This study determined the detergency properties of Catholyte, an electrochemically activated medium, on polyamide 6.6 as a possible alternative to conventional laundering detergents. Undyed polyamide 6.6 was used and ...This study determined the detergency properties of Catholyte, an electrochemically activated medium, on polyamide 6.6 as a possible alternative to conventional laundering detergents. Undyed polyamide 6.6 was used and soiled with keltex, corn starch, mineral oil, oleic acid, morpholine, vegetable fat, butanol, solvesso 150 and water. Some soiled fabric was retained as control and not laundered. Soiled fabric was laundered at 30 ~C as well as 40 ~C with either, distilled water, Catholyte, non-phosphate detergent, a 50/50 solution of Catholyte and non-phosphate detergent, or a 50/50 solution of Catholyte and phosphate detergent. Data were analyzed descriptively by using analysis of variance （ANOVA）, which fitted the factors of treatment and temperature, as well as all two-factor interactions between these variables. A probability value of 0.05 or less indicated significance. Catholyte was effective in removing soil and reached a/XE＊ value of 59.30, but was statistically different from the phosphate detergent. Temperature did not have a significant effect on soil removal from the fabric, but the interaction with a treatment had significant effects. Treatment alone had a significant soil removal effect on the fabric. Thus, the temperature was dependent on an interaction with the treatment. The non-phosphate detergent was efficient in removing soil from the fabric and slightly more efficient than either 50/50 Catholyte solution. The 50/50 Catholyte/non-phosphate detergent solution was slightly less effective than its phosphate containing counterpart. When considering the interaction between treatment and temperature, the 50/50 Catholyte/phosphate and 50/50 Catholyte/non-phosphate solutions were more efficient at 40 ~C. Thus the interaction between the solution and higher temperature proved to be a better combination. This was also the case for the Catholyte and the non-phosphate wash liquors. Catholyte, an environmentally friendly washing agent, is an attractive alternative to conventional laundry detergents because it removes soil efficiently from polyamide 6.6 fabric.展开更多
Development of catholytes with long-cycle lifespan,high interfacial stability,and fast electrochemical kinetics is crucial for the comprehensive deployment of high-energy density lithium metal batteries(LMBs)with cost...Development of catholytes with long-cycle lifespan,high interfacial stability,and fast electrochemical kinetics is crucial for the comprehensive deployment of high-energy density lithium metal batteries(LMBs)with cost-efficiency.In this study,a lithiated 2-mercaptopyridine(2-MP-Li)organosulfide was synthesized and used as the soluble catholyte for the first time.Under the routine working mode,the LMB using this 2-MP-Li catholyte possessed high capacity retention of 55.4%with a Coulombic efficiency(CE)of near 100%after 2,000 cycles.When a cell system was fully filled with 2-MP-Li catholyte,it yielded a double capacity with 15%improvement in the capacity retention,corresponding to 0.0182%capacity decay per cycle,as well as excellent rate performance even at 6 mA·cm^(−2).These superior achievements resulted from the enhanced interfacial stability of Li anode induced by the salt-type 2-MP-Li molecule and the avoiding of using neutral catholyte as the initial active material,thereby mitigating the side reactions originating from the polysulfide shuttle effect.Furthermore,density functional theory(DFT)calculation and kinetics investigations proved the pseudocapacitive characteristic and faster ion diffusion coefficient with this design.Besides,the fabricated energy storage device showed excellent performance but with low economic cost and easy processing.Such a LMB with an alterable amount of capacity has a high potential to be applied in flow-cell type batteries for large-scale grid energy storage in the future.展开更多
Acidic environments enhance CO_(2) utilization during CO_(2) electrolysis via a buffering effect that converts carbonates formed at the electrode surface back into CO_(2).Nevertheless,further investigation into acidic...Acidic environments enhance CO_(2) utilization during CO_(2) electrolysis via a buffering effect that converts carbonates formed at the electrode surface back into CO_(2).Nevertheless,further investigation into acidic CO_(2) electrolysis is required to improve its selectivity towards certain CO_(2) reduction reaction(CO_(2)RR)products,such as multicarbon(C2+)species,while enhancing its overall stability.In this study,liquid product recirculation in the catholyte and local OH−accumulation were identified as primary factors contributing to the degradation of gas diffusion electrodes mounted in closed‐loop catholyte configurations.We demonstrate that a single‐pass catholyte configuration prevents liquid product recirculation and maintains a continuous flow of acidic‐pH catholyte throughout the reaction while using the same volume as a closed‐loop setup.This approach improves electrode durability and maintains a Faradaic efficiency of 67%for multicarbon products over 4 h of CO_(2) electrolysis at−600 mA cm^(-2).展开更多
Electrodes,catalysts,membranes,if present,are three main components in constructing an MFC for harvesting desired maximum power density and achieving higher coulombic efficiency (CE).Great improvements have been made,...Electrodes,catalysts,membranes,if present,are three main components in constructing an MFC for harvesting desired maximum power density and achieving higher coulombic efficiency (CE).Great improvements have been made,based on previous researches,in developing and diversifying materials,aside from architectures.Electrodes most familiar to us are widely used carbon materials.For anodes,carbon matrix composites(e.g.,a combination of polyaniline(PANI)with TiO2 using carbon as substrate)have gained special attention,though carbon material itself can exhibit excellent performance by diversifying molecular structures such as carbon nanotubes(CNTs).In the meanwhile,the evolution of MFC architectures,heading to the direction of improving power generation,contributes to the combination of membranes and cathodes from separate modes to diverse assemblies,on which all sorts of catalysts,such as from commonly used Pt to iron phthalocyanine (Pc),metal tetramethoxyphenylporphyrin(TMPP),MnOx,or pyrolyzed iron(Ⅱ)phthalocyanine (pyr-FePc),can be immobilized through synthesis of these catalysts with polymer such as Nafion 117 (Dupont Co.,USA)or tetrafluoroethylen(eTeflon)containing functional groups or Polypyrrol(ePPy).In addition,catholytes with aqueous cathode immersed or flowing through the surface of air-cathode are favorably proposed containing transition metal redox couples or iron chelates.展开更多
Aqueous organic redox flow batteries(AORFBs),which exploit the reversible electrochemical reactions of water-soluble organic electrolytes to store electricity,have emerged as an efficient electrochemical energy storag...Aqueous organic redox flow batteries(AORFBs),which exploit the reversible electrochemical reactions of water-soluble organic electrolytes to store electricity,have emerged as an efficient electrochemical energy storage technology for the grid-scale integration of renewable electricity.pH-neutral AORFBs that feature high safety,low corrosivity,and environmental benignity are particularly promising,and their battery performance is significantly impacted by redox-active molecules and ion-exchange membranes(IEMs).Here,representative anolytes and catholytes engineered for use in pH-neutral AORFBs are outlined and summarized,as well as their side reactions that cause irreversible battery capacity fading.In addition,the recent achievements of IEMs for pH-neutral AORFBs are discussed,with a focus on the construction and tuning of ion transport channels.Finally,the critical challenges and potential research opportunities for developing practically relevant pH-neutral AORFBs are presented.展开更多
The relentless pursuit of sustainable and safe energy storage technologies hasdriven a departure from conventional lithium-based batteries toward other relevantalternatives. Among these, aqueous batteries have emerged...The relentless pursuit of sustainable and safe energy storage technologies hasdriven a departure from conventional lithium-based batteries toward other relevantalternatives. Among these, aqueous batteries have emerged as a promisingcandidate due to their inherent properties of being cost-effective, safe,environmentally friendly, and scalable. However, traditional aqueous systemshave faced limitations stemming from water's narrow electrochemical stabilitywindow (-1.23 V), severely constraining their energy density and viability inhigh-demand applications. Recent advancements in decoupling aqueous batteriesoffer a novel solution to overcome this challenge by separating the anolyteand catholyte, thereby expanding the theoretical operational voltage windowto over 3 V. One key component of this innovative system is the ion-selectivemembrane (ISM), acting as a barrier to prevent undesired crossover betweenelectrolytes. This review provides a comprehensive overview of recent advancementsin decoupling aqueous batteries, emphasizing the application of varioustypes of ISMs. Moreover, we summarize different specially designed ISMs andtheir performance attributes. By addressing the current challenges ISMs face,the review outlines potential pathways for future enhancement and developmentof aqueous decoupling batteries.展开更多
文摘This study determined the detergency properties of Catholyte, an electrochemically activated medium, on polyamide 6.6 as a possible alternative to conventional laundering detergents. Undyed polyamide 6.6 was used and soiled with keltex, corn starch, mineral oil, oleic acid, morpholine, vegetable fat, butanol, solvesso 150 and water. Some soiled fabric was retained as control and not laundered. Soiled fabric was laundered at 30 ~C as well as 40 ~C with either, distilled water, Catholyte, non-phosphate detergent, a 50/50 solution of Catholyte and non-phosphate detergent, or a 50/50 solution of Catholyte and phosphate detergent. Data were analyzed descriptively by using analysis of variance （ANOVA）, which fitted the factors of treatment and temperature, as well as all two-factor interactions between these variables. A probability value of 0.05 or less indicated significance. Catholyte was effective in removing soil and reached a/XE＊ value of 59.30, but was statistically different from the phosphate detergent. Temperature did not have a significant effect on soil removal from the fabric, but the interaction with a treatment had significant effects. Treatment alone had a significant soil removal effect on the fabric. Thus, the temperature was dependent on an interaction with the treatment. The non-phosphate detergent was efficient in removing soil from the fabric and slightly more efficient than either 50/50 Catholyte solution. The 50/50 Catholyte/non-phosphate detergent solution was slightly less effective than its phosphate containing counterpart. When considering the interaction between treatment and temperature, the 50/50 Catholyte/phosphate and 50/50 Catholyte/non-phosphate solutions were more efficient at 40 ~C. Thus the interaction between the solution and higher temperature proved to be a better combination. This was also the case for the Catholyte and the non-phosphate wash liquors. Catholyte, an environmentally friendly washing agent, is an attractive alternative to conventional laundry detergents because it removes soil efficiently from polyamide 6.6 fabric.
基金supported by the ZiQoo Chemical Co.,Ltd.All authors greatly acknowledge Associate Professor Akihiro Yoshida at Hirosaki University,Japan,to help measuring 1H NMR spectrum.Z.K.X.greatly acknowledges the Key Scientific Research Project of Universities in Henan Province(No.22A150023)Zhengzhou University Young Teacher Special Fund(No.226-33212552).
文摘Development of catholytes with long-cycle lifespan,high interfacial stability,and fast electrochemical kinetics is crucial for the comprehensive deployment of high-energy density lithium metal batteries(LMBs)with cost-efficiency.In this study,a lithiated 2-mercaptopyridine(2-MP-Li)organosulfide was synthesized and used as the soluble catholyte for the first time.Under the routine working mode,the LMB using this 2-MP-Li catholyte possessed high capacity retention of 55.4%with a Coulombic efficiency(CE)of near 100%after 2,000 cycles.When a cell system was fully filled with 2-MP-Li catholyte,it yielded a double capacity with 15%improvement in the capacity retention,corresponding to 0.0182%capacity decay per cycle,as well as excellent rate performance even at 6 mA·cm^(−2).These superior achievements resulted from the enhanced interfacial stability of Li anode induced by the salt-type 2-MP-Li molecule and the avoiding of using neutral catholyte as the initial active material,thereby mitigating the side reactions originating from the polysulfide shuttle effect.Furthermore,density functional theory(DFT)calculation and kinetics investigations proved the pseudocapacitive characteristic and faster ion diffusion coefficient with this design.Besides,the fabricated energy storage device showed excellent performance but with low economic cost and easy processing.Such a LMB with an alterable amount of capacity has a high potential to be applied in flow-cell type batteries for large-scale grid energy storage in the future.
基金supported by the EPFL,EMPA and the National Research Foundation of Singapore(Urban Solutions and Sustainability,Industry Alignment Fund[Pre‐Positioning]Programme)(A‐0004543‐00‐00)。
文摘Acidic environments enhance CO_(2) utilization during CO_(2) electrolysis via a buffering effect that converts carbonates formed at the electrode surface back into CO_(2).Nevertheless,further investigation into acidic CO_(2) electrolysis is required to improve its selectivity towards certain CO_(2) reduction reaction(CO_(2)RR)products,such as multicarbon(C2+)species,while enhancing its overall stability.In this study,liquid product recirculation in the catholyte and local OH−accumulation were identified as primary factors contributing to the degradation of gas diffusion electrodes mounted in closed‐loop catholyte configurations.We demonstrate that a single‐pass catholyte configuration prevents liquid product recirculation and maintains a continuous flow of acidic‐pH catholyte throughout the reaction while using the same volume as a closed‐loop setup.This approach improves electrode durability and maintains a Faradaic efficiency of 67%for multicarbon products over 4 h of CO_(2) electrolysis at−600 mA cm^(-2).
文摘Electrodes,catalysts,membranes,if present,are three main components in constructing an MFC for harvesting desired maximum power density and achieving higher coulombic efficiency (CE).Great improvements have been made,based on previous researches,in developing and diversifying materials,aside from architectures.Electrodes most familiar to us are widely used carbon materials.For anodes,carbon matrix composites(e.g.,a combination of polyaniline(PANI)with TiO2 using carbon as substrate)have gained special attention,though carbon material itself can exhibit excellent performance by diversifying molecular structures such as carbon nanotubes(CNTs).In the meanwhile,the evolution of MFC architectures,heading to the direction of improving power generation,contributes to the combination of membranes and cathodes from separate modes to diverse assemblies,on which all sorts of catalysts,such as from commonly used Pt to iron phthalocyanine (Pc),metal tetramethoxyphenylporphyrin(TMPP),MnOx,or pyrolyzed iron(Ⅱ)phthalocyanine (pyr-FePc),can be immobilized through synthesis of these catalysts with polymer such as Nafion 117 (Dupont Co.,USA)or tetrafluoroethylen(eTeflon)containing functional groups or Polypyrrol(ePPy).In addition,catholytes with aqueous cathode immersed or flowing through the surface of air-cathode are favorably proposed containing transition metal redox couples or iron chelates.
基金funded by the National Key Research and Development Program of China(Nos.2022YFB3805303,2022YFB3805304)the National Natural Science Foundation of China(Grant/Award Numbers:22308345,U20A20127)+1 种基金the Anhui Provincial Natural Science Foundation(No.2308085QB68)the Fundamental Research Funds for the Central Universities(No.WK2060000059).
文摘Aqueous organic redox flow batteries(AORFBs),which exploit the reversible electrochemical reactions of water-soluble organic electrolytes to store electricity,have emerged as an efficient electrochemical energy storage technology for the grid-scale integration of renewable electricity.pH-neutral AORFBs that feature high safety,low corrosivity,and environmental benignity are particularly promising,and their battery performance is significantly impacted by redox-active molecules and ion-exchange membranes(IEMs).Here,representative anolytes and catholytes engineered for use in pH-neutral AORFBs are outlined and summarized,as well as their side reactions that cause irreversible battery capacity fading.In addition,the recent achievements of IEMs for pH-neutral AORFBs are discussed,with a focus on the construction and tuning of ion transport channels.Finally,the critical challenges and potential research opportunities for developing practically relevant pH-neutral AORFBs are presented.
基金National Natural Science Foundation of China,Grant/Award Numbers:12304265,92372113,22309059China Postdoctoral Science Foundation,Grant/Award Number:2023MD744237+1 种基金the Young Talent Fund of Association for Science and Technology in Shaanxi,China,Grant/Award Number:20240514the Department of Science and Technology of Liaoning Province,Grant/Award Number:2022-MS-195。
文摘The relentless pursuit of sustainable and safe energy storage technologies hasdriven a departure from conventional lithium-based batteries toward other relevantalternatives. Among these, aqueous batteries have emerged as a promisingcandidate due to their inherent properties of being cost-effective, safe,environmentally friendly, and scalable. However, traditional aqueous systemshave faced limitations stemming from water's narrow electrochemical stabilitywindow (-1.23 V), severely constraining their energy density and viability inhigh-demand applications. Recent advancements in decoupling aqueous batteriesoffer a novel solution to overcome this challenge by separating the anolyteand catholyte, thereby expanding the theoretical operational voltage windowto over 3 V. One key component of this innovative system is the ion-selectivemembrane (ISM), acting as a barrier to prevent undesired crossover betweenelectrolytes. This review provides a comprehensive overview of recent advancementsin decoupling aqueous batteries, emphasizing the application of varioustypes of ISMs. Moreover, we summarize different specially designed ISMs andtheir performance attributes. By addressing the current challenges ISMs face,the review outlines potential pathways for future enhancement and developmentof aqueous decoupling batteries.
