首页 > 最新文献

Advanced Materials Technologies最新文献

英文 中文
Advanced Design and 3D Printing Strategies With Alginate-Nanoclay Nanocomposites: From Microstructure to Bioprinting
IF 6.4 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-14 DOI: 10.1002/admt.202401167
Weijian Hua, Cheng Zhang, Kellen Mitchell, Lily Raymond, Dale K. Hensley, Ryan Coulter, Erick Bandala, Jihua Chen, Changwoo Do, Danyang Zhao, Yifei Jin

Nanocomposites made from alginate and nanoclay are extensively applied for diverse biomedical applications. However, the lack of a clear understanding of the interactions between alginate and nanoclay makes it difficult to rationally design the nanocomposites for different material extrusion-based 3D bioprinting strategies. Here, a combined analytical model is proposed to accurately predict the interaction mechanisms between alginate and nanoclay through small-angle neutron scattering. These mechanisms are summarized into a phase diagram that can guide the design of alginate-nanoclay nanocomposites for different bioprinting applications. The rheological properties of various nanocomposites are measured to validate the proposed interaction mechanisms at the macroscale. Accordingly, three representative extrusion-based bioprinting strategies are linked with the nanocomposite design and applied to freeform fabricate complex structures. A roadmap is summarized to bridge the gap between biomaterial design and bioprinting processes, enabling the rapid and rational selection of biomaterial formula based on available 3D printing methods, and vice versa.

由海藻酸盐和纳米粘土制成的纳米复合材料被广泛应用于各种生物医学领域。然而,由于缺乏对海藻酸盐和纳米粘土之间相互作用的清晰认识,很难针对不同的材料挤压三维生物打印策略合理设计纳米复合材料。本文提出了一种组合分析模型,通过小角中子散射准确预测海藻酸盐和纳米粘土之间的相互作用机制。这些机制被归纳为一个相图,可指导设计用于不同生物打印应用的海藻酸盐-纳米粘土纳米复合材料。测量了各种纳米复合材料的流变特性,以验证所提出的宏观相互作用机制。因此,将三种具有代表性的基于挤压的生物打印策略与纳米复合材料设计联系起来,并应用于复杂结构的自由成型制造。总结出的路线图弥合了生物材料设计与生物打印工艺之间的差距,使人们能够根据现有的三维打印方法快速合理地选择生物材料配方,反之亦然。
{"title":"Advanced Design and 3D Printing Strategies With Alginate-Nanoclay Nanocomposites: From Microstructure to Bioprinting","authors":"Weijian Hua,&nbsp;Cheng Zhang,&nbsp;Kellen Mitchell,&nbsp;Lily Raymond,&nbsp;Dale K. Hensley,&nbsp;Ryan Coulter,&nbsp;Erick Bandala,&nbsp;Jihua Chen,&nbsp;Changwoo Do,&nbsp;Danyang Zhao,&nbsp;Yifei Jin","doi":"10.1002/admt.202401167","DOIUrl":"https://doi.org/10.1002/admt.202401167","url":null,"abstract":"<p>Nanocomposites made from alginate and nanoclay are extensively applied for diverse biomedical applications. However, the lack of a clear understanding of the interactions between alginate and nanoclay makes it difficult to rationally design the nanocomposites for different material extrusion-based 3D bioprinting strategies. Here, a combined analytical model is proposed to accurately predict the interaction mechanisms between alginate and nanoclay through small-angle neutron scattering. These mechanisms are summarized into a phase diagram that can guide the design of alginate-nanoclay nanocomposites for different bioprinting applications. The rheological properties of various nanocomposites are measured to validate the proposed interaction mechanisms at the macroscale. Accordingly, three representative extrusion-based bioprinting strategies are linked with the nanocomposite design and applied to freeform fabricate complex structures. A roadmap is summarized to bridge the gap between biomaterial design and bioprinting processes, enabling the rapid and rational selection of biomaterial formula based on available 3D printing methods, and vice versa.</p>","PeriodicalId":7292,"journal":{"name":"Advanced Materials Technologies","volume":"10 5","pages":""},"PeriodicalIF":6.4,"publicationDate":"2024-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143535855","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Efficient Large Area Semi-Transparent Dye-Sensitized Solar Cells (DSSCs) Printed with DMD400 Technology 用DMD400技术印刷的高效大面积半透明染料敏化太阳能电池(DSSCs)
IF 6.4 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-12 DOI: 10.1002/admt.202400637
Mahfoudh Raïssi, Himal Muwanwella, Falak Naz, Anaïs Bianchi, Didier Rousseau, Muhammad Tariq Sajjad

This work presents the development of fully printed, large-area, semi-transparent Dye-Sensitized Solar Cells (DSSCs) using TiO2 nanoparticles treated with TiCl4, a “D35” push-pull dye sensitizer, and I3/I redox mediator. Cells with areas of 4 and 200 cm2 were printed using hexagonal, stripe, and standard designs, employing digital materials deposition (DMD) technology. The porous films printed via DMD, confirmed by scanning electron microscopy (SEM), improved solar cells performance by enhancing the Open Circuit Voltage (Voc) and fill factor (FF). The hexagonal design, in particular, facilitated better electrolyte impregnation in the TiO2 mesoporous structure, boosting current density. This design yielded a power conversion efficiency (PCE) of 7.05% for 4 cm2 DSSCs, surpassing the stripe (5.50%) and standard (5.48%) designs. Its higher performance can be attributed to lower interfacial charge recombination rates and improvedcharge transfer and collection efficiency. Photophysical measurements indicated faster charge transfer rates in hexagonal cells (≈ 1.3  ×  109s−1) compared to the stripe (9.8  ×  108 s−1) and standard (9.5  ×  108 s−1) designs. Hence, our work highlights the potential of hexagonal design to improve both efficiency and transparency while reducing material consumption, offering a promising approach for manufacturing semi-transparent solar cells.

本研究提出了一种全印刷、大面积、半透明的染料敏化太阳能电池(DSSCs),该电池使用二氧化钛纳米颗粒经TiCl4(一种“D35”推挽式染料敏化剂)和I3 - /I -氧化还原介质处理。采用数字材料沉积(DMD)技术,使用六边形、条纹和标准设计打印面积为4和200 cm2的细胞。扫描电镜(SEM)证实,通过DMD打印的多孔膜通过提高开路电压(Voc)和填充因子(FF)改善了太阳能电池的性能。特别是六边形设计,有利于TiO2介孔结构中更好的电解质浸渍,提高电流密度。该设计为4平方厘米的DSSCs提供了7.05%的功率转换效率(PCE),超过了条形(5.50%)和标准(5.48%)设计。其较高的性能可归因于较低的界面电荷复合率和提高的电荷转移和收集效率。光物理测量表明,与条形电池(9.8 × 108 s−1)和标准电池(9.5 × 108 s−1)设计相比,六边形电池的电荷转移速率(≈1.3 × 109s−1)更快。因此,我们的工作强调了六边形设计在提高效率和透明度的同时减少材料消耗的潜力,为制造半透明太阳能电池提供了一种有前途的方法。
{"title":"Efficient Large Area Semi-Transparent Dye-Sensitized Solar Cells (DSSCs) Printed with DMD400 Technology","authors":"Mahfoudh Raïssi,&nbsp;Himal Muwanwella,&nbsp;Falak Naz,&nbsp;Anaïs Bianchi,&nbsp;Didier Rousseau,&nbsp;Muhammad Tariq Sajjad","doi":"10.1002/admt.202400637","DOIUrl":"https://doi.org/10.1002/admt.202400637","url":null,"abstract":"<p>This work presents the development of fully printed, large-area, semi-transparent Dye-Sensitized Solar Cells (DSSCs) using TiO<sub>2</sub> nanoparticles treated with TiCl<sub>4</sub>, a “D35” push-pull dye sensitizer, and I<sub>3</sub><sup>−</sup>/I<sup>−</sup> redox mediator. Cells with areas of 4 and 200 cm<sup>2</sup> were printed using hexagonal, stripe, and standard designs, employing digital materials deposition (DMD) technology. The porous films printed via DMD, confirmed by scanning electron microscopy (SEM), improved solar cells performance by enhancing the Open Circuit Voltage (Voc) and fill factor (FF). The hexagonal design, in particular, facilitated better electrolyte impregnation in the TiO<sub>2</sub> mesoporous structure, boosting current density. This design yielded a power conversion efficiency (PCE) of 7.05% for 4 cm<sup>2</sup> DSSCs, surpassing the stripe (5.50%) and standard (5.48%) designs. Its higher performance can be attributed to lower interfacial charge recombination rates and improvedcharge transfer and collection efficiency. Photophysical measurements indicated faster charge transfer rates in hexagonal cells (≈ 1.3  ×  10<sup>9</sup>s<sup>−1</sup>) compared to the stripe (9.8  ×  10<sup>8</sup> s<sup>−1</sup>) and standard (9.5  ×  10<sup>8</sup> s<sup>−1</sup>) designs. Hence, our work highlights the potential of hexagonal design to improve both efficiency and transparency while reducing material consumption, offering a promising approach for manufacturing semi-transparent solar cells.</p>","PeriodicalId":7292,"journal":{"name":"Advanced Materials Technologies","volume":"9 23","pages":""},"PeriodicalIF":6.4,"publicationDate":"2024-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/admt.202400637","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142762817","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Kelp Inspired High-Power Density Triboelectric Nanogenerator with Stacking Structure for Multiple Directional Ocean Wave Energy Harvesting 用于多方向海洋波能收集的具有堆叠结构的海带启发式高功率密度三电纳米发电机
IF 6.4 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-12 DOI: 10.1002/admt.202401183
Chao Sun, Xue Liu, Wei Zhong, Qinying Pan, Longyi Chen, Gengchen Zhang, Jia Wang, Xiaohong Dong, Jiang Shao

Ocean wave energy is one of the most promising green energies in the wild. However, it is still challenging to effectively collect wave energy due to its randomness and irregularity. In this work, a kelp inspired high-power density triboelectric nanogenerator (K-TENG) is presented for harvesting wave energy with characteristics in multiple directions. The proposed K-TENG consists of a series of stacked leaf-like units. The influence of configuration parameters, including pellet diameters, pellet numbers, unit sizes, oscillation frequency, swing amplitude, and wave directions on output performances of leaf-like units, are extensively investigated. Experimental data indicates that a single leaf-like unit can achieve a maximum output voltage of 623.14 V as well as a maximum current of 1.48 µA and realize energy harvesting from different wave directions. A K-TENG composed of 15 leaf-like units demonstrates a high-power density of 18.77 W m3 at a wave frequency of 2.5 Hz, which successfully powers a digital watch and 414 light-emitting diodes (LEDs). This work is hoped to provide a simple and reliable route to effectively harvest ocean wave energy.

{"title":"A Kelp Inspired High-Power Density Triboelectric Nanogenerator with Stacking Structure for Multiple Directional Ocean Wave Energy Harvesting","authors":"Chao Sun,&nbsp;Xue Liu,&nbsp;Wei Zhong,&nbsp;Qinying Pan,&nbsp;Longyi Chen,&nbsp;Gengchen Zhang,&nbsp;Jia Wang,&nbsp;Xiaohong Dong,&nbsp;Jiang Shao","doi":"10.1002/admt.202401183","DOIUrl":"https://doi.org/10.1002/admt.202401183","url":null,"abstract":"<p>Ocean wave energy is one of the most promising green energies in the wild. However, it is still challenging to effectively collect wave energy due to its randomness and irregularity. In this work, a kelp inspired high-power density triboelectric nanogenerator (K-TENG) is presented for harvesting wave energy with characteristics in multiple directions. The proposed K-TENG consists of a series of stacked leaf-like units. The influence of configuration parameters, including pellet diameters, pellet numbers, unit sizes, oscillation frequency, swing amplitude, and wave directions on output performances of leaf-like units, are extensively investigated. Experimental data indicates that a single leaf-like unit can achieve a maximum output voltage of 623.14 V as well as a maximum current of 1.48 µA and realize energy harvesting from different wave directions. A K-TENG composed of 15 leaf-like units demonstrates a high-power density of 18.77 W m<sup>−</sup><sup>3</sup> at a wave frequency of 2.5 Hz, which successfully powers a digital watch and 414 light-emitting diodes (LEDs). This work is hoped to provide a simple and reliable route to effectively harvest ocean wave energy.</p>","PeriodicalId":7292,"journal":{"name":"Advanced Materials Technologies","volume":"10 5","pages":""},"PeriodicalIF":6.4,"publicationDate":"2024-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143534001","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
A Novel Multiple Shape Memory Effect in PVDF-Based Ferroelectric Copolymers and Terpolymers 基于 PVDF 的铁电共聚物和三元共聚物中的新型多重形状记忆效应
IF 6.4 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-11 DOI: 10.1002/admt.202401281
Jiayi Jin, Zhaopeng Wang, Yuhong Zhu, Haitao Jiang, Rui Peng, Baojin Chu

Shape memory polymers (SMPs) have been extensively investigated because of their wide range of biomedical and robot applications. In most of SMPs, only one temporary shape can be formed and recovered through the mechanism of melting or glass transition. Herein, a multiple shape memory effect (mSME), i.e., formation of at least two temporary shapes, can be realized in polyvinylidene fluoride (PVDF)-based ferroelectric polymers by exploiting their expanded ferroelectric–paraelectric (F-P) phase transition temperature range. Although P(VDF-TrFE) (TrFE: trifluoroethylene) (55/45) copolymer is thought to be a normal ferroelectric, its ferroelectric phase transforms into a paraelectric phase through an intermediate relaxor ferroelectric-like state and mSME is observed in this extended phase transition temperature range. By incorporating CTFE (chlorotrifluoroethylene) into P(VDF-TrFE), P(VDF-TrFE-CTFE) becomes a relaxor ferroelectric with a further extended phase transition temperature range. The terpolymer exhibits improved mSME and at least three temporary shapes can be formed and recovered. A comparison of SME and structures of several PVDF-based copolymer and terpolymers suggests that the amount of polar phase is a critical factor affecting the SME. This study not only demonstrates mSME in ferroelectric polymers, which expands their application potential, but also provides an in-depth understanding of the shape memory mechanism of the polymers.

{"title":"A Novel Multiple Shape Memory Effect in PVDF-Based Ferroelectric Copolymers and Terpolymers","authors":"Jiayi Jin,&nbsp;Zhaopeng Wang,&nbsp;Yuhong Zhu,&nbsp;Haitao Jiang,&nbsp;Rui Peng,&nbsp;Baojin Chu","doi":"10.1002/admt.202401281","DOIUrl":"https://doi.org/10.1002/admt.202401281","url":null,"abstract":"<p>Shape memory polymers (SMPs) have been extensively investigated because of their wide range of biomedical and robot applications. In most of SMPs, only one temporary shape can be formed and recovered through the mechanism of melting or glass transition. Herein, a multiple shape memory effect (mSME), i.e., formation of at least two temporary shapes, can be realized in polyvinylidene fluoride (PVDF)-based ferroelectric polymers by exploiting their expanded ferroelectric–paraelectric (F-P) phase transition temperature range. Although P(VDF-TrFE) (TrFE: trifluoroethylene) (55/45) copolymer is thought to be a normal ferroelectric, its ferroelectric phase transforms into a paraelectric phase through an intermediate relaxor ferroelectric-like state and mSME is observed in this extended phase transition temperature range. By incorporating CTFE (chlorotrifluoroethylene) into P(VDF-TrFE), P(VDF-TrFE-CTFE) becomes a relaxor ferroelectric with a further extended phase transition temperature range. The terpolymer exhibits improved mSME and at least three temporary shapes can be formed and recovered. A comparison of SME and structures of several PVDF-based copolymer and terpolymers suggests that the amount of polar phase is a critical factor affecting the SME. This study not only demonstrates mSME in ferroelectric polymers, which expands their application potential, but also provides an in-depth understanding of the shape memory mechanism of the polymers.</p>","PeriodicalId":7292,"journal":{"name":"Advanced Materials Technologies","volume":"10 5","pages":""},"PeriodicalIF":6.4,"publicationDate":"2024-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143535854","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Multi-Layer LDPE Pouch Robots Enabled by Inkjet-Printed Masking Layers
IF 6.4 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-10 DOI: 10.1002/admt.202401052
Yifan You, Chen Dai, Ezequiel Goldschmidt, Ronald S. Fearing

Inflatable pouches are attractive as actuators and structural links in soft robots due to their low deflated profile and high deformation ratio. However, current pouch robot fabrication methods have relatively large minimum feature sizes and multi-layer fabrication challenges, limiting the integration of mechanisms with many independent degrees of freedom (DoF). A new monolithic prototype fabrication method utilizes inkjet printing of a masking ink layer, which prevents film bonding and thus defines inflatable regions. Multi-layer inflatable pouches of any planar geometry can be created using thermal fusing, with inter-layer connections and a minimum feature resolution of 0.3 mm. The multi-layer fabrication process enables the integration of pouches for bending actuation and structure, pneumatic channels, and external port connections. This high level of integration enables the fabrication of pouch robots with many independent DoFs. Specific examples using four layers of 38 micrometer thick Low-density polyethylene (LDPE) include 1) a 38 mm-wide 4-fingered robot hand with 8 independent DoFs which rotates a cube within its palm and 2) a 138 mm-long planar continuum manipulator with 10 independent DoFs for pick-and-place of a cylinder. These example designs demonstrate the capability of ink-patterned masking to achieve new levels of functionality for thin-film pouch robots.

{"title":"Multi-Layer LDPE Pouch Robots Enabled by Inkjet-Printed Masking Layers","authors":"Yifan You,&nbsp;Chen Dai,&nbsp;Ezequiel Goldschmidt,&nbsp;Ronald S. Fearing","doi":"10.1002/admt.202401052","DOIUrl":"https://doi.org/10.1002/admt.202401052","url":null,"abstract":"<p>Inflatable pouches are attractive as actuators and structural links in soft robots due to their low deflated profile and high deformation ratio. However, current pouch robot fabrication methods have relatively large minimum feature sizes and multi-layer fabrication challenges, limiting the integration of mechanisms with many independent degrees of freedom (DoF). A new monolithic prototype fabrication method utilizes inkjet printing of a masking ink layer, which prevents film bonding and thus defines inflatable regions. Multi-layer inflatable pouches of any planar geometry can be created using thermal fusing, with inter-layer connections and a minimum feature resolution of 0.3 mm. The multi-layer fabrication process enables the integration of pouches for bending actuation and structure, pneumatic channels, and external port connections. This high level of integration enables the fabrication of pouch robots with many independent DoFs. Specific examples using four layers of 38 micrometer thick Low-density polyethylene (LDPE) include 1) a 38 mm-wide 4-fingered robot hand with 8 independent DoFs which rotates a cube within its palm and 2) a 138 mm-long planar continuum manipulator with 10 independent DoFs for pick-and-place of a cylinder. These example designs demonstrate the capability of ink-patterned masking to achieve new levels of functionality for thin-film pouch robots.</p>","PeriodicalId":7292,"journal":{"name":"Advanced Materials Technologies","volume":"10 3","pages":""},"PeriodicalIF":6.4,"publicationDate":"2024-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143113909","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Graphene-Based Pressure Sensor Application in Non-Invasive Pulse Wave Velocity Continuous Estimation
IF 6.4 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-10 DOI: 10.1002/admt.202400876
Irene Buraioli, Stefania Vitale, Andrea Valerio, Alessandro Sanginario, Dario Leone, Sabrina Conoci, Artur Ciesielski, Alberto Milan, Danilo Demarchi, Paolo Samorì

Monitoring the cardiovascular health of patients and early diagnosis of heart diseases are highly sought after as they can represent a true cornerstone in tomorrow's healthcare surveillance. Here, an unprecedented non-invasive device prototype is reported for pulse wave velocity (PWV) measurement based on a piezoelectric graphene pressure sensor. PWV is a critical health indicator that estimates arterial stiffness by measuring the velocity of arterial pulse flow through the circulatory system. The sensor incorporates advanced electronic components and data analysis tools, enabling the measurement of pulse transit time (PTT), that is the time required for the pulse wave to travel between carotid and femoral artery sites. Significantly, the outcomes obtained through the novel method, which involved monitoring 10 patients within clinical environment, show statistical similarity to results obtained using established technology for the PWV estimation such as SphygmoCor. In particular, the mean difference between measurements done with the two techniques resulted in 0.1 m s−1, that is <2%, underscoring the reliability of the novel device. The technology holds big promise for enhancing cardiovascular healthcare delivery: it is wearable, potentially exploitable by a non-expert user, and it needs to be powered with just 0.2 V, thus it can become compatible even with applications in point-of-care settings.

{"title":"Graphene-Based Pressure Sensor Application in Non-Invasive Pulse Wave Velocity Continuous Estimation","authors":"Irene Buraioli,&nbsp;Stefania Vitale,&nbsp;Andrea Valerio,&nbsp;Alessandro Sanginario,&nbsp;Dario Leone,&nbsp;Sabrina Conoci,&nbsp;Artur Ciesielski,&nbsp;Alberto Milan,&nbsp;Danilo Demarchi,&nbsp;Paolo Samorì","doi":"10.1002/admt.202400876","DOIUrl":"https://doi.org/10.1002/admt.202400876","url":null,"abstract":"<p>Monitoring the cardiovascular health of patients and early diagnosis of heart diseases are highly sought after as they can represent a true cornerstone in tomorrow's healthcare surveillance. Here, an unprecedented non-invasive device prototype is reported for pulse wave velocity (PWV) measurement based on a piezoelectric graphene pressure sensor. PWV is a critical health indicator that estimates arterial stiffness by measuring the velocity of arterial pulse flow through the circulatory system. The sensor incorporates advanced electronic components and data analysis tools, enabling the measurement of pulse transit time (PTT), that is the time required for the pulse wave to travel between carotid and femoral artery sites. Significantly, the outcomes obtained through the novel method, which involved monitoring 10 patients within clinical environment, show statistical similarity to results obtained using established technology for the PWV estimation such as SphygmoCor. In particular, the mean difference between measurements done with the two techniques resulted in 0.1 m s<sup>−1</sup>, that is &lt;2%, underscoring the reliability of the novel device. The technology holds big promise for enhancing cardiovascular healthcare delivery: it is wearable, potentially exploitable by a non-expert user, and it needs to be powered with just 0.2 V, thus it can become compatible even with applications in point-of-care settings.</p>","PeriodicalId":7292,"journal":{"name":"Advanced Materials Technologies","volume":"10 5","pages":""},"PeriodicalIF":6.4,"publicationDate":"2024-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/admt.202400876","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143533422","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Magnetic Nozzle-Free Embedded 3D (MagNoFE3D) Printing
IF 6.4 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-10 DOI: 10.1002/admt.202401097
Franco N. Piñan Basualdo, Vasileios D. Trikalitis, Sabrina Visconti, Fanny Ficuciello, Constantinos Goulas, Jeroen Rouwkema, Sarthak Misra

The functional principle behind extrusion-based printing is the capability of flowing material through a nozzle on demand, which must solidify upon deposition, a behavior exhibited only by some materials. Embedded printing offers a solution to maintain shape fidelity during the deposition of a wider range of materials. However, the use of a moving nozzle in a support bath can lead to bath disturbance and the spreading of the ink. In this study, a novel embedded printing technique that eliminates the need for a nozzle by employing a magnetic sphere as the plotting moiety is introduced. The externally steered sphere creates a path by locally fluidizing the bath, allowing the simultaneously injected ink to flow into the space behind it. The method is benchmarked using water as an ink, achieving free-form printing without additional stabilization methods. The creation of solid structures is also demonstrated by printing a photocurable ink that is crosslinked and removed from the bath. Moreover, the plotting magnet can be incorporated into the printed part during the crosslinking, thus giving place to a magnetically responsive structure. This advancement paves the way for innovations in fields such as tissue engineering and microrobotics by enabling the fabrication of intricate and functional designs.

{"title":"Magnetic Nozzle-Free Embedded 3D (MagNoFE3D) Printing","authors":"Franco N. Piñan Basualdo,&nbsp;Vasileios D. Trikalitis,&nbsp;Sabrina Visconti,&nbsp;Fanny Ficuciello,&nbsp;Constantinos Goulas,&nbsp;Jeroen Rouwkema,&nbsp;Sarthak Misra","doi":"10.1002/admt.202401097","DOIUrl":"https://doi.org/10.1002/admt.202401097","url":null,"abstract":"<p>The functional principle behind extrusion-based printing is the capability of flowing material through a nozzle on demand, which must solidify upon deposition, a behavior exhibited only by some materials. Embedded printing offers a solution to maintain shape fidelity during the deposition of a wider range of materials. However, the use of a moving nozzle in a support bath can lead to bath disturbance and the spreading of the ink. In this study, a novel embedded printing technique that eliminates the need for a nozzle by employing a magnetic sphere as the plotting moiety is introduced. The externally steered sphere creates a path by locally fluidizing the bath, allowing the simultaneously injected ink to flow into the space behind it. The method is benchmarked using water as an ink, achieving free-form printing without additional stabilization methods. The creation of solid structures is also demonstrated by printing a photocurable ink that is crosslinked and removed from the bath. Moreover, the plotting magnet can be incorporated into the printed part during the crosslinking, thus giving place to a magnetically responsive structure. This advancement paves the way for innovations in fields such as tissue engineering and microrobotics by enabling the fabrication of intricate and functional designs.</p>","PeriodicalId":7292,"journal":{"name":"Advanced Materials Technologies","volume":"10 5","pages":""},"PeriodicalIF":6.4,"publicationDate":"2024-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/admt.202401097","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143533423","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Analog-Digital Hybridity of Resistive Switching in Ion-Irradiated BiFeO3 Memristor for Synergistic Neuromorphic Functionality and Artificial Learning
IF 6.4 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-09 DOI: 10.1002/admt.202400557
Suman Roy, Mousam Charan Sahu, Anjan Kumar Jena, Sameer Kumar Mallik, Roshan Padhan, Jyoti Ranjan Mohanty, Satyaprakash Sahoo

Memristors-based neuromorphic devices represent emerging computing architectures to perform complex tasks by outpacing the traditional Von-Neumann architectures in terms of speed, and energy efficiency. In this work, the resistive switching (RS) behavior of sol-gel grown and ion-irradiated BFO films is investigated under electrical stimulus. The Ag/BFO/FTO memristors emulate a combination of digital and analog RS behavior within a single device. The possible mechanism of analog digital hybridity is addressed by considering the formation of the conducting filament by oxygen vacancies, Ag+ ions and Schottky barrier height modulation. The ion-irradiated BFO samples are analyzed using the Raman, XRD, and XPS studies. To uphold bioinspired synaptic actions, crucial synaptic functionalities like pair-pulse facilitation and long-term potentiation/depression are effectively achieved. More intricate synaptic behaviors are also demonstrated such as spike-time-dependent plasticity and Pavlovian classical conditioning, which represent the prominent attributes of both learning and forgetting behavior. Additionally, high pattern recognition accuracy (96.1%) is achieved in an artificial neural network simulation by using the synaptic weights of the memristors. This synergistic effect of digital and analog RS in ion-irradiated BFO can be beneficial for the emulation of complex learning behavior as well as its incorporation into low-power neuromorphic computing.

{"title":"Analog-Digital Hybridity of Resistive Switching in Ion-Irradiated BiFeO3 Memristor for Synergistic Neuromorphic Functionality and Artificial Learning","authors":"Suman Roy,&nbsp;Mousam Charan Sahu,&nbsp;Anjan Kumar Jena,&nbsp;Sameer Kumar Mallik,&nbsp;Roshan Padhan,&nbsp;Jyoti Ranjan Mohanty,&nbsp;Satyaprakash Sahoo","doi":"10.1002/admt.202400557","DOIUrl":"https://doi.org/10.1002/admt.202400557","url":null,"abstract":"<p>Memristors-based neuromorphic devices represent emerging computing architectures to perform complex tasks by outpacing the traditional Von-Neumann architectures in terms of speed, and energy efficiency. In this work, the resistive switching (RS) behavior of sol-gel grown and ion-irradiated BFO films is investigated under electrical stimulus. The Ag/BFO/FTO memristors emulate a combination of digital and analog RS behavior within a single device. The possible mechanism of analog digital hybridity is addressed by considering the formation of the conducting filament by oxygen vacancies, Ag<sup>+</sup> ions and Schottky barrier height modulation. The ion-irradiated BFO samples are analyzed using the Raman, XRD, and XPS studies. To uphold bioinspired synaptic actions, crucial synaptic functionalities like pair-pulse facilitation and long-term potentiation/depression are effectively achieved. More intricate synaptic behaviors are also demonstrated such as spike-time-dependent plasticity and Pavlovian classical conditioning, which represent the prominent attributes of both learning and forgetting behavior. Additionally, high pattern recognition accuracy (96.1%) is achieved in an artificial neural network simulation by using the synaptic weights of the memristors. This synergistic effect of digital and analog RS in ion-irradiated BFO can be beneficial for the emulation of complex learning behavior as well as its incorporation into low-power neuromorphic computing.</p>","PeriodicalId":7292,"journal":{"name":"Advanced Materials Technologies","volume":"10 2","pages":""},"PeriodicalIF":6.4,"publicationDate":"2024-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143113954","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
3D Printing of Liquid Crystal Polymers for Space Applications
IF 6.4 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-09 DOI: 10.1002/admt.202400571
Caroline Houriet, Evelien Claassen, Chiara Mascolo, Haimo Jöhri, Abel Brieva, Szilvia Szmolka, Sébastien Vincent-Bonnieu, Agnieszka Suliga, Raphael Heeb, Silvan Gantenbein, Ugo Lafont, Thomas Rohr, Kunal Masania

Fused Filament Fabrication is a promising manufacturing technology for the circularity of space missions. Potential scenarios include in-orbit applications to maximize mission life and to support long-term exploration missions with in situ manufacturing and recycling. However, its adoption is restricted by the availability of engineering polymers displaying mechanical performance combined with resistance to space conditions. Here, a thermotropic Liquid Crystal Polymer (LCP) is reported as a candidate material with extrusion 3D printing. To expand its scope of applicability to structural parts for space applications, four different exposure conditions are studied: thermal cycling under vacuum, atomic oxygen, UV, and electron irradiations. While 1 MeV-electron irradiation leads to a green coloration due to annealable color centers, the mechanical performance is only slightly decreased in dynamic mode. It is also found that increased printing temperature improves transverse strength and resistance to thermal cycling with the trade-off of tensile stiffness and strength. Samples exposed to thermal cycling and the highest irradiation dose at lower printing temperatures still display a Young's modulus of 30 GPa and 503 MPa of tensile strength which is exceptionally high for a 3D-printed polymer. For the types of exposure studied, overall, the results indicate that LCP 3D-printed parts are well suited for space applications.

{"title":"3D Printing of Liquid Crystal Polymers for Space Applications","authors":"Caroline Houriet,&nbsp;Evelien Claassen,&nbsp;Chiara Mascolo,&nbsp;Haimo Jöhri,&nbsp;Abel Brieva,&nbsp;Szilvia Szmolka,&nbsp;Sébastien Vincent-Bonnieu,&nbsp;Agnieszka Suliga,&nbsp;Raphael Heeb,&nbsp;Silvan Gantenbein,&nbsp;Ugo Lafont,&nbsp;Thomas Rohr,&nbsp;Kunal Masania","doi":"10.1002/admt.202400571","DOIUrl":"https://doi.org/10.1002/admt.202400571","url":null,"abstract":"<p>Fused Filament Fabrication is a promising manufacturing technology for the circularity of space missions. Potential scenarios include in-orbit applications to maximize mission life and to support long-term exploration missions with in situ manufacturing and recycling. However, its adoption is restricted by the availability of engineering polymers displaying mechanical performance combined with resistance to space conditions. Here, a thermotropic Liquid Crystal Polymer (LCP) is reported as a candidate material with extrusion 3D printing. To expand its scope of applicability to structural parts for space applications, four different exposure conditions are studied: thermal cycling under vacuum, atomic oxygen, UV, and electron irradiations. While 1 MeV-electron irradiation leads to a green coloration due to annealable color centers, the mechanical performance is only slightly decreased in dynamic mode. It is also found that increased printing temperature improves transverse strength and resistance to thermal cycling with the trade-off of tensile stiffness and strength. Samples exposed to thermal cycling and the highest irradiation dose at lower printing temperatures still display a Young's modulus of 30 GPa and 503 MPa of tensile strength which is exceptionally high for a 3D-printed polymer. For the types of exposure studied, overall, the results indicate that LCP 3D-printed parts are well suited for space applications.</p>","PeriodicalId":7292,"journal":{"name":"Advanced Materials Technologies","volume":"10 4","pages":""},"PeriodicalIF":6.4,"publicationDate":"2024-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/admt.202400571","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143438727","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Reprogrammable 3D Shapes from 1D Metamaterial
IF 6.4 3区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-09 DOI: 10.1002/admt.202401113
Ezra Ben-Abu, Anna Zigelman, Yaron Veksler, Sefi Givli, Evgueni Filipov, Hod Lipson, Amir D. Gat

Three billion years of evolution have produced a vast variety of protein molecules, whose functions are directly dependent on their ability to assume and maintain specific shapes. Proteins are defined by the sequence and chemical characteristics of their amino acids, which dictate their 3D shape and function, ranging from enzymatic activity to immune responses. Here, we explore a synthetic form of linear structure that can be bent in a programmable way into various specific 3D shapes inspired by the way functional proteins are defined using genetic codes. This synthetic structure is based on non-circular multistable corrugated tubes, which can be fabricated at various length scales and cross-sectional shapes, thus enabling the modification of their properties. Additionally, the cross-section shape can be rewritten multiple times, allowing for the repair of structural damage and the rewriting of the properties of the structure's multi-stability. A numerical model is used to describe the bending energy landscape of different cross-sections. The proposed reprogrammable 3D shapes of a rewritable 1D metamaterial are promising candidates for futuristic robotic systems, complex deployable structures, catheter devices, and energy absorption and harvesting.

{"title":"Reprogrammable 3D Shapes from 1D Metamaterial","authors":"Ezra Ben-Abu,&nbsp;Anna Zigelman,&nbsp;Yaron Veksler,&nbsp;Sefi Givli,&nbsp;Evgueni Filipov,&nbsp;Hod Lipson,&nbsp;Amir D. Gat","doi":"10.1002/admt.202401113","DOIUrl":"https://doi.org/10.1002/admt.202401113","url":null,"abstract":"<p>Three billion years of evolution have produced a vast variety of protein molecules, whose functions are directly dependent on their ability to assume and maintain specific shapes. Proteins are defined by the sequence and chemical characteristics of their amino acids, which dictate their 3D shape and function, ranging from enzymatic activity to immune responses. Here, we explore a synthetic form of linear structure that can be bent in a programmable way into various specific 3D shapes inspired by the way functional proteins are defined using genetic codes. This synthetic structure is based on non-circular multistable corrugated tubes, which can be fabricated at various length scales and cross-sectional shapes, thus enabling the modification of their properties. Additionally, the cross-section shape can be rewritten multiple times, allowing for the repair of structural damage and the rewriting of the properties of the structure's multi-stability. A numerical model is used to describe the bending energy landscape of different cross-sections. The proposed reprogrammable 3D shapes of a rewritable 1D metamaterial are promising candidates for futuristic robotic systems, complex deployable structures, catheter devices, and energy absorption and harvesting.</p>","PeriodicalId":7292,"journal":{"name":"Advanced Materials Technologies","volume":"10 4","pages":""},"PeriodicalIF":6.4,"publicationDate":"2024-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/admt.202401113","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143438729","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Advanced Materials Technologies
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1