Thermosetting polymers exhibit outstanding mechanical properties,thermal stability,and chemical resistance due to their permanently cross-linked network structures.However,the irreversible nature of covalent cross-lin...Thermosetting polymers exhibit outstanding mechanical properties,thermal stability,and chemical resistance due to their permanently cross-linked network structures.However,the irreversible nature of covalent cross-linking renders these materials non-reprocessable and non-recyclable,posing significant environmental challenges.Although healable polymers based on dynamic covalent bonds and supramolecular interactions have emerged as promising alternatives,a broadly applicable strategy utilizing metal-ligand coordination in thermoset systems remains underexplored.In this work,we present a robust and healable thermoset system fabricated via ring-opening metathesis polymerization(ROMP)of commercially available chelating norbornene comonomers.Cross-linking is accomplished through O-donor coordination to Lewis acidic metal centers,yielding polydicyclopentadiene(PDCPD)-based networks that demonstrate high mechanical strength(up to 60.8 MPa)and effective self-healing performance.This methodology offers a simple and scalable approach to developing high-performance,sustainable thermosetting materials.展开更多
To evaluate their performance,we constructed organic solar cells using PTB7/Y6 and PTB7-b-PNDI active layers,which were deposited on PET substrates coated with PEDOT:PSS.The ternary solar cells demonstrated an excelle...To evaluate their performance,we constructed organic solar cells using PTB7/Y6 and PTB7-b-PNDI active layers,which were deposited on PET substrates coated with PEDOT:PSS.The ternary solar cells demonstrated an excellent power conversion efficiency after being stretched by 38%.The stretchable organic solar cells were spin-coated on the flexible substrate.The electrodes were formed via liquid metal dropcoating.Solar cell devices based on PET/PH1000/PEDOT:PSS and PTB7:Y6:5% BCP active layer materials show better stretchability than the normal solar cells.The PTB7:Y6:5% BCP-based stretchable organic solar cell achieves a high PCE of 12.3%,and a PCE of 7.8% after stretching.Incorporating block copolymer additives improves the mechanical properties of organic solar cells,thereby enabling superior stretchability.展开更多
As a natural biopolymer material,silk fibroin with unique mechanical properties can be used in the preparation of biocomposite hydrogels for strain sensors.But,the electromechanical properties of bio-composite hydroge...As a natural biopolymer material,silk fibroin with unique mechanical properties can be used in the preparation of biocomposite hydrogels for strain sensors.But,the electromechanical properties of bio-composite hydrogel strain sensors are still insufficient,such as the deterioration of electrical signals and low sensitivity,which need to develop a hydrogel with a stable transmission network for electric con-duction.Herein,a silk fibroin biocomposite hydrogel is prepared by incorporating tannic acid and MXene nanosheets into a polyacrylamide and silk fibroin double network.The electromechanical properties of hydrogels are improved by optimizing the proportion of material components.As a result,the double network structure and supramolecular interaction enhance the stretchability of hydrogels(692% fracture strain).The hydrogel also exhibits good biocompatibility and conductivity(0.85 S/m),which shows the application prospect in wearable sensors.The wireless strain sensor assembled by this biocomposite hy-drogel presents good portability and sensing performance,such as high sensitivity(gauge factor=6.04),wide working range(500% strain),and outstanding stability(1000 cycles at 100%strain).The results in-dicate that the hydrogel strain sensor can be used to monitor human body movement.The biocomposite hydrogel is expected to be applied in the field of wearable strain sensors,and this study can provide a new way for the design of flexible electronic materials.展开更多
Flexible electronic devices are often subjected to large and repeated deformation,so that their functional components such as metal interconnects need to sustain strains up to tens of percent,which is far beyond the i...Flexible electronic devices are often subjected to large and repeated deformation,so that their functional components such as metal interconnects need to sustain strains up to tens of percent,which is far beyond the intrinsic deformability of metal materials(~1%).To meet the stringent requirements of flexible electronics,metal/elastomer bilayers,a stretchable structure that consists of a metal film adhered to a stretchable elastomer substrate,have been developed to improve the stretch capability of metal interconnects.Previous studies have predicted that the metal/elastomer bilayers are much more stretchable than freestanding metal films.However,these investigations usually assume perfect bonding between the metal and elastomer layers.In this work,the effect of the metal/elastomer interface with a finite interfacial stiffness on the stretchability of bilayer structures is analyzed.The results show that the assumption of perfect interface(with infinite interfacial stiffness)may lead to an overestimation of the stretchability of bilayer structures.It is also demonstrated that increased adhesion between the metal and elastomer layers can enhance the stretchability of the metal layer.展开更多
The dimensional properties and uniarial stretchability of cotton interlock and interlock with missing needle are discussed on the basis of definition system for double knits. K values used widely to describe the dimen...The dimensional properties and uniarial stretchability of cotton interlock and interlock with missing needle are discussed on the basis of definition system for double knits. K values used widely to describe the dimensional properties of plain knitted structures are developed into the study of double knitted structures in this paper. K values are not constants, the numerical values of which will depend on the actual configuration of various knitted structures. It is suggested that the effect of knitted structures on dimensional properties and stretchability can be described by K values.展开更多
Stretchable electronics that monitor joint activity and treat diseases based on liquid metal could be used in the development of healthcare applications.Such devices can be seamlessly integrated with human skin.Howeve...Stretchable electronics that monitor joint activity and treat diseases based on liquid metal could be used in the development of healthcare applications.Such devices can be seamlessly integrated with human skin.However,most high-precision microstructures and complex patterns are difficult to fabricate due to the limitations of conventional fabrication solutions,resulting in suboptimal performance under practical conditions.Here,a liquid-metal stretchable system utilizing natural leaf veins was reported as microstructures,which was based on a biomimetic concept and utilized an all-solution process for the preparation of complex microstructures.The systems are ultra-high tensile(800%tensile strain),environmentally stable(20 days)and mechanically durable(300-cycle).The system can accurately recognize the wearer's finger bending level as well as simple gesture signals.At the same time,the system acts as a wearable heater,which can realize the fast heating behavior of heating up to 50℃in 3 min under the human body-safe voltage(1.5 V).The tensile stability is demonstrated by the heterogeneous integration of lasers(405 nm)with the system interconnects for a stretchable and wearable light source.展开更多
In the rapidly evolving field of wearable electronics,stretchy organic solar cells(OSCs)have emerged as promising candidates for portable power sources,necessitating materials with superior mechanical flexibility.Howe...In the rapidly evolving field of wearable electronics,stretchy organic solar cells(OSCs)have emerged as promising candidates for portable power sources,necessitating materials with superior mechanical flexibility.However,the inherent rigidity of conjugated backbones in top-performance photovoltaic polymers,such as PM6,poses a significant challenge,as it makes photovoltaic films prone to fracture under mechanical strain.Consequently,improving the mechanical properties of these films is a crucial research frontier for advancing stretchable photovoltaic technologies.This tutorial review provides a thorough examination of current strategies aimed at bolstering the mechanical resilience of polymer photovoltaic thin films,elucidated through a selection of pertinent examples leveraging the PM6-based systems.We first explore the prevalent strategy of incorporating third components,including vip polymer donors/acceptors and insulating polymers,to improve stretchability.We then discuss the structural design of PM6 aimed at reducing the backbone rigidity.Additionally,we summarize various predictive models for assessing the mechanical properties of these photovoltaic films.Finally,the future challenges and perspectives for stretchy OSCs are explored.展开更多
Achieving rubber-like stretchability in cellulose ionogels presents a substantial challenge due to the intrinsically extended chain configuration of cellulose.Inspired by the molecular configuration of natural rubber,...Achieving rubber-like stretchability in cellulose ionogels presents a substantial challenge due to the intrinsically extended chain configuration of cellulose.Inspired by the molecular configuration of natural rubber,we address this challenge by using cyanoethyl as a substitute for 1.5 hydroxyl on the D-glucose unit of cellulose.This strategy innovatively triggers the transformation of cellulose molecules into a coiled chain configuration,facilitating the creation of an ultra-stretchable ionogel free from any petrochemical polymers.The resultant ionogel demonstrates mechanical ductility comparable to that of a rubber band,achieving an elongation strain of nearly 1,000%while maintaining a tensile strength of up to 1.8 MPa and exhibiting a biomodulus akin to that of human skin,recorded at 63 kPa.Additionally,this stretchable ionogel presents skin-like self-healing behavior,favorable biocompatibility,and noteworthy thermoelectric properties,highlighted by a Seebeck coefficient of approximately 68 mV K−1.This study delineates a feasible molecular approach for developing stretchable ionogels from biomass resources,potentially revolutionizing self-powered stretchable electronics for integration with human tissues and skin.展开更多
Incorporating flexible conjugation breakers into conjugated polymers to develop intrinsically stretchable polymer semiconductors has garnered much attention.However,it still remains challenging to improve mechanical s...Incorporating flexible conjugation breakers into conjugated polymers to develop intrinsically stretchable polymer semiconductors has garnered much attention.However,it still remains challenging to improve mechanical stretchability without compromising the charge transport property of polymer semiconductors.Herein,we report an approach to enhance the mechanical stretchability of the polymer semiconductor while largely maintaining its semiconducting performance by incorporating di-2-thienylsulfide as the p-πconjugation units into the backbone of poly(3,6-di(thiophen-2-yl)diketopyrrolo-[3,4-c]pyrrole-1,4-dione-alt-thieno[3,2-b]thiophen)(PDPP-TT).Compared to the parent polymer PDPP-TT,the incorporation of the p-πconjugation units induces the twisting of the backbone and weakens the interchain packing order,resulting in higher crack onset strain and better mechanical durability.The polymer semiconductor in which the molar ratio of the repeat unit with di-2-thienylsulfides is 10%exhibits a crack onset strain greater than 100%and can retain its initial charge mobility after 1000 stretching-releasing cycles under 50%strain.Our studies show that incorporation of p-πconjugation units such as di-2-thienylsulfide into backbones of polymer semiconductors provides a feasible approach to balance the stretchability and charge mobility,thus making it a promising way for future development of stretchable polymer semiconductors.展开更多
With the emergence of Y-series small molecule acceptors,polymerizing the small molecule acceptors with aromatic linker units has attracted significant research attention,which has greatly advanced the photovoltaic per...With the emergence of Y-series small molecule acceptors,polymerizing the small molecule acceptors with aromatic linker units has attracted significant research attention,which has greatly advanced the photovoltaic performance of all-polymer solar cells.Despite the rapid increase in efficiency,the unique characteristics(e.g.,mechanical stretchability and flexibility)of all-polymer systems were still not thoroughly explored.In this work,we demonstrate an effective approach to simultaneously improve device performance,stability,and mechanical robustness of all-polymer solar cells by properly suppressing the aggregation and crystallization behaviors of polymerized Y-series acceptors.Strikingly,when introducing 50 wt%PYF-IT(a fluorinated version of PY-IT)into the well-known PM6:PY-IT system,the all-polymer devices delivered an impressive photovoltaic efficiency of 16.6%,significantly higher than that of the control binary cell(15.0%).Compared with the two binary systems,the optimal ternary blend exhibits more efficient charge separation and balanced charge transport accompanying with less recombination.Moreover,a high-performance 1.0 cm^(2)large-area device of 15%efficiency was demonstrated for the optimized ternary all-polymer blend,which offered a desirable PCE of 14.5%on flexible substrates and improved mechanical flexibility after bending 1000 cycles.Notably,these are among the best results for 1.0 cm^(2)all-polymer OPVs thus far.This work also heralds a bright future of all-polymer systems for flexible wearable energy-harvesting applications.展开更多
The development of strain sensors with high stretchability and stability is an inevitable requirement for achieving full-range and long-term use of wearable electronic devices.Herein,a resistive micromesh reinforced s...The development of strain sensors with high stretchability and stability is an inevitable requirement for achieving full-range and long-term use of wearable electronic devices.Herein,a resistive micromesh reinforced strain sensor(MRSS)with high stretchability and stability is prepared,consisting of a laser-scribed graphene(LSG)layer and two styrene-block-poly(ethylene-ran-butylene)-block-poly-styrene micromesh layers embedded in Ecoflex.The micromesh reinforced structure endows the MRSS with combined characteris-tics of a high stretchability(120%),excellent stability(with a repetition error of 0.8%after 11000 cycles),and outstanding sensitivity(gauge factor up to 2692 beyond 100%).Impressively,the MRSS can still be used continauously within the working range without damage,even if stretched to 300%.Furthermore,compared with different structure sensors,the mechanism of the MRSS with high stretchability and stability is elucidated.What's more,a multilayer finite element model,based on the layered structure of the LSG and the morphology of the cracks,is proposed to investigate the strain sensing behavior and failure mechanism of the MRSS.Finally,due to the outstanding performance,the MRSS not only performes well in monitoring full-range human motions,but also achieves intelligent recognitions of various respiratory activities and ges-tures assisted by neural network algorithms(the accuracy up to 94.29%and 100%,respectively).This work provides a new approach for designing high-performance resistive strain sensors and shows great potential in full-range and long-term intelligent health management and human-machine interac-tions applications.展开更多
Stretchable electronics have been recognized as intriguing next-generation electronics that possess huge market value,and stretchable electronic conductors(SECs)are essential for stretchable electronics,which not only...Stretchable electronics have been recognized as intriguing next-generation electronics that possess huge market value,and stretchable electronic conductors(SECs)are essential for stretchable electronics,which not only can serve as critical functional components but also are the indispensable electronic connections bridging various electronic components within stretchable electronic systems.Herein,we offer a comprehensive review of recent progress in SECs including the material categories,structure designs,fabrication techniques,and applications.The characteristics,performance enhancement strategies,and application requirements are emphasized.Based on the recent advances,the existing challenges and future prospects are outlined and discussed.展开更多
The scalable fabrication of stretchable conjugated polymer films via solution printing is essential for their practical application in largearea wearable electronics.However,the printed conjugated polymer films typica...The scalable fabrication of stretchable conjugated polymer films via solution printing is essential for their practical application in largearea wearable electronics.However,the printed conjugated polymer films typically exhibit high crystallinity,limiting their mechanical deformability.Herein,we propose a plasticizer-assisted printing strategy to simultaneously enhance the stretchability and electrical performance of films based on the conjugated polymer poly(3-(5-(5-methylselenophen-2-yl)thiophen-2-yl)-6-(5-methylthiophen-2-yl)-2,5-bis(4-octyltetradecyl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione)(P(TDPP-Se)).The incorporation of a plasticizer trioctyl trimellitate(TOTM)promotes P(TDPP-Se)aggregation in initial solution,facilitates chain alignment under flow field,and shorten solidification process,thereby restricting randomly polymer crystallization.Consequently,a low-crystallinity film with favorable edge-on orientation,strong chain alignment and improved chain dynamics is realized,which effectively alleviates crystallites fragmentation and crack propagation under large strain.The TOTM-plasticized film exhibits approximately 2-fold improvements in fracture strain and charge mobility,along with superior mobility retention under 100%strain in comparison to the neat film.This study provides a feasible approach for microstructure control in printed stretchable conjugated polymer film.展开更多
Permeable electronics promise improved physiological comfort,but remain constrained by limited functional integration and poor mechanical robustness.Here,we report a three-dimensional(3D)permeable electronic system th...Permeable electronics promise improved physiological comfort,but remain constrained by limited functional integration and poor mechanical robustness.Here,we report a three-dimensional(3D)permeable electronic system that overcomes these challenges by combining electrospun SEBS nanofiber mats,high-resolution liquid metal conductors patterned via thermal imprinting(50μm),and a strain isolators(SIL)that protects vertical interconnects(VIAs)from stress concentration.This architecture achieves ultrahigh air permeability(>5.09 m L cm^(-2)min^(-1)),exceptional stretchability(750%fracture strain),and reliable conductivity maintained through more than 32,500 strain cycles.Leveraging these advances,we have integrated multilayer circuits,strain sensors,and a three-axis accelerometer to achieve a fully integrated,stretchable,permeable wireless real-time gesture recognition glove.The system enables accurate sign language interpretation(98%)and seamless robotic hand control,demonstrating its potential for assistive technologies.By uniting comfort,durability,and high-density integration,this work establishes a versatile platform for nextgeneration wearable electronics and interactive human-robot interfaces.展开更多
The increasing demand for flexible displays and wearable electronics has driven extensive efforts to develop stretchable organic lightemitting diodes(OLEDs).A critical challenge in this field is the creation of emissi...The increasing demand for flexible displays and wearable electronics has driven extensive efforts to develop stretchable organic lightemitting diodes(OLEDs).A critical challenge in this field is the creation of emissive layers that combine high efficiency with mechanical robustness.Thermally activated delayed fluorescence(TADF)materials have attracted significant attention as third-generation emitters capable of achieving 100%internal quantum efficiency;however,their application in stretchable OLEDs has been limited.In this study,we propose an elastomer doping strategy.Polyurethane(PU)is incorporated into TADF polymers to improve their mechanical flexibility while maintaining a high luminescent efficiency.The resulting composite films exhibited excellent TADF characteristics and remarkable stretchability(75%).OLEDs fabricated from these materials achieved a maximum external quantum efficiency(EQE)of 14.26%and a peak luminance of 73570 cd·m^(-2),with the PUdoped devices showing a significantly suppressed efficiency roll-off.Additionally,a fully stretchable OLED architecture was designed and operated under tensile strain to maintain stable electroluminescent performance.These results demonstrate that elastomer doping is an effective strategy for balancing the mechanical compliance with optoelectronic performance,offering a promising pathway for the development of high-performance stretchable OLEDs for flexible electronics.展开更多
The soft nature has endowed conjugated polymers with promising applications in a wide range of field-effect transistor(FET)based flexible electronics.With unremitting efforts on revealing the molecular structure-prope...The soft nature has endowed conjugated polymers with promising applications in a wide range of field-effect transistor(FET)based flexible electronics.With unremitting efforts on revealing the molecular structure-property relationships,numerous novel conjugated polymers with high mobility and excellent mechanical property have been developed in the past decades.Incorporating hydrogen-bonding(H-bonding)units into semiconducting polymers is one of the most successful strategies for designing high-performance semiconducting materials.In this review,we aim to highlight the roles of H-bonding units in the performances of polymeric FETs from three aspects.These include(i)charge mobility enhancement for semiconducting polymers after incorporation of H-bonding units into the side chains,(ii)the effects of H-bonding units on the stretchability of conjugated polymers,and(iii)the improvement of self-healing properties of conjugated polymers containing dynamic hydrogen bonds due to the H-bonding units in the side chains or conjugated backbones.展开更多
Intrinsic stretchability is a promising attribute of polymer organic solar cells(OSCs).However,rigid molecular blocks typically exhibit poor tensile properties,rendering polymers vulnerable to mechanical stress.In thi...Intrinsic stretchability is a promising attribute of polymer organic solar cells(OSCs).However,rigid molecular blocks typically exhibit poor tensile properties,rendering polymers vulnerable to mechanical stress.In this study,we introduce a different approach utilizing all-small-molecule donors and acceptors to fabricate stretchable OSCs.An elastomer,styrene-b-ethylene-butylene-styrene(SEBS),was embedded to modulate film crystallization and stretchability.SEBS effectively confines the growth process of donors and acceptors,leading to enhancement of the crystallization quality,thus contributing to enhanced device efficiencies.Meanwhile,SEBS can absorb and release mechanical stress during stretching,thereby preventing mechanical degradation of donors and acceptors.The mechanical properties of the OSCs were significantly improved by the incorporation of SEBS.Notably,the crack-onset strain increased from 1.03% to 5.99% with SEBS embedding.These findings present a straightforward strategy for achieving stretchable OSCs using all small molecules,offering a different perspective for realizing stretchable devices.展开更多
Intrinsically stretchable semiconducting polymers play a vital role in the development of wearable electronics,featuring low-cost,large-area and high-density fabrication.Only single-stage dynamic chemical bond has bee...Intrinsically stretchable semiconducting polymers play a vital role in the development of wearable electronics,featuring low-cost,large-area and high-density fabrication.Only single-stage dynamic chemical bond has been widely incorporated into polymer backbones to afford stretchability while multiple dynamic bonds have not been investigated,making a formidable challenge to achieve high stretchability without compromising charge transport properties.Herein,we synthesize a series of stretchable polymer semiconductors incorporating urethane and bipyridine units,which can provide dynamic interconnected polymer network by combination of hydrogen bonds with metal coordination,simultaneously obtaining excellent stretchability and carrier mobilities.Compared with single-stage hydrogen bonds,multiple dynamic chemical bonds constructed by 10% hydrogen bonds and 0.25 equiv.metal coordination endowed the polymer semiconductors with an 58% enhancement in carrier mobility and a two-fold increase in crack-onset strain.Notably,the polymer exhibited stable carrier mobilities parallel to the stretching direction,with 91% of initial values even under 150% strain,which is the unprecedented value for intrinsically stretchable semiconducting polymers without blending of elastomers.Therefore,the introduction of multiple dynamic bonds provides an effective and promising approach for intrinsically stretchable and high-performance polymer semiconductor.展开更多
With the rapid development of flexible wearable electronics,the demand for stretchable energy storage devices has surged.In this work,a novel gradient-layered architecture was design based on single-pore hollow lignin...With the rapid development of flexible wearable electronics,the demand for stretchable energy storage devices has surged.In this work,a novel gradient-layered architecture was design based on single-pore hollow lignin nanospheres(HLNPs)-intercalated two-dimensional transition metal carbide(Ti_(3)C_(2)T_(x) MXene)for fabricating highly stretchable and durable supercapacitors.By depositing and inserting HLNPs in the MXene layers with a bottom-up decreasing gradient,a multilayered porous MXene structure with smooth ion channels was constructed by reducing the overstacking of MXene lamella.Moreover,the micro-chamber architecture of thin-walled lignin nanospheres effectively extended the contact area between lignin and MXene to improve ion and electron accessibility,thus better utilizing the pseudocapacitive property of lignin.All these strategies effectively enhanced the capacitive performance of the electrodes.In addition,HLNPs,which acted as a protective phase for MXene layer,enhanced mechanical properties of the wrinkled stretchable electrodes by releasing stress through slip and deformation during the stretch-release cycling and greatly improved the structural integrity and capacitive stability of the electrodes.Flexible electrodes and symmetric flexible all-solid-state supercapacitors capable of enduring 600%uniaxial tensile strain were developed with high specific capacitances of 1273 mF cm^(−2)(241 F g^(−1))and 514 mF cm^(−2)(95 F g^(−1)),respectively.Moreover,their capacitances were well preserved after 1000 times of 600%stretch-release cycling.This study showcased new possibilities of incorporating biobased lignin nanospheres in energy storage devices to fabricate stretchable devices leveraging synergies among various two-dimensional nanomaterials.展开更多
Soft polymer optical fiber(SPOF)has shown great potential in optical-based wearable and implantable biosensors due to its excellent mechanical properties and optical guiding characteristics.However,the multimodality c...Soft polymer optical fiber(SPOF)has shown great potential in optical-based wearable and implantable biosensors due to its excellent mechanical properties and optical guiding characteristics.However,the multimodality characteristics of SPOF limit their integration with traditional fiber optic sensors.This article introduces for the first time a flexible fiber optic vibration sensor based on laser interference technology,which can be applied to vibration measurement under high stretch conditions.This sensor utilizes elastic optical fibers made of polydimethylsiloxane(PDMS)as sensing elements,combined with phase generating carrier technology,to achieve vibration measurement at 50−260 Hz within the stretch range of 0−42%.展开更多
基金supported by the Strategic Priority Research Program of the Chinese Academy of Sciences(No.XDA0540000)the National Natural Science Foundation of China(Nos.22301294,52025031 and 22261142664)the USTC Research Funds of the Double First-Class Initiative(No.YD9990002030)。
文摘Thermosetting polymers exhibit outstanding mechanical properties,thermal stability,and chemical resistance due to their permanently cross-linked network structures.However,the irreversible nature of covalent cross-linking renders these materials non-reprocessable and non-recyclable,posing significant environmental challenges.Although healable polymers based on dynamic covalent bonds and supramolecular interactions have emerged as promising alternatives,a broadly applicable strategy utilizing metal-ligand coordination in thermoset systems remains underexplored.In this work,we present a robust and healable thermoset system fabricated via ring-opening metathesis polymerization(ROMP)of commercially available chelating norbornene comonomers.Cross-linking is accomplished through O-donor coordination to Lewis acidic metal centers,yielding polydicyclopentadiene(PDCPD)-based networks that demonstrate high mechanical strength(up to 60.8 MPa)and effective self-healing performance.This methodology offers a simple and scalable approach to developing high-performance,sustainable thermosetting materials.
基金Funded by the Natural Science Foundation of Fujian Province (No. 2019J01716)the Fujian Provincial Department of Science and Technology (No.2019L3008)。
文摘To evaluate their performance,we constructed organic solar cells using PTB7/Y6 and PTB7-b-PNDI active layers,which were deposited on PET substrates coated with PEDOT:PSS.The ternary solar cells demonstrated an excellent power conversion efficiency after being stretched by 38%.The stretchable organic solar cells were spin-coated on the flexible substrate.The electrodes were formed via liquid metal dropcoating.Solar cell devices based on PET/PH1000/PEDOT:PSS and PTB7:Y6:5% BCP active layer materials show better stretchability than the normal solar cells.The PTB7:Y6:5% BCP-based stretchable organic solar cell achieves a high PCE of 12.3%,and a PCE of 7.8% after stretching.Incorporating block copolymer additives improves the mechanical properties of organic solar cells,thereby enabling superior stretchability.
基金supported by the National Key Re-search and Development Program of China(No.2021YFA0715700)the National Natural Science Foundation of China(No.52003212).
文摘As a natural biopolymer material,silk fibroin with unique mechanical properties can be used in the preparation of biocomposite hydrogels for strain sensors.But,the electromechanical properties of bio-composite hydrogel strain sensors are still insufficient,such as the deterioration of electrical signals and low sensitivity,which need to develop a hydrogel with a stable transmission network for electric con-duction.Herein,a silk fibroin biocomposite hydrogel is prepared by incorporating tannic acid and MXene nanosheets into a polyacrylamide and silk fibroin double network.The electromechanical properties of hydrogels are improved by optimizing the proportion of material components.As a result,the double network structure and supramolecular interaction enhance the stretchability of hydrogels(692% fracture strain).The hydrogel also exhibits good biocompatibility and conductivity(0.85 S/m),which shows the application prospect in wearable sensors.The wireless strain sensor assembled by this biocomposite hy-drogel presents good portability and sensing performance,such as high sensitivity(gauge factor=6.04),wide working range(500% strain),and outstanding stability(1000 cycles at 100%strain).The results in-dicate that the hydrogel strain sensor can be used to monitor human body movement.The biocomposite hydrogel is expected to be applied in the field of wearable strain sensors,and this study can provide a new way for the design of flexible electronic materials.
文摘Flexible electronic devices are often subjected to large and repeated deformation,so that their functional components such as metal interconnects need to sustain strains up to tens of percent,which is far beyond the intrinsic deformability of metal materials(~1%).To meet the stringent requirements of flexible electronics,metal/elastomer bilayers,a stretchable structure that consists of a metal film adhered to a stretchable elastomer substrate,have been developed to improve the stretch capability of metal interconnects.Previous studies have predicted that the metal/elastomer bilayers are much more stretchable than freestanding metal films.However,these investigations usually assume perfect bonding between the metal and elastomer layers.In this work,the effect of the metal/elastomer interface with a finite interfacial stiffness on the stretchability of bilayer structures is analyzed.The results show that the assumption of perfect interface(with infinite interfacial stiffness)may lead to an overestimation of the stretchability of bilayer structures.It is also demonstrated that increased adhesion between the metal and elastomer layers can enhance the stretchability of the metal layer.
文摘The dimensional properties and uniarial stretchability of cotton interlock and interlock with missing needle are discussed on the basis of definition system for double knits. K values used widely to describe the dimensional properties of plain knitted structures are developed into the study of double knitted structures in this paper. K values are not constants, the numerical values of which will depend on the actual configuration of various knitted structures. It is suggested that the effect of knitted structures on dimensional properties and stretchability can be described by K values.
基金financially supported by the National Key Research and Development Program of China(No.2021YFA1401100)the National Natural Science Foundation of China(Nos.61825403 and 61921005)。
文摘Stretchable electronics that monitor joint activity and treat diseases based on liquid metal could be used in the development of healthcare applications.Such devices can be seamlessly integrated with human skin.However,most high-precision microstructures and complex patterns are difficult to fabricate due to the limitations of conventional fabrication solutions,resulting in suboptimal performance under practical conditions.Here,a liquid-metal stretchable system utilizing natural leaf veins was reported as microstructures,which was based on a biomimetic concept and utilized an all-solution process for the preparation of complex microstructures.The systems are ultra-high tensile(800%tensile strain),environmentally stable(20 days)and mechanically durable(300-cycle).The system can accurately recognize the wearer's finger bending level as well as simple gesture signals.At the same time,the system acts as a wearable heater,which can realize the fast heating behavior of heating up to 50℃in 3 min under the human body-safe voltage(1.5 V).The tensile stability is demonstrated by the heterogeneous integration of lasers(405 nm)with the system interconnects for a stretchable and wearable light source.
基金supported by the Science Fund for Distinguished Young Scholars of Tianjin Municipality(23JCJQJC00240)the National Natural Science Foundation of China(52121002)+1 种基金the Start-up Grant of Peiyang Scholar Program from Tianjin Universitythe Fundamental Research Funds for the Central Universities.
文摘In the rapidly evolving field of wearable electronics,stretchy organic solar cells(OSCs)have emerged as promising candidates for portable power sources,necessitating materials with superior mechanical flexibility.However,the inherent rigidity of conjugated backbones in top-performance photovoltaic polymers,such as PM6,poses a significant challenge,as it makes photovoltaic films prone to fracture under mechanical strain.Consequently,improving the mechanical properties of these films is a crucial research frontier for advancing stretchable photovoltaic technologies.This tutorial review provides a thorough examination of current strategies aimed at bolstering the mechanical resilience of polymer photovoltaic thin films,elucidated through a selection of pertinent examples leveraging the PM6-based systems.We first explore the prevalent strategy of incorporating third components,including vip polymer donors/acceptors and insulating polymers,to improve stretchability.We then discuss the structural design of PM6 aimed at reducing the backbone rigidity.Additionally,we summarize various predictive models for assessing the mechanical properties of these photovoltaic films.Finally,the future challenges and perspectives for stretchy OSCs are explored.
基金supported by the National Key Research and Development Program of China(Grant No.2023YFD2200504)the Central Guidance Fund for Local Science and Technology Development Projects(Grant No.2024JH6/100700013)+1 种基金the National Natural Science Foundation of China(Grant Nos.32171720 and 32371823)the National Science Fund for Distinguished Young Scholars(Grant No.31925028).
文摘Achieving rubber-like stretchability in cellulose ionogels presents a substantial challenge due to the intrinsically extended chain configuration of cellulose.Inspired by the molecular configuration of natural rubber,we address this challenge by using cyanoethyl as a substitute for 1.5 hydroxyl on the D-glucose unit of cellulose.This strategy innovatively triggers the transformation of cellulose molecules into a coiled chain configuration,facilitating the creation of an ultra-stretchable ionogel free from any petrochemical polymers.The resultant ionogel demonstrates mechanical ductility comparable to that of a rubber band,achieving an elongation strain of nearly 1,000%while maintaining a tensile strength of up to 1.8 MPa and exhibiting a biomodulus akin to that of human skin,recorded at 63 kPa.Additionally,this stretchable ionogel presents skin-like self-healing behavior,favorable biocompatibility,and noteworthy thermoelectric properties,highlighted by a Seebeck coefficient of approximately 68 mV K−1.This study delineates a feasible molecular approach for developing stretchable ionogels from biomass resources,potentially revolutionizing self-powered stretchable electronics for integration with human tissues and skin.
基金supported by NSFC(22322507,22075293)the Beijing Municipal Natural Science Foundation(Z220025)+2 种基金the Chinese Academy of Sciences(XDB0520000,XDB0960101,GJTD-2020-02,YSBR-110)supported by NSFC(22021002,22090021,T2441002,22422509)the Youth Innovation Promotion Association CAS(No.2022031).
文摘Incorporating flexible conjugation breakers into conjugated polymers to develop intrinsically stretchable polymer semiconductors has garnered much attention.However,it still remains challenging to improve mechanical stretchability without compromising the charge transport property of polymer semiconductors.Herein,we report an approach to enhance the mechanical stretchability of the polymer semiconductor while largely maintaining its semiconducting performance by incorporating di-2-thienylsulfide as the p-πconjugation units into the backbone of poly(3,6-di(thiophen-2-yl)diketopyrrolo-[3,4-c]pyrrole-1,4-dione-alt-thieno[3,2-b]thiophen)(PDPP-TT).Compared to the parent polymer PDPP-TT,the incorporation of the p-πconjugation units induces the twisting of the backbone and weakens the interchain packing order,resulting in higher crack onset strain and better mechanical durability.The polymer semiconductor in which the molar ratio of the repeat unit with di-2-thienylsulfides is 10%exhibits a crack onset strain greater than 100%and can retain its initial charge mobility after 1000 stretching-releasing cycles under 50%strain.Our studies show that incorporation of p-πconjugation units such as di-2-thienylsulfide into backbones of polymer semiconductors provides a feasible approach to balance the stretchability and charge mobility,thus making it a promising way for future development of stretchable polymer semiconductors.
基金This research was made possible thanks to the financial support of the National Natural Science Foundation of China(Nos.52073207 and 52121002)the Fundamental Research Funds for the Central Universities.L.Ye also appreciates the Peiyang Scholar Program of Tianjin University for support。
文摘With the emergence of Y-series small molecule acceptors,polymerizing the small molecule acceptors with aromatic linker units has attracted significant research attention,which has greatly advanced the photovoltaic performance of all-polymer solar cells.Despite the rapid increase in efficiency,the unique characteristics(e.g.,mechanical stretchability and flexibility)of all-polymer systems were still not thoroughly explored.In this work,we demonstrate an effective approach to simultaneously improve device performance,stability,and mechanical robustness of all-polymer solar cells by properly suppressing the aggregation and crystallization behaviors of polymerized Y-series acceptors.Strikingly,when introducing 50 wt%PYF-IT(a fluorinated version of PY-IT)into the well-known PM6:PY-IT system,the all-polymer devices delivered an impressive photovoltaic efficiency of 16.6%,significantly higher than that of the control binary cell(15.0%).Compared with the two binary systems,the optimal ternary blend exhibits more efficient charge separation and balanced charge transport accompanying with less recombination.Moreover,a high-performance 1.0 cm^(2)large-area device of 15%efficiency was demonstrated for the optimized ternary all-polymer blend,which offered a desirable PCE of 14.5%on flexible substrates and improved mechanical flexibility after bending 1000 cycles.Notably,these are among the best results for 1.0 cm^(2)all-polymer OPVs thus far.This work also heralds a bright future of all-polymer systems for flexible wearable energy-harvesting applications.
基金supported by National Natural Science Foundation of China(Nos.62201624,32000939,21775168,22174167,51861145202,U20A20168)Shenzhen Science and Technology Program(No.RCBS20221008093310024)+2 种基金Shenzhen Research Funding Program(No.JCYJ20190807160401657,JCYJ201908073000608)the Open Research Fund Program of Beijing National Research Center for Information Science and Technology(No.BR2023KF02010)support from Key Laboratory of Sensing Technology and Biomedical Instruments of Guangdong Province(No.2020B1212060077).
文摘The development of strain sensors with high stretchability and stability is an inevitable requirement for achieving full-range and long-term use of wearable electronic devices.Herein,a resistive micromesh reinforced strain sensor(MRSS)with high stretchability and stability is prepared,consisting of a laser-scribed graphene(LSG)layer and two styrene-block-poly(ethylene-ran-butylene)-block-poly-styrene micromesh layers embedded in Ecoflex.The micromesh reinforced structure endows the MRSS with combined characteris-tics of a high stretchability(120%),excellent stability(with a repetition error of 0.8%after 11000 cycles),and outstanding sensitivity(gauge factor up to 2692 beyond 100%).Impressively,the MRSS can still be used continauously within the working range without damage,even if stretched to 300%.Furthermore,compared with different structure sensors,the mechanism of the MRSS with high stretchability and stability is elucidated.What's more,a multilayer finite element model,based on the layered structure of the LSG and the morphology of the cracks,is proposed to investigate the strain sensing behavior and failure mechanism of the MRSS.Finally,due to the outstanding performance,the MRSS not only performes well in monitoring full-range human motions,but also achieves intelligent recognitions of various respiratory activities and ges-tures assisted by neural network algorithms(the accuracy up to 94.29%and 100%,respectively).This work provides a new approach for designing high-performance resistive strain sensors and shows great potential in full-range and long-term intelligent health management and human-machine interac-tions applications.
基金supported by the National Natural Science Foundation of China(52172170)Guangdong Natural Science Foundation for Distinguished Young Scholars(2023B1515020114)+2 种基金Fundamental Research Funds for the Central Universities(24lgqb003)Guangdong University Innovation and Enhancement Program(2024KTSCX003)Science and Technology Projects of Guangzhou(2025A04J4230).
文摘Stretchable electronics have been recognized as intriguing next-generation electronics that possess huge market value,and stretchable electronic conductors(SECs)are essential for stretchable electronics,which not only can serve as critical functional components but also are the indispensable electronic connections bridging various electronic components within stretchable electronic systems.Herein,we offer a comprehensive review of recent progress in SECs including the material categories,structure designs,fabrication techniques,and applications.The characteristics,performance enhancement strategies,and application requirements are emphasized.Based on the recent advances,the existing challenges and future prospects are outlined and discussed.
基金supported by the National Natural Science Foundation of China(No.52433009)the Fundamental Research Funds for the Central Universities(No.GK202501005)the State Key Laboratory of Polymer Science and Technology(No.PST-KF2025-07)。
文摘The scalable fabrication of stretchable conjugated polymer films via solution printing is essential for their practical application in largearea wearable electronics.However,the printed conjugated polymer films typically exhibit high crystallinity,limiting their mechanical deformability.Herein,we propose a plasticizer-assisted printing strategy to simultaneously enhance the stretchability and electrical performance of films based on the conjugated polymer poly(3-(5-(5-methylselenophen-2-yl)thiophen-2-yl)-6-(5-methylthiophen-2-yl)-2,5-bis(4-octyltetradecyl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione)(P(TDPP-Se)).The incorporation of a plasticizer trioctyl trimellitate(TOTM)promotes P(TDPP-Se)aggregation in initial solution,facilitates chain alignment under flow field,and shorten solidification process,thereby restricting randomly polymer crystallization.Consequently,a low-crystallinity film with favorable edge-on orientation,strong chain alignment and improved chain dynamics is realized,which effectively alleviates crystallites fragmentation and crack propagation under large strain.The TOTM-plasticized film exhibits approximately 2-fold improvements in fracture strain and charge mobility,along with superior mobility retention under 100%strain in comparison to the neat film.This study provides a feasible approach for microstructure control in printed stretchable conjugated polymer film.
基金supported in part by the National Key R&D Program of China under Grant 2024YFB4405300 and 2022YFA1204300the Natural Science Foundation of Hunan Province under Grant 2023JJ20016+2 种基金the National Natural Science Foundation of China under Grants of 52221001 and 62090035the Key Research and Development Plan of Hunan Province under grants of 2022GK3002 and 2023GK2012the Key Program of Science and Technology Department of Hunan Province under grant of 2020XK2001。
文摘Permeable electronics promise improved physiological comfort,but remain constrained by limited functional integration and poor mechanical robustness.Here,we report a three-dimensional(3D)permeable electronic system that overcomes these challenges by combining electrospun SEBS nanofiber mats,high-resolution liquid metal conductors patterned via thermal imprinting(50μm),and a strain isolators(SIL)that protects vertical interconnects(VIAs)from stress concentration.This architecture achieves ultrahigh air permeability(>5.09 m L cm^(-2)min^(-1)),exceptional stretchability(750%fracture strain),and reliable conductivity maintained through more than 32,500 strain cycles.Leveraging these advances,we have integrated multilayer circuits,strain sensors,and a three-axis accelerometer to achieve a fully integrated,stretchable,permeable wireless real-time gesture recognition glove.The system enables accurate sign language interpretation(98%)and seamless robotic hand control,demonstrating its potential for assistive technologies.By uniting comfort,durability,and high-density integration,this work establishes a versatile platform for nextgeneration wearable electronics and interactive human-robot interfaces.
基金supported by the National Natural Science Foundation of China(Nos.T2441002,22525506,U24A20137,and U22A6002)Strategic Priority Research Program of CAS(No.XDB0520101)+1 种基金National Key R&D Program of China(No.2023YFB3609000)CAS Project for Young Scientists in Basic Research(No.YSBR-053)。
文摘The increasing demand for flexible displays and wearable electronics has driven extensive efforts to develop stretchable organic lightemitting diodes(OLEDs).A critical challenge in this field is the creation of emissive layers that combine high efficiency with mechanical robustness.Thermally activated delayed fluorescence(TADF)materials have attracted significant attention as third-generation emitters capable of achieving 100%internal quantum efficiency;however,their application in stretchable OLEDs has been limited.In this study,we propose an elastomer doping strategy.Polyurethane(PU)is incorporated into TADF polymers to improve their mechanical flexibility while maintaining a high luminescent efficiency.The resulting composite films exhibited excellent TADF characteristics and remarkable stretchability(75%).OLEDs fabricated from these materials achieved a maximum external quantum efficiency(EQE)of 14.26%and a peak luminance of 73570 cd·m^(-2),with the PUdoped devices showing a significantly suppressed efficiency roll-off.Additionally,a fully stretchable OLED architecture was designed and operated under tensile strain to maintain stable electroluminescent performance.These results demonstrate that elastomer doping is an effective strategy for balancing the mechanical compliance with optoelectronic performance,offering a promising pathway for the development of high-performance stretchable OLEDs for flexible electronics.
基金supported by the National Key R&D Program of China(2018YFE0200700)NSFC(21790363,21871271,22090021,22075293,22021002,22071254).
文摘The soft nature has endowed conjugated polymers with promising applications in a wide range of field-effect transistor(FET)based flexible electronics.With unremitting efforts on revealing the molecular structure-property relationships,numerous novel conjugated polymers with high mobility and excellent mechanical property have been developed in the past decades.Incorporating hydrogen-bonding(H-bonding)units into semiconducting polymers is one of the most successful strategies for designing high-performance semiconducting materials.In this review,we aim to highlight the roles of H-bonding units in the performances of polymeric FETs from three aspects.These include(i)charge mobility enhancement for semiconducting polymers after incorporation of H-bonding units into the side chains,(ii)the effects of H-bonding units on the stretchability of conjugated polymers,and(iii)the improvement of self-healing properties of conjugated polymers containing dynamic hydrogen bonds due to the H-bonding units in the side chains or conjugated backbones.
基金financially supported by the National Natural Science Foundation of China(Nos.52303239 and 51933001)Natural Science Foundation of Shandong Province(Nos.ZR2022QB141 and 2023HWYQ-087).
文摘Intrinsic stretchability is a promising attribute of polymer organic solar cells(OSCs).However,rigid molecular blocks typically exhibit poor tensile properties,rendering polymers vulnerable to mechanical stress.In this study,we introduce a different approach utilizing all-small-molecule donors and acceptors to fabricate stretchable OSCs.An elastomer,styrene-b-ethylene-butylene-styrene(SEBS),was embedded to modulate film crystallization and stretchability.SEBS effectively confines the growth process of donors and acceptors,leading to enhancement of the crystallization quality,thus contributing to enhanced device efficiencies.Meanwhile,SEBS can absorb and release mechanical stress during stretching,thereby preventing mechanical degradation of donors and acceptors.The mechanical properties of the OSCs were significantly improved by the incorporation of SEBS.Notably,the crack-onset strain increased from 1.03% to 5.99% with SEBS embedding.These findings present a straightforward strategy for achieving stretchable OSCs using all small molecules,offering a different perspective for realizing stretchable devices.
基金the Fundamental Research Funds for the Central Universities(No.buctrc202103)the National Natural Science Foundation of China(Nos.52373170,22171019)+1 种基金Beijing Natural Science Foundation(No.2252015),SINOPEC(No.225057)Open Project Program of the State Key Laboratory of Fine Chemicals(No.KF2201,Dalian University of Technology)。
文摘Intrinsically stretchable semiconducting polymers play a vital role in the development of wearable electronics,featuring low-cost,large-area and high-density fabrication.Only single-stage dynamic chemical bond has been widely incorporated into polymer backbones to afford stretchability while multiple dynamic bonds have not been investigated,making a formidable challenge to achieve high stretchability without compromising charge transport properties.Herein,we synthesize a series of stretchable polymer semiconductors incorporating urethane and bipyridine units,which can provide dynamic interconnected polymer network by combination of hydrogen bonds with metal coordination,simultaneously obtaining excellent stretchability and carrier mobilities.Compared with single-stage hydrogen bonds,multiple dynamic chemical bonds constructed by 10% hydrogen bonds and 0.25 equiv.metal coordination endowed the polymer semiconductors with an 58% enhancement in carrier mobility and a two-fold increase in crack-onset strain.Notably,the polymer exhibited stable carrier mobilities parallel to the stretching direction,with 91% of initial values even under 150% strain,which is the unprecedented value for intrinsically stretchable semiconducting polymers without blending of elastomers.Therefore,the introduction of multiple dynamic bonds provides an effective and promising approach for intrinsically stretchable and high-performance polymer semiconductor.
基金supported by Natural Science and Engineering Research Council of Canada(RGPIN-2017-06737)Canada Research Chairs program,the National Key Research and Development Program of China(2017YFD0601005,2022YFD0904201)+1 种基金the National Natural Science Foundation of China(51203075)the China Scholarship Council(Grant No.CSC202208320361).
文摘With the rapid development of flexible wearable electronics,the demand for stretchable energy storage devices has surged.In this work,a novel gradient-layered architecture was design based on single-pore hollow lignin nanospheres(HLNPs)-intercalated two-dimensional transition metal carbide(Ti_(3)C_(2)T_(x) MXene)for fabricating highly stretchable and durable supercapacitors.By depositing and inserting HLNPs in the MXene layers with a bottom-up decreasing gradient,a multilayered porous MXene structure with smooth ion channels was constructed by reducing the overstacking of MXene lamella.Moreover,the micro-chamber architecture of thin-walled lignin nanospheres effectively extended the contact area between lignin and MXene to improve ion and electron accessibility,thus better utilizing the pseudocapacitive property of lignin.All these strategies effectively enhanced the capacitive performance of the electrodes.In addition,HLNPs,which acted as a protective phase for MXene layer,enhanced mechanical properties of the wrinkled stretchable electrodes by releasing stress through slip and deformation during the stretch-release cycling and greatly improved the structural integrity and capacitive stability of the electrodes.Flexible electrodes and symmetric flexible all-solid-state supercapacitors capable of enduring 600%uniaxial tensile strain were developed with high specific capacitances of 1273 mF cm^(−2)(241 F g^(−1))and 514 mF cm^(−2)(95 F g^(−1)),respectively.Moreover,their capacitances were well preserved after 1000 times of 600%stretch-release cycling.This study showcased new possibilities of incorporating biobased lignin nanospheres in energy storage devices to fabricate stretchable devices leveraging synergies among various two-dimensional nanomaterials.
文摘Soft polymer optical fiber(SPOF)has shown great potential in optical-based wearable and implantable biosensors due to its excellent mechanical properties and optical guiding characteristics.However,the multimodality characteristics of SPOF limit their integration with traditional fiber optic sensors.This article introduces for the first time a flexible fiber optic vibration sensor based on laser interference technology,which can be applied to vibration measurement under high stretch conditions.This sensor utilizes elastic optical fibers made of polydimethylsiloxane(PDMS)as sensing elements,combined with phase generating carrier technology,to achieve vibration measurement at 50−260 Hz within the stretch range of 0−42%.
