Solid polymer composite electrolytes possess the benefits of superior compatibility with electrodes and good thermal characteristics for more secure energy storage equipment.Herein,a new gel polymer electrolyte(GPE)co...Solid polymer composite electrolytes possess the benefits of superior compatibility with electrodes and good thermal characteristics for more secure energy storage equipment.Herein,a new gel polymer electrolyte(GPE)containing NH_(2)-MIL-53(Al),[PP_(13)][TFSI],LiTFSI,and PVDF-HFP was prepared using a simple method of solution casting.The effects of encapsulating different ratios of ionic liquid([PP_(13)][TFSI])into the micropores of functionalized metal-organic frameworks(NH_(2)-MIL-53(Al))on the electrochemical properties were compared.XRD,SEM,nitrogen adsorption-desorption isotherms,and electrochemical measurements were conducted.This GPE demonstrates a superior ionic conductivity of 8.08×10^(-4)S·cm^(-1)at 60℃and can sustain a discharge specific capacity of 156.6 mA·h·g^(-1)at 0.2 C for over 100 cycles.This work might offer a potential approach to alleviate the solid-solid contact with the solid-state electrolyte and electrodes and broaden a new window for the creation of all-solid-state batteries.展开更多
To address the limitations of the separate fluoride removal or detection in the existing materials,herein,amino-decorated metal organic frameworks NH_(2)-MIL-53(Al)have been succinctly fabricated by a sol-hydrothermal...To address the limitations of the separate fluoride removal or detection in the existing materials,herein,amino-decorated metal organic frameworks NH_(2)-MIL-53(Al)have been succinctly fabricated by a sol-hydrothermal method for simultaneous removal and determination of fluoride.As a consequence,the proposed NH_(2)-MIL-53(Al)features high uptake capacity(202.5 mg/g)as well as fast adsorption rate,being capable of treating 5 ppm of fluoride solution to below the permitted threshold in drinking water within 15 min.Specifically,the specific binding between fluoride and NH_(2)-MIL-53(Al)results in the release of fluorescent ligand NH2-BDC,conducive to the determination of fluoride via a concentration-dependent fluorescence enhancement effect.As expected,the resulting NH_(2)-MIL-53(Al)sensor exhibits selective and sensitive detection(with the detection limit of 0.31μmol/L)toward fluoride accompanied with a wide response interval(0.5-100μmol/L).More importantly,the developed sensor can be utilized for fluoride detection in practical water systems with satisfying recoveries from 89.6% to 116.1%,confirming its feasibility in monitoring the practical fluoride-contaminated waters.展开更多
A postsynthetic modification method was used to prepare salicylaldehyde functionalized metal-organicframeworks through the nucleophilic addition of salicylaldehyde with the amine group present in the frameworks ofNH2-...A postsynthetic modification method was used to prepare salicylaldehyde functionalized metal-organicframeworks through the nucleophilic addition of salicylaldehyde with the amine group present in the frameworks ofNH2-MIL-53（A1）. Hydroxyl groups were successfully grafted onto NI-I2-MIL-53（A1）, and imine groups were formed.Importantly, these hydroxyl and imine groups of the resulting NH2-MIL-53（A1）-SA can be used as the anchoringgroup to stabilise Au^3＋ ions and Au^0 nanoparticles（NPs）. By doing this, Au^3＋ ions and Au^0 NPs were successfully en-capsulated in the cages of NH2-MIL-53（A1） by a simple impregnation method. The resulting gold functionalizedNH2-MIL-53（AI） showed good catalytic activities in the one-pot synthesis of structurally divergent propargylaminesby three-component coupling reactions of aldehydes, amines and alkynes. Various aromatic/aliphatic aldehydes, aro-matic alkynes, and piperidine were able to undergo three-component coupling on NH2-MIL-53（A1）-Au. In addition,the catalyst NH2-M/L-53（A/）-Au was recovered easily by centrifugation and reused up to four times. Thus, it can beused for the environmentally friendly synthesis ofpropargylamines.展开更多
For all-solid-state lithium batteries(ASSLBs),polymer-blended solid composite electrolytes(SCEs)have drawn wide interest owing to their significance in improving the interfacial solid-solid contacts and inhibiting the...For all-solid-state lithium batteries(ASSLBs),polymer-blended solid composite electrolytes(SCEs)have drawn wide interest owing to their significance in improving the interfacial solid-solid contacts and inhibiting the growth of lithium dendrites.In this work,SCEs based on PVDF-HFP/PMMA matrix containing MOFs(NH2-MIL-53(Al))and LiTFSI were designed and synthesized employing an easy solution casting method.The synthesized samples were examined by XRD,SEM,EDS,and electrochemical tests.It was found that MPP-2 SCE not only has excellent ionic conductivity at 60℃ of 5.54×10^(−4) S cm^(−1),but also exhibits superior interfacial compatibility in Li||Li symmetric batteries,which can constantly cycle for about 800 h at 0.1 mA cm^(−2) with no short-circuiting.The assembled Li|MPP-2|LiFePO4 cell exhibited a first discharge specific capacity of up to 157.1 mAh g^(−1) at 60℃ and 0.2 C.This work may help to further advance the progress of ASSLBs in the future.展开更多
基金financially supported by National Natural Science Foundation of China(21701083)Postgraduate Research&Practice Innovation Program of Jiangsu Province(KYCX20_3137)。
文摘Solid polymer composite electrolytes possess the benefits of superior compatibility with electrodes and good thermal characteristics for more secure energy storage equipment.Herein,a new gel polymer electrolyte(GPE)containing NH_(2)-MIL-53(Al),[PP_(13)][TFSI],LiTFSI,and PVDF-HFP was prepared using a simple method of solution casting.The effects of encapsulating different ratios of ionic liquid([PP_(13)][TFSI])into the micropores of functionalized metal-organic frameworks(NH_(2)-MIL-53(Al))on the electrochemical properties were compared.XRD,SEM,nitrogen adsorption-desorption isotherms,and electrochemical measurements were conducted.This GPE demonstrates a superior ionic conductivity of 8.08×10^(-4)S·cm^(-1)at 60℃and can sustain a discharge specific capacity of 156.6 mA·h·g^(-1)at 0.2 C for over 100 cycles.This work might offer a potential approach to alleviate the solid-solid contact with the solid-state electrolyte and electrodes and broaden a new window for the creation of all-solid-state batteries.
基金supported by the National Key R&D Program of China(No.2017YFA0207202)the National Natural Science Foundation of China(No.51572263,No.51772299,No.41701259).
文摘To address the limitations of the separate fluoride removal or detection in the existing materials,herein,amino-decorated metal organic frameworks NH_(2)-MIL-53(Al)have been succinctly fabricated by a sol-hydrothermal method for simultaneous removal and determination of fluoride.As a consequence,the proposed NH_(2)-MIL-53(Al)features high uptake capacity(202.5 mg/g)as well as fast adsorption rate,being capable of treating 5 ppm of fluoride solution to below the permitted threshold in drinking water within 15 min.Specifically,the specific binding between fluoride and NH_(2)-MIL-53(Al)results in the release of fluorescent ligand NH2-BDC,conducive to the determination of fluoride via a concentration-dependent fluorescence enhancement effect.As expected,the resulting NH_(2)-MIL-53(Al)sensor exhibits selective and sensitive detection(with the detection limit of 0.31μmol/L)toward fluoride accompanied with a wide response interval(0.5-100μmol/L).More importantly,the developed sensor can be utilized for fluoride detection in practical water systems with satisfying recoveries from 89.6% to 116.1%,confirming its feasibility in monitoring the practical fluoride-contaminated waters.
文摘A postsynthetic modification method was used to prepare salicylaldehyde functionalized metal-organicframeworks through the nucleophilic addition of salicylaldehyde with the amine group present in the frameworks ofNH2-MIL-53（A1）. Hydroxyl groups were successfully grafted onto NI-I2-MIL-53（A1）, and imine groups were formed.Importantly, these hydroxyl and imine groups of the resulting NH2-MIL-53（A1）-SA can be used as the anchoringgroup to stabilise Au^3＋ ions and Au^0 nanoparticles（NPs）. By doing this, Au^3＋ ions and Au^0 NPs were successfully en-capsulated in the cages of NH2-MIL-53（A1） by a simple impregnation method. The resulting gold functionalizedNH2-MIL-53（AI） showed good catalytic activities in the one-pot synthesis of structurally divergent propargylaminesby three-component coupling reactions of aldehydes, amines and alkynes. Various aromatic/aliphatic aldehydes, aro-matic alkynes, and piperidine were able to undergo three-component coupling on NH2-MIL-53（A1）-Au. In addition,the catalyst NH2-M/L-53（A/）-Au was recovered easily by centrifugation and reused up to four times. Thus, it can beused for the environmentally friendly synthesis ofpropargylamines.
基金supported by National Natural Science Foundation of China(grant Nos.21701083,22179054)The Ministry of Science and Technology of the People's Republic of China(grant No.G2023014022L)Jiangsu Provincial Key Research and Development Program(grant No.BZ2023010).
文摘For all-solid-state lithium batteries(ASSLBs),polymer-blended solid composite electrolytes(SCEs)have drawn wide interest owing to their significance in improving the interfacial solid-solid contacts and inhibiting the growth of lithium dendrites.In this work,SCEs based on PVDF-HFP/PMMA matrix containing MOFs(NH2-MIL-53(Al))and LiTFSI were designed and synthesized employing an easy solution casting method.The synthesized samples were examined by XRD,SEM,EDS,and electrochemical tests.It was found that MPP-2 SCE not only has excellent ionic conductivity at 60℃ of 5.54×10^(−4) S cm^(−1),but also exhibits superior interfacial compatibility in Li||Li symmetric batteries,which can constantly cycle for about 800 h at 0.1 mA cm^(−2) with no short-circuiting.The assembled Li|MPP-2|LiFePO4 cell exhibited a first discharge specific capacity of up to 157.1 mAh g^(−1) at 60℃ and 0.2 C.This work may help to further advance the progress of ASSLBs in the future.
