ELECTROCHIMICA ACTA
·
2022
·
IF 7.336
Hongying Yang,Zhenfeng Cheng,Pengchao Wu,Yahui Wei,Jingyun Jiang,Qun Xu
Design and fabrication of 2D multi-metal oxalate materials with desired electrochemical activities are highly needed in electrocatalysis and supercapacitors . Herein, assisted by the deep eutectic solvothermal (DES) method, multi-metal oxalate consisting of Fe, Co, Ni, Cu, and Zn with different morphology was the controlled synthesis. It was found that the structure and composition of DES can control the nucleation and growth of multi-metal oxalate. High molecular PEG and gradually slow-release oxalic acid are in favor of the formation of 2D structure, while the low molecular EG and abundant oxalic acid are positive for the formation of 3D nanoparticles. The properties of the obtained multi-metal oxalates are confirmed by multi-analysis, which involves the single Ni-oxalate phase, morphological evolution ranging from particles to nanosheets, and complex composition up to five metal elements including Fe, Co, Ni, Cu as well as Zn. Notably, the well-designed 2D (FeCoNiCuZn)(C 2 O 4 )·2H 2 O nanosheets exhibit an ultralow overpotential of 334 mV at 100 mA cm −2 for OER as electrocatalyst with prolonged durability over 30 h at 10 mA cm −2 and a high specific capacity of 1337 C g −1 for aqueous supercapacitor.
研究领域:
材料化学
·
电化学
·
纳米材料
·
能源存储
·
催化化学
✓ 已验证
DOI
高影响因子
MACROMOLECULAR MATERIALS AND ENGINEERING
·
2021
·Vol. 306
·期 11
·2100456
·
IF 4.367
Zhiqiang Wu,Qiang Guo,Yang Liu,Huihui Zhou,Hua Zheng,Xingfeng Lei,Lei Gong,Yanhui Chen,Zhenguo Liu,Qiuyu Zhang
In order to meet the requirements of polymer dielectric materials for high thermal stability and excellent dielectric properties in the application of high-temperature film capacitors, a series of polyimide (PI) films are fabricated by introducing a self-synthesized aniline trimer (ACAT) with a conjugated structure in this work. Since the conjugated ACAT in the main chains of PI improves the electron polarization and carrier mobility of the PI molecular chains, the dielectric constant of the ACAT-PI films is greatly enhanced (4.4–7.4). Meanwhile, the dissipation factor does not increase apparently (0.002–0.013). The dielectric properties are stable even when the temperature is up to 200 °C, the thermal degradation temperature is as high as 450 °C, and the mechanical properties are also excellent (70–105 MPa). Among all the films, the PI film with 5 mol% ACAT exhibits the maximal energy density of 3.6 J cm −3 under the field of 426 kV mm −1 , the high tensile strength (90 MPa) and the excellent thermal stability ( T d5 = 515 °C). The work paves the way to prepare high-temperature polymer dielectric film materials with high energy storage density.
研究领域:
材料科学
·
高分子化学
·
介电物理
·
能源材料
·
功能高分子
✓ 已验证
DOI
高影响因子
POWDER TECHNOLOGY
·
2024
·
IF 4.5
Huifeng Xu,Pengfei Wang,Saiwei Luan,Lixia Cheng,Zhenxiao Fu,Xiuhua Cao,Lei Zhang,Shuhui Yu,Rong Sun
Conventionally, tetragonality in BaTiO 3 powder is attributed to grain size, disregarding the role of Ba/Ti ratio. However, our study reveals a significant impact of Ba/Ti ratio on tetragonality in BaTiO 3 . With an increase in Ba/Ti ratio from 0.990 to 1.010, particle size remains around 200 nm. Tetragonality initially rises from 1.006 to a maximum of 1.0092 at Ba/Ti = 1.000, then decreases to 1.005. Lower tetragonality is associated with Ba or Ti vacancies, using density functional theory (DFT), we analyzed the electron density and lattice distinction in BaTiO 3 powders. Both Ba and Ti vacancies affect lattice distortion, the Ti vacancies leading to more significant lattice expansion and lower tetragonality than Ba vacancies. Using this powder, we fabricated high-density BaTiO 3 ceramics and multi-layer ceramics capacitors (MLCCs) with X7R temperature stability (−55 to 125 °C, ±15% coefficient) and excellent reliability. This strategy has broad implications for tetragonal BaTiO 3 nanopowders and MLCCs development.
研究领域:
材料科学
·
无机非金属材料
·
电子陶瓷
·
固态化学
·
功能材料
✓ 已验证
DOI
高影响因子
SYNTHETIC METALS
·
2016
·
IF 2.299
Qiang Zhao,Junhua Chen,Fubin Luo,Lu Shen,Ying Wang,Kun Wu,Mangeng Lu
Nanostructure of ordered polyaniline-graphene (PANI-rGO PMAS ) hybrid nanomaterials is assembled based on poly(2-methoxyaniline-5-sulfonic acid) (PMAS) functionalized reduced graphene oxide (rGO PMAS ) nanosheets. The presence of PMAS not only improves dispersibility of reduced graphene oxide nanosheets, but also plays a key role for heterogeneous nucleation of polyaniline (PANI) nanorods . The formation mechanism of ordered PANI-rGO PMAS hybrid nanomaterials was studied in details by using field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) and ultraviolet-visible spectrophotometry (UV–vis). The conductivity of PANI-rGO PMAS hybrid with 17 wt% rGO PMAS is as high as 4480 S/m, compared with 2.93 S/m for pure PANI. The cyclic voltammetry tests indicate that, PANI-rGO PMAS containing 2 wt% rGO PMAS possesses fast response to redox reactions and excellent reversible stability. It has a high specific capacitance of 385 F g −1 at the scan rate of 10 mV s −1 with potential ranges from −0.2 to 0.8 V. This ordered polyaniline-graphene hybrid has potential applications for flexible supercapacitors, sensors, batteries, electromagnetic materials and thermoelectric materials, etc.
研究领域:
材料科学
·
纳米科技
·
高分子化学
·
电化学
·
能源材料
✓ 已验证
DOI
高影响因子
JOURNAL OF POWER SOURCES
·
2017
·
IF 6.395
Yongpeng Cui,Huanlei Wang,Nan Mao,Wenhua Yu,Jing Shi,Minghua Huang,Wei Liu,Shougang Chen,Xin Wang
The increasing demand for supercapacitors with high energy and power density has attracted extensive attention in designing advanced carbon materials with high accessible surface area, hierarchical porosity , and 2D/3D morphology. Here, we report a new approach to tune the morphology and structure of the nanocarbons by using methyl cellulose as the precursor. Due to the varying effect of different activating agents, the interconnected sheet-like carbon with a high surface area of up to 2285 m 2 g −1 and a thickness down to ∼4 nm can be obtained. These important characteristics make the nanocarbons demonstrate a high capacitance of 144 F g −1 at 1 A g −1 and 20 °C, and an excellent capacitance retention ratio of 64% at 100 A g −1 in ionic liquid . Because of the high fraction of meso/macropores for nanocarbons, an outstanding capacitance of 116 F g −1 can be achieved at 0 °C, with a high capacitance retention ratio of 39% at 100 A g −1 . A high energy of 16–17 and 9–10 W h kg −1 can be maintained at 20 and 0 °C when the supercapacitor is charged in less than 1s. The excellent electrochemical response of nanocarbons suggests that the proposed preparation process is promising for developing advanced carbon electrodes.
研究领域:
材料科学
·
电化学
·
纳米科技
·
能源存储
·
功能材料
✓ 已验证
DOI
高影响因子
CERAMICS INTERNATIONAL
·
2021
·Vol. 48
·期 3
·3636-3646
·
IF 4.527
Shunxiang Wang,Songwen Fang,Kexiang Zhang,Yongjin Zou,Zuoan Xiao,Fen Xu,Lixian Sun,Cuili Xiang
A poor electrical conductivity and short cycle life limits the wide application of transition metal oxides in energy storage applications. In this study, yolk-shell structured CuCo 2 S 4 was grown on NiO nanosheets (NiO@CuCo 2 S 4 ) via a hydrothermal method and vulcanization , which combined the synergistic interactions between Ni, Co, and Cu. The effect of varying the amount of the vulcanizing agent (thiourea) on the electrochemical performance of NiO@CuCo 2 S 4 was also investigated. Moreover, the amount of thiourea not only tuned the morphology of the composite, but significantly influenced its electrochemical performance. When the Cu 2+ : Co 2+ : thiourea molar ratio in the precursor solution was 1:2:6, the obtained NiO@CuCo 2 S 4 exhibited the best electrochemical performance of the various systems examined, with a specific capacitance of 1658 F g −1 being achieved at 1 A g −1 . Density functional theory calculations further confirmed the excellent synergistic effect between NiO and CuCo 2 S 4 . In addition, the asymmetric supercapacitor composed of a NiO@CuCo 2 S 4 positive electrode reached an ultrahigh energy density of 73 Wh kg −1 at a power density of 802 W kg −1 , as well as excellent cycling stability (i.e., 91% capacitance retention after 5000 cycles). These results suggest that NiO@CuCo 2 S 4 is a promising candidate for use in energy storage applications.
研究领域:
材料科学
·
电化学
·
纳米科技
·
能源存储
·
功能材料
✓ 已验证
DOI
高影响因子
JOURNAL OF SOLID STATE CHEMISTRY
·
2022
·
IF 3.656
Jiaying Zhang,Zhendong Yao,Wenzhen Zou,Qiang Shen,Meiqiang Fan,Tingli Ma
Transition trimetallic sulfide NiCoMn–S attracts great attention due to its high specific capacity for hybrid supercapacitors , as well as Ti 3 C 2 is considered essentially as a potential new electrode material with iconic two-dimensional layered structure and excellent conductivity. Herein, NiCoMn–S nanoparticles are composited with two-dimensional layered Ti 3 C 2 via simple one-step hydrothermal method , which is first applied as positive electrode in hybrid supercapacitors (HSCs). A large number of NiCoMn–S nanoparticles distribute on the surface of Ti 3 C 2 and even insert into the Ti 3 C 2 layers, providing abundant electrochemical active sites for redox reaction and enhancing the mechanical stability for composites. Moreover, the NiCoMn–S/Ti 3 C 2 composites show lower charge-transfer resistance than pure NiCoMn–S, illustrating that the two-dimensional layered structure of Ti 3 C 2 improve the conductivity and supply additional electronic channels for ion transportation. The NiCoMn–S/Ti 3 C 2 -3.4% delivers a specific capacity of 347.1 C g −1 at a specific density of 1 A g −1 , which is 28% higher than that of pure NiCoMn–S (270.2 C g −1 at 1 A g −1 ). Finally, a hybrid supercapacitor (HSC) is assembled by using NiCoMn–S/Ti 3 C 2 -3.4% as positive electrode and RGO as negative electrode, realizing a specific capacity of 164.3 C g −1 at 1 A g −1 and high specific energy of 16.2 Wh kg −1 at a specific power of 15 kW kg −1 .
研究领域:
材料科学
·
电化学
·
纳米材料
·
能源存储
·
功能材料
✓ 已验证
DOI
高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2022
·
IF 4.598
Dexi Liu,Shichang Xu,Yanmeng Cai,Yue Wang,Jiaqi Guo,Youlin Li
The conventional separation technologies, like chemical precipitation and adsorption processes, cannot quickly and selectively separate and recycle heavy metal ions from waste. Due to its rich sulfur content and excellent electrical conductivity, vanadium disulfide is a potential material for effectively removing lead from wastewater. The vanadium disulfide material with selective adsorption ability was introduced into CDI technology to construct a coupling technology with both advantages. The N -doped modified ZIF@vanadium disulfide (ZAC@VS 2 ) composites were successfully synthesized by hydrothermal method. Electrosorption experiments show that ZAC@VS 2 material presents the remarkable saturated adsorption capacity to lead(II) ions (239.52 mg/g) in the 500 mg/L PbCl 2 solution. In the triplex blend system (Fe 3+ /Pb 2+ /Na + ) with each solute density of 100 mg/L, the saturated adsorption efficiency of 85.4% to Pb 2+ can still be maintained. In addition, compared with the Langmuir(R 2 =0.873) adsorption isotherm model, the Freundlich model (R 2 =0.922) can be better used to fit the adsorption process, which proves that the adsorption process is multilayered and heterogeneous. XPS tests and competitive adsorption experiments show that the electric double layer (EDL) and complexation together promote the selective adsorption of heavy metal ions by ZAC@VS 2 . ZAC@VS 2 composite electrode shows excellent performance in the removal of lead ions in battery waste liquid, indicating the potential of introducing ZAC@VS 2 into CDI to remove lead ions.
研究领域:
环境科学
·
材料科学
·
水处理技术
·
重金属污染控制
·
电化学工程
✓ 已验证
DOI
高影响因子
Energy & Environmental Materials
·
2023
·Vol. 7
·期 3
·e12641
·
IF 15
Huachao Yang,Yiheng Qi,Zifan Wang,Qinghu Pan,Chuanzhi Zhang,Jianhua Yan,Kefa Cen,Zheng Bo,Kostya (Ken) Ostrikov
Safe operation of electrochemical capacitors (supercapacitors) is hindered by the flammability of commercial organic electrolytes. Non-flammable Water-in-Salt (WIS) electrolytes are promising alternatives; however, they are plagued by the limited operation voltage window (typically ≤2.3 V) and inherent corrosion of current collectors. Herein, a novel deep eutectic solvent (DES)-based electrolyte which uses formamide (FMD) as hydrogen-bond donor and sodium nitrate (NaNO 3 ) as hydrogen-bond acceptor is demonstrated. The electrolyte exhibits the wide electrochemical stability window (3.14 V), high electrical conductivity (14.01 mS cm −1 ), good flame-retardance, anticorrosive property, and ultralow cost (7% of the commercial electrolyte and 2% of WIS). Raman spectroscopy and Density Functional Theory calculations reveal that the hydrogen bonds between the FMD molecules and NO 3 − ions are primarily responsible for the superior stability and conductivity. The developed NaNO 3 /FMD-based coin cell supercapacitor is among the best-performing state-of-art DES and WIS devices, evidenced by the high voltage window (2.6 V), outstanding energy and power densities (22.77 Wh kg −1 at 630 W kg −1 and 17.37 kW kg −1 at 12.55 Wh kg −1 ), ultralong cyclic stability (86% after 30 000 cycles), and negligible current collector corrosion. The NaNO 3 /FMD industry adoption potential is demonstrated by fabricating 100 F pouch cell supercapacitors using commercial aluminum current collectors.
研究领域:
电化学
·
材料科学
·
能源存储
·
应用化学
·
物理化学
✓ 已验证
DOI
高影响因子
JOURNAL OF POWER SOURCES
·
2021
·
IF 9.127
Rui Xuan,Jinhui Li,Dongxu Huang,Tao Wang,Bo Zhang,Fangfang Niu,Guoping Zhang,Rong Sun,Ching-Ping Wong
With the continuous development of flexible electronic devices, the corresponding demands for electrochemical storage devices with flexibility and self-healing properties have been raised. However, the current supercapacitors still have great limitations in mechanical and self-healing performance. Herein, flexible and self-healing poly (2-acrylamido-2-methyl-1-propanesulfonic acid) (PAMPSA)/polyvinylimidazole (PVI)/LiCl polyelectrolyte is easily fabricated by a one-step copolymerization . The combined effect of electrostatic interaction and hydrogen bonding significantly enhances the mechanical and self-repairing ability of polyelectrolytes, showing excellent stretchability of 1137%, fracture stress of 154.57 kPa, and high healing efficiency of 91% at room temperature for 24 h. Besides, flexible electrode is prepared by adsorbing poly 3,4-ethylenedioxythiophene/polystyrene sulfonate on a polyurethane sponge. After assembly with a polyelectrolyte, the as-prepared supercapacitor proves excellent electrochemical performance. The area capacitance is 106 mF cm −2 at 50 mV s −1 and excellent cycle stability (97% capacity retention rate after 2000 cycles). In addition, the completely cut off supercapacitor can be successfully restored to 90% of the original capacitance, and still maintain a capacitance retention rate of up to 98% after 1000 cycles. This work provides a possible solution for designing low-cost intelligent and durable electrochemical storage device for smart clothing or electronic skin.
研究领域:
材料科学
·
高分子化学
·
电化学
·
柔性电子学
·
能源存储
✓ 已验证
DOI
高影响因子
IONICS
·
2018
·Vol. 25
·期 1
·241-251
·
IF 2.347
Wen Xinge,Dong Tao,Liu Ao,Zheng Shuohang,Chen Shimou,Han Yifan,Zhang Suojiang
As a polymer host, one polymeric ionic liquid poly(methyl methacrylate-1-vinyl-3-ethyl-imidazolium bis(trifluoromethylsulfonyl) imide) (abbr. P(MMA-co-VEImTFSI)) was successfully synthesized and characterized. Four poly(vinylidene fluoride-co-hexafluoropropylene) (abbr. PVDF-HFP)-based polymer electrolytes were prepared by blending 0, 5,15, and 25 wt% P(MMA-co-VEImTFSI). The electrochemical performances of the prepared electrolytes were studied carefully. The results revealed that increasing the polymeric ionic liquid content, the ionic conductivity of the polymer electrolytes could be enhanced and it obeyed the Arrhenius rule. The highest ionic conductivity of the polymer electrolytes was up to 2.09 × 10 −3 S cm −1 at room temperature. The polymer with 25 wt% polymeric ionic liquid showed an excellent electrochemical performance for supercapacitor electrolyte. After 2000 cycles, the retention of capacitance in P(MMA-co-VEImTFSI)-based polymer electrolyte was above 80%. It implied that the present P(MMA-co-VEImTFSI) polymeric ionic liquid was a decent component candidate in the high-performance polymer electrolytes.
研究领域:
材料科学
·
电化学
·
高分子化学
·
能源存储
·
功能材料
✓ 已验证
DOI
高影响因子
Energy Technology
·
2021
·Vol. 9
·期 12
·2100743
·
IF 3.631
Xin Hou,Penggang Ren,Zhong Dai,Zhengzheng Guo,Zengping Zhang,Aiyue Sun,Wenwei He,Fang Ren,Yanling Jin
Herein, nitrogen, oxygen codoped porous carbon nanofibers (CNFs) from corn residue-derived lignin are fabricated via the electrospinning method, followed by introduction of graphenes (GNs) via a simple “brush-coating and drying” process. The obtained GN-coated carbon nanofibers (CNFs@GNs) exhibit a 3D network architecture, abundance of heteroatoms, excellent electrical conductivity, high specific surface area (700.92 m 2 g −1 ), thus boosting the electrochemical performances. The CNFs@GNs electrode delivers a higher specific capacitance of 271.1 F g −1 than CNFs (200.3 F g −1 ) at 1 A g −1 . Furthermore, the assembled CNFs@GNs symmetric supercapacitor exhibits an energy density of 20.3 Wh kg −1 at the power density of 199.97 W kg −1 together with a high charge/discharge reversibility of 97.3% and Coulombic efficiency of 99.81% after 10 000 cycles. This “brush-coating and drying” strategy utilized here provides a convenient and efficient route for designing CNFs and GN composites and can be utilized in other active materials.
研究领域:
材料科学
·
纳米科技
·
电化学
·
能源存储
·
功能材料
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）