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A novel long persistent luminescent material CaGeO3:Tb3+ with photo-stimulation properties

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Journal of Rare Earths 2024年第7期42卷 1233-1239页

作者： Wei Meng Xiaoyan Fu Tongyan Lin Zewen Liu Naihui Chen Jiaxu Zhang Runyao Liu Rujun Yang Long Chen Hongwu Zhang school of chemistry and Material sciences Ludong University College of materials Science and Engineering Xiamen University of Technology College of materials Xiamen University

A novel green long afterglow material CaGeO3:Tb3+was synthesized by high temperature solid phase method.According to the experimental results,CaGeO3:Tb3+is a green long persistent luminescent（LPL）material with excellent performance.CaGeO3:Tb3+shows LPL emission peak at 442,490.9,548.7,588.5and 623.8 nm,corresponding to5D3to7F4and5D4to7FJ（J=6,5,4,3） transitions of Tb3+,Its CIE coordinates are（0.27,0.50）,indicating that the afterglow emission is close to the light of green region.In addition,after the excitation source is turned off,the afterglow time is longer than 90 min.After an interval of 7 h,the photo-stimulation luminescence（PSL） can be observed by using 980 nm laser cyclic excitation.The thermoluminescence（ThL） results show that there are three types of traps in the material and their depths are 0.666,0.774 and 0.892 eV respectively,which are caused by the doping of Tb3+.All the results show that CaGeO3:Tb3+is an excellent long afterglow luminescent material.

关键词： CaGeO3:Tb3+ Long persistent luminescence Photo-stimulation Rare earths Trap

Highly reversible Zn anode enabled by anticatalytic carbon layer with suppressed hydrogen evolution

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Rare Metals 2024年第7期43卷 3044-3054页

作者： Wen-Duo Zhang Chuang Sun Yu-Xuan Zhu Feng Gao Chao Lai school of chemistry and materials Science Jiangsu Normal University

Aqueous zinc-ion batteries（AZIBs） have emerged as a promising high-efficiency energy storage system due to the high energy density,low-cost and environmental friendliness.However,the practical application of AZIBs is severely restricted by the challenges faced by the Zn anode,which include uncontrollable dendrite growth,corrosion and hydrogen evolution reaction.Herein,a simple and convenient physical vapor deposition（PVD）method is reported for fabricating uniform graphite as a protection layer on the surface of Zn anode.The high conductivity graphite layer on Zn anode（denoted as Zn@C） not only benefits the uniform distribution of the electric field,but also provides numerous Zn nucleation sites to regulate and navigate Zn-ion stripping/plating behaviors.Additionally,the graphite layer with a poor catalytic activity endows the Zn@C anode with a highly suppressed hydrogen evolution.Consequently,a hydrogen and dendrite free anode is achieved with artificial anticatalytic carbon layer on Zn anode,exhibiting a high reversibility and excellent cycling stability over 2600 h at the current density of 5 mA·cm-2with a capacity of 2.5 mAh·cm-2and longtime cycling stability for assembled full cells.This work strategically designs the properties of the artificial interface layer to effectively address various challenges simultaneously,which presents insights for the future development of high-performance rechargeable AZIBs.

关键词： Zn metal anode Artificial anticatalytic layer Hydrogen suppression Dendrite free

Defect engineering of Fe–N doped crumpled graphene for improved ORR performance

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Progress in Natural Science:materials International 2024年第1期34卷 147-154页

作者： Yinli Liao Yingjie Zhu Ruyu Zou Qiong Yu Zhihong Tang school of materials and chemistry University of Shanghai for Science and Technology

As a promising alternative electrocatalyst to platinum for the oxygen reduction reaction（ORR）, an Fe-N/C electrocatalyst with more active sites was designed by using N-doped porous crumpled graphene as carbon precursor. More defects provided by the edges and cavities of the porous crumpled graphene facilitated the anchoring and inhibited the growth of Fe clusters, and hence introduced more active sites. Furthermore, crumpled structure combined with the pores provided abundant mass transfer channels, and the fast kinetics were ensured.Consequently, the porous crumpled graphene-based catalyst showed better ORR activity and good electrochemical stability. The half-wave potential(E1/2) of porous crumpled graphene-based catalyst was 0.69 V vs. RHE,and the current retention rate was above 97% after 20000s. In addition, the influence of different morphologies,degrees of defect, and compositions on the distribution of active sites and ORR performance of Fe-N/C were systematically studied, and the formation mechanism of Fe-N/C was proposed. This study provided valuable insights into designing more effective non-precious metal based electrocatalysts.

关键词： Fe-N/C electrocatalysts Oxygen reduction Planar structure Crumpled structure Porous crumpled structure

Ternary-phase layered cathodes toward ultra-stable and highrate sodium ion storage

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Rare Metals 2024年第4期43卷 1589-1598页

作者： Wen-Ji Yin Pei-Dan Su Qi Lu Xiao-Qiong Li Ji-Ming Peng Teng-Fei Zhou Ge-Meng Liang Yu-Liang Cao Hong-Qiang Wang Qing-Yu Li Si-Jiang Hu Guangxi Key Laboratory of Low Carbon Energy materials School of Chemistry and Pharmaceutical SciencesGuangxi Normal University Institutes of Physical Science and Information Technology Anhui University Department of chemistry and Pharmaceutical sciences Guilin Normal College College of chemistry and Chemical Engineering Huanggang Normal University school of Chemical Engineering and Advanced materials The University of Adelaide Engineering Research Center of Organosilicon Compounds and materials of Ministry of Education College of Chemistry and Molecular SciencesWuhan University

With the shortage of lithium resources,sodiumion batteries（SIBs） are considered one of the most promising candidates for lithium-ion batteries.P2-type and O3-type layered oxides are one of the few cathodes that can access high energy density.However,they usually exhibit structural change,capacity decay,and slow Na ion kinetic.Herein,we present layered ternary-phase cathodes with P2,P3 and O3 phases by a lattice doping strategy,which is demonstrated by X-ray diffraction（XRD） refinement.Combining the characteristics of P2,P3 and O3 phases,the layered composites show performance improvement during long-term battery cycling.In particular,Na0.7Li0.1Co0.3-Fe0.3Mn0.3O2（NLCFM） delivers a reversible capacity of120.1 mAh·g-1at 0.1C(1.0C=175 mA·g-1) with a superior capacity retention of 72.5% after 1000 cycles at10.0C.This work offers insights into the development of advanced cathode materials for SIBs.

关键词： Sodium-ion battery Cathode material Layered oxides Lattice doping Mixed phase

Construction of electron rich Fe active sites by FeCu alloy anchoring on carbon nitride for photocatalytic nitrogen reduction

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Rare Metals 2024年第4期43卷 1570-1579页

作者： Gang Dong Cong Huang Fei-Yang Chen Xue-Qin Liu Zhen Li Xiao-Li Su Tao Zeng Yun-Xia Chen Yi-Huang Chen Yang Wang school of materials Science and Engineering Jingdezhen Ceramic University Faculty of materials Science and chemistry China University of Geosciences College of chemistry and materials Engineering Wenzhou University

Given the clean and inexhaustible solar energy from solar light,photocatalytic ammonia synthesis is extremely appealing.However,high electron-hole recombination rates and insufficient active sites severely limited N2 photoreaction reduction.Herein,we designed and fabricated FeCu alloy nanoparticles anchored on carbon nitride nanosheets with excellent photocatalyt ic ammonia synthesis performance.As a coupler between Fe and carbon nitride,Cu promotes the separation of photogenerated charge carriers in carbon nitride under solar light irradiation,and renters the semiconductor a forceful electron donor for the Fe active sites.The accumulated electrons at Fe sites furtherly facilitated the adsorption and activation of the molecular nitrogen.Besides,the uniform dispersed FeCu alloy nanoparticles were on carbon nitride nanosheets enhanced the stability of photocataly tic nitrogen reduction reaction,making the artificial photocataly tic ammonia synthesis more sustainable for application.This work highlights that a direct electron transfer channel can be used to regulate the photochemical nitrogen fixation network.

关键词： Photocatalytic N 2 fixation Carbon nitride FeCu alloy Active sites Hydrogenation pathway

Recent advances in Ir/Ru-based perovskite electrocatalysts for oxygen evolution reaction

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Rare Metals 2024年第7期43卷 2891-2912页

作者： Zhi-Qi Jiang Cheng-Zhen Fan Jun-Yu Pan Li Shao Hao Chen Erum Pervaiz Yan Dong Tong-Zhou Wang Xue-Rong Zheng Ji-Hong Li Yi-Da Deng school of materials Science and Engineering Hainan University Department of Chemical Engineering School of Chemical and Materials Engineering (SCME)National University of Sciences & Technology (NUST) Key Laboratory of Advanced Energy materials chemistry (Ministry of Education) Nankai University

Oxygen evolution reaction(OER) is a kinetically harsh four-electron anode reaction that requires a large overpotential to provide current and is of great importance in renewable electrochemical technique.Ir/Rubased perovskite oxides hold great significance for application as OER electrocatalysts,due to that their multimetal-oxide forms can reduce the use of noble metals,and their compositional tunability can modulate the electronic structure and optimize OER performance.However,high operating potentials and corrosive environments pose a serious challenge to the development of durable Ir-based and Ru-based perovskite electrocatalysts.Tremendous efforts have been dedicated to improving the Ir/Ru-based perovskite activity to enhance the efficiency;however,progress in improving the durability of Ir/Ru-based perovskite electrocatalysts has been rather limited.In this review,the recent research progress of Ir/Ru-based perovskites is reviewed from the perspective of heteroatom doping,structural modulation,and formation of heterostructures.The dissolution mechanism studies of Ir/Ru and experimental attempts to improve the durability of Ir/Ru-based perovskite electrocatalysts are discussed.Challenges and outlooks for further developing Ru-and Irbased perovskite oxygen electrocatalysts are also presented.

关键词： Oxygen evolution reaction Ir/Ru-based perovskites Stability Electrocatalysts

Hydrochar and synthetic natural gas co-production for a full circular economy implementation via hydrothermal carbonization and methanation:An economic approach

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Journal of Environmental sciences 2024年第6期140卷 69-78页

作者： Judith González-Arias Guillermo Torres-Sempere Miriam González-Castaño Francisco MBaena-Moreno Tomás RReina Inorganic chemistry Department and materials sciences Institute University of Seville-CSICSevilleSpain materials sciences Institute(ICMSE) CSIC-University of SevilleSevilleSpain Department of chemistry and Chemical Engineering Chalmers University of TechnologyGothenburgSE 41296Sweden

Herein we study the economic performance of hydrochar and synthetic natural gas coproduction from olive tree pruning.The process entails a combination of hydrothermal carbonization and methanation.In a previous work,we evidenced that standalone hydrochar production via HTC results unprofitable.Hence,we propose a step forward on the process design by implementing a methanation,adding value to the gas effluent in an attempt to boost the overall process techno-economic aspects.Three different plant capacities were analyzed(312.5,625 and 1250 kg/hr).The baseline scenarios showed that,under the current circumstances,our circular economy strategy in unprofitable.An analysis of the revenues shows that hydrochar selling price have a high impact on NPV and subsidies for renewable coal production could help to boost the profitability of the process.On the contrary,the analysis for natural gas prices reveals that prices 8 times higher than the current ones in Spain must be achieved to reach profitability.This seems unlikely even under the presence of a strong subsidy scheme.The costs analysis suggests that a remarkable electricity cost reduction or electricity consumption of the HTC stage could be a potential strategy to reach profitability scenarios.Furthermore,significant reduction of green hydrogen production costs is deemed instrumental to improve the economic performance of the process.These results show the formidable techno-economic challenge that our society faces in the path towards circular economy societies.

关键词： Hydrothermal carbonization CO_(2)waste valorization Methanation Profitability analysis

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The Role of Renewable Protocatechol Acid in Epoxy Coating Modification: Significantly Improved Antibacterial and Adhesive Properties

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Chinese Journal of Polymer Science 2024年第1期42卷 63-72,I0008页

作者： Ming-Xuan Chen Jin-Yue Dai Li-Yue Zhang Shuai-Peng Wang Jing-Kai Liu Yong-Gang Wu Xin-Wu Ba Xiao-Qing Liu school of chemistry and materials Science Hebei UniversityBaoding 071000China Ningbo Institute of materials Technology and Engineering Chinese Academy of SciencesNingbo 315201China Key Laboratory of Marine materials and Related Technologies Chinese Academy of SciencesNingbo 315201China

It is of great significance to design epoxy coatings with superior antibacterial properties and high adhesive properties, as well as excellent processing, superior durability, and high transparency. However, it is still a challenge because of the common complex design and synthesis. Herein, the bio-based monomer protocatechuic acid(PCA) was used as raw material, the catechol structure with high bonding and antibacterial properties was introduced into the flexible alkane segment of ethylene glycol diglycidyl ether(EGDE) through an efficient, and green method, and it was cured with isophorone diamine(IPDA) to prepare corresponding thermosets. The cured resins exhibited excellent allaround qualities, particularly in bonding and antibacterial. When 30% PCA was added to pure epoxy resin, the adhesion between substrate and coating increased from 4.40 MPa to 13.60 MPa and the antibacterial rate of coating against E. coli and S. aureus could approach 100%. All of this is due to the fact that the catechol structure present in PCA has the ability to interact with various substrates and alter the permeability of bacterial cell membranes. The architecture of this method offers a fresh approach to dealing with the issues of challenging raw material selection and complex synthesis techniques.

关键词： Epoxy coatings Thermosets Catechol structure Antibacterial High adhesion

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Construction of plum-branch-like CoSe2@N-Doped carbon/carbon fiber with dual protective mechanisms for enhanced lithium storage

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Progress in Natural Science:materials International 2024年第3期34卷 495-502页

作者： Ying Wang Ming Zhang Lei Chen Yanjuan Li Qingqing Wang Xiaobin Wu Lingdi Shen Xiao Yan school of chemistry & materials Science Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials Jiangsu Normal University

Cobalt selenide（CoSe2） emerges as a highly promising anode material for lithium-ion batteries（LIBs） owing to its high theoretical capacity and cost-effectiveness. Despite these merits, its practical utilization faces challenges stemming from substantial volume fluctuations and limited electronic conductivity. To tackle these issues, a plumbranch-like structure of CoSe2@N-doped carbon that embedded in one-dimensional N-doped carbon fibers（CoSe2@NC/CFs）, is successfully synthesized through an in-situ confinement method. Well-defined CoSe2@NC nanoparticles, featuring diameters between 20～30 nm, are uniformly dispersed on both the inner and outer surfaces of the carbon fibers. The distinctive architecture of CoSe2@NC/CFs ensures an increased number of active sites, elevated electronic conductivity, alleviated volume expansion, and accelerated reaction kinetics.Consequently, the CoSe2@NC/CFs exhibits remarkable cycling performance and exceptional rate capability.Operating at a current density of 1000 mA g-1, the CoSe2@NC/CFs anode sustains a capacity of 664 mA h g-1with no obvious capacity decay over 500 cycles. Even at a high current density of 5000 mA g-1, it maintains a capacity of 445 mA h g-1with a mere 0.02 % capacity decay per cycle. This study introduces a novel approach to anode material design, showcasing significant advancements in lithium-ion battery technology.

关键词： Carbon fiber Electrochemical performances Electrode Lithium-ion battery Metal-selenide