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RESEARCH ON CHEMICAL INTERMEDIATES · 2025 · IF 3.5

Robust TiO2/Hβ catalyst for selective synthesis of cyclohexanone oxime from the oxidation of N-cyclohexylcyclohexanimine with O2 under mild conditions

Yan Jiaqi,Chen Wenkai,Ni Wenjin,Li Lu,Fu Jinfeng,Yang Qian,Yang Zhiyong

N -cyclohexylcyclohexanimine (N-CCA), a by-product of cyclohexylamine (CHA) oxidation to cyclohexanone oxime (CHO), was used as the starting reactant for the efficient conversion to CHO under an oxygen atmosphere, utilizing the constructed surface hydroxyl-rich Ti-based catalysts. Of these, the 20% TiO 2 /Hβ catalyst exhibited unique catalytic activity and stability, achieving 45.9% N-CCA conversion and 82.1% CHO selectivity, with the content of high-boiling by-products not exceeding 1.0%. The superior catalytic performance, as evidenced by characterization results, stems primarily from: (i) the combination of TiO 2 and Hβ, which promotes the formation of a high specific surface area with fine TiO 2 nanoparticles and high-density Ti δ+ active sites, which facilitate the adsorption and activation of N-CCA; (ii) the construction of rich hydroxyl groups, which enhances the Brønsted acid sites, thereby improving the generation of active oxygen species; (iii) the intercrystalline embedding of TiO 2 and Hβ, which forms Ti–O–Si bonds, effectively inhibiting Ti leaching and ensuring excellent catalyst stability. The conversion of N-CCA, the main by-product of CHA oxidation, to the desired CHO using an efficient and robust 20% TiO 2 /Hβ catalyst represents an attractive pathway.

研究领域: 催化 · 材料科学 · 化学反应工程 · 表面化学
✓ 已验证 产品关联 DOI 高影响因子
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2013 · IF 3.172

N-hydroxymethyl acrylamide polymer brush and its application in catalyzing coupling reaction

Zhihua Fu,Na Zhang,Jie Liu,Tiesheng Li,Wenjian Xu,Fei Wang,Tao Wang,Zhen Zhai,Linlin Liu,Luyan Mao,Yangjie Wu

Poly (N-hydroxy methyl acrylamide)-grafted silicon, glass, and quartz surfaces were successfully prepared by surface-initiated atom transfer radical polymerization (SI-ATRP) with methyl alcohol/water mixtures as solvents and CuCl/2,2-dipyridyl as a catalyst. The modified surfaces were characterized by water contact angle, atomic force microscope (AFM), Fluorescence spectrophotometer, Low-angle X-ray diffraction (LAXRD), and X-ray Photoelectron Spectroscopy (XPS). The results showed that the homogeneous and well hydrophilic N-hydroxymethyl acrylamide polymer brushes (NHAM-brushes), which had high hydrophilic properties and the added advantage of providing 3-D coatings with higher binding capacities, were obtained successfully. Cyclopalladated arylimine functionalized polymer brushes were also obtained by reacting HAM-brushes with N,N′-Carbonyldiimidazole (CDI) and cyclopalladated arylimine. The catalyst functionalized PHAM-brushes had good catalytic activity in heterogeneous compared to homogeneous catalyst and exhibited much improved stability and recyclability over time in Suzuki cross-coupling reaction.

研究领域: 材料科学 · 化学工程 · 表面化学
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2025 · IF 3.9

Preparation of Robust Thermal Protection Silicone Rubber by Constructing Interconnected C–Si Hybrid IPNs

Yang Zhang,Shitian Han,Bojie Fu,Shuai Li,Ziwen Sun,Zhengguang Heng,Shuang Xia,Yang Chen,Liwei Yan,Mei Liang,Huawei Zou

Flexible thermal protection materials are an important component of thermal protection systems. In order to obtain flexible thermal protection materials with excellent mechanical strength, adhesive strength, and ablation resistance, a novel bifunctional biphenyl-type epoxy (MNE) monomer with two epoxy groups and vinyl groups was synthesized and utilized to construct interconnected C–Si hybrid interpenetrating networks in silicone rubber. Benefiting from the formation of C–Si hybrid IPNs and the incorporation of polar groups and biphenyl units, when the content of MNE was 20% (MNE-20), the tensile strength, elongation at break, and bonding strength of MNE-20 were 2.44 MPa, 179%, and 1.98 MPa, respectively, which were 510% improved, 56% improved, and 519% improved compared to those of the pure PDMS. Meanwhile, the mass ablation rate of MNE-20 decreased to 0.019 g/s, 53.66% improved compared to that of pure PDMS, because pyrolysis gases were released across a broad temperature range and the quality of the pyrolysis carbon layer was significantly improved. This work provided a new strategy to design high-performance ablation-resistant elastomers, and the prepared materials have broad applications in fields such as aerospace sealing materials and high-temperature protective coatings.

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Journal of Energy Chemistry · 2019 · IF 5.162

Thiourea-assisted coating of dispersed copper electrocatalysts on Si photocathodes for solar hydrogen production

Pin Wang,Ziyu Yin,Linfeng Gao,Hui Li,Tongyu Zhang,Qing Shen,Jun Lv,Yingfang Yao,Wenjun Luo,Zhigang Zou

Photoelectrochemical water splitting can convert solar energy into clean hydrogen energy for storage. It is desirable to explore non-precious electrocatalysts for practical applications of a photoelectrode in a large scale. Here, we developed a facile spin-coating and in-situ photoelectrochemical reduction method to prepare a dispersed Cu electrocatalyst on a Si photocathode, which improves the performance remarkably. We find that thiourea in the precursor solution for spin-coating plays an important role in obtaining dispersed Cu particles on the surface of a Si photoelectrode. With thiourea in the precursor, the Cu/Si photocathode shows higher performance than the one without thiourea. Moreover, the Cu/Si photocathode also indicates good stability after 16 h illumination.

研究领域: 材料科学 · 能源化学
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CELLULOSE · 2017 ·Vol. 24 ·期 10 ·4189-4203 · IF 3.417

Thermoresponsive poly(poly(ethylene glycol) methylacrylate)s grafted cellulose nanocrystals through SI-ATRP polymerization

Zhang Xiuqiang,Zhang Jinlong,Dong Lili,Ren Suxia,Wu Qinglin,Lei Tingzhou

We report a series of thermoresponsive cellulose nanocrystals (CNCs) decorated with poly(poly(ethylene glycol) methylacrylate) copolymers (poly(PEGMA)- g -CNCs) synthesized by surface initiated-atom transfer radical polymerization (SI-ATRP). The chemical structures and surface morphologies were subsequently confirmed by FT-IR, XPS, and AFM measurements. With regard to thermally responsive behavior, poly(PEGMA)- g -CNCs show tunable lower critical solution temperature (LCST) values in the range of 34–66 °C by varying the feeding ratios of comonomers. The reversible morphological transformation from individual nano-rod structures to larger globule aggregates was further verified by AFM during the LCST transition. These functionalized CNCs have potential as smart film filters and biosensors.

研究领域: 材料科学 · 高分子化学
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Journal of Materials Chemistry A · 2022 ·Vol. 10 ·期 23 ·12632-12642 · IF 14.511

Phase-pure antiferroelectric AgNbO3 films on Si substrates: chemical solution deposition and phase transitions

Liang Shu,Xin Zhang,Wei Li,Jing Gao,Hongliang Wang,Yu Huang,Yue-Yu-Shan Cheng,Qian Li,Lisha Liu,Jing-Feng Li

AgNbO3-based antiferroelectric films have attracted emerging attention in the field of dielectric energy storage and possess promising applications in photocatalysis and microwave devices. Unfortunately, it remains a challenge to fabricate pure-phase AgNbO3 films on Si substrates, precluding their further integration into electronic devices. Here, we, for the first time, report phase-pure AgNbO3 films on Pt/Ti/SiO2/Si substrates by a chemical solution deposition (CSD) method. A facile CSD route without using the hazardous pyridine additive is demonstrated to obtain a stable AgNbO3 precursor for spin-coating films. By comprehensively controlling the heat treatment conditions, secondary phases are eliminated in the deposited films. The phase transitions of the AgNbO3 films are also investigated, where intriguingly the room temperature phase is determined to be the antiferroelectric M2 phase, rather than the commonly reported M1 phase in bulk AgNbO3. Meanwhile, the relative dielectric permittivity surpasses 300 at room temperature and maintains at ∼400 with low dielectric loss (<0.05; measured at frequencies of 0.1–1 MHz) over a wide temperature range of 150–350 °C, within a 5% variation. This work provides an easy-to-implement process of AgNbO3 films which may attract scientific interests and potential applications.

研究领域: 材料科学 · 电子工程 · 能源存储
✓ 已验证 DOI 高影响因子
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ACS Applied Materials & Interfaces · 2018 · IF 8.097

Conductive Binder for Si Anode with Boosted Charge Transfer Capability via n-Type Doping

Yan Zhao,Luyi Yang,Yunxing Zuo,Zhibo Song,Fang Liu,Ke Li,Feng Pan

Employing conductive binders in silicon (Si) anode has been considered as a fundamental solution to the pulverization of Si particles. Therefore, it is still a great challenge to improve the charge transfer capability of the conductive binder. Herein, a copolymer (PFPQ-COONa) is synthesized, characterized, and electrochemically tested as conductive binder for Si anode. It is found that PFPQ-COONa exhibits not only excellent cycling stability, but also satisfactory rate performance with relatively high areal loading, which outperforms currently reported single-component conductive binders. The superior electrochemical performance can be attributed to the molecular-level contact between binder and Si particles and to the enhanced intrinsic conductivity of PFPQ-COONa at reductive potential. This method provides a fresh perspective to design and develop conductive binder for high-capacity battery anode.

研究领域: 材料科学 · 电化学 · 电池技术
✓ 已验证 DOI PubMed 高影响因子
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Scientific Reports · 2020 ·Vol. 10 ·期 1 ·1-12 · IF 3.998

Cardanol derived P, Si and N based precursors to develop flame retardant phenolic foam

Bo Caiying,Shi Zhongyu,Hu Lihong,Pan Zheng,Hu Yun,Yang Xiaohui,Jia Puyou,Ren Xiaoli,Zhang Meng,Zhou Yonghong

A novel eco-friendly halogen-free cardanol-based flame retardant with P, Si, and N on the chain backbone (PSNCFR) was synthesized and incorporated into phenolic foams (PFs). PSNCFR was comprehensively investigated via Fourier transform infrared spectroscopy and nuclear magnetic resonance. PSNCFR endowed PFs with flame retardancy, contributed to generating a composite char defense against flames, and efficiently prevented smoking from PFs. PSNCFR introduction improved the flexural strength of the PFs to approximately 155% of that of pristine PF. PSNCFR-modified PFs displayed a high limiting oxygen index value of 41.9%. The results of cone calorimeter show that the mean heat release rate, mean effective heat of combustion, and total heat release of the PSNCFR-modified PFs reduced by 26.92%, 35.71%, and 31.25%, respectively. In particular, the total smoke production of the PSNCFR-modified PFs decreased by 64.55%, indicating excellent smoke inhibition. As for the mechanism, the condensation and gas phases during pyrolysis were responsible for the synergistic flame retardancy in the modified PFs. The findings demonstrate that PSNCFR can be used in PF preparation to overcome their drawbacks of internal brittleness and flammability.

研究领域: 材料科学 · 化学工程
✓ 已验证 DOI 高影响因子
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IONICS · 2019 ·Vol. 26 ·期 1 ·1-11 · IF 2.289

High-capacity flour-based nano-Si/C composite anode materials for lithium-ion batteries

Xu Ruhui,Zhang Keyu,Wei Runhong,Yuan Meimei,Zhang Yenan,Liang Feng,Yao Yaochun

A facile, low cost, and low equipment-requirement preparation route of Si/C composite was developed. Naturally porous flour was carbonized through a conformal carbonization process and a further activation process in vacuum, obtaining flour-derived porous carbon (FPC) with ample pores. FPC was used to load nano-silicon through electrostatic adsorption method. Si-FPC was coated by sucrose-derived carbon (SC) shell by aqueous evaporation method to obtain Si-FPC-SC. Benefitting from FPC’s good dispersion for silicon, 40%-Si-FPC delivers a reversible capacity of 1562 mAh g −1 , equivalent to 83% of pure nano-silicon’s reversible capacity, an outstanding rate performance of 761 mAh g −1 at 1 A g −1 current density. The final 30%-Si-FPC-SC exhibits a reversible capacity of 937 mAh g −1 at 0.1 A g −1 , a cyclic retention of 82.3% after 100 cycles. Furthermore, the synthetic method of Si/C composites offers a universal idea for the research of high-capacity anode materials for lithium-ion batteries.

研究领域: 材料科学 · 能源存储
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JOURNAL OF SOLID STATE ELECTROCHEMISTRY · 2019 ·Vol. 23 ·期 11 ·3145-3151 · IF 2.531

Li metal-free rechargeable all-solid-state Li2S/Si battery based on Li7P3S11 electrolyte

Xu Xiaoyan,Cheng Jun,Li Yuanyuan,Nie Xiangkun,Dai Linna,Ci Lijie

As high energy density and enhanced safety are required for the lithium-ion battery development, all-solid-state battery has attracted significant attention. Herein, we report an all-solid-state full battery consisting of a Li 7 P 3 S 11 solid electrolyte coated silicon anode, Li 2 S/graphene composite cathode, and Li 7 P 3 S 11 solid-state electrolyte. With a high capacity for the silicon anode and Li 2 S cathode, this battery yields a high theoretical specific energy density up to 1495 Wh kg −1 , which is higher than that of lithium-ion batteries based on oxide cathodes. Moreover, Li 2 S cathode is used as lithium source instead of using metallic lithium, avoiding interface reaction between lithium metal anode and sulfide electrolyte Li 7 P 3 S 11 . This all-solid-state battery system we proposed could avoid the safety issues associated with the use of lithium metal and be a promising candidate for an enhanced energy density, which would promote their applications in the fields of electric vehicles and portable electronics.

研究领域: 材料科学 · 储能 · 电化学 · 电池技术
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OZONE-SCIENCE & ENGINEERING · 2015 · IF 0.953

Effectiveness and Mechanisms of Fenton-like Si-FeOOH/H2O2 in 2,4-Dichlorophenol Wastewater Treatment

Shengtao Jiang,Jianzhong Zhu,Ying Ding,Shuli Bai,Yujiang Guan,Qingmei Ye

This research measured the effectiveness of Si-FeOOH as a type of heterogeneous Fenton-like catalyst made from alkaline precipitation methods, in catalyzing the degradation of 2,4-dichlorophenol (2,4-DCP) wastewater. Factors including catalyst dosage, pH, and hydrogen peroxide dosage were investigated, showing: with an initial concentration of 2,4-dichlorophenol at 100 mg/L, a dosage of catalyst at 0.1 g/L, a dosage of H2O2 at 1.5 ml/L, pH at 5 and indoors temperature at 25 ± 1 °C, the degradation rate of 2,4-dichlorophenol, CODCr and TOC has reached 94.21%, 83.67%, and 76.11%, separately. Comparisons were made with FeOOH used as catalyst, showing that Fenton-like Si-FeOOH is a better catalyst than FeOOH.

研究领域: 环境科学 · 化学工程 · 水处理技术 · 高级氧化工艺
✓ 已验证 DOI 高影响因子
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Materials · 2021 ·Vol. 14 ·期 11 ·2836 · IF 3.623

3D Yolk–Shell Structured Si/void/rGO Free-Standing Electrode for Lithium-Ion Battery

Jin Shao,Yi Yang,Xiaoyan Zhang,Liming Shen,Ningzhong Bao

In this study, we have successfully prepared a free-standing Si/void/rGO yolk–shell structured electrode via the electrostatic self-assembly using protonated chitosan. When graphene oxide (GO) is dispersed in water, its carboxyl and hydroxyl groups on the surface are ionized, resulting in the high electronegativity of GO. Meanwhile, chitosan monomer contains -NH2and -OH groups, forming highly electropositive protonated chitosan in acidic medium. During the electrostatic interaction between GO and chitosan, which results in a rapid coagulation phenomenon, Si/SiO2nanoparticles dispersed in GO can be uniformly encapsulated between GO sheets. The free-standing Si/void/rGO film can be obtained by freeze-drying, high-pressure compression, thermal reduction and HF etching technology. Our investigation shows that after 200 charge/discharge cycles at the current density of 200 mA·g−1, the specific discharge capacity of the free-standing electrode remains at 1129.2 mAh·g−1. When the current density is increased to 4000 mA·g−1, the electrode still has a specific capacity of 469.2 mAh·g−1, showing good rate performance. This free-standing electrode with a yolk–shell structure shows potential applications in the field of flexible lithium-ion batteries.

研究领域: 材料科学 · 电化学 · 能源存储 · 纳米材料 · 柔性电子器件
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