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High-entropy alloy nanocrystals boosting photocatalytic hydrogen evolution coupled with selective oxidation of cinnamyl alcohol

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Chinese Journal of Catalysis 2025年第1期68卷 326-335页

作者： Xianglin Xiang Bei Cheng Bicheng Zhu Chuanjia Jiang Guijie Liang Faculty of Materials Science and Engineering Kunming University of Science and TechnologyKunming 650093YunnanChina State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070HubeiChina Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of GeosciencesWuhan 430078HubeiChina College of Environmental Science and Engineering Nankai UniversityTianjin 300350China Hubei Key Laboratory of Low Dimensional Arts and Science Hubei University of Arts and ScienceXiangyang 441053HubeiChina

Photocatalysis provides a promising solution to the worldwide shortages of energy and industrially important raw materials by utilizing sunlight for coupled hydrogen(H_(2))production with controllable organic ***,we demonstrate that PtFeNiCoCu high-entropy alloy(HEA)nanocrystals can act as efficient cocatalysts for H_(2)evolution coupled with selective oxidation of cinnamyl alcohol to cinnamaldehyde by cubic cadmium sulfide(CdS)quantum dots(QDs)with uniform sizes of 4.0±0.5 *** nanocrystals were prepared via a simple solvothermal approach,and were successfully integrated with CdS QDs by an electrostatic self-assembly method to construct HEA/CdS *** optimized HEA/CdS sample presented an enhanced photocatalytic H_(2)production rate of 7.15 mmol g^(-1)h^(-1),which was 13 times that of pure CdS ***,a cinnamyl alcohol conversion of 96.2%with cinnamaldehyde selectivity of 99.5%was achieved after photoreaction for 3 *** integration of HEA with CdS QDs extended the optical absorption edge from 475 to 484 *** d-band center analysis,Pt atoms in the HEA are the active sites for H_(2)evolution,exhibiting higher catalytic activity than pure ***,the band structure of the CdS QDs enables the oxidative transformation of cinnamyl alcohol to cinnamaldehyde with high ***,femtosecond transient absorption spectroscopy shows that HEA can significantly promote the separation of photogenerated carriers in CdS,which is vital for achieving enhanced photocatalytic *** work inspires atomic-level design of photocatalytic materials for coordinated production of green energy carriers and value-added products.

关键词： Artificial photosynthesis d-Band center Photocatalytic hydrogen evolution Quantum dots Value-added organic synthesis

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Flexible three-dimensional-networked iron vanadate nanosheet arrays/carbon cloths as high-performance cathodes for magnesium ion batteries

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Science China materials 2022年第8期65卷 2197-2206页

作者： Han Tang Chunli Zuo Fangyu Xiong Cunyuan Pei Shuangshuang Tan Ping Luo Wei Yang Qinyou An Liqiang Mai State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and EngineeringWuhan University of TechnologyWuhan 430070China Hubei Provincial Key Laboratory of Green Materials for Light Industry Collaborative Innovation Center of Green Light-Weight Materials and ProcessingSchool of Materials and Chemical EngineeringHubei University of TechnologyWuhan 430070China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Foshan 528200China

Owing to their safety and low cost,magnesium ion batteries(MIBs)have attracted much attention in recent ***,the sluggish diffusion dynamics of magnesium ions hampers the search for appropriate cathode materials with excellent electrochemical ***,we design and synthesize a novel flexible three-dimensional-networked composite of iron vanadate nanosheet arrays/carbon cloths(3 D FeVO/CC)as a binder-free cathode for *** to bare FeVO nanosheets,the 3 D binder-free electrode with designed architecture enables a full range of electrochemical potential,including a high specific capacity of270 mA h g^(-1) and an increased life span(over 5000 cycles).Such achievable high-density energy originates from the synergistic optimization of electron and ion kinetics,while the durability benefits from the robust structure that prevents degradation in *** single-phase reaction mechanism of FeVO in the magnesium ion storage process is also explored by in-situ X-ray diffraction and Raman ***,a flexible MIB pouch cell(3 D FeVO/CCIMgNaTi_(3)O_(7)) is assembled and exhibits practical application *** work verifies that 3 D FeVO/CC is a potential candidate cathode material that can satisfy the requirements of highperformance *** also opens a new avenue to improve the electrochemical performance of cathode materials for MIBs.

关键词： iron vanadate nanosheet arrays flexibility cathode materials magnesium ion batteries

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Textured silicon nitride ceramics with enhanced properties fabricated by high pressure sintering

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Ceramics International 2025年

作者： Tao, Haoyu Qin, Xiaowei Sui, Jiahua Zou, Ji Wang, Weimin Ji, Wei Fu, Zhengyi Hubei Longzhong Laboratory Wuhan University of Technology Xiangyang Demonstration Zone Xiangyang China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China

Silicon nitride (Si3N4) ceramics with a textured morphology were prepared via high-pressure sintering in this study. The mechanical and thermal properties of the prepared materials in different orientations were investigated. Compared with the Si3N4 ceramics prepared at 1700 °C under low pressure of 50 MPa, the specimens prepared under high pressure of 200 MPa showed an obvious textured microstructure and a high fracture toughness (8.2 ± 0.5 MPa m1/2). Especially, the thermal conductivity was determined to be 105 W m−1 K−1 along the texture direction and 64 W m−1 K−1 in the vertical direction, respectively. The as-prepared Si3N4 with a morphological texture was anisotropic in hardness and toughness. High temperature and high pressure played a crucial role in the formation of Si3N4 ceramic texture and the enhancement of comprehensive properties. © 2025 Elsevier Ltd and Techna Group S.r.l.

关键词： Fracture toughness

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Pressure-controlled synergy between dehydrogenation and densification in TiH2 sintering

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Journal of the European Ceramic Society 2025年第14期45卷

作者： Hu, Tianxiao Lin, Mengting Zou, Ji Wang, Weimin Ji, Wei Fu, Zhengyi Hubei Longzhong Laboratory Wuhan University of Technology Xiangyang Demonstration Zone Xiangyang China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China

Titanium hydride (TiH2) ceramics have become key high-performance hydrogen storage materials. However, the sintering of TiH2 faces significant challenges due to the low temperature of dehydrogenation reaction (300–800 °C). In this study, high-pressure spark plasma sintering (HPSPS) technique was employed to successfully realize low-temperature high-density preparation by suppressing dehydrogenation and regulating densification kinetics under a high pressure (200 MPa). Under the optimized conditions (750 °C, 200 MPa, and 10 min), a fully dense single face-centered cubic (FCC) δ-Ti(H) phase bulk material was fabricated. The initial dehydrogenation temperature of samples fabricated by high-pressure spark plasma sintering (HPSPS) was higher than the dehydrogenation temperature of powder. Mechanistic analyses showed that high pressure inhibited hydrogen escape by compressing pores while promoting particle plastic flow and interfacial bonding. Increasing holding time from 5 to 10 min enhanced diffusion-dominated densification but exacerbated dehydrogenation-induced porosity under low-pressure conditions. The study shows that high pressure compaction can alleviate the contradiction between traditional high temperature densification and low temperature decomposition of TiH2, and offers a new strategy for the efficient densification of materials for low temperature decomposition. © 2025 Elsevier Ltd

关键词： Densification

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Magnetic field-enhanced photoelectrochemical water splitting of Co_(3)O_(4)/TiO_(2)for efficient oxygen evolution

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Science China materials 2024年第10期67卷 3168-3175页

作者： Ze-En Zhou Yi Lu Yi-Xuan Liu Shang Cao Ge Tian Zhi-Yi Hu Ling Shen Si-Ming Wu Jie Ying Wei Geng Xiao-Yu Yang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing&Shenzhen Research Institute&Laoshan Laboratory Wuhan University of TechnologyWuhan 430070China National Energy Key Laboratory for New Hydrogen-Ammonia Energy Technologies Foshan Xianhu LaboratoryFoshan 528200China Nanostructure Research Centre(NRC) Wuhan University of TechnologyWuhan 430070China School of Chemical Engineering and Technology Sun Yat-sen UniversityZhuhai 519082China

Effective separation of photogenerated carriers plays a vital role in governing the efficiency of photo-electrocatalytic ***,the advancement in enhancing the intrinsic carrier separation efficiency of semiconductors has shown limited ***,we reported the use of a magnetic field to improve the photoelectrochemical water splitting of a magnetic Co_(3)O_(4)/TiO_(2)photoanode by boosting the photogenerated carrier separation *** the presence of the magnetic field,oxygen evolution reaction occurs with a high photocurrent density of 0.86 mA cm^(−2)at 1.23 V versus VRHE,and an applied bias photon-to-current efficiency of 0.342%at 0.61 ***,the photoanode maintains its oxygen evolution reaction for more than 400 h with photocurrent decays by ca.10%.Observations made in this effort show that the enhancement of photo-electrocatalytic efficiency by a magnetic field is a consequence of the effect of the Lorentz force generated by the magnetic field on photogenerated carriers and ions near the Co_(3)O_(4)/TiO_(2)photoanode,which improves the carrier separation efficiency and the bubble release *** results suggest that manipulating photoelectrode carriers by using a magnetic field is a promising strategy to design high-performance photoelectrochemical for water splitting.

关键词： photoelectrochemical water splitting Co_(3)O_(4)/TiO_(2) carrier separation efficiency stability

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Defect Engineering on Carbon‑Based Catalysts for Electrocatalytic CO2 Reduction

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Nano-Micro Letters 2021年第1期13卷 56-78页

作者： Dongping Xue Huicong Xia Wenfu Yan Jianan Zhang Shichun Mu College of Materials Science and Engineering Zhengzhou UniversityZhengzhou 450001People’s Republic of China State Key Laboratory of Inorganic Synthesis and Preparative Chemistry and College of ChemistryJilin University2699 Qianjin StreetChangchun 130012People’s Republic of China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070People’s Republic of China

Electrocatalytic carbon dioxide(CO2)reduction(ECR)has become one of the main methods to close the broken carbon cycle and temporarily store renewable energy,but there are still some problems such as poor stability,low activity,and *** the most promising strategy to improve ECR activity is to develop electrocatalysts with low cost,high activity,and long-term ***,defective carbon-based nanomaterials have attracted extensive attention due to the unbalanced electron distribution and electronic structural distortion caused by the defects on the carbon ***,the present review mainly summarizes the latest research progress of the construction of the diverse types of defects(intrinsic carbon defects,heteroatom doping defects,metal atomic sites,and edges detects)for carbon materials in ECR,and unveil the structure-activity relationship and its catalytic *** current challenges and opportunities faced by high-performance carbon materials in ECR are discussed,as well as possible future *** can be believed that this review can provide some inspiration for the future of development of high-performance ECR catalysts.

关键词： Electrocatalytic CO2 reduction Carbon-based nanomaterials Intrinsic defects Heteroatom doping defects Metal atomic sites

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Structure and enhanced dielectric temperature stability of BaTiO3- based ceramics by Ca ion B site-doping

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Journal of Materiomics 2021年第2期7卷 295-301页

作者： Xuewen Jiang Hua Hao Yang Yang Enhao Zhou Shujun Zhang Ping Wei Minghe Cao Zhonghua Yao Hanxing Liu Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Xianhu Hydrogen ValleyFoshan528200China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing School of Materials Science and EngineeringWuhan University of TechnologyWuhan430070China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Material Science and EngineeringWuhan University of TechnologyWuhan430070China Institute for Superconducting and Electronic Materials Australian Institute of Innovative MaterialsUniversity of WollongongWollongongNSW2500Australia Nanostructure Research Centre Wuhan University of TechnologyWuhan430070China

Capacitor is an important part of many electronic devices,so the temperature stability as one key parameter of capacitor needs to be improved constantly for meeting the requirements of various application ***,combined with the X-ray diffraction(XRD),selected area electron diffraction(SAED)and Vienna Ab-initio Simulation Package(VASP)calculation,it was confirmed that Ca ion can substitute the Ti site in the BaTi1-xCaxO3-x[BTC100](0≤x≤0.05)ceramics synthesized by solid-phase method which greatly improved the low-temperature stability of dielectric ***,introducing Bi3þand Zn^(2+) into BTC4 to form(1-y)BaTi0.6Ca0.04O2.96-yBi(Zn_(0.5)Ti_(0.5))O_(3)[(1-y)BTC4-yBZT](0.1≤y≤0.2)ceramics can further improve the dielectric-temperature stability by means of diffused phase transition and core-shell *** importantly,the 0.85BTC4-0.15BZT ceramics with a pseudocubic perovskite structure possessed a temperature coefficient of capacitance at 25℃(TCC25℃)being less than±15%over a wide temperature range of 55℃-200℃and a temperate dielectric constant(ε=1060)and low dielectric loss(tanδ=1.5%),which measure up to the higher standard in the current capacitor industry such as X9R requirements.

关键词： BaTiO3 Ca substituted X9R capacitors Dielectric properties

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Nitrogen‐doped tin oxide electron transport layer for stable perovskite solar cells with efficiency over 23%

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Interdisciplinary materials 2022年第2期1卷 309-315页

作者： Yanping Mo Chao Wang Xuntian Zheng Peng Zhou Jing Li Xinxin Yu Kaizhong Yang Xinyu Deng Hyesung Park Fuzhi Huang Yi‐Bing Cheng State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhanP.R.China Solar Hydrogen Production Lab Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong LaboratoryFoshanP.R.China International School of Materials Science and Engineering Wuhan University of TechnologyWuhanP.R.China Department of Materials Science and Engineering Graduate School of Semiconductor Materials and Devices EngineeringPerovtronics Research CenterLow Dimensional Carbon Materials CenterUlsan National Institute of Science and TechnologyUlsanRepublic of Korea

Tin oxide has made a major breakthrough in high-efficiency perovskite solar cells(PSCs)as an efficient electron transport layer by the low-temperature chemical bath deposition ***,tin oxide often contains pernicious defects,resulting in unsatisfactory ***,we develop high-quality tin oxide films via a nitrogen-doping strategy for high-efficiency and stable planar *** aligned energy level at the interface of doped SnO_(2)/perovskite,more excellent charge extraction and reduced nonradiative recombination contribute to the enhanced efficiency and ***,the power conversion efficiency of the devices based on N‐SnO_(2) film increases to 23.41% from 20.55% of the devices based on the pristine SnO_(2).The N-SnO_(2) devices show an outstanding stability retaining 97.8% of the initial efficiency after steady-state output at a maximum power point for 600s under standard AM1.5G continuous illumination without encapsulation,while less than 50% efficiency remains for the devices based on pristine SnO_(2).This simple scalable strategy has shown great promise toward highly efficient and stable PSCs.

关键词： electron transport layer N doping perovskite solar cell SnO_(2)

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Achieving enhanced thermoelectric and mechanical performance in p-type bismuth telluride through constrained hot deformation

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Ceramics International 2025年

作者： Chen, Quansheng Ji, Chen Yu, Jian Hua, Lin Zhao, Wenyu State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China School of Automotive Engineering Wuhan University of Technology Wuhan430070 China School of Materials Science and Engineering Jiujiang University Jiujiang332005 China Hubei Key Laboratory of Advanced Technology for Automobile Components Wuhan University of Technology Wuhan430070 China

Bi2Te3-based alloys remain the only commercially available thermoelectric (TE) materials. However, their practical applications are severely constrained by the inferior mechanical performance of the zone melting (ZM) ingot. Herein, a simple constrained hot deformation (CHD) technology was developed to prepare the p-type Bi0.5Sb1.5Te3 polycrystalline materials derived from ZM ingots. It was discovered that the deformation process has negligible impact on the phase composition, but can efficiently refine the grains to approximately 5 μm through the dynamic recrystallization and simultaneously introduce high-density dislocations. Although the donor-like effect induced by deformation would obviously deteriorate the electrical conductivity, the recovery effect triggered by high deformation temperature can effectively optimize the carrier concentration and thus alleviate the degradation of power factor. The material deformed at 773 K maintains a relatively high power factor ∼3.33 mW K−2 m−1 at 300 K, together with a significantly decreased lattice thermal conductivity ∼0.59 W m−1 K−1, and an improved zT ∼1.1 was obtained ultimately. More importantly, the deformed materials show a significant improvement in mechanical performance due to the grain refinement. A maximum average Vickers hardness of 0.67 GPa was achieved for the material deformed at 723 K, which is ∼40 % higher than that of the ZM ingot. Our work indicates the simple CHD is an efficient technology to synergistically enhance both TE and mechanical properties of Bi2Te3-based ZM ingot. © 2025 Elsevier Ltd and Techna Group S.r.l.

关键词： Polycrystalline materials

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One-step preparation of porous aminated-silica nanoparticles and their antibacterial drug delivery applications

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Journal of materials Science & technology 2020年第15期47卷 139-146页

作者： Yongren Wu Shun Chen Yang Liu Zhiwei Lu Shaokun Song Yang Zhang Chuanxi Xiong Lijie Dong Center for Smart Materials and Devices State Key Laboratory of Advanced Technology for Materials Synthesis and ProcessingWuhan University of TechnologyWuhan430070China

Porous functionalized silica nanoparticles have attracted the interest of researchers as they are excellent carriers for antibacterial drug delivery *** this work,porous aminated-silica nanoparticles(SiO2-NH2 NPs) were prepared via one-step approach through the ammonia-catalyzed hydrolysis of tetraethylorthosilicate(TEOS) and(3-aminopropyl) triethoxysilane(APTES) in a mixed water-ethanol *** obtained SiO2-NH2 NPs displayed a spherical morphology and relatively uniform size distribution,while the morphology and structure of SiO2-NH2 NPs were mainly determined by the order of the reagents added and the pH value of the *** characterization,the results showed that there were a large number of-NH2 groups on the surface of porous SiO2-NH2 NPs and that the porous SiO2-NH2 NPs had a large surface area of 476 m2 g-1 with an average pore width of 4.3 *** an absorbing-releasing experiment and bacterial test,those SiO2-NH2 NPs were found to exhibit efficient absorption and release of drugs as well as a pH-de pendent release pattern of epirubicin-loaded SiO2-NH2 ***,SiO2-NH2@capsaicin NPs exhibited antibacterial *** porous SiO2-NH2 NPs could be a candidate for drug delivery for antibacterial applications owing to their tailored porous structure and high surface area.

关键词： Porous aminated-silica nanoparticles Surface area Drug delivery Antibacterial property

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