Surfaces and Interfaces
·
2025
·
IF 6.3
Chunlin Chen,Xiyi Ma,Guoqing Xiao,Mingtan Wang,Junjie Cao,Jing Gou,Hongxin Yan
Waterborne epoxy coatings are favored for their environmental friendliness and low volatile organic compounds (VOC) emissions. However, traditional waterborne epoxy coatings have limitations in terms of barrier properties and self-healing ability, resulting in poor long-term corrosion protection. To overcome this shortcoming, a novel green composite based on PDA@Ce-MOF@TA-Fe (PCTF) was developed in this study, aiming to construct a high-performance coating system with enhanced corrosion protection, pH responsiveness, and self-healing properties. The EIS measurements demonstrated a significant enhancement in the barrier property and self-healing capability of the waterborne epoxy coating incorporated with the PCTF composite (PCTF/WEC). After 40 days of immersion in corrosive conditions, the impedance of the PCTF/WEC coating remains at 9.82 × 10 8 Ω·cm 2 , which is much higher than that of the WEC coating alone (1.47 × 10 6 Ω·cm 2 ). PCTF/WEC coating also shows excellent pH response in acidic environments (pH = 3). Salt spray tests and UV irradiation tests confirm the coating's good weathering resistance. This study provides a promising strategy for the development of long-lasting and environmentally friendly anti-corrosion coatings.
✓ 已验证
产品关联
DOI
高影响因子
ACS Sustainable Chemistry & Engineering
·
2025
·
IF 7.3
Rongdi Wu,Jitong Han,Weichao Chen,Xin Yu,Ruixin Gao,Chunming Zhang
A biomimetic, fluorine-free, three-layer aqueous coating for cotton─composed of an Fe2+/Cu2+-catalyzed polydopamine (PDA) primer, a chitosan–SiO2 (CS) aerogel midlayer, and a thin polydimethylsiloxane (PDMS) overcoat─was developed to impart durable superhydrophobicity, rapid photothermal self-healing, antibacterial activity, and efficient oil–water separation. Treated cotton exhibited a static water contact angle (WCA) of 170° and retained a WCA of >155° after 2500 Martindale abrasion cycles or 30 ISO 105-C06 wash cycles; the WCA was restored to ≥160° after ambient storage or within 20 min under natural sunlight as surface temperatures approached ≈50 °C. PDA-mediated Cu2+ chelation (5 mM) produced >99% inhibition of Escherichia coli and Staphylococcus aureus; gravity-driven oil–water separation efficiencies exceeded 98% with >96% retention after 12 cycles. Preliminary scalability and environmental impact analyses, including material inventories and PDMS release estimates, support the potential for industrial translation. This fluorine-free, beetle-exoskeleton-inspired strategy offers a scalable route to multifunctional, sustainable textile finishing and environmental remediation.
✓ 已验证
产品关联
DOI
高影响因子
RSC Advances
·
2025
·Vol. 15
·期 44
·37273-37287
·
IF 4.6
Ya Gao,Haoping Huo,Jianlin Li,Nengqing Wang,Haonan Gao,Yingbo Wang
Eradicating cutaneous infections induced by pathogenic microorganisms, such as bacteria, fungi, and viruses, via conventional topical drug delivery is challenging owing to limited epidermal penetration. To overcome this limitation, we fabricated a poly(ethylene glycol) diacrylate (PEGDA) microneedle array coated with a carboxymethyl chitosan (CMC) film embedded within situ-synthesized polydopamine-modified silver nanoparticles (PDA@Ag NPs) for enhanced antibacterial efficacy. This design utilizes microneedle (MN)-mediated skin perforation to enhance drug permeation, combined with rapid film dissolution for the efficient release of the payload. The experimental findings revealed that the PDA@Ag-CMC/PEGDA MNs possess favorable biocompatibility along with dual photothermal and photodynamic functionalities. Mild photothermal therapy (PTT) triggered by these MNs promotes the production of antibacterial reactive oxygen species (ROS), resulting in a high antibacterial rate of up to 98% against both Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) under NIR irradiation at a PDA@Ag concentration of 40 μg mL−1. To assess transdermal delivery performance, lidocaine hydrochloride (LiH) (78 μg per MN array) was incorporated into the CMC film as a model drug. Physiological conditions confirmed accelerated LiH release from the PDA@Ag-LiH-CMC/PEGDA system upon aqueous exposure. This minimally invasive approach demonstrated promising broad-spectrum antibacterial activity, suggesting that the PDA@Ag-LiH-CMC/PEGDA platform could serve as a viable clinical solution for managing polymicrobial skin infections and alleviating wound pain.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
TALANTA
·
2023
·
IF 6.1
Qing Li,Yu-Meng Guo,Xiang-Yi He,Guang-Li Li
The reliable and accurate detection of glyphosate is urgently demanded because it is related to food and environmental safety. In this contribution, a PDA-PEI/Cu 2+ complex that possesses peroxidase-mimetic activity and stimulus-responsive fluorescence was fabricated by coordinating Cu 2+ with polydopamine-polyethyleneimine copolymer dots (PDA-PEI CPDs). With the introduction of Cu 2+ , the fluorescence intensity of PDA-PEI CPDs dropped sharply owing to the electron transfer effect. As a peroxidase-mimicking nanozyme , the PDA-PEI/Cu 2+ complex owns catalytic capacity to oxidize the colorless 3,3′,5,5′-tetramethylbenzidine (TMB) into blue oxTMB, leading a further fluorescence quenching by internal filtering effect by oxTMB. Once the glyphosate participated, the fluorescence signal of PDA-PEI CPDs is recovered significantly because of the formation of more stable Glyp-Cu 2+ complexes, meanwhile the peroxidase-mimicking activity of PDA-PEI/Cu 2+ complex could be strongly hindered. According to this principle, a novel and extremely convenient ‘turn off’ colorimetric and ‘turn on’ fluorescence sensing platform can be established for dual-mode detection of glyphosate. The favorable sensitivity and selectivity and were verified in the analysis of glyphosate in the environment through the marriage of dual-signal sensing platform. The detection limit of the dual-mode glyphosate sensing platform was 103.82 ng/mL for colorimetric assay and 16.87 ng/mL for fluorescent assay, respectively. Satisfactory recoveries in the range of 96.40%–104.66% were obtained, indicating the potential of this method for application in complicated real sample. Thereby, this strategy broadens the applications of polydopamine nanomaterials and holds a promising application in determination of pesticide residues .
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2022
·
IF 6.371
Na Zhang,Shuangshuang Peng,Zhiyu Liu,Ye Li,Ju Huang,Jing Li,Hongri Wan,Shuai Zhou,Zhaojian Gao,Teng Chen
In this paper, Ag NPs-decorated magnetic Fe 3 O 4 @PDA nanocomposites have been successfully prepared. The spherical Fe 3 O 4 nanoparticles with an average size approximately 340 nm were modified by dopamine under mild conditions. Dopamine was self-polymerized surrounding Fe 3 O 4 nanoparticles and transformed into poly dopamine (PDA) layers. The PDA-encapsulated magnetic (Fe 3 O 4 @PDA) nanoparticles could in-situ reduce silver ammonium ions by the catechol groups in PDA layers. The Ag NPs with an average size ranging from 20 nm to 36 nm were densely decorated on the thin PDA shell. The resultant Fe 3 O 4 @PDA-Ag nanocomposites were employed as highly efficient catalysts for the reduction of different organic pollutants in the appearance of sodium borohydride. The Fe 3 O 4 @PDA-Ag nanocomposites also demonstrated extraordinary cycling stability when the catalyst was recycled several times for the reduction of MB. The antimicrobial tests indicated Fe 3 O 4 @PDA-Ag nanocomposites could efficiently prohibit the growth of microorganism, including various bacteria and fungi. The minimal inhibitory concentrations (MIC) for Fe 3 O 4 @PDA-Ag nanocomposites against different bacteria and fungi were also determined. The excellent catalytic activity, magnetic recyclability, and antimicrobial performance make Fe 3 O 4 @PDA-Ag a feasible candidate for the remediation of wastewater which contains multiple water soluble organic pollutants and pathogenic microorganism.
✓ 已验证
产品关联
DOI
高影响因子
COMPOSITES SCIENCE AND TECHNOLOGY
·
2022
·
IF 9.879
Huasong Xu,Congzhen Xie,Bin Gou,Rui Wang,Jiangang Zhou,Licheng Li
Field-grading polymer nanocomposites have drawn significant attention in high voltage electrical industries due to their excellent nonlinear conductive or dielectric properties . But composites with both nonlinear properties are rarely reported, and desirable nonlinear performance associated with excess fillers in the composite is at the expense of electric breakdown strength . In this work, BaTiO 3 nanoparticles were decorated successively using double-shell layers of TiO 2 and polydopamine, which are developed as novel nanofillers (BT@TiO 2 @PDA) for field-grading applications. Subsequently, BNNSs were prepared by liquid phase exfoliation, serving as the inhibitor of breakdown phase growth in the composites. Finally, novel epoxy nanocomposites (EP/BT@TiO 2 @PDA-OB) with BT@TiO 2 @PDA and oriented BNNSs were fabricated by a simple hot-pressing method. Results show that the hierarchically designed nanoparticles can make the composites possess not only nonlinear dielectric properties due to high ε r of BT and improved interfacial polarization , but also nonlinear conductive properties resulted from the organic semiconductor PDA shell. Nonlinear effective medium theory (EMT) was utilized to explain the nonlinear dielectric properties, and the hopping transport model considering Pool-Frenkel effect was applied to explain the nonlinear conductive properties. In addition, electric breakdown tests reveal that EP/BT@TiO 2 @PDA-OB has significantly enhanced breakdown strength (45.7 kV/mm) as compared to that of pristine epoxy resin (29.4 kV/mm) and EP/BT@TiO 2 @PDA-RB (randomly dispersed BNNSs, 36.2 kV/mm). It is expected that these results can open new avenues for the design of novel composites with both nonlinear conductive properties and dielectric properties as well as high breakdown strength.
✓ 已验证
产品关联
DOI
高影响因子
Materials
·
2022
·Vol. 15
·期 6
·2039
·
IF 3.748
Yueqi Zhang,Bin Du,Yuting Wu,Zhiwei Liu,Jiang Wang,Jianjie Xu,Zhaoyang Tong,Xihui Mu,Bing Liu
Bacterial infection is a significant cause of morbidity and mortality to humans worldwide. Thus, a method for nonspecific, sensitive, and rapid enrichment of such bacteria is essential for bacteria detection and treatment. This study demonstrates a self-made core-shell Fe3O4@Polydopamine@Polyethyleneimine magnetic beads (Fe3O4@PDA@PEI MBs) with a high density positive charge-based magnetic separation scheme for the broad-spectrum rapid enrichment of microorganisms in the liquid phase. MBs with a high-density positive charge have a strong electrostatic attraction to most microorganisms in nature. Our scheme is as follows: (1) wrapping dopamine (DA) on the iron oxide through self-polymerization and wrapping PEI on the outermost shell layer in a mode of crosslinking with the PDA; (2) subsequently, the Fe3O4@PDA@PEI MBs were used to concentrate microorganisms from the sample solution; (3) performing magnetic separation and calculating the adsorption efficiency. The as-prepared Fe3O4@PDA@PEI MBs composite was carefully characterized by zeta potential analysis, Value stream-mapping (VSM), transmission electron microscopy (TEM), and Fourier transforms infrared spectrometry (FT-IR). In this study, both gram-positive and gram-negative bacteria could be captured in three minutes through electrostatic interaction. Furthermore, the adsorption efficiency on gram-negative (>98%) is higher than that on gram-positive (>95%), allowing for a simple, rapid assay to enrich organisms in resource-limited settings.Keywords:magnetic beads;bacterial enrichment;magnetic separation;electrostatic interaction
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ACS Applied Materials & Interfaces
·
2023
·
IF 9.5
Yang Wang,Zhen Chen,Yixin Wu,Yu Li,Ziyu Yue,Minghua Chen
Lithium-ion batteries (LIBs) have achieved a triumph in the market of portable electronic devices since their commercialization in the 1990s due to their high energy density. However, safety issue originating from the flammable, volatile, and toxic organic liquid electrolytes remains a long-standing problem to be solved. Alternatively, composite solid electrolytes (CSEs) have gradually become one of the most promising candidates due to their higher safety and stable electrochemical performance. However, the uniform dispersity of ceramic filler within the polymer matrix remains to be addressed. Generally, all-solid-state lithium metal batteries without any liquid components suffer from poor interfacial contact and low ionic conductivity, which seriously affect the electrochemical performance. Here we report a CSE consisting of lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), polydopamine (PDA) coated Li6.4La3Zr1.4Ta0.6O12 (LLZTO) (denoted as PDA@LLZTO) microfiller, polyacrylonitrile (PAN), and poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP). Introducing only 4 μL of liquid electrolyte at the electrode|electrolyte interface, the CSE-based cells exhibit high ionic conductivity (0.4 × 10–3 S cm–1 at 25 °C), superior cycle stability, and excellent thermal stability. Even under low temperatures, the impressive electrochemical performance (78.8% of capacity retention after 400 cycles at 1 C, 0 °C, and decent capacities delivered even at low temperature of −20 °C) highlights the potential of such quasi-solid-state lithium metal batteries as a viable solution for the next-generation high-performance lithium metal batteries.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ACS Applied Energy Materials
·
2021
·
IF 6.024
Rui Wang,Congzhen Xie,Shoukang Luo,Huasong Xu,Bin Gou,Jiangang Zhou,Hao Yang
Polymer-based dielectric materials with high energy storage performance have become an important part of electric power and electronic systems. But due to the low intrinsic dielectric constant of polymers, it is usually needed to mingle high dielectric constant nanofillers to improve their dielectric properties. However, the addition of nanoparticles often results in higher dielectric loss and lower breakdown strength. Herein, using a simple method of surface modification of BaTiO3, silica and polydopamine are coated on the surface of BaTiO3, significantly improving the dielectric properties of the polymer. Meanwhile, the composite with a sandwich structure is prepared by using BaTiO3@SiO2@PDA/PVDF as the central layer and pure PVDF as the two outer layers, achieving an ultrahigh breakdown strength (633 MV/m). The sandwich-structured composite with 1 wt % BaTiO3@SiO2@PDA has the highest discharge energy density (15.4 J/cm3). The simulation results reveal that the sandwich structure not only acts as an interface carrier barrier but also optimizes the electric field concentration inside the composite, which reduces the probability of electric breakdown. This work can broaden the way for dielectric films to be used in the field of high energy density, and the modification strategy can also provide ideas for other fields.
✓ 已验证
产品关联
DOI
高影响因子
EUROPEAN POLYMER JOURNAL
·
2020
·
IF 3.862
Qinting Chen,Bin Yang,Mengya Ding,Yang Pan,Jiasheng Qian,Zhengzhi Zheng,Bin Wu,Jibin Miao,Ru Xia,Youlei Tu,You Shi
In this work, SiO 2 @PDA nanoparticles obtained by in - situ coating polydopamine (PDA) on the surface of spherical SiO 2 nanoparticles were adopted to prepare the polyvinylidene fluoride (PVDF) composite films via thermally-induced phase separation (TIPS) method with diphenyl carbonate (DPC) as the diluent. PDA was proved to cover evenly on the surface of SiO 2 nanoparticles, which was favorable to the dispersion of hydrophilic nanoparticles in the matrix. Effect of the presence of SiO 2 @PDA nanoparticles on crystallization behavior, thermal stability, mechanical properties and hydrophilicity of the composite films was intensively investigated. Heterogeneous nucleating effect on the crystallization of PVDF coupled with elevated crystallinity was found upon the incorporation of SiO 2 @PDA without altering the crystal form of PVDF. The rigidity, tensile strength as well as thermal stability of the composite films containing SiO 2 @PDA were significantly improved in comparison to both neat film and those containing unmodified nanoparticles. In addition, the hydrophilicity of PVDF composite films’ surface was remarkably enhanced with an increasing SiO 2 @PDA content, which helped to reduce the protein adsorption of the composite films considerably. The present study would supply an insight into the fabrication of PVDF composite films with desirable performance and capabilities.
✓ 已验证
产品关联
DOI
高影响因子
PEST MANAGEMENT SCIENCE
·
2021
·Vol. 77
·期 11
·4960-4970
·
IF 4.845
Wenneng Wu,Minghui Wan,Qiang Fei,Yu Tian,Saijie Song,He Shen,Jian Shen
BACKGROUND Stimuli-responsive pesticide controlled release system provides a new strategy for the development of high-efficiency pesticides formulation. RESULTS In this article, we report a novel polydopamine surface modified MXene-Ti 3 C 2 T x nanocarrier for pesticide delivery and plant protection. Polydopamine modified Ti 3 C 2 T x (PDA@Ti 3 C 2 T x ) nanocarrier was prepared by biomimetic self-polymerization of dopamine on the surface of Ti 3 C 2 T x . A typical pesticide, emamectin benzoate (EB), was loaded on PDA@Ti 3 C 2 T x through physisorption process, with a high pesticide loading rate of 45.37%. PDA@Ti 3 C 2 T x exhibited excellent photothermal conversion effect ( η = 34.5%). Under the irradiation of near-infrared (NIR) laser, EB would sustained release from PDA@Ti 3 C 2 T x nanocarrier to surrounding medium. Compared with free EB, EB@PDA@Ti 3 C 2 T x exhibited prolonged persistence period, which can keep antipest activity at 14 days post spraying. In addition, PDA@Ti 3 C 2 T x nanocarrier and EB@PDA@Ti 3 C 2 T x nanoformulation are of good safety, showing no side effect to the seed germination and seedling growth. CONCLUSION This research developed a novel nanocarrier for water-insoluble pesticide delivery, realizing NIR-responsive controlled release and sustained antipest activity.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2019
·Vol. 30
·期 19
·18246-18258
·
IF 2.195
Yu Zongxue,Feng XiaoFang,Min Xia,Li XiuHui,Shao LiangYan,Zeng HaoJie
In the study, the reduced graphene oxide/graphitic Bi 12 O 17 Cl 2 –TiO 2 heterojunctions sheet membrane(RGO/PDA/Bi 12 O 17 Cl 2 –TiO 2 ) was fabricated by the dopamine modification and assembling the RGO/PDA/Bi 12 O 17 Cl 2 –TiO 2 composites on the surface of commercial CA(cellulose acetate) membrane to degrade methylene blue (MB) and p-chlorophenol (4-CP) to harmless products. These membrane materials were comprehensively characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and UV–vis diffuse reflectance spectra (DRS). The results showed that RGO/PDA/Bi 12 O 17 Cl 2 –TiO 2 nanofiber membrane exhibited extremely high degradation performance with a good distribution of RGO/PDA/Bi 12 O 17 Cl 2 –TiO 2 on the CA nanofiber membrane surface. Besides, the complete photodegradation of 100 mL MB (15 mg L −1 ) solution and 100 mL 4-CP (15 mg L −1 ) solution with artificial visible-light was achieved after 100 min and 160 min, respectively. The RGO/PDA/Bi 12 O 17 Cl 2 –TiO 2 -CA composite membrane revealed the ability of continuous and simultaneous flow-through separation of oil/water emulsion and degradation of soluble organic dye under visible-light irradiation in a short time. Moreover, the nanofiber membranes exhibited excellent stability and reusability for MB-containing oil–water mixed emulsion separation has great potential to be applied in industrial application.
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）