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Spatial confinement of free-standing graphene sponge enables excellent stability of conversion-type Fe_(2)O_(3)anode for sodium storage

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Chinese Chemical Letters 2025年第3期36卷 544-549页

作者： Jun Dong Senyuan Tan Sunbin Yang Yalong Jiang Ruxing Wang Jian Ao Zilun Chen Chaohai Zhang 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 430068China State Key Laboratory of New Textile Materials and Advanced Processing Technologies Wuhan Textile UniversityWuhan 430200China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Nanjing University of Aeronautics and Astronautics Nanjing 210016China

Conversion-type anode materials are highly desirable for Na-ion batteries(NIBs)due to their high theoretical ***,the active materials undergo severe expansion and pulverization during the sodiation,resulting in inferior cycling ***,a self-supporting three-dimensional(3D)graphene sponge decorated with Fe_(2)O_(3)nanocubes(rGO@Fe_(2)O_(3))is ***,the 3D graphene sponge with resilience and high porosity benefits to accommodate the volume expansion of the Fe_(2)O_(3)nanocubes and facilitates the rapid electrons/ions transport,enabling spatial confinement to achieve outstanding ***,the free-standing rGO@Fe_(2)O_(3)can be directly used as an electrode without additional binders and conductive additives,which helps to obtain a higher energy *** on the total mass of the rGO@Fe_(2)O_(3)material,the rGO@Fe_(2)O_(3)anode presents a specific capacity of 859 mAh/g at 0.1 A/*** also delivers an impressive cycling performance(327 mAh/g after 2000 cycles at 1 A/g)and a superior rate capacity(162mAh/g at 20 A/g).The coin-type Na_(3)V_(2)(PO_(4))_(3)@C//rGO@Fe_(2)O_(3)NIB exhibits an energy density of 265.3Wh/*** unique 3D ionic/electronic conductive network may provide new strategies to design advanced conversion-type anode materials for high-performance NIBs.

关键词： Conversion-type anode Spatial confinement Fe_(2)O_(3) Graphene network Self-supporting Sodium-ion batteries

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NaTiO_(x)-modified high-nickel layered oxide cathode for stable sodium-ion batteries

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Carbon Energy 2025年第1期7卷 283-291页

作者： Yingcong Liu Xing Zhou Dongwei He Xiaowei Liu Chao Yang Dawei Xu Meilong Wang Ruitao Sun Bin Zhang Jingjing Xie Jin Han Wen Chen Ya You State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Yibin Libode New Materials Co.Ltd SichuanChina International School of Materials Science and Engineering School of Materials Science and MicroelectronicsWuhan University of TechnologyWuhan 430070China

The O3-type layered cathode with high Ni content has attracted much attention because of its high capacity and simple synthesis ***,surface side reaction and O3-P3 phase transitions would occur during Na+insertion/extraction,resulting in unsatisfying electrochemical ***,O3-Na[Ni_(0.6)Co_(0.2)Mn_(0.2)]O_(2)(NNCM622)cathode is modified by a NaTiOx coating layer in a wet chemistry method,which reduces the parasitic reaction and facilitates Na+***,the partially doped Ti improves structural stability by restraining the irreversible multiple-phase *** a result,the modified NNCM622 cathode obtains a high specific capacity of 143.4 mAh g^(−1)and an improved capacity retention of 69%after 300 *** work offers new prospects for stabilizing the NNCM622 cathode with a feasible coating strategy.

关键词： cathode high-nickel layered oxides sodium-ion battery surface modification

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Simultaneously improving the strength and ductility of AZ91/GNPs composites through decorating graphene nanoplatelets with MgO

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Journal of materials Science & technology 2024年第16期183卷 133-151页

作者： Pingbo Wang Jun Shen Tijun Chen Jiqiang Ma Qinglin Li Shaokai Zheng State Key Laboratory of Solidification Processing Northwestern Polytechnical UniversityXi’an 710072China State Key Laboratory of Advanced Processing and Recycling of Non-ferrous Metals Lanzhou University of TechnologyLanzhou 730050China

Magnesium matrix composites(MgMCs)have always suffered low strengthening efficiency and poor ductility due to the difficulties in pursuing the well-bonded ***,graphene nanoplatelets(GNPs)were decorated with magnesium oxide nanoparticles(MgO NPs)through chemical co-precipitation and then incorporated into AZ91 alloy to fabricate MgMCs via powder *** effect of MgO on the interface of the Mg/graphene system was investigated based on the first-principles calculations,and the result indicated that modifying GNPs with MgO NPs was helpful in improving the Mg-GNP interface *** interface structural analysis revealed that the MgO NPs were firmly bonded with both GNPs andα-Mg through the distortion area bonding and semi-coherent interfacial bonding,severing as a bridge to fasten the interface bonding of *** addition,the MgO NPs on GNPs acted as a barrier to prevent GNPs from seriously reacting with the AZ91 *** a result,the AZ91/MgO@GNPs composite was endowed with enhancements of 31%and 10%in the yield strength,and increments of 71%and 61%in elongation compared with the AZ91 alloy and AZ91/GNPs composite,respectively,exhibiting a more significant potential in optimizing the strength-toughness tradeoffcompared with the AZ91/***,the possible strengthening and toughening mechanisms were also discussed in *** work offers a relatively novel surface modification strategy to modulate the Mg-GNP interface for a simultane-ous improvement of strength and ductility.

关键词： Graphene nanoplatelets Magnesium oxide First-principles calculations Magnesium matrix composites Powder thixoforging

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Universal Encapsulation Adhesive for Lead Sedimentation and Attachable Perovskite Solar Cells with Enhanced Performance

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Energy & Environmental materials 2024年第3期7卷 303-310页

作者： Xuehao Zhu Haoyu Cai Cong Bai Zhengzhe Wu Wenjian Shen Yiming Xiong Juan Zhao Fuzhi Huang Yibing Cheng Jie Zhong Research Centre for Advanced Thin Film Photovoltaics State Key Laboratory of Advanced Technology for Materials Synthesis and ProcessingWuhan University of TechnologyWuhan 430070China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Foshan 528216China School of Automobile Engineering Wuhan University of TechnologyWuhan 430070China

In this work,a modified polyurethane adhesive(PUA)was prepared to realize a convenient encapsulation strategy for lead sedimentation and attachable perovskite solar cells(A-PSCs).The modified PUA can completely self-heal within 45 min at room temperature with an efficient lead ion-blocking rate of 99.3%.The PUA film can be coated on a metal electrode with slight efficiency improvement from 23.96%to 24.15%.The thermal stability at 65℃and the humidity stability at 55%relative humidity(RH)are superior to the devices encapsulated with *** PUA film has strong adhesion to the flexible substrate and the initial efficiency of the flexible perovskite module(17.2%)encapsulated by PUA remains 92.6%within 1825 *** results suggest that PUA encapsulation is universal for rigid and flexible PSCs with enhanced stability and low lead ***,it was found that flexible PSCs can be well attached to various substrates with PUA,providing a facile route for the A-PSCs in various scenarios without additional encapsulation and installation.

关键词： adhesive attachable device flexible module lead leakage polyurethane

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Facile synthesis of hybridized Co/Fe-ZIF under solvent-free conditions for efficient oxidation evolution reaction electrocatalysis

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Nano Research 2025年第1期18卷 362-372页

作者： YinSheng Xu Zihan Li Zhonghan Cheng Somboon Chaemchuen State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Department of Chemical Engineering Faculty of EngineeringMahidol UniversityNakhon Pathom 73170Thailand State Key Laboratory of Silicate Materials for Architectures Wuhan University of TechnologyWuhan 430070China School of Materials Science and Engineering Wuhan University of TechnologyWuhan 430070China

Developing non-noble catalyst synthesis under green conditions with efficient electrochemical reactions is a challenging task in green energy *** meet this challenge,the synthesis of hybridized non-noble cobalt and iron in the zeolitic-imidazole framework(Co/Fe-ZIF)through a solid-state thermal(SST)method is *** the obtained Co/Fe-ZIF structure,iron atoms are uniformly dispersed and randomly hybridized with primary cobalt atoms and imidazole linker,similar to the structure of *** hybridized Co/Fe-ZIF shows potential as an electrocatalyst for oxidation evolution reaction(OER).The optimal iron-incorporating catalyst,Co/Fe_(0.2)-ZIF,demonstrates remarkable performance with a minimized overpotential of 285 mV at the current density(j)of 10 mA·cm^(-2)in 1 M *** synergistic effect of iron and cobalt ions on the catalyst provides active sites that bind to intermediate(OOH^(*))more strongly and facilitate high electron charge transfer,enhancing efficient ***,the synergistic Co/Fe_(0.2-)ZIF catalyst demonstrates excellent durable reaction time compared to non-iron catalyst(ZIF-67)and conventional catalyst(RuO_(2)).

关键词： zeolitic-imidazole frameworks solid-state thermal method solvent-free synthesis electrocatalyst oxidation evolution reaction

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Grain-refining fabrication of nanocrystalline(La_(0.2)Nd_(0.2)Sm_(0.2)Gd_(0.2)Eu_(0.2))_(2)Zr_(2)O_(7)high-entropy ceramics by ultra-high pressure sintering

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Journal of materials Science & technology 2023年第36期167卷 205-212页

作者： Zhangtian Wu Wei Ji Jinyong Zhang Yanan Yuan Ji Zou Weimin Wang Zhengyi Fu State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Hubei Longzhong Laboratory Wuhan University of Technology Xiangyang Demonstration ZoneXiangyang 441000China

As an important A_(2)B_(2)O_(7)-type ceramic,(La_(0.2)Nd_(0.2)Sm_(0.2)Gd_(0.2)Eu_(0.2))_(2)Zr_(2)O_(7)high-entropy pyrochlore pos-sesses promising properties such as high melting point,high chemical durability,and low thermal ***,the low sintering ability limits its application in thermal barrier coating and radioactive waste *** usually needs long-term high-temperature soaking to achieve full density,but with inevitable grain *** this work,dense and grain-refined nanocrystalline(La_(0.2)Nd_(0.2)Sm_(0.2)Gd_(0.2)Eu_(0.2))_(2)Zr_(2)O_(7)ceramics were prepared with ultra-high pressure sintering(UHPS)method under 10 GPa at a low temperature of 800℃.The densification behavior,microstructure evo-lution,and properties of the UHPS-ed samples were then *** grain size of as-prepared(La_(0.2)Nd_(0.2)Sm_(0.2)Gd_(0.2)Eu_(0.2))_(2)Zr_(2)O_(7)ceramic was only 151 nm,which is 40%smaller than that of raw *** addition,it exhibited advantageous properties including both high hardness and aqueous *** deformation under ultra-high pressure was believed as the dominant densification mechanism responsible for grain refinement and property improvement.

关键词： High-entropy ceramics Ultra-high pressure sintering Grain refining Nanocrystalline Plastic deformation

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

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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

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

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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

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In-situ defect passivation assisted three-step printing of efficient and stable formamidine-lead bromide solar cells

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Journal of Energy Chemistry 2024年第9期96卷 396-405页

作者： Hang Yang Tao Zhou Haoyu Cai Wenjian Shen Hao Chen Yongjun Liu Juan Zhao Yi-Bing Cheng Jie Zhong State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070HubeiChina Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Foshan 528216GuangdongChina School of Automobile Engineering Wuhan University of TechnologyWuhan 430070HubeiChina

Perovskite solar cells(PSCs)emerge as the most promising photovoltaics(PV)for their high performance and potential convenient cost-effective production routes comparing to the sophomore PV *** printed PSCs with simplified device architecture and fabrication procedures could further enhance the competitive strength of PSC *** this work,we present an in-situ defect passivation(ISDP)assisted full-printing of high performance formamidine-lead bromide(FAPbBr_(3))*** three rapid printing steps are involved for electron transporting layer(ETL),perovskite and carbon to form a complete solar cell on the low-cost fluorine-doped tin oxide(FTO)***-chain polymer monomethyl ether polyethylene glycol is particularly utilized as the ISDP passivator,leading to conformal coating on the rough FTO and defect passivation for both ETL and perovskite during printing.A high efficiency of 10.85%(certified 10.14%)and a high V_(oc)up to 1.57 V are achieved for the printed *** unencapsulated PSCs maintain above 90%of the initial efficiency after continuously heating at 85℃for 1000 h and over 80%of the efficiency after the maximum power point tracking for 3500 *** fully printed semitransparent PSCs with carbon grids(CGs)show average visible light transmittance over 33%and an efficiency of 8.81%.

关键词： Formamidinium lead bromide Fully printed Lowcosts Carbon electrode Semitransparent

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Acidic oxygen evolution reaction:Mechanism,catalyst classification,and enhancement strategies

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Interdisciplinary materials 2023年第1期2卷 53-90页

作者： Qianli Ma Shichun Mu Fuel cell Materials Laboratory Foshan Xianhu LaboratoryFoshanChina State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhanChina

As the most desirable hydrogen production device,the highly efficient acidic proton exchange membrane water electrolyzers(PEMWE)are severely limited by the sluggish kinetics of oxygen evolution reaction(OER)at the *** IrO2 is a commercial acid-stable OER catalyst with poor activity and high cost,which has motivated the development of ***,hitherto most of the designed acidic OER catalysts have disadvantages of low activity or stability,which cannot meet the requirement of industrial ***,exploring suitable strategies to enhance the activity and stability of cost-effective acidic OER catalysts is crucial for developing the PEMWE *** this review,the main OER mechanisms,different types of catalysts,and their activity and stability characteristics are summarized and discussed,and then possible strategies to improve activity and stability are ***,the problems and prospects of such catalysts are generalized to shed some light on the future research of advanced catalysts for acidic OER.

关键词： catalyst hydrogen energy oxygen evolution reaction proton exchange membrane water electrolyzer water oxidation

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