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ELECTROCHIMICA ACTA · 2015 · IF 4.504

Lithium sodium vanadium phosphate and its phase transition as cathode material for lithium ion batteries

Peng Li,Lianyi Shao,Pengfei Wang,Xi Zheng,Haoxiang Yu,Shangshu Qian,Miao Shui,Nengbing Long,Jie Shu

In this work, Li 2 NaV 2 (PO 4 ) 3 is successfully synthesized by using a simple solid-state reaction method. Structural analysis shows that this sample is a hybrid product consisted of rhombohedral Li 3 V 2 (PO 4 ) 3 phase and rhombohedral Na 3 V 2 (PO 4 ) 3 phase As a cathode material for lithium ion batteries, Li 2 NaV 2 (PO 4 ) 3 exhibits an initial reversible capacity of 108.9   mAh   g −1 at 35   mA   g −1 in the potential range between 3.0 and 4.3   V, with an average working potential at 3.75   V. The lithium-ion diffusion coefficient in Li 2 NaV 2 (PO 4 ) 3 is measured to be 1.86–3.27   ×   10 −15   cm 2   s −1 . In addition, the electrochemical reaction between Li 2 NaV 2 (PO 4 ) 3 and Li is also investigated by various in-situ and ex-situ techniques. Viewed from the in-situ and ex-situ results, it is concluded that the electrochemical reactions of Li 2 NaV 2 (PO 4 ) 3 with Li are associated with the formation of rhombohedral LiV 2 (PO 4 ) 3 phase and rhombohedral NaV 2 (PO 4 ) 3 phase during the lithium ion extraction process and its reverse lithium insertion process is reversible for structural evolution. The highly stable structure ensures the electrochemical reversibility of Li 2 NaV 2 (PO 4 ) 3 cathode material in lithium ion batteries.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 固体化学
✓ 已验证 DOI 高影响因子
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Journal of Environmental Chemical Engineering · 2021 ·Vol. 9 ·期 4 ·105292 · IF 5.909

0D/1D Z-scheme g-C3N4 quantum dot/WO3 composite for efficient Cr (VI) photoreduction under visible light

Jie Zhou,Wenyi Cai,Jing Ding,Hui Wan,Guofeng Guan

The appropriate construct of Z-scheme heterostructure composite with high photocatalytic activity has created new opportunities for environmental protection. Herein, graphitic carbon nitride quantum dots/tungsten trioxide (CNQDs/WO 3 ) was firstly fabricated using CNQDs decorated onto the surface of WO 3 nanorod grown along the [110] orientation in hydrothermal environment to construct a Z-scheme heterostructure composite. By various characterization methods, the crystal structure, micro morphology, atomic valence state and surface functional groups of the catalyst were systematically revealed. The results indicated that Z-scheme heterojunctions between CNQDs and WO 3 were successfully constructed. Compared with pure WO 3 , CNQDs/WO 3 exhibited prominent photoreduction performance under visible light irradiation. The optimal 5% CNQDs/WO 3 could reduce almost 100% Cr (VI) under acidic condition with the best photocatalytic activity within 90 min. More than this, 5% CNQDs/WO 3 also displayed excellent stability and recyclability even after five cycles of photoreduction experiments. Based on the free radical quenching experiments, the possible photoreduction reaction mechanism had been proposed in detail. The Z-scheme heterostructure provided the possibility of the generation, rapidly transfer and efficient separation of photogenerated electrons, which were major active species in the Cr (VI) photoreduction process.

研究领域: 环境催化 · 材料化学 · 纳米科技 · 光催化 · 环境污染治理 · 半导体异质结
✓ 已验证 DOI 高影响因子
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POLYMER TESTING · 2020 · IF 3.275

Epoxy nanocomposites with high thermal conductivity and low loss factor: Realize 3D thermal conductivity network at low content through core-shell structure and micro-nano technology

Rui Wang,Congzhen Xie,Bin Gou,Huasong Xu,Shoukang Luo,Jiangang Zhou,Leilei Zeng

Dielectric polymers with high thermal conductivity are very promising in the fields of aerospace and electronic device packaging. However, composites with excellent dielectric properties usually have low thermal conductivity. It is usually to fill the polymer with thermal conductivity particles to improve the thermal conductivity, but the high content of filler often reduces the mechanical properties of the polymer. In this paper, the traditional insulating polymer epoxy resin was used as the matrix, by covering the surface of silicon carbide with graphene to form a core-shell structure and co-filled with nano diamonds to achieve the preparation of high-performance epoxy resin at low content. The results showed that at the filling content of 30 wt%, the thermal conductivity of epoxy nanocomposites showed a dramatic thermal conductivity enhancement of 1263%, the energy storage modulus increased by 1.1 GPa, and the dielectric loss remained unchanged at 50 Hz. The advantages of the composite are the structural design and surface modification of the filler, which not only take advantage of its inherent advantages, but also improve the interface area with the epoxy matrix. The composite materials with excellent properties are expected to provide theoretical guidance for the application of high thermal conductivity dielectric materials.

研究领域: 材料科学 · 高分子化学 · 复合材料工程 · 电子封装材料 · 介电材料 · 热管理材料
✓ 已验证 DOI 高影响因子
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Small · 2023 ·Vol. 19 ·期 40 ·2303227 · IF 13.3

Sodium-Ion Substituted Water Molecule in Layered Vanadyl Phosphate Enhancing Electrochemical Kinetics and Stability of Zinc Ion Storage

YuanZhe Wu,Quan Zong,Chaofeng Liu,Yanling Zhuang,Daiwen Tao,Jiangying Wang,Jingji Zhang,Qilong Zhang,Guozhong Cao

Vanadyl phosphate (VOPO 4 ·2H 2 O) has been regarded as one of the most promising cathode materials for aqueous Zn-ion batteries due to its distinct layered structure. However, VOPO 4 ·2H 2 O has not yet demonstrated the exceptional Zn ion storage performance owing to the structural deterioration during repeated charging/discharging process and poor intrinsic conductivity. In this work, 2D sodium vanadyl phosphate (NaVOPO 4 ·0.83H 2 O, denoted as NaVOP) is designed as a cathode material for Zn-ion batteries, in which sodium ions are preinserted into the interlayer, replacing part of water. Benefiting from the in situ surface oxidization, improved electronic conductivity, and increased hydrophobicity, the NaVOP electrode exhibits a high discharge capacity of 187 mAh g −1 at 0.1 A g −1 after activation, excellent rate capability and enhanced cycling performance with 85% capacity retention after 1500 cycles at 1 A g −1 . The energy storage mechanism of the NaVOP nanoflakes based on the rapid Zn 2+ and H + intercalation pseudocapacitance are investigated via multiple ex situ characterizations.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机化学 · 纳米材料
✓ 已验证 DOI 高影响因子
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ELECTROCHIMICA ACTA · 2019 · IF 5.383

Semi-continuous electrochemical extraction of lithium from brine using CF-NMMO/AC asymmetric hybrid capacitors

Xiaoyu Zhao,Guangyu Li,Minghui Feng,Yanfei Wang

Compared to traditional extraction of lithium using solar evaporation, the electrochemical extraction is advantageous in many aspects, including elevated efficiency, superior selectivity, and low environmental pollution. In this study, LiNi 0·038 Mo 0·012 Mn 1·95 O 4 (LNMMO) with good lattice structure and nano morphology was successfully prepared and confirmed by XRD (X-ray diffraction), SEM-Mapping (scanning electron microscope mapping), SEM (scanning electron microscope), and EDX (Energy-dispersive X-ray spectroscopy) analyses. The pairing of LNMMO with activated carbon (AC) yielded obvious cost-effective and environmentally friendly composite when compared to conventional Noble metals used for battery anodes, such as Ag and Pt. A hybrid supercapacitor was assembled using delithiated LNMMO cathode (NMMO) and AC anode to form NMMO/AC. The cell showed high capacity, high rate performance, and excellent cyclic stability. A continuous flow NMMO/AC hybrid supercapacitor (CF-NMMO/AC) was developed for selective capture of Li + in aqueous solution by combining NMMO/AC hybrid supercapacitor with self-designed continuous flow control system. The device delivered high Li + extraction efficiencies reaching 14.4 mg/g per one cycle in simulated brine by consuming only 7.91  W h/mol Li + . The overall process produced 97.2% Li + in simulated brine at optimized operating conditions. Overall, CF-NMMO/AC system provided higher efficiency, superior selectivity, and moderate energy utilization for Li + recovery from brine.

研究领域: 电化学 · 环境科学 · 材料科学 · 能源工程 · 分离科学 · 可持续技术
✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Addressable planar arrays of highly-luminescent 1,4-bis(5-phenyloxazol-2-yl)benzene nanowires via mask-confined graphoepitaxy for optoelectronic applications

Wei Zhou,Wanglong Mao,Pingyang Huang,Xiong Huang,Haoyuan Xu,Bo Wu,Xiaofang Jiang,Xiangtao Chen,Hanyu Liu,Guofu Zhou,Jinyou Xu

This study introduces a facile method for the controlled growth of addressable planar arrays of highly luminescent, catalyst-free 1,4-bis(5-phenyloxazol-2-yl)benzene (POPOP) nanowires. By employing a hollow mask over a faceted sapphire substrate, simultaneous control over the position and orientation of the nanowires is achieved through a mask-confined graphoepitaxial growth, offering substantial advantages over traditional post-growth assembly techniques. High-temperature annealing creates parallel nanogrooves on the sapphire surface, inducing a graphoepitaxial effect that aligns the nanowires with a consistent [102] crystallographic axis. The hollow mask further aids in precisely localizing nanowire growth through its shadowing effect. Optoelectronic investigations reveal that these nanowires emit intense and stable blue photoluminescence at room temperature, with a broad spectrum spanning from 400 to 600 nm. This luminescence is achieved through excitation by continuous-wave ultraviolet light or two-photon absorption using femtosecond infrared light. Notably, the emission quantum efficiency of POPOP nanowires reaches 59 %, a remarkable improvement over the 12 % observed in powder counterparts when excited with 405 nm light. Transit absorption spectra indicate that ground state bleaching and excited state absorption display consistent kinetics within a 100 ps time window, suggesting the same origin from singlet excitons. The precise alignment and positioning of these nanowires make them viable for in-situ integration into photodetectors with rapid ultraviolet light responses. This study advances the controlled growth of catalyst-free nanowire arrays and enhances the understanding of the optoelectronic properties of POPOP nanowires.

研究领域: 材料科学 · 纳米科技 · 光电子学 · 凝聚态物理 · 表面科学 · 有机半导体
✓ 已验证 DOI 高影响因子
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2019 · IF 14.229

In-situ synthesis of monodispersed CuxO heterostructure on porous carbon monolith for exceptional removal of gaseous Hg0

Liyuan Zhang,Shu Yang,Yuekun Lai,Hui Liu,Yiang Fan,Cao Liu,Haiying Wang,Liyuan Chai

Gaseous Hg 0 is one of the most deadly and hard-to-dispose pollutants. The oxidation of Hg 0 is a promising route, but the rational design and synthesis of highly efficient catalysts still remain grand challenges. Herein, CuO@Cu 2 O (or Cu x O) heterostructured nanoparticles uniformly monodispersing on porous carbon monolith were designed and successfully synthesized using oligo( m -phenylenediamine)-Cu 2+ complex as raw material. The Cu x O-carbon catalyst contains ∼28 wt% of Cu. Based on density functional theory calculation, the CuO@Cu 2 O junction interfaces can accelerate the Hg 0 oxidation by significantly reducing the energy barriers of reaction. Only 1 mg of the catalyst can catalyze the oxidation of more than 90 % of Hg 0 with [HCl] = 0.5 ppm, [O 2 ] = 6 vol%, T = 150 °C. The poisoning effect of either SO 2 or H 2 O on the catalysts is weak. Moreover, a long-term test confirmed that the Hg 0 oxidation rate can maintain more than 90 % even in the co-presence of SO 2 (5000 ppm) and H 2 O (10 vol%).

研究领域: 环境催化 · 材料化学 · 大气污染控制 · 纳米材料 · 表面科学
✓ 已验证 DOI 高影响因子
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CARBOHYDRATE POLYMERS · 2018 · IF 5.158

Dopamine-induced functionalization of cellulose nanocrystals with polyethylene glycol towards poly(L-lactic acid) bionanocomposites for green packaging

Le Li,Rui-Ying Bao,Tao Gao,Zheng-Ying Liu,Bang-Hu Xie,Ming-Bo Yang,Wei Yang

Improving the physical properties of biobased polymers using bionanofillers is essential to preserve its biodegradability. This work presents a dopamine-induced functionalization of cellulose nanocrystals (CNCs) with polyethylene glycol (PEG), to enhance the crystallization, mechanical and barrier properties of poly( L -lactic acid) (PLLA) bionanocomposites. The effect of molecular weight of grafted PEG on the properties of PLLA is also studied. PEGylation of CNCs significantly enhance the crystallization of PLLA, especially for CNCs functionalized with PEG of lower molecular weight, which lead to balanced strength and ductility, and 66.4% reduction in the oxygen permeability coefficient at a low content of 0.5 wt %. Moreover, 168% improvement of ductility for PLLA can be obtained by CNCs functionalized with longer PEG chains. The surface functionalization of CNCs proposed here opens up a green avenue towards designing and fabricating fully bio-based, high-barrier and low-cost polymer nanocomposites for packaging applications.

研究领域: 高分子材料 · 纳米复合材料 · 生物基包装 · 材料科学 · 聚合物改性 · 结晶动力学
✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2019 · IF 8.355

Supramolecular chemistry assisted construction of ultra-stable solvent-resistant membranes for angstrom-sized molecular separation

Yanqiu Zhang,Hongguang Sun,Hussain Sadam,Yuyan Liu,Lu Shao

Organic solvent nanofiltration (OSN) membrane is an embryonic technology in chemical engineering for simultaneously purifying organic solvents and recycling nano-scale molecules. Although the inherent nano-cavity cyclodextrins (CDs) as powerful molecular hosts in supramolecular science ensure promise for separation technology, the limited synthesis toolbox and material choice impede the CDs deployment in membrane separations, especially for OSN applications. Herein, biocompatible β-cyclodextrin (β-CD) and mussel-inspired polydopamine (pDA) were discovered as the building blocks to simultaneously construct OSN membranes assisted by the host-guest interactions of supramolecular chemistry and hydrogen-bonds via one-step “green” process. Honeycomb microstructures were formed in this process, which adds the molecular transportation pathways. Such biopolymer membranes can remain extraordinarily stable in organic solvent environments, whilst achieving high rejection against angstrom-sized molecule with different charges toward environmental and energy benefits.

研究领域: 高分子科学 · 膜分离技术 · 化学工程 · 纳米材料 · 绿色化学 · 生物医用材料 · 超分子化学
✓ 已验证 DOI 高影响因子
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IONICS · 2022 ·Vol. 29 ·期 2 ·505-518 · IF 2.961

Fe-doped Sn@ 3D carbon lithium-ion battery anode mesoporous material with sodium alginate as the carbon source

Yang Dongping,Xiong Deping,Feng Zuyong,Wen Kunhua,Wu Kaidan,He Miao,Feng Yefeng

Sn-based materials receive a lot of attention because of their high theoretical specific capacity, acceptable price, and good electrical conductivity. However, Sn-based materials have a large volume expansion in the circulation process, leading to the rapid decay of capacity. According to the ion diffusion time formula: t  = L2/2D, where L is the diffusion length or the particle size, and D is the diffusion constant of the ions and the electrons. It can be seen that reducing the particle size can significantly improve the multiplier performance of the material. At present, the main methods for preparing nano-sized metal/carbon composites are the high-energy ball grinding method, hydrothermal method, calcined metal, and organic matter precursor. In this paper, sodium alginate was used as a precursor system for the Fe-doped Sn @3D carbon composite material, which was applied to the lithium-ion battery anode to obtain excellent electrochemical performance (1133.5 mAhg −1 after 200 cycles at 0.2 Ag −1 ). The increase in the specific surface area of Fe-doped Sn @3D carbon also increases the charge transfer efficiency and further improves the multiplier performance of the electrode. Meanwhile, the nano-size and structure can better buffer the volume expansion and protect the structure of the electrode.

研究领域: 材料科学 · 电化学 · 纳米材料 · 能源存储 · 功能材料 · 复合材料
✓ 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
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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
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