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Ferroelectric catalytic BaTiO3-based composite insoles to promote healing of infected wounds: Analysis of antibacterial efficacy and angiogenesis 基于 BaTiO3 的铁电催化复合鞋垫可促进感染伤口的愈合:抗菌效果和血管生成分析
IF 24.5 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-06-18 DOI: 10.1002/idm2.12194
Qiong Liu, Xudan Liu, Linfeng Fan, Xinna Bai, Hao Pan, Hang Luo, Dou Zhang, Haitao Huang, Chris R. Bowen

Our feet are often subjected to moist and warm environments, which can promote the growth of harmful bacteria and the development of severe infection in wounds located in the foot. As a result, there is a need for new and innovative strategies to safely sterilize feet, when shoes are worn, to prevent any potential foot-related diseases. In this paper, we have produced a non-destructive, biocompatible and convenient-to-use insole by embedding a BaTiO3 (BT) ferroelectric material into a conventional polydimethylsilane (PDMS) insole material to exploit a ferroelectric catalytic effect to promote the antibacterial and healing of infected wounds via the ferroelectric charges generated during walking. The formation of reactive oxygen species generated through a ferroelectric catalytic effect in the PDMS-BT composite is shown to increase the oxidative stress on bacteria and decrease both the activity of bacteria and the rate of formation of bacterial biofilms. In addition, the ferroelectric field generated by the PDMS-BT insole can enhance the level of transforming growth factor-beta and CD31 by influencing the endogenous electric field of a wound, thereby promoting the proliferation, differentiation of fibroblasts and angiogenesis. This work therefore provides a new route for antimicrobial and tissue reconstruction by integrating a ferroelectric biomaterial into a shoe insole, with significant potential for health-related applications.

我们的双脚经常处于潮湿和温暖的环境中,这可能会促进有害细菌的生长,并导致足部伤口发生严重感染。因此,我们需要新的创新策略,在穿鞋时对足部进行安全消毒,以预防任何潜在的足部相关疾病。在本文中,我们将 BaTiO3(BT)铁电材料嵌入到传统的聚二甲基硅烷(PDMS)鞋垫材料中,利用铁电催化作用,通过行走时产生的铁电荷促进感染伤口的抗菌和愈合,从而制作出一种无损伤、生物相容性好且使用方便的鞋垫。通过铁电催化作用在 PDMS-BT 复合材料中产生的活性氧的形成,可以增加细菌的氧化应激,降低细菌的活性和细菌生物膜的形成速度。此外,PDMS-BT 鞋垫产生的铁电场可通过影响伤口的内生电场来提高转化生长因子-β 和 CD31 的水平,从而促进成纤维细胞的增殖、分化和血管生成。因此,这项研究通过将铁电生物材料集成到鞋垫中,为抗菌和组织重建提供了一条新途径,在健康相关应用领域具有巨大潜力。
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引用次数: 0
Self-adhesive and biocompatible dry electrodes with conformal contact to skin for epidermal electrophysiology 用于表皮电生理学的自粘性和生物相容性干电极,可与皮肤保形接触
IF 24.5 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-06-16 DOI: 10.1002/idm2.12198
Xiaoxue Lin, Zeping Ou, Xuewei Wang, Can Wang, Yunfei Ouyang, Ibrahim M. Mwakitawa, Feng Li, Rui Chen, Yaru Yue, Jihe Tang, Wei Fang, Shanshan Chen, Bing Guo, Jianyong Ouyang, Tatyana Shumilova, Yongli Zhou, Liang Wang, Chengwu Zhang, Kuan Sun

Long-term biopotential monitoring requires high-performance biocompatible wearable dry electrodes. But currently, it is challenging to establish a form-preserving fit with the skin, resulting in high interface impedance and motion artifacts. This research aims to present an innovative solution using an all-green organic dry electrode that eliminates the aforementioned challenges. The dry electrode is prepared by introducing biocompatible maltitol into the chosen conductive polymer, poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate). Thanks to the secondary doping and plasticizer effect of maltitol, the dry electrode exhibits good stretchability (62%), strong self-adhesion (0.46 N/cm), high conductivity (102 S/cm), and low Young's modulus (7 MPa). It can always form a conformal contact with the skin even during body movements. Together with good electrical properties, the electrode enables a lower skin contact impedance compared to the current standard Ag/AgCl gel electrode. Consequently, the application of this dry electrode in bioelectrical signal measurement (electromyography, electrocardiography, electroencephalography) and long-term biopotential monitoring was successfully demonstrated.

长期生物电位监测需要高性能、生物兼容的可穿戴干电极。但目前,建立与皮肤的外形贴合是一项挑战,会导致高界面阻抗和运动伪影。本研究旨在利用一种全绿色有机干电极提出一种创新解决方案,以消除上述挑战。干电极的制备方法是在所选导电聚合物聚(3,4-亚乙二氧基噻吩):聚(苯乙烯磺酸)中引入生物相容性麦芽糖醇。由于麦芽糖醇的二次掺杂和增塑作用,干电极具有良好的拉伸性(62%)、较强的自粘性(0.46 N/cm)、高导电率(102 S/cm)和较低的杨氏模量(7 MPa)。即使在身体运动时,它也能始终与皮肤形成贴合接触。与目前的标准银/氯化银凝胶电极相比,该电极具有良好的电气性能,可实现较低的皮肤接触阻抗。因此,这种干电极在生物电信号测量(肌电图、心电图、脑电图)和长期生物电位监测中的应用得到了成功验证。
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引用次数: 0
Three-dimensional bioprinting biphasic multicellular living scaffold facilitates osteochondral defect regeneration 三维生物打印双相多细胞活支架促进骨软骨缺损再生
IF 24.5 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-06-02 DOI: 10.1002/idm2.12181
Xingge Yu, Mazaher Gholipourmalekabadi, Xudong Wang, Changyong Yuan, Kaili Lin

Due to tissue lineage variances and the anisotropic physiological characteristics, regenerating complex osteochondral tissues (cartilage and subchondral bone) remains a great challenge, which is primarily due to the distinct requirements for cartilage and subchondral bone regeneration. For cartilage regeneration, a significant amount of newly generated chondrocytes is required while maintaining their phenotype. Conversely, bone regeneration necessitates inducing stem cells to differentiate into osteoblasts. Additionally, the construction of the osteochondral interface is crucial. In this study, we fabricated a biphasic multicellular bioprinted scaffold mimicking natural osteochondral tissue employing three-dimensional (3D) bioprinting technology. Briefly, gelatin-methacryloyl (GelMA) loaded with articular chondrocytes and bone marrow mesenchymal stem cells (ACs/BMSCs), serving as the cartilage layer, preserved the phenotype of ACs and promoted the differentiation of BMSCs into chondrocytes through the interaction between ACs and BMSCs, thereby facilitating cartilage regeneration. GelMA/strontium-substituted xonotlite (Sr-CSH) loaded with BMSCs, serving as the subchondral bone layer, regulated the differentiation of BMSCs into osteoblasts and enhanced the secretion of cartilage matrix by ACs in the cartilage layer through the slow release of bioactive ions from Sr-CSH. Additionally, GelMA, serving as the matrix material, contributed to the reconstruction of the osteochondral interface. Ultimately, this biphasic multicellular bioprinted scaffold demonstrated satisfactory simultaneous regeneration of osteochondral defects. In this study, a promising strategy for the application of 3D bioprinting technology in complex tissue regeneration was proposed.

由于组织血统的差异和各向异性的生理特点,再生复杂的骨软骨组织(软骨和软骨下骨)仍然是一个巨大的挑战,这主要是由于软骨和软骨下骨再生的要求不同。软骨再生需要大量新生成的软骨细胞,同时保持其表型。相反,骨再生需要诱导干细胞分化成成骨细胞。此外,骨软骨界面的构建也至关重要。在这项研究中,我们利用三维(3D)生物打印技术制作了一种模仿天然骨软骨组织的双相多细胞生物打印支架。简而言之,装载了关节软骨细胞和骨髓间充质干细胞(ACs/BMSCs)的明胶-甲基丙烯酰(GelMA)作为软骨层,保留了ACs的表型,并通过ACs和BMSCs之间的相互作用促进BMSCs分化为软骨细胞,从而促进软骨再生。载入 BMSCs 的 GelMA/锶替代氙石(Sr-CSH)作为软骨下骨层,通过 Sr-CSH 中生物活性离子的缓慢释放,调节 BMSCs 向成骨细胞的分化,并增强软骨层中 ACs 对软骨基质的分泌。此外,作为基质材料的 GelMA 也有助于骨软骨界面的重建。最终,这种双相多细胞生物打印支架实现了令人满意的骨软骨缺损同步再生。这项研究为三维生物打印技术在复杂组织再生中的应用提出了一种前景广阔的策略。
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引用次数: 0
Exploring the mathematic equations behind the materials science data using interpretable symbolic regression 利用可解释的符号回归探索材料科学数据背后的数学方程式
IF 24.5 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-05-29 DOI: 10.1002/idm2.12180
Guanjie Wang, Erpeng Wang, Zefeng Li, Jian Zhou, Zhimei Sun

Symbolic regression (SR), exploring mathematical expressions from a given data set to construct an interpretable model, emerges as a powerful computational technique with the potential to transform the “black box” machining learning methods into physical and chemistry interpretable expressions in material science research. In this review, the current advancements in SR are investigated, focusing on the underlying theories, fundamental flowcharts, various techniques, implemented codes, and application fields. More predominantly, the challenging issues and future opportunities in SR that should be overcome to unlock the full potential of SR in material design and research, including graphics processing unit acceleration and transfer learning algorithms, the trade-off between expression accuracy and complexity, physical or chemistry interpretable SR with generative large language models, and multimodal SR methods, are discussed.

符号回归(SR)是从给定数据集中探索数学表达式以构建可解释模型的方法,它是一种强大的计算技术,具有将 "黑箱 "加工学习方法转化为材料科学研究中物理和化学可解释表达式的潜力。在这篇综述中,我们将重点研究 SR 的基础理论、基本流程图、各种技术、实施代码和应用领域,并对 SR 的当前进展进行研究。更主要的是,讨论了 SR 中应克服的挑战性问题和未来机遇,以释放 SR 在材料设计和研究中的全部潜力,包括图形处理单元加速和迁移学习算法、表达准确性和复杂性之间的权衡、使用生成式大型语言模型的物理或化学可解释 SR 以及多模态 SR 方法。
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引用次数: 0
Recent progress in heterostructured materials for room-temperature sodium-sulfur batteries 室温钠硫电池用异质结构材料的最新进展
IF 24.5 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-05-28 DOI: 10.1002/idm2.12177
Haobin Song, Yifan Li, Xue L. Li, Yixiang Li, Dong-sheng Li, Deli Wang, Shaozhuan Huang, Hui Ying Yang

Room-temperature sodium-sulfur (RT Na-S) batteries are a promising next-generation energy storage device due to their low cost, high energy density (1274 Wh kg−1), and environmental friendliness. However, RT Na-S batteries face a series of vital challenges from sulfur cathode and sodium anode: (i) sluggish reaction kinetics of S and Na2S/Na2S2; (ii) severe shuttle effect from the dissolved intermediate sodium polysulfides (NaPSs); (iii) huge volume expansion induced by the change from S to Na2S; (iv) continuous growth of sodium metal dendrites, leading to short-circuiting of the battery; (v) huge volume expansion/contraction of sodium anode upon sodium plating/stripping, causing uncontrollable solid-state electrolyte interphase growth and “dead sodium” formation. Various strategies have been proposed to address these issues, including physical/chemical adsorption of NaPSs, catalysts to facilitate the rapid conversion of NaPSs, high-conductive materials to promote ion/electron transfer, good sodiophilic Na anode hetero-interface homogenized Na ions flux and three-dimensional porous anode host to buffer the volume expansion of sodium. Heterostructure materials can combine these merits into one material to realize multifunctionality. Herein, the recent development of heterostructure as the host for sulfur cathode and Na anode has been reviewed. First of all, the electrochemical mechanisms of sulfur cathode/sodium anode and principles of heterostructures reinforced Na-S batteries are described. Then, the application of heterostructures in Na-S batteries is comprehensively examined. Finally, the current primary avenues of employing heterostructures in Na-S batteries are summarized. Opinions and prospects are put forward regarding the existing problems in current research, aiming to inspire the design of advanced and improved next-generation Na-S batteries.

室温钠硫(RT Na-S)电池因其低成本、高能量密度(1274 Wh kg-1)和环境友好性而成为一种前景广阔的下一代储能设备。然而,RT Na-S 电池面临着硫阴极和钠阳极带来的一系列重大挑战:(i) S 和 Na2S/Na2S2 的反应动力学缓慢;(ii) 溶解的中间体多硫化钠(NaPSs)产生严重的穿梭效应;(iii) 从 S 到 Na2S 的变化引起巨大的体积膨胀;(iv) 钠金属枝晶的持续增长,导致电池短路; (v) 钠阳极在钠电镀/剥离时的巨大体积膨胀/收缩,导致固态电解质相间生长和 "死钠 "的形成无法控制。为解决这些问题,人们提出了各种策略,包括 NaPSs 的物理/化学吸附、促进 NaPSs 快速转化的催化剂、促进离子/电子转移的高导电性材料、良好的钠阳极异质界面均化 Na 离子通量以及缓冲钠体积膨胀的三维多孔阳极主机。异质结构材料可以将这些优点集于一身,实现材料的多功能性。本文综述了以异质结构为宿主的硫阴极和钠阳极的最新发展。首先,介绍了硫阴极/钠阳极的电化学机理和异质结构增强 Na-S 电池的原理。然后,全面考察了异质结构在 Na-S 电池中的应用。最后,总结了目前在 Na-S 电池中采用异质结构的主要途径。针对目前研究中存在的问题提出了看法和展望,旨在启发设计先进和改进的下一代 Na-S 电池。
{"title":"Recent progress in heterostructured materials for room-temperature sodium-sulfur batteries","authors":"Haobin Song,&nbsp;Yifan Li,&nbsp;Xue L. Li,&nbsp;Yixiang Li,&nbsp;Dong-sheng Li,&nbsp;Deli Wang,&nbsp;Shaozhuan Huang,&nbsp;Hui Ying Yang","doi":"10.1002/idm2.12177","DOIUrl":"https://doi.org/10.1002/idm2.12177","url":null,"abstract":"<p>Room-temperature sodium-sulfur (RT Na-S) batteries are a promising next-generation energy storage device due to their low cost, high energy density (1274 Wh kg<sup>−1</sup>), and environmental friendliness. However, RT Na-S batteries face a series of vital challenges from sulfur cathode and sodium anode: (i) sluggish reaction kinetics of S and Na<sub>2</sub>S/Na<sub>2</sub>S<sub>2</sub>; (ii) severe shuttle effect from the dissolved intermediate sodium polysulfides (NaPSs); (iii) huge volume expansion induced by the change from S to Na<sub>2</sub>S; (iv) continuous growth of sodium metal dendrites, leading to short-circuiting of the battery; (v) huge volume expansion/contraction of sodium anode upon sodium plating/stripping, causing uncontrollable solid-state electrolyte interphase growth and “dead sodium” formation. Various strategies have been proposed to address these issues, including physical/chemical adsorption of NaPSs, catalysts to facilitate the rapid conversion of NaPSs, high-conductive materials to promote ion/electron transfer, good sodiophilic Na anode hetero-interface homogenized Na ions flux and three-dimensional porous anode host to buffer the volume expansion of sodium. Heterostructure materials can combine these merits into one material to realize multifunctionality. Herein, the recent development of heterostructure as the host for sulfur cathode and Na anode has been reviewed. First of all, the electrochemical mechanisms of sulfur cathode/sodium anode and principles of heterostructures reinforced Na-S batteries are described. Then, the application of heterostructures in Na-S batteries is comprehensively examined. Finally, the current primary avenues of employing heterostructures in Na-S batteries are summarized. Opinions and prospects are put forward regarding the existing problems in current research, aiming to inspire the design of advanced and improved next-generation Na-S batteries.</p>","PeriodicalId":100685,"journal":{"name":"Interdisciplinary Materials","volume":"3 4","pages":"565-594"},"PeriodicalIF":24.5,"publicationDate":"2024-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/idm2.12177","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141730368","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synergistic adsorption and catalytic effects of Ti3C2Tx/CoO/MoO3 composite on lithium polysulfides for high-performance lithium–sulfur batteries 用于高性能锂硫电池的 Ti3C2Tx/CoO/MoO3 复合材料对多硫化锂的协同吸附和催化效应
IF 24.5 Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-05-27 DOI: 10.1002/idm2.12178
Bin Fan, Weikun Chen, Kaining Li, Qingya Wei, Qian He, Wei Liu, Bigui Zhou, Jun Yuan, Yingping Zou

The shuttle effect of lithium polysulfides (LiPSs) and their sluggish kinetic processes lead to rapid capacity fading and poor cycling stability in lithium–sulfur (Li–S) batteries, limiting their commercial viability. This study proposes a functionalized separator with adsorption and synergistic catalysis ability for Li–S batteries. The modified separator comprises Ti3C2Tx sheets, CoO, and MoO3. Experimental and theoretical calculations demonstrate that Ti3C2Tx/CoO/MoO3 composite not only effectively inhibits the shuttle effect of LiPSs, ensuring efficient utilization of active materials, but also enhances reversibility and reaction kinetics among LiPSs. The full exposure of active sites in the Ti3C2Tx/CoO/MoO3 composite and the synergistic action of different catalysts enable efficient capture and conversion of LiPSs molecules at the material surface. Besides, the lithium–sulfur batteries with Ti3C2Tx/CoO/MoO3@PP separator exhibited only a 0.042% capacity decay per cycle at 0.5 C (800 cycles). Moreover, a high areal capacity of 6.85 mAh cm−2 was achieved at high sulfur loading (7.9 mg cm−2) and low electrolyte-to-sulfur ratio (10 μL mg−1).

锂多硫化物(LiPSs)的穿梭效应及其缓慢的动力学过程导致锂硫(Li-S)电池的容量快速衰减和循环稳定性差,从而限制了其商业可行性。本研究为锂硫电池提出了一种具有吸附和协同催化能力的功能化隔膜。这种改性隔膜由 Ti3C2Tx 片、CoO 和 MoO3 组成。实验和理论计算证明,Ti3C2Tx/CoO/MoO3 复合材料不仅能有效抑制锂离子电池的穿梭效应,确保活性材料的高效利用,还能增强锂离子电池之间的可逆性和反应动力学。Ti3C2Tx/CoO/MoO3 复合材料中活性位点的充分暴露和不同催化剂的协同作用使材料表面能有效捕获和转化锂多糖分子。此外,采用 Ti3C2Tx/CoO/MoO3@PP 隔膜的锂硫电池在 0.5 摄氏度(800 次循环)的条件下,每次循环的容量衰减仅为 0.042%。此外,在高硫负荷(7.9 毫克厘米-2)和低电解质硫比(10 μL 毫克-1)条件下,实现了 6.85 毫安时厘米-2 的高单位容量。
{"title":"Synergistic adsorption and catalytic effects of Ti3C2Tx/CoO/MoO3 composite on lithium polysulfides for high-performance lithium–sulfur batteries","authors":"Bin Fan,&nbsp;Weikun Chen,&nbsp;Kaining Li,&nbsp;Qingya Wei,&nbsp;Qian He,&nbsp;Wei Liu,&nbsp;Bigui Zhou,&nbsp;Jun Yuan,&nbsp;Yingping Zou","doi":"10.1002/idm2.12178","DOIUrl":"https://doi.org/10.1002/idm2.12178","url":null,"abstract":"<p>The shuttle effect of lithium polysulfides (LiPSs) and their sluggish kinetic processes lead to rapid capacity fading and poor cycling stability in lithium–sulfur (Li–S) batteries, limiting their commercial viability. This study proposes a functionalized separator with adsorption and synergistic catalysis ability for Li–S batteries. The modified separator comprises Ti<sub>3</sub>C<sub>2</sub>T<i><sub>x</sub></i> sheets, CoO, and MoO<sub>3</sub>. Experimental and theoretical calculations demonstrate that Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub>/CoO/MoO<sub>3</sub> composite not only effectively inhibits the shuttle effect of LiPSs, ensuring efficient utilization of active materials, but also enhances reversibility and reaction kinetics among LiPSs. The full exposure of active sites in the Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub>/CoO/MoO<sub>3</sub> composite and the synergistic action of different catalysts enable efficient capture and conversion of LiPSs molecules at the material surface. Besides, the lithium–sulfur batteries with Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub>/CoO/MoO<sub>3</sub>@PP separator exhibited only a 0.042% capacity decay per cycle at 0.5 C (800 cycles). Moreover, a high areal capacity of 6.85 mAh cm<sup>−2</sup> was achieved at high sulfur loading (7.9 mg cm<sup>−2</sup>) and low electrolyte-to-sulfur ratio (10 μL mg<sup>−1</sup>).</p>","PeriodicalId":100685,"journal":{"name":"Interdisciplinary Materials","volume":"3 5","pages":"726-737"},"PeriodicalIF":24.5,"publicationDate":"2024-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/idm2.12178","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142170310","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Outside Back Cover: Volume 3 Issue 3 封底外页第 3 卷 第 3 期
Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-05-26 DOI: 10.1002/idm2.12197

Outside Back Cover: Surface defects have been considerable issues for the perovskite quantum dots light-emitting diodes (PeQLEDs). In the work of doi:10.1002/idm2.12164, Tong et al. report an in-situ surface passivation to PeQDs by introducing the metal cations competitive lattice occupancy assisted with acid-etching, achieving an external quantum efficiency of 8.42% for pure blue PeQLEDs.

封底外侧:表面缺陷一直是包晶量子点发光二极管(PeQLEDs)面临的重要问题。在 doi:10.1002/idm2.12164 号论文中,Tong 等人报告了通过引入金属阳离子竞争性晶格占位并辅助酸蚀,对 PeQDs 进行原位表面钝化的方法,使纯蓝色 PeQLED 的外部量子效率达到 8.42%。
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引用次数: 0
Outside Front Cover: Volume 3 Issue 3 封面外页:第 3 卷第 3 期
Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-05-26 DOI: 10.1002/idm2.12179

Outside Front Cover: In the study documented in doi:10.1002/idm2.12160, a pioneering S-type UiO-66-NH2/ZnS(en)0.5 heterostructure photocatalyst is engineered to enhance charge separation and oxygen activation. As depicted in the image, when subjected to solar light, the catalyst efficiently transforms gaseous NO pollutants into nitrates via a superoxidemediated pathway. This advancement represents a significant stride towards rejuvenating environmental well-being, instilling optimism for a more pristine and sustainable earth for all.

封面外页:doi:10.1002/idm2.12160》中记载的研究中,设计了一种开创性的 S 型 UiO-66-NH2/ZnS(en)0.5 异质结构光催化剂,以增强电荷分离和氧活化。如图所示,在太阳光的照射下,催化剂通过超氧化途径将气态氮氧化物污染物有效地转化为硝酸盐。这一进步标志着在恢复环境健康方面迈出了重要一步,为所有人创造一个更加纯净和可持续发展的地球注入了乐观精神。
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引用次数: 0
Inside Front Cover: Volume 3 Issue 3 封面内页:第 3 卷第 3 期
Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-05-26 DOI: 10.1002/idm2.12195

Inside Front Cover: The cover image depicts a close-up view of a wrinkle morphology 3D substrate-based conducting polymer hydrogel elastomer. This novel design, detailed in the article with doi:10.1002/idm2.12161, addresses the limitations of traditional conducting polymer hydrogels, particularly their brittleness and viscoelasticity. By utilizing digital light processing (DLP) technology and in-situ polymerization, an interconnection network hydrogel is formed, resulting in a material with reduced viscoelasticity, quick response time, low hysteresis, and stable cyclic performance. The wrinkle morphology effectively enhances the elastomer's flexibility and geometric freedom, while the 3D gradient structure boosts its sensitivity, positioning this material as a promising candidate for flexible sensor applications.

封面内页:封面图片描绘了基于三维基底的导电聚合物水凝胶弹性体的皱纹形态特写。这种新颖的设计(doi:10.1002/idm2.12161)解决了传统导电聚合物水凝胶的局限性,尤其是其脆性和粘弹性。通过利用数字光处理(DLP)技术和原位聚合,形成了一种互连网络水凝胶,从而使材料具有更低的粘弹性、更快的响应时间、更低的滞后性和更稳定的循环性能。皱纹形态有效增强了弹性体的柔韧性和几何自由度,而三维梯度结构则提高了其灵敏度,使这种材料成为柔性传感器应用的理想候选材料。
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引用次数: 0
Inside Back Cover: Volume 3 Issue 3 封底内页第 3 卷 第 3 期
Q1 CHEMISTRY, PHYSICAL Pub Date : 2024-05-26 DOI: 10.1002/idm2.12196

Inside Back Cover: In the review of doi:10.1002/idm2.12162, twisted van der Waals layered materials form regular moiré superlattice patterns at their interfaces. The interfacial physical and mechanical behavior is significantly influenced by the in-plane and out-of-plane deformation fields dependent on moiré superlattices.

封底内页:在 doi:10.1002/idm2.12162 的综述中,扭曲的范德华层材料在其界面上形成规则的摩尔纹超格图案。界面的物理和机械行为受到取决于摩尔超晶格的面内和面外变形场的显著影响。
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引用次数: 0
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