ACS Nano
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2020
·
IF 14.588
Xinliang Li,Mian Li,Qi Yang,Hongfei Li,Hailong Xu,Zhifang Chai,Ke Chen,Zhuoxin Liu,Zijie Tang,Longtao Ma,Zhaodong Huang,Binbin Dong,Xiaowei Yin,Qing Huang,Chunyi Zhi
Nonbattery behavior related phase transition of electrodes is usually not favorable for any batteries because it results in performance degradation at all times. Here, we demonstrate a zinc hybrid-ion battery (ZHIB) with an unusual capacity enhancement even within 18 000 cycles by employing V2CTX MXene as the cathode, enormously differing from all reported counterparts with capacity degradation initiated within hundreds of cycles. The dominated mechanisms are determined to be MXene delamination and an unexpected phase transition during cycling. Both the original cathode and secondary derivative contribute to capacity simultaneously, resulting in the unusual capacity enhancement. Consequently, the specific capacity of 508 mAh g–1 (highest for all reported aqueous zinc-ion batteries) and high energy density of 386.2 Wh kg–1 are realized. Also, the quasi-solid-state batteries fabricated can output stably at −20 °C and in bending, twisting, stabbing, and cutting conditions. Our work brings an effective approach, that is, utilizing “unstable” electrode materials, which should usually be avoided, to achieve continuously enhanced performance of a battery. The idea to use both original and secondary materials for energy storage may be developed to be a general method to achieve extraordinary cycling stability of batteries.
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COMPOSITES SCIENCE AND TECHNOLOGY
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2019
·
IF 6.309
Zhongyang Wang,Kai Sun,Peitao Xie,Yao Liu,Qilin Gu,Runhua Fan
The insulator-conductor percolative composites have been mostly constructed to achieve high permittivity and negative permittivity. In this work, permittivity transition from positive to negative is investigated in acrylic polyurethane-aluminum (APu/Al) percolative composites at radio frequency. Both the high permittivity and negative permittivity are accompanied with low loss due to the self-passivated nature of aluminum . The reactance and ac conductivity are studied to explain the dielectric properties , which provides an essential insight into the universal principles of high permittivity and negative permittivity behaviors in percolative composites. Meanwhile, when the conductive filler content exceeds the percolation threshold, a derived formula of permittivity has been put forward on the basis of the existing theoretical framework of percolation theory. Resourceful dielectric properties of APu/Al percolative composites will make them as potential alternatives for capacitors and metamaterials.
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POWDER METALLURGY
·
2019
·
IF 1.149
Jiaxin Li,Yuhong Chen,Yongquan Li,Zhangjun Bai,Kang Wang
Alloys with composition of Ta-10 wt.% W and Ta-10 wt.% W-6 wt.% Al, respectively, were prepared by the hot-press sintering process. The oxidation behaviour at 900°C and 1000°C was studied. The oxidation weight gain curves of the Ta–10%W alloy followed the linear law and the final oxidation product was Ta2O5 solid solution. Meanwhile, due to the addition of Al, the oxidation weight gain curves of the Ta–10%W–6%Al alloy followed the parabolic law. The final oxidation products at 900°C formed a dense outer layer Al2O3 and an inner layer. However, after being oxidised at 1000°C, the oxidation products included Al2O3, AlTaO4 and Ta22W4O67. Since the dense Al2O3 oxide film was consumed by the generation of AlTaO4, the inward diffusion of oxygen cannot be prevented. The oxidation resistance degraded at 1000°C. The addition of Al significantly improved the oxidation resistance of the Ta-W-based alloy system.
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Nanoscale
·
2019
·Vol. 11
·期 36
·16781-16787
·
IF 6.97
Na Li,Zheng Yi,Ning Lin,Yitai Qian
The application of Si-based anode materials is hindered by their extreme volume change, poor cycling stability, and low coulombic efficiency. Solving these problems generally requires a combination of strategies, such as nanostructure designing or surface coating. However, these strategies increase the difficulty of the fabrication process. Herein, a simple and one-pot replacement reaction route was designed to produce an Al2O3 layer anchored on mesoporous Si nanospheres (Si@Al2O3) by employing Al nanospheres with a naturally formed Al2O3 layer as a reducing agent and self-sacrificial template. The obtained Si@Al2O3 was mesoporous, with enough porous space to buffer the volume change and provide a fast lithium ion transfer channel. Furthermore, the coated Al2O3 layer could stabilize the structure and SEI layer of the mesoporous Si nanospheres, endowing the Si@Al2O3 nanospheres with improved initial coulombic efficiency, cycling performance and rate capability. As a result, a high capacity of 1750.2 mA h g−1 at 0.5 A g−1 after 120 cycles and 1001.7 mA h g−1 at 2 A g−1 after 500 cycles were delivered for lithium ion batteries. The good performance could be attributed to the mesoporous structure and the outer-coated Al2O3 layer.
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MATERIALS & DESIGN
·
2018
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IF 4.525
Yajie Chen,Wenchao Zhang,Chunpei Yu,Debin Ni,Kefeng Ma,Jiahai Ye
NiCo 2 O 4 has been selected as an oxidizer to realize the nanothermite film for the first time in this study. The NiCo 2 O 4 /Al core-shell nanowires (NWs) thermite film has been fabricated using a facile hydrothermal-annealing synthesis method and a controllable magnetron sputtering process. The as-obtained NiCo 2 O 4 /Al NWs thermite film shows a uniform structure and distribution on the substrate, with a favorable interfacial contact between the bimetallic oxide and the fuel at the nanoscale . It is found that the quantity of Al plays a key role in the total heat release magnitude. The maximal heat release of the NiCo 2 O 4 /Al nanothermite film has reached 2076.0 J/g at the optimal Al deposited thickness of 450 nm with the obtained optimum Al/NiCo 2 O 4 molar ratio of 4.9. Moreover, this design strategy is highly compatible with microelectromechanical systems (MEMs) and it can be applied to realize other nanothermites composed by bimetallic oxide and fuel.
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ENERGY & FUELS
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2018
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IF 3.024
Da Wang,Yuyang Wang,Xiaoyu Li,Lei Chen,Guangci Li,Xuebing Li
In situ catalytic hydrogenolysis of lignin is an efficient method for lignin valorization. Herein, a novel in situ lignin catalytic hydrogenolysis technique in alkaline aqueous solution over a NiAl alloy catalyst under mild conditions was systematically suited. Ni served as the active phase and could be exposed by etching Al atoms with alkaline aqueous solution. Meanwhile, H2 resources could be in situ generated and easily arrived at the adjacent exposed Ni sites to be activated. The in situ lignin hydrogenolysis system exhibits attractive depolymerization results under mild conditions, with an 86.8% conversion degree and 18.9 wt % yield of aromatic monomers at 220 °C, much higher than the traditional hydrogenolysis method using a commercial Raney Ni catalyst under high pressure external H2. The mechanism studies with lignin model compounds suggest that alkaline aqueous solution could promote the cleavage of C–O–C bonds and hinder the hydrogenation of the benzene ring. In addition, a moderate amount of exposed Ni sites as well as rich active hydrogen species are determinant for efficient lignin depolymerization.
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BIOMEDICINE & PHARMACOTHERAPY
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2018
·
IF 3.457
Xiang-Feng Guo,Ji-Peng Liu,Si-Quan Ma,Peng Zhang,Wen-De Sun
5-Fluorouracil (5-Fu) and cisplatin (DDP) as important therapies in treatment of human gastric cancer have been widely determined. However, the therapeutic effects are usually hampered due to drug resistance or toxicity at high concentrations for application. Avicularin (AL, quercetin-3-α- l -arabinofuranoside), a bio-active flavonol isolated from a number of plants, has been reported to display diverse pharmacological properties. In this study, we explored the hypothesis by which AL reversed 5-Fu or DDP resistance in gastric cancer and the underlying molecular mechanism. Here, in vitro, the drug-resistant cancer cells were incubated to AL or DDP alone or the combination of AL and DDP. Then, MTT, colony formation, Hoechst 33258 , flow cytometry and western blot analysis were used to investigate the effects of AL in the regulation of drug-resistance gastric cancer cells. The results indicated that AL treatment markedly re-sensitizes the drug resistant cells (SGC-7901/5-Fu and SGC-7901/DDP) to cytotoxicity of 5-Fu or DDP. Molecular mechanism analysis indicated that AL and DDP combination treatment enhanced apoptosis in SGC-7901/DDP cells, accompanied with the up-regulation of cleaved Caspase-3 and PARP, as well as the activation of pro-apoptotic signals, including Bax and BOK. Significantly, down regulation of Bax or BOK expressions using Bax siRNA or BOK siRNA decreased the inhibitory role of DDP in apoptosis of SGC-7901/DDP cells pretreated with AL, demonstrating that AL-reversed DDP resistance was associated with Bax and BOK expression. In vivo, AL and DDP combination significantly reduced gastric tumor growth. Immunohistochemical analysis indicated that co-treatment of AL and DDP significantly induced apoptosis, and reduced tumor cell proliferation in tumor tissue samples. Furthermore, we also found that the Bax, BOK, cleaved Caspase-3 and PARP expression in tumor tissues were highly induced by AL and DDP co-treatment. Together, our findings may provide a novel combination therapeutic strategy in treatment of human gastric cancer.
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BIOMETALS
·
2018
·Vol. 31
·期 6
·1051-1059
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IF 2.478
Luo Junchong,Li Xiaowen,Li Xinran,He Yongming,Zhang Mengdan,Cao Changyu,Wang Kai
To investigate the effect of Selenium Rich Yeast ( SeY ) on hepatotoxicity of Aluminium (Al), SeY (0.1 mg/kg) was orally administrated to aluminium-exposed mice (10 mg/kg) for 28 days. The risk of oxidative stress was assessed by detecting the total antioxidant capacity (T-AOC), catalase activity, H 2 O 2 content, and mRNA levels of the Keap1/Nrf-2/HO-1 pathway. Inflammatory reactions were assessed by detecting the mRNA levels of inflammatory biomarkers. Our results showed that SeY protected against the liver histological changes induce by Al. The body weight gain of mice treated with SeY + Al restore to normal compare with mice exposed to Al alone. Al treatment significantly decreased the activities of antioxidant enzymes, reduced T-AOC levels, and up-regulated the mRNA level of Nrf2 and HO-1, thereby ultimately leading to peroxidation. SeY shown a significant protective effect against oxidative stress caused by Al. In addition, Al exposure induced inflammatory responses in rat liver by promoting the release of inflammatory cytokines (TNF-a, NF-kB, TNF-R1, IL-1, IL-6, and COX-2). SeY protected against changes in liver by regulating the mRNA expression levels of inflammatory factors. These results suggested that Se protected the liver from the Al-induced hepatotoxicity by regulating the mRNA level of Keap1/Nrf2/HO-1, and inhibited inflammatory responses by down-regulating the expression level of inflammatory cytokine.
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METALLURGICAL AND MATERIALS TRANSACTIONS A-PHYSICAL METALLURGY AND MATERIALS SCIENCE
·
2018
·Vol. 49
·期 8
·3683-3691
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IF 1.887
Cai Xiaoping,Liu Yanan,Wang Xiaohong,Jiao Xinyang,Wang Jianzhong,Akhtar Farid,Feng Peizhong
Open-cell Fe-Al intermetallic foams were successfully prepared by a simple and energy-saving thermal explosion (TE) process. The effects of the Fe/Al molar ratio (Fe-(40–50) at. pct Al) and thermal treatment temperature on the TE temperature profile, phase composition, pore characteristics, and oxidation resistance of the prepared foams were investigated. The results showed that the Al content significantly influenced the ignition ( T ig ) and combustion ( T c ) temperatures of the TE process; in particular, as the Al content decreased, T ig increased gradually from 623 °C to 636 °C and T c decreased from 1059 °C to 981 °C. FeAl was identified as the dominant phase in the thermally treated foams. The Fe-Al intermetallic foams displayed an open porosity of 60 vol pct, with pores connected with each other to form an open pore structure. The formation of the pores was attributed to the expansion of interparticle pores in the pressed body during the TE reaction. X-ray photoelectron spectroscopy analysis of the Fe-50Al foam showed that the Al 2p and O 1s binding energies were 74.5 eV and at 531.4 eV, respectively. The formation of a surface alumina layer in the early stages of the oxidation process resulted in the parabolic oxidation rate law, and the Fe-50Al foams exhibited an excellent resistance to oxidation at 650 °C in air. These results suggest that the synthesized Fe-Al foams represent promising materials for applications involving an oxidizing environment and high temperatures.
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JOURNAL OF THE ELECTROCHEMICAL SOCIETY
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2018
·Vol. 165
·期 11
·E616
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IF 3.662
Junfeng Li,Mingyong Wang,Jiguo Tu,Shuqiang Jiao
The direct preparation of metallic Sm or alloys from raw oxide Sm2O3 is an attracting but challenging process. The stable electrochemical behavior and low solubility of Sm2O3 limit the extraction of Sm element in molten salts. Here, it is found that metallic Sm is hardly obtained by electro-deoxidation and aluminothermic reduction of solid Sm2O3 pellet according to experiment and calculation. Through the novel electrochemical reduction of solid Sm2O3-Al pellet, Al3Sm alloy with ∼0.4 Sm/Al molar ratio is successfully prepared in calcium chloride melt at 1173 K. The reduction potential of Sm2O3-Al pellet to Al-Sm alloy is more positive than that of calcium. Al plays an indispensable role in the reduction of Sm2O3. The preparation process of alloy can be well identified as two steps: Sm(III) → Sm(II) and Sm(II) → Sm(0). Sm2O3 is firstly converted to Sm(II) based on the combination of electrochemical and aluminothermic reduction. Then, Al3Sm is formed by electrochemical reduction and alloying with Al.
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International Journal of Environmental Research and Public Health
·
2018
·Vol. 15
·期 5
·872
·
IF 2.145
Yuhui Jiang,Yixuan Shang,Shuyao Yu,Jianguo Liu
Hexachlorobenzene (HCB) contamination of soils remains a significant environmental challenge all over the world. Reductive stabilization is a developing technology that can decompose the HCB with a dechlorination process. A nanometallic Al/CaO (n-Al/CaO) dispersion mixture was developed utilizing ball-milling technology in this study. The dechlorination efficiency of HCB in contaminated soils by the n-Al/CaO grinding treatment was evaluated. Response surface methodology (RSM) was employed to investigate the effects of three variables (soil moisture content, n-Al/CaO dosage and grinding time) and the interactions between these variables under the Box-Behnken Design (BBD). A high regression coefficient value (R2= 0.9807) and lowpvalue (<0.0001) of the quadratic model indicated that the model was accurate in predicting the experimental results. The optimal soil moisture content, n-Al/CaO dosage, and grinding time were found to be 7% (m/m), 17.7% (m/m), and 24 h, respectively, in the experimental ranges and levels. Under optimal conditions, the dechlorination efficiency was 80%. The intermediate product analysis indicated that dechlorination was the process by stepwise loss of chloride atoms. The main pathway observed within 24 h was HCB → pentachlorobenzene (PeCB) → 1,2,3,4-tetrachlorobenzene (TeCB) and 1,2,4,5-TeCB. The results indicated that the moderate soil moisture content was crucial for the hydrodechlorination of HCB. A probable mechanism was proposed wherein water acted like a hydrogen donor and promoted the hydrodechlorination process. The potential application of n-Al/CaO is an environmentally-friendly and cost-effective option for decontamination of HCB-contaminated soils.Keywords:nanometallic Al/CaO;ball milling;dechlorination;response surface methodology
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Nature Communications
·
2018
·Vol. 9
·期 1
·1-11
·
IF 12.353
Wan Fang,Zhang Linlin,Dai Xi,Wang Xinyu,Niu Zhiqiang,Chen Jun
Rechargeable aqueous zinc-ion batteries are promising energy storage devices due to their high safety and low cost. However, they remain in their infancy because of the limited choice of positive electrodes with high capacity and satisfactory cycling performance. Furthermore, their energy storage mechanisms are not well established yet. Here we report a highly reversible zinc/sodium vanadate system, where sodium vanadate hydrate nanobelts serve as positive electrode and zinc sulfate aqueous solution with sodium sulfate additive is used as electrolyte. Different from conventional energy release/storage in zinc-ion batteries with only zinc-ion insertion/extraction, zinc/sodium vanadate hydrate batteries possess a simultaneous proton, and zinc-ion insertion/extraction process that is mainly responsible for their excellent performance, such as a high reversible capacity of 380 mAh g –1 and capacity retention of 82% over 1000 cycles. Moreover, the quasi-solid-state zinc/sodium vanadate hydrate battery is also a good candidate for flexible energy storage device.
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