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Preparation and Characterization of pH-Responsive Charge Reversal Nanocomposite for miRNA Delivery

Journal of Wuhan University of technology(materials Science) 2024年第4期39卷 1048-1052页

作者：余丹 YE Liyuan LI Binbin MOU Fangzhi 殷义霞 State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Hainan Institute Wuhan University of TechnologySanya 572000China Biomedical Materials and Engineering Research Center of Hubei Province Wuhan University of TechnologyWuhan 430070China

pH-responsive charge reversal loaded miRNA nanocomposite was prepared by electrostatic *** morphology,particle size and zeta potential of the nanocomposites were analyzed by transmission electron microscopy and dynamic light *** synthesis of the polymer was analyzed by^(1)*** zeta-potential changes and cellular uptake effects of the nanocomplexes under different pH environments were *** experimental results show that the surface morphology of the nanocomposite is spherical,and the average particle size is about 135 *** the pH value of the solution gradually decreases,the surface charge of the nanocomposite reverses from negative charge to positive charge(from-9.4 to+17.1 mV).Cellular uptake mediated by pH-responsive nanocomposite is selective for tumor cells,and the cellular uptake effect in tumor cells at pH 6.5 was approximately 3 times higher than that at pH *** pH responsive charge reversal nanocomposite has promising application prospects for gene delivery in the weak acid environment of tumors.

关键词： charge conversion siRNA delivery pH responsive cancer therapy

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Unveiling oscillatory nature for sustainable fuel production

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National Science Review 2024年第5期11卷 90-91页

作者： Ning Han Ye Wang Bao-Lian Su Department of Materials Engineering State Key Laboratory of Physical Chemistry of Solid Surfaces Collaborative Innovation Center of Chemistry for Energy Materials National Engineering Laboratory for Green Chemical Productions of Alcohols Ethers and Esters College of Chemistry and Chemical Engineering Xiamen University Laboratory of Inorganic Materials Chemistry(CMI) University of Namur State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology

A century ago, in 1923, Franz Fischer and Hans Tropsch introduced the groundbreaking Fischer–Tropsch (FT) synthesis, a heterogeneous catalytic process used to convert synthesis gas (syngas,CO+H2) into multi-carbon hydrocarbons [1]. Over the past 100 years, FT synthesis has emerged as a pivotal method for converting non-petroleum resources into exceptionally clean fuels or valuable chemicals via syngas [2–4].

关键词： production nature fuel oscillatory sustainable unveiling

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Efficient overall photosynthesis of H_(2)O_(2) by the BTz@Mn_(0.2)Cd_(0.8)S S-scheme heterojunction

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Science China Chemistry 2024年第6期67卷 1953-1960页

作者： Zhongyue Chen Sijie Wan Bei Cheng Wang Wang Yao Xiang Jiaguo Yu Shaowen Cao State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan430070China Hubei Technology Innovation Center for Advanced Composites Wuhan University of TechnologyWuhan430070China Hospital of Wuhan University of Technology Wuhan University of TechnologyWuhan430070China Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of GeosciencesWuhan430074China

The photosynthesis of hydrogen peroxide(H_(2)O_(2))through the selective 2e^(-)oxygen reduction reaction(ORR)from O_(2)and H_(2)O stands out as an environmentally sustainable and cost-effective method for generating this essential ***,the widespread application of most photocatalysts is impeded by their reliance on sacrificial *** this context,we present a noteworthy advancement in the form of a step-scheme(S-scheme)heterojunction involving a donor-acceptor(D-A)-conjugated polymer and manganese cadmium sulfide(BTz@MCS).This innovative configuration enables efficient photocatalytic H_(2)O_(2)production within a non-sacrificial system,showcasing an impressive H_(2)O_(2)yield of 5,368μmol g^(-1)h^(-1)and an apparent quantum yield of 4.5%at 420 *** insights gained from in-situ irradiated X-ray photoelectron spectroscopy(ISIXPS),in-situ diffuse reflectance infrared Fourier transformations spectroscopy(DRIFTS),and density function calculations(DFT),it is revealed that the sp^(2)C between thiazole-thiazole rings at the BTz and the concentrated holes at the MCS function as spatially separated redox *** centers catalyze the selective 2e^(-)ORR and 4e^(-)water oxidation reaction(WOR)*** O_(2)generated from the WOR is subsequently utilized by the ORR cycle,enabling the overall photosynthesis of H_(2)O_(2)with accelerated total reaction ***,the high photocatalytic performance of the developed catalyst is attributed to well-designed S-scheme heterojunctions with tuned band *** spatially separated redox centers and effective transfer of photogenerated charge carriers facilitated by the internal electric field significantly enhance reaction *** study introduces a promising avenue for photocatalytic H_(2)O_(2)production without sacrificial agents,providing valuable insights into the underlying mechanisms in S-scheme heterojunctions.

关键词： hydrogen peroxide non-sacrificial redox centers S-scheme heterojunction

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Enhanced Electrochemical Performances of Ni Doped Cr_(8)O_(21)Cathode materials for Lithium-ion Batteries

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Journal of Wuhan University of technology(materials Science) 2023年第6期38卷 1242-1247页

作者： TANG Guoli LIU Hanxing YU Zhiyong YANG Bo KONG Linghua School of Materials Science and Engineering Wuhan University of TechnologyWuhan 430070China International School of Materials Science and Engineering Wuhan University of TechnologyWuhan 430070China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan 430070China

Cathode materials,nickel doped Cr_(8)O_(21),were synthesized by a solid-state *** effects of Ni doping on the electrochemical performances of Cr_(8)O_(21) were *** experimental results show that the discharge capacities of the samples depend on the nickel contents,which increases firstly and then decreases with increasing Ni *** Ni_(0.5)Cr_(7.5)O_(21)delivers a first capacity up to 392.6 m Ah·g^(-1)at *** addition,Ni doped sample also demonstrates enhanced cycling stability and rate capability compared with that of the bare Cr_(8)O_(21).At 1 C,an initial discharge capacity of 348.7 m Ah·g^(-1)was achieved for Ni_(0.5)Cr_(7.5)O_(21),much higher than 271.4 m Ah·g^(-1)of the un-doped sample,with an increase of more than 28%.Electrochemical impedance spectroscopy results confirm that Ni doping reduces the growth of interface resistance and charge transfer resistance,which is conducive to the electrochemical kinetic behaviors during charge-discharge.

关键词： Cr_(8)O_(21) cathode material doping electrochemical performances lithium-ion batteries

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The Shock Response and Spall Mechanism of Mg-Al-Zn Alloy:Molecular Dynamics Study

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Acta Mechanica Solida Sinica 2022年第3期35卷 495-503页

作者： Xiaoyue Yang Shuang Xu Lisheng Liu Hubei Key Laboratory of Theory and Application of Advanced Materials Mechanics Wuhan University of TechnologyWuhan 430070China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

Shock responses of Mg-Al-Zn alloy are investigated by the molecular dynamics(MD)*** wave propagation,plastic deformation behavior and failure mechanism along the[0001]and[1010]orientations are *** both orientations,simulation results show that the shock wave has an obvious double-wave structure(plastic-elastic)under a piston velocity of 1200 m/s.A higher Hugoniot elastic limit(HEL)is observed for[0001]-oriented *** the shock pressure is along the[1010]direction,the distance between plastic and elastic waves is closer,and higher dislocation density and more twins are ***,the spall strength for[1010]-oriented shock is predicted to be *** addition,the wave interactions,HEL and spall strength predicted for Mg-Al-Zn alloy are compared with the experimental results and MD simulation results of Mg single crystal in the *** is concluded that the shock performance of Mg-Al-Zn is better than that of Mg single crystal.

关键词： Mg-Al-Zn Shock compression Molecular dynamics Hugoniot elastic limit Spall strength

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In situ confined vertical growth of Co_(2.5)Ni_(0.5)Si_(2)O_(5)(OH)_(4)nanoarrays on rGO for an efficient oxygen evolution reaction

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Nano materials Science 2023年第4期5卷 351-360页

作者： Yang Mu Xiaoyu Pei Yunfeng Zhao Xueying Dong Zongkui Kou Miao Cui Changgong Meng Yifu Zhang State Key Laboratory of Fine Chemicals School of Chemical EngineeringDalian University of TechnologyDalian116024China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan430070China

Rational design of oxygen evolution reaction(OER)catalysts at low cost would greatly benefit the *** advantage of earth-abundant elements Si,Co and Ni,we produce a unique-structure where cobalt-nickel silicate hydroxide[Co_(2.5)Ni_(0.5)Si_(2)O_(5)(OH)_(4)]is vertically grown on a reduced graphene oxide(rGO)support(CNS@rGO).This is developed as a low-cost and prospective OER *** to cobalt or nickel silicate hydroxide@rGO(CS@rGO and NS@rGO,respectively)nanoarrays,the bimetal CNS@rGO nanoarray exhibits impressive OER performance with an overpotential of 307 mV@10 mA cm^(-2).This value is higher than that of CS@rGO and NS@*** CNS@rGO nanoarray has an overpotential of 446 mV@100 mA cm^(-2),about 1.4 times that of the commercial RuO_(2)*** achieved OER activity is superior to the state-of-the-art metal oxides/hydroxides and their *** vertically grown nanostructure and optimized metal-support electronic interactions play an indispensable role for OER performance improvement,including a fast electron transfer pathway,short proton/electron diffusion distance,more active metal centers,as well as optimized dualatomic electron *** advantage of interlay chemical regulation and the in-situ growth method,the advanced-structural CNS@rGO nanoarrays provide a new horizon to the rational and flexible design of efficient and promising OER electrocatalysts.

关键词： Co_(2.5)Ni_(0.5)Si_(2)O_(5)(OH)_(4)@rGO Vertical grown nanoarrays Geometric and electronic structure regulation Metal-support interactions Oxygen evolution reaction

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Enhanced Electrical Properties of Bi_(2−x)Sb_(x)Te_(3) Nanoflake Thin Films Through Interface Engineering

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Energy & Environmental materials 2024年第6期7卷 359-366页

作者： Xudong Wu Junjie Ding Wenjun Cui Weixiao Lin Zefan Xue Zhi Yang Jiahui Liu Xiaolei Nie Wanting Zhu Gustaaf Van Tendeloo Xiahan Sang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China NRC(Nanostructure Research Centre) Wuhan University of TechnologyWuhan 430070China EMAT(Electron Microscopy for Materials Science) University of AntwerpGroenenborgerlaan 171Antwerp 2023Belgium

The structure–property relationship at interfaces is difficult to probe for thermoelectric materials with a complex interfacial *** thermoelectric materials with a simple,structurally-uniform interface provides a facile way to understand how these interfaces influence the transport ***,we synthesized Bi_(2−x)Sb_(x)Te_(3)(x=0,0.1,0.2,0.4)nanoflakes using a hydrothermal method,and prepared Bi_(2−x)Sb_(x)Te_(3) thin films with predominantly(0001)interfaces by stacking the nanoflakes through spin *** influence of the annealing temperature and Sb content on the(0001)interface structure was systematically investigated at atomic scale using aberration-corrected scanning transmission electron *** and Sb doping facilitate atom diffusion and migration between adjacent nanoflakes along the(0001)*** such it enhances interfacial connectivity and improves the electrical transport *** reactions create new interfaces that increase the scattering and the Seebeck *** to the simultaneous optimization of electrical conductivity and Seebeck coefficient,the maximum power factor of the Bi_(1.8)Sb_(0.2)Te_(3) nanoflake films reaches 1.72 mW m^(−1)K^(−2),which is 43%higher than that of a pure Bi_(2)Te_(3) thin film.

关键词： Bi_(2)Te_(3) nanoflakes interface engineering scanning transmission electron microscopy thermoelectric thin film

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Deep learning-enhanced NIR-II fluorescence volumetric microscopy for dynamic 3D vascular imaging

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Journal of Innovative Optical Health Sciences 2025年第3期18卷 154-164页

作者： Shiyi Peng Yuhuang Zhang Xuanjie Mou Tianxiang Wu Mingxi Zhang Jun Qian State Key Laboratory of Extreme Photonics and Instrumentation International Research Center for Advanced PhotonicsCentre for Optical and Electromagnetic ResearchCollege of Optical Science and EngineeringZhejiang UniversityHangzhou 310058P.R.China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070P.R.China

Three-dimensional (3D) visualization of dynamic biological processes in deep tissue remains challenging due to the trade-off between temporal resolution and imaging depth. Here, we present a novel near-infrared-II (NIR-II, 900–1880nm) fluorescence volumetric microscopic imaging method that combines an electrically tunable lens (ETL) with deep learning approaches for rapid 3D imaging. The technology achieves volumetric imaging at 4.2 frames per second (fps) across a 200 μm depth range in live mouse brain vasculature. Two specialized neural networks are utilized: a scale-recurrent network (SRN) for image enhancement and a cerebral vessel interpolation (CVI) network that enables 16-fold axial upsampling. The SRN, trained on two-photon fluorescence microscopic data, improves both lateral and axial resolution of NIR-II fluorescence wide-field microscopic images. The CVI network, adapted from video interpolation techniques, generates intermediate frames between acquired axial planes, resulting in smooth and continuous 3D vessel reconstructions. Using this integrated system, we visualize and quantify blood flow dynamics in individual vessels and are capable of measuring blood velocity at different depths. This approach maintains high lateral resolution while achieving rapid volumetric imaging, and is particularly suitable for studying dynamic vascular processes in deep tissue. Our method demonstrates the potential of combining optical engineering with artificial intelligence to advance biological imaging capabilities.

关键词： NIR-II fluorescence bioimaging volumetric microscopy deep learning reconstruction dynamic vascular imaging

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Continuous Fe^(3+)releasing enabled complete reconstruction of Ni-based MOF for promoted water oxidation in industrial alkali

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Science China Chemistry 2024年第9期67卷 2949-2957页

作者： Zhaojian Wang Wei Zhang Wenzhong Huang Ruohan Yu Changliang Chen Liqiang Mai Liang Zhou State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Sanya Science and Education Innovation Park Wuhan University of TechnologySanya 572000China Hubei Longzhong Laboratory Wuhan University of Technology(Xiangyang Demonstration Zone)Xiangyang 441000China

Most oxygen evolution reaction(OER)electrocatalysts show poor stability under industrial alkaline conditions(20–30 wt.%KOH).Therefore,it is essential to develop stable,efficient,and low-cost OER catalysts for industrial water ***,we present a straightforward approach for the complete electrochemical reconstruction of Ni-BDC,a Ni-based metal-organic framework,for *** method involves the continuous release of Fe^(3+)from Fe foam counter electrode in a high-concentration(6.0 M,25 wt.%)KOH *** continuously Fe^(3+)releasing not only realizes in situ Fe^(3+)doping,but also introduces abundant defects in the obtained catalyst during cyclic voltammetry activation,thereby accelerating the electrochemical *** reconstructed OER catalyst(Fe-doped nickel hydroxide/oxyhydroxide nanosheets supported on Ni foam,Fe-NiO_(x)(OH)y/NF)manifests a low overpotential of 217 mV at 10 mA cm^(-2)and 263 m V at 100 m A cm^(-2)in 1.0 M ***,the Fe-NiO_(x)(OH)_(y)/NF also demonstrates high stability in 30 wt.%*** strategy of regulating the electrochemical reconstruction process sheds light on the construction of stable and efficient OER catalysts for industrial water electrolysis.

关键词： oxygen evolution reaction industrial alkaline conditions metal-organic framework complete reconstruction

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Bioactive citrate-based polyurethane tissue adhesive for fast sealing and promoted wound healing

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Regenerative Biomaterials 2024年第1期3卷 69-81页

作者： Yan Li Jiawei Liu Chenxi Lian He Yang Mingjiang Zhang Youfa Wang Honglian Dai State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Biomedical Materials and Engineering Research Center of Hubei ProvinceWuhan University of TechnologyWuhan 430070China Chaozhou Branch of Chemistry and Chemical Engineering Guangdong Laboratory Chaozhou 521000China Shenzhen Research Institute of Wuhan University of Technology Shenzhen 518000China

As a superior alternative to sutures,tissue adhesives have been developed significantly in recent ***,existing tissue adhesives struggle to form fast and stable adhesion between tissue interfaces,bond weakly in wet environments and lack *** this study,a degradable and bioactive citrate-based polyurethane adhesive is constructed to achieve rapid and strong tissue *** hydrophobic layer was created with polycaprolactone to overcome the bonding failure between tissue and adhesion layer in wet environments,which can effectively improve the wet bonding *** citrate-based polyurethane adhesive provides rapid,non-invasive,liquid-tight and seamless closure of skin incisions,overcoming the limitations of sutures and commercial tissue *** addition,it exhibits biocompatibility,biodegradability and hemostatic *** degradation product citrate could promote the process of angiogenesis and accelerate wound *** study provides a novel approach to the development of a fast-adhering wet tissue adhesive and provides a valuable contribution to the development of polyurethane-based tissue adhesives.

关键词： tissue adhesive polyurethane citrate wet adhesion

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