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RSC Advances · 2018 ·Vol. 8 ·期 44 ·24900-24905 · IF 2.936

Porous carbon adsorption layer enabling highly reversible redox-reaction of a high potential organic electrode material for sodium ion batteries

Yanjie Wang,Chun Fang,Ying Huang,Qing Liu,Ruirui Zhao,Xuli Ding,Yunhui Huang

Organic compounds have been utilized in rechargeable batteries as electrode materials on account of their designable structures and reversible redox properties. However, most of them suffer from problems with dissolution resulting in poor electrochemical performance. In this work, we adapt a sodium salt of tetracyanoquinodimethane (NaTCNQ) to work as a high redox potential cathode material in sodium ion batteries (SIBs). A porous carbon coated separator is demonstrated to be an adsorption layer and prevents the dissolved active material from migrating to the anode side. The NaTCNQ cell assembled with a carbon layer containing 5% activated carbon (AC) exhibits a higher initial capacity and greatly improved cycling stability. Using a conductive adsorption layer in organic redox batteries is a promising pathway to develop high performance organic electrode materials for SIBs.

研究领域: 电化学 · 能源材料 · 纳米材料 · 电池技术 · 功能材料
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Smart films based on semiconductor heterojunctions of mechanoluminescent sulfide and sulfur oxide for stress sensing and anti-counterfeiting applications

Yiheng Yue,Guocheng Pan,Jun Wan,Zhen Xiao,Yang Zhang,Shiqing Xu,Gongxun Bai

Mechanoluminescent (ML) materials offer significant potential for remote stress sensing and distribution. However, creating highly sensitive and responsive ML materials remains a challenge. In this study, mechanoluminescent semiconductor materials have been successfully prepared as Mn 2+ doped ZnS-SrZnOS heterojunction composites. These materials exhibit high-resolution stress distribution visualization and rapid response, captured via camera recording. Notably, they possess a low stress triggering threshold, reaching the KPa level, and respond within milliseconds. Furthermore, it was found that by adjusting the doping concentration of Mn 2+ within the heterojunction, the material utilizes its bimodal emission capability to manipulate the fluorescence shift and achieve optical anti-counterfeiting. The synthesis of smart films by combining the material with polydimethylsiloxane matrix had enabled the achievement of collision detection, information hiding and optical anti-counterfeiting. These results suggest that the prepared smart films have wide range of optical sensing applications.

研究领域: 材料科学 · 纳米科技 · 光学传感 · 功能材料 · 固态物理 · 表面与界面科学
✓ 已验证 DOI 高影响因子
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DIAMOND AND RELATED MATERIALS · 2019 · IF 2.29

Magnesium silicate hydroxide modified by carbon from hydrothermal carbonization of gelatin for tribological application

Qiuying Chang,Hao Zhang,Rongqin Gao

A new nanocomposite was prepared by combining Magnesium silicate hydroxide (MSH) with decomposed gelatin under one-pot hydrothermal synthesis conditions. The chemical reaction process involved the MSH formation and the gelation decomposing into carbonaceous species. The characterization of resultant nanoparticles revealed that the nanocomposite was a combination of hydrogenated amorphous carbon and MSH. And the addition of gelatin during synthesis increased the content of granular nanoparticles in nanocomposite samples. The results of tribological experiments of MSH modified by carbon (MSH@C) as lubricant additive showed that the nanocomposites presented much better anti-wear property and friction stability than the MSH without modification. Thus MSH@C nanocomposites were expected to be a promising candidate for lubricant additives. The amorphous carbon film was detected on the wear scar which might account for the significant tribological property.

研究领域: 材料科学 · 纳米科技 · 表面工程 · 摩擦学 · 复合材料
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CHINESE JOURNAL OF ANALYTICAL CHEMISTRY · 2017 ·Vol. 45 ·期 6 ·830-836 · IF 0.795

Cobalt Hexacyanoferrate-modified Graphene Platform Electrode and Its Electrochemical Sensing toward Hydrogen Peroxide

Hong-Cai ZHAO,Pu ZHANG,She-Hong LI,Hong-Xia LUO

A large area graphene platform electrode (GPE) was fabricated by transferring chemical vapor deposition (CVD) grown graphene on Cu foils onto polyethylene terephthalate (PET) substrates with the aid of polymethyl methacrylate (PMMA). Cobalt hexacyanoferrate (CoHCF) was electrodeposited on GPE by cyclic voltammetry. The morphology and electrochemical properties of CoHCF/GPE were studied by scanning electron microscope (SEM), electrochemical impedance spectroscopy (EIS) and the electrochemical measurements. The CoHCF/GPE showed favorable sensing effect toward H 2 O 2 . A novel non-enzyme H 2 O 2 sensor was constructed. Under the optimal experimental conditions, the proposed sensor responded to the addition of H 2 O 2 very quickly (about 2 s) with a wide linear rang (0.005–1.2 mM) and a low detection limit (7.1 nM). This sensor was easy to be fabricated and showed excellent stability and anti-interference ability.

研究领域: 电化学 · 生物传感器 · 纳米材料 · 分子诊断 · 转化医学 · 即时检测
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2019 ·Vol. 44 ·期 31 ·16348-16358 · IF 4.084

Mesoporous g-C3N4/Zn–Ti LDH laminated van der Waals heterojunction nanosheets as remarkable visible-light-driven photocatalysts

Dandan Sun,Dechao Chi,Zekang Yang,Zipeng Xing,Junwei Yin,Zhenzi Li,Qi Zhu,Wei Zhou

Mesoporous g-C 3 N 4 /Zn–Ti layered double hydroxide (LDH)-laminated van der Waals heterojunction nanosheets were prepared by a facile one-step in situ hydrothermal method . Due to the strong electrostatic interactions between the positively charged Zn–Ti LDH and negatively charged g-C 3 N 4 nanocrystal , a laminated van der Waals heterostructure was successfully formed between Zn–Ti LDH and g-C 3 N 4 . The mesoporous g-C 3 N 4 /Zn–Ti LDH-laminated van der Waals heterojunction, which had a narrow bandgap of 2.41 eV extended the photoresponse to the visible light region. The obtained heterojunctions showed excellent visible-light-driven photocatalytic performance for the complete removal of ceftriaxone sodium (up to ∼97%) and a high hydrogen production rate (∼161.87 μmol h −1  g −1 ). This was mainly attributed to the formation of the laminated van der Waals heterojunctions, which favoured charge separation and the absorption of visible light, and the mesoporous structure, which provided more surface active sites. This facile strategy for preparing mesoporous g-C 3 N 4 /Zn–Ti LDH-laminated van der Waals heterojunctions offers new insights for the fabrication of high-performance van der Waals heterojunction photocatalytic materials.

研究领域: 材料科学 · 光催化 · 纳米材料 · 环境化学 · 能源化学
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2020 · IF 16.683

Spatially controlled oxygen storage materials improved the syngas selectivity on chemical looping methane conversion

Dewang Zeng,Yu Qiu,Min Li,Li Ma,Dongxu Cui,Shuai Zhang,Rui Xiao

Chemical looping redox cycle of oxygen storage materials offers a versatile platform to convert methane to value-added products in a clean and efficient manner. However, the highly dynamic nature of the oxygen diffusion process restrains the selective formation of the target products over a long reaction period. In this work, we show the oxygen storage materials-comprising of iron oxides and zirconium oxide support, with the nickel catalyst controllably deposited—that significantly enhanced the syngas selectivity. Mechanistic study indicated the oxygen releasing rate can be well controlled within a long reaction period by the specific spatial structure, demonstrating a new strategy to tune the oxygen diffusion in chemical looping process. Through the observed spatial effects, this work can be also extended to develop more oxygen storage materials for the other chemical looping applications, e.g. methane reforming, methane oxidative coupling, ethane oxidative dehydrogenation, etc .

研究领域: 催化化学 · 能源化学 · 材料化学 · 化学工程 · 多相催化
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Nanoscale · 2021 ·Vol. 13 ·期 23 ·10393-10401 · IF 7.79

Surfactant-mediated morphology evolution and self-assembly of cerium oxide nanocrystals for catalytic and supercapacitor applications

Xiaodong Hao,Shuai Zhang,Yang Xu,Liangyu Tang,Kazutoshi Inoue,Mitsuhiro Saito,Shufang Ma,Chunlin Chen,Bingshe Xu,Tadafumi Adschiri,Yuichi Ikuhara

Surfactant plays a remarkable role in determining the growth process (facet exposition) of colloidal nanocrystals (NCs) and the formation of self-assembled NC superstructures, the underlying mechanism of which, however, still requires elucidation. In this work, the mechanism of surfactant-mediated morphology evolution and self-assembly of CeO2 nanocrystals is elucidated by exploring the effect that surfactant modification has on the shape, size, exposed facets, and arrangement of the CeO2 NCs. It is directly proved that surfactant molecules determine the morphologies of the CeO2 NCs by preferentially bonding onto Ce-terminated {100} facets, changing from large truncated octahedra (mostly {111} and {100} exposed), to cubes (mostly {100} exposed) and small cuboctahedra (mostly {100} and {111} exposed) by increasing the amount of surfactant. The exposure degree of the {100} facets largely affects the concentration of Ce3+ in the CeO2 NCs, thus the cubic CeO2 NCs exhibit superior oxygen storage capacity and excellent supercapacitor performance due to a high fraction of exposed active {100} facets with great superstructure stability.

研究领域: 材料化学 · 纳米科学 · 催化化学 · 电化学 · 无机功能材料
✓ 已验证 DOI 高影响因子
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CERAMICS INTERNATIONAL · 2017 ·Vol. 43 ·期 16 ·14176-14182 · IF 2.986

Polyaceticzirconium for zirconia continuous fibers: Polymeric evolution process and the relationship between polymeric structure and rheological behavior

Lin Wang,Benxue Liu,Luyi Zhu,Yongshuai Xie,Yadong Lv,Chonghe Xu,Xiaotong Jin,Xinqiang Wang,Guanghui Zhang,Dong Xu

Polyaceticzirconium (PEZ) sol, which is the precursor of zirconia (ZrO 2 ) continuous fibers, has been synthesized by means of the reaction between zirconium oxychloride octahydrate (ZrOCl 2 ·8H 2 O) and potassium acetate (CH 3 COOK) in methanol. The polymeric structures and the rheological behaviors of the sols with different molar ratios of ZrOCl 2 ·8H 2 O/CH 3 COOK are different and would affect the spinnability and stability significantly. Herein, the polymeric structures and rheological behaviors of the PEZ sols with the molar ratios of 1:1, 1:1.5, 1:1.8 and 1:2 were investigated by Fourier transform infrared (FT-IR), 1 H nuclear magnetic resonance spectrum ( 1 H-NMR), thermogravimetry and differential thermal analysis (TG/DTA) and rheological measurements. The results showed the carboxyl group acted as a chelating ligand instead of bidentate ligand, and the water molecule coordinated to Zr 4+ was deprotoned gradually with the decrease of the molecular ratios. The different polymeric structures lead to a different rheological behaviors of the sols. It is divided into three types, the Newton fluid with a low viscosity produced by the charged linear polymeric structures, the shear thinning fluid with a high viscosity produced by the three-dimensional polymeric structures and the shear thinning fluids with a proper viscosity produced by the linear twining polymeric structures. Through the experimental guidance, we successfully synthesized a sol with suitable viscosity and stability, and used it to fabricate high quality ZrO 2 fibers.

研究领域: 材料科学 · 无机化学 · 高分子化学 · 纤维工程 · 溶胶-凝胶技术
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INTERNATIONAL JOURNAL OF REFRACTORY METALS & HARD MATERIALS · 2020 · IF 3.407

Microstructure refinement and mechanical properties improvement in the W-Y2O3 alloys via optimized freeze-drying

Weiqiang Hu,Zhi Dong,Hui Wang,Tansir Ahamad,Zongqing Ma

Oxide-dispersion-strengthened (ODS) tungsten based alloys with high performance were synthesized by optimized freeze-drying with PVP and PEG polymer dispersant additives and subsequent low temperature sintering . The pre-freezing principle developed firstly in our work shows that fast cooling rate and polymer dispersant additives contribute to the refinement and uniformity of precursor powders. The optimized freeze-dried W-Y 2 O 3 composite powders possess an average grain size of 9 nm, which can be attributed to the steric hindrance provided by polymer dispersants during freeze-drying and voids left by the decomposition of polymer dispersants during calcination . After sintering at low temperature, the W-Y 2 O 3 alloys have ultrafine W grain (210 nm) and nano second phase particles (<50 nm) dispersed in W matrix while maintaining a high relative density of 97.8%. These factors mentioned above lead to the microhardness and compressive strength as high as 721 ± 31 HV 0.2 , 814 MPa respectively, accompanied by a high total deformation plasticity of above 50%. These results indicate that the optimized freeze-drying and subsequent low temperature sintering is a promising way to fabricate ODS tungsten based alloys with high performance.

研究领域: 材料科学 · 金属学与冶金工程 · 纳米材料 · 复合材料 · 结构材料
✓ 已验证 DOI 高影响因子
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JOURNAL OF POWER SOURCES · 2017 · IF 6.395

Bulk heterojunction perovskite solar cells based on room temperature deposited hole-blocking layer: Suppressed hysteresis and flexible photovoltaic application

Zhiliang Chen,Guang Yang,Xiaolu Zheng,Hongwei Lei,Cong Chen,Junjie Ma,Hao Wang,Guojia Fang

Perovskite solar cells have developed rapidly in recent years as the third generation solar cells. In spite of the great improvement achieved, there still exist some issues such as undesired hysteresis and indispensable high temperature process. In this work, bulk heterojunction perovskite-phenyl-C 61 -butyric acid methyl ester solar cells have been prepared to diminish hysteresis using a facile two step spin-coating method. Furthermore, high quality tin oxide films are fabricated using pulse laser deposition technique at room temperature without any annealing procedure. The as fabricated tin oxide film is successfully applied in bulk heterojunction perovskite solar cells as a hole blocking layer. Bulk heterojunction devices based on room temperature tin oxide exhibit almost hysteresis-free characteristics with power conversion efficiency of 17.29% and 14.0% on rigid and flexible substrates , respectively.

研究领域: 材料科学 · 光伏技术 · 纳米材料 · 能源材料 · 半导体器件 · 薄膜制备
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Green Energy & Environment · 2021 ·Vol. 8 ·期 2 ·589-600 · IF 8.207

Metal organic framework supported niobium pentoxide nanoparticles with exceptional catalytic effect on hydrogen storage behavior of MgH2

Liuting Zhang,Farai Michael Nyahuma,Haoyu Zhang,Changshan Cheng,Jiaguang Zheng,Fuying Wu,Lixin Chen

Nb 2 O 5 nanoparticles with an average particle size of 10 nm supported on a rhombic dodecahedral metal organic framework (MOF) were successfully synthesized by a facile one-pot hydrothermal reaction and subsequent calcination process. Experimental results demonstrated that the prepared catalyst drastically improved the hydrogen storage behavior of MgH 2 . 7 wt% Nb 2 O 5 @MOF doped MgH 2 started to desorb hydrogen at 181.9 °C and 6.2 wt% hydrogen could be released within 2.6 min and 6.3 min at 275 °C and 250 °C, respectively. The fully dehydrogenated composite also displayed excellent hydrogenation by decreasing the onset absorption temperature to 25 °C and taking up 4.9 wt% and 6.5 wt% hydrogen within 6 min at 175 °C and 150 °C, respectively. Moreover, the corresponding activation energy was calculated to be 75.57 ± 4.16 kJ mol −1 for desorption reaction and 51.38 ± 1.09 kJ mol −1 for absorption reaction. After 20 cycles, 0.5 wt% hydrogen capacity was lost for the MgH 2 +7 wt% Nb 2 O 5 @MOF composite, much lower than 1.5 wt% of the MgH 2 +7 wt% Nb 2 O 5 composite. However, the addition of Nb 2 O 5 @MOF had limited effect on reducing the dehydrogenation enthalpy of MgH 2 . Microstructure analysis revealed that Nb 2 O 5 particles were uniformly distributed on surface of the MgH 2 matrix and synergistically improved the hydrogen storage property of MgH 2  with MOF.

研究领域: 材料科学 · 无机化学 · 纳米催化 · 能源存储 · 氢能源 · 固态储氢
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COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING · 2020 · IF 6.444

High micromechanical interlocking graphene oxide/carboxymethyl cellulose composite architectures for enhancing the interface adhesion between carbon fiber and epoxy

Baowei Qiu,Tong Sun,Muxuan Li,Yang Chen,Shengtai Zhou,Mei Liang,Huawei Zou

The interface performance of carbon fiber (CF) reinforced polymer composites (CFRPs) is one of the key factors that affect their properties. In order to improve the interface adhesion between CF and epoxy (EP), a green method is proposed. Carboxymethyl cellulose (CMC) and graphene oxide (GO) are introduced to the CF surface through the hydrogen bonds, and they can form high micromechanical interlocking composite architectures, which can enhance the micromechanical interaction in the interface of CF and EP. It is found that CMC and GO can significantly improve the interfacial shear strength (IFSS) and interlaminar shear strength (ILSS) of EP/CF composite. This means that it has great potential to improve the interface of CFRPs and strengthen their performance by natural cellulose fibers. This modification method does no harm to CF and is environmental friendliness, which lays a research foundation for using natural cellulose to enhance the interface performance of CFRPs.

研究领域: 复合材料科学 · 高分子材料 · 界面工程 · 纳米材料 · 绿色制造
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