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Biomass-Based Discrete Furan Oligomers as materials for Electrochromic Devices

ACS Sustainable Chemistry and engineering 2024年第1期12卷 459-469页

作者： Atayde, Eduardo C. Fong, Guan-Lun Yeh, Jyun-Yi Matsagar, Babasaheb M. Wang, Yu-Cheng Chen, De-Chian Peng, Chi-How Li, Yi-Pei Yamauchi, Yusuke Ho, Kuo-Chuan Wu, Kevin C.-W. Molecular Science and Technology Program Taiwan International Graduate Program (TIGP-MST) Academia Sinica No. 128 Sec. 2 Academia Road Taipei 11529 Taiwan Department of Chemistry National Tsing Hua University No. 101 Sec. 2 Kuang-Fu Road Hsinchu 30013 Taiwan Department of Chemical Engineering National Taiwan University No. 1 Sec. 4 Roosevelt Road Taipei 10617 Taiwan Sustainable Chemical Science and Technology Program Taiwan International Graduate Program (TIGP-SCST) Academia Sinica No. 128 Sec. 2 Academia Road Taipei 11529 Taiwan School of Chemical Engineering and Australian Institute for Bioengineering and Nanotechnology (AIBN) The University of Queensl Brisbane 4072 QLD Australia Department of Materials Process Engineering Graduate School of Engineering Nagoya University Nagoya 464-8603 Japan Institute of Polymer Science and Engineering National Taiwan University No.1 Sec. 4 Roosevelt Rd. Taipei 10617 Taiwan Department of Chemical Engineering and Materials Science Yuan Ze University No. 135 Yuandong Rd. Taoyuan 320 Taiwan

Electrochromic devices (ECDs) are materials that can undergo reversible changes in transmittance when exposed to different applied potentials. While many conjugated heterocyclic oligomers, such as oligothiophenes, have been developed for this purpose, there is no reported study on the use of discrete oligomeric furans as ECD materials. In this work, we introduce a furan trimer that can be utilized as a discrete electrochromic material, which transitions from light yellow to red and has a very high coloration efficiency of 1940 cm²/C at 507 nm. We propose that the reversible π-stack formation of the oligomer radical cations is behind this phenomenon, as evidenced by both experimental and computational results. The derivability of this oligomer from biomass and its facile synthesis make it an interesting alternative for other existing organic electrochromic materials. © 2023 American Chemical Society

关键词： electrochromism furan oligomer hydroxyalkylation−alkylation reaction solvatochromism π-stacks

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engineering Hydrogels for Efficient Solar Desalination and Water Purification

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Accounts of materials Research 2021年第5期2卷 374-384页

作者： Youhong Guo Guihua Yu Materials Science and Engineering Program Texas Materials InstituteThe University of Texas at AustinAustinTexas 78712United States

CONSPECTUS:Safe and adequate water is a global challenge due to the growing population and pollution in the wake of natural *** to clean water is a cornerstone for the further development of our modern ***-powered desalination and water purification have attracted much research attention due to the high solar-to-thermal conversion efficiency and ease of implementation in multiple scales,from compact,stand-alone devices for individual households to large,centralized dimensions for ***,the generation of water vapor at low temperatures below the boiling point is usually a slow process under natural *** production rate of clean water relies on the efficiencies of solar energy conversion and utilization,which can be enhanced in two directions:systems optimization and materials *** from bottom heating and volumetric heating,interfacial evaporation has been adopted recently to systematically reduce energy loss by localizing heat near the evaporation surface using photothermal ***,carbonaceous materials,narrow bandgap semiconductors,and polymers with different structures were designed to achieve thermal management and water *** this Account,we highlight the recent progress of hydrogels as a highly tunable material platform for solar-powered desalination and water *** begin by introducing how gelation chemistry endows hydrogels with desirable properties and multiscale tunability from molecular to macroscopic ***,we review three major strategies to promote efficient solar-to-vapor conversion in terms of reducing water evaporation enthalpy,optimizing heat distribution,and tailoring the evaporation ***,by selecting polymeric backbones with hydratable functional groups,the water state in hydrogels can be regulated to facilitate intermediate water,which has a lower evaporation enthalpy compared to that of the bulk *** polymer−water interaction can be

关键词： enthalpy corners backbone

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Characterization of Spicule Structure 152nd

Characterization of Spicule Structure

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152nd Annual Meeting and Exhibition of The Minerals, Metals and materials Society, TMS 2023

作者： Tavangarian, Fariborz Gray, Jennifer L. Clark, Trevor Gao, Chao Mechanical Engineering Program School of Science Engineering and Technology Pennsylvania State University Harrisburg MiddletownPA17057 United States Materials Research Institute The Pennsylvania State University University Park PA16802 United States Department of Mechanical and Industrial Engineering Norwegian University of Science and Technology Trondheim7034 Norway

ISBN: (纸本)9783031225239

Nature has been a great source of inspiration for engineers and scientists for centuries. It provides unique ideas to overcome the unmet needs of human beings. Spicules are structural elements of Euplectella Aspergillum sponges that reside in the deep ocean. They have an exceptional microstructure that provides excellent mechanical properties. Although spicules are composed of a brittle material, silica (SiO2), they behave differently under load compared to other ceramics. This behavior is due to their concentric cylindrical structure. To produce a similar structure with potential engineering and biomedical applications, one needs to investigate its microstructure in depth. In this study, we examined the microstructure of spicules to understand their architecture as a foundation to better design biomedical implants for tissue engineering applications. © 2023, The Minerals, Metals & materials Society.

关键词： Microstructure

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Effect of Concentration and Residence Time of Joncryl■ADR4368 on Melt Processability of Poly(3-hydroxybutyrate)

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Journal of Renewable materials 2024年第12期12卷 2079-2094页

作者： Jéssica da Silva Chagas JoséElson Soares Filho Natália Fernanda Inocêncio Silva Marcelo Massayoshi Ueki Eliton Souto de Medeiros Renate Maria Ramos Wellen Mauricio Pinheiro de Oliveira Gelsoneide da Silva Gois Yêda Medeiros Bastos de Almeida Amélia S.F.Santos Post-Graduation Program in Materials Engineering(PPCEM) Federal University of Paraíba(UFPB)João PessoaPB 58051-900Brazil Laboratory of Materials and Biosystems(LAMAB) Federal University of Paraíba(UFPB)João PessoaPB 58051-900Brazil Department of Materials Engineering Federal University of Sergipe(UFS)Jardim Rosa ElzeSão CristóvãoSE 49100-000Brazil Institute of Science and Technology Federal University of São Paulo(UNIFESP)São Josédos CamposSP 12231-280Brazil Department of Chemical Engineering Federal University of Pernambuco(UFPE)Cidade UniversitáriaRecifePE 50670-901Brazil

Poly(3-hydroxybutyrate)(PHB)is a biothechnological and biodegradable thermoplastic polymer from the polyhydroxyalkanoates(PHAs)family,whose chain regularity,high molecular weight,and physical and mechanical properties comparable to polypropylene(PP)are characteristics that have made PHB a prominent commercial ***,its susceptibility to thermal degradation and hydrolysis has limited many *** address the challenges associated with processing,a random copolymer of 95.86 mol%3-hydroxybutyrate and 4.14 mol%3-hydroxyvalerate(referred as PHB)was compounded without(neat PHB)and with 0.25,0.5,1,and 1.5 wt%of chain extender(Joncryl■ADR 4368),consisting of multifunctional epoxy groups,and melt mixed in an internal mixer at 170℃,50 rpm,and residence times of 5,10,and 15 *** effect of chain extender concentration and residence time on the effectiveness of Joncryl■ADR 4368 to recover the pristine PHB properties were investigated through torque rheometry,melt flow index(MFI),differential scanning calorimetry(DSC),tensile testing,and thermogravimetric *** results indicated that an increase in residence time strongly influenced the prevalence of thermomechanical degradation reactions over chain extension reactions of PHB during processing in the molten *** residence times favored chain extension,while longer times favored chain *** trend led to no enhancement of PHB mechanical properties processed for 10 and 15 min,regardless of additive content *** flow index,thermogravimetric analysis and tensile strength exhibited an asymptotic behavior with the increase in additive concentration,exhibiting a noteworthy improvement in tensile strength and temperature at the highest rate of thermal degradation(TMAX),and a decrease in melt flow index of neat PHB with only 0.25 wt%of additive mixed for 5 *** results found in this work allow additional data for processing PHB by manipulating the ratios of multifunctional chain

关键词： PHB chain extender degradation epoxy groups viscosity

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Approach for enhancing sensitivity of tin-oxo cluster resist for high NA extreme UV lithography 41

Approach for enhancing sensitivity of tin-oxo cluster resist...

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Advances in Patterning materials and Processes XLI 2024

作者： Ku, Yejin Kim, Gayoung Kim, Min Seung Lee, Jin-Kyun Kim, Jiho Park, Byeong-Gyu Lee, Sangsul Lee, Seohyeon Jung, Byung Jun Lee, Changhyeon Kim, Hyunseok Hur, Su-Mi Koh, Chawon Nishi, Tsunehiro Kim, Hyun-Woo Program in Environment and Polymer Engineering Inha University Incheon22212 Korea Republic of Department of Polymer Science and Engineering Inha University Incheon22212 Korea Republic of Pohang Accelerator Laboratory Postech Pohang37673 Korea Republic of Department of Materials Science and Engineering University of Seoul Seoul02504 Korea Republic of Department of Polymer Engineering Graduate School Chonnam National University Gwangju61186 Korea Republic of School of Polymer Science and Engineering Chonnam National University Gwangju61186 Korea Republic of Department of Materials Science and Engineering Yonsei University Seoul03722 Korea Republic of Samsung Electronics Co. Ltd. Semiconductor R&d Center Gyeonggi-do 18448 Korea Republic of

ISBN: (纸本)9781510672208

High numerical aperture (NA) EUV lithography is considered as the most-promising candidate for next generation lithography protocol that will play a crucial role in meeting the demand on the enhanced semiconductor performance and productivity. While this technology enables the fabrication of sub-10 nm patterns, the increased NA has posed challenges, such as reduced depth of focus and narrower process margins. To overcome these hurdles, it is essential to apply thinner resist films while ensuring that the resulting small patterns maintain sufficient physical and chemical durability. Moreover, considering that thinner films absorb fewer photons, the resist molecular structure should be designed to compensate sensitivity burdens. Here, an approach has been proposed to enhance sensitivity by accelerating the solubility change of a well-known tinbased nanocluster resist. To accomplish this goal, it is important to increase not only the number of secondary electrons but also reaction sites and promote radical-based chemical reactions. We aimed at experimentally validating this concept by utilizing elements with high EUV absorbance and highly reactive functional groups with tin radicals. As a model resist, we chose a tin-oxo cage material consisting of a divalent cation containing 12 tin atoms and two counter anions. Our findings indicate that the introduction of unsaturated groups capable of building bridging bonds with radicals leads to fast solubility change at a lower exposure dose, thus enhancing sensitivity. This research offers a promising direction for the development of resists tailored for High NA EUV lithography. © COPYRIGHT SPIE. Downloading of the abstract is permitted for personal use only.

关键词： Tin

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Mo-terminated edges in two-dimensional molybdenum disulfide for site-specific hydrolysis and DNA cleavage

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materials Today 2025年 86卷 162-171页

作者： Wang, Cong Wu, Menghan Li, Muqing Zhao, Yingcan Zhao, Mingchuang Zhang, Yunhao Bai, Yichao Gao, Jianxiang Wang, Xiaoxia Tian, Xilin Zhang, Han Chang, Liang Zou, Xiaolong Liu, Bilu Kang, Feiyu Terrones, Mauricio Lei, Yu Institute of Materials Research Shenzhen Key Laboratory of Advanced Layered Materials for Value-added Applications Guangdong Provincial Key Laboratory of Thermal Management Engineering and Materials & Center of Double Helix Tsinghua Shenzhen International Graduate School Tsinghua University Shenzhen518055 China Institute of Materials Research & Shenzhen Geim Graphene Center Shenzhen Key Laboratory of Advanced Layered Materials for Value-added Applications Tsinghua-Berkeley Shenzhen Institute and Tsinghua Shenzhen International Graduate School Tsinghua University Shenzhen518055 China Environmental Science Program Department of Life Sciences Beijing Normal University-Hong Kong Baptist University United International College Guangdong519087 China Tsinghua Shenzhen International Graduate School Tsinghua University Shenzhen518055 China Department of Physics Department of Chemistry Department of Materials Sciences Center for 2-Dimensional and Layered Materials The Pennsylvania State University University ParkPA16802 United States International Collaborative Laboratory of 2D Materials for Optoelectronics Science and Technology of Ministry of Education Institute of Microscale Optoelectronics Shenzhen University Shenzhen518060 China

The hydrolysis of DNA serves as the foundational principle for gene engineering that enable precise gene cleavage at the molecular level. This process typically occurs in biological nucleases, which exhibit nucleobase-selective and catalytic hydrolysis capabilities rarely replicated in abiotic nanomaterials. Here, we demonstrate that molybdenum-terminated (Mo-terminated) edges of molybdenum disulfide (MoS2) possess the unique ability to abstract a proton (H+) from water molecules, thereby facilitating catalytic hydrolysis reactions that cleave the phosphodiester bonds in DNA through the action of hydroxide ions. The enhanced proton absorption at Mo-terminated edges of MoS2 significantly reduces the activation energy required for the DNA hydrolysis reaction. Furthermore, the favorable interaction between the Mo-terminated edges and thymine nucleobases promotes both charge transfer and P-O bond cleavage, enabling targeted DNA hydrolysis at 'TTTTTTT' sequences under dark conditions. This discovery underscores the potential of MoS2 as a stable, efficient nanosystem for precise genetic editing, heralding advanced applications in the field of gene engineering. © 2025 The Author(s)

关键词： Activation energy

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Cr-modified CuAlBe shape memory alloy: Role of microstructure, thermodynamic parameters, superelasticity, dissipated energy and corrosion resistance

Journal of Alloys and Metallurgical Systems

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Journal of Alloys and Metallurgical Systems 2024年 7卷

作者： Silva, David D.S. Candido, Gemierson V.M. Alves, Ricardo F. Dias, Elisabeth A.M.G.S. Oliveira, Danniel F. Federal University of São Carlos Graduate Program in Materials Science and Engineering SP São Carlos13565-905 Brazil Colorado School of Mines George S. Ansell Department of Metallurgical and Materials Engineering GoldenCO80401 United States Federal University of Paraíba Graduate Program in Mechanical Engineering PB João Pessoa58051-900 Brazil Federal University of Rio Grande do Norte Graduate Program in Materials Science and Engineering RN Natal59078-970 Brazil Federal University of Paraíba Graduate Program in Materials Science and Engineering PB João Pessoa58051-900 Brazil

This study reports the effects of Cr addition on the microstructure, superelasticity and corrosion resistance improvement of CuAlBe shape memory alloy. Analysis via structural, morphological, thermal, mechanical and electrochemical characterizations were performed. The analyses revealed austenite as the stable phase at room temperature for all samples. The increase in the Cr content caused a slight increase in the recovery rate and dissipated energy. Electrochemical results demonstrate that a small addition of Cr (0.1–0.3 wt%) increase the corrosion resistance due the decreases of the corrosion current density and increase of the corrosion potential. © 2024 The Authors

关键词： Corrosion resistance

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Positive-tone Tin-oxo Nanoclusters for Extreme UV lithography 42

Positive-tone Tin-oxo Nanoclusters for Extreme UV lithograph...

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Advances in Patterning materials and Processes XLII

作者： Kim, Gayoung Ku, Yejin Jeon, Subin Lee, Jin-Kyun Lee, Seohyun Jung, Byung Jun Lee, Sung-Il Ryu, Choonghan Park, Kangho Jung, Yun Lim Jeong, Changyoung Choi, Jin Program in in Environment and Polymer Engineering Inha University Incheon22212 Korea Republic of Program in Semiconductor Convergence Inha University Incheon22212 Korea Republic of Department of Polymer Science and Engineering Inha University Incheon22212 Korea Republic of Department of Materials Science and Engineering University of Seoul Seoul02504 Korea Republic of Samsung Electronics Co. Ltd. Semiconductor R&D Center Suwon18448 Korea Republic of

ISBN: (纸本)9781510686427

In this study, we propose a strategy to achieve positive metal oxide resists (pMORs) based on tin-oxo nanoclusters (TOCs) for extreme ultraviolet (EUV) lithography in high-performance semiconductor integrated circuit manufacturing. TOC possesses Lewis acidic properties and becomes more strongly acidic upon ligand dissociation when exposed to high-energy radiation, such as electron beam (e-beam) and EUV. During the subsequent development process using an aqueous solution of tetramethylammonium hydroxide (TMAH), a Lewis base, the exposed regions undergo Lewis acid-base interactions, leading to increased hydrophilicity. Ultimately, this results in enhanced solubility, enabling the formation of positive-tone patterns. To address the limitations of TOCs, particularly in terms of process margin and chemical stability, we mixed TOCs with small organic molecules containing phenolic hydroxyl groups, which act as Lewis bases. This modification effectively mitigated the shortcomings of TOCs. A TOC formulation containing 10% dendritic polyphenol (DPP) exhibited an improved dissolution contrast while simultaneously enhancing chemical stability. Using this in EUV lithography, we successfully achieved high resolution positive-tone patterns with a line width of 13 nm. © 2025 SPIE.

关键词： Extreme ultraviolet lithography

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Achieving Near-Intrinsic Exciton Linewidth at Room Temperature in Monolayer WS2 Coupled with a Mie Resonator

Achieving Near-Intrinsic Exciton Linewidth at Room Temperatu...

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CLEO: science and Innovations, S and I 2022

作者： Fang, Jie Yao, Kan Zheng, Yuebing Materials Science & Engineering Program Texas Materials Institute The University of Texas at Austin AustinTX78712 United States Walker Department of Mechanical Engineering The University of Texas at Austin AustinTX78712 United States

ISBN: (纸本)9781557528209

Strong multiparticle interactions at room temperature (RT) lead to broadened homogeneous exciton linewidths in 2D semiconductors, degrading the quality of excitonic mode and emission. By coupling a Mie resonator with monolayer WS2, we achieve narrowed linewidths at RT, approaching the theoretical limit at 0 Kelvin. © Optica Publishing Group 2022, © 2022 The Author(s)

关键词： Linewidth

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Intercalated Graphene and Colloidal Quantum Dots as a novel Architecture for UV/ Vis/NIR Multispectral Photodetection

Intercalated Graphene and Colloidal Quantum Dots as a novel ...

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2024 IEEE Research and Applications of Photonics in Defense Conference, RAPID 2024

作者： Shang, J.Y. Ahn, S. Shang, J.Y. Mena, O. Vazquez University of California Department of Nanoengineering 9500 Gilman DriveLa Jolla San Diego92093 United States Program in Materials Science and Engineering University of California 9500 Gilman DriveLa Jolla San Diego92093 United States

We present a compact hybrid architecture of intercalated graphene and PbS quantum dots with independent electrical contacts for each graphene layer that allowing for detection of different spectral bands for each grap... 详细信息

ISBN: (纸本)9798350373097

关键词： Nanocrystals

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