INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2024
·
IF 8.1
Zhongxuan Lin,Zhenluo Yuan,Huanhuan Zhang,Shuyan Guan,Xiaojiao Wang,Shiqian Zhao,Guangxin Fan,Yanping Fan,Baozhong Liu
Lowering the dehydrogenation temperature and maintaining high dehydrogenation capacity are greatly hindering the practical application of α-AlH 3 for the hydrogen fuel cell industry. Herein, the layered accordion-like V 2 C MXene is synthesized and doped into α-AlH 3 by mild ball milling . The 1 wt.% V 2 C-catalyzed α-AlH 3 possesses excellent dehydrogenation performance with a low initial decomposition temperature of 70.5 °C and a high hydrogen release capacity of 8.1 wt.%. Furthermore, 7.8 wt.% of hydrogen could be quickly released from α-AlH 3 -1 wt.% V 2 C composite within 15 min at 120 °C, with a lower activation energy of 69.5 kJ/mol than that of as-received sample. The excellent dehydrogenation performance is attributed to the high activity of the zero valence V catalyst which is transformed from the multivalent V during ball milling and to promote dissociation and reorganization of hydrogen. This effective approach significantly enhances the dehydrogenation of α-AlH 3 , providing a hopeful approach for modifying metal hydrides .
研究领域:
材料科学
·
无机化学
·
能源化学
·
纳米材料
·
储氢材料
✓ 已验证
DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
·
2021
·
IF 8.067
Fengnian Zhang,Fuhao Cheng,Chufei Cheng,Meng Guo,Yufeng Liu,Yang Miao,Feng Gao,Xiaomin Wang
Abatract A series of compositionally complex fluorite oxides (CCFOs) were prepared by ball milling the mixture of ZrO 2 , HfO 2 , Y 2 O 3 , La 2 O 3 , and Pr 6 O 11 followed by conventional solid-state sintering. Both XRD and TG-DSC results demonstrated that single-phase (Zr 0.2 Hf 0.2 Pr 0.2 Y 0.2 La 0.2 )O 2-δ was formed at 1400 °C. Elements in bulk ceramic were uniformly distributed without evident accumulation according to SEM-EDS pictures. TEM results revealed that polycrystalline ceramic powder was assignable to cubic Fm-3m fluorite structure. The electrical conductivity ( σ ) was measured via EIS technology and activation energy ( E a ) of CCFOs was calculated in Arrhenius plots. In the temperature range of 300-750 °C, CCFOs preserved the same conduction mechanism and (Zr 0.1667 Hf 0.1667 Pr 0.1667 Y 0.25 La 0.25 )O 2-δ possessed higher σ and lower E a than other high entropy fluorite oxides which is related to the incorporation of Pr element or the connection of cation-V o complex.
研究领域:
材料科学
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无机非金属材料
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固体离子学
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功能陶瓷
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能源材料
✓ 已验证
DOI
高影响因子
NEW JOURNAL OF CHEMISTRY
·
2022
·Vol. 46
·期 19
·9432-9439
·
IF 3.925
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
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纳米材料
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能源存储
·
电池技术
✓ 已验证
DOI
高影响因子
CERAMICS INTERNATIONAL
·
2020
·Vol. 46
·期 16
·24799-24804
·
IF 3.83
Pengfei Pan,Xu Wang,Yaqi Ji,Wumei Dong,Lei Zhang,Ling Wang,Ming Zhang
A simple, efficient and low-cost method to synthesize zirconia nanopowders dispersed with graphene by wet ball milling was reported in this paper. The raw material for ball milling is cheap graphite powder rather than expensive graphene. Graphite powders were exfoliated into graphene nanosheets (GNSs) in the process of ball milling, as a result of strong shear forces and moderate impact forces between graphite powders, milling balls, and ZrO 2 nanoparticles . The mixed powders were milled for 3, 10, 20, 30, 40, and 50 h, respectively. Moreover, the morphology, composition and structure of the mixed powders milled were characterized by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy, Raman spectroscopy , Fourier transform infrared spectroscopy , and field emission transmission electron microscopy . Results showed that the graphite powders were exfoliated effectively, and the GNSs were dispersed uniformly in the zirconia simultaneously. The presence of zirconia nanoparticles significantly improved the efficiency of ball milling exfoliation.
研究领域:
材料科学
·
纳米技术
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无机非金属材料
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复合材料
✓ 已验证
DOI
高影响因子
SOLID STATE IONICS
·
2017
·
IF 2.354
Leyu Zhan,Yao Zhang,Xiangyang Zhuang,Hui Fang,Yunfeng Zhu,Xinli Guo,Jian Chen,Zengmei Wang,Liquan Li
The x LiBH 4 -Li 3 N ( x = 1, 2, 4) composites were investigated on their lithium ionic conductivities . They maintained the original phase structures of orthorhombic LiBH 4 and hexagonal β-Li 3 N during ball milling according to the analyses by X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). Electrochemical impedance spectra (EIS) tests showed that LiBH 4 -Li 3 N composites lift the lithium ionic conductivities from that of bulk LiBH 4 by nearly 100 times at low temperature. LiBH 4 -Li 3 N offers 1.06 × 10 − 5 S cm − 1 of conductivity while bulk LiBH 4 possesses only 2.05 × 10 − 7 S cm − 1 at 323 K. Cyclic voltammetry (CV) tests indicated that the voltage window of composites could attain 3 V, which is much more stable than Li 3 N (< 1 V). No thermodynamic incident appears in DSC curves except for the orthorhombic-hexagonal transition endothermic peak of LiBH 4 in the x LiBH 4 -Li 3 N composites. It confirms the phases stabilities of the x LiBH 4 -Li 3 N ( x = 1, 2, 4) composites before and after CV tests. In-situ solid state Nuclear Magnetic Resonance (NMR) tests on LiBH 4 -Li 3 N illustrated that the high conductivity in low temperature should not come from high-temperature phase of LiBH 4 . Therefore, the enhancement of lithium ionic mobility of the composite might be attributed to both Li 3 N and the interfaces between small crystallites where transmission electron microscope (TEM) morphology showed the appearance of amorphous grain boundary.
研究领域:
材料科学
·
固态离子学
·
能源化学
·
电化学
·
纳米材料
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固体电解质
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锂离子电池
✓ 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
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
CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Yuqing Sun,Adeel Abbas,Hongxiang Wang,Chang Tan,Zhihao Li,Yujie Zong,Hui Sun,Chunlei Wang,Hongchao Wang
Quaternary Cu 2 MnSnSe 4 alloys with low intrinsic thermal conductivity are identified as promising middle-temperature thermoelectric materials. However, zT is depressed by the poor electrical performance. To overcome this issue, here, a series of Cu 2.1 Mn 0.9 SnSe 4 samples are prepared by ball-milling method which appears as a time-saving technique and lattice strain variation is observed by changing the annealing time ( x = 0, 1, 2, 3, 4 days). The vacancy defects concentration of Cu, with lowest vacancy defects formation energy, is changed with the competition between compression and tension-strain state, consistent with the first principles calculations, which optimizes the carrier transport. As a result, about 4 times increment of the carrier mobility is found. Moreover, the lattice strain of several nanometers is observed with TEM analysis, which scatters phonon strongly. A lowest κ L value of 0.57 W m −1 K −1 at 673 K is obtained for x = 3 sample, which is close to the amorphous limit. The interactive effect of enhanced mobility and strong scattering of phonons, contributing to a record zT ∼ 0.48 at 673 K for x = 3 sample. Lattice strain engineering is an effective tactic to simultaneously optimize the electrical and thermal transport.
研究领域:
材料科学
·
凝聚态物理
·
功能材料
·
能源材料
·
半导体物理
✓ 已验证
DOI
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2013
·Vol. 38
·期 25
·10932-10938
·
IF 3.548
H. Wang,J. Zhang,J.W. Liu,L.Z. Ouyang,M. Zhu
In this study, alkali hydroxides (NaOH, LiOH, KOH) were attempted as new-type catalytic additives to improve the hydrogen storage properties of MgH 2 by ball milling . It is shown that the additives readily react with the MgH 2 to form perovskite-structured NaMgH 3 and KMgH 3 , but not the LiMgH 3 . Although the in-situ formed perovskite hydrides remain stable during hydriding/dehydriding cycles, both NaMgH 3 and KMgH 3 show predominant catalytic role on the hydriding and dehydriding of MgH 2 . In contrast, the LiOH modified MgH 2 presents much inferior sorption kinetics because of the absence of LiMgH 3 . The catalytic mechanism of perovskite hydrides can be explained by the high hydrogen mobility in the perovskite structure . This study shows that such cheap hydroxides could be used as efficient catalysts to improve the hydrogen storage properties of high-capacity metal hydrides and complex hydrides .
研究领域:
材料科学
·
无机化学
·
能源化学
·
氢能存储
·
金属氢化物
·
固态储氢
·
催化化学
✓ 已验证
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2017
·
IF 3.133
Jing Lin,Zhanyi Cao,Lianshan Sun,Fei Liang,Limin Wang
Ti 1.4 V 0.6 Ni + x LiAlH 4 ( x = 0.5, 1, 1.5, 2, 2.5, wt.%) composites were prepared by ball-milling, and the effects of LiAlH 4 content on structure and electrochemical properties of the composites were investigated systematically. The addition of LiAlH 4 to the Ti 1.4 V 0.6 Ni alloy significantly affected the morphology and size of the composite particles . The electrochemical cycling stability and rate dischargeability of the composite electrodes benefitted from adding some LiAlH 4 ( x = 1), which however deteriorated when the LiAlH 4 content increased further. The positive effect of LiAlH 4 on the electrochemical performance of the studied alloy was caused by suppression of the dissolution of active components of the Ti 1.4 V 0.6 Ni hydrogen storage alloy.
研究领域:
材料科学
·
金属功能材料
·
能源存储
·
电化学
·
氢能技术
✓ 已验证
DOI
高影响因子
Energy Technology
·
2020
·Vol. 8
·期 10
·2000606
·
IF 3.404
Yu Wang,Nachuan Yang,Yi Shuai,Kanghua Chen
Na 3 PS 4 -based materials, which have relatively high conductivities, make promising Na-ion solid electrolytes for realizing all-solid-state sodium batteries. Herein, Na 2.9375 PS 3.9375 Cl 0.0625 solid electrolytes’ power is prepared by a mechanical ball milling process and subsequent heat treatment process using low-cost Na, NaCl, P 2 S 5 , and S as raw materials. In addition, its electrical conductivity and electrochemical performance by compounding with polyethylene oxide–NaClO 4 are studied. The results show that Na 2.9375 PS 3.9375 Cl 0.0625 solid electrolyte heated at 550 °C with polyethylene oxide–NaClO 4 exhibits Na-ion conductivity of 8.75 × 10 −4 S cm −1 . The pragmatic and cost-effective raw materials grant the solid electrolyte with high-performance and higher practical value.
研究领域:
材料科学
·
电化学
·
能源存储
·
固体离子学
·
无机非金属材料
✓ 已验证
DOI
高影响因子
JOURNAL OF POWER SOURCES
·
2017
·
IF 6.395
Xiubo Xie,Ming Chen,Peng Liu,Jiaxiang Shang,Tong Liu
Nickel sulfides decorated reduced graphene oxide (rGO) has been produced by co-reducing Ni 2+ and graphene oxide (GO), and is subsequently ball milled with Mg nanoparticles (NPs) produced by hydrogen plasma metal reaction (HPMR). The nickel sulfides of about 800 nm completely in situ change to MgS, Mg 2 Ni and Ni multiple catalysts after first hydrogenation/dehydrogenation process at 673 K. The Mg-5wt%NiS/rGO nanocomposite shows the highest hydrogen desorption kinetics and capacity properties, and the catalytic effect order of the additives is NiS/rGO, NiS and rGO. At 573 K, the Mg-NiS/rGO nanocomposite can quickly desorb 3.7 wt% H 2 in 10 min and 4.5 wt% H 2 in 60 min. The apparent hydrogen absorption and desorption activation energies of the Mg-5wt%NiS/rGO nanocomposite are decreased to 44.47 and 63.02 kJ mol −1 , smaller than those of the Mg-5wt%rGO and Mg-5wt%NiS samples. The best hydrogen desorption properties of the Mg-5wt%NiS/rGO nanocomposite can be explained by the synergistic catalytic effects of the highly dispersed MgS, Mg 2 Ni and Ni catalysts on the rGO sheets, and the more nucleation sites between the catalysts, rGO sheets and Mg matrix.
研究领域:
材料科学
·
纳米科技
·
能源化学
·
催化化学
·
储氢材料
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）