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ADVANCED FUNCTIONAL MATERIALS · 2024 ·Vol. 34 ·期 32 ·2401535 · IF 18.5

Self-Recoverable, Highly Repeatable, and Thermally Stable Mechanoluminescence for Dual-Mode Information Storage and Photonic Skin Applications

Shiye Qin,Wanyuan Wei,Birong Tian,Zhidong Ma,Shaofan Fang,Yongsheng Wang,Jiachi Zhang,Zhaofeng Wang

Mechanically driven light generation is an intriguing phenomenon holding great promise in various fields. However, the existing mechanoluminescence (ML) materials always suffer from poor self-recoverability, low repeatability, and environmental disturbance, severely hindering their practical applications. In this work, a self-activating ML system based on interfacial triboelectrification is created by compositing the Ca 6 BaP 4 O 17 :0.02Ce 3+ powders into a flexible polydimethylsiloxane (PDMS) matrix. With no need for pre-irradiation, the composite film emits self-activating and self-charging ML simultaneously in response to the rubbing or stretching stimuli. Accordingly, the Ca 6 BaP 4 O 17 :0.02Ce 3+ /PDMS exhibits desirable self-recovery and repeatable ML performance, which could still be recorded (or observed by naked eyes) even after ca. 1000 stretching cycles with a fast self-recovery period of < 0.1 s. Furthermore, the Ca 6 BaP 4 O 17 :0.02Ce 3+ /PDMS possesses good thermal stability in a temperature range from 298 to 473 K. The developed Ca 6 BaP 4 O 17 :0.02Ce 3+ /PDMS is applicable to various fields, and the dual-mode information storage and photonic skin devices are created as representatives. Compared to the existing oxide-based ML materials (the ML signal disappears after only several or tens of rapid mechanics cycles), this work breaks through the bottleneck issues on the self-recoverability, repeatability, and thermal stability, which significantly advances the ML field.

研究领域: 材料科学 · 光学工程 · 电子工程
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JOURNAL OF APPLIED POLYMER SCIENCE · 2025 · IF 2.8

UPy-Functionalized Conductive Polyurethane Elastomer With Notable Thermal Stability and Partial Mechanical Recovery Properties

Shuai Yuan,Jian Hu,Jin Yang

A series of UPy-functionalized conductive polyurethane elastomers (UCPUs) were synthesized by using p-phenylene diisocyanate (PPDI) and 2-ureido-4[1H]-pyrimidinone (UPy) as hard segments and extending the molecular chain by aniline trimer (AT). To improve the thermal stability and mechanical properties of UCPUs, aminopropyl terminated polydimethylsiloxane (PDMS) has also been introduced into soft segments. The correlation between microphase separation structure and thermal stability, mechanical properties, and self-healing performance was investigated using multiple characterization techniques such as DSC, DMA, XRD, SAXS, ATR-FTIR, POM, and so on. The addition of UPy constructed a dynamic cross-linked network and slightly reduced the heat resistance of UCPUs. The introduction of PDMS significantly improved the thermal stability and mechanical properties. The tensile strength, thermal stability, and self-healing efficiency of the UCPU-40% (U5) with the most balanced performance can reach 33.9 MPa, 303°C, and 21%, respectively. All UCPUs have excellent processability and recyclability, and their electrical conductivity can also be controlled by changing the doping amount of (1S)-(+)-10-camphorsulfonic acid (CSA). This developed UPy-functionalized conductive polyurethane with notable thermal stability and partial mechanical recovery properties may provide a new reference for preparing heat-resistant conductive polyurethane material.

研究领域: 材料科学 · 高分子化学 · 物理化学
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Nature Communications · 2022 ·Vol. 13 ·期 1 ·1-10 · IF 17.694

Ag9GaSe6: high-pressure-induced Ag migration causes thermoelectric performance irreproducibility and elimination of such instability

Liu Jing-Yuan,Chen Ling,Wu Li-Ming

The argyrodite Ag 9 GaSe 6 is a newly recognized high-efficiency thermoelectric material with an ultralow thermal conductivity; however, liquid-like Ag atoms are believed to cause poor stability and performance irreproducibility, which was evidenced even after the 1 st measurement run. Herein, we demonstrate the abovementioned instability and irreproducibility are caused by standard thermoelectric sample hot-pressing procedure, during which high pressure promotes the 3-fold-coordinated Ag atoms migrate to 4-fold-coordinated sites with higher-chemical potentials. Such instability can be eliminated by a simple annealing treatment, driving the metastable Ag atoms back to the original sites with lower-chemical potentials as revealed by the valence band X-ray photoelectron chemical potential spectra and single crystal X-ray diffraction data. Furthermore, the hot-pressed-annealed samples exhibit great stability and TE property repeatability. Such a stability and repeatability has never been reported before. This discovery will give liquid-like materials great application potential.

研究领域: 材料科学 · 热电学 · 固体物理学
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JOURNAL OF LUMINESCENCE · 2020 · IF 3.28

Reproducible mechanical-to-optical energy conversion in Mn (II) doped sphalerite ZnS

Ronghua Ma,Xiaoyan Wei,Chunfeng Wang,Shaohui Mao,Bing Chen,Yonghong Shao,Yu Fu,Keyu Yan,Dengfeng Peng

Mechanoluminescenece (ML) is a dynamic luminescence phenomenon of materials under various mechanical stimulation. Impurity doped ZnS shows high ML repeatability without any needs for extra excitation sources, thus making it very promising in applications like stress sensing and battery-free new light source . Lots of progress has been made in the last decades, however, the reproducible ML (RML) mechanism is still unclear to explain some basic phenomena like how the electron is excited to conduction band when undergoing mechanical actions or how the excitation energy is transferred to the dopants so efficiently. Based on comparative study of photoluminescence (PL) and ML in Mn 2+ doped ZnS prepared via melt-salt method, the RML energy routes in sphalerite ZnS: Mn 2+ is proposed herein, and further, a general mechanism is supposed which could apply to other RML systems. The excitation of RML is possibly generated by electron transfer during bond rebuilding in plastic deformation while the highly efficient energy transfer is realized through hole and electron capture by the dopant. According to this mechanism, we provide some prospects for further optimization of RML performance as well as discovery of new RML materials.

研究领域: 材料科学 · 光学
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JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY · 2012 ·Vol. 51 ·期 5 ·1205-1214 · IF 3.919

A facile method for the preparation of thermally remendable cross-linked polyphosphazenes

Xinjian Cheng,Cheng Peng,Daohong Zhang,Shuzheng Liu,Aiqing Zhang,Hui Huang,Jiansheng Lian

Novel cross-linked polyphosphazenes with remendable capacity have been synthesized through the Diels-Alder reactions. Their structure and properties were characterized by NMR, FT-IR, GPC, DSC, TGA SEM, and polarizing microscope. The process of Diels-Alder reaction (D-A reaction) and retro-Diels-Alder reaction (retro-D-A reaction) have been investigated by FT-IR, UV, and DSC. The cross-linked polyphosphazenes exhibited remendable capability only need a thermal treatment when they were cut by blade, any other treatments such as additional monomer or catalyst, surface treatment or pressure were not needed. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013

CAS / MDL: 617-89-0 940-71-6
研究领域: 材料科学 · 高分子化学
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SENSORS AND ACTUATORS B-CHEMICAL · 2015 · IF 4.097

A fluorescent bis-NBD derivative of calix[4]arene: Switchable response to Ag+ and HCHO in solution phase

Shaofei Zhang,Hui Yang,Ying Ma,Yu Fang

A bis-nitrobenzoxadiazole (NBD) derivative of calix[4]arene (L 1 ) and a control compound (L 2 ), mono-NBD derivative of the calixarene were designed and prepared via click chemistry. Fluorescence studies demonstrated that L 1 as created can function as a switch with the presence of Ag + in THF, of which the free state of L 1 emits at ∼527   nm, but the binding state at 576   nm. Based upon this discovery, L 1 was studied as a chemo-sensor of Ag + in a mixture solvent of THF and H 2 O with a detection limit (DL) of ∼6.2   ×   10 −7   mol/L. Presence of other commonly found metal ions shows little effect upon the determination. Moreover, the L 1 in the Ag + -L 1 complex could be fully released with introduction of HCHO, a bases for the sensitive and selective detection of the toxic chemical. The DL of this test is 6.6   ×   10 −7   mol/L. Interestingly, binding and releasing of the fluorescent ligand could be repeated for at least 5 times. Furthermore, both sensing could be performed in a visualized manner. It is believed that the fluorescent compound as created should have a potential to find real-life applications.

CAS / MDL: 98-54-4
研究领域: 化学 · 分析化学
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LWT-FOOD SCIENCE AND TECHNOLOGY · 2022 · IF 6.056

Mechanical, microstructural, and rheological characterization of gelatin-dialdehyde starch hydrogels constructed by dual dynamic crosslinking

Tianqi Cui,Yuxue Sun,Yue Wu,Jiarong Wang,Yangyue Ding,Jianjun Cheng,Mingruo Guo

Novel gelatin/dialdehyde starch (GDS) hydrogels based on gelatin were prepared using dialdehyde starch as a macromolecular crosslinking agent. Fourier transform infrared spectroscopy , Raman spectroscopy , and X-ray diffraction showed that the dynamic hydrogel network was formed by covalent imine bonds and hydrogen bonds between dialdehyde starch and gelatin. The synergistic physical and chemical cross-linking endowed the hydrogels with excellent mechanical properties (maximum compressive stress was 0.55 MPa), fatigue resistance (they maintained their shape after ten compression cycles), toughness (54.6 kN/m 2 ), and self-recoverability of the polymeric network. In the rheological tests, all the storage modulus were higher than loss modulus, indicating that they are elastic gels and not viscous sols. The polymer network of GDS hydrogels could recover rapidly when subjected to oscillating shear strain. In addition, with increasing dialdehyde starch concentration, the hydrogels had higher swelling stability and a denser microstructure. Given these excellent properties, the hydrogels have potential application prospects as cell culture scaffolds and carriers of bioactive substance.

CAS / MDL: 9000-70-8
研究领域: 材料科学 · 生物医学工程
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Advanced Science · 2022 ·Vol. 9 ·期 12 ·2105742 · IF 17.521

Tough, Instant, and Repeatable Adhesion of Self-Healable Elastomers to Diverse Soft and Hard Surfaces

Ke Li,Xingjie Zan,Chen Tang,Zhuangzhuang Liu,Jianghuan Fan,Gang Qin,Jia Yang,Wei Cui,Lin Zhu,Qiang Chen

Repeatability and high adhesion toughness are usually contradictory for common polymer adhesives. Repeatability requires temporary interactions between the adhesive and the substrate, while high adhesion toughness is usually achieved by permanent bonding. Integrating these two features into one adhesive system is still a daunting challenge. Here, the development of a series of viscoelastic elastomers composed of a soft and hard segment is reported, which exhibit tough, instant, yet repeatable adhesion to a variety of soft and hard surfaces. Such a combination of mutually exclusive properties is attributed to the synergy of high mobility of polymer chains and massive viscoelastic dissipation of the elastomers around the interface. By optimizing the relaxation time and mechanical dissipation, the resulting adhesives can achieve a tough yet repeatable adhesion toughness above 2000 J m −2 , superior to the best-in-class commercial adhesives. Numerous acrylate monomers are proven applicable to the preparation of such adhesives, validating the universality of the fabrication method. The application of these elastomers as adhesive and protective layers in soft electronics by virtue of their universal and tough adhesion to various soft and hard substrates is also demonstrated.

研究领域: 材料科学 · 化学工程 · 软电子学
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Nature Communications · 2023 ·Vol. 14 ·期 1 ·1-13 · IF 16.6

Protein fibers with self-recoverable mechanical properties via dynamic imine chemistry

Sun Jing,He Haonan,Zhao Kelu,Cheng Wenhao,Li Yuanxin,Zhang Peng,Wan Sikang,Liu Yawei,Wang Mengyao,Li Ming,Wei Zheng,Li Bo,Zhang Yi,Li Cong,Sun Yao,Shen Jianlei,Li Jingjing,Wang Fan,Ma Chao,Tian Yang,Su Juanjuan,Chen Dong,Fan Chunhai,Zhang Hongjie,Liu Kai

The manipulation of internal interactions at the molecular level within biological fibers is of particular importance but challenging, severely limiting their tunability in macroscopic performances and applications. It thus becomes imperative to explore new approaches to enhance biological fibers’ stability and environmental tolerance and to impart them with diverse functionalities, such as mechanical recoverability and stimulus-triggered responses. Herein, we develop a dynamic imine fiber chemistry (DIFC) approach to engineer molecular interactions to fabricate strong and tough protein fibers with recoverability and actuating behaviors. The resulting DIF fibers exhibit extraordinary mechanical performances, outperforming many recombinant silks and synthetic polymer fibers. Remarkably, impaired DIF fibers caused by fatigue or strong acid treatment are quickly recovered in water directed by the DIFC strategy. Reproducible mechanical performance is thus observed. The DIF fibers also exhibit exotic mechanical stability at extreme temperatures (e.g., −196 °C and 150 °C). When triggered by humidity, the DIFC endows the protein fibers with diverse actuation behaviors, such as self-folding, self-stretching, and self-contracting. Therefore, the established DIFC represents an alternative strategy to strengthen biological fibers and may pave the way for their high-tech applications.

CAS / MDL: 111-30-8
研究领域: 材料科学 · 生物技术 · 高分子科学 · 机械工程
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Polymers · 2024 ·Vol. 16 ·期 21 ·3045 · IF 4.7

Effects of Isocyanate Structure on the Properties of Polyurethane: Synthesis, Performance, and Self-Healing Characteristics

Hairui Wang,Lan Cao,Xiaolei Wang,Xiurui Lang,Wenwen Cong,Long Han,Hongyu Zhang,Huibin Zhou,Jujie Sun,Chengzhong Zong

Polyurethane (PU) plays a critical role in elastomers, adhesives, and self-healing materials. We selected the most commonly used aromatic isocyanates, 4,4′-methylene diphenyl diisocyanate (MDI) and tolylene-2,4-diisocyanate (TDI), and the most commonly used aliphatic isocyanates, hexamethylene diisocyanate (HDI), isophorone diisocyanate (IPDI), and dicyclohexylmethane-4,4′-diisocyanate (HMDI), as raw materials, combined with polytetramethylene ether glycol (PTMG) and 1,4-butanediol (BDO) to successfully synthesize five PU materials. The effects of isocyanate structure on polymerization rate, hydrogen bonding, thermal properties, phase separation, wettability, self-healing performance, adhesion, and mechanical properties were systematically investigated. The results show that isocyanates with higher symmetry facilitate hydrogen bonding, but excessive flexibility and crystallinity may inhibit its formation. MDI-based PU exhibits the highest hydrogen bonding index (HBI) of 4.10, along with the most distinct phase separation and the highest tensile strength of 23.4 MPa. HMDI-based PU demonstrates the best adhesion properties, with the highest lap shear strength of 7.9 MPa, and also exhibits excellent scratch healing ability. IPDI-based PU shows good self-healing performance, recovering 88.7% of its original tensile strength and 90.6% of its original lap shear strength after heating at 80 °C for 24 h. Furthermore, all the samples can be reprocessed by melt or solution methods, showing excellent recyclability.

CAS / MDL: 77-58-7 4098-71-9
研究领域: 材料科学 · 化学工程
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JOURNAL OF POLYMER RESEARCH · 2025 ·Vol. 32 ·期 4 ·1-14 · IF 2.8

Castor oil-segmented polyurethanes with disulfide bonds: excellent self-healing and mechanical properties

Xian Changqing,Deng Tao,Sun Bocun,Yang Wenbo,Li Boyan,Li Youbing,Xia Tian,Yang Chaolong,Yang Yi

Self-healing polyurethanes are garnering attention as a smart material, and has significant application potential in aerospace, biomedical, and electronics fields. In this paper, castor oil is selected as a soft segment in place of petroleum-based polyol to enhance the mechanical properties of polyurethane while improving the mobility of molecular chains. Meanwhile, a polyurethane with good self-healing properties was successfully prepared by selecting 2,2`-Diaminodiphenyl disulfide (DTDA) containing disulfide bonds as a chain extender. As the proportion of DTDA increases, the initial thermal decomposition temperature of polyurethane decreases by 21°C. Cutting and tensile tests confirmed the high mechanical properties and self-healing characteristics of the polyurethane network. And the self-healing efficiency of the polyurethane materials was improved by prolonging the healing time and increasing the healing temperature. As the content of disulfide bonds and hard segments increased, the tensile strength of polyurethane increases progressively, the elongation at break decreased, and the R(stress) and R(strain) of each specimen tended to increase and then decrease. The healing efficiency of the specimen with a disulfide bond content of 13.45% was optimal, with both R(stress) and R(strain) reaching more than 99%.

CAS / MDL: 77-58-7
研究领域: 材料科学 · 化学工程
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Advanced Materials Interfaces · 2018 ·Vol. 5 ·期 20 ·1800571 · IF 4.834

Direct Writing and Repairable Paper Flexible Electronics Using Nickel–Liquid Metal Ink

Hao Chang,Rui Guo,Ziqiao Sun,Hongzhang Wang,Yi Hou,Qian Wang,Wei Rao,Jing Liu

Liquid metals such as gallium and its alloys can be printed on various substrates to form electronic circuits. However, up to now there are still few methods for the direct writing of liquid metals on common printed paper. Here, a novel conductive material prepared by adding metal powder to a gallium alloy is introduced. The proposed material exhibits low liquidity, excellent plasticity, significantly enhanced adhesivity to paper substrates, which guarantee the stable and flexible electrical connection. The oxide film wrapping the nickel powder forms a skeleton for additional oxidation products, resulting in superior adhesion to paper. In addition, several paper flexible electronic applications are showcased to demonstrate the practical value and reparability of this material. This work paves the way for the design of a facile method of preparing paper electronics.

CAS / MDL: 7440-02-0
研究领域: 材料科学 · 柔性电子 · 电子工程
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