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Insights into laser powder bed fused β-type titanium alloy: Investigating corrosion behavior and wear properties after post-heat treatment

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Journal of materials Research and technology 2025年 37卷 1596-1605页

作者： Xuan Luo Yuhao Li Chao Yang Chao Zhao Hongwei Ma Tao Song Minghan Sun Xiaotao Liu Dongdong Li Ning Li State Key Laboratory of Materials Processing and Die & Mould Technology Huazhong University of Science and Technology Wuhan 430074 China National Engineering Research Center of Near-net-shape Forming for Metallic Materials Guangdong Provincial Key Laboratory for Processing and Forming of Advanced Metallic Materials South China University of Technology Guangzhou 510640 China

The systematic evaluation of corrosion resistance and wear behavior represents a critical imperative for advancing biomedical titanium alloys in implant applications. This study systematically examines the corrosion-wear characteristics of laser powder bed fusion (LPBF)-fabricated β-type Ti-34.5Nb-6.9Zr-4.9Ta-1.4Si (TNZTS) alloy after post heat treatment, comparing with LPBF-processed Ti–35Nb–7Zr–5Ta (TNZT) and Ti–6Al–4V counterparts. Electrochemical analysis reveals the TNZTS system's good corrosion resistance, stemming primarily from stabilized passivation film formation. The incorporation of Si did not significantly affect the corrosion performance of TNZT alloy. In addition, the TNZTS alloy with hard S2 phase showes improvement in wear resistance, as manifested by shallower and narrower wear tracks and a lower specific wear rate. This study provides foundational insights into the novel β-type Ti–Nb–Zr–Ta–Si alloy with excellent corrosion resistance and wear properties, positioning it as a promising candidate for load-bearing orthopedic implant applications.

关键词： Laser powder bed fusion Biomedical titanium alloy Corrosion Wear property Electrochemistry

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Designing polymer nanocomposites with high energy density using machine learning

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npj Computational materials 2021年第1期7卷 999-1007页

作者： Zhong-Hui Shen Zhi-Wei Bao Xiao-Xing Cheng Bao-Wen Li Han-Xing Liu Yang Shen Long-Qing Chen Xiao-Guang Li Ce-Wen Nan State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Center of Smart Materials and DevicesWuhan University of TechnologyWuhanChina International School of Materials Science and Engineering Wuhan University of TechnologyWuhanChina Hefei National Laboratory for Physical Sciences at the Microscale Department of Physics and CAS Key Laboratory of Strongly-Coupled Quantum Matter Physics University of Science and Technology of China HefeiChina Department of Materials Science and Engineering The Pennsylvania State UniversityUniversity ParkPAUnited States School of Materials Science and Engineering State Key Lab of New Ceramics and Fine ProcessingTsinghua UniversityBeijingChina

Addressing microstructure-property relations of polymer nanocomposites is vital for designing advanced dielectrics for electrostatic energy ***,we develop an integrated phase-field model to simulate the dielectric response,charge transport,and breakdown process of polymer ***,based on 6615 high-throughput calculation results,a machine learning strategy is schemed to evaluate the capability of energy *** find that parallel perovskite nanosheets prefer to block and then drive charges to migrate along with the interfaces in x-y plane,which could significantly improve the breakdown strength of polymer *** verify our predictions,we fabricate a polymer nanocomposite P(VDF-HFP)/Ca_(2)Nb_(3)O_(10),whose highest discharged energy density almost doubles to 35.9 J cm^(−3) compared with the pristine polymer,mainly benefit from the improved breakdown strength of 853 MVm^(−1).This work opens a horizon to exploit the great potential of 2D perovskite nanosheets for a wide range of applications of flexible dielectrics with the requirement of high voltage endurance.

关键词： polymer energy perovskite

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Microstructure and mechanical properties of B 4 C–TiB 2 –SiC-BN composites fabricated by in-situ reaction spark plasma sintering

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Journal of materials Research and technology 2025年 37卷 389-396页

作者： Zeping Wang Wen Zhang Jinyong Zhang Lin Ren Fan Zhang Weimin Wang Zhengyi Fu Hubei Longzhong Laboratory Wuhan University of Technology Xiangyang Demonstration Zone Xiangyang 441000 China State Key Laboratory of Advanced Technology for Materials Synthesis and Progressing. Wuhan University of Technology Wuhan 430070 China

B 4 C-TiB 2 -SiC-BN composites are fabricated by employing B 4 C, Si 3 N 4 , and TiC as raw powders via in-situ reaction spark plasma sintering. The densification behavior, microstructure, and mechanical properties of composites with different additive amounts of (Si 3 N 4 +TiC) are investigated. It is confirmed that the in-situ reaction during the sintering procedure of the composites effectively promotes the densification process. Toughening mechanisms including crack deflection, crack branching, crack bridging coupled with BN pull-out lead to the improvement of flexural strength and fracture toughness. As a result, the composites exhibit optimal performance when 15 wt% (Si 3 N 4 +TiC) are added, with the bulk density, flexural strength, fracture toughness and Vickers hardness of 2.59 g/cm 3 , 705 MPa, 4.4 MPa m 1/2 , and 27.8 GPa, respectively. This provides a novel route to preserve the lightweight characteristics and simultaneously enhance the mechanical performance of B 4 C-based composites.

关键词： B 4 C-TiB 2 -SiC-BN composites In-situ reaction Toughening mechanisms Mechanical properties

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Phosphorus modulated porous CeO_(2)nanocrystallines for accelerated polysulfide catalysis in advanced Li-S batteries

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Journal of materials Science & technology 2022年第36期131卷 212-220页

作者： Xuefeng Tao Zhao Yang Menghao Cheng Rui Yan Fan Chen Sujiao Cao Shuang Li Tian Ma Chong Cheng Wei Yang College of Polymer Science and Engineering State Key Laboratory of Polymer Materials EngineeringSichuan UniversityChengdu 610065China State Key Laboratory of Advanced Processing and Recycling of Non-ferrous Metals Lanzhou University of TechnologyLanzhou 730050China Department of Ultrasound National Clinical Research Center for GeriatricsWest China HospitalSichuan UniversityChengdu 610041China

The insulating nature of sulfur species,sluggish reaction kinetics,and uncontrolled dissolution of lithium polysulfide(LiPS)intermediates during the complex and multiphase sulfur redox process,have severely inhibited the applications of Li-S *** this study,we report a rational strategy to accelerate the polysulfide catalysis via constructing phosphorus modulated porous CeO_(2)(P-CeO_(2))for advanced Li-S *** morphology and surface analysis demonstrate that the P-CeO_(2)consists of abundant Pmodulated porous CeO_(2)*** battery performance reveals that the introduction of P will lead to an improved initial capacity of 1027 mA hg^(-1)than that of bare CeO_(2)(895.7 mA hg^(-1))at 0.2 *** addition,the P-CeO_(2)cathode can maintain a low capacity decay ratio of 0.10%per cycle after 500 cycles at 1.0 *** coin battery tests suggest that the P-CeO_(2)cathode presents faster oxidation-reduction kinetics of LiPS and quick diffusion of Li^+***,the studies of redox processes and chemical interactions of LiPS have demonstrated the P-CeO_(2)cathode displays stronger adsorption of Li_(2)S_(6),higher redox peak current,and earlier precipitation of Li_(2)S than the bare CeO_(2).This study demonstrates for the first time that the P-modulation of metal oxide surface can simultaneously promote the catalytic reaction kinetics and chemical interaction of *** anticipate that this P-modulation method can be extended to many other nanostructured metal catalytic sites for developing affordable advanced Li-S batteries.

关键词： Metal oxides P-modulated porous CeO_(2) Polysulfide catalytic materials Shuttle effects Lithium-sulfur batteries

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Multi-functional layered double hydroxides supported by nanoporous gold toward overall hydrazine splitting

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Frontiers of Chemical Science and Engineering 2024年第1期18卷 61-69页

作者： Yongji Qin Huijie Cao Qian Liu Shaoqing Yang Xincai Feng Hao Wang Meiling Lian Dongxing Zhang Hua Wang Jun Luo Xijun Liu ShenSi Lab Shenzhen Institute for Advanced StudyUniversity of Electronic Science and Technology of ChinaShenzhen 518110China Institute for New Energy Materials and Low-Carbon Technologies School of Materials Science and EngineeringTianjin University of TechnologyTianjin 300384China State Key Laboratory of Featured Metal Materials and Life-cycle Safety for Composite Structures Guangxi Key Laboratory of Processing for Non-ferrous Metals and Featured MaterialsSchool of ResourcesEnvironment and MaterialsGuangxi UniversityNanning 530004China Institute for Advanced Study Chengdu UniversityChengdu 610106China China National Coal Group Corporation Beijing 100120China Tianjin Engineering Research Center of Civil Aviation Energy Environment and Green Development School of Transportation Science and EngineeringCivil Aviation University of ChinaTianjin 300300China

Layered double hydroxides have demonstrated great potential for the oxygen evolution reaction,which is a crucial half-reaction of overall water ***,it remains challenging to apply layered double hydroxides in other electrochemical reactions with high efficiency and ***,we report two-dimensional multifunctional layered double hydroxides derived from metalorganic framework sheet precursors supported by nanoporous gold with high porosity,which exhibit appealing performances toward oxygen/hydrogen evolution reactions,hydrazine oxidation reaction,and overall hydrazine *** as-prepared catalyst only requires an overpotential of 233 mV to reach 10 mA·cm^(-2) toward oxygen evolution *** overall hydrazine splitting cell only needs a cell voltage of 0.984 V to deliver 10 mA·cm^(-2),which is far more superior than that of the overall water splitting system(1.849 V).The appealing performances of the catalyst can be contributed to the synergistic effect between the metal components of the layered double hydroxides and the supporting effect of the nanoporous gold substrate,which could endow the sample with high surface area and excellent conductivity,resulting in superior activity and stability.

关键词： layered double hydroxide oxygen evolution reaction hydrazine oxidation reaction overall hydrazine splitting hydrogen production

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Oriented Growth for Efficient and Scalable Perovskite Solar Cells by Vapor-Solid Reaction

SSRN

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SSRN 2023年

作者： Duan, Changyu Zhong, Jialing Hu, Shenghan Dou, Yichen Lu, Jianfeng Cheng, Yi-Bing Ku, Zhiliang State Key Laboratory of Advanced Technologies for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China State Key Laboratory of Silicate Materials for Architectures Wuhan University of Technology Wuhan430070 China

The precise control and understanding of crystal orientation in perovskite polycrystalline films are crucial for the development of efficient and stable devices. However, achieving this control remains a significant challenge. Herein, we have developed a PbI2 oriented growth strategy, combining with in-situ vapor-solid reaction transformations, to achieve oriented growth of full-vacuum perovskite films. GIWAXS analysis revealed the general pattern of PbI2 oriented vapor growth and in-situ vapor-solid reaction transformation in this two-step process. The resulting preferred orientation has effectively reduced trap states density, optimizing the carrier dynamics. As a result, champion efficiencies of 22.11% (0.148 cm2), 20.60% (1 cm2) and 19.41% (5 × 5 cm2 mini-modules) are achieved, which are the highest value for perovskite based on vapor-solid reaction. Additionally, the oriented growth method is applicable to a variety of guide layers and is extended to 30 × 30 cm2 film, demonstrating the universality and scalability of the method. © 2023, The Authors. All rights reserved.

关键词： Perovskite solar cells

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Boosting Ion Conduction and Moisture Stability Through Zn2+ Substitution of Chloride Electrolytes for All-Solid-state Lithium Batteries

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advanced Energy materials 2025年

作者： Lei, Peng Wu, Gang Liu, Hong Qi, Xiang Wu, Meng Li, Dabing Li, Yang Gao, Lei Nan, Ce-Wen Fan, Li-Zhen Beijing Key Laboratory for Advanced Energy Materials and Technologies Institute of Advanced Materials and Technology University of Science and Technology Beijing Beijing100083 China State Key Laboratory of New Ceramics and Fine Processing School of Materials Science and Engineering Tsinghua University Beijing100084 China

The recently emerged chloride solid electrolytes have garnered significant attention due to their superior ionic conductivity, wide electrochemical stability window, and exceptional compatibility with high-voltage oxide cathodes. Nevertheless, the currently cost-effective Zr-based chloride solid electrolytes face significant challenges, including low ionic conductivity and poor moisture stability. Herein, a versatile Zn2+-doped Zr-based chloride electrolyte is presented, designed to meet the aforementioned requirements. The optimized Li2.4Zr0.8Zn0.2Cl6 exhibits an improved ionic conductivity of 1.13 mS cm−1 at 30 °C. Simultaneously, the Li2.4Zr0.8Zn0.2Cl6 also demonstrates impressive moisture stability, maintaining its structural integrity after exposure to humid air. The mechanism underlying the enhanced moisture stability of Li2.4Zr0.8Zn0.2Cl6 is further elucidated by density functional theory calculations. Most notably, whether coupled with LiCoO2 or LiNi0.8Mn0.1Co0.1O2 cathodes, Li2.4Zr0.8Zn0.2Cl6-based all-solid-state batteries demonstrate exceptional cycling stability and rate performance. This high ionic conduction and moisture-resistant chloride electrolyte holds great promise for significantly advancing the commercialization of all-solid-state lithium batteries. © 2025 Wiley-VCH GmbH.

关键词： Solid-state Batteries

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Nonsolvent-Induced Electrospun Fibers with Crater-Like Surface and High-Loading Polytriphenylamine-Derived as a Flexible Cathode for Lithium-Ion Batteries

SSRN

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SSRN 2023年

作者： Xiong, Yufeng Li, Yingjiang Hu, Zhengfei Sun, Zhengquan Cheng, Yiliang Zhang, Yang Dong, Lijie Center for Smart Materials and Devices State Key Laboratory of Advanced Technology for Materials Synthesis and Processing School of Materials Science and Engineering Wuhan University of Technology Wuhan430070 China

Fabricating electrodes simultaneously possessing remarkable flexibility, excellent mechanical properties, and high energy density remains a significant challenge in flexible lithium-ion batteries (LIBs). Herein, a series of flexible organic composite films were prepared with high-loading polytriphenylamine (PTPA) and the derivatives (PTPA-PO) as active material, along with carbon nanotubes (CNTs) serving as conductive filler. The fabrication employed the polyethylene oxide (PEO) assisted nonsolvent (or poor solvent) induced phase separation electrospinning (NIPSE) method. Subsequently, the fiber morphology and electrochemical applications of the flexible organic composite films were systematically studied. Notably, the 60% PTPA-PO/20% CNTs/PEO flexible electrode with a high-loading active material of 60 wt% exhibits a significant discharge capacity of 146.6 mAh·g-1 and a favorable discharge platform ~ 3.7 V vs. Li. Furthermore, the inherent flexibility of electrode contributes to efficient and stable transport of ions and electrons, resulting in a fine capacity retention of 93.3% after 100 cycles. The improvement of electrochemical performance can be rationalized by the unique internal conductive network and crater-like surface structure of the fibers formed through the NIPSE method. This work provides an efficient method to fundamentally improve the energy storage performance and flexibility of LIBs. © 2023, The Authors. All rights reserved.

关键词： Electrospinning

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界面工程实现Au@MoS_(2)核壳异质结在等离激元学和光电子学领域卓越的热载流子输运动力学

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Science China materials 2023年第10期66卷 3931-3940页

作者：刘然朱翔宇刘盛洪欧阳德才马小茜夏芳芳余一梦张悍吴劲松刘世元梁文锡李渊翟天佑 State Key Laboratory of Materials Processing and Die&Mould Technology School of Materials Science and EngineeringHuazhong University of Science and TechnologyWuhan 430074China Wuhan National Laboratory for Optoelectronics Huazhong University of Science and TechnologyWuhan 430074China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Nanostructure Research CenterWuhan University of TechnologyWuhan 430070China School of Engineering and Materials Science Queen Mary University of LondonMile End RoadLondonE14NSUK State Key Laboratory of Digital Manufacturing Equipment and Technology School of Mechanical Science and EngineeringHuazhong University of Science and TechnologyWuhan 430074China Shenzhen Huazhong University of Science and Technology Research Institute Shenzhen 518057China

贵金属和二维半导体构建的异质结为等离激元纳米结构产生的热载流子提供了独特的电荷传输路径,有望应用于各种等离激元和光电子器件.然而,传统异质结构的电荷转移速度和效率通常受限于有限的界面面积和不可避免的界面污染.本文中,具有... 详细信息

贵金属和二维半导体构建的异质结为等离激元纳米结构产生的热载流子提供了独特的电荷传输路径,有望应用于各种等离激元和光电子器件.然而,传统异质结构的电荷转移速度和效率通常受限于有限的界面面积和不可避免的界面污染.本文中,具有原子级清洁和较大接触界面的新型Au@MoS_(2)核壳异质结构能够实现超快和高效的热电子转移.飞秒瞬态吸收光谱研究表明,Au@MoS_(2)中从金纳米颗粒到MoS_(2)的热电子注入时间常数小于244 fs,而机械转移方法制备的Au/MoS_(2)对照样品的热电子注入时间常数为493 fs,同时,电荷转移效率从Au/MoS_(2)的3.33%提升至Au@MoS_(2)的25.3%.开尔文探针力显微镜和离散偶极近似研究进一步证明了上述结果,明显改善的电荷转移归因于原子级清洁和完全封装的异质结界面.这项研究提供了贵金属-二维半导体异质结构内固有电荷转移的基本理解,从而展现了Au@MoS_(2)这一新型异质结结构在等离激元和光电子器件中的应用前景.

关键词： 2D materials MoS_(2) heterostructures optoelectronics plasmonics

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Solid-state stepwise temperature-programmable synthesis of bioinspired Fe-N-C oxygen reduction electrocatalyst featuring Fe-N_(5)configuration

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Nano Research 2025年第3期18卷 654-665页

作者： Wei Sang Somboon Chaemchuen Longyang Zhang Zechen Wang Xingchuan Li Cocoro Andrew Nagasaka Mo Xiong Naoki Ogiwara Cheng Chen Zhao Wang Jian Zhang Francis Verpoort Shichun Mu Zongkui Kou Tingting Wang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Department of Basic Science School of Arts and SciencesThe University of TokyoKomabaMeguro-kuTokyo 153-8902Japan MOE Key Laboratory for Non-Equilibrium Synthesis and Modulation of Condensed Matter School of PhysicsXi’an Jiao tong UniversityXi’an 710049China Sanya Science and Education Innovation Park of Wuhan University of Technology Sanya 572000China Department of Chemical Engineering Faculty of EngineeringMahidol UniversityNakhon Pathom 73170Thailand School of Mathematical&Physical Sciences Wuhan Textile UniversityWuhan 430200China Joint Institute of Chemical Research(FFMiEN) Peoples Friendship University of Russia(RUDN University)6 Miklukho-Maklaya Str.117198 MoscowRussia National Research Tomsk Polytechnic University Lenin Avenue 30634050 TomskRussia Hubei Key Laboratory of Ferro &Piezo-electric Materials and DevicesFaculty of Physics and Electronic SciencesHubei UniversityWuhan 430062China School of Chemistry and Chemical Engineering Hainan UniversityHaikou 57022China

The bioinspired Fe-N-C features an asymmetric Fe-N_(5)configuration to produce active metal-oxygen intermediates by introducing axial N ligand into a symmetric Fe-N_(4) structure,enabling highly active oxygen reduction reaction(ORR).However,the artificial creation of active Fe-N_(5)configuration with a direct,facile and green method has been rarely developed yet,as current techniques involve complex processes and costly ***,we advance a novel solid-state stepwise temperature-programmable(SST)route to directly produce bioinspired Fe-N_(5)-*** then demonstrate that such a Fe-N_(5)-C exhibits a quite higher half-wave potential(0.92 V)with 22-fold faster ORR kinetics(15.6 mA·cm^(−2)@0.85 V)over that of the commercial Pt/C ***,we perform density functional theory(DFT)to find that the Fe is discharged with an extra 0.1 e^(−)through the axially coordinate N ligand,which significantly enhances the ability to activate O_(2) and enables an easier desorption of the crucial intermediate ^(*)OH on the Fe-N_(5)configuration over the conventional Fe-N_(4) structure.

关键词： single atom catalysts Fe-N_(5)coordination solvent-free synthesis oxygen reduction reaction(ORR) metal-air battery

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