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Single-atom Zn confined in hierarchical hollow microstructure as an acid/base-resistant microwave absorption materials

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Nano Research 2024年第8期17卷 6785-6794页

作者： Yue Lou Jiao Li Xiaokun Li Zhenyu Zhu Zhan Shi Biao Xu School of chemistry and Chemical Engineering Nanjing University of Science and TechnologyNanjing 210094China state key laboratory of inorganic synthesis and Preparative chemistry College of ChemistryJilin UniversityChangchun 130012China

Developing acid/base-resistant and low-price microwave-absorbing materials with lighter weight is highly desired for practical applications in extreme ***,we demonstrate the successful synthesis of the N-doped porous carbon(NC)material with hierarchical pore structure by the spray pyrolysis *** large specific surface area(SBET=707.53 m^(2)·g^(−1))of materials enables multiple scattering of incident electromagnetic waves,and N doping greatly enhances the electrical conductivity of the ***,single-atom Zn can adjust the local electronic structure of adjacent sites such as carbon and nitrogen atoms,induce the center of polarization,and thus change the dielectric and electronic properties of the host *** porous carbon coating of single-atom Zn avoids the deterioration of electromagnetic parameters caused by the accumulation of magnetic particles under high-temperature *** the same time,they can also be used in various complex environments,such as acidic and basic ***,NC-1000,with high surface area,low density,and good chemical stability,obtained a minimum reflection loss(RLmin)of−50.5 dB and an effective absorption bandwidth(EAB)exceeding 5.1 GHz at the thickness of 1.9 *** soaking in the strong acid and base solution,the electromagnetic wave absorption performance of the material decreased bylable raw materials and a simple preparation scheme are expected to expedite industrial mass production for this novel type of materials.

关键词： hierarchical hollow microstructure microwave absorption metal-organic framework(MOF) impedance matching singleatom Zn acid/base-resistant

Zeolites for the separation of ethylene,ethane,and ethyne

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Frontiers of Chemical Science and Engineering 2024年第9期18卷 137-146页

作者： Binyu Wang Qiang Li Haoyang Zhang Jia-Nan Zhang Qinhe Pan Wenfu Yan state key laboratory of inorganic synthesis&Preparative chemistry College of ChemistryJilin UniversityChangchun 130012China key laboratory of Advanced Energy Catalytic and Functional Materials preparation College of Materials Science and EngineeringZhengzhou UniversityZhengzhou 450012China key laboratory of Advanced Materials of Tropical Island Resources(Ministry of Education) School of Chemistry and Chemical EngineeringHainan UniversityHaikou 570228China

The cost-effective separation of ethylene(C_(2)H_(4)),ethyne(C_(2)H_(2)),and ethane(C_(2)H_(6))poses a significant challenge in the contemporary chemical *** contrast to the energy-intensive high-pressure cryogenic distillation process,zeolite-based adsorptive separation offers a low-energy *** review provides a concise overview of recent advancements in the adsorptive separation of C_(2)H_(4),C_(2)H_(2),and C_(2)H_(6)using zeolites or zeolite-based *** commences with an examination of the industrial significance of these compounds and the associated separation ***,it systematically examines the utilization of various types of zeolites with diverse cationic species in such separation *** then it explores how different zeolitic structures impact adsorption and separation capabilities,considering principles such as cation-πinteraction,π-complexation,and steric separation concerning C_(2)H_(4),C_(2)H_(2),and C_(2)H_(6)***,it discusses methods to enhance the separation performance of zeolites and zeolite-based adsorbents,encompassing structural design,modifications,and ion exchange ***,it summarizes current research trends and future directions,highlighting the potential application value of zeolitic materials in the field of C_(2)H_(4),C_(2)H_(2),and C_(2)H_(6)separation and offering recommendations for further investigation.

关键词： zeolite ethylene ethane cation-πinteraction π-complexation

Mechanism of interfacial effects in sodium-ion storage devices

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Nano Research 2024年第3期17卷 1313-1326页

作者： Yifan Wei Lingxing Zan Huicong Xia Wenfu Yan Jia-Nan Zhang College of Materials Science and Engineering Zhengzhou UniversityZhengzhou 450001China key laboratory of Advanced Energy Catalytic and Functional Material preparation of Zhengzhou City Zhengzhou 450001China key laboratory of Chemical Reaction Engineering of Shaanxi Province College of Chemistry&Chemical EngineeringYan’an UniversityYan’an 716000China state key laboratory of inorganic synthesis and Preparative chemistry and College of chemistry Jilin UniversityChangchun 130012China

Rechargeable sodium-ion batteries(SIBs)are considered as the next-generation secondary *** performance of SIB is determined by the behavior of its electrode surface and the electrode–electrolyte interface during charging and ***,the characteristics of these surfaces and interfaces should be analyzed to realize large-scale energy storage systems with high energy density and long-cycle *** various studies have investigated the properties of electrode materials,few studies have focused on the construction of stable and efficient SIB interfaces,and even fewer have explored the mechanisms of interfacial effects;however,the strategies of regulating interfacial effects are yet to be completely ***,the results obtained thus far are insufficient to draw systematic *** present study reviews the literature on the mechanism of interfacial effects in Na+storage *** interfaces in a sodium-ion storage device include a heterogeneous interface between electrode materials,a solid electrolyte interphase,and a cathode electrolyte *** interfacial effects during the intercalation,transformation,and alloy reactions and the resulting overall battery performance were theoretically *** this review,we aim to provide a theoretical basis for optimizing the structures of electrode surface and electrode–electrolyte interface to optimize the performance of *** addition,the challenges of investigating interfacial effects and several possible helpful methods and opportunities for studying the mechanisms of interfacial effects in SIBs will be presented.

关键词： sodium-ion storage interfacial effects solid electrolyte interphase cathode electrolyte interphase

Rational design of new in situ reduction of Ni(II)catalytic system for low-cost and large-scale preparation of porous aromatic frameworks

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Carbon Energy 2024年第5期6卷 105-113页

作者： Shanshan Wang Yue Wu Wenxiang Zhang Hao Ren Guangshan Zhu Heping Ma School of Chemical Engineering and Technology Xi'an Jiaotong UniversityXi'anChina state key laboratory of inorganic synthesis and Preparative chemistry College of ChemistryJilin UniversityChangchunChina College of chemistry Northeast Normal UniversityChangchunChina

Porous aromatic framework 1(PAF-1)is an extremely representative nanoporous organic framework owing to its high stability and exceptionally high surface ***,the synthesis of PAF-1 is catalyzed by the Ni(COD)2/COD/bpy system,suffering from great instability and high ***,we developed an in situ reduction of the Ni(II)catalytic system to synthesize PAF-1 in low cost and high *** active Ni(0)species produced from the NiCl_(2)/bpy/NaI/Mg catalyst system can effectively catalyze homocoupling of tetrakis(4-bromophenyl)methane at the room temperature to form PAF-1 with high Brunauer-Emmett-Teller(BET)-specific surface area up to 4948 m^(2) g^(−1)(Langmuir surface area,6785 m2 g−1).The possible halogen exchange and dehalogenation coupling mechanisms for this new catalytic process in PAF's synthesis are discussed in *** efficiency and universality of this innovative catalyst system have also been demonstrated in other PAFs'*** work provides a cheap,facile,and efficient method for scalable synthesis of PAFs and explores their application for high-pressure storage of Xe and Kr.

关键词： adsorption carbon material nickel catalysis porous aromatic framework porous organic polymer

Celebrating 40 Years of Chemical Research in Chinese Universities

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Chemical Research in Chinese Universities 2024年第4期40卷 561-563页

作者： YU Jihong WANG Dan state key laboratory of inorganic synthesis and Preparative chemistry International Center of Future ScienceJilin UniversityChangchun 130012P.R.China state key laboratory of Biochemical Engineering Key Laboratory of Biopharmaceutical Preparation and DeliveryInstitute of Process EngineeringChinese Academy of SciencesBeijing 100190P.R.China

Chemical Research in Chinese Universities was founded in 1984 as a comprehensive academic journal in the field of *** has since become a repository of intellectual treasures,documenting the evolving landscape of chemical science within the academic *** the past 40 years,Chemical Research in Chinese Universities has witnessed the rapid development of chemical research in universities.

关键词： chemistry. landscape journal

Enhancing the Efficiency and Durability of Perovskite Solar Cells by Donor-Acceptor Covalent Organic Framework with Thiazolo[5,4-d]thiazole Unit

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CCS chemistry 2024年第7期6卷 1721-1730页

作者： Liyi Yao Shuainan Liu Lin Li Bangdi Ge Wenyu Jiao Siyu Zong Xiaowei Song Donglei Zhou Zhiqiang Liang state key lab of inorganic synthesis and Preparative chemistry College of ChemistryJilin UniversityChangchun 130012 state key laboratory of Integrated Optoelectronics College of Electronic Science and EngineeringJilin UniversityChangchun 130012 Electron Microscopy Center Jilin UniversityChangchun 130012

Donor-Acceptor(D-A)alignment is considered a productive strategy to improve the charge separation efficiency of covalent organic frameworks(COFs)and enhance the charge-transfer yield(CTY)of ***,organic molecules containing heteroatoms can produce coordination interaction with PbI2 of perovskite precursor to affect the crystallization process,thereby impeding the decomposition and improving the stability of perovskite ***,a thiazolo[5,4-d]thiazole(TZ)-based D-A type COF_(TPDA-TZDA) was designed and synthesized from N,N,N′,N′-tetrakis(4-aminophenyl)-1,4-benzenediamine(TPDA)and 4,4′-(thiazolo[5,4-d]thiazole-2,5-diyl)dibenzaldehyde(TZDA).Upon incorporation into the FAPbI3 layer,COF_(TPDA-TZDA) not only restrained the perovskite defects and enhanced the grain size of perovskite films through the coordination effect of the N atoms of TZDA but also ameliorated the charge transport within the perovskite film,which was the benefit of the D-A structure of COF_(TPDA-TZDA).As a result,incorporation of COF_(TPDA-TZDA) into the perovskite solar cells(PSCs)led to a remarkable power conversion efficiency(PCE)of up to 23.51%.Furthermore,even after being stored in high relative humidity(RH≈60%)for 480 h,these PSCs maintained over 90.55%of their original *** work sets the foundation for the development of highly efficient and stable PSCs by utilizing TZ-based D-A type COFs.

关键词： thiazolo[5,4-d]thiazole perovskite solar cells donor-acceptor covalent organic frameworks charge-transfer

Metal-metal bonds in Zintl clusters:synthesis,structure and bonding in[Fe_(2)Sn_(4)Bi_(8)]^(3-)and[Cr_(2)Sb_(12)]^(3-)

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Chinese Chemical Letters 2024年第8期35卷 558-566页

作者： Ya-Nan Yang Zi-Sheng Li Sourav Mondal Lei Qiao Cui-Cui Wang Wen-Juan Tian Zhong-Ming Sun John E.McGrady state key laboratory of Element-Organic chemistry Tianjin Key Lab for Rare Earth Materials and ApplicationsSchool of Materials Science and EngineeringNankai UniversityTianjin 300350China Department of chemistry University of OxfordInorganic Chemistry LaboratoryOxfordOX13QRUnited Kingdom

We report here the synthesis and characterization of two new members of the M2 E 12 family of endohe-dral Zintl clusters,[Fe_(2)Sn_(4)Bi_(8)]^(3-)and[Cr_(2)Sb_(12)]^(3-),both of which contain open-shell metal dimers encap-sulated inside a triple-decker cluster of main-group *** 75-electron[Fe_(2)Sn_(4)Bi_(8)]^(3-)cluster has a D4h-symmetric structure,while[Cr_(2)Sb_(12)]^(3-),despite having the same 75-electron count,is strongly dis-torted to a geometry that resembles a CrSb_(8)crown capped by a CrSb_(4)*** structural differences between the two are driven by the increasing availability of 3d electron density in the earlier transi-tion metal,which leads,ultimately,to different electronic configurations in the two *** trends precisely mirror those observed in the ME_(10)and ME_(12)families containing a single transition metal ion.

关键词： Zintl anions Endohedral clusters Metal-metal bond Second-order Jahn-Teller effect DFT calculation

Recyclable High-performance Carbon Fiber Reinforced Epoxy Composites Based on Dithioacetal Covalent Adaptive Network

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Chinese Journal of Polymer Science 2024年第10期42卷 1514-1524,I0011页

作者： Gui-Lian Shi Ting-Cheng Li Dao-Hong Zhang Jun-Heng Zhang key laboratory of Catalysis and Energy Materials chemistry of Ministry of Education&Hubei key laboratory of Catalysis and Materials Science Hubei R&D Center of Hyperbranched Polymers Synthesis and ApplicationsSouth-Central Minzu UniversityWuhan430074China state key laboratory of New Textile Materials and Advanced Processing Technologies Wuhan Textile UniversityWuhan430200China Ministry-of-Education key laboratory for the Green preparation and Application of Functional Materials Hubei UniversityWuhan430062Chin

Recycling of carbon fiber reinforced composites is important for sustainable development and the circular *** the use of dynamic chemistry,developing high-strength recyclable CFRPs remains a major challenge due to the mutual exclusivity between the dynamic and mechanical properties of ***,we developed a high-strength recyclable epoxy resin(HREP)based on dynamic dithioacetal covalent adaptive network using diglycidyl ether bisphenol A(DGEBA),pentaerythritol tetra(3-mercapto-propionate)(PETMP),and vanillin epoxy resin(VEPR).At high temperatures,the exchange reaction of thermally activated dithioacetals accelerated the rearrangement of the network,giving it significant reprocessing ***,HREP exhibited excellent solvent resistance due to the increased cross-linking *** this high-strength recyclable epoxy resin as the matrix and carbon fiber modified with hyperbranched ionic liquids(HBP-AMIM+PF6-)as the reinforcing agent,high performance CFRPs were successfully *** tensile strength,interfacial shear strength(IFSS)and interlaminar shear strength(ILSS)of the optimized formulation(HREP20/CF-HBPPF6)were 1016.1,70.8 and 76.0 MPa,*** addition,the CFRPs demonstrated excellent solvent and acid/*** CFRPs could completely degrade within 24 h in DMSO at 140℃,and the recycled CF still maintained the same tensile strength and ILSS as the original after multiple degradation cycles.

关键词： Epoxy resin Hyperbranched ionic liquid Recycling Carbon fiber Composites

Electrostatic Interaction-directed Construction of Hierarchical Nanostructured Carbon Composite with Dual Electrical Conductive Networks for Zinc-ion Hybrid Capacitors with Ultrastability

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Energy & Environmental Materials 2024年第1期7卷 184-192页

作者： Changyu Leng Zongbin Zhao Xuzhen Wang Yuliya V.Fedoseeva Lyubov G.Bulusheva Alexander V.Okotrub Jian Xiao Jieshan Qiu state key lab of Fine Chemicals School of Chemical EngineeringLiaoning Key Lab for Energy Materials and Chemical Engineering Dalian University of TechnologyDalian 116024China Nikolaev Institute of inorganic chemistry Siberian Branch of the Russian Academy of Sciences3 Acad.Lavrentiev Ave.Novosibirsk 630090Russia College of Chemical Engineering Beijing University of Chemical Technology Beijing 100029China

Metal-organic framework(MOF)-derived carbon composites have been considered as the promising materials for energy ***,the construction of MOF-based composites with highly controllable mode via the liquid-liquid synthesis method has a great challenge because of the simultaneous heterogeneous nucleation on substrates and the self-nucleation of individual MOF nanocrystals in the liquid ***,we report a bidirectional electrostatic generated self-assembly strategy to achieve the precisely controlled coatings of single-layer nanoscale MOFs on a range of substrates,including carbon nanotubes(CNTs),graphene oxide(GO),MXene,layered double hydroxides(LDHs),MOFs,and SiO_(2).The obtained MOF-based nanostructured carbon composite exhibits the hierarchical porosity(V_(meso)/V_(micro)∶2.4),ultrahigh N content of 12.4 at.%and"dual electrical conductive networks."The assembled aqueous zinc-ion hybrid capacitor(ZIC)with the prepared nanocarbon composite as a cathode shows a high specific capacitance of 236 F g^(-1)at 0.5 A g^(-1),great rate performance of 98 F g^(-1)at 100 A g^(-1),and especially,an ultralong cycling stability up to 230000 cycles with the capacitance retention of 90.1%.This work develops a repeatable and general method for the controlled construction of MOF coatings on various functional substrates and further fabricates carbon composites for ZICs with ultrastability.

关键词： carbon composite electrostatic interaction metal-organic framework coating self-assembly zinc-ion hybrid capacitor