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Enhanced oxidation resistance of high-entropy diborides by multi-component synergistic effects 通过多组分协同效应增强高熵二硼化物的抗氧化性
IF 6.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-20 DOI: 10.1007/s40843-024-3045-4
Zhongyu Tang  (, ), Zihao Wen  (, ), Lei Zhuang  (, ), Hulei Yu  (, ), Yanhui Chu  (, )

Oxidation resistance is critical for high-entropy diborides (HEBs) to be used as thermal structural components under oxygen-containing high-temperature environments. Here, we successfully realize the exploitation of (Zr, Ta, Cr, W) B2 HEBs with superior oxidation resistance by comprehensively screening their compositions. To be specific, 21 kinds of HEB-xTM (x = 0–25 mol%, TM = Zr, Ta, Cr, and W) samples are fabricated via an ultrafast high-temperature sintering technique. The as-fabricated HEB-5Cr samples show the best oxidation resistance at 1673 K among all the samples. Subsquent oxidation investigations further confirm the as-fabricated HEB-5Cr samples possess superior oxidation resistance with the parabolic oxidation behavior across 1473–1773 K. Such superior oxidation resistance is believed to result from the multi-component synergistic effects. Particularly, the Ta5+ and W4+ cations with high ionic field strengths can promote the formation of 4B–O–4B linkages between [BO4] tetrahedrons by charge balance, which can stabilize the three-dimensional skeletal structure of B2O3 glass and consequently result in an improved viscosity of the B2O3 glassy layer. In addition, the ZrO2 and Cr2O3 with high melting points can dissolve into the B2O3 glass to increase its glass transition temperature, leading to an enhanced viscosity of the B2O3 glassy layer.

要在含氧高温环境下用作热结构组件,高熵二硼化物(HEBs)的抗氧化性至关重要。在此,我们通过全面筛选具有优异抗氧化性的(Zr、Ta、Cr、W)B2 HEB 的成分,成功实现了对其的开发利用。具体来说,我们通过超快高温烧结技术制备了 21 种 HEB-xTM (x = 0-25 mol%,TM = Zr、Ta、Cr 和 W)样品。在所有样品中,制备的 HEB-5Cr 样品在 1673 K 时的抗氧化性最好。随后的氧化研究进一步证实,经加工的 HEB-5Cr 样品具有优异的抗氧化性,在 1473-1773 K 之间的氧化行为呈抛物线状。特别是具有高离子场强的 Ta5+ 和 W4+ 阳离子可通过电荷平衡促进 [BO4] 四面体之间形成 4B-O-4B 连接,从而稳定 B2O3 玻璃的三维骨架结构,进而提高 B2O3 玻璃层的粘度。此外,熔点较高的 ZrO2 和 Cr2O3 可以溶解到 B2O3 玻璃中,提高其玻璃化转变温度,从而提高 B2O3 玻璃层的粘度。
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引用次数: 0
Elongated antiferromagnetic skyrmion in two-dimensional RuF4 二维 RuF4 中的拉长反铁磁天线
IF 6.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-20 DOI: 10.1007/s40843-024-3020-y
Mu Lan  (, ), Rong Wang  (, ), Shihao Wei  (, ), Lezhong Li  (, ), Wenning Ren  (, ), Xing Zhang  (, ), Xi Zhang  (, ), Gang Xiang  (, )

Two-dimensional (2D) antiferromagnetic (AFM) skyrmions are free from stray magnetic field and skyrmion Hall effect, and can be driven by a small current density up to a high speed, desirable for low-power spintronic applications. However, most 2D AFM skyrmions are realized in complex heterostructured materials, which impedes the dense integration of spintronic devices. Here, we propose that 2D AFM skyrmions can be achieved in ruthenium tetrafluoride (RuF4) monolayer using hybrid functional theory combined with atomistic spin dynamics simulations. Our study indicates that 2D RuF4 is dynamically stable and its nondegenerate vibration modes in optical branches are either Raman or infrared active. Furthermore, 2D RuF4 acts as an indirect bandgap semiconductor with an out-of-plane AFM state. Notably, the presence of a weak Dzyaloshinskii-Moriya interaction in 2D RuF4 leads to a spin spiral ground state at low temperatures, enabling the formation of AFM skyrmions with possible length modulation by an external magnetic field. Our results give insight into 2D RuF4 and may provide an intriguing platform for 2D AFM skyrmion-based spintronic applications.

二维(2D)反铁磁性(AFM)天线离子不受杂散磁场和天线霍尔效应的影响,可以通过较小的电流密度实现高速驱动,是低功耗自旋电子应用的理想之选。然而,大多数二维 AFM 天幕都是在复杂的异质结构材料中实现的,这阻碍了自旋电子器件的密集集成。在这里,我们利用混合函数理论结合原子自旋动力学模拟,提出了在四氟化钌(RuF4)单层中实现二维原子力显微镜天幕的方法。我们的研究表明,二维 RuF4 具有动态稳定性,其光学分支中的非enerate 振动模式具有拉曼或红外活性。此外,二维 RuF4 还是一种具有平面外 AFM 状态的间接带隙半导体。值得注意的是,二维 RuF4 中存在微弱的 Dzyaloshinskii-Moriya 相互作用,这导致了低温下的自旋螺旋基态,从而形成了可通过外部磁场进行长度调制的 AFM 天线。我们的研究结果使人们对二维 RuF4 有了深入的了解,并可能为基于二维 AFM 天线的自旋电子应用提供一个有趣的平台。
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引用次数: 0
A customized zeolitic imidazolate framework enabling bionic preconcentration of ultralow CO2 可实现超低二氧化碳仿生预浓缩的定制沸石咪唑酸盐框架
IF 6.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-20 DOI: 10.1007/s40843-024-3044-0
Hongyang Jin  (, ), Ziyang Wang  (, ), Guangli Yu  (, ), Junchao Dong  (, ), Shuai Zhao  (, ), Fengchao Cui  (, ), Hao Zhang  (, ), Guolong Lu  (, ), Xiaoqin Zou  (, ), Zhiyong Chang  (, )

Advancing our understanding of global climate, particularly in polar regions, requires accurate detection of carbon dioxide (CO2) in ice cores and deep sea environments. However, detecting trace levels of CO2 in these areas presents significant challenges. We introduce a novel preconcentration approach using functionalized zeolitic imidazolate framework, ZIF-8(CN), for the detection of ultra-low CO2. ZIF-8(CN) has small pores (4.4 Å) and cyano groups (–CN), enabling highly selective adsorption of CO2 (36.2 cm3 g−1) over N2 (1.6 cm3 g−1) at 298 K. The mechanism involves unique –CN⋯CO2⋯–CN interactions within the pore structure. When cast into a film on an aluminum substrate, ZIF-8(CN) demonstrates exceptional CO2 preconcentration capability (1 ppm in N2) with an extraordinary preconcentration factor of 748, outperforming traditional ZIF and zeolite materials. Additionally, a ZIF-8(CN) preconcentrator is designed and fabricated with bionic gas flow of fractal structure which optimizes the gas-film contact, and thus its performance is further improved by 115%.

要深入了解全球气候,尤其是极地地区的气候,就必须准确探测冰芯和深海环境中的二氧化碳(CO2)。然而,在这些地区检测痕量二氧化碳水平是一项重大挑战。我们介绍了一种利用功能化沸石咪唑啉框架 ZIF-8(CN)进行超低二氧化碳检测的新型预浓缩方法。ZIF-8(CN) 具有小孔(4.4 Å)和氰基(-CN),在 298 K 下可高度选择性地吸附 CO2(36.2 cm3 g-1)而不是 N2(1.6 cm3 g-1)。当在铝基底上铸成薄膜时,ZIF-8(CN) 显示出卓越的二氧化碳预浓缩能力(在 N2 中为 1 ppm),预浓缩系数高达 748,优于传统的 ZIF 和沸石材料。此外,ZIF-8(CN) 预浓缩器的设计和制造采用了分形结构的仿生气流,优化了气膜接触,因此其性能进一步提高了 115%。
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引用次数: 0
Reversible electrochromism in α-In2Se3 through ferroelectric switching induced phase transition 通过铁电转换诱导相变实现 α-In2Se3 中的可逆电致色性
IF 8.1 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-19 DOI: 10.1007/s40843-024-3060-1
Zhongshen Luo, Qingyuan Wang, Runcang Feng, Shun Wang, Zhou Zhou, Yiqi Hu, Qiankun Li, Qingyu Yan, Zhijian Feng, Yanfei Hou, Tianhao Ying, Yuyan Weng, Liang Fang, Lu You

Electrochromic materials change color or opacity when subjected to electrical stimuli, often through reversible chemical reactions or phase transitions. Their optical switch capabilities make them promising for applications like smart windows and glasses, thus garnering widespread attention in recent years. Van der Waals layered ferroelectric α-In2Se3, known for its rich polymorphs, is a promising candidate for exploring physical property modulation via phase transformations. However, the discovery of electrochromism in In2Se3 has been impeded by similar optical constants among its polymorphs. Herein, we report the experimental observation of reversible electrochromism in α-In2Se3 thin flakes accompanied by ferroelectric polarization switching. Microscopic structural characterizations reveal that the color change stems from a crystalline-to-amorphous phase transition. An improved Kramer-Kronig analysis was employed to quantify the change in optical constants of the flake. A disordered polarization switching model, inherent to the crystal symmetry of α-In2Se3, was proposed to explain the electrically driven amorphization. This work delivers distinct insight into the unique electrochromic behavior and unveils opportunities of relevant applications for the van der Waals layered ferroelectric.

电致变色材料在受到电刺激时会改变颜色或不透明度,通常是通过可逆的化学反应或相变实现的。电致变色材料的光学开关功能使其在智能窗户和眼镜等应用中大有可为,因此近年来受到广泛关注。范德华层铁电体 α-In2Se3 以其丰富的多晶体而闻名,是探索通过相变调制物理性质的理想候选材料。然而,In2Se3 多晶体之间相似的光学常数阻碍了电致变色的发现。在此,我们报告了在α-In2Se3薄片中伴随铁电极化转换的可逆电致色性实验观测结果。显微结构表征显示,颜色变化源于晶体到非晶体的相变。改进的克雷默-克罗尼格分析法被用来量化薄片光学常数的变化。研究人员提出了α-In2Se3 晶体对称性固有的无序偏振切换模型,以解释电驱动的非晶化现象。这一研究成果为独特的电致变色行为提供了独特的见解,并为范德华层状铁电体的相关应用提供了机会。
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引用次数: 0
Noncationic polymer-assisted carrier for nucleic acid drug delivery 用于核酸药物输送的非阳离子聚合物辅助载体
IF 8.1 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-15 DOI: 10.1007/s40843-024-3048-0
Miao Su, Junbin Chen, Yueqiang Zhu, Chaoran Chen, Yuxi Zhang, Xianzhu Yang

Nucleic acid drugs are emerging as a novel biotherapeutic modality for disease treatment, targeting nucleic acids to regulate the protein translation process and thereby facilitating disease management. They hold significant promise in biomedical applications and treatment avenues. Given their negative charge, high molecular weight, and hydrophilic properties, nucleic acid drugs require carriers to traverse multiple biological barriers and facilitate intracellular delivery. Cationic material-based carriers present an unprecedented opportunity to address these challenges through electrostatic interactions with nucleic acids. However, concerns regarding the biosafety and cytotoxic responses of cationic materials have emerged in early clinical studies. As a result, the use of non-cationic polymer carriers, by controlling or circumventing the use of cationic materials, represents a promising approach for nucleic acid delivery. In this review, we highlight various designs of non-cationic polymer carriers that go beyond the principle of electrostatic interactions, including conjugation, chemical bonding, physical crosslinking, hydrophobic interactions, and coordination bonding with nucleic acids. Additionally, we discuss strategies for enhancing the efficiency of nucleic acid delivery and therapeutic effects of non-cationic polymer carriers, focusing on targeted delivery, cellular internalization, and endosomal escape.

核酸药物正在成为治疗疾病的一种新型生物治疗方式,它以核酸为靶点,调节蛋白质的翻译过程,从而促进疾病的治疗。核酸药物在生物医学应用和治疗领域大有可为。鉴于核酸药物的负电荷、高分子量和亲水特性,它们需要载体来穿越多种生物屏障并促进细胞内输送。阳离子材料载体通过与核酸的静电相互作用,为应对这些挑战提供了前所未有的机会。然而,在早期临床研究中出现了对阳离子材料的生物安全性和细胞毒性反应的担忧。因此,通过控制或规避使用阳离子材料,使用非阳离子聚合物载体是一种很有前景的核酸递送方法。在本综述中,我们将重点介绍非阳离子聚合物载体的各种设计,这些设计超越了静电相互作用的原理,包括与核酸的共轭、化学键、物理交联、疏水相互作用和配位键。此外,我们还讨论了提高核酸递送效率和非阳离子聚合物载体治疗效果的策略,重点是靶向递送、细胞内化和内膜逸出。
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引用次数: 0
Ultrastrong multifunctional assembled 2D materials 超强多功能组装二维材料
IF 6.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-14 DOI: 10.1007/s40843-024-3085-x
Yury Gogotsi
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引用次数: 0
Switchable K–O bonds unveiling anomalous ferroelastic transitions in a polar hybrid crystal 可转换 K-O 键揭示极性杂化晶体中的反常铁弹性跃迁
IF 6.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-13 DOI: 10.1007/s40843-024-2918-8
Yao-Bin Li  (, ), Wei-Jian Xu  (, ), Xiao-Xian Chen  (, ), De-Xuan Liu  (, ), Zhi-Shuo Wang  (, ), Wei-Xiong Zhang  (, )

Hybrid ferroelastic crystals have garnered considerable interest due to their promising potential as mechanical switches and sensors. The anomalous ferroelastic phase transitions, in which ferroelasticity occurs in the high-temperature phase rather than the low-temperature phase, are of particular interest, but they are sporadically-documented and none of them is involved in breaking of the chemical bonds. Herein, a hydroxyl-containing cation, i.e., Me3NOH+, is employed to construct a three-dimensional hybrid crystal (Me3NOH)2KBiCl6 (1). This crystal undergoes distinct two-step structural phase transitions with space-group changes of Pna21P1121P63mc, belonging to an anomalous temperature-reversed mm2F2 ferroelastic transition and a normal 6mmF2 ferroelastic transition, respectively. The anomalous ferroelastic transition is entirely driven by switchable K–O coordination bonds involving breaking and reformation. Notably, the dynamic behavior of Me3NOH+ cations along with the distortion of inorganic framework enables the manifestation of unusual “high-low-medium” second-harmonic generation-switching behaviors. This study presents the enormous benefits of switchable coordination bonds for inducing anomalous ferroelastic phase transitions, offering valuable insight for the exploration of new multifunctional ferroelastic materials.

混合铁弹性晶体因其作为机械开关和传感器的巨大潜力而备受关注。其中,铁弹性发生在高温相而非低温相的反常铁弹性相变尤其引人关注,但这些相变只有零星的文献记载,而且都不涉及化学键的断裂。本文采用含羟基阳离子,即 Me3NOH+ 来构建三维杂化晶体 (Me3NOH)2KBiCl6 (1)。该晶体经历了明显的两步结构相变,空间群变化为 Pna21-P1121-P63mc,分别属于反常的温度反转 mm2F2 铁弹性转变和正常的 6mmF2 铁弹性转变。反常铁弹性转变完全由涉及断裂和重构的可切换 K-O 配位键驱动。值得注意的是,Me3NOH+ 阳离子的动态行为以及无机框架的畸变使得不寻常的 "高-低-中 "二次谐波发生切换行为得以体现。这项研究展示了可切换配位键在诱导反常铁弹性相变方面的巨大优势,为探索新型多功能铁弹性材料提供了宝贵的启示。
{"title":"Switchable K–O bonds unveiling anomalous ferroelastic transitions in a polar hybrid crystal","authors":"Yao-Bin Li \u0000 (,&nbsp;),&nbsp;Wei-Jian Xu \u0000 (,&nbsp;),&nbsp;Xiao-Xian Chen \u0000 (,&nbsp;),&nbsp;De-Xuan Liu \u0000 (,&nbsp;),&nbsp;Zhi-Shuo Wang \u0000 (,&nbsp;),&nbsp;Wei-Xiong Zhang \u0000 (,&nbsp;)","doi":"10.1007/s40843-024-2918-8","DOIUrl":"10.1007/s40843-024-2918-8","url":null,"abstract":"<div><p>Hybrid ferroelastic crystals have garnered considerable interest due to their promising potential as mechanical switches and sensors. The anomalous ferroelastic phase transitions, in which ferroelasticity occurs in the high-temperature phase rather than the low-temperature phase, are of particular interest, but they are sporadically-documented and none of them is involved in breaking of the chemical bonds. Herein, a hydroxyl-containing cation, <i>i.e.</i>, Me<sub>3</sub>NOH<sup>+</sup>, is employed to construct a three-dimensional hybrid crystal (Me<sub>3</sub>NOH)<sub>2</sub>KBiCl<sub>6</sub> (1). This crystal undergoes distinct two-step structural phase transitions with space-group changes of <i>Pna</i>2<sub>1</sub>–<i>P</i>112<sub>1</sub>–<i>P</i>6<sub>3</sub><i>mc</i>, belonging to an anomalous temperature-reversed <i>mm</i>2<i>F</i>2 ferroelastic transition and a normal 6<i>mmF</i>2 ferroelastic transition, respectively. The anomalous ferroelastic transition is entirely driven by switchable K–O coordination bonds involving breaking and reformation. Notably, the dynamic behavior of Me<sub>3</sub>NOH<sup>+</sup> cations along with the distortion of inorganic framework enables the manifestation of unusual “high-low-medium” second-harmonic generation-switching behaviors. This study presents the enormous benefits of switchable coordination bonds for inducing anomalous ferroelastic phase transitions, offering valuable insight for the exploration of new multifunctional ferroelastic materials.\u0000</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":773,"journal":{"name":"Science China Materials","volume":"67 10","pages":"3408 - 3414"},"PeriodicalIF":6.8,"publicationDate":"2024-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208957","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Photothermal phase change material microcapsules via cellulose nanocrystal and graphene oxide co-stabilized Pickering emulsion for solar and thermal energy storage 通过纤维素纳米晶和氧化石墨烯共稳定皮克林乳液实现光热相变材料微胶囊,用于太阳能和热能储存
IF 6.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-12 DOI: 10.1007/s40843-024-3040-5
Wang Sun  (, ), Zhe Zhang  (, ), Zhen Zhang  (, ), Nisha He  (, ), Qiang Wei  (, ), Liu Feng  (, ), Zhenghao Wang  (, ), Jie Wu  (, ), Can Liu  (, ), Shiyu Fu  (, ), Yelin Hou  (, ), Gilles Sèbe, Guofu Zhou  (, )

Phase change materials (PCMs) have attracted significant attention in thermal management due to their ability to store and release large amounts of heat during phase transitions. However, their widespread application is restricted by leakage issues. Encapsulating PCMs within polymeric microcapsules is a promising strategy to prevent leakage and increase heat transfer area with matrices. Moreover, photothermal PCM microcapsules are particularly desirable for solar energy storage. Herein, we fabricated photothermal PCM microcapsules with melamine-formaldehyde resin (MF) as shell using cellulose nanocrystal (CNC) and graphene oxide (GO) co-stabilized Pickering emulsion droplets as templates. CNC displays outstanding Pickering emulsifying ability and can facilitate the fixation of GO at the oil-water interface, resulting in a stable CNC/GO co-stabilized PCM Pickering emulsion. A polydopamine (PDA) layer was coated in-situ on the emulsion droplets via oxidization self-polymerization of dopamine. Meanwhile, GO was reduced to reduced GO (rGO) due to the reducing ability of PDA. The outmost MF shell of the PCM microcapsules was formed in-situ through the polymerization and crosslinking of MF prepolymer. The resulted PCM@CNC/rGO/PDA/MF microcapsules exhibit uniform sizes in the micrometer range, excellent leakage-proof performance, high phase change enthalpy (175.4 J g−1) and PCM encapsulation content (84.2%). Moreover, the presence of rGO and PDA endows PCM@CNC/rGO/PDA/MF microcapsules with outstanding photothermal conversion performance. The temperature of PCM@CNC/rGO/PDA/MF microcapsule slurries (15wt.%) can reach 73°C after light irradiation at 1 W cm−2. Therefore, photothermal PCM@CNC/rGO/PDA/MF microcapsules are promising for solar energy harvesting, thermal energy storage, and release in various applications, such as energy-efficient buildings and smart textiles.

相变材料(PCM)能够在相变过程中储存和释放大量热量,因此在热管理领域备受关注。然而,它们的广泛应用受到泄漏问题的限制。将 PCM 封装在聚合物微胶囊中是一种很有前景的策略,可以防止泄漏并增加与基质的热传导面积。此外,光热 PCM 微胶囊尤其适用于太阳能储存。在此,我们以三聚氰胺-甲醛树脂(MF)为外壳,以纤维素纳米晶(CNC)和氧化石墨烯(GO)共稳定的皮克林乳液液滴为模板,制作了光热 PCM 微胶囊。CNC 具有出色的皮克林乳化能力,可促进 GO 在油水界面的固定,从而形成稳定的 CNC/GO 共稳定 PCM 皮克林乳液。通过多巴胺的氧化自聚合作用,在乳液液滴上原位涂覆了聚多巴胺(PDA)层。同时,由于 PDA 的还原能力,GO 被还原成还原型 GO(rGO)。通过 MF 预聚物的聚合和交联,PCM 微胶囊的最外层 MF 壳在原位形成。所制备的 PCM@CNC/rGO/PDA/MF 微胶囊在微米范围内尺寸均匀,具有优异的防漏性能、高相变焓(175.4 J g-1)和 PCM 封装率(84.2%)。此外,rGO 和 PDA 的存在使 PCM@CNC/rGO/PDA/MF 微胶囊具有出色的光热转换性能。在 1 W cm-2 的光照射下,PCM@CNC/rGO/PDA/MF 微胶囊浆料(15 wt.%)的温度可达 73°C。因此,光热PCM@CNC/rGO/PDA/MF微胶囊在太阳能收集、热能储存和释放等方面具有广阔的应用前景,如节能建筑和智能纺织品。
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引用次数: 0
Chiral perturbation in D-O-A organic phosphors towards efficient circularly polarized electroluminescence D-O-A 有机荧光粉中的手性扰动,实现高效圆极化电致发光
IF 8.1 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-12 DOI: 10.1007/s40843-024-3042-1
Ying Yang, Shuai Xiao, Yan Zhou, Changsheng Shi, Lulin Xu, Xiangji Liao, Ning Su, Ning Sun, You-Xuan Zheng, Liming Ding, Junqiao Ding

Chiral organic phosphors with room-temperature phosphorescence (RTP) show a great potential in high-performance circularly polarized organic light-emitting diodes (CP-OLEDs). As a proof of concept, herein, we report a pair of chiral RTP enantiomers (S/R)-CP-RTP-D1 with acridine as the donor (D), triazine as the acceptor (A), oxygen as the bridge, and (S/R)-2-methylbutane as the chiral alkyl chain. It is found that the effective chiral perturbation can endow (S/R)-CP-RTP-D1 with mirror symmetric chiroptical properties, while maintaining the characteristic RTP emission. Consequently, the corresponding doped and non-doped CP-OLEDs based on (S/R)-CP-RTP-D1 achieve obvious circularly polarized electroluminescence (CPEL) signals, revealing promising external quantum efficiencies of 14.9% and 13.0% with the dissymmetry factors ∣gEL∣ of 7.00 × 10−4 and 9.87 × 10−4, respectively. These results highlight that chiral perturbation in D-O-A organic phosphors is a reliable strategy towards efficient CPEL.

具有室温磷光(RTP)的手性有机荧光粉在高性能圆偏振有机发光二极管(CP-OLED)中显示出巨大的潜力。作为概念验证,我们在本文中报告了一对手性 RTP 对映体 (S/R)-CP-RTP-D1,其中吖啶为供体(D),三嗪为受体(A),氧为桥,(S/R)-2-甲基丁烷为手性烷基链。研究发现,有效的手性扰动可以赋予 (S/R)-CP-RTP-D1 镜像对称的千光特性,同时保持 RTP 发射的特征。因此,基于(S/R)-CP-RTP-D1 的相应掺杂和非掺杂 CP-OLED 实现了明显的圆偏振电致发光(CPEL)信号,外部量子效率分别达到 14.9% 和 13.0%,不对称因子 ∣gEL∣ 分别为 7.00 × 10-4 和 9.87 × 10-4。这些结果表明,D-O-A 有机荧光粉中的手性扰动是实现高效 CPEL 的可靠策略。
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引用次数: 0
A highly linear stretchable MXene-based biocompatible hydrogel–elastomer hybrid with tissue-level softness 具有组织级柔软度的高线性可拉伸 MXene 生物相容性水凝胶-弹性体混合物
IF 6.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-08-09 DOI: 10.1007/s40843-024-2985-8
Shu Wan  (, ), Haizhou Huang  (, ), Zisheng He  (, ), Yizhou Ye  (, ), Shen Li  (, ), Shi Su  (, ), Jiaxin Shen  (, ), Longxiang Han  (, ), Peng Wan  (, ), Xu Ran  (, ), Li Chen  (, ), Xuefeng He  (, ), Litao Sun  (, ), Hengchang Bi  (, )

Maintaining low modulus while endowing the wide-range linear stretchability to wearable or implantable devices is crucial for these devices to reduce the mechanical mismatch between the devices and human skin/tissue interfaces. However, improving linear stretchability often results in an increased modulus of stretchable electronic materials, which hinders their conformability in long-term quantifiable monitoring of organs. Herein, we develop a hybrid structure involving interlocking low-modulus porous elastomers (Ecoflex-0030) and MXene-based hydrogels with crosslinking networks of polyvinyl alcohol, sodium alginate, and MXene. This hydrogel–elastomer structure exhibits superior performance compared with previous reports, with a wide linear stretchability strain range from 0 to 1000% and maintaining a low modulus of 6.4 kPa. Moreover, the hydrogel–elastomer hybrids can be utilized as highly sensitive strain sensors with remarkable characteristics, including high sensitivity (gauge factor ∼3.52), a linear correlation between the resistance and strain (0–200%), rapid response (0.18 s) and recovery times (0.21 s), and excellent electrical reproducibility (1000 loading–unloading cycles). Those electrical and mechanical properties allow the sensor to act as a suitable quantifiable equipment in organ monitoring, human activities detecting, and human–machine interactions.

在保持低模量的同时,赋予可穿戴或植入设备大范围的线性拉伸性,对于这些设备减少设备与人体皮肤/组织界面之间的机械不匹配至关重要。然而,提高线性拉伸性往往会导致可拉伸电子材料的模量增大,从而影响其在器官长期量化监测中的适配性。在此,我们开发了一种混合结构,其中包括互锁的低模量多孔弹性体(Ecoflex-0030)和基于 MXene 的水凝胶,以及聚乙烯醇、海藻酸钠和 MXene 的交联网络。与之前的报告相比,这种水凝胶-弹性体结构表现出更优越的性能,线性拉伸应变范围从 0% 到 1000%,并保持 6.4 kPa 的低模量。此外,水凝胶-弹性体混合物还可用作高灵敏度的应变传感器,具有显著的特性,包括高灵敏度(测量系数∼3.52)、电阻与应变之间的线性相关(0-200%)、快速响应(0.18 秒)和恢复时间(0.21 秒),以及出色的电气再现性(1000 次加载-卸载循环)。这些电气和机械特性使传感器成为器官监测、人体活动检测和人机交互的合适量化设备。
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引用次数: 0
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