期刊文献+
共找到36,545篇文章
< 1 2 250 >
每页显示 20 50 100
Accelerating Oxygen Electrocatalysis Kinetics on Metal-Organic Frameworks via Bond Length Optimization 被引量:2
1
作者 Fan He Yingnan Liu +10 位作者 Xiaoxuan Yang Yaqi Chen Cheng‑Chieh Yang Chung‑Li Dong Qinggang He Bin Yang Zhongjian Li Yongbo Kuang Lecheng Lei Liming Dai Yang Hou 《Nano-Micro Letters》 SCIE EI CAS CSCD 2024年第9期279-290,共12页
Metal-organic frameworks(MOFs)have been developed as an ideal platform for exploration of the relationship between intrinsic structure and catalytic activity,but the limited catalytic activity and stability has hamper... Metal-organic frameworks(MOFs)have been developed as an ideal platform for exploration of the relationship between intrinsic structure and catalytic activity,but the limited catalytic activity and stability has hampered their practical use in water splitting.Herein,we develop a bond length adjustment strategy for optimizing naphthalene-based MOFs that synthesized by acid etching Co-naphthalenedicarboxylic acid-based MOFs(donated as AE-CoNDA)to serve as efficient catalyst for water splitting.AE-CoNDA exhibits a low overpotential of 260 mV to reach 10 mA cm^(−2)and a small Tafel slope of 62 mV dec^(−1)with excellent stability over 100 h.After integrated AE-CoNDA onto BiVO_(4),photocurrent density of 4.3 mA cm^(−2)is achieved at 1.23 V.Experimental investigations demonstrate that the stretched Co-O bond length was found to optimize the orbitals hybridization of Co 3d and O 2p,which accounts for the fast kinetics and high activity.Theoretical calculations reveal that the stretched Co-O bond length strengthens the adsorption of oxygen-contained intermediates at the Co active sites for highly efficient water splitting. 展开更多
关键词 metal-organic frameworks Bond length adjustment Spin state transition Orbitals hybridization Water splitting
下载PDF
Synergistic catalysis of the N-hydroxyphthalimide on flower-like bimetallic metal-organic frameworks for boosting oxidative desulfurization
2
作者 Jing He Kun Zhu +5 位作者 Wei Jiang Dong-Ao Zhu Lin-Hua Zhu Hai-Yan Huang Wen-Shuai Zhu Hua-Ming Li 《Petroleum Science》 SCIE EI CAS CSCD 2024年第1期674-682,共9页
Synergic catalytic effect between active sites and supports greatly determines the catalytic activity for the aerobic oxidative desulfurization of fuel oils.In this work,Ni-doped Co-based bimetallic metal-organic fram... Synergic catalytic effect between active sites and supports greatly determines the catalytic activity for the aerobic oxidative desulfurization of fuel oils.In this work,Ni-doped Co-based bimetallic metal-organic framework(CoNi-MOF)is fabricated to disperse N-hydroxyphthalimide(NHPI),in which the whole catalyst provides plentiful synergic catalytic effect to improve the performance of oxidative desulfurization(ODS).As a bimetallic MOF,the second metal Ni doping results in the flower-like morphology and the modification of electronic properties,which ensure the exposure of NHPI and strengthen the synergistic effect of the overall catalyst.Compared with the monometallic Co-MOF and naked NHPI,the NHPI@CoNi-MOF triggers the efficient activation of molecular oxygen and improves the ODS performance without an initiator.The sulfur removal of dibenzothiophene-based model oil reaches 96.4%over the NHPI@CoNi-MOF catalyst in 8 h of reaction.Furthermore,the catalytic product of this aerobic ODS reaction is sulfone,which is adsorbed on the catalyst surface due to the difference in polarity.This work provides new insight and strategy for the design of a strong synergic catalytic effect between NHPI and bimetallic supports toward high-activity aerobic ODS materials. 展开更多
关键词 metal-organic frameworks DOPED BIMETALLIC N-HYDROXYPHTHALIMIDE Aerobic processes Oxidative desulfurization
下载PDF
Metal-organic frameworks and their composites for advanced lithium-ion batteries:Synthesis,progress and prospects
3
作者 Chengcai Liu Borong Wu +7 位作者 Tao Liu Yuanxing Zhang Jingwen Cui Lingjun Huang Guoqiang Tan Ling Zhang Yuefeng Su Feng Wu 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2024年第2期449-470,I0011,共23页
Metal-organic frameworks(MOFs)are among the most promising materials for lithium-ion batteries(LIBs)owing to their high surface area,periodic porosity,adjustable pore size,and controllable chemical composition.For ins... Metal-organic frameworks(MOFs)are among the most promising materials for lithium-ion batteries(LIBs)owing to their high surface area,periodic porosity,adjustable pore size,and controllable chemical composition.For instance,their unique porous structures promote electrolyte penetration,ions transport,and make them ideal for battery separators.Regulating the chemical composition of MOF can introduce more active sites for electrochemical reactions.Therefore,MOFs and their related composites have been extensively and thoroughly explored for LIBs.However,the reported reviews solely include the applications of MOFs in the electrode materials of LIBs and rarely involve other aspects.A systematic review of the application of MOFs in LIBs is essential for understanding the mechanism of MOFs and better designing related MOFs battery materials.This review systematically evaluates the latest developments in pristine MOFs and MOF composites for LIB applications,including MOFs as the main materials(anode,cathode,separators,and electrolytes)to auxiliary materials(coating layers and additives for electrodes).Furthermore,the synthesis,modification methods,challenges,and prospects for the application of MOFs in LIBs are discussed. 展开更多
关键词 metal-organic frameworks ELECTRODES Electrolytes SEPARATORS Lithium-ion batteries
下载PDF
Hollow Metal-Organic Framework/MXene/Nanocellulose Composite Films for Giga/Terahertz Electromagnetic Shielding and Photothermal Conversion
4
作者 Tian Mai Lei Chen +2 位作者 Pei‑Lin Wang Qi Liu Ming‑Guo Ma 《Nano-Micro Letters》 SCIE EI CAS CSCD 2024年第9期161-179,共19页
With the continuous advancement of communication technology,the escalating demand for electromagnetic shielding interference(EMI)materials with multifunctional and wideband EMI performance has become urgent.Controllin... With the continuous advancement of communication technology,the escalating demand for electromagnetic shielding interference(EMI)materials with multifunctional and wideband EMI performance has become urgent.Controlling the electrical and magnetic components and designing the EMI material structure have attracted extensive interest,but remain a huge challenge.Herein,we reported the alternating electromagnetic structure composite films composed of hollow metal-organic frameworks/layered MXene/nanocellulose(HMN)by alternating vacuum-assisted filtration process.The HMN composite films exhibit excellent EMI shielding effectiveness performance in the GHz frequency(66.8 dB at Kaband)and THz frequency(114.6 dB at 0.1-4.0 THz).Besides,the HMN composite films also exhibit a high reflection loss of 39.7 dB at 0.7 THz with an effective absorption bandwidth up to 2.1 THz.Moreover,HMN composite films show remarkable photothermal conversion performance,which can reach 104.6℃under 2.0 Sun and 235.4℃under 0.8 W cm^(−2),respectively.The unique micro-and macrostructural design structures will absorb more incident electromagnetic waves via interfacial polarization/multiple scattering and produce more heat energy via the local surface plasmon resonance effect.These features make the HMN composite film a promising candidate for advanced EMI devices for future 6G communication and the protection of electronic equipment in cold environments. 展开更多
关键词 metal-organic frameworks MXene NANOCELLULOSE Electromagnetic shielding Photothermal conversion
下载PDF
Expediting^(*)OH accumulation kinetics on metal-organic frameworks-derived CoOOH with CeO_(2) “accelerator” for electrocatalytic 5-hydroxymethylfurfural oxidation valorization
5
作者 Peiyun Zhou Haokun Pan +3 位作者 Guangtong Hai Xiang Liu Xiubing Huang Ge Wang 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2024年第11期721-732,共12页
In this work,nickel foam supported CeO_(2)-modified CoBDC(BDC stands for terephthalic acid linker)metal-organic frameworks(NF/CoBDC@CeO_(2)) are prepared by hydrothermal and subsequent impregnation methods,which can b... In this work,nickel foam supported CeO_(2)-modified CoBDC(BDC stands for terephthalic acid linker)metal-organic frameworks(NF/CoBDC@CeO_(2)) are prepared by hydrothermal and subsequent impregnation methods,which can be further transformed to NF/CoOOH@CeO_(2) by reconstruction during the electrocatalytic test.The obtained NF/CoOOH@CeO_(2) exhibits excellent performance in electrocatalytic oxidation of 5-hydroxymethylfurfural(HMF) because the introduction of CeO_(2) can optimize the electronic structure of the heterointerface and accelerate the accumulation of ^(*)OH.It requires only a potential of 1.290 V_(RHE) to provide a current density of 50 mA cm^(-2) in 1.0 M KOH+50 mM HMF,which is 222 mV lower than that required in 1,0 M KOH(1.512 V_(RHE)).In addition,density-functional theory calculation results demonstrate that CeO_(2) biases the electrons to the CoOOH side at the heterointerface and promotes the adsorption of ^(*)OH and ^(*)HMF on the catalyst surface,which lower the reaction energy barrier and facilitate the electrocata lytic oxidation process. 展开更多
关键词 CeO_(2) metal-organic frameworks 5-Hydroxymethylfurfural oxidation reaction HETEROINTERFACE Reconstruction
下载PDF
Regulating interfacial behavior of zinc metal anode via metal-organic framework functionalized separator
6
作者 Ruotong Li Liang Pan +6 位作者 Ziyu Peng Ningning Zhao Zekun Zhang Jing Zhu Lei Dai Ling Wang Zhangxing He 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2024年第6期213-220,I0006,共9页
Aqueous zinc ion batteries(AZIBs)are one of the promising energy storage devices.However,uncontrolled dendrite and side reactions have seriously hindered its further application.In this study,the metal-organic framewo... Aqueous zinc ion batteries(AZIBs)are one of the promising energy storage devices.However,uncontrolled dendrite and side reactions have seriously hindered its further application.In this study,the metal-organic framework(MOF)functionalized glass fiber separator(GF-PFC-31)was used to regulate interfacial behavior of zinc metal anode,enabling the development of high-performance AZIBs.In PFC-31,there areπ-πinteractions between two adjacent benzene rings with a spacing of 3.199 A.This spacing can block the passage of[Zn(H_(2)O)_6]^(2+)(8.6 A in diameter)through the GF-PFC-31 separator to a certain extent,which promotes the deposition process of Zn ions.In addition,the sulfonic acid group(-S03H)contained in GF-PFC-31 can form a hydrogen bonding network with H_(2)O,which can provide a desolvation effect and reduce the side reaction.Consequently,GF-PFC-31 separator achieves uniform deposition of Zn ions.The Zn‖GF-PFC-31‖Zn symmetric cell exhibits stable cycle life(3000 h at 1.2 mA cm^(-2),2000 h at 0.3 mA cm^(-2),and 2000 h at 5.0 mA cm^(-2)),and Zn‖GF-PFC-31‖MnO_(2) full cell with GF-PFC-31 separator can cycle for 1000 cycles at 1.2 A g^(-1)with capacity retention rate of 82.5%.This work provides a promising method to achieve high-performance AZIBs. 展开更多
关键词 Aqueous zinc ion batteries Interfacial behavior metal-organic framework Sulfonic acid group SEPARATOR
下载PDF
Temperature-feedback two-photon-responsive metal-organic frameworks for efficient photothermal therapy
7
作者 Xianshun Sun Xin Lu +4 位作者 Wenyao Duan Bo Li Yupeng Tian Dandan Li Hongping Zhou 《中国科学技术大学学报》 CAS CSCD 北大核心 2024年第6期53-59,I0011,共8页
The realization of real-time thermal feedback for monitoring photothermal therapy(PTT)under near-infrared(NIR)light irradiation is of great interest and challenge for antitumor therapy.Herein,by assembling highly effi... The realization of real-time thermal feedback for monitoring photothermal therapy(PTT)under near-infrared(NIR)light irradiation is of great interest and challenge for antitumor therapy.Herein,by assembling highly efficient photothermal conversion gold nanorods and a temperature-responsive probe((E)-4-(4-(diethylamino)styryl)-1-methylpyridin-1-ium,PyS)within MOF-199,an intelligent nanoplatform(AMPP)was fabricated for simultaneous chemodynamic therapy and NIR light-induced temperature-feedback PTT.The fluorescence intensity and temperature of the PyS probe are linearly related due to the restriction of the rotation of the characteristic monomethine bridge.Moreover,the copper ions resulting from the degradation of MOF-199 in an acidic microenvironment can convert H_(2)O_(2)into•OH,resulting in tumor ablation through a Fenton-like reaction,and this process can be accelerated by increasing the temperature.This study establishes a feasible platform for fabricating highly sensitive temperature sensors for efficient temperature-feedback PTT. 展开更多
关键词 metal-organic framework TWO-PHOTON temperature feedback photothermal therapy chemodynamic therapy
下载PDF
Improvement of ionic conductivity of solid polymer electrolyte based on Cu-Al bimetallic metal-organic framework fabricated through molecular grafting
8
作者 Liu-bin SONG Tian-yuan LONG +5 位作者 Min-zhi XIAO Min LIU Ting-ting ZHAO Yin-jie KUANG Lin JIANG Zhong-liang XIAO 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2024年第9期2943-2958,共16页
A composite solid electrolyte comprising a Cu-Al bimetallic metal-organic framework(CAB),lithium salt(LiTFSI)and polyethylene oxide(PEO)was fabricated through molecular grafting to enhance the ionic conductivity of th... A composite solid electrolyte comprising a Cu-Al bimetallic metal-organic framework(CAB),lithium salt(LiTFSI)and polyethylene oxide(PEO)was fabricated through molecular grafting to enhance the ionic conductivity of the PEO-based electrolytes.Experimental and molecular dynamics simulation results indicated that the electrolyte with 10 wt.%CAB(PL-CAB-10%)exhibits high ionic conductivity(8.42×10~(-4)S/cm at 60℃),high Li+transference number(0.46),wide electrochemical window(4.91 V),good thermal stability,and outstanding mechanical properties.Furthermore,PL-CAB-10%exhibits excellent cycle stability in both Li-Li symmetric battery and Li/PL-CAB-10%/LiFePO4 asymmetric battery setups.These enhanced performances are primarily attributable to the introduction of the versatile CAB.The abundant metal sites in CAB can react with TFSI~-and PEO through Lewis acid-base interactions,promoting LiTFSI dissociation and improving ionic conductivity.Additionally,regular pores in CAB provide uniformly distributed sites for cation plating during cycling. 展开更多
关键词 polyethylene oxide Cu−Al bimetallic metal-organic framework solid lithium metal battery molecular grafting ionic conductivity
下载PDF
Photophysics of metal-organic frameworks:A brief overview
9
作者 刘晴硕 余俊宏 胡建波 《Chinese Physics B》 SCIE EI CAS CSCD 2024年第1期122-133,共12页
Metal-organic frameworks(MOFs),which are self-assembled porous coordination materials,have garnered considerable attention in the fields of optoelectronics,photovoltaic,photochemistry,and photocatalysis due to their d... Metal-organic frameworks(MOFs),which are self-assembled porous coordination materials,have garnered considerable attention in the fields of optoelectronics,photovoltaic,photochemistry,and photocatalysis due to their diverse structures and excellent tunability.However,the performance of MOF-based optoelectronic applications currently falls short of the industry benchmark.To enhance the performance of MOF materials,it is imperative to undertake comprehensive investigations aimed at gaining a deeper understanding of photophysics and sequentially optimizing properties related to photocarrier transport,recombination,interaction,and transfer.By utilizing femtosecond laser pulses to excite MOFs,time-resolved optical spectroscopy offers a means to observe and characterize these ultrafast microscopic processes.This approach adds the time coordinate as a novel dimension for comprehending the interaction between light and MOFs.Accordingly,this review provides a comprehensive overview of the recent advancements in the photophysics of MOFs and additionally outlines potential avenues for exploring the time domain in the investigation of MOFs. 展开更多
关键词 metal-organic framework(MOF) ultrafast spectroscopy PHOTOPHYSICS carrier dynamics
下载PDF
Metal-organic framework-derived porous carbon for the advanced aqueous zinc-ion hybrid capacitor
10
作者 LIU Wei-fang HU Zi-han ZHANG Qi 《Journal of Central South University》 SCIE EI CAS CSCD 2024年第7期2268-2279,共12页
Aqueous zinc ion hybrid capacitors(ZIHCs)are considered one of the most promising electrochemical energy storage systems due to their high safety,environmental friendliness,low cost,and high power density.However,the ... Aqueous zinc ion hybrid capacitors(ZIHCs)are considered one of the most promising electrochemical energy storage systems due to their high safety,environmental friendliness,low cost,and high power density.However,the low energy density and the lack of sustainable design strategies for the cathodes hinder the practical application of ZIHCs.Herein,we design the N and O co-doped porous carbon cathode by annealing metal-organic framework(ZIF-8).ZIF-8 retains the original dodecahedral structure with a high specific surface(2814.67 m^(2)/g)and I_(G)/I_(D) ratio of 1.0 during carbonization and achieves self-doping of N and O heteroatoms.Abundant defect sites are introduced into the porous carbon to provide additional active sites for ion adsorption after the activation of carbonized ZIF-8 by KOH treatment.The ZIHCs assembled with modified ZIF-8 as the cathode and commercial zinc foil as the anode show an energy density of 125 W∙h/kg and a power density of 79 W/kg.In addition,this ZIHCs device achieves capacity retention of 77.8%after 9000 electrochemical cycles,which is attributed to the diverse pore structure and plentiful defect sites of ZIF-8-800(KOH).The proposed strategy may be useful in developing high-performance metal-ion hybrid capacitors for large-scale energy storage. 展开更多
关键词 zinc ion hybrid capacitor CATHODE metal-organic framework(ZIF-8) KOH activation
下载PDF
Metal-Organic Framework Enabling Poly(Vinylidene Fluoride)-Based Polymer Electrolyte for Dendrite-Free and Long-Lifespan Sodium Metal Batteries
11
作者 Yusi Lei Liang Yue +4 位作者 Yuruo Qi Yubin Niu Shujuan Bao Jie Song Maowen Xu 《Energy & Environmental Materials》 SCIE EI CAS CSCD 2024年第1期68-76,共9页
Sodium dentrite formed by uneven plating/stripping can reduce the utilization of active sodium with poor cyclic stability and,more importantly,cause internal short circuit and lead to thermal runaway and fire.Therefor... Sodium dentrite formed by uneven plating/stripping can reduce the utilization of active sodium with poor cyclic stability and,more importantly,cause internal short circuit and lead to thermal runaway and fire.Therefore,sodium dendrites and their related problems seriously hinder the practical application of sodium metal batteries(SMBs).Herein,a design concept for the incorporation of metal-organic framework(MOF)in polymer matrix(polyvinylidene fluoride-hexafluoropropylene)is practiced to prepare a novel gel polymer electrolyte(PH@MOF polymer-based electrolyte[GPE])and thus to achieve high-performance SMBs.The addition of the MOF particles can not only reduce the movement hindrance of polymer chains to promote the transfer of Na^(+)but also anchor anions by virtue of their negative charge to reduce polarization during electrochemical reaction.A stable cycling performance with tiny overpotential for over 800 h at a current density of 5 mA cm^(-2)with areal capacity of 5 mA h cm^(-2)is achieved by symmetric cells based on the resulted GPE while the Na_(3)V_(2)O_(2)(PO_(4))_(2)F@rGO(NVOPF)|PH@MOF|Nacell also displays impressive specific cycling capacity(113.3 mA h g^(-1)at 1 C)and rate capability with considerable capacity retention. 展开更多
关键词 dendrite-free gel polymer electrolyte metal organic framework sodium batteries
下载PDF
Engineering Spin States of Isolated Copper Species in a Metal-Organic Framework Improves Urea Electrosynthesis 被引量:8
12
作者 Yuhang Gao Jingnan Wang +4 位作者 Yijun Yang Jian Wang Chuang Zhang Xi Wang Jiannian Yao 《Nano-Micro Letters》 SCIE EI CAS CSCD 2023年第9期536-549,共14页
The catalytic activities are generally believed to be relevant to the electronic states of their active center, but understanding this relationship is usually difficult. Here, we design two types of catalysts for elec... The catalytic activities are generally believed to be relevant to the electronic states of their active center, but understanding this relationship is usually difficult. Here, we design two types of catalysts for electrocatalytic urea via a coordination strategy in a metal–organic frameworks: Cu^(Ⅲ)-HHTP and Cu^(Ⅱ)-HHTP. Cu^(Ⅲ)-HHTP exhibits an improved urea production rate of 7.78 mmol h^(−1)g^(−1) and an enhanced Faradaic efficiency of 23.09% at-0.6 V vs. reversible hydrogen electrode, in sharp contrast to Cu^(Ⅱ)-HHTP.Isolated CuⅢspecies with S = 0 spin ground state are demonstrated as the active center in Cu^(Ⅲ)-HHTP, different from Cu^(Ⅱ) with S = 1/2 in Cu^(Ⅱ)-HHTP. We further demonstrate that isolated Cu^(Ⅲ)with an empty dx2-y20orbital in Cu^(Ⅲ)-HHTP experiences a single-electron migration path with a lower energy barrier in the C–N coupling process, while Cu^(Ⅱ)with a single-spin state( d_(x2-y2)^(1)) in Cu^(Ⅱ)-HHTP undergoes a two-electron migration pathway. 展开更多
关键词 ELECTROCATALYSIS Urea synthesis metal-organic framework Spin catalysis C-N coupling
下载PDF
Dual-conductive metal-organic framework@MXene heterogeneity stabilizes lithium-ion storage 被引量:2
13
作者 Lanju Sun Honglei Wang +7 位作者 Shengliang Zhai Jikai Sun Xu Fang Hongyan Yang Dong Zhai Chengcheng Liu Wei-Qiao Deng Hao Wu 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2023年第1期368-376,I0009,共10页
Although a few pristine metal-organic frameworks(MOFs) of graphene analogue topology exhibit high intrinsic electrical conductivity, their use in lithium-ion batteries(LIBs) is still hampered by unfavorable Li+adsorpt... Although a few pristine metal-organic frameworks(MOFs) of graphene analogue topology exhibit high intrinsic electrical conductivity, their use in lithium-ion batteries(LIBs) is still hampered by unfavorable Li+adsorption energy(ΔEa). In this paper, an electroconductive ferrocene-based MOF@MXene heterostructure is built to provide stable anodes for Li+storage. Charge density difference and planar average potential charge density show substantial redistribution of charges at the interfaces, transferring from MXene to MOF layers. Moreover, density functional theory(DFT) calculations reveal that the interaction between MXene and MOF significantly increases the ΔEa. As a result, the heterostructure anode exhibits high capacities and outstanding cycling stability with a capacity retention of 80% after 5000 cycles at 5 A g^(-1), outperforming mono-component MXene and MOF. Furthermore, the heterostructure anode is built into a full cell with a commercial NCM 532 cathode, delivering a high energy density of 611 Wh kg^(-1)and power density of 7600 W kg^(-1). The developed conductive MOF@MXene heterogeneity for improved LIB offers valuable insights into the design of advanced electrode materials for energy storage. 展开更多
关键词 MXene metal-organic framework HETEROSTRUCTURE Lithium-ion battery Adsorption energy
下载PDF
Tuning the electronic structure of a metal-organic framework for an efficient oxygen evolution reaction by introducing minor atomically dispersed ruthenium 被引量:2
14
作者 Yuwen Li Yuhang Wu +5 位作者 Tongtong Li Mengting Lu Yi Chen Yuanjing Cui Junkuo Gao Guodong Qian 《Carbon Energy》 SCIE CSCD 2023年第2期61-71,共11页
The establishment of efficient oxygen evolution electrocatalysts is of great value but also challenging.Herein,a durable metal–organic framework(MOF)with minor atomically dispersed ruthenium and an optimized electron... The establishment of efficient oxygen evolution electrocatalysts is of great value but also challenging.Herein,a durable metal–organic framework(MOF)with minor atomically dispersed ruthenium and an optimized electronic structure is constructed as an efficient electrocatalyst.Significantly,the obtained NiRu_(0.08)-MOF with doping Ru only needs an overpotential of 187 mV at 10 mA cm^(-2) with a Tafel slop of 40 mV dec^(-1) in 0.1M KOH for the oxygen evolution reaction,and can work continuously for more than 300 h.Ultrahigh Ru mass activity is achieved,reaching 56.7 Ag^(-1)_(Ru) at an overpotential of 200 mV,which is 36 times higher than that of commercial RuO_(2).X-ray adsorption spectroscopy and density function theory calculations reveal that atomically dispersed ruthenium on metal sites in MOFs is expected to optimize the electronic structure of nickel sites,thus improving the conductivity of the catalyst and optimizing the adsorption energy of intermediates,resulting in significant optimization of electrocatalytic performance.This study could provide a new avenue for the design of efficient and stable MOF electrocatalysts. 展开更多
关键词 ELECTROCATALYSIS electronic structure metal-organic framework oxygen evolution reaction
下载PDF
Research progress on the substrate for metal-organic framework(MOF) membrane growth for separation 被引量:1
15
作者 Wufeng Wu Xilu Hong +2 位作者 Jiang Fan Yanying Wei Haihui Wang 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2023年第4期299-313,共15页
During the last decade, metal-organic frameworks(MOFs) have been applied in various fields due to their unique chemical and functional advantages. One of the widespread research hotspots is MOF-based membranes for sep... During the last decade, metal-organic frameworks(MOFs) have been applied in various fields due to their unique chemical and functional advantages. One of the widespread research hotspots is MOF-based membranes for separations, specifically continuous defect-free MOF membranes, which are usually grown on porous substrates. The substrate not only serves as the MOF layer support but also has a great influence on the membrane fabrication process and the final separation performance of the resultant membrane. In this review, we mainly introduce the progress focused on the substrates for MOF membranes fabrication. The substrate modifications and seeding methods aimed at synthesizing highquality MOF membranes are also summarized systematically. 展开更多
关键词 Membrane separation MOF membrane metal-organic frameworks SUPPORT Synthesis
下载PDF
Metal-organic frameworks based single-atom catalysts for advanced fuel cells and rechargeable batteries 被引量:1
16
作者 Yifei Wu Peng Hu +5 位作者 Fengping Xiao Xiaoting Yu Wenqi Yang Minqi Liang Ziwei Liang Aixin Zhu 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2023年第5期501-534,I0012,共35页
The next-generation energy storage systems such as fuel cells,metal-air batteries,and alkali metal(Li,Na)-chalcogen(S,Se)batteries have received increasing attention owing to their high energy density and low cost.How... The next-generation energy storage systems such as fuel cells,metal-air batteries,and alkali metal(Li,Na)-chalcogen(S,Se)batteries have received increasing attention owing to their high energy density and low cost.However,one of the main obstacles of these systems is the poor reaction kinetics in the involved chemical reactions.Therefore,it is essential to incorporate suitable and efficient catalysts into the cell.These years,single-atom catalysts(SACs)are emerging as a frontier in catalysis due to their maximum atom efficiency and unique reaction selectivity.For SACs fabrication,metal-organic frameworks(MOFs)have been confirmed as promising templates or precursors due to their high metal loadings,structural adjustability,porosity,and tailorable catalytic site.In this review,we summarize effective strategies for fabricating SACs by MOFs with corresponding advanced characterization techniques and illustrate the key role of MOFs-based SACs in these batteries by explaining their reaction mechanisms and challenges.Finally,current applications,prospects,and opportunities for MOFs-based SACs in energy storage systems are discussed. 展开更多
关键词 metal-organic frameworks Single-atom catalysts Rechargeable batteries ELECTROCATALYSTS Coordination configuration
下载PDF
Interfacial Engineering of Defect-Rich and Multi-Heteroatom-Doped Metal-Organic Framework-Derived Manganese Fluoride Anodes to Boost Lithium Storage 被引量:1
17
作者 Xiaohong Tan Jiawei Liu +3 位作者 Jiating Huang Yilin Li Akif Zeb Xiaoming Lin 《Energy & Environmental Materials》 SCIE EI CAS CSCD 2023年第5期449-459,共11页
Manganese fluoride(MnF2)is a high-performance lithium-ion battery anode material with an excellent structural stability,low synthesis cost,and better manufacturing convenience.However,its low theoretical capacity(577 ... Manganese fluoride(MnF2)is a high-performance lithium-ion battery anode material with an excellent structural stability,low synthesis cost,and better manufacturing convenience.However,its low theoretical capacity(577 mAh g^(-1)),weak conductivity of fluoride,and poor recyclability limit its practical application.Fortunately,oxygen vacancies(Ov)and heteroatomic doping are among the most promising strategies to modulate the inherent reduced electronic conductivity and kinetic response of electrode materials in order to boost their lithium storage capacity.Herein,self-templating,self-optimizing,and self-supporting metal-organic framework template approach with the introduction of oxygen vacancies by substitution of exogenous heteroatoms is proposed,where triple heteroatom-doped(N,O,and F)carbon-encapsulated MOF-derived manganese fluoride(Ov-ZMF@NOFs)microstructures are designed.Interestingly,the exogenously introduced triple heteroatomic carbon matrix forms a fluffy three-dimensional mechanical structure,interlaced conducting networks,efficient conducting pathways,and intense electrochemical dynamics at the periphery of the manganese fluoride nanoparticles.Benefiting from the above-mentioned features,the Ov-ZMF@NOFs exhibit expected electrochemical properties with ultra-long recyclability(high reversible capacity of 419 mAh g^(-1)at 6 A g^(-1))and good rate performance(capacity of 232 mAh g^(-1)at a current density of 16 A g^(-1)).Theoretical calculations underline the essential contribution of multiple heteroatoms doping in boosting the electrode conductivity and reducing the lithium-ion migration energy barrier.Combining controllable vacancy engineering and heteroatom doping technology at the nanoscale provides a new philosophy and concept for the design and fabrication of next-generation high-energy lithium-ion battery materials. 展开更多
关键词 anode lithium-ion batteries metal-organic framework multi-heteroatomic doping oxygen vacancies
下载PDF
Structural survey of metal-covalent organic frameworks and covalent metal-organic frameworks 被引量:1
18
作者 Chaozhi Xiong Zhenwu Shao +3 位作者 Jia’nan Hong Kexin Bi Qingsong Huang Chong Liu 《International Journal of Minerals,Metallurgy and Materials》 SCIE EI CAS CSCD 2023年第12期2297-2309,共13页
This review offers an overview of the latest developments in metal-covalent organic framework(MCOF)and covalent metal-organic framework(CMOF)materials,whose construction entails a combination of reversible coordinatio... This review offers an overview of the latest developments in metal-covalent organic framework(MCOF)and covalent metal-organic framework(CMOF)materials,whose construction entails a combination of reversible coordination and covalent bonding adapted from metal-organic frameworks(MOFs)and covalent organic frameworks(COFs),respectively.With an emphasis on the MCOF and CMOF structures,this review surveys their building blocks and topologies.Specifically,the frameworks are classified based on the dimensions of their components(building blocks),namely,discrete building blocks and one-dimensional infinite building blocks.For the first category,the materials are further divided into collections of two-and three-dimensional networks based on their topologies.For the second category,the recently emerging MCOFs with woven structures are covered.Finally,the state-of-the-art in MCOF and CMOF chemistry has been laid out for promising avenues in future developments. 展开更多
关键词 metal–covalent organic frameworks covalent metal-organic frameworks TOPOLOGY building block
下载PDF
Zinc-Based Metal-Organic Frameworks for High-Performance Supercapacitor Electrodes:Mechanism Underlying Pore Generation 被引量:1
19
作者 Shigeyuki Umezawa Takashi Douura +6 位作者 Koji Yoshikawa Daisuke Tanaka Vlad Stolojan S.Ravi P.Silva Mika Yoneda Kazuma Gotoh Yasuhiko Hayashi 《Energy & Environmental Materials》 SCIE EI CAS CSCD 2023年第2期100-112,共13页
Heat treatment of metal-organic frameworks(MOFs)has provided a wide variety of functional carbons coordinated with metal compounds.In this study,two kinds of zinc-based MOF(ZMOF),C_(16)H_(10)O_(4)Zn(ZMOF1)and C_(8)H_(... Heat treatment of metal-organic frameworks(MOFs)has provided a wide variety of functional carbons coordinated with metal compounds.In this study,two kinds of zinc-based MOF(ZMOF),C_(16)H_(10)O_(4)Zn(ZMOF1)and C_(8)H_(4)O_(4)Zn(ZMOF2),were prepared.ZMOF1 and ZMOF2 were carbonized at 1000℃,forming CZMOF1 and CZMOF2,respectively.The specific surface area(S_(BET))of CZMOF2 was~2700 m^(2)g^(−1),much higher than that of CZMOF1(~1300 m^(2)g^(−1)).A supercapacitor electrode based on CZMOF2 achieved specific capacitances of 360,278,and 221 F g^(−1)at 50,250,and 1000 mA g^(−1)in an aqueous electrolyte(H2SO_(4)),respectively,the highest values reported to date for ZMOF-derived electrodes under identical conditions.The practical applicability of the CZMOF-based supercapacitor was verified in non-aqueous electrolytes.The initial capacitance retention was 78%after 100000 charge/discharge cycles at 10 A g^(−1).Crucially,the high capacitance of CZMOF2 arises from pore generation during carbonization.Below 1000℃,pore generation is dominated by the Zn/C ratio of ZMOFs,as carbon atoms reduce the zinc oxides formed during carbonization.Above 1000℃,a high O/C ratio becomes essential for pore generation because the oxygen functional groups are pyrolyzed.These findings will provide insightful information for other metal-based MOFderived multifunctional carbons. 展开更多
关键词 metal-organic frameworks pore generation porous carbons SUPERCAPACITOR zinc oxides
下载PDF
Novel in-capsule synthesis of metal-organic framework for innovative carbon dioxide capture system 被引量:1
20
作者 Wei Yu Ming Gao +5 位作者 Guanhe Rim Tony G.Feric Mark L.Rivers Ammar Alahmed Aqil Jamal Ah-Hyung Alissa Park 《Green Energy & Environment》 SCIE EI CAS CSCD 2023年第3期767-774,共8页
Metal-Organic Frameworks(MOFs)have been developed as solid sorbents for CO_(2) capture applications and their properties can be controlled by tuning the chemical blocks of their crystalline units.A number of MOFs(e.g.... Metal-Organic Frameworks(MOFs)have been developed as solid sorbents for CO_(2) capture applications and their properties can be controlled by tuning the chemical blocks of their crystalline units.A number of MOFs(e.g.,HKUST-1)have been developed but the question remains how to deploy them for gas-solid contact.Unfortunately,the direct use of MOFs as nanocrystals would lead to serious problems and risks.Here,for the first time,we report a novel MOF-based hybrid sorbent that is produced via an innovative in-situ microencapsulated synthesis.Using a custom-made double capillary microfluidic assembly,double emulsions of the MOF precursor solutions and UV-curable silicone shell fluid are produced.Subsequently,HKUST-1 MOF is successfully synthesized within the droplets enclosed in the gas permeable microcapsules.The developed MOF-bearing microcapsules uniquely allow the deployment of functional nanocrystals without the challenge of handling ultrafine particles,and further,can selectively reject undesired compounds to protect encapsulated MOFs. 展开更多
关键词 ENCAPSULATION metal-organic frameworks(MOFs) Carbon capture In-situ microencapsulated synthesis
下载PDF
上一页 1 2 250 下一页 到第
使用帮助 返回顶部