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CHEMICAL ENGINEERING JOURNAL · 2019 · IF 8.355

Ultrafast kinetics net electrode assembled via MoSe2/MXene heterojunction for high-performance sodium-ion batteries

Enze Xu,Yan Zhang,Hui Wang,Zhifeng Zhu,Junjie Quan,Yajing Chang,Pengcheng Li,Dabin Yu,Yang Jiang

Establishing advanced sodium-ion batteries (SIBs) with high energy density and eco-friendly electrode materials are still far from satisfactory due to the large-size of sodium-ions and sluggish redox kinetics during electrochemical processes. Herein, a novel ultrafast kinetics net electrode assembled via MoSe 2 /MXene heterojunction is synthesized by a simple hydrothermal method followed by thermal annealing. Featuring the Van der Waals force interaction between MoSe 2 and MXene , the volumetric change during the sodium ions insertion/extraction courses is effectively restrained, and the reaction kinetics is greatly enhanced further. Meanwhile, both the high electrical and ion conductivity (lower diffusion barrier between Na + /MXene ~0.066 eV) provided by the unique MXene based net heterostructure of our hybrid materials, as evidenced by DFT calculations, are beneficial to the transportation of sodium ions, thus enabling an outstanding rate and long-cycling capability. As a result, the fabricated cells exhibit high reversible capacities of 490 mAh g −1 at 1 A g −1 , as well as 250 mAh g −1 at a high current of 10 A g −1 with a coulombic efficiency of 99.8%, indicating the excellent electrochemical performance of our hybrid materials, especially at high current. This novel net MoSe 2 /MXene heterostructure, combined with our simple synthesis strategy together, are expected to have great potential in sodium-ions storage application.

研究领域: 材料科学 · 电化学 · 能源存储 · 纳米材料 · 固态物理
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CARBOHYDRATE POLYMERS · 2018 · IF 5.158

Chitosan derivative-based self-healable hydrogels with enhanced mechanical properties by high-density dynamic ionic interactions

Ningxiao Yuan,Lu Xu,Bo Xu,Jianhao Zhao,Jianhua Rong

Chitosan derivative-based self-healable hydrogels with enhanced mechanical properties are reported, which were prepared by polymerization of acrylic acid (AAc) in 2-hydroxypropyltrimethyl ammonium chloride chitosan (HACC) solution. The PAAc/HACC hydrogels exhibit tensile fracture stress as high as 3.31 MPa and a Young's modulus of 2.53 MPa. They can maintain their original shape after 30 repeated compression cycles under various strain conditions, with a compression stress of more than 60 MPa at 99% strain. The damaged PAAc/HACC hydrogels can heal together in the presence of a NaCl salt solution with a self-healing efficiency of up to 61%. In addition, the PAAc/HACC hydrogels have high ionic conductivity and can serve as electrolytes for supercapacitors. The analysis suggests that all these good properties of the PAAc/HACC hydrogels mainly result from their high-density dynamic ionic interactions structure.

研究领域: 高分子材料科学 · 生物医学工程 · 功能材料 · 组织工程 · 药物递送系统 · 再生医学 · 电化学器件
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2024 · IF 9.4

A self-healing composite solid electrolyte with dynamic three-dimensional inorganic/organic hybrid network for flexible all-solid-state lithium metal batteries

Ying Jiang,Kai Chen,Jinping He,Yuxue Sun,Xiaorong Zhang,Xiaoxing Yang,Haiming Xie,Jun Liu

Composite solid electrolytes (CSEs), which combine the advantages of solid polymer electrolytes and inorganic solid electrolytes, are considered to be promising electrolytes for all-solid-state lithium metal batteries. However, the current CSEs suffer from defects such as poor inorganic/organic interface compatibility, lithium dendrite growth, and easy damage of electrolyte membrane, which hinder the practical application of CSEs. Herein, a CSE (PBHL@LLZTO@DDB) with polyurethane (PBHL) as the polymer matrix and Li 6.4 La 3 Zr 1.4 Ta 0.6 O 12 (LLZTO) modified by silane coupling agent (DDB) as inorganic fillers (LLZTO@DDB) has been prepared. Disulfide bond exchange reactions between PBHL and LLZTO@DDB enable PBHL@LLZTO@DDB to form a dynamic three-dimensional (3D) inorganic/organic hybrid network, which promotes the uniform dispersion of LLZTO in PBHL@LLZTO@DDB, improves the Li + conductivity (1.24 ± 0.08 × 10 −4  S cm −1 at 30 ℃), and broadens the electrochemical stability window (5.16 V vs. Li + /Li). Moreover, a combination of hydrogen bonds and disulfide bonds endows PBHL@LLZTO@DDB with excellent self-healing properties. As such, both all-solid-state symmetric and full cells exhibit excellent cycle performance at ambient temperature. More importantly, the healed PBHL@LLZTO@DDB can almost completely restore its original electrochemical properties, indicating its application potential in flexible electronic products.

研究领域: 材料科学 · 电化学 · 能源存储 · 高分子化学 · 固态离子学
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MATERIALS CHEMISTRY AND PHYSICS · 2022 · IF 4.778

Multilevel halide perovskite memristors based on optical & electrical resistive switching effects

Zehan Liu,Pengpeng Cheng,Yongfei Li,Ruyan Kang,Jian Zhou,Jia Zhao,Zhiyuan Zuo

With the aim of addressing the growing challenge of approaching the end of Moore's law and von Neumann bottleneck, the evolution of neuromorphic computing based on memristors that emulate the behaviors of the brain has attracted great attention. Organic-inorganic hybrid lead halide perovskites with inherent hybrid ionic-electronic conduction ability have been proposed as promising candidates for memristors to replace traditional charge-based memory. Here we propose MA 0.85 Cs 0.15 PbI 3 memristors with high surface crystallinity and stable operation in the atmospheric environment by mixing inorganic cation Cs + and organic cation MA + . The prepared memristors present excellent resistive switching performances including low operation voltage, high ON/OFF ratio, stable endurance, long retention, and robustness under ambient condition. Besides that, four distinct resistance states have been obtained in the above devices by modifying the operation voltages. Moreover, the resistance switching processes can be controlled both by electrical field and light illumination. Finally, this research provides utilization potentiality in the optical and electrical two-dimension controlled multilevel information devices with a total of five stable resistance states. The present work would offer an effective way to develop multifunctional high-density data-storage applications by storing multiple resistance states in a single unit cell.

研究领域: 材料科学 · 纳米电子学 · 凝聚态物理 · 信息存储技术 · 类脑计算
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JOURNAL OF ALLOYS AND COMPOUNDS · 2015 · IF 2.999

Carbon nanotubes modified for ZnCo2O4 with a novel porous polyhedral structure as anodes for lithium ion batteries with improved performances

Qiang Ru,Xiong Song,Yudi Mo,Lingyun Guo,Shejun Hu

Carbon nanotubes (CNTs) are adopted to modify ZnCo 2 O 4 (ZCO) electrode, and a novel porous polyhedral structure ZCO/CNTs composites are prepared by a facile and scalable hydrothermal process, and the pure ZCO with cubic structure is also synthesized for comparison. The as-prepared materials are characterized by field emission scanning electron microscopy (FESEM). The results demonstrate that the introduced of CNTs has great effects on the nanostructure and electrochemical performance of the samples. The CNTs among the polyhedral structure ZCO/CNTs composites can provide better mechanical robustness, more contact between Li + and electrodes, and more effective electron transmission than the pure ZCO with cubic structure. When tested as anode materials for lithium ion batteries , the ZCO/CNTs composites exhibit a high initial coulombic efficiency of 83.9%, a high specific capacity of ∼864.6 mAh g −1 at a current rate of 100 mA g −1 after 150 cycles, as well as a good rate capability at elevated current rates, such as, ∼924.3 and ∼605.7 mAh g −1 at current rates of 500 and 2000 mA g −1 , respectively. This work would be meaningful in the preparation of complex oxides/carbon composites with porous nanostructure as anodes for LIBs.

研究领域: 材料科学 · 电化学 · 纳米科技 · 能源存储 · 功能材料
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CURRENT APPLIED PHYSICS · 2023 · IF 2.4

Three-terminal nonvolatile memory photodetectors based on rationally engineered heterostructured tin zinc oxide nanowires

WenXin Zhang,Hao Li,Haofei Cong,Ruifu Zhou,Yuanbin Qin,Peilong Xu,Xuhai Liu,Fengyun Wang

One-dimensional wide band-gap metal oxide semiconductors demonstrate enormous potential in high-performance ultraviolet photodetectors. Here, via tuned zinc oxide (ZnO) concentration ratio and heterojunction structure as well as decent V TH value, we electrospun tin zinc oxide (SnZnO X ) nanowires for photoelectronic conversion function. The constructed optimized photodetectors based on Sn 8 Zn 2 O X nanowires can exhibit a remarkable detectivity of 1.77 × 10 16 Jones, excellent responsivity of 2.23 × 10 3 A/W and relative high sensitivity over 10 4 . In addition to the excellent photodetection performance, Sn 8 Zn 2 O X nanowire devices exhibit nonvolatile memory effect , which can maintain the light-induced low resistance state at 5 V without light. Moreover, a voltage of 30 V was applied to Sn 8 Zn 2 O X nanowires devices to realize light-writing state switching to bias-erasing state, and the device could come back to their initial high resistance state. These results indicate SnZnO X nanowires devices possess a tremendous potential in the circuit design of the artificial visual system.

研究领域: 材料科学 · 纳米电子学 · 光电子学 · 半导体器件 · 人工视觉系统
✓ 已验证 DOI 高影响因子
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Journal of Materials Chemistry A · 2014 ·Vol. 2 ·期 37 ·15546-15552 · IF 0

Flexible quantum dot-sensitized solar cells with improved efficiencies based on woven titanium wires

Yitan Li,Lin Wei,Cuncun Wu,Chang Liu,Yanxue Chen,Hong Liu,Jun Jiao,Liangmo Mei

Uniform zinc oxide (ZnO) nanosheet arrays were grown on woven titanium wires using a low temperature hydrothermal method. Photoanodes were prepared by depositing CdS and CdSe quantum dots onto the ZnO nanosheet arrays by a successive ionic layer adsorption and reaction (SILAR) method. Solar cells were assembled using these nanostructured photoanodes and their photovoltaic performance was characterized. The effect of using SILAR cycles for the deposition of quantum dots on the performance of these nanostructured solar cells was investigated systematically. The overall light-to-electricity conversion efficiency of 0.98% was achieved under 100 mW cm−2 illumination for flexible CdS/CdSe co-sensitized solar cells using conventional Pt foils as counter electrodes. To further improve the performance of the flexible solar cells, PbS and Cu2S counter electrodes based on Pb and Cu foils were fabricated. The best conversion efficiencies of flexible CdS/CdSe co-sensitized solar cells using Cu2S and PbS counter electrodes were 3.4% and 2.5%, which demonstrated a significant enhancement in values for short circuit current, open circuit voltage, and fill factor compared to those obtained with the commonly used Pt and Au electrodes.

研究领域: 材料科学 · 纳米科技 · 能源材料 · 光电化学 · 半导体器件
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JOURNAL OF POWER SOURCES · 2024 · IF 8.1

Enhanced electrochemical performance of a cost-effective Sm2O3-coated spinel LiNi0.5Mn1.5O4 cathode for high-voltage lithium-ion batteries

Zhengwu Wang,Yannan Zhang,Bao Zhang,Dong Yang,Kai Zhou,Yixue Huang,Fei Wang,Jianguo Duan,Xianshu Wang,Peng Dong,Yingjie Zhang

Spinel LiNi 0.5 Mn 1.5 O 4 (LNMO) has gained significant attention as a promising cathode material for lithium-ion batteries due to its high working voltage (>4.7 V) and energy density . However, challenges such as electrolyte decomposition-induced material interface erosion and transition metal dissolution under high operating voltage hinder its commercial use. In this study, a thin and uniform Sm 2 O 3 layer has been successfully deposited on the surface of LNMO using a wet chemical method . A comprehensive investigation of surface morphology , crystal structure, and electrochemical performance of the modified LNMO is conducted. The results demonstrate that the Sm 2 O 3 surface modification acts as a robust multifunctional protective layer, effectively shielding against hydrofluoric acid-induced chemical attack and enhancing the migration efficiency of lithium ions . Notably, the capacity retention rate of LNMO@Sm 2 O 3 (3 wt%) remains up to 88 % after 280 cycles, significantly surpassing the uncoated counterpart. The coated material exhibits a capacity of 114 mAh g −1 even under 10 C rate conditions. Moreover, the AC impedance values and manganese dissolution of the modified material in the organic electrolyte are considerably lower than those of the uncoated counterpart. Theoretical calculations strongly support the experimental findings, revealing higher Mn vacancy formation energy and density of states at the Fermi energy level for the Sm 2 O 3 -modified electrodes. This research contributes to the field of surface modification and paves the way for further enhancements in the electrochemical performance of other high-voltage manganese-based lithium-ion batteries (LIBs).

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 纳米技术 · 表面工程 · 锂电池
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JOURNAL OF MEMBRANE SCIENCE · 2018 · IF 6.578

Long-side-chain type imidazolium-functionalized fluoro-methyl poly(arylene ether ketone) anion exchange membranes with superior electrodialysis performance

Junbin Liao,Jiajie Zhu,Shanshan Yang,Nengxiu Pan,Xinyan Yu,Chao Wang,Jun Li,Jiangnan Shen

Developing highly ion conductive and desirable electrodialysis (ED) performance anion exchange membranes (AEMs) is of great significance. In this work, we report a strategy for fabricating novel AEMs based on a series of fluoro-methyl poly(arylene ether ketone)s having long-side-chain imidazolium groups for ED. Having hydrophilic conductive flexible side-chain imidazolium groups and rigid hydrophobic backbone within AEM matrix, the optimized AEM (PAEK-60-im) shows low water uptake of 24.9% at 80 °C and desirable ion conductivity of 22.01 mS cm –1 at 30 °C. In NaCl removal application of ED, PAEK-60-im shows the NaCl removal ratio of 69.66% within 120 min, outperforming commercial AEM-Type II (68.98%). Accordingly, it has a higher current efficiency of 83.7% but lower energy consumption of 5.9 kWh kg –1 , compared with the commercial one (82.0%; 6.6 kWh kg –1 ). In particular, in selectrodialysis application, possibly owing to the synergistic effect of pore-size sieving effect resulting from macro-separation morphology and hydration energy difference of SO 4 2– ions (–1000 kJ mol –1 ) and Cl – ions (–317 kJ mol –1 ) in feeding solution, PAEK-60-im shows significantly superior monovalent anion perm-selectivity (Cl − /SO 4 2− ) of 7.70 at 30 min, relative to commercial anion-selective Neosepta ACS (5.27) and many other reported mono-valent anion selective AEMs having elegant surface modified layers. The superior ED performance of the homogeneous PAEK-60-im is suggestive of its potential separation application.

研究领域: 材料科学 · 化学工程 · 电化学 · 膜技术
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Advanced Electronic Materials · 2021 ·Vol. 8 ·期 4 ·2100997 · IF 7.295

Combustion Synthesized Electrospun InZnO Nanowires for Ultraviolet Photodetectors

Junyu He,Peilong Xu,Ruifu Zhou,Hao Li,Hongliang Zu,Jun Zhang,Yuanbin Qin,Xuhai Liu,Fengyun Wang

Ultraviolet (UV) photodetectors play an important role in numerous commercial and scientific applications. The UV photodetectors based on binary-cation indium zinc oxide (InZnO) thin films exhibit great performance enhancement, compared with their single-cation counterparts. However, UV photodetectors based on 1D InZnO nanowires could potentially exhibit more superior optoelectrical performance, due to the large surface-to-volume ratio and favorable carrier transport characteristics of nanowires. This work has combined combustion synthesis with electrospinning technique to efficiently fabricate InZnO nanowire-based UV photodetectors. At the annealing temperature of 375 °C, the newly designed InZnO nanowire photodetectors exhibit excellent photoelectric performance under the irradiation of 310 nm UV light, including a photo-to-dark current ratio of 1.2 × 10 4 , a photo responsivity of 2.8 × 10 3 A W –1 , and a high detectivity of 2.4 × 10 16 Jones. This study not only demonstrates the opportunity to construct new-generation transparent electronics based on 1D metal oxide nanowires but also sheds new light on how to further decrease the annealing temperature of metal oxide nanowire devices for low-temperature fabrication processes.

研究领域: 材料科学 · 纳米科技 · 光电子学 · 半导体器件 · 功能材料
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JOURNAL OF POWER SOURCES · 2024 · IF 8.1

Study on the influence of different manganese sources on the formation of P2/β Bi-phase cathode materials for sodium ion batteries

Yixuan Zhang,Guo-Qiang Liu,Danlei Qiao,Jiaguan Chen,Qiang Sun,Lei Wen

This work focuses on the effect of the of Mn 3+ /Mn 4+ ratio in the reactants on the structure and electrochemical properties of NaMn 0.9 Cu 0.1 O 2 cathode materials for sodium-ion batteries. By systematically varying the manganese valence states in the reactants, we observed a phase transition from the β-phase to the P2-phase with increasing Mn 3+ concentrations in the reactants, contrary to the expected favorability of the β-phase at higher Mn 3+ levels. This finding suggests a complex interplay between the valence states of the reactants and phase formation mechanisms, which needs further investigation. Additionally, electrochemical testing indicated that the phase composition significantly impacts the electrochemical performance of the material. Specifically, the M0 sample, possessing the optimal P2/β ratio, exhibited excellent electrochemical performances, achieving a high initial discharge capacity of 155.1 mA h g −1 and remains 88.1 % after 40 cycles. These results emphasize the importance of precursor selection and valence management in the development of high-performance cathode materials for sodium-ion batteries.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 固态化学
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2018 ·Vol. 29 ·期 16 ·13925-13930 · IF 2.324

Structure, morphology and electrical conductivity of Sm and Bi co-doped CeO2 electrolytes synthesized by co-precipitation method

Li Tianjing,Shi Qingle

In this paper, explain a new relationships between Bi 3+ content, the phase crystal, microstructure and conductivity for Sm and Bi co-doped Ce 0.8− x Sm 0.2 Bi x O 1.9−1/2 x ( x  = 0, 0.05, 0.1, 0.15, 0.2) electrolytes prepared by co-precipitation method. The XRD patterns showed that this compounds exhibit a fluorite-type cubic structure after the samples calcined at 700 °C for 4 h and the cell volumes of increased when the Bi content increased. In addition, for the samples sintered at 1400 °C for 4 h, the Bi doping improves the relative density, the grain size and the average thermal expansion coefficient (TEC). More in details, the relative density and TEC increase with the Bi content. Form the AC impedance spectroscopy measurements, the conductivity of the sintered samples is found to improve with the increasing of Bi content (for x  ≤ 0.15), which is ascribed to the increasing of the number of oxygen ion vacancies and the increase in the unit cell volume. However, the conductivity decreases when the Bi content is further increased (0.15 <  x  ≤ 0.2), which is ascribed the reduction of the number of free oxygen vacancies. The highest conductivity at 800 °C is 5.6 × 10 −2  S/cm and the activation energy is 0.83 eV for Ce 0.65 Sm 0.2 Bi 0.15 O 1.825 , indicating that this would be a promising electrolyte for the intermediate temperature-solid oxide fuel cell applications.

研究领域: 材料科学 · 无机非金属材料 · 固态离子学 · 能源材料 · 燃料电池
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