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CHEMICAL COMMUNICATIONS · 2015 ·Vol. 51 ·期 15 ·3227-3230 · IF 6.834

Exploration of Na2.65Ti3.35Fe0.65O9 as anode materials for Na-ion batteries

Maowen Xu,Jun-Ke Hou,Yu-Bin Niu,Guan-Nan Li,Yu-Tao Li,Chang Ming Li

Na2.65Ti3.35Fe0.65O9 rods were prepared by a simple solid-state route and coated with carbon to enhance their electronic conductivity. For the first time, Na2.65Ti3.35Fe0.65O9 was explored as an anode material for Na-ion batteries to deliver a discharge capacity of 137.5 mA h g−1 at a current rate of 40 mA g−1. The charge/discharge capacity of a carbon-coated sample increased by 46.3% to achieve 201.1 mA h g−1.

研究领域: 材料科学 · 电化学 · 能源存储
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IONICS · 2019 ·Vol. 26 ·期 2 ·627-637 · IF 2.289

Ni and F co-modification to enhance the electrochemical properties of Li4Ti5O12 anode materials for lithium-ion batteries

Zhai Huanhuan,Shuai Yi,Wang Yu,Chen Kanghua

As a negative electrode material, the main drawbacks of Li 4 Ti 5 O 12 (LTO) are its low electric conductivity and poor Li-ion diffusion coefficient. Fortunately, elements modification to address these problems is an effective method. Herein, we firstly report Ni and F co-modified LTO material which is synthesized via a solid-state reaction. Powder X-ray diffraction, scanning electron microscopy, and X-ray photoelectron spectroscopy were conducted to investigate the structure and morphology. Afterwards, we surprisingly find that Ni and F co-modification can reduce the overall charge transfer resistance of LTO for part of Ti 4+ converts into Ti 3+ and Ni 2+ ions supply the charge carriers. When test in battery, a superior discharge capacity of 236.1 mAh g −1 at 0.036 A g −1 is obtained, much higher than that of pristine LTO (196.9 mAh g −1 ). Furthermore, it still retains a discharge capacity of 174.6 mAh g −1 after 200 cycles at 0.18 A g −1 and exhibits an excellent rate performance.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 固体化学
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CHEMICAL COMMUNICATIONS · 2016 ·Vol. 52 ·期 64 ·9969-9971 · IF 6.567

Exploration of a calcium–organic framework as an anode material for sodium-ion batteries

Yan Zhang,Yubin Niu,Min-Qiang Wang,Jingang Yang,Shiyu Lu,Jin Han,Shu-Juan Bao,Maowen Xu

In this communication, we designed and synthesized a novel calcium–organic framework and presented it as an anode material for sodium-ion batteries. The results show that it delivers a reversible capacity of higher than 140 mA h g−1 even after 300 cycles. The remarkable performance is attributed to the high structural stability and extremely low solubility of the calcium–organic framework in electrolytes.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 功能材料
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NEW JOURNAL OF CHEMISTRY · 2022 ·Vol. 46 ·期 19 ·9432-9439 · IF 3.925

A scalable ball milling strategy to endow SnS anode electrodes with free volume property for enhanced electrochemical performance

Huibin Guan,Dong Feng,Qi Liu,Tianbiao Zeng

Among the tin-based composites, stannous sulfide (SnS) is a prospective material to serve as an anode for lithium-ion batteries (LiBs) owing to its high theoretical-capacity, layer-structure for fast Li+ diffusion paths, and low toxicity. However, severe volume expansion/shrinkage exfoliates the electrode coating, leading to the severe loss of active materials. Herein, free volume was introduced into SnS to relieve the sequelae of volume expansion/shrinkage creatively, which effectively improved the cyclability of the SnS-based anode. The as-synthesized SnS/G-15% exhibited overall optimal electrochemical performances, i.e., the highest reversible capacity and best cyclability over pure SnS, SnS/G-5% and SnS/G-25%. Ex situ scanning electron microscopy images also illustrated that no cracks were generated in the cycled SnS/G-15% electrode. This work highlights an efficient and cost effective approach for the synthesis of long-cycle life and high-cyclability anodes.

研究领域: 材料科学 · 电化学 · 纳米材料 · 能源存储 · 电池技术
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY · 2019 · IF 3.218

Lath-shaped biomass derived hard carbon as anode materials with super rate capability for sodium-ion batteries

Xiaoxia Ren,Shou-Dong Xu,Shibin Liu,Liang Chen,Ding Zhang,Li Qiu

Biomass wastes or biomass derived hard carbon materials with the advantages of green, as well as economic and high reversible capacity have became the promising anode materials for sodium ion batteries (SIBs). Despite this, the poor rate capability hinders their further development. Here, we synthesized lath-shaped hard carbon materials derived from peanut shells by a two-step approach, namely a hydrothermal pretreatment for different treatment time first, and then a carbonized process at 800   °C. Morphology and structural characterizations (SEM, XRD and Raman) prove the hydrothermal pretreatment has a great influence on morphology transformation, the layer spacing, as well as the defect concentration which can enhance the adsorption sites of Na + and shorten the transport route of sodium ions . The PSDHCs-4 (hydrothermal treatment for 4   h) electrode can deliver the highest reversible capacity of 256   ±   5 mAh g −1 , and show the best capacity retention of 97   ±   2% at the current rate of 0.1 C after 100   cycles. More importantly, PSDHCs-4 electrode shows the excellent rate performances with a reversible capacity of 261, 244, 206, 163, 125, and 100 mAh g −1 at the current rates of 0.1, 0.2, 0.5, 1.0, 2.0 and 5.0 C, respectively. These remarkable electrochemical properties indicate that PSDHCs-4 material should be a promising anode material for SIBs.

研究领域: 材料科学 · 电化学 · 能源存储 · 纳米材料 · 可持续能源 · 碳材料
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JOURNAL OF ALLOYS AND COMPOUNDS · 2017 · IF 3.133

Rational design of graphene-encapsulated NiCo2O4 core-shell nanostructures as an anode material for sodium-ion batteries

Yanrong Wang,Hui Huang,Qingshui Xie,Yuanpeng Wang,Baihua Qu

Sodium-ion batteries (SIBs) have gained more and more interest for grid-level energy storage applications compared with current lithium-ion batteries (LIBs). In this paper, well-uniform and dispersed spindle-shaped NiCo 2 O 4 particles were synthesized by solvothermal method, and then graphene-encapsulated NiCo 2 O 4 (NiCo 2 O 4 @G) was formed core-shell nanostructures , which greatly enhanced the electronic and ionic (electro-active) conduction and also effectively buffering to accommodate the strain. Benefit from its structure feature, the prepared NiCo 2 O 4 @G core-shell nanostructures composite shows good cycling with a capacity of up to ∼400 mAh g −1 (100 mA g −1 ) in 100 cycles for NIBs anode. The facile synthesis process and excellent SIBs behaviors in this paper are expected to be extended in developing other anode materials in battery system.

研究领域: 材料科学 · 电化学 · 能源存储 · 纳米材料 · 电池技术
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JOURNAL OF POWER SOURCES · 2017 · IF 6.395

Comparative study of Pb1-xBaxLi2Ti6O14 (0≤x≤1) as lithium storage materials for secondary batteries

Haoxiang Yu,Minghe Luo,Hua Lan,Lei Yan,Shangshu Qian,Wuquan Ye,Miao Shui,Nengbing Long,Jie Shu

The preparation and characterization of Pb 1- x Ba x Li 2 Ti 6 O 14 ( x  = 0, 1/4, 1/2, 3/4, 1) as anode materials for lithium ion batteries are investigated in this research. The structure, morphology and electrochemical properties are compared with each other by changing the Pb/Ba atomic ratio in Pb 1- x Ba x Li 2 Ti 6 O 14 . It can be observed that each sample shows the same orthorhombic structure with Cmca space group. Moreover, it can also be found that the working potential, conductivity, cycling and rate performances of as-received samples gradually change along with the evolution of x in Pb 1- x Ba x Li 2 Ti 6 O 14 ( x  = 0, 1/4, 1/2, 3/4, 1). Electrochemical evaluation shows that the operating potential of the as-received sample gradually decreases with increasing x value in Pb 1- x Ba x Li 2 Ti 6 O 14 and its initial charge capacity increases reversely. Moreover, different Pb/Ba atomic ratio also brings different cycling stability for Pb 1- x Ba x Li 2 Ti 6 O 14 . Especially for Pb 3/4 Ba 1/4 Li 2 Ti 6 O 14 , it presents better electrochemical properties than other samples. After 120 cycles, the reversible capacity of Pb 3/4 Ba 1/4 Li 2 Ti 6 O 14 is maintained at 129.7 mAh g −1 with capacity retention of 88.3%. In addition, its electrochemical reversibility is also demonstrated by in-situ X-ray investigation.

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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Advanced Energy and Sustainability Research · 2021 ·Vol. 2 ·期 6 ·2000095 · IF 0

Layered Structure Na2Ti3O7 as a Promising Anode Material for Sodium-Ion Batteries

Jun Pan,Nana Wang,Dan Lv,Wujie Dong,Jian Yang,Fuqiang Huang

Sodium-ion batteries (SIBs), as next-generation energy storage devices, can be made by a similar production process to lithium-ion batteries (LIBs). The key to accelerating their commercialization is to discover appropriate high-performance electrode materials with low cost, nontoxicity, and simple synthetic features. Herein, layered-structure Na 2 Ti 3 O 7 , with the advantages of appropriate charge/discharge plateaus, superior stability, environmental friendliness, and ease of preparation using cheap raw materials, is selected for assembly in full-cell battery packs to evaluate its suitability for practical application. When evaluated in a coin cell, it has a capacity of 77.2 mAh g −1 at 1 A g −1 after 10 000 cycles with capacity retention of 99.9%, demonstrating its excellent stability. In the case of a soft-pack battery, it retains 22.3 mAh g −1 at 0.1 A g −1 and 18.1 mAh g −1 at 0.05 A g −1 after 50 cycles. After cycling, there is no sodium dendrite formation or active material shedding, further confirming its safety in practical application. Therefore, Na 2 Ti 3 O 7 as another intercalation/deintercalation mechanism material has application potential in the future.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 纳米材料 · 电池技术
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CERAMICS INTERNATIONAL · 2016 ·Vol. 43 ·期 1 ·363-367 · IF 2.758

Porous Fe2O3 nanotubes as advanced anode for high performance lithium ion batteries

Mingchen Sun,Mengfei Sun,Hongxun Yang,Wanghua Song,Yu Nie,Shengnan Sun

One-dimensional porous Fe 2 O 3 nanotubes with 2   µm length, 220   nm outer diameter and 65   nm wall thickness were firstly synthesized via a low temperature hydrothermal method followed by thermal treatment. As advanced anode for lithium ion batteries , porous Fe 2 O 3 nanotubes exhibit obviously enhanced electrochemical properties in terms of lithium storage capacity (1050.1   mA   h   g −1 at 100   mA   g −1 rate), initial coulombic efficiency (78.4%), cycle performances (90.6% capacity retention at 50th cycle), and rate capability (613.7   mA   h   g −1 at 1000   mA   g −1 rate). This enhancement could be attributed to the one-dimensional nanostructure of porous Fe 2 O 3 nanotubes which could increase contact area between electrolyte and active materials, shorten migration path for Li + ions and electrons, and accommodate the volume variations via additional void space during cycling.

研究领域: 材料科学 · 电化学 · 纳米科技 · 能源存储 · 无机功能材料
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JOURNAL OF ALLOYS AND COMPOUNDS · 2018 · IF 3.779

One-step solid-phase synthesis of binder-free molybdenum disulfide/carbon fibers paper anode for high-performance lithium-ion batteries

Wenyuan He,Xuejun Zheng,Jinfeng Peng,Qiang Zhang,Dazhao Pei,Xinyang Yan

A facile one-step solid-phase synthesis strategy is developed for synthesizing a binder-free molybdenum disulfide/carbon fibers paper (MoS 2 /CFP) anode. The microstructure, composition, morphology and electrochemical performances were investigated. It is found that the thin MoS 2 layers are well anchored on the interlaced carbon fibers to form MoS 2 /CFP, which has mesoporous structure and large specific surface area of ∼18.8 m 2 g -1 . As a result, the obtained MoS 2 /CFP anode exhibits a reversible capacity of 261 mAh·g −1 with 31.2% loading ratio of MoS 2 . After subtracting the capacity of CFP, the MoS 2 in the composite anode delivers a reversible capacity of 539 mAh·g −1 and shows better cycle stability than commercial MoS 2 after 100 cycles at 100 mA g −1 . The remarkable electrochemical performances could be attributed to the buffer space among carbon fibers for the volume changes of MoS 2 as well as the highly conductive carbon fibers network, suggesting that the MoS 2 /CFP is a promising binder-free anode for lithium-ion batteries.

研究领域: 材料科学 · 电化学 · 纳米材料 · 能源存储 · 电池技术
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JOURNAL OF POWER SOURCES · 2014 · IF 5.211

Phase composition and electrochemical performance of sodium lithium titanates as anode materials for lithium rechargeable batteries

Kaiqiang Wu,Jie Shu,Xiaoting Lin,Lianyi Shao,Peng Li,Miao Shui,Mengmeng Lao,Nengbing Long,Dongjie Wang

A series of Na x Li 4−x Ti 6 O 14 (0 ≤ x ≤ 4) are prepared by solid-state method and their structures, morphologies and electrochemical properties are compared by changing the Na/Li atomic ratio. It can be found that two single-phase samples of Na 2 Li 2 Ti 6 O 14 and Na 4 Ti 6 O 14 and three multi-phase samples of Li 4 Ti 6 O 14 (Li 4 Ti 5 O 12 /TiO 2 ), NaLi 3 Ti 6 O 14 (Na 2 Li 2 Ti 6 O 14 /Li 4 Ti 5 O 12 /TiO 2 ) and Na 3 LiTi 6 O 14 (Na 2 Li 2 Ti 6 O 14 /Na 2 Ti 3 O 7 ) can be formed by using a stoichiometric ratio of starting materials based on the formula of Na x Li 4−x Ti 6 O 14 . Besides, different Na/Li atomic ratios in Na x Li 4−x Ti 6 O 14 also induce the morphology evolution shifting from round-shape to polyhedron-shape, and then to square-shape with the increase of Na content. Electrochemical tests show that Li 4 Ti 6 O 14 delivers the highest charge capacities of 116 mAh g −1 at 100 mA g −1 , 91.5 mAh g −1 at 200 mA g −1 , 77.5 mAh g −1 at 300 mA g −1 and 66.9 mAh g −1 at 400 mA g −1 among five samples. For comparison, Na 4 Ti 6 O 14 only reveals the reversible capacities of 38.6 mAh g −1 at 100 mA g −1 , 30.2 mAh g −1 at 200 mA g −1 , 24.8 mAh g −1 at 300 mA g −1 and 20.9 mAh g −1 at 400 mA g −1 . It suggests that Li 4 Ti 6 O 14 is the most potential lithium storage material among all the Na x Li 4−x Ti 6 O 14 samples.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 功能材料
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JOURNAL OF ALLOYS AND COMPOUNDS · 2021 · IF 5.316

Electrolytic preparation of porous TiSi2/Si nanocomposites and the electrochemical performances as lithium-ion battery anode

Jiaxu Cheng,Jinghan Qiao,Zongyang Yang,Bowen Zhu,Jianguo Duan,Ding Wang,Rui Huang,Yingjie Zhang,Zhongren Zhou,Peng Dong

One of the key efficient strategies to optimize the silicon micro-structure and to improve the lithium-storage electrochemical performance is to introduce the metallic phase into silicon matrix to realize the silicon-metal recombination as well as the nanocrystallization of silicon structure. The present research introduced metallic titanium to synthesis TiSi 2 /Si nanocomposites by the aid of electrolyzing SiO 2 /TiO 2 in molten salt. The reduced nanocomposites exhibited excellent lithiation stability with the initial discharging specific capacity of 2107 mA h/g and the first columbic efficiency of 89.96%. Particularly benefiting from the compositional TiSi 2 phase and the structural superiority of silicon nanowires surrounded by the alloyed nanoparticles , the as-obtained anode also delivered a high rate capacity. The major objective of this study is to establish the technology for molten salt electrolytic preparation of TiSi 2 /Si nanocomposites for lithium-ion batteries and further to offer solutions for modifying the silicon anode materials .

研究领域: 材料科学 · 电化学 · 纳米科技 · 能源存储 · 无机非金属材料
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