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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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RSC Advances · 2021 ·Vol. 11 ·期 16 ·9450-9458 · IF 3.361

Phosphorus modification of cobalt–iron nanoparticles embedded in a nitrogen-doped carbon network for oxygen reduction reaction

Rui Zhang,Zheng Wang,Lin Zhu,Weixin Lv,Wei Wang

For the electrochemical reduction of oxygen the development of heteroatom-doped carbon-based transition metal catalysts has become a recognized strategy to replace traditional noble metal catalysts. In this work a catalyst consisting of CoFe nanoparticles encapsulated in N-doped carbon-based materials (NC) supported by carbon nanotubes (CNTs), i.e. Fe3Co1@NC/CNTs, was modified via treatment with a phosphate salt to synthesize a P-Fe3Co1@NC/CNTs catalyst. The P-Fe3Co1@NC/CNTs exhibits with 5.29 mA cm−2 an enhanced current density which is comparable to a Pt/C catalyst. In addition, a stability and methanol resistance better than the Pt/C catalyst were observed which is ascribed to the carbon encapsulation and the synergies between the two transition metals. Finally, the reaction mechanism of P-doping was studied and discussed. These results provide possible directions for carbon-based catalysts and doping with heteroatoms for the improvement of catalytic activity. Moreover, the zinc–air battery assembled with P-Fe3Co1@NC/CNTs as the air-cathode exhibited a high-power density of 73 mW cm−2, which is comparable to that of Pt/C (71 mW cm−2) and a specific capacity of 763 mA h g−1. The prepared catalyst could potentially serve to take the place of precious metal catalysts in rechargeable Zn–air batteries.

研究领域: 电催化 · 材料化学 · 能源化学 · 纳米材料 · 电化学能源存储 · 燃料电池 · 金属-空气电池
✓ 已验证 DOI 高影响因子
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2017 ·Vol. 28 ·期 16 ·11563-11568 · IF 2.019

Borosiloxane boron diffusion for p-emitter formation on n-type silicon wafers

Sun Xinjie,Tong Hua,Yuan Xiao,Liu Cui,Yuan Shuanglong,Chen Guorong,Yang Yunxia

Thermal boron diffusion, which forms highly doped and shallow p-emitters on phosphor-doped silicon wafers, is one of the primary processes in commercial-scale production of n-type cells. Here, we report on the use of nontoxic and nonvolatile borosiloxane sols as the spin-on boron source. In comparison to the tribromide (BBr 3 ) boron diffusion that is applied in the production of most commercial n-type cells, borosiloxane boron diffusion may have potential advantages in terms of cost, safety, operability, etc. The borosiloxane sols studied here were formed from a cross-linking reaction between boron acid and a mixture of two types of silicon alkoxides, methyltriethoxysilane (MTEOS) and dimethyldiethoxysilane (DMDEOS). The MTEOS/DMDEOS ratio was found to be the key factor determining the synthetic period, net structure, thermal transformation property, and coating behavior of the borosiloxane sols. In combination with the spin-coating method, the performance of borosiloxane boron diffusion into phosphor-doped silicon wafers (1–3 Ω·cm) was systematically investigated by varying the borosiloxane composition (boron/silicon or MTEOS/DMDEOS ratio) and the diffusion process parameters (temperature, ambience, and period of individual sub-steps), and by relating them to the resulting sheet resistance and boron doping profile. The results show that under the diffusion conditions in conventional cell production lines, the formed p-emitters can have variable sheet resistance in the range of 35–582 Ω/□ and boron doping depth of 100–300 nm.

研究领域: 材料科学 · 半导体物理 · 光伏技术 · 表面工程 · 纳米材料 · 化学气相沉积 · 微电子学
✓ 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
✓ 已验证 DOI 高影响因子
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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
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2017 ·Vol. 134 ·期 35 ·45258 · IF 1.86

Polysiloxane/polyacrylate composite latexes with balanced mechanical property and breathability: Effect of core/shell mass ratio

Jie Shen,Jian-wu Sun,Yang Hu,Cheng-you Kan

Polysiloxane/polyacrylate (PSi/PA) core/shell latexes are fabricated, and the particle morphology, the film structure, as well as the properties of the latex films are investigated by comparing with blend latexes, and the relationship between structure and property is proposed. Results indicate that the structure and property of the latex films heavily depend on the particle morphology. The sea–island latex films with uniform distribution of PSi phases can be formed from the PSi/PA core/shell latexes, and with the mass ratio from 1:1 to 1:4, their tensile strength and elongation at break are close to the pure PA latex film, while the elastic recovery and water vapor permeability improve notably. It is found that the phase segregation occurs in the blend latex films, and although the blend latex films provide better water vapor breathability, their mechanical properties sacrifice obviously. Therefore, the various properties must be balanced for practical applications and the core/shell latexes are competitive for meeting the balanced requirements. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 45258.

研究领域: 高分子科学 · 材料化学 · 功能材料 · 胶体与界面化学 · 薄膜材料
✓ 已验证 DOI 高影响因子
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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
✓ 已验证 DOI 高影响因子
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JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC · 2014 · IF 2.745

Immobilization of horseradish peroxidase (HRP) on polyimide nanofibers blending with carbon nanotubes

Teng Zhang,Xiao-Ling Xu,Yi-Ning Jin,Jian Wu,Zhi-Kang Xu

Carbon nanotubes are widely applied in electronics, which offers great potential for enhancing the activity of redox enzyme. In this work, polyimide (PI) was blended with multiwalled carbon nanotubes (MWCNTs) and then electrospun into nanofibers for the immobilization of horseradish peroxidase (HRP), a redox enzyme. SEM and TEM were used to characterize the surface morphology of the PI/MWCNTs nanofibers and to analyze the protruding parts induced by the blending of MWCNT. The results indicate that, compared to the virgin PI nanofibers, the blending of MWCNTs increases the retention activity of immobilized HRP from 2.38% to 12.50%. Circular dichroism and UV–vis molecular absorption spectrometry were used to explore the interactions between HRP and MWCNTs . It seems that MWCNTs increase the enzyme activity by the facilitation of electron transfer among the catalytic intermediates “HRP I”, “HRP II” and MWCNTs.

研究领域: 生物化学 · 纳米生物技术 · 酶工程 · 生物材料 · 分析化学
✓ 已验证 DOI 高影响因子
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SENSORS AND ACTUATORS B-CHEMICAL · 2022 · IF 9.221

In2O3 sensing electrode prepared by salt melt method for impedancemetric-type NH3 sensor

Yueying Gao,Weiwei Meng,Ling Wang,Yuehua Li,Lei Dai

Salt melt synthesis is a kind of inorganic material synthesis method developed in modern times, which has certain potential advantages and development prospects. The sensing electrode (SE) material In 2 O 3 was synthesized by the salt melt method. The composition and morphology of the synthesized products under different conditions were studied in detail by combining XRD , SEM and TEM characterization. The results show that the salt melt method can facilely synthesize high-purity In 2 O 3 powder at a lower temperature, and its morphology changes regularly with the change of reaction conditions. The effects of synthesis times and temperatures on the gas-sensing performance of In 2 O 3 were discussed. The sensor based on In 2 O 3 (380 °C − 30 min)-SE exhibited superior gas-sensing performance in the range of NH 3 concentration of 50–500 ppm. The NH 3 response characteristics exhibited little effect at different relative humidity (RH) and oxygen partial pressure conditions. In addition, the sensor exhibited good repeatability and selectivity .

研究领域: 材料科学 · 传感器技术 · 无机合成 · 气体传感 · 功能材料
✓ 已验证 DOI 高影响因子
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RSC Advances · 2017 ·Vol. 7 ·期 64 ·40650-40657 · IF 3.108

One-step in situ synthesis of strontium ferrites and strontium ferrites/graphene composites as microwave absorbing materials

Wei Chen,Qingyun Liu,Xixi Zhu,Min Fu

Strontium ferrites/graphene (SrFe12O19/G) composites were synthesized by a facile one-step surfactant assisted hydrothermal method. The structure, magnetic properties and electromagnetic parameters of the as-prepared composites were evaluated. Uniform SrFe12O19 nanoparticles with a diameter of 60–70 nm were well distributed on the graphene. The formation of SrFe12O19 nanoparticles and the reduction of graphene oxide were accomplished simultaneously. The re-stacking of graphene sheets and the aggregation of SrFe12O19 nanoparticles were inhibited. The as-obtained composites exhibited better absorbing properties than the pristine SrFe12O19 particles due to the synergistic effect of SrFe12O19 and graphene. The minimum reflection loss (RL) of SrFe12O19/G composites with the thickness of 3 mm reached −34.8 dB at 13.6 GHz, and the effective absorption bandwidth (RL < −10 dB) was 5.7 GHz. However, the minimum RL of the SrFe12O19 particles only reached −13.5 dB, and the effective absorption bandwidth was 4.6 GHz. A possible mechanism for the enhanced absorbing performance was proposed.

研究领域: 材料科学 · 纳米材料 · 电磁学 · 功能材料 · 复合材料
✓ 已验证 DOI 高影响因子
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DALTON TRANSACTIONS · 2022 ·Vol. 52 ·期 2 ·376-383 · IF 4.569

H2/D2 separation in gas chromatography through a MOF-on-MOF strategy using γ-AlOOH@Al(OH)(1,4-NDC)@ZIF-67 as the stationary phase via additive effects of chemical affinity quantum sieving and kinetic sieving

Enming Ping,Lingyun Kong,Mengyao Liu,Yunshan Zhou,Lijuan Zhang,Nan Chen

The reaction of porous γ-Al2O3 particles acting as both a sacrificial template and an aluminum source with 1,4-naphthalene diacid (H2NDC) resulted in the formation of γ-AlOOH@Al(OH)(1,4-NDC) composites, in which ZIF-67 was then loaded by the in situ crystallization method, leading to the formation of γ-AlOOH@Al(OH)(1,4-NDC)@ZIF-67 composites. The deliberately designed composite was used to separate H2/D2 at 77 K in a 1 m chromatographic column. The results demonstrated that the optimized composite can achieve the effective separation of H2/D2 in gas chromatography due to the additive effects of kinetic sieving and chemical affinity quantum sieving of Al(OH)(1,4-NDC) and ZIF-67. By optimizing chromatographic separation conditions, the resolution R reached 2.02 with the separation time t = 7.72 min. The composite also showed satisfactory repeatability and reproducibility.

研究领域: 材料科学 · 分离科学 · 物理化学 · 纳米材料 · 能源化学
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