SEPARATION SCIENCE AND TECHNOLOGY
·
2019
·
IF 1.354
Mei Wang,Na Rao,Yuqing Liu,Jiale Li,Qunpeng Cheng,Jianfen Li
TETA or TETA-AEP mixtures were used as an activator to enhance CO2 capture in the MDEA solution. The effect of amount and type of activators, and the viscosity of absorbents on CO2 capture were discussed. The results showed that the positive effect of TETA-AEP mixtures on CO2 capture in the MDEA solution was greater than that of TETA. The optimal absorbent was No. V, whose CO2 absorption capacity/desorption efficiency was 3.08 times/1.18 times of No. І. The viscosity had a little influence on CO2 absorption and an obvious effect on CO2 desorption.
研究领域:
化学工程
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
Energy & Environmental Materials
·
2020
·Vol. 5
·期 1
·245-252
·
IF 0
Chunli Wang,Lianshan Sun,Bingbing Tian,Yong Cheng,Limin Wang
As important ingredients in lithium-ion battery, the Coulombic efficiency and power density greatly impact the electrochemical performances. Although recent literatures have reported nano-porous materials to enhance the specific capacities, intrinsic drawbacks such as poor initial Coulombic efficiency and low volumetric capacity could not be avoided. Herein, we propose a strategy to prepare carbon supported MoO 2 spheres used for lithium-ion battery with high volumetric capacity density. A high initial Coulombic efficiency of 76.5% is obtained due to limited solid electrolyte interface film formed on the exposed surface. Meantime, the sample with an optimal carbon content and a proper structural strength reveals a higher reversible capacity of 956 mA h g −1 than the theoretical capacity of crystalline MoO 2 (838 mA h g −1 ) and a high capacity retention ratio of 96.4% after 100 cycles at 0.5 A g −1 . And an effective compaction capacity density (under 5 MPa) of 670 mA h cm −3 of the spheres proves its potential value in practical applications.
研究领域:
材料科学
·
电化学
·
能源存储
·
纳米材料
·
电池技术
✓ 已验证
DOI
Journal of Materials Chemistry A
·
2016
·Vol. 4
·期 27
·10593-10600
·
IF 8.262
Wei Wen,Jin-Ming Wu,Yin-Zhu Jiang,Jun-Qiang Bai,Lu-Lu Lai
Li-ion microbatteries find wide applications in microdevices. It is important to develop electrode materials with high areal capacity, excellent rate capability and superior safety for microbatteries. TiO2 nanowire arrays satisfy the requirements of high areal capacity, short transport lengths and superior safety for microbatteries, but their areal/volumetric capacity is hindered by the insufficient surface area. TiO2 nanotrees can effectively eliminate these disadvantages of TiO2 nanowires; however, the electrochemical performances of TiO2 nanotrees for Li-ion microbatteries remain unexplored. It is highly desired yet challenging to construct two-dimensional TiO2 nanobranches with an ultrathin thickness and large length on nanoarrays, to maximize the surface area and structural hierarchy of electrodes. Herein, we developed a novel synthetic strategy to fabricate TiO2 nanotrees by depositing anatase/TiO2(B) mixed phase ultrathin nanobelts onto single-crystalline anatase nanowire arrays. The nanobelt branches were several nanometers in thickness and 200–260 nm in length. The growth process and the electrochemical mechanism were investigated. The unique nanoarchitecture and optimal phase structure endow the electrode with high areal capacity and rate capability, which is the best performance for TiO2 nanowire arrays ever documented. The 2nd discharge capacity of the TiO2 nanotrees at 0.1 mA cm−2 is ca. 267 μA h cm−2, corresponding to a volumetric capacity of 330 mA h cm−3. The TiO2 nanotrees have an areal capacity of 205, 141, 97 and 69 μA h cm−2 at a current density of 0.5, 2.0, 5.0 and 10.0 mA cm−2, respectively. The capacity can remain stable for 400 charge–discharge cycles at 1.0 mA cm−2. The present strategy may give hints to elegant electrode designs for energy applications.
研究领域:
材料科学
·
电化学
·
纳米科技
·
能源存储
·
微电子器件
✓ 已验证
DOI
高影响因子
JOURNAL OF RARE EARTHS
·
2017
·Vol. 36
·期 3
·304-310
·
IF 2.429
Shengting Kuang,Zhifeng Zhang,Yanling Li,Haiqin Wei,Wuping Liao
The extraction and separation of heavy rare earths (REs) using newly synthesized α-aminophosphonic acid extractant 2-ethylhexyl-3-(2-ethylhexylamino)pentan-3-yl phosphonic acid (HEHAPP, H A ) in n-heptane were investigated from chloride medium. The extraction stoichiometries of lanthanum , gadolinium , yttrium and lutetium are determined to be RE A 3 by the slope analysis method. The favorable separation factors of adjacent heavy REs(Ⅲ), i.e. β Y/Ho , β Er/Y , β Tm/Er , β Yb/Tm and β Lu/Yb , are determined to be 1.87, 1.36, 3.21, 3.22 and 1.93, respectively, when extracted from a binary system at proper condition. The loading capacities of H A for Ho, Er, Yb and Lu increase in the order Ho < Er < Yb < Lu with the values being 0.201, 0.205, 0.216 and 0.229 mol/L, respectively. So H A would be a potential extractant for the separation of heavy REs(Ⅲ). Among inorganic acids such as H 2 SO 4 , HNO 3 and HCl, HCl is tested to be the most effective stripping agent.
研究领域:
湿法冶金
·
稀土化学
·
分离科学与技术
·
无机化学
·
萃取化学
✓ 已验证
DOI
高影响因子
JOURNAL OF MATERIALS CHEMISTRY
·
2011
·Vol. 21
·期 32
·12068-12077
·
IF 5.101
Dongyang Chen,Shuanjin Wang,Min Xiao,Yuezhong Meng,Allan S. Hay
A novel dihydroxyl monomer bearing 18 electron rich phenyl rings were synthesized and polymerized with other monomers bearing electron deficient phenyl rings to give dense and selective sites in macromolecules for post-sulfonation, which was successfully conducted in ClSO3H/CH2Cl2 solution at room temperature in a subsequential step. The chemical structures were confirmed by 1H NMR and FT-IR spectra. The ionic exchange capacity (IEC) was controlled to be from 0.65 to 1.21 mequiv g−1 to afford considerable proton conductivity. Distinct phase separation was observed in the resulting membranes from SAXS profiles. The SPAEK-5 with an IEC of 1.21 mequiv g−1 gave better proton conductivity than Nafion 117 at all tested temperatures under 100% relative humidity. The membranes exhibited an exceeding stability when immersing in Fenton's reagent (3 wt.% H2O2 + 2 ppm FeSO4) at 80 °C. These properties make them promising candidates for electrochemical applications.
研究领域:
材料科学
·
高分子化学
·
膜科学
·
电化学
·
能源材料
✓ 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
Green Energy & Environment
·
2020
·Vol. 7
·期 1
·53-65
·
IF 6.395
Hong-Li Ding,Hai-Tao Yu,Xiao-dong Wang,Chen-Feng Guo,Bing Zheng,Ying Xie,Ting-Feng Yi
SrLi 2 Ti 6 O 14 (SLTO) coated with different amount of ZrO 2 was successfully prepared. The as-obtained composites are stacked by a series of particles with a pure phase structure and a good crystallinity. Furthermore, ZrO 2 coating not only enhances the structural stability of the materials but also facilitates the diffusion of lithium through the SEI film. As a result, the redox polarization was reduced, and the reversibility of the electrochemical reaction was enhanced. Particularly, SLTO-ZrO 2 -2 sample delivers a high initial lithiation capacity of 283.6 mA h g −1 , and the values maintain at 251.7, 228.0, 207.4, 175.3, and 147.7 mA h g −1 at the current densities of 0.13, 0.26, 0.54, 1.31, and 2.62 A g −1 , respectively. Our experiment also confirmed that SLTO materials coated with ZrO 2 are suitable for high power density applications, and the lithiation specific energy efficiency of SLTO-ZrO 2 -2 is 200% as high as that of pure SLTO at a power density of 1257 W kg −1 .
研究领域:
材料科学
·
电化学
·
能源存储
·
无机非金属材料
·
固态离子学
✓ 已验证
DOI
高影响因子
JOURNAL OF POWER SOURCES
·
2019
·
IF 7.467
Liming Jin,Jie Ni,Chao Shen,Fenglai Peng,Qiang Wu,Donghao Ye,Junsheng Zheng,Gaoran Li,Cunman Zhang,Zhoupeng Li,Jim P. Zheng
A metallically conductive TiB 2 is developed to construct multifunctional separator toward improved lithium-sulfur (Li–S) battery performance. Coupled with two-dimensional graphene, the obtained TiB 2 @G separator fulfills a synergistic combination of strong physical and chemical sulfur immobilization as well as a high-efficiency sulfur reutilization, thus establishing a robust barrier against the polysulfide shuttling and enabling a fast and durable sulfur electrochemistry . As a result, cells based on TiB 2 @G separator exhibit a high sulfur utilization with 1350 mA h g −1 capacity at 0.05C, superb rate capability up to 5.0C, and excellent cyclability with a high capacity retention over 85% after 300 cycles at 0.5C. Moreover, significantly mitigated self-discharge and considerably high areal capacity of 5.8 mA h cm −2 can be also achieved, indicating the great promise of this separator design for the development of high-performance Li–S batteries.
研究领域:
电化学
·
能源材料
·
纳米材料科学
·
储能技术
·
电池化学
✓ 已验证
DOI
高影响因子
CERAMICS INTERNATIONAL
·
2019
·Vol. 45
·期 8
·10633-10639
·
IF 3.45
Guorong Hu,Zhichen Xue,Zhongyuan Luo,Zhongdong Peng,Yanbing Cao,Weigang Wang,Yuexi Zeng,Yong Huang,Yong Tao,Tianfan Li,Zhiyong Zhang,Ke Du
The Li-rich cathode material for long cycle performance and long-term storage performance is a challenge for next-generation lithium-ion batteries due to the rapid capacity degradation over cycling and the formation of residual lithium on the surface during long-term storage. Herein, an elevated performance of Li 1.2 Mn 0.54 Ni 0.13 Co 0.13 O 2 materials via CeO 2 inlay is reported, which was prepared from Li 1.2 Mn 0.54 Ni 0.13 Co 0.13 O 2 by sol-gel inlay with CeO 2 . It was proved by scanning electron microscopy, high-resolution transmission electron microscopy, X-ray diffraction and X-ray photoelectron spectroscopy that cerium oxide cladding not only covered the surface of the material but also diffused into the interior of the material change crystal structure. Cerium oxide on the cladding not only reduces the material's contact with water and carbon dioxide in the air, but also prevents the material from being corroded by electrolyte during electrochemical test. The position of the transition metal atom is replaced Ce atoms, which increases the unit cell volume and the stability of the Li-rich material during the cycling. The results show that the storage property and the electrochemical cycling property of the material have been improved obviously. The CeO 2 inlaid lithium rich material discharged 204.6 mAh/g for the first time at the current of 1C, and 164.4 mAh/g after 150 charge and discharge cycles with corresponding capacity retention rate of 80.35%, compared with the retention rate of 57.26% for pristine Li-rich material capacity. After being stored in humid air for 40 days, the CeO 2 inlaid lithium-rich material showed better electrochemical performance than the pristine one. It is powerfully demonstrated that the CeO 2 inlay strategy here holds huge promise for surface modification of electrode materials for lithium-ion batteries.
研究领域:
材料科学
·
电化学
·
锂离子电池
·
能源存储
·
无机非金属材料
✓ 已验证
DOI
高影响因子
Journal of Energy Chemistry
·
2016
·Vol. 26
·期 3
·481-487
·
IF 2.322
Zhen Zhang,Pengfei Zhou,Huanju Meng,Chengcheng Chen,Fangyi Cheng,Zhanliang Tao,Jun Chen
LiNi 0.915 Co 0.075 Al 0.01 O 2 (NCA) with Zr(OH) 4 coating is demonstrated as high performance cathode material for lithium ion batteries (LIBs). The coated materials are synthesized via a simple dry coating method of NCA with Zr(OH) 4 powders, and then characterized with scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). Experimental results show that amorphous Zr(OH) 4 powders have been successfully coated on the surface of spherical NCA particles, exhibiting improved electrochemical performance . 0.50 wt% Zr(OH) 4 coated NCA delivers a capacity of 197.6 mAh/g at the first cycle and 154.3 mAh/g after 100 cycles with a capacity retention of 78.1% at 1 C rate. In comparison, the pure NCA shows a capacity of 194.6 mAh/g at the first cycle and 142.5 mAh/g after 100 cycles with a capacity retention of 73.2% at 1 C rate. Electrochemical impedance spectroscopy (EIS) results show that the coated material exhibits a lower resistance, indicating that the coating layer can efficiently suppress transition metals dissolution and decrease the side reactions at the surface between the electrode and electrolyte. Therefore, surface coating with amorphous Zr(OH) 4 is a simple and useful method to enhance the electrochemical performance of NCA-based materials for the cathode of LIBs.
研究领域:
电化学
·
材料科学
·
能源存储
·
电池技术
·
无机非金属材料
·
固态化学
✓ 已验证
DOI
高影响因子
ELECTROCHIMICA ACTA
·
2021
·
IF 6.901
Xiaozhong Zhou,Zhaoyi Qi,Yuyuan Jiang,Pengfei Yan,Juanxia Ding,Haiyan Wang,Hongkai Lu,Dongxu Liu,Kaifa Dong,Yougen Tang,Dongfei Sun,Ziqiang Lei
SiO x is regarded as a promising anode material for the next-generation lithium-ion batteries with high energy density. However, the reduplicative volume changes during cycling cause the pulverizations of Si, leading to decreased utilization of active Si component and poor cycling performance. Herein, a facile and scalable Fe-Cr decorating strategy is reported to boost the lithium storage of SiO x anode. Our comprehensive characterizations indicate that there are strong interactions between Fe-Cr and SiO x during a facile ball milling process. After cycling, Fe-Cr nanoparticles are dispersed in the in-situ formed lithium silicates and Li 2 O matrix, which can maintain superior conductivity of lithium ion and electron for the active components through point-to-point connections. This unique structure boosts the electrochemical de-alloying process of the low-valent Li x Si (0 ≤ x ≤ 2), and increases effective utilization of the active Si component during cycling, resulting in improvement of reversible capacity and cycling stability. This bm SiO x -FeCr electrode can deliver high reversible specific capacity (1370 m Ah g −1 at 200 mA g −1 ), good rate capability (653.8 m Ah g −1 at 2000 mA g −1 ), and superior cycling stability. This work provides a promising route for improving the utilization of active Si component and the structural stability of SiO x -based anodes.
研究领域:
材料科学
·
电化学
·
纳米材料
·
能源存储
·
电池技术
·
固态物理
✓ 已验证
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2022
·
IF 6.371
Huicai Xie,Quanyi Liu,Xiaohua Luo,Shengcan Ma,Xinqiang Gao,Zhenxing Li,Zhaojun Mo,Jun Shen
For more practical applications, research on magnetic refrigeration has been gradually focused on developing refrigerants with large magnetocaloric effect (MCE) under low magnetic fields (≤2 T). EuTiO 3 exhibits considerable low-field MCE near ordering temperature, meanwhile the magnetic switch from antiferromagnetic to ferromagnetic (AFM-FM) in it provides the feasibility of improving the magnetocaloric performance. In this study, a series of Eu(Ti,Nb,M)O 3 (M=Cu or Zn) compounds were synthesized, and the crystal structure, magnetic properties together with cryogenic MCEs were investigated in detail. The co-substitution contributes to an FM coupling domination in all the compounds. Besides, significantly enhanced and giant low-field MCEs were detected in these compounds. Under the field change of 1 T, all the samples possess remarkable magnetic entropy change (>15 J·kg -1 ·K -1 ) around 5 K without hysteresis. The corresponding refrigerating capacities are calculated to be 68.0, 72.6, 76.0, and 69.6 J·kg -1 , respectively, exhibiting an increase of 149–178% than EuTiO 3 . The outstanding magnetocaloric performances make the Eu(Ti,Nb,M)O 3 (M=Cu or Zn) compounds competitive candidates for cryogenic magnetic refrigeration.
研究领域:
材料科学
·
凝聚态物理
·
功能材料
·
低温工程
·
磁学
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）