ELECTROCHIMICA ACTA
·
2019
·
IF 5.383
Aijia Wei,Wen Li,Qian Chang,Xue Bai,Rui He,Lihui Zhang,Zhenfa Liu,Yanji Wang
Mg 2+ /F − co-doped LiNi 0.5 Mn 1.5 O 4 cathode material was synthesized by a facile one-step solid-state process. The effect of Mg 2+ /F − co-doping on grain morphology, phase structure, and electrochemical properties was studied by a series of characterizations. Scanning-electron-microscopy images show that Mg 2+ /F − co-doped LiNi 0.5 Mn 1.5 O 4 (denoted LNMO-MF) particles grow larger than pure LiNi 0.5 Mn 1.5 O 4 particles. X-ray diffraction, Raman spectra , Fourier transformation infrared spectroscopy , X-ray photoelectron spectroscopy, and cyclic-voltammetry tests indicate that all samples mainly display a Fd -3m space group and more Mn 3+ ions in the LNMO-MF sample after Mg 2+ /F − co-doping, which is conducive to increasing the cationic disorder degree and enhancing the electronic conductivity of electrode material. Results show that the LNMO-MF cathode material delivers an excellent rate performance with discharge capacities of 142, 144, 140 136, 132, 124, 115, and 100 mAh g −1 at 0.2, 0.5, 1, 2, 3, 5, 7, and 10C (1C = 140 mAh g −1 ), respectively. Remarkably, LNMO-MF also shows cycling stability with a capacity retention of 86.2% at 5C after 400 cycles, which is much higher than that of pure LiNi 0.5 Mn 1.5 O 4 (67.7%). The improvement of LNMO-MF's electrochemical properties could be ascribed to the Mg 2+ /F − co-doping, delivering a more stable structure, better crystallinity , the highest Li + diffusion coefficient , and the lowest charge-transfer resistance.
研究领域:
材料科学
·
电化学
·
无机非金属材料
·
能源存储
·
锂离子电池
·
固态化学
·
功能材料
✓ 已验证
DOI
高影响因子
MATERIALS CHEMISTRY AND PHYSICS
·
2019
·
IF 2.781
Yunjiao Li,Shilei Wang,Yongxiang Chen,Tongxing Lei,Shiyi Deng,Jie Zhu,Jinping Zhang,Jia Guo
Cadmium oxides (CdO), an important semiconductor material , have many superior properties when used as a cathode material for nickel-cadmium batteries. Here, the coating and the doped co-modified LiNi 0.8 Co 0.15 Al 0.05 O 2 cathode are constructed by a continuous wet chemical process and a high-temperature sintering process, wherein the Cd 2+ are uniformly doped in a gradient form and the CdO protective layer is distributed on the outer surface of secondary particles. The Cd-modified NCA material has more stable interfacial and crystal lattice structure, thereby inhibiting harmful phase transitions and side-reactions. Accordingly, the modified sample has excellent electrochemical performance and maintaining a complete spherical morphology during long cycling compared to the pristine sample. In addition, as a pillar ion, cadmium increases the plate spacing and lithium-ion diffusion kinetics. The electrochemical results show that the capacity retention of the modified sample Cd-2000 reached 96.5% and 90.6% after 100 cycles and 200 cycles respectively at 1 C. At the high current rate of 8 C, the initial capacity and retention (100 cycles, 3.0–4.3 V) reach 166.2 mAh g −1 and 95.2%, respectively. Besides, the results of electrochemical impedance spectroscopy (EIS) reveal that CdO modification could decrease the resistance of the cell polarization and impedance increment upon cycling.
研究领域:
材料科学
·
电化学
·
能源存储
·
无机化学
·
半导体材料
✓ 已验证
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2022
·
IF 6.371
Liying Xian,Min Li,Daping Qiu,Chuang Qiu,Cheng Yue,Feng Wang,Ru Yang
Layered P-type structures are integral to most competitive cathodes for sodium-ion batteries (SIBs). However, the performance of P2-type cobalt-based layered materials is unsatisfactory owing to a low initial discharge capacity caused by Na deficiency. Here, Mn-doped Na x CoO 2 with a P3 structure is synthesized by using a modified solvent-thermal method with calcination . A structural analysis shows that partial Mn doping can effectively control P3 phase formation and increase d -layer spacing, thereby improving the diffusion of Na + . In addition, enhanced electrochemical performance is observed in optimized P3-type Na 0.26 Co 0.48 Mn 0.52 O 2 (NCMO-1), which exhibits a reversible specific capacity of 64 mAh g −1 at 3 A g −1 and a good capacity retention of 58% after 500 cycles. Furthermore, the Na-ion full cell constructed with an NCMO-1 cathode and a hard carbon anode yields a competitive energy density of 175.9 Wh kg −1 at 0.4 A g −1 with excellent cycle stability. Thus, this work provides a new viewpoint on the development of P3 structural materials with higher electrochemical performance for SIBs.
研究领域:
材料科学
·
电化学
·
能源存储
·
无机化学
·
固态化学
✓ 已验证
DOI
高影响因子
CERAMICS INTERNATIONAL
·
2024
·Vol. 50
·期 22
·44983-44992
·
IF 5.1
Shuai Zhao,Hai-lin Ren,Yang Su,Cheng-wei Li,Xiao-min Wang
High-nickel layered cathode materials for lithium-ion batteries have received widespread attention in new energy vehicles for their excellent specific energy and cost advantages, and are considered to be the most promising cathode materials for high-energy density lithium-ion batteries. Despite its many advantages, poor thermal stability and rapid capacity degradation have greatly limited its large-scale application. Ion doping is considered to be an effective way to improve its drawbacks, and in this paper, a series of W-doped LiNi 0.9 Co 0.1 O 2 cathode materials were prepared using WO 3 as a tungsten source. Among them, 1 mol% W doping was the most effective, and its reversible capacity of 204.44 mA g −1 still had 93.25 % capacity retention after 100 this cycles at 1C. Combined with DFT calculations , it is found that the introduction of W does not change the original layered structure and the material transitions from semi-metallic to metallic at lower doping concentrations, resulting in more electrons occupying the Fermi energy levels to enhance its electrical conductivity and leading to an elevated spin state and a lower oxidation state of Ni.
研究领域:
材料科学
·
电化学
·
能源存储
·
固态化学
·
计算材料学
✓ 已验证
DOI
高影响因子
JOURNAL OF POWER SOURCES
·
2018
·
IF 6.945
Jing Gao,Chunshui Sun,Lei Xu,Jian Chen,Chong Wang,Decai Guo,Hao Chen
Due to flexible property and light weight, the lithiated Nafion membrane swollen with PC (PC-Li-Nafion) has been employed as both solid-state electrolyte and separator to fabricate solid-state Li-S cells. The electrochemical measurements of PC-Li-Nafion membrane show that its Li-ion transference number is 0.928, ionic conductivity of 2.1 × 10 −4 S cm −1 can be achieved at 70 °C and its electrochemical window is 0 ∼ +4.1 V vs. Li + /Li. It is observed that the Li dendrites are suppressed by using PC-Li-Nafion membrane due to its single-ion conducting property. The amounts of Li-Nafion resin binder and conductive carbon in the cathode are optimized as 40% and 10% respectively to make a balance of ionic and electronic conductivities . A thin-layer Li-Nafion resin with a thickness of around 2 μm is fabricated between the cathode and PC-Li-Nafion membrane to improve the interfacial contact and further enhance the specific capacity of the cell. When measured at 70 °C, the Li-S cell delivers a reversible specific capacity of 1072.8 mAh g −1 (S) at 0.05 C and 895 mAh g −1 (S) at 1 C. The capacity retention at 1 C is 89% after 100 cycles. These results suggest that high-performance solid-state Li-S cells can be fabricated with the Li-Nafion polymer electrolyte .
研究领域:
电化学
·
能源材料
·
固态电池
·
聚合物电解质
·
锂离子电池
·
电极界面工程
·
储能技术
✓ 已验证
DOI
高影响因子
Small
·
2019
·Vol. 15
·期 50
·1904854
·
IF 10.856
Junchao Zheng,Zhuo Yang,Alvin Dai,Linbo Tang,Hanxin Wei,Yunjiao Li,Zhenjiang He,Jun Lu
Although the high energy density and environmental benignancy of LiNi 0.8 Co 0.15 Al 0.05 O 2 (NCA) holds promise for use as cathode material in Li-ion batteries, present low rate capabilities, and fast capacity fade limit its broad commercial applications. Here, it is reported that surface modification of NCA cathode ( R-3m ) with 5 nm-thick nanopillar layers and Fm-3m structures significantly improves electrode structure, morphology, and electrochemical performance. The formation of nanopillar layers increases cycling and working voltage stability of NCA by shielding the host material from hydrofluoric acid and improves structural stability with the electrolyte. The modified NCA cathode exhibits an enhanced 89% capacity retention at a rate of 1 C over that of pristine NCA (75.2%) after 150 cycles and effectively suppresses working voltage fade (a drop of 0.025 V after 300 cycles) during repeated charge–discharge cycles. In addition, the diffusion barrier of Li ions in NCA crystals at 0.80 V is noticeably smaller than that of Li ions in pristine NCA (0.87 eV). These findings demonstrate that this unique surface structure design considerably enhances cycle and rate performance of NCA, which has potential applications in other Ni-rich layered cathode materials.
研究领域:
材料科学
·
电化学
·
能源存储
·
锂离子电池
·
纳米材料
✓ 已验证
DOI
高影响因子
IONICS
·
2016
·Vol. 22
·期 8
·1343-1351
·
IF 2.119
Li Qi-Ling,Xu Wang-Qiong,Bai Hong-Li,Guo Jun-Ming,Su Chang-Wei
ZnO-coated LiMn 2 O 4 cathode materials were prepared by a combustion method using glucose as fuel. The phase structures, size of particles, morphology, and electrochemical performance of pristine and ZnO-coated LiMn 2 O 4 powders are studied in detail by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), galvanostatic charge-discharge test, and X-ray photoelectron spectroscopy (XPS). XRD patterns indicated that surface-modified ZnO have no obvious effect on the bulk structure of the LiMn 2 O 4 . TEM and XPS proved ZnO formation on the surface of the LiMn 2 O 4 particles. Galvanostatic charge/discharge test and rate performance showed that the ZnO coating could improve the capacity and cycling performance of LiMn 2 O 4 . The 2 wt% ZnO-coated LiMn 2 O 4 sample exhibited an initial discharge capacity of 112.8 mAh g −1 with a capacity retention of 84.1 % after 500 cycles at 0.5 C. Besides, a good rate capability at different current densities from 0.5 to 5.0 C can be acquired. CV and EIS measurements showed that the ZnO coating effectively reduced the impacts of polarization and charge transfer resistance upon cycling.
研究领域:
材料科学
·
电化学
·
能源存储
·
无机化学
·
纳米材料
✓ 已验证
DOI
高影响因子
ELECTROCHIMICA ACTA
·
2015
·
IF 4.504
Xinhe Yang,Zicheng Zuo,Haiyan Wang,Quanbin Chen,Hui Zhang,Zhenlei Huang,Borong Wu,Henghui Zhou
A one-step synthesis method is developed to prepare the Li[Ni 0.5 Co 0.2 Mn 0.3 ]O 2 (NCM 523) cathode with uniform tungsten-coating layer for lithium-ion battery . Such modified material shows similar properties with the bare NCM 523 in terms of the primary particles, secondary structure , and specific capacity. With W coating layer , the NCM 523 gives remarkable improvement in the long-term capacity retention in the half-cell testing, which is sharply inconsistent with the result from the full-battery tests, indicating a contradiction between the half-cell and full-battery tests in some case. After further investigations, such conflict between the half-cell and full-cell tests in evaluating the W-coating strategy is attributed to the dissolution of Li 2 WO 4 layer in the electrolyte, which probably destroys the solid electrolyte interface (SEI) on the graphite anode and irreversibly consumes the active lithium ions for renovating SEI in full-cell testing. These results will benefit researchers in the area of lithium-ion batteries to fully understand the differences between the half-cell and full-cell testing, and develop the effective strategies for cathode modifications.
研究领域:
电化学
·
材料科学
·
能源存储
·
电池技术
·
表面改性
·
固态离子学
✓ 已验证
DOI
高影响因子
IONICS
·
2020
·Vol. 26
·期 9
·4257-4265
·
IF 2.394
Jiang Huize,Han Yu,Wang Hui,Zhu Yuhao,Guo Qingpeng,Jiang Haolong,Zheng Chunman,Xie Kai
The poor interface between the active materials, solid electrolytes, and conductive additives in composite cathode materials is the key factor restricting the performance of the all-solid-state lithium-sulfur battery. Here, the composite cathode material was prepared through the method of one-step ball milling. The sulfide electrolyte Li 3 PS 4 (LPS) was formed on the surface of the active material Li 2 S while the conductive additives were incorporated, and the conductive ions and electronic network were constructed simultaneously. After adding an appropriate amount of carbon nanotubes (cnt), the composite cathode exhibited high specific capacity of 1145.2 mAh g −1 after 30 times of cycling at a current density of 0.2 mA cm −2 , and the battery with ultrahigh areal Li 2 S loading also displays high capacity of 962.6 mA g −1 . The composite cathode with high Li 2 S content (56.3%) was prepared, with excellent performance exhibited: the capacity is 741 mAh g −1 after 30 times of cycling at a current density of 0.2 mA cm −2 .
Without additional sulfide electrolyte, the composite cathode materials were prepared by one-step ball milling with lithium sulfide, phosphorus pentasulfide, acetylene black, and carbon nanotubes as raw materials.
研究领域:
材料科学
·
电化学
·
能源存储
·
固态离子学
·
纳米复合材料
✓ 已验证
DOI
高影响因子
Energy Technology
·
2022
·Vol. 11
·期 11
·2200376
·
IF 4.149
Peng Xu,Decheng Zhao,Shupei Liu,Jinghui Ren,Jian Zhou,Ning Wang,Zhoulu Wang,Xiang Liu,Yutong Wu,Yi Zhang
Selenium cathodes are expected to become next-generation energy storage materials due to their high electronic conductivity and volumetric capacity. However, their commercial applications are hindered by polyselenides dissolution and low Se utilization. Herein, a biomass compound, namely lychee seed, is used as a sustainable precursor to design hierarchically porous carbon by a single-step carbonization activation method. With a unique hierarchical porous structure, the lychee seed–derived activated carbon (LSDAC) used to encapsulate selenium delivers a reversible capacity of 446 mA h g −1 at 2 C and 291 mA h g −1 at 5 C after 1000 cycles. The Se/LSDAC electrodes show the most favorable fast-charging and good cycling behavior compared to the previously reported biomass-based carbon materials. By increasing the Se area loading to 9.5 mg cm −2 , the Se/LSDAC cathode maintains an areal capacity of 3.7 mA h cm −2 (3.2 mA cm −2 areal current density) after 80 cycles. High Se loading and economical and fast-charging cathode designs in Li–Se batteries are inspired.
研究领域:
电化学储能
·
材料科学
·
纳米能源材料
·
可持续能源技术
·
先进电池技术
✓ 已验证
DOI
高影响因子
JOURNAL OF POWER SOURCES
·
2020
·
IF 8.247
Tianjiang Sun,Qingshun Nian,Shibing Zheng,Xuming Yuan,Zhanliang Tao
Aqueous zinc-ion batteries (ZIBs) are gaining widespread attention owing to their intrinsic safety and low cost. However, it is still a challenge that finding robust cathode materials to build a high-energy-density aqueous ZIBs. Here, we synthesize a novel layered K 0.41 MnO 2 ·0.5H 2 O (KMO) cathode material for aqueous ZIBs. The constructed Zn//KMO battery shows an ultrahigh discharge capacity of 425 mAh g −1 and a remarkable energy density of 503 Wh kg −1 at 175 mA g −1 , as well as an good durability over 1500 cycles with no obvious capacity fading. A comprehensive study suggests that the water molecules can intercalate into layered KMO with H + and Zn 2+ ions during discharging process. The co-intercalating water not only facilitates ions insertion, but serves as pillars to stabilize the structure of KMO. This work demonstrates the mechanism about water cointercalation and provides a way for designing high-energy-density aqueous ZIBs.
研究领域:
电化学储能
·
材料科学
·
能源化学
·
无机化学
·
电池技术
✓ 已验证
DOI
高影响因子
Advanced Sustainable Systems
·
2024
·Vol. 8
·期 8
·2400098
·
IF 6.5
Fuyu Xiao,Wenbin Lai,Shihan Zeng,Lingjun He,Mingyang Ge,Fenqiang Luo,Peixun Xiong,Hui Lin,Chuyuan Lin,Yongjin Luo,Jixiang Zhang,Qingrong Qian,Qinghua Chen,Lingxing Zeng
The resource scarcity and pollution leakage risk caused by discarding the spent power lithium-ion batteries has aroused growing concern. Recovering and regenerating the cathode material from spent power lithium-ion batteries in an easy and environmentally friendly manner remains a significant challenge and an area of focus in battery research. Hence, a green and convenient method to recover FePO 4 from spent LiFePO 4 cathode powder by using Na 2 S 2 O 8 as an oxidizer and as cathode materials for lithium/sodium-ion batteries (LIBs/SIBs) is reported. Benefiting from the remarkable graphene oxide (GO) and vanadium oxide (V 2 O 5 ) coating, the regenerated FePO 4 –V 2 O 5 –graphene oxide (FePO 4 –V 2 O 5 –GO) is suitable for Li/Na storage (153 mAh g −1 at 0.2C/118 mAh g −1 at 0.5C). The high capacity retention, that stable for 300 cycles in LIBs and 300 cycles for SIBs, is also realized due to the stable structure. This work provides a green strategy for regenerating the cathode of spent lithium-ion batteries and designing cathodes of alkali metal ion batteries.
研究领域:
材料科学
·
电化学
·
能源存储
·
环境科学
·
资源回收
·
纳米材料
·
电池技术
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）