检索结果-内蒙古大学图书馆

Homologous CoS2 interface with directed electron transfer and strong chloridion repulsion for efficient seawater oxidation

引用

Science China Chemistry 2025年第5期68卷 1869-1878页

作者： Yuan Tian Jiang-Bo Chen Jie Ying Ge Tian Yu-Xuan Xiao Yi Lu Si-Ming Wu Wei Geng Ling Shen Xiao-Yu Yang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing and School of Materials Science and Engineeringand Shenzhen Research Institute & Laoshan LaboratoryWuhan University of Technology School of Chemical Engineering and Technology Sun Yat-sen University National Energy Key Laboratory for New Hydrogen-Ammonia Energy Technologies Foshan Xianhu Laboratory

Seawater electrolysis is a highly promising method to produce high energy density hydrogen,especially in dry areas that have scarce freshwater ***,application of seawater electrolysis is confronted by two major problems associated with catalysts employed for the anodic oxygen evolution reaction（OER） including the competitive hypochlorite evolution reaction（HCER） and strong chloridion（Cl-） triggered *** studies aimed at overcoming these problems,a facile method has been developed to synthesize a homologous CoS2heterojunction as an OER *** to a difference in work functions at the interface and increased electron density,this material has directed electron transfer and strong chloridion repulsion properties,*** have shown that CoS2achieves low overpotentials of 289 and 322 mV at 10 mA cm-2current density in respective alkaline（1 M KOH） and alkaline simulated seawater ***,the outstanding stability of CoS2is reflected in a negligible decline in activity during promotion of the OER for 100 *** of density functional theory calculations reveal that the homologous CoS2heterojunction promotes directed electron transport for optimizing adsorption/desorption of reactive species and heightens the Cl-adsorption energy for strongly repulsing Cl-,phenomena that enhance OER performance in alkaline simulated seawater.

关键词： metal sulfide homologous heterojunction directed transfer chloride ion repulsion seawater electrolysis

来源：评论

学校读者我要写书评

暂无评论

Low sintering shrinkage porous ceramics: Principles, progress, and perspectives

引用

Journal of advanced Ceramics 2025年第2期14卷 1-36页

作者： Jie Xu Yueqi Shao Xiaoying Feng Xiaoyan Zhang Hao Li Jinlong Yang Feng Gao State Key Laboratory of Solidification Processing MIIT Key Laboratory of Radiation Detection Materials and DevicesSchool of Materials Science and EngineeringNorthwestern Polytechnical UniversityXi’an 710072China Institute for Advanced Materials and Technology University of Science and Technology BeijingBeijing 100083China State Key Lab of New Ceramics and Fine Processing School of Materials Science and EngineeringTsinghua UniversityBeijing 100084China

Porous ceramics are lightweight materials with diverse pore structures and are widely applied in areas such as thermal insulation, sound absorption, filtration, catalysis, and energy storage. However, excessive shrinkage during the sintering process of porous ceramics leads to cracking and deterioration, posing significant challenges for achieving complex shapes. Despite its importance, the field of low sintering shrinkage porous ceramics has not received sufficient attention. This review systematically discusses the principles and progress in the development of low sintering shrinkage porous ceramics. First, we introduce the characteristics of various preparation methods, including partial sintering, particle-stabilized foaming, gel-casting, foam-gelcasting, and additive manufacturing (AM). We then explain three primary principles of low sintering shrinkage from the perspectives of the volume effect and mass transfer processes. This review focuses on the properties and applications of typical low sintering shrinkage ceramics such as mullite and alumina, particularly their mechanical properties and thermal conductivity as thermal insulation and ceramic cores. Finally, we summarize the current state and present future perspectives on low sintering shrinkage porous ceramics.

关键词： porous ceramics low sintering shrinkage volume expansion mass transfer process pore structure properties

来源：评论

学校读者我要写书评

暂无评论

Review and prospects on the low-voltage Na_(2)Ti_(3)O_(7) anode materials for sodium-ion batteries

引用

Journal of Energy Chemistry 2024年第1期88卷 446-460,I0011页

作者： Jun Dong Yalong Jiang Ruxing Wang Qiulong Wei Qinyou An Xiaoxing Zhang Hubei Key Laboratory for High-efficiency Utilization of Solar Energy and Operation Control of Energy Storage System Hubei University of TechnologyWuhan 430068HubeiChina State Key Laboratory of New Textile Materials and Advanced Processing Technologies Wuhan Textile UniversityWuhan 430200HubeiChina Xiamen Key Laboratory of High-Performance Metals and Materials College of MaterialsXiamen UniversityXiamen 361005FujianChina State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070HubeiChina

Due to its low cost and natural abundance of sodium,Na-ion batteries(NIBs)are promising candidates for large-scale energy storage *** development of ultralow voltage anode materials is of great significance in improving the energy density of ***-voltage anode materials,however,are severely lacking in *** all the reported insertion oxides anodes,the Na_(2)Ti_(3)O_(7) has the lowest operating voltage(an average potential of 0.3 V ***^(+)/Na)and is less likely to deposit sodium,which has excellent potential for achieving NIBs with high energy densities and high *** significant progress has been made,achieving Na_(2)Ti_(3)O_(7) electrodes with excellent performance remains a severe *** paper systematically summarizes and discusses the physicochemical properties and synthesis methods of Na_(2)Ti_(3)O_(7).Then,the sodium storage mechanisms,key issues and challenges,and the optimization strategies for the electrochemical performance of Na_(2)Ti_(3)O_(7) are classified and further ***,remaining challenges and future research directions on the Na_(2)Ti_(3)O_(7) anode are *** review offers insights into the design of high-energy and high-safety NIBs.

关键词： Sodium-ion batteries Low-voltage anode materials Na_(2)Ti_(3)O_(7) Electrochemical performances Electrochemical mechanism

来源：评论

学校读者我要写书评

暂无评论

Structural and Luminescent Properties of Mg_(0.25-x)Al_(2.57)O_(3.79)N_(0.21):xMn^(2+)Green-Emitting Transparent Ceramic Phosphor

引用

Journal of Wuhan University of technology(materials Science) 2024年第3期39卷 533-540页

作者：郝留成 MIAO Xiaojun LI Kai ZHONG Jianying 涂兵田 YANG Zhangfu 王皓 Pinggao Group Co. LtdPingdingshan 467001China State Key Lab of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Hubei Longzhong Laboratory Xiangyang 430070China School of Materials Science and Engineering Anhui University of Science and TechnologyHuainan 232001China

A series of spinel-type Mg_(0.25-x)Al_(2.57)O_(3.79)N_(0.21):xMn^(2+)(MgAlON:xMn^(2+))phosphors were synthesized by the solid-state reaction *** transparent ceramic phosphors were fabricated by pressureless sintering followed by hot-isostatic pressing(HIP).The crystal structure,luminescence and mechanical properties of the samples were systematically *** transparent ceramic phosphors with tetrahedrally coordinated Mn^(2+)show strong green emission centered around 515 nm under blue light *** the Mn^(2+)concentration increases,the crystal lattice expands slightly,resulting in a variation of crystal field and a slight red-shift of green emission *** weak absorption peaks in the transmittance spectra originate from the spin-forbidden ^(4)T_(1)(^(4)G)→^(6)A_(1) transition of Mn^(2+).The decay time was found to decrease from 5.66 to 5.16 ms with the Mn^(2+)*** present study contributes to the systematic understanding of crystal structure and properties of MgAlON:xMn^(2+)green-emitting transparent ceramic phosphor which has a potential application in high-power light-emitting diodes.

关键词： transparent ceramic phosphor green emission MgAlON photoluminescence

来源：评论

学校读者我要写书评

暂无评论

Molecular Engineering of g-C_(3)N_(4)with Dibenzothiophene Groups as Electron Donor for Enhanced Photocatalytic H_(2)-Production

引用

Chinese Journal of Structural Chemistry 2022年第6期41卷 48-54页

作者： Shanren Tao Sijie Wan Qinyang Huang Chengming Li Jiaguo Yu Shaowen Cao State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

The construction of donor-acceptor(D-A)molecular structure is an attractive strategy to enhance the photocatalytic performance of polymeric ***,dibenzothiophene(DBT)-4-carbaldehyde as the precursor is introduced into g-C_(3)N_(4)(TCN)prepared by two-step thermal polymerization to construct an intramolecular D-A type copolymer(TCN-DBT_(x)).DFT calculation and experimental results reveal that DBT plays the role of electron donor unit to modify g-C_(3)N_(4).The incorporation of DBT not only adjusts the band gap to improve reduction ability,but also induces an internal electric field with extendingπ-conjugated system for effective charge *** a result,TCN-DBT_(x)exhibits much better photocatalytic performance with an optimal hydrogen production rate of 3334μmol h^(-1)g^(-1),which is 2.5 times that of *** work provides a protocol for preparing high-performance g-C_(3)N_(4)-based photocatalysts toward various applications.

关键词： carbon nitride donor-acceptor photocatalysis charge transfer

来源：评论

学校读者我要写书评

暂无评论

Graphitic carbon nitride/La,Rh co-doped SrTiO_(3)S-scheme heterojunction for photocatalytic CO_(2)reduction

引用

Rare Metals 2024年第11期43卷 5880-5890页

作者： Si-Jie Wan Yan-Ting Hou Wang Wang Guo-Qiang Luo Chuan-Bin Wang Rong Tu Shao-Wen Cao Chaozhou Branch of Chemistry and Chemical Engineering Guangdong Laboratory Chaozhou 521000China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Hubei Technology Innovation Center for Advanced Composites Wuhan University of TechnologyWuhan 430070China

Photocatalytic reduction of CO_(2)has attracted considerable interest owing to its potential to resolve the energy and environmental ***,the lack of proficient photocatalysts has restricted the application of solar-driven photocatalytic CO_(2)***,we reported an S-scheme heterojunction by combining g-C_(3)N_(4)with La^(3+)and Rh^(3+)co-doped SrTiO_(3)through the electrostatic self-assembly method for the efficient photocatalytic CO_(2)*** comparison with g-C_(3)N_(4),the asprepared CN/LRSTO-30 wt%S-scheme heterojunction not only possesses a broadened visible-light response due to the defect states in La,Rh co-doped SrTiO_(3)induced by codoped La^(3+)and Rh^(3+)but also has more adsorption sites for the capture and activation of CO_(2)***,separation and transfer efficiency of the photoinduced charge carriers is much enhanced in the CN/LRSTO-30wt%S-scheme heterojunction via its robust internal electric field,which is firmly demonstrated by in situ irradiation X-ray photoelectron spectroscopy ***,the prepared S-scheme heterojunction achieves impressive photocatalytic CO_(2)reduction performance with an average CO and CH4 evolution rate of4.1-1.8μmol·g^(-1)·h^(-1),respectively,which are~1.9 and~22.5-fold higher than those of pure g-C_(3)N_(4).This study provides innovative perspectives on the design of creative S-scheme heterojunctions for applications in photocatalytic CO_(2)reduction.

关键词： g-C_(3)N_(4) La Rh co-doped SrTiO_(3) S-scheme heterojunction Separation of photogenerated charge carriers Photocatalytic CO_(2)reduction

来源：评论

学校读者我要写书评

暂无评论

Microstructure and Mechanical Property of (TiNbTaZrHf)C Synthesized by In-situ Reaction

引用

Journal of Wuhan University of technology(materials Science) 2022年第2期37卷 177-183页

作者： ZHOU Qing ZHANG Jinyong FU Zhengyi WANG Dangqiang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

The(TiNbTaZrHf)C high entropy carbide(HEC)was successfully synthesized by complete commercial transition metal powders,obtained fine sintered bulks without additives by in-situ reaction element synthesis method.(TiNbTaZrHf)C bulk shows a face centered cubic rock salt structure with homogeneous single-phase FCC structure in composition and *** optimum sintering temperature is about 1900℃at which the best mechanical properties are *** mechanical properties of(TiNbTaZrHf)C ceramic block are better than those of binary transition metal carbides,and it has obvious high entropy *** a small amount of Al as sintering additive,the mechanical properties of(TiNbTaZrHf)C ceramics continue to improve,the bending strength of the samples at each temperature is increased by at least 38%,and the highest is 486 *** elastic modulus and hardness of the sample at 1900℃are also slightly increased by 4%and 14%,*** above conclusions illustrate that the properties of high entropy ceramics are greatly improved by in-situ reaction sintering.

关键词： high entropy carbide in-situ reaction microstructure mechanical property sintering additive

来源：评论

学校读者我要写书评

暂无评论

Isomeric Fluorene-based Heteroundecenes with Different Side Chains Anchoring Positions for Small Molecule Acceptors

引用

Journal of Wuhan University of technology(materials Science) 2022年第1期37卷 136-147页

作者： WANG Wei ZHAN Chun XIAO Shengqiang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

Two isomeric fluorene-based heteroundecenes of bis(thienocyclopenthieno[3,2-b]thieno)fluorene(BT2T-F)and bis(dithieno[3,2-b:2’,3’-d]thiophene)cyclopentafluorene(B3T-F)have been designed and *** side chains of 4-hexylphenyl anchor on the 5th and 8th positions in B3T-F while on the 4th and 9th positions in BT2T-F,in which the former is closer to the center of the fused *** corresponding acceptor-donor-acceptor(A-D-A)type small molecule acceptors(SMAs)of BT2T-FIC and B3T-FIC were prepared by linking BT2T-F and B3T-F as fused ring donor units with the acceptor unit of 2-(5,6-difluoro-3-oxo-2,3-dihydroinden-1-ylidene)malononitrile(IC-2F),respectively.B3T-FIC presents a superior crystallinity with intense face-on π-π stacking in its neat film while BT2T-FIC is more *** blended with PBDB-T-2Cl as a polymer donor,the optimized PBDB-T-2Cl:BT2T-FIC device exhibits an averaged power conversion efficiency(PCE)of 10.56%while only 7.53%in the PBDB-T-2Cl:B3T-FIC *** improved short-circuit current(J_(sc))and fill factor(FF)of the PBDB-T-2Cl:BT2T-FIC device are the main contribution of its higher performance,which is attributed to its more efficient and balanced charge transport and better carrier recombination *** that BT2T-FIC blend and B3T-FIC blend films both take a preferential face-on orientatedπ-πstacking with comparable distances,the suitable SMA domain size obtained in the BT2T-FIC blend could account for its more efficient photovoltaic *** results highlight the importance of side-chain strategy in developing efficient SMAs with huge fused ring cores.

关键词： polymer solar cells small molecule acceptor side chains morphology

来源：评论

学校读者我要写书评

暂无评论

Pressureless densification and properties of high-entropy boride ceramics with B_(4)C additions

引用

Journal of materials Science & technology 2024年第23期190卷 1-9页

作者： Fawei Wang Liang Xu Ji Zou Jingjing Liu Huayue Liang Wei Ji Weimin Wang Zhengyi Fu Hubei Longzhong Laboratory Wuhan University of Technology Xiangyang Demonstration ZoneXiangyang 441000China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China School of Materials Science and Engineering Wuhan University of TechnologyWuhan 430070China

High entropy boride ceramics have great potential as structural materials serving in extreme ***,their applications are limited by the difficulty of *** the present study,dense(Ti_(0.2)Zr_(0.2)Hf_(0.2)Nb_(0.2)Ta_(0.2))B_(2)ceramics with B_(4)C additions were prepared through pressureless sintering at as low as 1900℃.Calculations based on the CALPHAD approach predict that(Ti_(0.2)Zr_(0.2)Hf_(0.2)Nb_(0.2)Ta_(0.2))B_(2)starts to melt at about 3315℃whilst B_(4)C additions reduce the temperature and broaden the tempera-ture region where solid and liquid *** showed that the introduction of B_(4)C could trigger the densification of(Ti_(0.2)Zr_(0.2)Hf_(0.2)Nb_(0.2)Ta_(0.2))B_(2)at a lower temperature and promote their densification *** relative density of samples with 5 wt%of B_(4)C additions sintered at 1900 and 2000℃was 97.7%and 99.7%,*** the sintering temperature was further increased to 2100℃,the liquid phase was reactively formed,leading to the rapid grain coarsening in samples with B_(4)C *** by well-dispersed B_(4)C grains,the sample with 5 wt%B_(4)C sintered at 2000℃exhibited excellent mechanical properties with the Vickers hardness,flexural strength,and fracture toughness of 21.07±2.09 GPa,547±45 MPa,and 5.24±0.14 MPa m^(1/2),which are comparable or even higher than counterparts sintered under pressure.

关键词： High entropy boride ceramic Microstructure Pressureless sintering Densification Mechanical properties

来源：评论

学校读者我要写书评

暂无评论

synthesis of magnetic targeted delivery microcapsules and its anti-corrosion self-healing behavior in epoxy resin coatings

引用

Corrosion Communications 2023年第2期10卷 27-37页

作者： Yingxiang Ma Dan Jiang Yuping Yang Li Ma Jian Zhou Guosheng Huang Cunguo Lin State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology State Key Laboratory for Marine Corrosion and Protection Luoyang Ship Material Research Institute

This study proposed a tung-oil based magnetic targeted delivery microcapsules （MDTMs） to enhance the efficiency of self-healing coatings （SHC）.Magnetic particles were used as function particles and emulsifier in synthesis of microcapsules （MC）.DSC,OM,SEM,TEM,VSM,NSS,EIS and SKP were used to characterize the compounds,structure,healing behavior and anti-corrosion *** indicate that magnetically driven SHC （MD-SHC） reduces 50%migration path of the released tung oil,and increases the release rate of tung oil after the coating is mechanically *** and EIS results suggest that the healing part has impressive anti-corrosion performance,scratches were filled with a large amount of tung oil in a short time,and the released tung oil had formed a complete oil film on scratches at 24 h with higher polarization resistance （Rp）.Rpof MD-SHC（2.5×10～5–3.6×10～5Ωcm2） is 2.0–2.8 times of that the SHC （1.1×10～5–1.8×10～5Ωcm2）.The enrichment in MD-SHC at the interface decreases bonding strength from 7 to 4.5 MPa as the mass additive of microcapsules reaches 15 wt.%.The current work proves the effectiveness of MD-SHC in improving self-healing ability.

关键词： Self-healing coatings Corrosion Microcapsules Magnetic particle Electrochemical impedance spectroscopy

来源：评论

学校读者我要写书评

暂无评论

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

请选择保存的检索档案：

请选择收藏分类：

通借通还

建议与咨询 留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

请选择保存的检索档案： 新增检索档案 确定 取消

请选择收藏分类： 新增自定义分类 确定 取消

通借通还

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

请选择保存的检索档案：

请选择收藏分类：