Benefiting from the low cost and high abundance of potassium resources,K-based batteries have attracted numerous research interest as a more sustainable battery chemist,particularly when considering the enormous deman...Benefiting from the low cost and high abundance of potassium resources,K-based batteries have attracted numerous research interest as a more sustainable battery chemist,particularly when considering the enormous demand for sustainable energy storage while limiting Li sources for Li-based batteries.However,the much larger size of the K-ion usually leads to the serious electrodes'volumetric expansion with rapid capacity fading,making the pursuit of electrodes for potassium storage with high capacity and high stability a significant challenge.The polymer electrode materials have been considered promising materials to address these issues due to their porous characteristics,insolubility in electrolytes,and flexible structural design at a molecular level.In this review,we outline the recent advancements in redox-active polymer electrodes,including anode and cathode,materials for K-based batteries,including crystalline porous coordination polymers,crystalline covalent organic polymers,amorphous polymers,and polymer composites.We discuss the electrode designs,electrochemical performances,and K-ion storage mechanism,with a focus on their structure-function correlations.With this knowledge,we propose the perspectives and challenges in designing advanced polymer electrode materials for K-based batteries.We expect this review will shed light on the further development of reliable polymer electrode materials.展开更多
Electron transfer processes at polymer electrolyte/electrode interfaces play a central role in modern electrochemical devices of energy conversion,however,current understanding of electron transfers through electroche...Electron transfer processes at polymer electrolyte/electrode interfaces play a central role in modern electrochemical devices of energy conversion,however,current understanding of electron transfers through electrochemical interfaces was established exclusively based on the studies of liquid/solid electrochemical interfaces.Thus,similarities and differences of liquid and polymer electrolyte/electrode interfaces need to be mapped out to guide the design of device level electrochemical interfaces.In this work,we employ the sulfonate adsorption/desorption as a probe reaction to understand the electron-transfer steps in polymer and liquid electrolytes.Through cyclic voltametric investigations on the well-define single-crystal Pd_(ML)Pt(111)electrode,we demonstrate that the oxidative adsorption and reductive desorption of sulfonates at the polymer electrolyte/electrode interface are chemically distinct from those in liquid electrolytes,with the former occurring mostly via the proton-coupled pathway while the latter proceeding mainly through the solvation-mediated pathway.Importantly,the sulfonate adsorption/desorption behaviors of alkylsulfonates become increasingly similar to those in Nafion with longer alkyl chains,suggesting that the interfacial hydrophobicity and solvation environment conferred by the perfluorinated polymer play a decisive role in the electron-transfer mechanism.Results reported in this study highlight the mechanistic distinctions between electron-transfer processes at electrochemical interfaces involving polymer and liquid electrolytes,and provide a framework for understanding electron-transfer processes at polymer electrolyte/electrode interfaces.展开更多
Redox polymers are a class of high-capacity, low-cost electrode materials for electrochemical energy storage, butthe mechanisms governing their cycling stability are not well understood. Here we investigate the effect...Redox polymers are a class of high-capacity, low-cost electrode materials for electrochemical energy storage, butthe mechanisms governing their cycling stability are not well understood. Here we investigate the effect of anionson the longevity of a p-dopable polymer through comparing two aqueous zinc-based electrolytes. Galvanostaticcycling studies reveal the polymer has better capacity retention in the presence of triflate anions than that withsulfate anions. Based on electrode microstructural analysis and evolution profiles of the cell stacking pressure, theorigin of capacity decay is ascribed to mechanical fractures induced by volume change of the polymer activematerials during repeated cycling. The volume change of the polymer with the triflate anion is 61% less than thatwith the sulfate anion, resulting in fewer cracks in the electrodes. The difference is related to the different anionsolvation structures—the triflate anion has fewer solvated water molecules compared with the sulfate anion,leading to smaller volume expansion. This work highlights that anions with low solvation degree are preferablefor long-term cycling.展开更多
A Microbial fuel cell(MFC)with metal free polymer/graphite electrodes(150 mm×150 mm)was constructed.The electrodes with flowing channels,which were different in roughness,were designed.No additional catalyst was ...A Microbial fuel cell(MFC)with metal free polymer/graphite electrodes(150 mm×150 mm)was constructed.The electrodes with flowing channels,which were different in roughness,were designed.No additional catalyst was coated on the electrode,therefore the MFC was cheaper and possessed good durability with high performance.The effect of roughness,K3Fe(CN)6 concentration and sprayed air on the performance of the constructed MFC was investigated.Results showed that the roughness of electrode can significantly affect the performance of MFC.The power density of MFC increased by 1.56 times owing to the arithmetic mean roughness which has increased by 1.41 times.With an increasing K3Fe(CN)6 concentration,the performance of MFC also improves.The MFC with K3Fe(CN)6 only(30 mM)showed the highest power density of 1260 mW/m2,which is by 21.4 times and 1.3 times higher than those of MFCs with spraying air only(59 mW/m2)and with K3Fe(CN)6+air(1005 mW/m2),respectively.This showed that the appropriate concentration of K3Fe(CN)6 can significantly improve the power density,while the air has a negative effect when it is sprayed onto K3Fe(CN)6 catholyte.A coulombic efficiency of 34.2%and an energy efficiency of 13.3%with a COD degradation rate of 73.5%were achieved with MFC using K3Fe(CN)6 only.The overpotentials of MFC were also calculated.It can be seen that both theηohmic andηconcentration were very low as compared to theηactivation,and theηconcentration can be ignored because its effect was less than 3 mV.The theoretical calculation suggested that with an increasing conversion rate of K3Fe(CN)6,the cathode potential decreased and reached 0.31 V at a conversion rate of 0.99.While the anode behaves differently for constant pH and changeable pH as the reaction progresses,which reveals that the buffer solution and removal of protons play an important role in maintaining the anode potential.展开更多
Benefiting from the diversity and subjective design feasibility of molecular structure, flexibility,lightweight, molecular level controllability, resource renewability and relatively low cost, polymeric electrode mate...Benefiting from the diversity and subjective design feasibility of molecular structure, flexibility,lightweight, molecular level controllability, resource renewability and relatively low cost, polymeric electrode materials are promising candidates for the next generation of sustainable energy resources and have attracted extensive attention for the foreseeable large scale applications. The conductive polymers have been utilized as electrode materials in the pioneer reports, which, however, have the disadvantages of low stability, low reversibility and slope voltage due to the delocalization of charges in the whole conjugated systems. The discovery of carbonyl materials aroused the interest of organic and polymeric materials for batteries again. This review presents the recent progress in carbonyl polymeric electrode materials for lithium-ion batteries, sodium-ion batteries and magnesium-ion batteries. This comprehensive review is expected to be helpful forarousing more interest of organic materials for met展开更多
A manufacturing method is proposed for carbon based composite double polymer compliant electrode.The stiffness of this compliant electrode is changed by adjusting the mass fraction of carbon black and the ratios betwe...A manufacturing method is proposed for carbon based composite double polymer compliant electrode.The stiffness of this compliant electrode is changed by adjusting the mass fraction of carbon black and the ratios between Ecoflex20 and RT625.Tensile machine is used to test its ductility and hardness.The conductivity is measured through the source table.Finally,it is printed on the dielectric elastomers(DE)film,and the high-voltage amplifier is used for dielectric elastomers actuators(DEAs)dynamics testing.The results show that the compliant electrode has high tensile properties(>200%),low stiffness(<300 kPa)and well conductivity(0.0493 S/cm).It is proved that the DEAs displacement output is up to 1.189 mm by this compliant electrode under dynamic response,which is 1.64 times and 1.32 times of the same type.Moreover,this formula extends the curing time of the original compliant electrode ink.It can provide a reference for the production of compliant electrode and DEAs in the future.展开更多
In this paper,the functional polymeric active materials were prepared by the grafting copolymerization and their structure and properties were studied.The results show that the structure and properties of these ac- ti...In this paper,the functional polymeric active materials were prepared by the grafting copolymerization and their structure and properties were studied.The results show that the structure and properties of these ac- tive materials have the relative large effects on the properties of gadolinium ion selective electrodes.展开更多
Organic electrode materials are promising for lithium-ion batteries(LIBs) because of their environmental friendliness and structural diversity.However,they always suffer from limited capacity,poor cycling stability,an...Organic electrode materials are promising for lithium-ion batteries(LIBs) because of their environmental friendliness and structural diversity.However,they always suffer from limited capacity,poor cycling stability,and rate performance.Herein,hexaazatrinaphthalene-based azo-linked hyperbranched polymer(HAHP) is designed and synthesized as a cathode for LIBs.However,the densely stacked morphology lowers the chance of the active sites participating in the redox reaction.To address this issue,the singlewalled carbon nanotube(SWCNT) template is used to induce the growth of nanosized HAHP on the surface of SWCNTs.The HAHP@SWCNT nanocomposites have porous structures and highly accessible active sites.Moreover,the strong π-π interaction between HAHP and highly conductive SWCNTs effectively endows the HAHP@SWCNT nanocomposites with improved cycling stability and fast charge-discharge rates.As a result,the HAHP@SWCNT nanocomposite cathode shows a high specific capacity(320.4 mA h g^(-1)at 100 mA g^(-1)),excellent cycling stability(800 cycles;290 mA h g^(-1)at 100 mA g^(-1),capacity retained 91%) and outstanding rate performance(235 mA h g^(-1)at 2000 mA g^(-1),76% capacity retention versus 50 mA g^(-1)).This work provides a strategy to combine the macromolecular structural design and micromorphology control of electrode materials for obtaining organic polymer cathodes for high-performance LIBs.展开更多
Organic redox-active polymers provide promising alternatives to metal-containing inorganic compounds in Li-ion batteries(LIBs),whereas suffer from low actual capacities,poor rate/power capabilities,and inferior cyclin...Organic redox-active polymers provide promising alternatives to metal-containing inorganic compounds in Li-ion batteries(LIBs),whereas suffer from low actual capacities,poor rate/power capabilities,and inferior cycling stability.Herein,poly(anthraquinonyl sulfide)-coated carbon nanotubes(CNT@PAQS)are readily performed by in situ polymerization to form core-sheath nanostructures.Remarkably,flower-like PAQS nanosheets are interwoven around CNTs to synergistically create robust 3D hierarchical networks with abundant cavities,internal channels,and sufficiently-exposed surfaces/edges,thereby promoting electron transport and making more active sites accessible for electrolytes and vip ions.Apparently,the as-fabricated CNT@PAQS cathode delivers the large reversible capacity(200.5 mAh g^(-1)at 0.05 A g^(-1)),high-rate capability(161.5 mAh g^(-1)at 5.0 A g^(-1)),and impressive cycling stability(retaining 88.0%over 1000 cycles).In addition,an asymmetric full-battery using CNT@PAQS as a cathode and cyclized polyacrylonitrile-encapsulated CNTs as an anode is assembled that delivers a high energy density of 86.3 Wh kg^(-1),and retains 81.3%of initial capacity after 1000 cycles.This work opens up an efficient strategy to combine highly conductive and redox-active phases into core-sheath heterostructures to unlock the barrier of high-rate charge storage.The further integration of two polymer-based electrodes into asymmetric full cells would also consolidate the development of low-cost,sustainable,and powerful batteries.展开更多
Affordable,easily recycled organics with electroactive centers have drawn attention in the pursuit of high-performance aqueous zinc organic batteries(AZOBs).However,intrinsic barriers such as high solubility,unde-sira...Affordable,easily recycled organics with electroactive centers have drawn attention in the pursuit of high-performance aqueous zinc organic batteries(AZOBs).However,intrinsic barriers such as high solubility,unde-sirable potential,and inferior conductivity hinder their further development.To this end,we have designed an advanced cathode material for AZOBs,comprising an n-type polymer with a three-dimensional(3D)building block(HAT-TP)formed by polymerizing 2,3,6,7,10,11-hexacyano-1,4,5,8,9,12-hexazepenanthrene(HAT-CN)and 3D 2,3,6,7,14,15-hexaaminotriptycene(THA-NH 2).The introduction of a 3D architecture not only bolsters the insolubility but also exposes redox-active sites for cation coordination,while the material's extended conjugated system promotes electronic delocalization to increase the redox potential and conductivity.As a result,a HAT-TP battery exhibits a notable initial discharge voltage of 1.32 V at 0.1 A g^(-1),followed by a midpoint voltage of 1.17 V.Remarkably,an ultrastable capacity retention ratio of up to 93.4%is achieved,even after 40,000 cycles at 5 A g^(-1).Theoretical simulations reveal that the elevated discharge potential results from the strong electronic delocalization of HAT-TP,which improves the affinity with cations.Ex situ characterizations and theoretical calculations verify that the reversible Zn^(2+)/H^(+)co-storage mechanism involves only electroactive C=N sites and the best possible coordination paths between them.展开更多
Herein,we introduce a redox conjugated covalent organic polymer(p-HATN,HATN=hexaazatrinaphthylene)anode bearing HATN species for long-lifespan aqueous alkaline and acidic batteries.The p-HATN features intriguing super...Herein,we introduce a redox conjugated covalent organic polymer(p-HATN,HATN=hexaazatrinaphthylene)anode bearing HATN species for long-lifespan aqueous alkaline and acidic batteries.The p-HATN features intriguing superhydrophilicity and unique wide pH adaptability,while the conjugated network and amorphous cross-linked structure further endow p-HATN with improved electron transport,facile ion diffusion and superior acid-alkali tolerability.As a result,p-HATN exhibits fast surface-controlled redox activity and superior stability for K^(+)and H^(+)ions storage with remarkable capacity retentions in three-electrode cells(88%capacity retention in 13 M KOH over 30000 cycles;nearly 100%capacity retention in 0.5 M H_(2)SO_(4)over 54000 cycles).Moreover,the assembled p-HATN//Ni(OH)_(2)cell with 13 M KOH and p-HATN//PbO_(2)cell with 0.5 M H_(2)SO_(4)also achieve ca-pacity retentions of 83%retention over 55000 cycles and 92%over 15000 cycles,respectively,outperforming most similar systems.This work sheds light on the rational design of advanced polymer anodes for long-lifespan alkaline and acidic batteries.展开更多
Anion-selective electrodes based on dissociated ion-exchangers such as lipophilicquaternary ammonium or phosphonium species always display classical Hofmeister be-havior in the following order: ClO<sub>4</sub...Anion-selective electrodes based on dissociated ion-exchangers such as lipophilicquaternary ammonium or phosphonium species always display classical Hofmeister be-havior in the following order: ClO<sub>4</sub><sup>-</sup>】SCN<sup>-</sup>】I<sup>-</sup>】Br<sup>-</sup>】NO<sub>2</sub><sup>-</sup>】Cl<sup>-</sup>】SO<sub>4</sub><sup>2-</sup>.A new sol-vent polymeric membrane electrode based on Schiff base complexes of Co（Ⅱ）[Co（Ⅱ）S]and showing excellent selectivity toward iodide ion is for the first time prepared inour work. The resulting electrodes exhibit fairly low detection limits andpotentiometric anion-selectivity sequences deviated from the Hofmeister pattern.Bis（salicylaldehyde） ethylenediiminecobalt（Ⅱ） [Co（Ⅱ）（salen）], bis（salicylaldehyde）-phenyldiiminecobalt（Ⅱ） [Co（Ⅱ）（salophen）],展开更多
We discuss the efficiency of an electro-optic （EO） polymer sensor with interdigitated coplanar electrodes. The developed EO sensor is used to detect terahertz radiation via EO sampling. Results show that the sensor ...We discuss the efficiency of an electro-optic （EO） polymer sensor with interdigitated coplanar electrodes. The developed EO sensor is used to detect terahertz radiation via EO sampling. Results show that the sensor improves more significantly detection sensitivity than does a sensor with sandwich configurations.展开更多
This paper reports the use of an electrochemically polymerized Toluidine Blue (TB) film electrode.The film on platinum electrode surface was analyzed with ESCA.The heterogeneous electron transfer processes of myoglobi...This paper reports the use of an electrochemically polymerized Toluidine Blue (TB) film electrode.The film on platinum electrode surface was analyzed with ESCA.The heterogeneous electron transfer processes of myoglobin at the polymerized TB film electrode have been investigated using in situ UV-visible spectroelectrochemistry.The formal potential(E°′)and electron transfer number(n)of myoglobin were calculated as E°′=0.045 V(vs.NHE)and n=0.99.The exhaustive reduction and oxidation electrolyses are achieved in 130 s and 110 s respectively,during a potential step between-0.4 V and+0.4 V.A formal heterogeneous electron transfer rate constant(ksh)of 1.09× 10^(-4) cm/s and a transfer coefficient(α)of 0.47 were obtained by cyclic voltabsorptometry,which indicated that myoglobin underwent a quasi-reversible electrode process at the polymerized TB film electrode.展开更多
Electrochemical CO_(2) reduction driven by renewable electricity is one of the promising strategies to store sus-tainable energy as fuels.However,the selectivity of value-added multi-carbon products remains poor for f...Electrochemical CO_(2) reduction driven by renewable electricity is one of the promising strategies to store sus-tainable energy as fuels.However,the selectivity of value-added multi-carbon products remains poor for further application of this process.Here,we regulate CO adsorption by forming a Nafion layer on the copper(Cu)electrode that is repulsive to OH^(-),contributing to enhanced selectivity of CO_(2) reduction to C_(2) products with the suppression of C 1 products.The operando Raman spectroscopy indicates that the local OH^(-)would adsorb on part of active sites and decrease the adsorption of CO.Therefore,the electrode with repulsive to OH^(-)can adjust the concentration of OH^(-),leading to the increased adsorption of CO and enhanced C–C coupling.This work shows that electrode design could be an effective strategy for improving the selectivity of CO_(2) reduction to multi-carbon products.展开更多
Organic carbonyl electrode materials offer promising prospects for future energy storage systems due to their high theoretical capacity,resource sustainability,and structural diversity.Although much progress has been ...Organic carbonyl electrode materials offer promising prospects for future energy storage systems due to their high theoretical capacity,resource sustainability,and structural diversity.Although much progress has been made in the research of high-performance carbonyl electrode materials,systematic and in-depth studies on the underlying factors affecting their electrochemical properties are rather limited.Herein,five polyimides containing different types of diamine linkers are designed and synthesized as cathode materials for Li-ion batteries.First,the incorporation of carbonyl groups increases the active-site density in both conjugated and non-conjugated systems.Second,increased molecular rigidity can improve the accessibility of the active sites.Third,the introduction of the conjugated structure between two carbonyl groups can increase the reactivity of the active sites.Consequently,the incorporation of carbonyl structures and conjugated structures increases the capacity of polyimides.PTN,PAN,PMN,PSN,and PBN exhibit 212,198,199,151,and 115mAh g^(−1)at 50mAg^(−1),respectively.In addition,the introduction of a carbonyl structure and a conjugated structure is also beneficial for improving cycling stability and rate performance.This work can deepen the understanding of the structure–function relationship for the rational design of polyimide electrode materials and can be extended to the molecular design of other organic cathode materials.展开更多
The most prevalent among nervous system tumors significantly jeopardize patient health.For nerve integrity preservation after tumor removal,continuous intraoperative neurophysiological monitoring(CINM)is indispensable...The most prevalent among nervous system tumors significantly jeopardize patient health.For nerve integrity preservation after tumor removal,continuous intraoperative neurophysiological monitoring(CINM)is indispensable during microsurgery.The paper highlights the articles about the development of a system that employs soft and stretchable organic electronic materials for CINM.This innovative system harnesses soft and stretchable organic electronic materials and deploys conductive polymer electrodes with low impedance and modulus.These electrodes facilitate uninterrupted near-field action potential recording during surgery,resulting in enhanced signal-to-noise ratios and reduced invasiveness.Additionally,the system's multiplexing capabilities enable precise nerve localization,even in the absence of anatomical landmarks.展开更多
基金financially supported by the Guangdong Basic and Applied Basic Research Foundation(Nos.2022B1515020001,2024A1515010277)the National Natural Science Foundation of China(Nos.22109052,52202221)+1 种基金Guangzhou Science and Technology Program(No.2024A04J3899)the Fundamental Research Funds for the Central Universities(No.21624410)。
文摘Benefiting from the low cost and high abundance of potassium resources,K-based batteries have attracted numerous research interest as a more sustainable battery chemist,particularly when considering the enormous demand for sustainable energy storage while limiting Li sources for Li-based batteries.However,the much larger size of the K-ion usually leads to the serious electrodes'volumetric expansion with rapid capacity fading,making the pursuit of electrodes for potassium storage with high capacity and high stability a significant challenge.The polymer electrode materials have been considered promising materials to address these issues due to their porous characteristics,insolubility in electrolytes,and flexible structural design at a molecular level.In this review,we outline the recent advancements in redox-active polymer electrodes,including anode and cathode,materials for K-based batteries,including crystalline porous coordination polymers,crystalline covalent organic polymers,amorphous polymers,and polymer composites.We discuss the electrode designs,electrochemical performances,and K-ion storage mechanism,with a focus on their structure-function correlations.With this knowledge,we propose the perspectives and challenges in designing advanced polymer electrode materials for K-based batteries.We expect this review will shed light on the further development of reliable polymer electrode materials.
基金supported by the National Key R&D Program of China(No.2021YFA1501003)。
文摘Electron transfer processes at polymer electrolyte/electrode interfaces play a central role in modern electrochemical devices of energy conversion,however,current understanding of electron transfers through electrochemical interfaces was established exclusively based on the studies of liquid/solid electrochemical interfaces.Thus,similarities and differences of liquid and polymer electrolyte/electrode interfaces need to be mapped out to guide the design of device level electrochemical interfaces.In this work,we employ the sulfonate adsorption/desorption as a probe reaction to understand the electron-transfer steps in polymer and liquid electrolytes.Through cyclic voltametric investigations on the well-define single-crystal Pd_(ML)Pt(111)electrode,we demonstrate that the oxidative adsorption and reductive desorption of sulfonates at the polymer electrolyte/electrode interface are chemically distinct from those in liquid electrolytes,with the former occurring mostly via the proton-coupled pathway while the latter proceeding mainly through the solvation-mediated pathway.Importantly,the sulfonate adsorption/desorption behaviors of alkylsulfonates become increasingly similar to those in Nafion with longer alkyl chains,suggesting that the interfacial hydrophobicity and solvation environment conferred by the perfluorinated polymer play a decisive role in the electron-transfer mechanism.Results reported in this study highlight the mechanistic distinctions between electron-transfer processes at electrochemical interfaces involving polymer and liquid electrolytes,and provide a framework for understanding electron-transfer processes at polymer electrolyte/electrode interfaces.
文摘Redox polymers are a class of high-capacity, low-cost electrode materials for electrochemical energy storage, butthe mechanisms governing their cycling stability are not well understood. Here we investigate the effect of anionson the longevity of a p-dopable polymer through comparing two aqueous zinc-based electrolytes. Galvanostaticcycling studies reveal the polymer has better capacity retention in the presence of triflate anions than that withsulfate anions. Based on electrode microstructural analysis and evolution profiles of the cell stacking pressure, theorigin of capacity decay is ascribed to mechanical fractures induced by volume change of the polymer activematerials during repeated cycling. The volume change of the polymer with the triflate anion is 61% less than thatwith the sulfate anion, resulting in fewer cracks in the electrodes. The difference is related to the different anionsolvation structures—the triflate anion has fewer solvated water molecules compared with the sulfate anion,leading to smaller volume expansion. This work highlights that anions with low solvation degree are preferablefor long-term cycling.
基金The authors would like to thank the Federal Ministry of Education and Research(Bundesministerium für Bildung und Forschung),BMBF,Germany,for funding parts of this study under the contract No.02WER1317D.
文摘A Microbial fuel cell(MFC)with metal free polymer/graphite electrodes(150 mm×150 mm)was constructed.The electrodes with flowing channels,which were different in roughness,were designed.No additional catalyst was coated on the electrode,therefore the MFC was cheaper and possessed good durability with high performance.The effect of roughness,K3Fe(CN)6 concentration and sprayed air on the performance of the constructed MFC was investigated.Results showed that the roughness of electrode can significantly affect the performance of MFC.The power density of MFC increased by 1.56 times owing to the arithmetic mean roughness which has increased by 1.41 times.With an increasing K3Fe(CN)6 concentration,the performance of MFC also improves.The MFC with K3Fe(CN)6 only(30 mM)showed the highest power density of 1260 mW/m2,which is by 21.4 times and 1.3 times higher than those of MFCs with spraying air only(59 mW/m2)and with K3Fe(CN)6+air(1005 mW/m2),respectively.This showed that the appropriate concentration of K3Fe(CN)6 can significantly improve the power density,while the air has a negative effect when it is sprayed onto K3Fe(CN)6 catholyte.A coulombic efficiency of 34.2%and an energy efficiency of 13.3%with a COD degradation rate of 73.5%were achieved with MFC using K3Fe(CN)6 only.The overpotentials of MFC were also calculated.It can be seen that both theηohmic andηconcentration were very low as compared to theηactivation,and theηconcentration can be ignored because its effect was less than 3 mV.The theoretical calculation suggested that with an increasing conversion rate of K3Fe(CN)6,the cathode potential decreased and reached 0.31 V at a conversion rate of 0.99.While the anode behaves differently for constant pH and changeable pH as the reaction progresses,which reveals that the buffer solution and removal of protons play an important role in maintaining the anode potential.
基金the National 1000-Talents Programthe National Natural Science Foundation of China(Nos. 51773071, 51203067, 51603063)+1 种基金Wuhan Science and Technology Bureau(No. 2017010201010141)the Fundamental Research Funds for the Central Universities(No. HUST: 2017KFYXJJ023)for financial support
文摘Benefiting from the diversity and subjective design feasibility of molecular structure, flexibility,lightweight, molecular level controllability, resource renewability and relatively low cost, polymeric electrode materials are promising candidates for the next generation of sustainable energy resources and have attracted extensive attention for the foreseeable large scale applications. The conductive polymers have been utilized as electrode materials in the pioneer reports, which, however, have the disadvantages of low stability, low reversibility and slope voltage due to the delocalization of charges in the whole conjugated systems. The discovery of carbonyl materials aroused the interest of organic and polymeric materials for batteries again. This review presents the recent progress in carbonyl polymeric electrode materials for lithium-ion batteries, sodium-ion batteries and magnesium-ion batteries. This comprehensive review is expected to be helpful forarousing more interest of organic materials for met
基金Science and Technology Talent Project of Xi’an Science and Technology Bureau,Shaanxi Province(No.2020KJRC0049)。
文摘A manufacturing method is proposed for carbon based composite double polymer compliant electrode.The stiffness of this compliant electrode is changed by adjusting the mass fraction of carbon black and the ratios between Ecoflex20 and RT625.Tensile machine is used to test its ductility and hardness.The conductivity is measured through the source table.Finally,it is printed on the dielectric elastomers(DE)film,and the high-voltage amplifier is used for dielectric elastomers actuators(DEAs)dynamics testing.The results show that the compliant electrode has high tensile properties(>200%),low stiffness(<300 kPa)and well conductivity(0.0493 S/cm).It is proved that the DEAs displacement output is up to 1.189 mm by this compliant electrode under dynamic response,which is 1.64 times and 1.32 times of the same type.Moreover,this formula extends the curing time of the original compliant electrode ink.It can provide a reference for the production of compliant electrode and DEAs in the future.
文摘In this paper,the functional polymeric active materials were prepared by the grafting copolymerization and their structure and properties were studied.The results show that the structure and properties of these ac- tive materials have the relative large effects on the properties of gadolinium ion selective electrodes.
基金supported by the National Natural Science Foundation of China(Grant No.51903100)the Science and Technology Development Plan of Jilin Province,China(Grant No.20210402060GH)。
文摘Organic electrode materials are promising for lithium-ion batteries(LIBs) because of their environmental friendliness and structural diversity.However,they always suffer from limited capacity,poor cycling stability,and rate performance.Herein,hexaazatrinaphthalene-based azo-linked hyperbranched polymer(HAHP) is designed and synthesized as a cathode for LIBs.However,the densely stacked morphology lowers the chance of the active sites participating in the redox reaction.To address this issue,the singlewalled carbon nanotube(SWCNT) template is used to induce the growth of nanosized HAHP on the surface of SWCNTs.The HAHP@SWCNT nanocomposites have porous structures and highly accessible active sites.Moreover,the strong π-π interaction between HAHP and highly conductive SWCNTs effectively endows the HAHP@SWCNT nanocomposites with improved cycling stability and fast charge-discharge rates.As a result,the HAHP@SWCNT nanocomposite cathode shows a high specific capacity(320.4 mA h g^(-1)at 100 mA g^(-1)),excellent cycling stability(800 cycles;290 mA h g^(-1)at 100 mA g^(-1),capacity retained 91%) and outstanding rate performance(235 mA h g^(-1)at 2000 mA g^(-1),76% capacity retention versus 50 mA g^(-1)).This work provides a strategy to combine the macromolecular structural design and micromorphology control of electrode materials for obtaining organic polymer cathodes for high-performance LIBs.
基金supported by National Natural Science Foundation of China(52173091 and 51973235)Program for Leading Talents of National Ethnic Affairs Commission of China(MZR21001)+1 种基金Hubei Provincial Natural Science Foundation of China(2021CFA022)Wuhan Science and Technology Bureau(2020010601012198).
文摘Organic redox-active polymers provide promising alternatives to metal-containing inorganic compounds in Li-ion batteries(LIBs),whereas suffer from low actual capacities,poor rate/power capabilities,and inferior cycling stability.Herein,poly(anthraquinonyl sulfide)-coated carbon nanotubes(CNT@PAQS)are readily performed by in situ polymerization to form core-sheath nanostructures.Remarkably,flower-like PAQS nanosheets are interwoven around CNTs to synergistically create robust 3D hierarchical networks with abundant cavities,internal channels,and sufficiently-exposed surfaces/edges,thereby promoting electron transport and making more active sites accessible for electrolytes and vip ions.Apparently,the as-fabricated CNT@PAQS cathode delivers the large reversible capacity(200.5 mAh g^(-1)at 0.05 A g^(-1)),high-rate capability(161.5 mAh g^(-1)at 5.0 A g^(-1)),and impressive cycling stability(retaining 88.0%over 1000 cycles).In addition,an asymmetric full-battery using CNT@PAQS as a cathode and cyclized polyacrylonitrile-encapsulated CNTs as an anode is assembled that delivers a high energy density of 86.3 Wh kg^(-1),and retains 81.3%of initial capacity after 1000 cycles.This work opens up an efficient strategy to combine highly conductive and redox-active phases into core-sheath heterostructures to unlock the barrier of high-rate charge storage.The further integration of two polymer-based electrodes into asymmetric full cells would also consolidate the development of low-cost,sustainable,and powerful batteries.
基金supported by the National Natural Science Foundation of China(52203215)the Natural Science Research Start-up Foundation of Recruiting Talents of Nanjing University of Posts and Telecommunications(Grant No.NY225035).
文摘Affordable,easily recycled organics with electroactive centers have drawn attention in the pursuit of high-performance aqueous zinc organic batteries(AZOBs).However,intrinsic barriers such as high solubility,unde-sirable potential,and inferior conductivity hinder their further development.To this end,we have designed an advanced cathode material for AZOBs,comprising an n-type polymer with a three-dimensional(3D)building block(HAT-TP)formed by polymerizing 2,3,6,7,10,11-hexacyano-1,4,5,8,9,12-hexazepenanthrene(HAT-CN)and 3D 2,3,6,7,14,15-hexaaminotriptycene(THA-NH 2).The introduction of a 3D architecture not only bolsters the insolubility but also exposes redox-active sites for cation coordination,while the material's extended conjugated system promotes electronic delocalization to increase the redox potential and conductivity.As a result,a HAT-TP battery exhibits a notable initial discharge voltage of 1.32 V at 0.1 A g^(-1),followed by a midpoint voltage of 1.17 V.Remarkably,an ultrastable capacity retention ratio of up to 93.4%is achieved,even after 40,000 cycles at 5 A g^(-1).Theoretical simulations reveal that the elevated discharge potential results from the strong electronic delocalization of HAT-TP,which improves the affinity with cations.Ex situ characterizations and theoretical calculations verify that the reversible Zn^(2+)/H^(+)co-storage mechanism involves only electroactive C=N sites and the best possible coordination paths between them.
基金supported by the National Natural Science Foundation of China(No.52273222)
文摘Herein,we introduce a redox conjugated covalent organic polymer(p-HATN,HATN=hexaazatrinaphthylene)anode bearing HATN species for long-lifespan aqueous alkaline and acidic batteries.The p-HATN features intriguing superhydrophilicity and unique wide pH adaptability,while the conjugated network and amorphous cross-linked structure further endow p-HATN with improved electron transport,facile ion diffusion and superior acid-alkali tolerability.As a result,p-HATN exhibits fast surface-controlled redox activity and superior stability for K^(+)and H^(+)ions storage with remarkable capacity retentions in three-electrode cells(88%capacity retention in 13 M KOH over 30000 cycles;nearly 100%capacity retention in 0.5 M H_(2)SO_(4)over 54000 cycles).Moreover,the assembled p-HATN//Ni(OH)_(2)cell with 13 M KOH and p-HATN//PbO_(2)cell with 0.5 M H_(2)SO_(4)also achieve ca-pacity retentions of 83%retention over 55000 cycles and 92%over 15000 cycles,respectively,outperforming most similar systems.This work sheds light on the rational design of advanced polymer anodes for long-lifespan alkaline and acidic batteries.
基金National Natural Science Foundation of ChinaElectroanalytical Chemistry Laboratory, Changchun Institute of Applied Chemistry, Academia Sinica.
文摘Anion-selective electrodes based on dissociated ion-exchangers such as lipophilicquaternary ammonium or phosphonium species always display classical Hofmeister be-havior in the following order: ClO<sub>4</sub><sup>-</sup>】SCN<sup>-</sup>】I<sup>-</sup>】Br<sup>-</sup>】NO<sub>2</sub><sup>-</sup>】Cl<sup>-</sup>】SO<sub>4</sub><sup>2-</sup>.A new sol-vent polymeric membrane electrode based on Schiff base complexes of Co（Ⅱ）[Co（Ⅱ）S]and showing excellent selectivity toward iodide ion is for the first time prepared inour work. The resulting electrodes exhibit fairly low detection limits andpotentiometric anion-selectivity sequences deviated from the Hofmeister pattern.Bis（salicylaldehyde） ethylenediiminecobalt（Ⅱ） [Co（Ⅱ）（salen）], bis（salicylaldehyde）-phenyldiiminecobalt（Ⅱ） [Co（Ⅱ）（salophen）],
基金supported by the National Natural Science Foundation of China(Nos.60871073 and 61201075)China Postdoctoral Science Foundation(No.2012M511507)
文摘We discuss the efficiency of an electro-optic （EO） polymer sensor with interdigitated coplanar electrodes. The developed EO sensor is used to detect terahertz radiation via EO sampling. Results show that the sensor improves more significantly detection sensitivity than does a sensor with sandwich configurations.
基金Project supported by the National Natural Science Foundation of China
文摘This paper reports the use of an electrochemically polymerized Toluidine Blue (TB) film electrode.The film on platinum electrode surface was analyzed with ESCA.The heterogeneous electron transfer processes of myoglobin at the polymerized TB film electrode have been investigated using in situ UV-visible spectroelectrochemistry.The formal potential(E°′)and electron transfer number(n)of myoglobin were calculated as E°′=0.045 V(vs.NHE)and n=0.99.The exhaustive reduction and oxidation electrolyses are achieved in 130 s and 110 s respectively,during a potential step between-0.4 V and+0.4 V.A formal heterogeneous electron transfer rate constant(ksh)of 1.09× 10^(-4) cm/s and a transfer coefficient(α)of 0.47 were obtained by cyclic voltabsorptometry,which indicated that myoglobin underwent a quasi-reversible electrode process at the polymerized TB film electrode.
基金This work was supported by the following projects:INTERNATIONAL COOPERATION Projects of the Ministry of Science and Technology(2014DFE60170)the Strategic Japanese-Swiss Science and Technology Program from the Swiss National Science Foundation(project No.IZJSZ2_180176)+4 种基金the Sino-Swiss Science and Technology Cooperation(SSSTC)2016 project from the Swiss National Science Foundation(project No.IZLCZ2_170294)the National Natural Science Foundation of China(Grant No.61674084)the Overseas Expertise Introduction Project for DisciplineInnovation of Higher Education of China(Grant No.B16027)Tianjin Science and Technology Project(Grant No.18ZXJMTG00220)the Fundamental Research Fund for the Central Universities of China.
文摘Electrochemical CO_(2) reduction driven by renewable electricity is one of the promising strategies to store sus-tainable energy as fuels.However,the selectivity of value-added multi-carbon products remains poor for further application of this process.Here,we regulate CO adsorption by forming a Nafion layer on the copper(Cu)electrode that is repulsive to OH^(-),contributing to enhanced selectivity of CO_(2) reduction to C_(2) products with the suppression of C 1 products.The operando Raman spectroscopy indicates that the local OH^(-)would adsorb on part of active sites and decrease the adsorption of CO.Therefore,the electrode with repulsive to OH^(-)can adjust the concentration of OH^(-),leading to the increased adsorption of CO and enhanced C–C coupling.This work shows that electrode design could be an effective strategy for improving the selectivity of CO_(2) reduction to multi-carbon products.
基金The authors thank the financial support from the National Natural Science Foundation of China(No.51903100)the Science and Technology Development Plan of Jilin Province,P.R.China(No.20210402060GH and 20230201138GX).
文摘Organic carbonyl electrode materials offer promising prospects for future energy storage systems due to their high theoretical capacity,resource sustainability,and structural diversity.Although much progress has been made in the research of high-performance carbonyl electrode materials,systematic and in-depth studies on the underlying factors affecting their electrochemical properties are rather limited.Herein,five polyimides containing different types of diamine linkers are designed and synthesized as cathode materials for Li-ion batteries.First,the incorporation of carbonyl groups increases the active-site density in both conjugated and non-conjugated systems.Second,increased molecular rigidity can improve the accessibility of the active sites.Third,the introduction of the conjugated structure between two carbonyl groups can increase the reactivity of the active sites.Consequently,the incorporation of carbonyl structures and conjugated structures increases the capacity of polyimides.PTN,PAN,PMN,PSN,and PBN exhibit 212,198,199,151,and 115mAh g^(−1)at 50mAg^(−1),respectively.In addition,the introduction of a carbonyl structure and a conjugated structure is also beneficial for improving cycling stability and rate performance.This work can deepen the understanding of the structure–function relationship for the rational design of polyimide electrode materials and can be extended to the molecular design of other organic cathode materials.
文摘The most prevalent among nervous system tumors significantly jeopardize patient health.For nerve integrity preservation after tumor removal,continuous intraoperative neurophysiological monitoring(CINM)is indispensable during microsurgery.The paper highlights the articles about the development of a system that employs soft and stretchable organic electronic materials for CINM.This innovative system harnesses soft and stretchable organic electronic materials and deploys conductive polymer electrodes with low impedance and modulus.These electrodes facilitate uninterrupted near-field action potential recording during surgery,resulting in enhanced signal-to-noise ratios and reduced invasiveness.Additionally,the system's multiplexing capabilities enable precise nerve localization,even in the absence of anatomical landmarks.
