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Eu3+ doped hydroxyapatite nanowires enabling solid-state electrolytes with enhanced ion transport

Journal of materials Science & technology 2024年第19期186卷 104-109页

作者： Xiaoyue Wang Hong Zhang Lin Xu Liqiang Mai State Key Laboratory of Advanced Technology for Materials Synthesis and Processing School of Materials Science and EngineeringWuhan University of TechnologyWuhan 430070China Hubei Longzhong Laboratory Wuhan University of Technology(Xiangyang Demonstration Zone)Xiangyang 441000China Hainan Institute Wuhan University of TechnologySanya 572000China

The polymer-based solid-state electrolytes (PSEs) are promising for solid-state batteries but they have deficiencies such as low ionic conductivity, low lithium-ion transference number, and unstable electrode/electrolyte interface. Herein, we designed a hydroxyapatite nanowire doped with high-valence cations in anticipation of the formation of positively charged active sites on the nanowire surface. The higher surface activity can reduce the reaction activation energy on the nanowire surface and adsorb the anions in the PSEs as a way to improve the ionic conductivity and Li+ transference number of the PSEs. The active sites on the surface of the nanowires anchor the anions, thus increasing the Li+ transference number to 0.38, which effectively improves the ionic conductivity of the PSE to 1.58 × 10-4 S cm-1 at room temperature. At the same time, the composite polymer electrolyte has a wide electrochemical window. The lithium symmetric cell stably cycles for 800 h at a current density of 0.1 mA cm-2, and the LiFePO4||Li full cell steadily cycles for 180 cycles at a rate of 0.5 C with a capacity retention of 94.2 %. The ion doping strategy to change the surface electrical behavior of nanowires provides an idea to improve the ionic conductivity of solid-state electrolytes.

关键词： Nanowires Ion doping Active site Polymer-based solid-state electrolyte

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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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Unraveling the Role of Nitrogen-Doped Carbon Nanowires Incorporated with MnO_(2)Nanosheets as High Performance Cathode for Zinc-Ion Batteries

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Energy & Environmental materials 2023年第3期6卷 205-213页

作者： Xiaohui Li Qiancheng Zhou Ze Yang Xing Zhou Dan Qiu Huajun Qiu Xintang Huang Ying Yu Institute of Nanoscience and Technology College of Physical Science and TechnologyCentral China Normal UniversityWuhan 430079China State Key Laboratory of Advanced Technology for Materials Synthesis and processing Wuhan University of Technology Wuhan 430070China

Manganese-based cathode materials are considered as a promising candidate for rechargeable aqueous zinc-ion batteries(ZIBs).Suffering from poor conductive and limited structure tolerance,various carbon matrix,especially N-doped carbon,were employed to incorporate with MnO_(2)for greatly promoted electrochemical ***,the related underlying mechanism is still unknown,which is unfavorable to guide the design of high performance ***,by incorporating layered MnO_(2)with N-doped carbon nanowires,a free-standing cathode with hierarchical core-shell structure(denoted as MnO_(2)@NC)is *** from the N-doped carbon and rational architecture,the MnO_(2)@NC electrode shows an enhanced specific capacity(325 mAh g^(−1)at 0.1 A g^(−1))and rate performance(90 mAh g^(−1)at 2 A g^(−1)),as well as improved cycling ***,the performance improvement mechanism of MnO_(2)incorporated by N-doped carbon is investigated by X-ray photoelectron spectroscopy(XPS),Raman spectrums and density functional theory(DFT)*** N atom elongates the Mn-O bond and reduces the valence of Mn^(4+)ion in MnO_(2)crystal by delocalizing its electron ***,the electrostatic repulsion will be weakened when Zn^(2+)/H^(+)insert into the host MnO_(2)lattices,which is profitable to more cation insertion and faster ion transfer kinetics for higher capacity and rate *** work elucidates a fundamental understanding of the functions of N-doped carbon in composite materials and shed light on a practical pathway to optimize other electrode materials.

关键词： core-shell nanostructure MnO_(2)nanosheets N-doped carbon Zn ion batteries

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4D printing for future manufacturing

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Science China materials 2023年第11期66卷 4517-4518页

作者： Chaolin Tan Ji Zou Zhengyi Fu Singapore Institute of Manufacturing Technology(SIMTech) Agency for ScienceTechnology and Research(A*STAR)Singapore 636732Singapore State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

Additive manufacturing(AM),also called three-dimensional(3D)printing,offers disruptive design freedom and manufacturing flexibility due to the layer-wise incremental formation manner of *** in AM techniques provide unique advantages and feasibilities for overcoming challenges arising from fabricating parts with complexities in geometry,materials,and properties.

关键词： printing properties freedom

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Ionic liquids-assisted in-situ targeted defect-healing strategy for high-performance sprayed perovskite modules

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Journal of Energy Chemistry 2025年第5期104卷 756-764页

作者： Jize Wang Xinxin Yu Cong Geng Wangnan Li Ying Liang Bin Li Yong Peng Yi-Bing Cheng State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070HubeiChina Hubei Key Laboratory of Low Dimensional Optoelectronic Materials and Devices Hubei University of Arts and ScienceXiangyang 441053HubeiChina Hubei Longzhong Laboratory Wuhan University of Technology(Xiangyang Demonstration Zone)Xiangyang 441000HubeiChina

In the process of spraying coating perovskite films,the"coffee ring"effect(CRE)leads to the problem of excessive organic ammonium salt accumulation in local areas that cannot be completely *** introduce an in-situ targeted defect-healing strategy by incorporating butylamine formate(BAFa)ionic liquid into the spray *** liquids,due to their long carbon chain structure,tend to target flow towards the CRE region during the droplet evaporation *** coordination between the lone pair electrons in the C=O group of BAFa and Pb^(2+)effectively reduces defects in perovskite and suppresses non-radiative recombination ***,amine ligands,which are repelled to the film surface and grain boundaries,form a thin insulating monolayer in the CRE areas,forcing charge carriers to transport through areas of the perovskite with fewer *** approach enables the crystallization control and defect-heal over the Cs_(0.19)FA_(0.81)PbI_(3-x-y)Br_(x)Cl_(y)perovskite ***,the champion perovskite solar cell achieved a power conversion efficiency of 22.04%,while mini-modules with an effective area of 64.8 cm^(2)reached a peak power conversion efficiency of 18.35%,demonstrating the significant potential for commercializing large-area perovskite solar cells.

关键词： Ion liquid Spray-coating Perovskite solar cell "Coffee-ring"effect Targeted defect-healing

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Ultraviolet Photodetector based on Sr_(2)Nb_(3)O_(10) Perovskite Nanosheets

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Journal of Wuhan University of technology(materials Science) 2024年第2期39卷 282-287页

作者：张斌斌 JIA Mengmeng LIANG Qi WU Jinsong ZHAI Junyi 李宝文 School of Materials Science and Engineering Wuhan University of TechnologyWuhan 430070China CAS Center for Excellence in Nanoscience Beijing Institute of Nanoenergy and NanosystemsChinese Academy of SciencesBeijin 100083China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

Liquid-phase exfoliation was employed to synthesize Sr_(2)Nb_(3)O_(10) perovskite nanosheets with thicknesses down to 1.76 *** electron microscopy(TEM),atomic force microscope(AFM),X-ray photoelectron spectrometer(XPS),and other characterization techniques were used to evaluate the atomic structure and chemical composition of the exfoliated nanosheets.A UV photodetector based on individual Sr_(2)Nb_(3)O_(10) nanosheets was prepared to demonstrate the application of an ultraviolet(UV) *** UV photodetector exhibited outstanding photocurrent and responsivity with a responsivity of 3×10^(5) A·W^(-1) at 5 V bias under 280 nm illumination,a photocurrent of 60 nA,and an on/off ratio of 3×10^(2).

关键词： perovskite nanosheets liquid-phase exfoliation ultraviolet photodetector

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Metal-nitrogen-doped hybrid ionic/electronic conduction triple-phase interfaces for high-performance all-solid-state lithium-sulfur batteries

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Nano Research 2023年第8期16卷 10956-10965页

作者： Hao Li Jiangping Song Fanglin Wu Rui Wang Dan Liu Haolin Tang A State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Department of Chemistry School of ChemistryChemical Engineering and Life SciencesWuhan University of TechnologyWuhan 430070China

The point-to-point contact mechanism in all-solid-state Li-S batteries(ASSLSBs)is not as efficient as a liquid electrolyte which has superior mobility in the electrode,resulting in a slower reaction kinetics and inadequate ionic/electronic conduction network between the S(or Li_(2)S),conductive carbon,and solid-state electrolytes(SSEs)for achieving a swift(dis)charge ***,a series of hybrid ionic/electronic conduction triple-phase interfaces with transition metal and nitrogen co-doping were *** graphitic ordered mesoporous carbon frameworks(TM-N-OMCs;TM=Fe,Co,Ni,and Cu)serve as hosts for Li_(2)S and Li_(6)PS_(5)Cl(LPSC)and provide abundant reaction sites on the triple *** from both experimental and computational research display that the combination of Cu-N co-dopants can promote the Li-ion diffusion for rapid transformation of Li_(2)S with adequate ionic(6.73×10^(−4)S·cm^(−1))/electronic conductivities(1.77×10^(−2)S·cm^(−1))at 25℃.The as-acquired Li_(2)S/Cu-N-OMC/LPSC electrode exhibits a high reversible capacity(1147.7 mAh·g^(−1))at 0.1 C,excellent capacity retention(99.5%)after 500 cycles at 0.5 C,and high areal capacity(7.08 mAh·cm^(−2)).

关键词： all-solid-state lithium-sulfur batteries triple-phase interfaces ordered mesoporous carbons mixed ion/electron conductivities Li_(6)PS_(5)Cl solid electrolyte

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Methylthio side-chain modified quinoidal benzo-[1,2-b:4,5-b']dithiophene derivatives for high-performance ambipolar organic field-effect transistors

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Science China Chemistry 2024年第10期67卷 3357-3365页

作者： Li Chen Xiaoqi Luo Nuoya Li Shaoqian Peng Qing Jiang Di Wu Jianlong Xia State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Center of Smart Materials and DevicesWuhan University of TechnologyWuhan 430070China School of Chemistry Chemical Engineering and Life ScienceWuhan University of TechnologyWuhan 430070China Department of Chemistry National University of SingaporeSingapore 117543Singapore

Quinoidal small molecule semiconductors hold huge potential in ambipolar organic field-effect transistors(OFETs)and organic spintronic ***,two quinoidal molecules with methylthio side chains were synthesized to develop molecular semiconductors with high ambipolar mobility,designated QBDTS and *** theoretical calculation results reveal that QBDTS has a closed-shell structure while QTBDTS showed an open-shell structure with a biradical character(y0)of 0.46 and its magnetic properties were further investigated using electron paramagnetic resonance(EPR)and superconducting quantum interference device(SQUID)*** methyl side chains showed a large impact on the molecular orbital *** HOMO/LUMO levels of QBDTS and QTBDTS were measured to be-5.66/-4.56 and-5.27/-4.48 eV,respectively,which are favorable for ambipolar charge transport in ***,the spin-coated QBDTS displayed hole and electron mobilities of 0.01 and 0.5 cm^(2)V^(-1)s^(-1)while QTBDTS showed a record high hole mobility of 1.8 cm^(2)V^(-1)s^(-1)and electron mobility of 0.3 cm^(2)V^(-1)s^(-1).Moreover,comparative studies of the thin film morphologies also manifested the beneficial influence of methyl side chains on film crystallinity and molecule *** results strongly proved that methyl side chain engineering can be a simple but efficient strategy for modulating electronic properties and molecular stacking *** work also represents a big advancement for quinoidal molecular semiconductors in ambipolar OFET applications.

关键词： side-chain modification quinoidal molecules ambipolar diradicals organic field-effect transistors

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An artificial interphase enables stable PVDF-based solid-state Li metal batteries

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Nano Research 2024年第3期17卷 1482-1490页

作者： Mengjun Wu Jiangping Song Jiaheng Lei Haolin Tang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Department of Chemistry School of ChemistryChemical Engineering and Life SciencesWuhan University of TechnologyWuhan 430070China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Foshan 528200China

Composite polymer electrolytes(CPEs)have attracted much attention for high energy density solid-state lithium-metal batteries owing to their flexibility,low cost,and easy ***,the unstable Li/CPE interface is always challengeable for the practical utilization of ***,a polymer interlayer containing K+prepared by ultraviolet(UV)-curing precursor solution is coated on Li surface to stabilize the interface between poly(vinylidene difluoride)(PVDF)composite electrolytes and Li *** from the physical barrier of the interlayer,the continuous decomposition of PVDF is restrained and the intimate contact between electrode and electrolyte is also achieved to reduce the interface ***,the added K+is utilized to further regulate smooth Li *** a consequence,the symmetric Li|Li cell with coated Li demonstrates steady cycling at 0.4 mAh·cm^(-2) and a high critical current density of 1 mA·cm^(-2).The assembled Li|LiFePO_(4) cell presents outstanding cycling stability(capacity retention of 90%after 400 cycles at 1 C)and good rate *** associated pouch cell performs impressive flexibility and *** work provides a convenient strategy to achieve stable Li/PVDF interface for high-performance PVDF-based solid state Li metal batteries.

关键词： interfacial modification solid-state batteries composite polymer electrolytes interfacial compatibility lithium dendrite

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BiOBr/COF S-scheme photocatalyst for H_(2)O_(2) production via concerted two-electron pathway

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Journal of materials Science & technology 2023年第35期166卷 241-249页

作者： Haozhen Zhang Jingjing Liu Yong Zhang Bei Cheng Bicheng Zhu Linxi Wang Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of Geosciences68 Jincheng StreetWuhan 430078China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

Constructing step-scheme(S-scheme)heterojunctions has become a popular strategy for efficient pho-tocatalytic H_(2)O_(2) ***,we in situ grew BiOBr nanosheets(NSs)on a Schiff-base covalent organic framework(COF)with largeπ-conjugated structures to prepare S-scheme BiOBr/COF photocat-alysts for H_(2)O_(2) *** highest photocatalytic H_(2)O_(2) production performance of the composite sample constituting the S-scheme heterojunction is 3749μmol g−1 h−1,which was 1.85 and 27 times the rates of COF and BiOBr,*** construction of S-scheme heterojunction contributed to ef-ficient carrier transfer and separation in space and enhanced redox ***,the lying-down O_(2)-adsorption configuration on the COF surface favors the concerted two-electron O_(2) reduction process,which greatly reduced the reduction potential requirement for O_(2)-to-H_(2)O_(2) *** synergy be-tween the S-scheme heterojunction and the unique O_(2)-COF interaction boosted photocatalytic H_(2)O_(2) pro-duction activity.

关键词： S-scheme heterojunction Photocatalytic H_(2)O_(2)production Covalent organic frameworks Concerted two-electron O_(2)reduction O_(2)-adsorption configuration

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