JOURNAL OF MATERIALS SCIENCE
·
2025
·
IF 3.9
Wang Yanting,Song Shiyu,Liao Xilin,Zhou Pei wen,Li Runchuan,Xing Mengxing,Lin Jia-Horng,Li Liang,Liu Rangtong
The rapid development of science and technology has led to the aggravation and complexity of electromagnetic radiation pollution. Therefore, multifunctional electromagnetic interference shielding materials have become increasingly indispensable. Based on the advantages of textile materials, the modular coupling assembly strategy was utilized to achieve the structural regulation of the multifunctional PP conductive composite film and effectively endowed it with excellent EMI shielding performance. In this study, the adhesive property of polydopamine was utilized to enhance the chemical reactivity of PP films. The construction of porous conductive structures and core–shell conductive structures of PPy inside and outside PP fibers was achieved by controlling the polymerization rate of pyrrole in a low-temperature environment. The macroscopic encapsulation of the hydrophobic layer enhanced the bonding strength between the PP substrate and the conductive layer. The results show that different concentrations of pyrrole affected the microstructure and EMI shielding performance. When the concentration of pyrrole was 0.8 mol/L, the surface contact angle and surface resistance of the PP composite film were 138.42° and 73 Ω, respectively. In addition, the shielding value of the PP composite film was as high as 28.02 dB, which could effectively shield 99.84% of electromagnetic waves. This preparation strategy of coupling multiple functional layers to realize multifunctional composite films provides research ideas for the structural design of multi-purpose smart wearable electromagnetic protection composite materials.
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DOI
高影响因子
Nature Communications
·
2025
·
IF 15.7
Yang Sinian,Zhao Shunshun,Xu Haojie,Wang Xinwei,Huang Xuanrui,Yang Qi,Chen Yong,Wang Guoxiu,Chen Shimou
Aqueous zinc-ion batteries have emerged as a promising system for safe and sustainable energy storage. However, their practical application is hindered by detrimental interfacial side reactions and inadequate low-temperature performance. Herein, we report the design of a gradient chaotropic ionic liquid (IL)-based aqueous electrolyte (Emim⁺-TFA⁻/OTf⁻-Zn 2+ -H 2 O), which can simultaneously fulfil the conflicting demands of dendrite-free zinc deposition and low-temperature operation. By forming an antifreeze electrolyte with a hydrophobic yet salt-philic interface, the proposed formulation overcomes the limitations of conventional IL-based systems that rely on H 2 O-lean compositions, complex additives, or elaborate solvent mixtures. Thus, the assembled zinc-ion cells exhibit improved zinc plating/stripping stability. At a current density of 0.1 mA cm −2 and 0.1 mAh cm −2 , the Zn | |Zn symmetric cells endure prolonged zinc plating/stripping, exceeding 13,000 h at −30 °C and 6690 h at −40 °C. In full cells, Zn | |VO 2 @VO maintains nearly 100% capacity retention over 3500 cycles at 0.2 A g −1 and −40 °C. This gradient chaotropic Zn 2+ electrolyte design provides a versatile platform for effective antifreeze Zn 2+ solvation chemistry and accelerated interfacial ion transport, enabling high-performance zinc batteries in subzero environments.
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DOI
PubMed
高影响因子
JOURNAL OF NANOBIOTECHNOLOGY
·
2025
·
IF 12.6
Huang Xiaobin,Yi Yakun,Zhou Ke,Liu Lei,Wu Hai-Chen
MicroRNAs (miRNAs) play crucial roles in the pathogenesis of diverse diseases; however, their extremely low abundance in complex biological systems makes highly sensitive and specific multiplexed detection particularly challenging. Here, we report an enzyme-assisted nanopore sensor that enables simultaneous and ultrasensitive detection of multiple miRNAs. Capture DNA (cDNA) immobilized on streptavidin-coated magnetic beads specifically hybridizes with target miRNAs, opening the cDNA hairpin and facilitating the binding of alkaline phosphatase (ALP)-labeled detection DNA to form stable complexes. ALP catalyzes the dephosphorylation of designed phosphorylated peptide probes, inducing conformational and charge changes that yield distinct current blockade signatures in the presence of cucurbit [ 7 ]uril within the nanopore. This strategy reduces background interference via magnetic separation and amplifies detection signals through enzymatic reactions, thereby markedly improving sensitivity for low-abundance miRNAs. The sensor achieves a broad dynamic range from 10.0 fM to 10.0 nM across three target miRNAs, with femtomolar-level limits of detection. By integrating molecular separation, enzymatic amplification, and nanopore sensing, this platform provides a robust approach for precise miRNA analysis, offering strong potential for early disease diagnosis.
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DOI
PubMed
高影响因子
JOURNAL OF ELECTRONIC MATERIALS
·
2025
·Vol. 54
·期 7
·5189-5195
·
IF 2.5
Wang Cong,Li Yue,Li Yahao,Zheng Xiaoxi,Yang Xuelin
Lithium metal is recognized as a promising alternative anode material for next-generation Li batteries. However, the growth of lithium dendrites due to uneven deposition of lithium and the side reactions caused by unstable solid–electrolyte interphase (SEI) films have seriously hindered the development of lithium metal batteries. Therefore, we cast a bifunctional dual-layer protective film of graphene oxide (GO) and SnF 2 onto a Li plate to address the above problems. As a result of the synergistic effect between the SnF 2 -derived LiSn alloy and GO layer, the symmetric cell with modified Li electrodes exhibited extraordinary cyclic stability close to 2900 h when cycled at 0.5 mA cm −2 and 0.5 m Ah cm −2 . Ultralow interfacial impedance of only 3.6 Ω was also obtained at the 50th cycle. This work presents a simple but effective modification strategy to improve the stability of lithium metal battery anodes.
研究领域:
材料科学
·
电化学
·
能源存储
·
纳米材料
·
电池技术
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产品关联
DOI
高影响因子
Science China-Materials
·
2025
·
IF 7.4
Peng Chunli,Tang Baoling,Zhang Xuejie,Molokeev Maxim S.,Zhang Haoran,Lei Bingfu
Near-infrared (NIR) spectroscopy has significantly advanced NIR light sources. However, creating NIR emitters with optimal luminescence properties, high thermal stability, and adjustable emission peaks poses a critical challenge for future smart NIR devices. We introduced a chemical unit cosubstitution strategy by incorporating Ca 2+ and Sn 4+ ions into the garnet structure. Through this approach, Y 3− y Ca y Ga 4.95− y Sn y G 12 :0.05Cr 3+ ( y = 0–1) phosphors were developed by modulating the A&C ligands, resulting in emission centers ranging from 708 to 768 nm. The modified local environment of Cr 3+ accounts for the increased light intensity (2.71 times) and broadening observed. Furthermore, this study investigated the impact of varying Cr 3+ concentrations (Y 2.6 Ca 0.4 Ga 4.6− x Sn 0.4 G 12 : x Cr 3+ ) on the production of high-performance phosphors. Compared with Y 3 Ga 4.93 G 12 :0.07Cr 3+ , the optimized phosphor exhibited exceptional external quantum efficiency (EQE = 34.96%). The luminescence enhancement is attributed to an increase in radiative transitions caused by octahedral Jahn-Teller distortion, whereas the notable thermal stability (91.3% at 423 K) is attributed to the presence of weak electron-phonon coupling (EPC) and oxygen vacancy (O V ) defects. Finally, by combining it with a 450 nm blue LED chip, we constructed a near-infrared phosphor-converted LED (NIR pc-LED) device with superior electroluminescence efficiency (18.8% @ 100 mA), increasing the ultralow quenching rate (< 5% intensity loss after 30 days of operation) and demonstrating remarkable performance in plant lighting applications.
研究领域:
材料科学
·
光学材料
·
固态照明
·
光子学
·
植物生物技术
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DOI
高影响因子
CHINESE JOURNAL OF POLYMER SCIENCE
·
2019
·Vol. 38
·期 4
·342-348
·
IF 2.804
Yang Ying,Shan Tong,Cao Jian,Wang Hua-Chun,Wang Ji-Kang,Zhong Hong-Liang,Xu Yun-Xiang
Two conjugated polymers (PuIDTBD and PuIDTQ) with unsymmetric side chains have been prepared for polymer solar cells using two other polymers (PIDTBD and PIDTQ) with symmetric side chains as control compounds. The combination of methyl and 4-hexylphenyl side chains on the same bridged carbon can ensure good solubility, decrease π - π stacking distances, and bring proper miscibility with PC 71 BM simultaneously. Therefore, the corresponding polymer solar cells (PSCs) based on donor polymers with unsymmetric side chains exhibited enhanced short-circuit current density ( J SC ) and power conversion efficiency (PCE) compared with those of control polymers. The PIDTBD and PIDTQ based devices possessed low PCE of 2.13% and 1.48%, while PCEs of devices based on PuIDTBD and PuIDTQ were improved to 3.93% and 4.12%, respectively. The results demonstrate that unsymmetric side chain engineering of conjugated polymers is an effective approach to achieve high performance PSCs.
研究领域:
材料科学
·
能源科学
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DOI
高影响因子
Food Analytical Methods
·
2019
·Vol. 12
·期 12
·2777-2784
·
IF 2.413
Li Hong,Zhao Chunxi,Tian Hao,Yang Yaling,Li Wanyi
An uncomplicated, valid, and convenient way for detection of lycopene and β-carotene in fruit juice samples using acid–base-induced deep eutectic solvent (DES) liquid-liquid microextraction (DES-ABLLME) prior to HPLC was developed. The ternary fatty acid DESs were prepared by C 9 :C 10 :C 11 (2:1:1), which serve as hydrogen bond donors and hydrogen bond acceptors synchronously. In extraction procedure, NH 3 ·H 2 O was used as the emulsifier and reacted with DESs with a milk solution, which can significantly increase the extraction efficiency. HCl was used as the de-emulsifier, which could break the state of emulsification. At optimum conditions, the calibration graphs were linear in the concentration range from 0.1 to 100 μg mL −1 for lycopene and from 0.025 to 5.00 μg mL −1 for β-carotene. The limits of detection (LODs) were 0.05 and 0.002 μg mL −1 for lycopene and β-carotene, respectively. The RSD values were varied from 1.3 to 4.1%. Finally, the proposed method was applied to analyze β-carotene and lycopene in fruit juices.
研究领域:
食品科学
·
分析化学
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DOI
高影响因子
Scientific Reports
·
2020
·Vol. 10
·期 1
·1-12
·
IF 3.998
Wu Yifan,Li Lingtong,Chen Shaopeng,Qin Jun,Chen Xiaolang,Zhou Dengfeng,Wu Hong
Poly( D -lactic acid) (PDLA) with different polyethylene glycol (PEG) segment synthesized PDLA-PEG-PDLA triblock copolymer through the ring-opening reaction of D -LA and PEG will be used as a toughening modifier. The microstructure, crystal structures and crystallization behaviors of this triblock copolymer were investigated by Fourier transform infrared (FTIR) spectroscopy, nuclear magnetic resonance (NMR) spectroscopy, X-ray diffraction (XRD), differential scanning calorimetry (DSC) and polarized optical microscopy (POM). The triblock copolymer is synthesized from the appearance of CH 2 stretching vibration peak at 2910 cm −1 and C-O stretching vibration peak at 1200 cm −1 from PEG in FTIR spectra. Moreover, the chemical shift that is about 3.6 ppm in 1 H NMR and 68.8ppm in 13 C NMR proves this matter. The results of XRD and DSC reveal that PDLA and PEG are crystallized separately, and are not fully compatible, and microphase separation has occurred in this triblock copolymer. PEG can induce the triblock copolymer to accelerate the rate of crystallization, allowing it to crystallize more completely in the same amount of time. When the molecular weight of PEG is 6000 or the ratio of D -LA/PEG is 1/1, the crystallizability of PDLA-PEG-PDLA triblock copolymer is the best.
研究领域:
材料科学
·
高分子化学
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DOI
PubMed
高影响因子
CELLULOSE
·
2022
·Vol. 29
·期 17
·9089-9104
·
IF 6.123
Zhao Yang,Jin Bo,Zheng Tian,Peng Rufang
A novel natural macromolecule stabilizer, tea polyphenol, was developed based on the scavenging effect of nitroxide radical to enhance the thermal stability of nitrocellulose. The structural of tea polyphenols was confirmed by infrared spectroscopy, and their good thermal stability of tea polyphenols in nitrocellulose was confirmed by methyl violet paper test and vacuum stability test. The iso-thermogravimetric test showed that tea polyphenols could prolong the safe storage life of nitrocellulose. The inhibition of tea polyphenols on the autocatalytic thermal decomposition of nitrocellulose in the early stage of nitrocellulose thermal decomposition was confirmed by SEM images at different stages of nitrocellulose thermal decomposition. The thermal interaction between tea polyphenols and nitrocellulose was further analyzed by non-isothermal thermal analysis. Experiments confirmed that tea polyphenols can enhance the thermal stability of nitrocellulose. Their addition increased the T 0 of nitrocellulose by 2.0–9.4 ℃, the T bp 0 by 1.4–9.6 ℃, and the activation energy of nitrocellulose by 5.38–9.77 kJ·mol –1 .
研究领域:
材料科学
·
化学工程
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DOI
高影响因子
MICROCHIMICA ACTA
·
2019
·Vol. 186
·期 6
·1-7
·
IF 5.479
Zhang Limei,Qin Ju,Yang Qiang,Wei Siqi,Yang Rui
Carbon dots (CDs) were hydrothermally prepared from gelatin as the sole precursor. The CDs were hybridized with CoOOH nanosheets (NSs) to obtain a fluorescent probe (CD-CoOOH) for ascorbic acid (AA). The blue luminescence of the CDs, with excitation/emission maxima of 350/443 nm, is quenched by the NSs. If the NSs are reduced to Co 2+ by addition of AA, the CD-CoOOH hybrid is disintegrated and fluorescence recovers. The hybrid nanoprobe has a linear response in the 0.8–12.5 μM and 12.5–690 μM AA concentration ranges and a 0.025 μM limit of detection. Compared to previously reported methods for detecting AA, this methods has a wider linear range and a lower detection limit. The nanoprobe was utilized to quantify AA in spiked human serum samples and gave satisfactory results. The strategy was also applied to the construction of an “AND” logic gate, which avoided perplexed material decorations and chemical tracking.
Scheme 1. Schematic illustrations of the preparation of CDs and of the working principle for determination of ascorbic acid (AA).
研究领域:
分析化学
·
生物医学工程
·
材料科学
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PubMed
高影响因子
Cell Death Discovery
·
2023
·Vol. 9
·期 1
·1-11
·
IF 7
Zhang Libo,Ren Zhen,Lü Jinhui,Mo Xinhai,Lin Jie,Li Ya,Ma Wenjing,Liu Pengfei,Shen Yajing,Zhao Qian,Qian Lu,Cheng Xiaoxin,Yu Zuoren,Zhang Bo
Nanomaterials have been well demonstrated to have the potential to be used for tumor cell-targeted drug delivery. Targeted inhibition of miR-221 was proved to promote the sensitivity of triple genitive breast cancer (TNBC) cells to chemo-drugs. In order to improve the chemotherapeutic effect in TNBC, herein, we developed a novel kind of nanoparticles shelled with PLGA and loaded with perfluoropentane (PFP), paclitaxel (PTX), and anti-miR-221 inhibitor, which was named PANP. Ultrasound-triggered vaporization of PFP in PANPs was utilized for real-time imaging track of the nanoparticles in vivo. In addition, macrophages were applied for the internalization of PANPs to form RAW-PANP with strong chemotaxis to accumulate around cancer cells. Nanoparticles with different contents did not cause M2 polarization compared with the control group but caused polarization toward M1. We compared the inherent tumor-homing behavior of macrophages containing different contents with that of normal macrophages and no significant abnormalities were observed. After injection into the tumor-burden mice, RAW-PANPs showed enrichment within tumor tissues. Upon the ultrasound cavitation-triggered burst, PTX was released in the tumor. Meanwhile, the release of anti-miR-221 improved the sensitivity of tumor cells to PTX. As a result, RAW-PANPs showed high efficiency in suppressing TNBC cell proliferation in vitro and inhibiting tumor growth and progression in vivo. The treatments did not induce liver, heart, or kidney injury. In conclusion, the current study not only developed a macrophage-carried, ultrasound-triggered, cancer cell-targeted chemotherapeutic system, but also demonstrated a miRNA-based technique to promote drug sensitivity of cancer cells, which holds strong potential to treat patients with TNBC, especially for those suffering drug-resistance. The innovation of this study is to use macrophages to deliver nanoparticles to the tumors and then use ultrasound locally to burst the nanoparticles to release the miRNA and PTX.
研究领域:
癌症生物学
·
药学
·
生物医学工程
·
纳米技术
·
治疗诊断学
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DOI
PubMed
高影响因子
JOURNAL OF NANOPARTICLE RESEARCH
·
2015
·Vol. 17
·期 3
·1-17
·
IF 2.184
Hou Lin,Feng Qianhua,Wang Yating,Zhang Huijuan,Jiang Guixiang,Yang Xiaomin,Ren Junxiao,Zhu Xiali,Shi Yuyang,Zhang Zhenzhong
Graphene oxide (GO) with strong optical absorption in the near-infrared (NIR) region has shown great potential both in photothermal therapy and drug delivery. In this work, hyaluronic acid (HA)-functionalized GO (HA-GO) was successfully synthesized and controlled loading of mitoxantrone (MIT) onto HA-GO via π – π stacking interaction was investigated. The results revealed that drug-loaded nanosheets with high loading efficiency of 45 wt% exhibited pH-sensitive responses to tumor environment. Owing to the receptor-mediated endocytosis, cellular uptake analysis of HA-GO showed enhanced internalization. In vivo optical imaging test demonstrated that HA-GO nanosheets could enhance the targeting ability and residence time in tumor site. Moreover, the anti-tumor activity of free MIT, MIT/GO, and MIT/HA-GO in combination with NIR laser was investigated using human MCF-7 cells. In vitro cytotoxicity study revealed that HA-GO could stand as a biocompatible nanocarrier and MIT/HA-GO demonstrated remarkably higher toxicity than free MIT and MIT/GO, with IC 50 of 0.79 µg ml −1 . Tumor cell-killing potency was enhanced when MIT/HA-GO were combined with NIR irradiation, and the IC 50 of MIT/HA-GO plus laser irradiation was 0.38 µg ml −1 . In vivo, MIT/HA-GO plus NIR laser irradiation with the tumor growth inhibition of 93.52 % displayed greater anti-tumor effect compared with free MIT and MIT/GO with or without laser irradiation. Therefore, the MIT/HA-GO nanosheets may potentially be useful for further development of synergistic cancer therapy.
研究领域:
生物医学工程
·
纳米医学
·
肿瘤学
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DOI
高影响因子
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