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SYNTHETIC METALS · 2025 · IF 4.6

A highly stretchable, stable and sensitive PEDOT:PSS-P(HEMA-co-AA) hydrogel for strain sensors

Yu Lin,Gen Li,Juan Teng,Haibo Wang,Ximei Liu

As a crucial component of flexible electronic devices, poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS)-based hydrogels for strain sensors have garnered extensive attention for their potential in the field of wearable sensors due to their inherent conductivity and flexibility. However, challenges such as poor mechanical strength, limited sensitivity, and poor durability have hindered the widespread application of PEDOT:PSS hydrogels in high-performance strain sensors. In this study, we develop a novel PEDOT:PSS-P(HEMA-co-AA) hydrogel that addresses common limitations in hydrogel applications, demonstrating remarkable stretchability, low hysteresis, and reliable conductivity. The hydrogel is synthesized using a semi-interpenetrating polymer network (SIPN) strategy, combining the linear conducting polymer PEDOT:PSS with a chemically cross-linked network based on 2-hydroxyethyl methacrylate (HEMA) and acrylic acid (AA). This hybrid structure notably contributes to the hydrogel's mechanical properties, achieving a stretchability of 195 %, while maintaining a rapid response time of 0.20 seconds and exceptional cyclic stability over 1000 cycles under 100 % strain. Moreover, the hydrogel demonstrates promising strain-sensing capabilities, positioning it as a strong candidate for future applications in wearable electronics and flexible sensors. The adoption of the SIPN strategy, along with the synergistic combination of PEDOT:PSS and P(HEMA-co-AA), paves a new pathway for enhancing the mechanical performance and sensing properties of hydrogels in strain-sensing technologies.

研究领域: 材料科学 · 柔性电子 · 生物医学工程
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Micromachines · 2021 ·Vol. 12 ·期 3 ·252 · IF 2.891

Stretchable MXene/Thermoplastic Polyurethanes based Strain Sensor Fabricated Using a Combined Electrospinning and Electrostatic Spray Deposition Technique

Feiyu Fang,Han Wang,Huaquan Wang,Xiaofei Gu,Jun Zeng,Zixu Wang,Xindu Chen,Xin Chen,Meiyun Chen

In this work, a novel flexible electrically resistive-type MXene/Thermoplastic polyurethanes(TPU) based strain sensors was developed by a composite process of electrospinning (ES) and electrostatic spray deposition (ESD). Compared with other deposition processes, the sensing layer prepared by ESD has better adhesion to the ES TPU nanofiber membrane and is not easy to crack during the stretching process, thereby greatly improving the working range of the strain sensor. Furthermore, we obtained the sandwich structure easily by ES on the surface of the sensing layer again. This will help make the stress distribution more uniform during the stretching process and further increase the strain sensing range. The ESD-ES strain sensors were attached on skin to monitor various human motions. The results demonstrate that our ESD-ES strain sensors have wide application prospects in smart wearable device.Keywords:strain sensor;electrospinning;electrostatic spray deposition;MXene

CAS / MDL: 67-63-0
研究领域: 材料科学 · 电子工程
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COMPOSITES COMMUNICATIONS · 2024 · IF 6.5

Stretchable, fast response and adhesive MXene-based hydrogels for wearable strain sensor

Yifan Zhang,Wenlong Pan,Yuliao Dong,Jianning Ding,Lin Xu

Conductive hydrogels have emerged as significant materials within the domain of soft electronics, attributed to their remarkable stretchability, high sensitivity, and rapid response characteristics. In this study, we successfully developed a novel conductive hydrogel, named NAM, which integrates MXene nanosheets into a P(NIPAm-AAc) network to create a dynamic crosslinked structure. This NAM hydrogel exhibits exceptional mechanical properties, including a tensile strength exceeding 1400% and the ability to adhere to objects of different materials. It also demonstrates satisfactory electrical conductivity (0.233 S/m) and high sensitivity (GF=3.384), with rapid response and recovery time of 60 ms. The NAM hydrogel sensors are capable of detecting a wide range of strains (0-800%) and maintaining excellent repeatability in cyclic loading-unloading. They can effectively monitor subtle facial micro-expressions, laryngeal vocalizations, and human motion data, and can be integrated into soft robotic systems for enhanced functionality. The findings suggest significant potential applications for the NAM hydrogel in soft robotics, flexible electronic skin, smart health monitoring, and biomedicine, highlighting its multifunctional capabilities in the realm of soft electronics.

研究领域: 材料科学 · 生物医学工程 · 软体机器人
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JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION · 2020 · IF 2.69

The preparation of multifunction chitosan adhesive hydrogel by “one- step” method

Ruixue Liu,Yingbo Li,Jichao Chen,Xiaojing Zhang,Zhibin Niu,Yadong Sun

Chitosan adhesive hydrogels have attracted interest because of their unique properties. However, it is still a challenge to use simple and unmodified chitosan to synthesize multifunctional hydrogels with adhesive, self-healing and strain sensing properties. Here, a multifunctional hydrogel of Ca2+-chitosan/polyacrylamide(Ca2+- CS/PAAm)with adhesive self-healing and strain sensing properties was carried out by one-step preparation method. The hydrogel has the ability to adhere to a variety of materials, wherein the adhesion strength to rubber surface is 48.4 kPa. The hydrogel has excellent strain sensing capability on finger bending or cyclic stretching, the sensitivity factor is 0.41 ± 0.015. The cut hydrogel healed completely at room temperature within 4 h, and the healing hydrogel can be stretched to 5 times of its original length. This makes Ca2+-CS/PAAm hydrogel to be great potential in the application of strain sensors, wound dressing and skin adhesives.

研究领域: 生物材料 · 医学工程 · 高分子化学
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NANOTECHNOLOGY · 2018 ·Vol. 29 ·期 17 ·175502 · IF 3.404

Photoelastic colloidal gel for a high-sensitivity strain sensor

Hui Pan,Zhixin Chen,Shenmin Zhu,Chun Jiang,Di Zhang

Nanoparticles, having the ability to self-assemble into an ordered structure in their suspensions, analogous to liquid crystals, have attracted extensive attention. Herein, we report a new type of colloidal gel with an ordered crystal structure assembled from 1D and 2D nanoparticles. The material has high elasticity and, more interestingly, it shows significant photoelasticity. Its refractive index can be tuned under external stress and exhibits an ultra-wide dynamic range (Δn) of the order of 10−2. Due to the large Δn, the material shows an extremely high strain sensibility of 720 nm/ε, an order of magnitude higher than the reported ones.

研究领域: 材料科学 · 纳米技术
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CARBOHYDRATE POLYMERS · 2023 · IF 11.2

Strain-induced orientation facilitates the fabrication of highly stretchable and tough xylan-based hydrogel for strain sensors

Lisong Hu,Yitong Xie,Shishuai Gao,Xiaoyu Shi,Chenhuan Lai,Daihui Zhang,Chuanwei Lu,Yi Liu,Lei Du,Xuezhi Fang,Feng Xu,Chunpeng Wang,Fuxiang Chu

Stretchable and tough polysaccharide-based functional hydrogels have gained popularity for various applications. However, it still remains a great challenge to simultaneously own satisfactory stretchability and toughness, particularly when incorporating renewable xylan to offer sustainability. Herein, we describe a novel stretchable and tough xylan-based conductive hydrogel utilizing the natural feature of rosin derivative. The effect of different compositions on the mechanical properties and the physicochemical properties of corresponding xylan-based hydrogels were systematically investigated. Owing to the multiple non-covalent interactions among different components to dissipate energies and the strain-induced orientation of rosin derivative during the stretching, the highest tensile strength , strain, and toughness of xylan-based hydrogels could reach 0.34 MPa, 2098.4 %, and 3.79 ± 0.95 MJ/m 3 , respectively. Furthermore, by incorporating MXene as the conductive fillers, the strength and toughness of hydrogels were further enhanced to 0.51 MPa and 5.95 ± 1.19 MJ/m 3 . Finally, the synthesized xylan-based hydrogels were able to serve as a reliable and sensitive strain sensor to monitor the movements of human beings. This study provides new insights to develop stretchable and tough conductive xylan-based hydrogel, especially utilizing the natural feature of bio-based resources.

研究领域: 材料科学 · 生物工程
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2023 · IF 4.2

Facile Strategy to In Situ Synthesize Gallic Acid-Modified Lignin and Its Utilization for Fabricating Conductive and Self-Adhesive Hydrogels as Strain Sensors

Xiaoyu Shi,Kai Wang,Shishuai Gao,Daihui Zhang,Chenhuan Lai,Can Jin,Mi Li,Chunpeng Wang,Qiang Yong,Fuxiang Chu

As lignin is one of the most abundant renewable resources, utilization to fabricate functional hydrogels has gained increasing attention. However, the heterogeneous structure and the few available functional groups of lignin limited its applications. Herein, we presented a simple strategy to synthesize gallic acid (GA)-modified lignin as a key component to prepare conductive hydrogels. The addition of GA during the organic solvent pretreatment of poplar changed the structure of lignin and increased the total content of phenolic hydroxyl groups from 3.20 to 3.89 mmol/g (EOL-G30). Moreover, the enzymatic hydrolysis of pretreated poplar was enhanced from 49.1 to 55.2% (OP-G30) at a low enzyme loading of 5 FPU/g. When using GA-modified lignin to prepare hydrogels, the resulting hydrogel exhibited excellent self-adhesion to various substrates and demonstrated effective free radical scavenging capabilities. When incorporating sodium chloride (NaCl) as conductive ions, the hydrogels exhibit reliable strain-sensing capability. Moreover, they also displayed robust functionality in a low-temperature environment (−20 °C). This study has presented valuable insights to realize in situ modification of lignin and fabricate lignin-based functional materials, offering new perspectives for the biorefinery industry.

研究领域: 材料科学 · 生物化学 · 可再生资源工程
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Journal of Materials Chemistry C · 2023 ·Vol. 11 ·期 12 ·4235-4242 · IF 6.4

A highly stable elastic electrode via direct covalent crosslinking for strain sensors

Linping Wang,Ben-Lin Hu,Fengyuan Zhang,Yinxia Zhang,Junming Li,Tianhua Xu,Run-Wei Li

Electrodes are essential components in electronic devices. One challenge in developing wearable electronics involves obtaining elastic electrodes with high mechanical and electrical stability. Poor mechanical and electrical stability in stretchable polymer electrodes often stems from instability of the nodes in the polymer network based on poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS), which has typically been used in elastic electrodes. In this study, soft and long chains were covalently crosslinked to the PSS chains directly via esterification between sulfonic acid and epoxy groups, and is used as the first effective example of the direct covalent-crosslinking of PEDOT:PSS to enhance the mechanical and electrical stability of elastic electrodes. By varying the crosslinking temperature and long chain ratio, the optimal PEDOT:PSS films showed a conductivity of 13 100 S m−1 and a stretchability of up to 50%. The R/R0 values of these films up to 50% strain were lower than 1.5. Elastic capacitive strain sensors using these crosslinked PEDOT:PSS films as electrodes showed a high linearity of up to 50% strain and excellent stability during cyclic testing. Our study provides a valid solution for enhancing the mechanical and electrical stability of elastic electrodes, indicating the potential of stable elastic PEDOT:PSS electrodes in thin film devices for electronic skin applications.

研究领域: 材料科学 · 电子工程 · 可穿戴技术
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Cell Reports Physical Science · 2022 · IF 7.832

Self-sensing polymer composite containing a continuous and periodic graphene monolayer

Jigang Du,Yang Zhang,Xubing Wu,Wei Li,Bingxue Jiang,Song Wang,Khak Ho Lim,Qingyue Wang,Pei Zhao,Wen-Jun Wang,Pingwei Liu

Embedding the capability of self-sensing to polymeric materials provides tremendous opportunities for developing smart materials with highly important applications. However, a facile method that can introduce this capability to different polymers beyond strain sensing remains elusive. Here, we report a strategy of incorporating a continuous graphene sheet as an electric probe into polymer matrices for developing self-sensing composites. The resulted composite demonstrates impressively high conductivities of 290 S/m at a graphene volume fraction ( V G ) of 0.00068, a good electrical recovery at a cyclic elastic strain of 30% and a strain-sensing upper limit of 80%. Moreover, the glass transition, melting, and photodegradation process of different polymers can also be monitored in situ , and the corresponding glass transition temperature ( T g ) and melting point ( T m ) can be calculated. Our work paves the way for the development and application of novel self-sensing polymer composites with high sensitivity and versatility based on two-dimensional (2D) materials.

研究领域: 材料科学 · 智能材料 · 纳米技术
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POLYMER · 2024 · IF 4.1

Multifunctional inorganic-organic phase-change hydrogel with excellent light-to-thermal energy conversion and strain sensing capabilities for medical thermotherapy and monitoring

Yongsheng Li,Xiao Wu,Yujie Liao,Hong Shao,Yongqian Chen,Wenbin Yang,Pengfei Lv,Yuanlin Zhou,Changyu Tang

Flexible light/electrically responsive inorganic-organic phase-change materials (PCMs) have promising applications in thermal management and wearable health monitoring. Herein, flexible hydrogel PCMs with excellent light-to-thermal energy conversion efficiency and strain sensing capability were synthesized by loading sodium acetate trihydrate (SAT)/expanded graphite (EG)/borax/carboxymethylcellulose sodium (CMC) (termed SEBC) composites into a polyacrylamide (PAM)/chitosan (CS)/graphene (GNPs) (termed PCG) bi-networked hydrogel via a facile one-step strategy. The resulting composites showed excellent self-adhesion properties, tensile cycling stability, thermal stability, high melting enthalpy (119.7 J/g), and low water loss rate (0.41 %, at 70 °C). Benefiting from the light-absorbing ability and electrical conductivity of EG and GNPs, the hydrogel composite exhibited a high light-to-thermal energy conversion efficiency of 92.2 % and meanwhile can absorb excessive thermal energy to regulate the thermotherapy temperature on human joints under infrared light. Besides, the hydrogel composite can act as a strain sensor with an excellent gauge factor value of 2.73 by changing conductive network (EG and GNP) resistance to monitor the recovery of patient's joint activities. This multifunctional inorganic-organic phase-change hydrogels present good potential for personalized healthcare.

CAS / MDL: 9012-76-4 6131-90-4
研究领域: 材料科学 · 生物医学工程
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MACROMOLECULAR CHEMISTRY AND PHYSICS · 2024 ·Vol. 225 ·期 22 ·2400224 · IF 2.5

High-Performance Multipedal Shape Strain Sensors for Human Motion and Electrophysiological Signal Monitoring

Gen Li,Rongtai Wan,Shuhan Liu,Lina Wang,Mangmang Yu,Jiang Zhong,Hanjun Yang,Ximei Liu,Baoyang Lu

Strain sensors from conducting polymer hydrogel have been widely employed in various wearable devices, electronic skins, and biomedical applications. These sensors provide outstanding flexibility and high sensitivity by integrating conducting polymer with hydrogels, making them particularly suitable for monitoring human motion and physiological signals like heart rate or muscle activity. Despite their extensive application potential, conducting polymer hydrogel face several technical challenges in practical use, including poor mechanical properties, lack of long-term stability, and difficulty in customizable design. This work introduces a method for fabricating a multipedal strain sensor using poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS)/polyvinyl alcohol (PVA) dimethyl sulfoxide (DMSO)hydrogels through screen printing and demonstrates its application in human motion monitoring. The multipedal strain sensor demonstrates a low Young's modulus (200 kPa), high stretchability (400%), and excellent mechanical cyclic stability (3000 cycles). Furthermore, this strain sensor is further applied to detect human movements such as chewing, smiling, fist clenching, arm bending, and carotid pulse monitoring. Comparative analysis between the multipedal-designed sensor and the non-designed sensor highlights the enhanced sensing capabilities of the multipedal sensor. The design of this multipedal sensor holds the potential to broaden the design concepts for strain sensors and offers new insights for wearable devices and electronic skins.

CAS / MDL: 67-68-5
研究领域: 生物医学工程 · 材料科学 · 柔性电子
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POLYMER · 2020 · IF 4.231

Graphene assisted ion-conductive hydrogel with super sensitivity for strain sensor

Yi Wang,Guanghui Gao,Xiuyan Ren

Hydrogels flexible wearable sensors have gained widespread attention. However, there was a great challenge to prepare the flexible hydrogel sensor with rapid response, wide strain monitoring ranges, great sensitivity and self-adhesion. Therefore, the greatly sensitive and rapidly responsive strain sensor with wide monitoring range and self-adhesion was prepared by introducing sodium caseinate (SC) and reduced graphene oxide (rGO) into the polyacrylamide hydrogel due to ions and electrons provide two different ways of conducting electricity. Casein not only imparted excellent adhesion to the hydrogel, but also provided a good ionic conductive pathway. In addition, the introduction of rGO could offer an electronic pathway. Therefore, the obtained hydrogel exhibited excellent rapid response (190 ms), high sensitivity (Gauge factor, GF = 13.14) and wide strain monitoring range (0.1–1100%). As a result, SC/rGO/PAAm hydrogels could detect sensitive locomotor signals (for example speaking) and large-scale mankind movements for example knee bending). It was believed that the ion and electron conduction would provide a new mechanism to preparing greatly sensitive hydrogel strain sensor.

研究领域: 材料科学 · 生物医学工程
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