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JOURNAL OF RAMAN SPECTROSCOPY · 2016 ·Vol. 48 ·期 2 ·243-250 · IF 2.395

Laser-induced plasmonic heating on silver nanoparticles/poly(N-isopropylacrylamide) mats for optimizing SERS detection

Lin Wang,Yan Zhang,Wenqi Zhang,Tianrui Ren,Feng Wang,Haifeng Yang

Silver nanoparticle (AgNP)/poly( N -isopropylacrylamide) (PNIPAAm) composite solution was electrospun followed by crosslinking to fabricate AgNP/PNIPAAm composite nanofiber mats. Embedded AgNPs were found to align along the PNIPAAm nanofibers, which generate more hotspots upon laser-induced plasmonic heating. This kind of AgNP/PNIPAAm mats show enhanced surface-enhanced Raman scattering (SERS) effect upon continuous pulsed laser irradiation, showing a ‘laser heating sensitive’ SERS effect. Laser-induced plasmonic heating can also tune the temperature-responsive interaction between PNIPAAm and analytes and has been applied in the on-site ‘laser heating sensitive’ separation and SERS detection of analytes. The composite nanofiber mats also showed good reproducibility and stability. What is more, this ‘laser heating sensitivity’ has also been applied in the direct SERS detection of adenosine in urea solution without urea interference. Together with the advantages of ease of large-scale fabrication, stable and ‘laser heating sensitivity’, AgNP/PNIPAAm mats might find application in sensitive multicomponent biosensing. Copyright © 2016 John Wiley & Sons, Ltd.

研究领域: 材料科学 · 分析化学 · 生物医学工程
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CORROSION · 2013 ·Vol. 69 ·期 7 ·672-680 · IF 1.772

Inhibition of Iron Corrosion in HCl Solutions by N-[2-[(2-Aminoethyl) Amino] Ethyl]-9-Octadecenamide

Jiang Y.Y.,Chen Y.,Ye Z.Y.,Chen H.,Zhang Z.,Zhang J.Q.,Cao C.N.

N-[2-[(2-aminoethyl) amino] ethyl]-9-octadecenamide (AAOA) has been synthesized in the lab, then tested as an effective and economic acid inhibitor for A3 steel in an acid medium with electrochemical techniques (electrochemical impedance and polarization curve). The results show that AAOA acts as a good mixed-type inhibitor for A3 steel in 1 M hydrochloric acid (HCl) solution, and the inhibition efficiency reaches 94% at the concentration of 200 mg/L. The corrosion current density of A3 steel increases with the increasing temperature from 20°C to 60°C. Meanwhile, Langmuir isotherm is found to provide the description of the adsorption behavior of AAOA, and the value of adsorption free energy (ΔG 0 ) is as low as low as −37.3 kJ/mol. One can assume the adsorption of inhibitor molecules on the metal surface is by chemisorption, which has been understood taking into account some other adsorption parameters (ΔH 0 , ΔS 0 ) and the activation parameters (E a , ΔH * , ΔG * ).

研究领域: 材料科学 · 腐蚀与防护 · 电化学
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MATERIALS RESEARCH BULLETIN · 2024 · IF 5.3

In-situ preparation of Ag2S nanoparticle-anchored BiVO4 nanosheet p-n heterostructure on three-dimensional flexible substrate for enhancement of photocatalytic activity

Chuanyun Yang,Xingjian Zhang,Zhengdao Li,Zhishuai Wang,Jiping Shi,Haiquan Xie,Ting Li,Yong Zhou

A series of hybrid films were designed and fabricated by in situ growth of Ag 2 S nanoparticles with varying content on BiVO 4 nanosheets deposited on stainless steel mesh. The formation of a p-n heterojunction between Ag 2 S and BiVO 4 enabled an extended spectral response range and facilitated the separation of charge carriers through a single directional pathway for electron transport. Exploiting these advantages, Ag 2 S/BiVO 4 composites were employed in various photocatalytic applications under simulated solar irradiation. The results demonstrated, in terms of water purification, that the composite not only possessed photocatalytic ability to degrade RhB or Cr(VI) individually but also exhibited significantly enhanced photocatalytic efficiency in simultaneously removing mixed pollutants containing RhB and Cr(VI). In terms of CO 2 conversion, Ag 2 S/BiVO 4 also displayed a stronger photocatalysis capability compared to pure BiVO 4 film. Furthermore, the immobilized Ag 2 S/BiVO 4 film exhibited improved mechanical strength and long-term stability, making it highly suitable for practical applications.

研究领域: 材料科学 · 环境科学
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Materials Research Express · 2019 ·Vol. 6 ·期 9 ·095704 · IF 1.449

Dehydration behaviours of isopropyl group initiate the surface wettability transition of temperature sensitive poly(N-isopropylacrylamide) hydrogel

Meng Xia,Shenxin Pan,Yujie Sun,Qiuzhu Luo,Zhengping Fang,Peixin He,Jing Fu,Yuhong Zhang

As a new generation of smart materials, poly(N-isopropylacrylamide) (PNIPAM) is studied for its wettability transition mechanism, which is necessary for the development of the next generation of wettability transition materials. Herein, we minutely report the effects of temperature on the wettability of solid-oil-water and solid-water-air interfaces for the first time. The PNIPAM hydrogel surface (PHS) became less hydrophilic and less lipophobic with the temperature increasing, and the sharply changes in wettability occur range from 28 °C to 32 °C. Furthermore, unlike previous assumptions, our data about resonance Raman spectroscopy and molecular dynamics simulation suggest that dehydration of isopropyl is more likely to be a cause of drastic changes in wettability. This study suggests a novel foundation to comprehend the wetting behavior of smart PNIPAM gelation surface.

研究领域: 材料科学 · 生物医学工程
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JOURNAL OF ALLOYS AND COMPOUNDS · 2021 · IF 5.316

Construction of N-doped C@MoS2 heteroshell with the yolk of Sn nanoparticles as high-performance anodes for sodium-ion batteries

Peiyuan Mao,Yong Wang,Pandeng Xiao,Wen Zhang,Shun Rao,Zhi Wang

Herein, we demonstrate the reasonable design and preparation of yolk-heteroshell Sn@N-doped C@MoS 2 nanospheres as anode materials in sodium-ion battery. Through an effective multi-step strategy, Sn nanoparticles are encapsulated in N-doped C nanocage surrounded by ultra-thin MoS 2 nanosheets to form Sn@N-doped C@MoS 2 nanospheres. In this novel structure, Sn nanoparticles with high theoretical capacity improve the space utilization inside the heteroshell; the N-doped carbon nanocage as the skeleton not only inhibits the mutual accumulation of Sn and MoS 2 , but also improves conductivity; the outer MoS 2 ultra-thin sheets can consolidate C@MoS 2 heteroshell, provide numerous active sites and favor the fast diffusion of Na + /e - . Notably, the combination of carbon nanocage and MoS 2 sheets in the yolk-heteroshell structure can effectually buffer the volume expansion of Sn nanoyolks and reinforce C@MoS 2 heteroshell while reducing the carbon content. Therefore, the yolk-heteroshell structure plays a crucial role in enhanced reversible capacity and cyclic stability of Sn@N-doped C@MoS 2 nanospheres, which activates their sodium storage potential. The yolk-heteroshell Sn@N-doped C@MoS 2 nanospheres exhibit high reversible capacity of 488.4 mAh g −1 at 0.1 A g −1 after 300 cycles and long-cycle stability of 350.6 mAh g −1 at 0.5 A g −1 after 500 cycles. Moreover, their full cell delivers a stable reversible discharge capacity of about 80.1 mAh g −1 after 30 cycles at 0.5 C. This work provides a feasible yolk-heteroshell strategy for Sn-based composite nanomaterials .

研究领域: 材料科学 · 电化学
✓ 已验证 DOI 高影响因子
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RESEARCH ON CHEMICAL INTERMEDIATES · 2015 ·Vol. 42 ·期 3 ·2211-2220 · IF 1.221

A simple and efficient approach for highly selective preparation of nitrocyclohexane from cyclohexane with tert-butyl nitrite catalyzed by N-hydroxyphthalimide

Liu Shuilin,You Kuiyi,Jian Jian,Luo Qing,Liu Pingle,Ai Qiuhong,Luo He’an

A simple and effective approach for highly selective preparation of nitrocyclohexane from cyclohexane using tert-butyl nitrite as a nitrating agent under atmospheric pressure has been successfully developed in this work. The results indicate that the N -hydroxyphthalimide catalyst gave the best results with 27.3 % of cyclohexane conversion and 88.0 % of selectivity to nitrocyclohexane under optimal reaction conditions. The present reaction provides a novel strategy for the synthesis of nitroalkanes from the nitration of low-carbon alkanes because of the mild reaction condition, simple experimental procedure and high selectivity towards the desired product. This method may be very significant to establish such a synthesis method for aliphatic nitro-compounds from the low-carbon alkanes in organic fields.

研究领域: 有机化学 · 合成化学
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ENERGY & FUELS · 2022 · IF 4.654

Investigation on the Stability of Janus SiO2-n Nanoparticle-Assisted Nonionic Surfactant-Stabilized Foam and Its Application in Enhanced Oil Recovery

Daofan Wang,Han Jia,Qiuxia Wang,Xiaolong Wen,Ziwei Wei,Qiang Wang,Fangning Fan,Shijie Wen,Kaihe Lv,Dexin Liu

The stability of the foam directly impacts the final efficiency of the foam flooding in enhanced oil recovery (EOR). In the present work, a series of Janus SiO2-n nanoparticles (JSn NPs) with various modification degrees were successfully prepared and employed to improve the stability of the nonionic surfactant polyethylene glycolmonoisodecylether (PMIE)-stabilized foam. The PMIE–JS3 system with a much low JS3 NP concentration (0.1 wt %) displayed extraordinary foamability and stabilizing foam ability via the foam volume, half-life, relative volume decay, and optical microscope photograph measurements. Then, the dynamic surface tension and dilatational viscoelasticity tests were conducted to explore the mechanism. It was found that the PMIE–JS3 system with great interfacial activity and intensive interfacial film highly facilitated the generation of the foam and improved the foam stability. Moreover, the PMIE–JS3-stabilized foam exhibited outstanding stability, even under the influence of crude oil. The sandpack flooding tests indicated that the PMIE–JS3-stabilized foam could effectively plug the high-permeability channels to modify the water injection profile and consequently greatly enhanced tertiary oil recovery (∼15.3% of the initial oil in place).

研究领域: 化学工程 · 石油工程 · 材料科学
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED ELECTROCHEMISTRY · 2024 · IF 2.4

N, S co-doped lignin graded porous carbon as efficient Pt-free counter electrodes for dye-sensitized solar cells

Li Jingzhe,Zhang Jiaxin,Ling Yikai,Long Min,Tian Rui,Liang Ti,Nong Guangzai

Pt counter electrodes are essential components of dye-sensitized solar cells (DSSCs). However, their high cost and poor stability limit the development of these cells. In the quest for alternative materials to replace Pt, this study utilized sodium lignosulfonate as the primary raw material and successfully prepared N, S co-doped hierarchical porous carbon by adjusting the ratio of thiourea. This carbon was then fabricated into a counter electrode to replace Pt. The results showed that the N, S co-doped hierarchical porous carbon exhibited superior electrochemical performance compared to single-atom doped carbon. When used as the counter electrode in DSSCs, it achieved a power conversion efficiency of 8.62%, which is higher than the 7.98% efficiency of Pt. Furthermore, it demonstrated greater stability than Pt in stability tests. These findings confirm that N, S co-doped hierarchical porous carbon could replace Pt, thereby advancing the scientific understanding of DSSCs and promoting their application and development. Graphical Abstract

研究领域: 材料科学 · 能源材料 · 太阳能电池
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CARBON · 2022 · IF 11.307

Surface-confined polymerization to construct binary Fe3N/Co–N–C encapsulated MXene composites for high-performance zinc-air battery

Dangcheng Su,Yuanhua Xiao,Yingliang Liu,Shengang Xu,Shaoming Fang,Shaokui Cao,Xuezhao Wang

2D MXenes (transition metal carbides, Ti 3 C 2 T x ) with large surface area and metallic conductivity are widely used as supporters in catalysts. Unfortunately, the single MXene sheets would deteriorate in the presence of oxygen and water, which is almost the same as the environment of oxygen reduction reaction (ORR). Herein, an “armor” was constructed to encapsulate the oxidizable MXene by a confined in-situ oxidative polymerization strategy, employing the electrostatic interaction between the exfoliated MXene sheets (negatively charged) and oxidant (Fe 3+ , positively charged). The ultra-dispersed binary Fe 3 N and Co sits coupled with the large surface area MXene supporter synergy to endow more exposed active sites, meanwhile, the density functional theory (DFT) studies reveal that a moderate binding strength between the intermediates and the binary active sites was effectively modulated to enhance the ORR performance. The synthesized Fe 3 N/Co–N–C@MXene exhibits an impressive half-wave potential (E 1/2 , 0.871V) and a lower Tafel slope of 52.56 mV dec −1 than that of Pt–C-20% (74.89 mV dec −1 ). The Fe 3 N/Co–N–C@MXene based ZAB exhibits a four times higher peak power density (189.16 mW cm −2 ) than the Pt–C-20% based ZABs and superior cycle stability within 320 h. Furthermore, the assembled flexible ZABs shows high flexibility and stability in different bending scenarios.

研究领域: 材料科学 · 电化学 · 纳米催化 · 能源存储与转换 · 功能材料
✓ 已验证 DOI 高影响因子
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JOURNAL OF MEMBRANE SCIENCE · 2024 · IF 8.4

Aryl-ether-free polyphenylene-based anion exchange membranes incorporating N-cyclic quaternary ammoniums for enhanced alkaline fuel cell performance

Xiaomeng Chu,Haoxi Zhang,Cuizhi Zhang,Runan Shao,Zitong Huang,Hongfu Lv,Shaojie Liu,Lei Liu,Nanwen Li,Song Zhao

Selecting appropriate polymer backbones is crucial for the advancement of anion exchange membranes (AEMs) that exhibit both high ionic conductivity and robust chemical stability. In this study, we synthesized rigid and chemically inert aryl-ether-free polyphenylene-based polymer backbones containing alkaline-resistant N-cyclic cations, i.e. dimethyl piperidinium (DMP) or 6-azonia-spiro[5.5]undecane (ASU), as high-performance AEMs. The procedure encompassed several key steps: superacid-catalyzed Friedel-Crafts polycondensation, bromomethylation, azidation, and Cu(I)-mediated azide-alkyne cycloaddition. The synthesized BP-ASU(DMP)-x copolymers demonstrated excellent film-forming capabilities to afford robust AEMs as compared to polyolefin-based counterparts. Owing to the significant incompatibility between the hydrophobic backbones and the hydrophilic cations, the BP-ASU(DMP)-x membranes exhibited a well-defined microphase-separated morphology, resulting in exceptionally high hydroxide conductivity, up to 157.2 mS cm −1 at 80 °C in water. More importantly, BP-ASU-150 membrane exhibited no chemical degradation and a conductivity retention of >97 % when immersed in 1 M NaOH solution at 80 °C for 4000 h. Compared to the poly(2,6-dimethyl-1,4-phenylene oxide) (PPO) and polyolefin-based counterparts, the achieved outstanding alkaline stability is related to aryl-ether-free polyphenylene and alkali-stable N-cyclic cations, highlighting the importance of polymer backbones for AEM materials. Finally, all the polyphenylene-based AEMs with incorporated N-cyclic cations were assembled in single H 2 /O 2 AEMFCs, with the BP-ASU-150 membrane demonstrating a peak power density (PPD) of 860.4 mW cm −2 at a current density of 1363 mA cm −2 . We concluded that the BP-ASU(DMP) AEMs demonstrated superior performance across various metrics due to exceptional stability and robustness of polyphenylene polymers, highlighting their potential as backbones for high-performance AEM materials.

研究领域: 材料科学 · 能源化学
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BIOMACROMOLECULES · 2024 · IF 5.5

Facile Preparation of Heteropolypeptides from Crude Mixtures of α-Amino Acid N-Carboxyanhydrides

Xiao Sun,Aoting Li,Ning Li,Guonan Ji,Ziyuan Song

Heteropolypeptides bearing two or more functional side chains are promising polymeric materials for various biomedical applications. However, conventional preparation of heteropolypeptides relies on the synthesis and purification of each N-carboxyanhydride (NCA) monomer in a separate manner, which substantially increases the time and cost. Herein, we report the facile preparation of heteropolypeptides with up to 86% yield within several hours, which are obtained from a mixture of crude NCA monomers. The combination of n-hexane precipitation and biphasic segregation effectively removed >90% impurities from crude NCA mixtures, allowing for the successful polymerization process. Various heteropolypeptides with monomodal distribution and narrow dispersity were efficiently prepared, whose compositions were predetermined by the feeding ratios of amino acids. We believe that this work significantly simplifies the preparation of various heteropolypeptides, boosting the downstream studies of these promising materials.

研究领域: 高分子科学 · 材料科学 · 生物技术 · 化学工程
✓ 已验证 DOI PubMed 高影响因子
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APPLIED SURFACE SCIENCE · 2020 · IF 6.182

Cu/Al2O3 catalyst prepared by a double hydrolysis method for a green, continuous and controlled N-methylation reaction of nitroarenes with methanol

Hao Zhang,Junyan Wang,Minjie Liu,Di Liu

Cu/Al 2 O 3 catalyst was developed by a double hydrolysis precipitation. Over the Cu/Al 2 O 3 catalyst, a continuous mode of N-methylations of nitroarenes with methanol was successfully achieved under the exogenous base- and H 2 - free condition. Methylation process of nitroarenes could be controlled just by adjusting reaction conditions, affording the desired N-monomethylanilines or N, N-dimethylanilines, respectively. The characterization displayed that the double hydrolysis precipitation method made active metal Cu surface enrichment and high dispersion, meanwhile endow Cu/Al 2 O 3 with more developed pore system, which were responsible for the higher performance of our catalyst relative to Cu/Al 2 O 3 -CP. Compared with the reported batch mode, our procedure possessed the merits of low cost, environment-friendliness, better controllability and wide universality.

研究领域: 催化化学 · 绿色化学工程
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