(OH)2/MXA),is constructed via a facile selfassembled approach and used as an efficient free-standing polysulfides reservoir.The interconnected three-dimensional(3D)porous network with void space and strong interfacial interaction not only enables high sulfur loading but facilitates fast ion and electron transport.Experimental and theoretical results confirm the hetero-framework exhibits outstanding immobilization and conversion ability for polysulfides due to its polar surface and bifunctional catalytic activities toward both formation and decomposition of Li2S.The optimized Co(OH)2/MXA cathode delivers excellent rate capability(407 mAh·g-1at 5C)with a sulfur loading of 2.7 mg·cm-2,and ultra-stable cycling performance as an extremely small capacity decay of~0.005%per cycle within 1700 cycles at 1C is achieved with a high sulfur loading of 6.7 mg·cm-2.More significantly,our design structural/componential methodology here promises the MXene-based aerogel electrodes for LiS batteries and beyond. 展开更多
关键词 MXene aerogel Co(OH)2sheets Hetero-architecture Self-standing hosts Li-S batteries
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Porous carbon nanofibers derived from low-softening-point coal pitch towards all-carbon potassium ion hybrid capacitors 认领 引用 被引量:7
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作者 Guang-Yuan Wang Xiao-Hong Wang +3 位作者 Jin-Feng Sun Ya-Min Zhang Lin-Rui Hou Chang-Zhou Yuan 《Rare Metals》 SCIE EI CAS CSCD 2022年第11期3706-3716,共11页
Potassium ion hybrid capacitors(PIHC)have promising applications in medium and large-scale energy storage systems due to their high energy/power density,abundant potassium resource and low cost.However,the slow kineti... Potassium ion hybrid capacitors(PIHC)have promising applications in medium and large-scale energy storage systems due to their high energy/power density,abundant potassium resource and low cost.However,the slow kinetics of battery-type anodes originating from the large-size K+results in a mismatch between the two electrodes,rendering the modest energy density of PIHC.Herein,we first develop an electrospinning strategy to successfully synthesize fibrous precursor by using the HNO3pre-oxidized low-softening-point coal pitch as the low-cost raw material.With further carbonization or KOH activation,the two types of carbon nanofibers(CNF)are fabricated as anode and cathode materials,respectively,towards the dual-carbon PIHC devices.Thanks to its threedimensional interconnected porous conducting network and large layer spacing,the resulted CNF anode material is endowed with high reversible capacities,excellent rate and long cycle stability.Meanwhile,the activated CNF cathode with a large surface area of 2169 m2·g-1exhibits excellent capacitive performance.A PIHC constructed with the two fibrous electrodes delivers an energy density of110.0 Wh·kg-1at 200.0 W kg-1,along with a capacitance retention of 83.5%after 10,000 cycles at 1.0 A·g-1.The contribution here provides a cost-efficiency avenue and platform for advanced dual-carbon PIHC. 展开更多
关键词 Potassium ion hybrid capacitors(PIHC) Low-softening-point coal pitch Carbon nanofibers(CNF) Dual-carbon devices Long durability
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