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JOURNAL OF POWER SOURCES · 2022 · IF 9.794

Improving interfacial stability by in situ protective layer formation in 4.2V poly(ethylene oxide) based solid state lithium batteries

Wei Feng,Huirong Liu,Mingliang Zhao,Jianling Li,Feiyu Kang

The poly(ethylene oxide) based composite solid electrolyte(PEO-CSE) is an effective solution for developing high-performance solid-state lithium battery . However, the poly(ethlene oxide)(PEO) based solid-state lithium battery using 4.0 V cathode suffers from severe interfacial instability problems. In this work, we add additive lithium difluorophosphate(LiPO 2 F 2 ) into the PEO-CSE to form a stable and low resistance interphase at the cathode/electrolyte interface during charge/discharge process. The electrochemical stability window of PEO-CSE increases to ∼5.0 V. Besides, the electrochemical performance of PEO based solid-state lithium battery with LiCoO 2 as cathode is excellent. The discharge capacity of LiCoO 2 /Li cell with LiPO 2 F 2 reaches 108.5 mAh g −1 at 1.0C. In contrast, the discharge capacity that without LiPO 2 F 2 is only 60.0 mAh g −1 . Meanwhile, the PEO-CSE with LiPO 2 F 2 cell delivers stable cycle performance at 4.2 V. The capacity retention maintains 88.5% compared with 16.1%(without LiPO 2 F 2 ) after 100 cycles. Furthermore, it's still maintains 83.3% after 150 cycles. In addition, the cathode/electrolyte interface is analyzed by transmission electron microscope(TEM) and X-ray photoelectron spectroscopy(XPS). Galvanostatic intermittent titration test(GITT) is used to analyze the dynamic diffusion performance. This strategy provides a simple and effective way to improve the high voltage stability of the cathode/electrolyte interface.

研究领域: 电化学 · 材料科学 · 能源存储 · 固态电池 · 界面工程
✓ 已验证 DOI 高影响因子
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2019 · IF 6.361

Co nanoparticles supported on three-dimensionally N-doped holey graphene aerogels for electrocatalytic oxygen reduction

Kai-Wen Cao,Hao Huang,Fu-Min Li,Hong-Chang Yao,Juan Bai,Pei Chen,Pu-Jun Jin,Zi-Wei Deng,Jing-Hui Zeng,Yu Chen

The reactive and stable catalysts for the oxygen reduction reaction are highly desirable for low temperature fuel cells. The commercial oxygen reduction reaction electrocatalysts generally reply on noble metal based nanomaterials, which suffer from inherent cost and selectivity issues. At present, it still remains challenge for designing efficient non-noble metal-based oxygen reduction reaction electrocatalysts. Herein, we successfully synthesize Co nanoparticles supported on three-dimensionally N-doped holey graphene aerogels hybrids by the high-temperature calcination of the graphene aerogels-polyallylamine-Co II hybrids. The component optimized hybrids show the excellent electrocatalytic activity for oxygen reduction reaction in alkaline media, which is comparable to commercial Pt/C electrocatalyst. Meanwhile, the hybrids also show eminent tolerance for CO and methanol, attributing to their excellent oxygen reduction reaction selectivity. The three-dimensionally interconnected structure of graphene aerogels, N-doping, uniform dispersion and high crystallinity of Co nanoparticles, and holey structure of graphene contribute to the striking oxygen reduction reaction activity of hybrids.

研究领域: 材料科学 · 电化学 · 纳米催化 · 能源材料 · 燃料电池
✓ 已验证 DOI 高影响因子
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APPLIED SURFACE SCIENCE · 2018 · IF 4.439

Hydrothermal growing of cluster-like ZnO nanoparticles without crystal seeding on PET films via dopamine anchor

Deshan Cheng,Mantang He,Wenbin Li,Jihong Wu,Jianhua Ran,Guangming Cai,Xin Wang

Growing of ZnO nanoparticles on PET films without crystal seeding has been achieved by employing polydopamine as the anchor. The PDA layer was formed on the surface of PET film by the polymerization of dopamine. The PDA-PET was dipped into zinc precursors for hydrothermal growth of ZnO nanoparticles. Cluster-like ZnO nanoparticles were obtained and the special structure was affected by the growing time and zinc ion concentration. The surface morphology, structure and properties were characterized, and the functions including antimicrobial activity and UV protection of the ZnO-coated PET film were investigated. The developed facile hydrothermal approach without seeding will benefit the development of UV resistant and antimicrobial PET films.

研究领域: 材料科学 · 纳米技术 · 表面功能化 · 生物医用材料 · 高分子材料
✓ 已验证 DOI 高影响因子
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NEW JOURNAL OF CHEMISTRY · 2017 ·Vol. 41 ·期 22 ·13319-13326 · IF 3.269

Facile synthesis, crystal structure and bioactivity evaluation of two novel barium complexes based on 2,4,6-trichlorophenoxyacetic acid and o-ferrocenylcarbonyl benzoic acid

Xiuling Xu,Fan Hu,Qi Shuai

Two novel Ba(II) complexes [Ba(TCPA)2(H2O)4] 1 and [Ba(H2O)8]·2(o-FcCOC6H4COO)·6H2O 2 [HTCPA = 2,4,6-trichlorophenoxyacetic acid and o-HOOCC6H4-COFc = o-ferrocenylcarbonyl benzoic acid] have been synthesized by a facile microwave method. The solid-state structures were well established by means of X-ray crystallography as well as routine analysis of the infrared spectrum (FTIR), elemental analysis, field emission scanning electron microscopy (FESEM) and thermogravimetric analysis (TG). Different polyhedra of tricapped triangular prisms for 1 and dodecahedra for 2 were present. It is worth noting that the central Ba(II) ion in 1 is nine-coordinated by two carboxylate oxygen atoms from TCPA ligands and seven oxygen atoms from coordinated water molecules. By contrast, the eight-coordinated Ba(II) in 2 forms barium-water clusters assembled by O–H⋯O hydrogen-bonds contributed by coordinated water molecules. The uncoordinated o-OOCC6H4-COFc ligands in 2 play a key role in the process of charge balance. FESEM images exhibited different surface appearances between the ligand and barium complexes, that is: flower-like HTCPA, branch-like o-HOOCC6H4-COFc, block-like complex 1 and corner-truncated cubes for complex 2. The allelopathic activity of the complexes and their corresponding ligands was evaluated against two herbaceous plants of barnyard grass and turnip (Raphanus sativus). All the tested compounds showed certain activity with good RI values. An antifungal bioassay was also carried out in vitro on three strains of Botrytis cinerea Pers., Glomerella cingulata Schr and Cytospora sp. Complex 1 and HTCPA can work against all three tested fungi, whereas o-HOOCC6H4-COFc and 2 only worked for Botrytis cinerea Pers. The complex presented in this paper has potential applications in weed control, and this work provides an experimental basis for future studies on Ba-based pesticides.

研究领域: 无机化学 · 金属配合物化学 · 农业化学 · 晶体工程 · 植物生理学 · 农药学 · 生物活性评估
✓ 已验证 DOI 高影响因子
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POLYMERS FOR ADVANCED TECHNOLOGIES · 2011 ·Vol. 22 ·期 12 ·2237-2243 · IF 1.776

Enhancement of a hyperbranched charring and foaming agent on flame retardancy of polyamide 6

Chenhao Ke,Juan Li,Keyi Fang,Qiliang Zhu,Jin Zhu,Qing Yan

A hyperbranched polyamine was prepared using an A 2 + B 3 approach. It acted as a hyperbranched charring and foaming agent (HCFA) in combination with ammonium polyphosphate (APP) to form a new intumescent flame retardant (IFR) system for polyamide 6 (PA6). Effect of HCFA on flame retardant and thermal degradation properties of IFR-PA6 was investigated by limiting oxygen index (LOI), UL-94 vertical burning, cone calorimeter, and thermogravimetric analysis (TGA) tests. The IFR system presented the most effective flame retardancy in PA6 when the weight ratio of APP to HCFA was 2:1. The LOI value of IFR-PA6 could reach 36.5 with V-0 rating when the IFR loading was 30 wt%. Even if the loading decreased to 25 wt%, IFR-PA6 could still maintain V-0 rating with an LOI value of 31. TGA curves indicated that APP would interact with both PA6 and HCFA in PA6/APP/HCFA composite under heating. The interaction between APP and HCFA improved the char formation ability of IFR system and then much more char was formed for PA6/APP/HCFA composite than for PA6/APP. Therefore, better flame retardancy was achieved. Moreover, the structure and morphology of char residue were studied by Fourier transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS), and scanning electron microscopy (SEM). The results indicated that compact and foaming char layer containing P-O-C structure was formed for PA6/APP/HCFA system during combustion. Copyright © 2010 John Wiley & Sons, Ltd.

研究领域: 高分子化学 · 材料科学 · 阻燃材料 · 热稳定性 · 聚合物复合材料
✓ 已验证 DOI 高影响因子
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Small · 2023 ·Vol. 19 ·期 24 ·2207362 · IF 13.3

Splashing-Assisted Femtosecond Laser-Activated Metal Deposition for Mold- and Mask-Free Fabrication of Robust Microstructured Electrodes for Flexible Pressure Sensors

Yaqiang Ji,Yuan Zhang,Jiaqi Zhu,Pai Geng,Jonathan E. Halpert,Liang Guo

Flexible pressure sensors play an indispensable role in flexible electronics. Microstructures on flexible electrodes have been proven to be effective in improving the sensitivity of pressure sensors. However, it remains a challenge to develop such microstructured flexible electrodes in a convenient way. Inspired by splashed particles from laser processing, herein, a method for customizing microstructured flexible electrodes by femtosecond laser-activated metal deposition is proposed. It takes advantage of the catalyzing particles scattered during femtosecond laser ablation and is particularly suitable for moldless, maskless, and low-cost fabrication of microstructured metal layers on polydimethylsiloxane (PDMS). Robust bonding at the PDMS/Cu interface is evidenced by the scotch tape test and the duration test over 10 000 bending cycles. Benefiting from the firm interface, the developed flexible capacitive pressure sensor with microstructured electrodes presents several conspicuous features, including a sensitivity (0.22 kPa −1 ) 73 times higher than the one using flat Cu electrodes, ultralow detection limit (<1 Pa), rapid response/recovery time (4.2/5.3 ms), and excellent stability. Moreover, the proposed method, inheriting the merits of laser direct writing, is capable of fabricating a pressure sensor array in a maskless manner for spatial pressure mapping.

研究领域: 生物医学工程 · 柔性电子学 · 微纳加工 · 传感器技术 · 材料科学
✓ 已验证 DOI 高影响因子
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Journal of Energy Chemistry · 2021 · IF 9.676

Insights into the enhanced structure stability and electrochemical performance of Ti4+/F− co-doped P2-Na0.67Ni0.33Mn0.67O2 cathodes for sodium ion batteries at high voltage

Pengfei Zhou,Jing Zhang,Zhennan Che,Zuhao Quan,Ju Duan,Xiaozhong Wu,Junying Weng,Jinping Zhao,Jin Zhou

P2-Na 0.67 Ni 0.33 Mn 0.67 O 2 is considered as a promising cathode material for sodium-ion battery (SIBs) because of its high capacity and discharge potential. However, its practical use is limited by Na + /vacancy ordering and P2-O2 phase transition. Herein, a Ti 4+ /F − co-doping strategy is developed to address these issues. The optimal P2-Na 0.67 Ni 0.33 Mn 0.37 Ti 0.3 O 1.9 F 0.1 exhibits much enhanced sodium storage performance in the high voltage range of 2.0–4.4 V, including a cycling stability of 77.2% over 300 cycles at a rate of 2 C and a high-rate capability of 87.7 mAh g −1 at 6 C. Moreover, the P2-Na 0.67 Ni 0.33 Mn 0.37 Ti 0.3 O 1.9 F 0.1 delivers reversible capacities of 82.7 and 128.1 mAh g −1 at −10 and 50 °C at a rate of 2 C, respectively. The capacity retentions over 200 cycles at −10 °C is 94.2%, implying more opportunity for practical application. In-situ X-ray diffraction analysis reveals that both P2-O2 phase transitions and Na + /vacancy ordering is suppressed by Ti 4+ /F − co-doping, which resulting in fast Na + diffusion and stable phase structure. The hard carbon//P2-Na 0.67 Ni 0.33 Mn 0.37 Ti 0.3 O 1.9 F 0.1 full cell exhibits a high energy density of 310.2 Wh kg −1 and remarkable cyclability with 82.1% retention after 300 cycles at 1 C in the voltage range of 1.5–4.2 V. These results demonstrate that the co-doping Ti 4+ /F − is a promising strategy to improve the electrochemical properties of P2-Na 0.67 Ni 0.33 Mn 0.67 O 2 , providing a facile tactic to develop high performance cathode materials 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 · 电池技术
✓ 已验证 DOI 高影响因子
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JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS · 2016 ·Vol. 105 ·期 6 ·1369-1378 · IF 2.881

In vitro and in vivo degradation of potential anti-adhesion materials: Electrospun membranes of poly(ester-amide) based on l-phenylalanine and p-(dioxanone)

Bing Wang,Jun Dong,Lijing Niu,Wenyan Chen,Dongliang Chen,Chengyi Shen,Jiang Zhu,Xiaoming Zhang

Electrospun membranes of poly(p-dioxanone-co- l -phenylalanine) (PDPA) hold potential as an anti-adhesion material. Since adjustable degradation properties are important for anti-adhesion materials, in this study, the in vitro and in vivo degradation processes of PDPA electrospun membranes were investigated in detail. The morphological analysis of these membranes revealed the main degradation conditions of PDPA membranes. The weight remaining and molecular weight variation showed that the overall degradation rate of the membranes could be adjusted by modulating the molecular structure of the PDPAs. Especially, α-chymotrypsin could catalyze the degradation process of PDPAs. Based on these results, the in vitro degradation mechanism was demonstrated, and confirmed by 1 H NMR of the hydrolysis products. Finally, the in vivo degradation and biocompatibility of different PDPAs were investigated. The kinetic study showed that the in vitro and in vivo molecular weight loss of PDPAs have the first-order characteristics. The in vivo degradation rate of the most Phe-containing PDPA-3 is the slowest, and this result relates to the biocompatibilities of PDPAs. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 105B: 1369–1378, 2017.

研究领域: 生物材料学 · 组织工程 · 高分子科学 · 生物医学工程 · 药物递送 · 再生医学 · 生物降解
✓ 已验证 DOI 高影响因子
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Colloid and Interface Science Communications · 2019 · IF 1.87

Influence of TiO2 nanostructure size and surface modification on surface wettability and bacterial adhesion

Gaoqi Wang,Ding Weng,Chaolang Chen,Lei Chen,Jiadao Wang

The aim of the study was to explore the synergistic effects of nanostructure size and surface treatment of TiO 2 coatings on its wettability and bacteria adhesion. The coatings were fabricated by TiO 2 particles with a diameter ranging from 25 nm to 300 nm. The surface wettability of coatings was tuned by chemical treatment. The anti-adhesion property of as-prepared coatings was evaluated with Streptococcus mutans in two types of solutions: phosphate buffer solution (PBS) and PBS with 1 wt% sucrose. The results show that particle size and surface treatment have significant influences on the wettability (with contact angles of 0–160°) and bacterial adhesion. The coating prepared by chemically modified 25 nm particles has a superhydrophobic property, and could inhibit bacterial adhesion in aqueous solutions with sucrose or not. The study also provides a facile, universal and low-cost process to fabricate anti-adhesion coating, which is applicable for diverse of substrates.

研究领域: 生物材料学 · 纳米医学 · 表面科学 · 微生物学 · 口腔生物学
✓ 已验证 DOI 高影响因子
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MATERIALS SCIENCE IN SEMICONDUCTOR PROCESSING · 2021 · IF 3.927

An optimized passivation mechanism at the copper film recess for achieving efficient planarization of copper chemical mechanical polishing

Nengyuan Zeng,Chenwei Wang,Chong Luo,Hongdong Zhao,Yuling Liu,Wantang Wang,Tengda Ma

This article proposed an improvement plan for the slurry to reduce the dishing caused during copper chemical mechanical polishing (CMP) of the interconnect structure. According to the difference in the pressure between the concave and convex parts of the copper film in the high-hardness polishing pad, polishing slurries were designed with a distinct difference in the polishing removal rate under high and low platen pressures to improve their planarization efficiency. 2 wt% GLY (glycine) and 1 wt% H 2 O 2 can provide a chemical dissolution effect, adding 0.1% TAZ (1,2,4-triazole) to slow down the corrosion mainly for the recession, by adjusting the slurry pH to 7. The polishing results showed that the slurry had a high copper removal rate (6772 Å/min) at high pressure (3.0 psi) and a much lower removal rate (3273 Å/min) at low pressure (1.2 psi). The pattern wafer polished with this slurry obtained relatively low dishing. The other comparison groups showed slight differences in copper removal rate at high and low pressure and a deeper dishing of the polished pattern wafer. In this paper, based on the analysis of static dissolution experiments, electrochemical experiments, and XPS experiments of copper films in different slurries, the chemical reaction mechanism of copper films in the solution system of GLY and H 2 O 2 was studied at different pH values. In addition, the inhibition mechanism of TAZ on the copper surface at different slurry pH values was proposed, including the properties of the TAZ molecule adsorption film on the copper surface, the uniformity of the surface coverage, and the thickness of the passivation layer . The results can reflect the polishing results to a certain extent despite some deviations, but it can also be used as a more reasonable argument to explain the optimization scheme of the slurry proposed in this article.

研究领域: 材料科学 · 微电子制造 · 表面化学 · 半导体工艺 · 腐蚀与防护
✓ 已验证 DOI 高影响因子
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Journal of Materiomics · 2022 ·Vol. 8 ·期 5 ·1001-1008 · IF 8.589

Silver particle interlayer with high dislocation density for improving the joining of BaZr0.1Ce0.7Y0.1Yb0.1O3-δ electrolyte and AISI 441 interconnect

Xiaoyang Wang,Chun Li,Qihan Zhou,Mingshen Li,Mushi Zheng,Junlei Qi,Xiaoqing Si,Jian Cao

One of the critical challenges for the protonic ceramic fuel cell stack is sealing electrolytes and interconnects. However, the traditional Ag CuO sealant will aggravate the oxidation along the interconnect surface and result in brittle compound layers at the BaZr 0.1 Ce 0.7 Y 0.1 Yb 0.1 O 3- δ (BZCYYb) electrolyte interface. The present work demonstrates that a silver particle interlayer with high dislocation density can be adopted to join BZCYYb electrolyte to the interconnect (AISI 441 stainless) in air instead of traditional Ag CuO sealant. Elevating temperatures result in a sufficient bonding at the Ag/BZCYYb interface, and a defect-free joint is obtained at 950 °C. Atomic bonding at Ag/BZCYYb interface is confirmed by TEM. Also, a dense and thin oxide layer (2–3 μm) is formed along the AISI 441 interface. Ag particles in the interlayer provide the main driving force for the sintering joining. The massive dislocations promote the recovery and recrystallization of the Ag interlayer, as well as the interdiffusion of BZCYYb/Ag. After aging in the wet oxidizing atmosphere at 600 °C for 300 h, joints remain intact and dense, indicating superior oxidation resistance and aging performance. Besides, the joint shear strength (25.3 MPa) is 59 % higher than that of the joint brazed by traditional Ag CuO.

研究领域: 材料科学 · 固态离子学 · 能源材料 · 电化学 · 连接技术 · 高温材料
✓ 已验证 DOI 高影响因子
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PROPELLANTS EXPLOSIVES PYROTECHNICS · 2024 ·Vol. 50 ·期 3 ·e202400232 · IF 1.7

Analysis of Combustion Properties of Tungsten/Copper Oxide Pyrotechnic Delay Composition

Bo Hao,Caixian Xu,Geng Chen,Yuangen Lu,Li Zhang

In response to issues such as poor accuracy and unstable delay times encountered in the practical use of tungsten-based delay compositions, an analysis of the combustion performance of tungsten-based delay compositions with the addition of copper oxide was conducted. This study selected five tungsten-based composite delay compositions prepared by blending tungsten-based delay compositions with copper oxide at different content, aiming to investigate the influence of varying copper oxide proportions on the combustion characteristics of tungsten-based delay compositions. Microscopic morphologies and thermal decomposition behaviors of the tungsten/copper oxide delay compositions were analyzed using scanning electron microscopy (SEM) and differential scanning calorimetry (DSC), while combustion products were examined by X-ray diffraction (XRD). The results indicate that copper oxide exerts a strong catalytic decomposition effect on tungsten-based delay compositions. Specifically, a low concentration of copper oxide enhances the combustion rate of tungsten-based delay compositions, while an increase in copper oxide content subsequently slows down the combustion rate. Notably, tungsten-based delay compositions with 9% copper oxide content demonstrate high precision, good stability, and a relatively slow combustion rate, offering a wider range of adjustability for controlling the combustion speed of delay compositions and providing a feasible method for managing the delay time range in practical applications.

研究领域: 材料科学 · 火工品技术 · 燃烧学 · 无机化学 · 功能材料
✓ 已验证 DOI 高影响因子
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