COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2025
·
IF 5.4
Yunle Yao,Rui Pan,Hua Cheng,Yi Gong,Lin Chen,Xian Zhang,Meng Xue,Xingyou Tian
Encapsulation is a crucial technology for isolating and protecting moisture-sensitive materials. However, traditional organic-inorganic composite films often exhibit poor adhesion at the interface and high gas permeability, making stable operation difficult. In this work, an enhanced atomic layer deposition (EALD) method was used to uniformly deposit a layer of thickness-controlled alumina on a Polyethylene Naphthalate (PEN) film with oxygen-containing polar groups(CTPEN) on its surface, successfully producing a high-barrier composite film (EALD-Al 2 O 3 /CTPEN) with Al-O-C chemical bonds. The designed CTPEN film significantly enhanced the adhesion of alumina, thereby improving the performance of the composite film. Moreover, the mechanical properties of the composite film were significantly enhanced, with the elongation at break of EALD-Al 2 O 3 /CTPEN at 72 % being considerably higher than that of ALD-Al 2 O 3 /PEN at 44 %, and the tensile strength reaching 220 MPa. At the same time, EALD-Al 2 O 3 /CTPEN maintained excellent light transmission, exceeding 85 %. Humidity -sensitive resistors encapsulated with EALD-Al 2 O 3 /CTPEN exhibited stable operating performance in both air and humidity-sensitive environments, confirming the superior barrier properties of the composite film. This EALD-Al 2 O 3 /CTPEN composite layer holds promise as a prospective encapsulation layer for future flexible devices.
研究领域:
材料科学
·
高分子物理
·
表面工程
·
柔性电子
·
薄膜技术
✓ 已验证
产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2023
·
IF 15.1
Jili Yuan,Hao Yin,Xin Ge,Ronglan Pan,Caijuan Huang,Dechao Chen,Lin Hu,Haibo Xie
The coordination environment of transition metals in single-atom catalysts (SACs) is crucial for tuning the pathway of the electrocatalytic oxygen reduction reaction (ORR). However, it is significantly difficult to simultaneously and precisely control the first and second coordination structure near the metal active center. Herein, we report that the activated carbon black was used to anchor transition metals’ single atoms with a similar first and second coordination structure. As a result, Co-SACs exhibit an extraordinary performance for ORR to produce H 2 O 2 , where a current density of around ∼2.8 mA cm −2 at 0.1 V vs RHE by rotating ring-disk electrodes and a high yield rate of 110.2 mmol g metal −1 h −1 at the potential of 0.3 V vs RHE in a gas diffusion electrodes (GDEs) cell, with a high positive onset potential of 0.65 V vs RHE and a >80% selectivity of H 2 O 2 at the potential range from 0.25 to 0.65 V vs RHE, respectively. The combined experimental observations and theoretical calculations indicate that the catalytic active center lies in the Co-C 3 /O 1 moiety of the adjacent epoxy group. The possible position of the epoxy group in the second coordination sphere was further revealed. Moreover, Co-SACs were employed in an electrocatalytic GDEs cell for distributed generation of H 2 O 2 in the acidic media, and coupling Fe-SACs-based Fenton filter or electro-Fenton setup with the H 2 O 2 electrolytic generator delivers an efficient and distributable wastewater treatment system. Our study provides a promising and alternative route for on-site H 2 O 2 production coupling the practical application process.
研究领域:
催化化学
·
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
Materials Chemistry Frontiers
·
2019
·Vol. 3
·期 3
·456-463
·
IF 0
Bin Xiao,Wen-hai Zhang,Hai-feng Xia,Zhi-teng Wang,Lin-bo Tang,Chang-sheng An,Zhen-jiang He,Hui Tong,Jun-chao Zheng
V2(PO4)O is a novel promising anode material because of its stable crystal structure, low cost, and environmentally friendliness. However, its low electronic and ionic conductivity result in poor specific capacity and rate performance, hindering its industrial application. In this study, V2(PO4)O/C@CNT hollow spheres (HSs) with a core–shell structure were successfully synthesized by a simple spray drying method. Pluronic® F-127 acted as a carbon source and template, and induced the V2(PO4)O particles to form HSs. The V2(PO4)O/C@CNT HSs were composed of uniform HSs of about 0.4–0.6 μm in diameter and carbon nanotubes (CNTs). The HS structure enhances the electronic conductivity and lithium ion transport rate of V2(PO4)O/C materials and thus helps improve the electrochemical performance. CNTs not only increase the electronic conductivity and lithium ion transport rate, but also hinder the aggregation of the HSs. These activities enhance the electrochemical performance. The lithium ion storage behavior of V2(PO4)O/C@CNT HSs is systematically studied in the potential range 0.01–3.0V. The V2(PO4)O/C@CNT HS anode can achieve a high reversible capacity of 894.9 mA h g−1 at 0.1 A g−1 and can obtain a reversible capacity of 490.4 mA h g−1 at a high rate of 5 A g−1, perhaps the best electrochemical performance demonstrated so far for a V2(PO4)O anode material (specific capacity and rate performance), indicating its promise for application as an anode material in advanced lithium-ion batteries.
研究领域:
材料科学
·
能源存储
✓ 已验证
产品关联
DOI
CHEMICAL ENGINEERING JOURNAL
·
2025
·
IF 13.2
Yongjiang Li,Ailing Zhang,Yanhui Wang,Donglei Fan,Yichao Lin,Jie Liu,Tao Tang
Phosphorus containing flame-retardants with low oxidation states are widely used in Flexible polyurethane foam (FPUF) due to their excellent gas-phase flame retardancy. However, achieving good migration resistance in prepared flame retardant while balancing or even improving the mechanical properties (such as ductility, good rebound ability) and flame retardancy of FPUF remains a challenging issue. To solve the above problem, we have designed diphenylphosphine oxide silicon glycol (DPPSG) that combines a phosphorus-based flame retardant group with a Si-O-C bond structure. Chemically linking DPPSG into the molecular chain of flexible polyurethane foam and mechanical properties at the same time. On one hand, DPPSG has good compatibility with polyether polyols 330, reacting uniformly with isocyanates and participating in the foaming and gelation process of FPUF. This ensures its enduring flame retardancy. On the other hand, the tensile strength and elongation at break of the flame retardant foam (10DPPSG foam) prepared by adding 10% DPPSG of polyether polyol 330 increased by 71.4% and 77.6% respectively. Moreover, even after 100 cycles of compression rebound testing, 10DPPSG foam exhibited excellent elasticity with a permanent compression deformation rate of only 4.9%. This work provides a new approach to develop FPUF that achieves a balance between mechanical and flame-retardant properties.
研究领域:
材料科学
·
高分子化学
✓ 已验证
产品关联
DOI
高影响因子
ADVANCED FUNCTIONAL MATERIALS
·
2024
·Vol. 34
·期 33
·2400302
·
IF 18.5
Anding Xu,Mianying Huang,Chenxi Liu,Teng Li,Xue Li,Songping Wu,Zhiguang Xu,Yurong Yan
Constructing Sb atomic clusters with obvious size effect in Sb/C composites has great potential for boosting electrochemical reactivity toward ultrahigh rate and long-term sodium storage. However, how to balance the contradiction between ultra-small size of Sb atomic clusters and high loading in a specific Sb/C composite is an unprecedented challenge. Here, a facile in situ vaporization-reduction strategy is presented for preparing Sb atomic clusters@N, S co-doped carbon networks (Sb ACs@NSC). Featuring the high content of Sb atomic clusters (45.30 wt%, ICP) with superior electrochemical activity, robust Sb─O─C bond and N, S co-doped conductive carbon matrix, the Sb ACs@NSC electrode possessed ultrafast electrochemical kinetics and impressive long-term cycling stability for providing unprecedented rate capability of 245.7 mAh g −1 at ultrahigh rate of 80 A g −1 and maintaining highlighted capacity of 306.7 mAh g −1 after 1000 cycles under 10 A g −1 , outperforming all reported Sb-based materials for SIBs. The DFT calculations further revealed that the Sb─O─C bond and N, S co-doped carbon matrix are beneficial for stable adsorption capabilities and fast electrochemical kinetics of Na + . The designing compromised dense Sb atomic clusters and powerful interface bond will light on developing advanced atomic materials for energy storage and conversion.
研究领域:
材料科学
·
电化学
✓ 已验证
产品关联
DOI
高影响因子
FUEL
·
2021
·
IF 6.609
Yishuang Wu,Zixiang Lin,Xun Zhu,Xun Hu,Mortaza Gholizadeh,Hongqi Sun,Yong Huang,Shu Zhang,Hong Zhang
Catalytic hydrogenolysis of lignin to phenolic monomers has received a lot of attention, but it is still a challenge because the cleavage of the strong C(sp 2 )-O/C bonds between structural units is usually under harsh conditions, resulting in the presence of the competing reaction of hydrogenation. Herein, hydrogenolysis of an herbaceous lignin into phenolic monomers was performed over Ru supported on various (non)-functionalized graphitized carbon nanotubes (CNT, CNT-OH, CNT-COOH, and CNT-NH 2 ), which were featured by different hydrogenation performances originally from the diverse metal-support interactions. Among the investigated supports, CNT-NH 2 enables the formation of the finest Ru nanoparticles with an average size of 1.86 nm, leading to the highest yield of phenolic monomers from lignin hydrogenolysis. The best hydrogenolysis performance of Ru@CNT-NH 2 was mainly from the partial hydrogenation of C(sp 2 )-O/C bonds to C(sp 3 )-O/C bonds in lignin, thus reducing their bond dissociation energy (BDE). The intimacy between hydrogenolysis and hydrogenation was further proved by depolymerization of a lignin β-O-4 model compound.
研究领域:
化学工程
·
催化科学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
2019
·
IF 7.65
Shizong Wang,Haiyang Liu,Jianlong Wang
In this study, nitrogen, sulfur and oxygen co-doped carbon armored cobalt sulfide (Co/Co 9 S 8 @N-S-O-C) composite was synthesized, characterized and used to activate peroxymonosulfate (PMS) for the degradation of sulfamethoxazole (SMX). SMX (0.04 mM) can be completely degraded within 20 min in the presence of 0.8 mM PMS and 0.1 g/L Co/Co 9 S 8 @N-S-O-C composite. The first-order kinetics constant of SMX degradation was 0.307 min -1 , and the mineralization of SMX was 30.1 %. The Quenching experiments of the free radicals and the identification of degradation products demonstrated that sulfate radicals played a dominant role in SMX degradation. The degradation rate of SMX increased with temperature, and activation energy was calculated to be 48.6 kJ/mol. The degradation rate of SMX increased firstly then decreased with increase of pH. Chloridion and humic acid decreased the degradation rate of SMX no matter what their initial concentration was. The effect of carbonate on SMX degradation depended on its initial concentration. Co/Co 9 S 8 @N-S-O-C composite showed good stability, the removal efficiency of SMX was 98.4 % in the fifth experiment. Based on the characterization results of the catalyst before and after use, it was concluded that cobalt, sulfur, pyridnic N and graphitic N were responsible for PMS activation.
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2021
·
IF 6.953
Ying Liao,Yu Chen,Caiyan Wan,Guangxian Zhang,Fengxiu Zhang
A halogen-free, formaldehyde-free, efficient, durable, N P flame retardant, the ammonium salt of meglumine phosphoric ester acid (ASMPEA), was prepared. The Fourier-transform infrared spectroscopy (FTIR) and nuclear magnetic resonance spectroscopy ( 1 H NMR, 13 C NMR, and 31 P NMR) results indicated that ASMPEA was grafted onto cotton fibers by P-O-C covalent bonds. The LOI value of 30 wt% ASMPEA-treated cotton fabric was 40.2%, and after 50 laundering cycles (LCs), the LOI value decreased to 29.4%, indicating that the cotton fibers treated with ASMPEA were endowed with excellent durable flame retardancy. Thermogravimetry (TG), cone calorimetry, and vertical flammability test results showed that ASMPEA-treated cotton decomposed into phosphoric acid or polyphosphoric acid during combustion, which promoted the thermal degradation and charring of treated cotton fabrics and hindered the spread of flames. Scanning electron microscopy (SEM), X-ray diffraction (XRD), and energy-dispersive spectrometry (EDS) verified that ASMPEA infiltrated the cotton fiber without obviously affecting its surface morphology or crystal structure; however, the mechanical properties of the treated cotton fabric decreased slightly. These results confirm that ASMPEA achieved excellent durable flame retardancy when used to coat cotton fabric.
研究领域:
材料科学
·
纺织工程
·
阻燃性
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF POWER SOURCES
·
2026
·
IF 8.4
Guanghui Zhou,Yumeng Jia,Kai Chen,Haiguang Gao,Jian Zang,Yucheng Huang,Juan Xu,Jianyu Cao
Organic cathode materials present a highly viable alternative, offering abundant resources, environmental compatibility, and highly designable molecular structures. However, conventional organic materials suffer from high solubility and low electronic conductivity. To overcome these inherent drawbacks, we propose a structural design strategy based on constructing extended π-conjugated molecular frameworks with high-density electrochemically reversible groups. Inspired by this strategy, we synthesized a novel sulfur-linked C3-symmetric conjugated organic compound, tris-benzothioxanthenedione 2,3-b (denoted as 6S6O), via a facile condensation reaction. The unique structure of 6S6O provides multiple high-density C=O/C=N moieties for reversible lithium storage, excellent solvent tolerance, and high intrinsic conductivity due to electron delocalization. Electrochemical testing demonstrates outstanding performance in a Li//6S6O half-cell, delivering a high reversible capacity of 352 mAh g −1 at 0.1 A g −1 , corresponding to a high energy density of ∼748.6 Wh kg −1 . Importantly, the electrode demonstrates excellent rate capability (retaining 65.3% capacity with a 20-fold current increase) and superior long-term cycling stability, maintaining 77.5% capacity retention over 2409 cycles at 2 A g −1 . Ex situ characterization and DFT calculations confirm a highly reversible, capacitive-controlled Li + storage mechanism involving the C=O and C=N bonds of the quinone/pyrazine units. The results validate the effectiveness of the extended π-conjugated design for developing high-performance organic cathode materials.
✓ 已验证
产品关联
DOI
高影响因子
Small Structures
·
2022
·Vol. 3
·期 10
·2200078
·
IF 11.343
Danni Wang,Xiaoqiong Du,Biao Zhang
It has been widely recognized that ether electrolytes show great advantages in building robust solid–electrolyte interphases (SEIs) for stable anode performance. However, its extension to the graphite electrode is hampered by the ether solvent cointercalation, leading to a lower capacity and higher potential than those in ester counterparts having neat cation insertion. Herein, the ether solvent molecules by optimizing the O/C atomic ratio through tailoring the end group and chain length are screened. Such a modification alters the solvation strength between K ions and the solvent, which dictates the intercalation behavior in graphite. In particular, an ethylene glycol diethyl ether-derived electrolyte is developed, which prevents the solvent cointercalation and induces the formation of binary intercalation compound KC 8 . Meanwhile, the novel ether electrolyte helps build a uniform and robust SEI, significantly boosting the rate capability and long-term stability of graphite anode. This study resolves the dilemma of ether electrolyte in realizing the stable and high-capacity graphite anode for facilitating its application in potassium-ion batteries.
研究领域:
材料科学
·
电化学
·
电池技术
✓ 已验证
DOI
高影响因子
MATERIALS AND CORROSION-WERKSTOFFE UND KORROSION
·
2021
·Vol. 73
·期 2
·242-253
·
IF 2.097
Liying Song,Hao Shi,Peng Han,Xiaohong Ji,Qingli Cheng
A self-healing coating containing an electrospun nanofibre encapsulating 3,4,5-trihydroxy benzoic acid cyclohexyl ester (GACE) was prepared. Scanning electron microscopy and transmission electron microscopy demonstrated that the nanofibre had a core–shell structure. The shell thickness of the electrospun fibre was approximately 270 nm, while the core thickness was approximately 380 nm. The self-healing process of the coating containing GACE nanofibres over a carbon steel surface was simulated in a 3.5 wt% NaCl solution for 30 days. Fourier-transform infrared spectroscopy analysis revealed that the synthesised GACE reacted with iron ions and formed a stable Fe–O–C compound, which could repair the scratched coating. The self-repair performance was evaluated through electrochemical measurements, and then a healing model was developed.
研究领域:
材料科学
·
表面化学
·
纳米技术
✓ 已验证
产品关联
DOI
高影响因子
WASTE MANAGEMENT
·
2021
·
IF 7.145
Huayi Chen,Xingjian Yang,Yonglin Liu,Xueming Lin,Jinjin Wang,Zhen Zhang,Na Li,Yongtao Li,Yulong Zhang
Waste chicken feathers are the ideal precursor for the production of low-cost N-enriched biochar. KOH-modified N-enriched biochar (KNB) containing 15.92 wt% N was successfully prepared using waste chicken feathers. The adsorption kinetics results showed that KNB had rapid Cd (2 h) and Pb (1 h) adsorption rates. The Cd and Pb adsorption capacities of KNB (the values of K F were 22.324 (Cd) and 119.654 (Pb) mg 1−(1/n) ·L 1/n ·g −1 ) were 7.07 and 26.52 times higher than those of the original biochar based on the adsorption isotherm results. The KNB was stable at pH 3–6 and had stronger co-adsorption capacities in double-ion systems. Based on the adsorption experiments and various characterization methods, we concluded that the primary Cd and Pb adsorption mechanisms of KNB involved electrostatic interactions, cation-π interactions, complexation, and K + exchange. The precipitation mechanism could partially account for Pb adsorption but not for Cd adsorption. KOH modification enhanced the electronegativity of biochar and then increased the electrostatic attraction. Surface O- and N-containing functional groups were involved in Cd and Pb adsorption. Graphitic-N, oxidised-N, and O C O were the main active adsorption groups, the relative contents of which increased after KOH modification, thus increasing the Cd and Pb adsorption performance. Therefore, KNB can be used as a fast and highly efficient adsorption agent to remove Cd and Pb from wastewater containing either Cd and Pb or a combination of these two metals.
研究领域:
环境科学
·
材料科学
·
废水处理
✓ 已验证
产品关联
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）