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Chemical exfoliation of layered Al5C3N for the synthesis of AlN nanosheets. 层状Al5C3N的化学剥落制备AlN纳米片。
IF 9.6 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-01-01 Epub Date: 2025-12-08 DOI: 10.1038/s43246-025-01019-3
Nima Amousa, Melina Poll, Louis Godeffroy, Pedro Berastegui, Norbert H Nickel, Namrata Sharma, Olivier Donzel-Gargand, Thomas Dittrich, Steffen Fengler, Sebastian Wintz, Tristan Petit, Ulf Jansson, Jesus Gonzalez-Julian

Two-dimensional (2D) aluminum nitride (AlN) represents a promising material with unique properties predicted by density functional theory (DFT), characterized by a honeycomb lattice where Al and N atoms exhibit threefold in-plane coordination. However, the synthesis of free-standing AlN nanosheets has been challenging due to the crystal configurations of the well-known bulk AlN, which presents a hexagonal wurtzite structure with a tetrahedral coordination, preventing its exfoliation to obtain nanosheets. Herein, we propose a facile method involving the preparation of layered-structured aluminum carbonitrides, Al5C3N, followed by exfoliation into AlN nanosheets, offering a potential route for producing 2D AlN. The Al5C3N precursor was chemically etched in hydrofluoric acid (HF), breaking the Al-C bonds and exposing the AlN nanosheets. The development of this synthesis method opens up opportunities towards the preparation of 2D AlN and the investigation of its unique properties for applications in sensors and microelectronics.

二维(2D)氮化铝(AlN)是一种具有密度泛函理论(DFT)预测的独特性能的有前途的材料,其特征是蜂窝晶格,其中Al和N原子在平面内表现出三重配位。然而,由于众所周知的大块AlN的晶体结构,它呈现出具有四面体配位的六边形纤锌矿结构,阻止了其剥离以获得纳米片,因此独立式AlN纳米片的合成一直具有挑战性。在此,我们提出了一种简单的方法,包括制备层状结构的铝碳氮化物Al5C3N,然后剥离成AlN纳米片,为生产二维AlN提供了一条潜在的途径。在氢氟酸(HF)中化学蚀刻Al5C3N前驱体,破坏Al-C键并暴露出AlN纳米片。这种合成方法的发展为制备二维AlN和研究其在传感器和微电子领域的独特性能提供了机会。
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引用次数: 0
Near-zero hysteresis van der Waals MnAl2S4 field-effect transistors with low minimal threshold voltage degradation and high thermal stability. 具有低最小阈值电压退化和高热稳定性的近零迟滞范德华MnAl2S4场效应晶体管。
IF 9.6 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-01-01 Epub Date: 2026-01-09 DOI: 10.1038/s43246-025-01020-w
Seyed Mehdi Sattari-Esfahlan, Yury Illarionov, Fang Xu, Alexandros Provias, Saeed Mirzaei, Jan Michalička, Theresia Knobloch, Ondřej Man, Yangbo Zhou, Tibor Grasser

The integration of high-quality, ultrathin van der Waals (vdW) dielectrics with 2D semiconductors remains a critical bottleneck in the development of reliable, ultra-scaled field-effect transistors (FETs). Here, we report a comprehensive study of MoS2-based FETs employing layered rhombohedral MnAl2S4 as the gate insulator, a previously unexplored vdW dielectric that can be isolated down to the monolayer limit. Devices fabricated in both top-gated (TG) and bottom-gated (BT) configurations exhibit excellent electrical performance, featuring low gate leakage, minimal hysteresis ( < 2 mV) under high electric fields up to 11 MV cm-1 across a wide range of gate voltage sweep rates (0.001-10 Vs-1). We observed a consistent counterclockwise hysteresis and an anomalous bias temperature instability (BTI), possibly caused by the diffusion of Mn interstitials and S vacancies formed inside the MnAl2S4 film during growth. Notably, we show that threshold voltage degradation at high temperatures was observed to be negligible, and hysteresis dynamics and very small BTI are reproducible over a long time, demonstrating the high reliability of our devices. In addition, the vdW interface between MnAl2S4 and MoS2 in our device is of good quality and is expected to provide a small density of insulator defects, a promising gate dielectric for reliable 2D devices.

高质量的超薄范德华(vdW)电介质与二维半导体的集成仍然是开发可靠的超尺度场效应晶体管(fet)的关键瓶颈。在这里,我们报告了一项基于mos2的fet的综合研究,采用层状菱形MnAl2S4作为栅极绝缘体,这是一种以前未开发的vdW介电体,可以被隔离到单层极限。采用顶门控(TG)和底门控(BT)结构制造的器件具有优异的电气性能,具有低栅极泄漏,最小磁滞(-1)在宽范围的栅极电压扫描速率(0.001-10 Vs-1)。我们观察到一个一致的逆时针滞后和一个反常的偏置温度不稳定性(BTI),可能是由于Mn间隙的扩散和S空位在MnAl2S4薄膜生长过程中形成的。值得注意的是,我们发现高温下的阈值电压退化可以忽略不计,迟滞动力学和非常小的BTI在很长一段时间内都是可重复的,这证明了我们的设备的高可靠性。此外,我们的器件中MnAl2S4和MoS2之间的vdW接口质量良好,有望提供小密度的绝缘体缺陷,这是一种有前途的栅极介质,用于可靠的2D器件。
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引用次数: 0
Resolving the fundamentals of the J-integral concept by multi-method in situ nanoscale stress-strain mapping. 用多方法原位纳米应力-应变映射解决j积分概念的基本原理。
IF 7.5 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-01-01 Epub Date: 2025-02-22 DOI: 10.1038/s43246-025-00752-z
Michael Meindlhumer, Markus Alfreider, Noel Sheshi, Anton Hohenwarter, Juraj Todt, Martin Rosenthal, Manfred Burghammer, Enrico Salvati, Jozef Keckes, Daniel Kiener

The integrity of structural materials is oftentimes defined by their resistance against catastrophic failure through dissipative plastic processes at the crack tip, commonly quantified by the J-integral concept. However, to date the experimental stress and strain fields necessary to quantify the J-integral associated with local crack propagation in its original integral form were inaccessible. Here, we present a multi-method nanoscale strain- and stress-mapping surrounding a growing crack tip in two identical miniaturized fracture specimens made from a nanocrystalline FeCrMnNiCo high-entropy alloy. The respective samples were tested in situ in a scanning electron microscope and a synchrotron X-ray nanodiffraction setup, with detailed analyzes of loading states during elastic loading, crack tip blunting and general yielding, corroborated by a detailed elastic-plastic finite element model. This complementary in situ methodology uniquely enabled a detailed quantification of the J-integral along different integration paths from experimental nanoscale stress and strain fields. We find that conventional linear-elastic and elastic-plastic models, typically used to interpret fracture phenomena, have limited applicability at micron to nanoscale distances from propagating cracks. This for the first time unravels a limit to the path-independence of the J-integral, which has significant implications in the development and assessment of modern damage-tolerant materials and microstructures.

结构材料的完整性通常由其在裂纹尖端的耗散塑性过程中抵抗灾难性破坏的能力来定义,通常由j积分概念量化。然而,到目前为止,量化与局部裂纹扩展相关的j积分的原始积分形式所需的实验应力场和应变场是无法获得的。在这里,我们在两个相同的由纳米晶FeCrMnNiCo高熵合金制成的小型化断裂样品中,展示了围绕裂纹尖端生长的多方法纳米尺度应变和应力映射。分别在扫描电子显微镜和同步x射线纳米衍射装置上进行了原位测试,详细分析了弹性加载、裂纹尖端钝化和一般屈服的加载状态,并通过详细的弹塑性有限元模型进行了验证。这种互补的原位方法独特地实现了从实验纳米尺度应力和应变场沿不同积分路径的j积分的详细量化。我们发现,通常用于解释断裂现象的传统线弹性和弹塑性模型在距离裂纹扩展的微米至纳米尺度上的适用性有限。这是第一次揭示了j积分的路径独立性的限制,这对现代损伤容忍材料和微结构的开发和评估具有重要意义。
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引用次数: 0
Evaluation of in situ tissue-engineered arteriovenous grafts suitable for cannulation in a large animal model. 在大型动物模型中评估适合插管的原位组织工程动静脉移植物。
IF 7.5 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-01-01 Epub Date: 2025-07-16 DOI: 10.1038/s43246-025-00879-z
Paul J Besseling, Wojciech Szymczyk, Martin Teraa, Raechel J Toorop, Paul A A Bartels, Boris Arts, Rob C H Driessen, Arturo M Lichauco, Hidde C Bakker, Joost O Fledderus, Gert J de Borst, Patricia Y W Dankers, Carlijn V C Bouten, Marianne C Verhaar

The sustainability of vascular access for hemodialysis is limited by frequent interventions and the inability of synthetic grafts to self-heal. Tissue engineering offers a solution through biodegradable grafts that remodel into autologous tissue. Here we assess electrospun polycarbonate-bis urea (PC-BU) vascular scaffolds (6mm-inner-Ø), reinforced with 3D-printed polycaprolactone coils, in a goat model, and compared them to expanded polytetrafluoroethylene (ePTFE) controls. The tissue-engineered grafts were repeatedly cannulated starting two weeks after implantation and were evaluated using computed tomography and histological analyses. By 12 weeks, the PC-BU grafts remodel into autologous tissue while maintaining structural integrity, maintaining integrity without dilations, ruptures, or aneurysms. Cannulation does not interfere with scaffold degradation or neo-tissue formation. Although the patency rate is lower for the PC-BU grafts (50%) compared to ePTFE (100%), the engineered grafts exhibit a self-healing response not seen in ePTFE. These findings demonstrate the potential of PC-BU tissue-engineered grafts as healing, functional vascular access solutions for hemodialysis, supporting cannulation during tissue transformation.

血液透析血管通路的可持续性受到频繁干预和合成移植物不能自愈的限制。组织工程提供了一种解决方案,通过可生物降解的移植物改造成自体组织。在这里,我们在山羊模型中评估了用3d打印聚己内酯线圈增强的电纺聚碳酸酯-双尿素(PC-BU)血管支架(内层6mm -Ø),并将其与膨胀聚四氟乙烯(ePTFE)对照进行了比较。组织工程移植物在植入后两周开始反复插管,并使用计算机断层扫描和组织学分析进行评估。到12周时,PC-BU移植物重塑成自体组织,同时保持结构完整性,保持完整性,无扩张、破裂或动脉瘤。插管不干扰支架降解或新组织形成。尽管与ePTFE(100%)相比,PC-BU移植物的通畅率(50%)较低,但工程移植物表现出ePTFE所没有的自愈反应。这些发现证明了PC-BU组织工程移植物作为血液透析的愈合、功能性血管通路解决方案的潜力,以及在组织转化过程中支持插管的潜力。
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引用次数: 0
Disorder-induced universality and scaling in hole-doped iron-based superconductors. 空穴掺杂铁基超导体的无序诱导普适性和标度。
IF 7.5 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-01-01 Epub Date: 2025-07-10 DOI: 10.1038/s43246-025-00843-x
Omar Chmaissem, Ryan Stadel, Keith M Taddei, Daniel Bugaris, Dmitry D Khalyavin, Pascal Manuel, Duck Young Chung, Mercouri G Kanatzidis, Raymond Osborn, Stephan Rosenkranz

Iron-based superconductors exhibit various magnetic and electronic phases that are highly sensitive to structural and chemical modifications. Elucidating the origins of these phases remains a central challenge. Here, using neutron and x-ray diffraction, we uncover a universal phase diagram that identifies disorder as a hidden tuning parameter governing these phase transitions. By analyzing nine hole-doped phase diagrams, we observe the emergence of a double-Q tetragonal magnetic phase in proximity to ideal FeAs4 tetrahedral configurations, thereby demonstrating a strong link between bond-angle stabilization and magnetic transitions. Beyond stabilizing the double-Q phase, atomic disorder also influences charge doping and magnetic anisotropy. We further observe similar scaling behavior of the transition temperatures of the double-Q and the more prevalent orthorhombic single-Q magnetic phases, evidencing a unified origin of structural and magnetic properties linked to itinerant nesting instability. Our findings establish a comprehensive basis for understanding how chemical disorder, charge doping, and structural features collectively shape the magnetic and superconducting properties of iron-based superconductors.

铁基超导体表现出对结构和化学修饰高度敏感的各种磁相和电子相。阐明这些阶段的起源仍然是一个核心挑战。在这里,使用中子和x射线衍射,我们发现了一个通用相图,将无序识别为控制这些相变的隐藏调谐参数。通过分析9个空穴掺杂相图,我们观察到在理想的FeAs4四面体结构附近出现了双q四面体磁相,从而证明了键角稳定与磁跃迁之间的紧密联系。除了稳定双q相外,原子无序性还影响电荷掺杂和磁各向异性。我们进一步观察到双q相和更普遍的正交单q相的转变温度相似的标度行为,证明了与流动嵌套不稳定性相关的结构和磁性能的统一起源。我们的发现为理解化学无序、电荷掺杂和结构特征如何共同塑造铁基超导体的磁性和超导性奠定了全面的基础。
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引用次数: 0
Stabilization of adhesions controls F-actin architecture in mechanotransduction. 机械转导中粘附的稳定控制f -肌动蛋白结构。
IF 9.6 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-01-01 Epub Date: 2025-12-11 DOI: 10.1038/s43246-025-01006-8
Keith R Carney, Remi Sondaz, Wesley Sturgess, Kabilan Sakthivel, Jungkyu Kim, Vinay Swaminathan, Tamara C Bidone

A cell's ability to sense and respond to the mechanical properties of the extracellular matrix (ECM) is essential for maintaining tissue homeostasis, and its disruption contributes to diseases such as fibrosis, cardiovascular disorders, and cancer. Effective mechanical coupling between the plasma membrane, the underlying filamentous actin (F-actin) cytoskeleton, and integrin-based adhesion complexes (IACs) is required to link ECM mechanics to cell morphology, yet the underlying mechanisms remain incompletely understood. Here, we combine computational modeling and high-resolution imaging to show that integrin-ECM bonds determine F-actin cytoskeleton organization. On soft substrates, short-lived IACs bonds allow rapid actin retrograde flow and dense branching, restricting protrusion and limiting cell spreading. In contrast, stiff substrates or Mn²⁺-mediated integrin activation stabilize adhesions, promote filament alignment, and drive membrane protrusion for cell spreading. These cytoskeletal transitions arise from feedback between adhesion strength and the spatial positioning of the F-actin barbed ends relative to the leading-edge membrane. This positioning determines whether filaments polymerize into linear bundles or branch into dendritic networks, each generating distinct protrusive forces that regulate cell spreading. Collectively, our findings establish integrin-ECM bond stability as a key regulator of F-actin cytoskeleton organization and cell morphology.

细胞感知和响应细胞外基质(ECM)机械特性的能力对于维持组织稳态至关重要,其破坏会导致纤维化、心血管疾病和癌症等疾病。质膜、潜在的丝状肌动蛋白(F-actin)细胞骨架和基于整合素的粘附复合物(IACs)之间需要有效的机械耦合才能将ECM力学与细胞形态联系起来,但其潜在机制仍未完全了解。在这里,我们结合计算模型和高分辨率成像来显示整合素- ecm键决定f -肌动蛋白细胞骨架组织。在软底物上,短寿命的IACs键允许肌动蛋白快速逆行流动和密集分支,限制突出和限制细胞扩散。相比之下,刚性底物或Mn 2 +介导的整合素激活稳定了粘附,促进了纤维排列,并驱动膜突出以促进细胞扩散。这些细胞骨架转变是由粘附强度和f -肌动蛋白倒钩端相对于前缘膜的空间定位之间的反馈引起的。这种定位决定了细丝是聚合成线状束还是分支成树突网络,每一种都产生不同的突出力来调节细胞的扩散。总之,我们的研究结果表明,整合素- ecm键的稳定性是f -肌动蛋白细胞骨架组织和细胞形态的关键调节因子。
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引用次数: 0
Exploring cluster formation in uranium oxidation using high resolution X-ray spectroscopy at elevated temperatures. 利用高分辨率x射线光谱在高温下探索铀氧化中的团簇形成。
IF 7.5 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-01-01 Epub Date: 2025-04-17 DOI: 10.1038/s43246-025-00795-2
Elena F Bazarkina, Stephen Bauters, Yves Watier, Stephan Weiss, Sergei M Butorin, Kristina O Kvashnina

Uranium dioxide (UO2) is a complex material with significant relevance to nuclear energy, materials science, and fundamental research. Understanding its high-temperature behavior is crucial for developing new uranium-based materials and improving nuclear fuel efficiency in nuclear reactors. Here we study the evolution of uranium state during the oxidation of UO2 in air at temperatures up to 550 °C using the in situ X-ray absorption spectroscopy in high energy resolution fluorescence detection mode at the U M4 edge, combined with electronic structure calculations. Our data reveal a complex sequence of events occurring over minutes and hours at elevated temperatures, including changes in the electronic and local structure, 5 f electron occupancy, the formation of U cuboctahedral clusters, and the creation of U4O9 and U3O7 mixed U oxide phases. These findings highlight the fundamental role of clustering processes and pentavalent uranium in both the oxidation process and the stabilization of uranium materials.

二氧化铀(UO2)是一种复杂的材料,与核能、材料科学和基础研究有着重要的关系。了解其高温行为对于开发新的铀基材料和提高核反应堆的核燃料效率至关重要。本文利用高能分辨率荧光检测模式下的原位x射线吸收光谱技术,结合电子结构计算,研究了在高达550℃的温度下UO2在空气中氧化过程中铀态的演变。我们的数据揭示了在高温下发生的一系列复杂事件,包括电子和局部结构的变化,5f电子占用,U立方体簇的形成,以及U4O9和U3O7混合U氧化物相的形成。这些发现突出了聚类过程和五价铀在铀材料氧化过程和稳定化中的基本作用。
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引用次数: 0
Harnessing the bio-adhesive power of natural deep eutectic solvents for trichome-inspired pest control. 利用天然深共晶溶剂的生物粘附力来控制毛虫。
IF 7.5 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-01-01 Epub Date: 2025-05-19 DOI: 10.1038/s43246-025-00823-1
Abinaya Arunachalam, Tim Oosterhoff, Isabel Breet, Peter Dijkstra, Roshan Akdar Mohamed Yunus, Daniele Parisi, Bram Knegt, Mirka Macel, Marleen Kamperman

The carnivorous Drosera species employ hair-like appendages called trichomes that secrete a deadly adhesive consisting of an acidic polysaccharide, sugars, organic acids, and water to capture prey insects. Here, we develop a sustainable alternative to chemical pesticides using hyaluronic acid in a sugar-based natural deep eutectic solvent to mimic the composition and trapping mechanism of the Drosera mucilage. We formulate trichome biomimetic adhesives that become sprayable with added water to lower their viscosity, which can then regain the required adhesiveness as water evaporates up to the equilibrium content. Using a custom indentation setup, we measure promising adhesion energies between 9.5-14.5 µJ over one week, along with the formation of elongated fibrils (>2.3 cm) for the best-performing sample. Additionally, the material shows no phytotoxicity for over two weeks and effectively immobilizes western flower thrips through multiple contact points with the material in Petri dish bioassays, highlighting its efficacy and trapping mechanism akin to natural trichomes.

肉食性的Drosera物种使用毛发状的附属物,称为毛状体,分泌一种由酸性多糖、糖、有机酸和水组成的致命粘合剂来捕获猎物昆虫。在这里,我们开发了一种可持续的化学农药替代品,使用糖基天然深层共熔溶剂中的透明质酸来模拟Drosera粘液的组成和捕获机制。我们配制的毛状体仿生胶黏剂,加入水后可喷洒,以降低其粘度,当水蒸发到平衡含量时,可恢复所需的黏性。使用定制的压痕装置,我们在一周内测量到有希望的粘附能在9.5-14.5µJ之间,同时形成了性能最佳的样品的细长原纤维(>2.3 cm)。此外,该材料在超过两周的时间内没有植物毒性,并且在培养皿生物测定中通过与材料的多个接触点有效地固定了西部花蓟马,突出了其功效和类似于天然毛的捕获机制。
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引用次数: 0
Investigation of hybrid plasmons in a highly crystalline Bi2Se3/C60 heterostructure using low-loss electron energy loss spectroscopy. 利用低损耗电子能量损失光谱研究高结晶Bi2Se3/C60异质结构中的杂化等离子体。
IF 9.6 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-01-01 Epub Date: 2025-07-29 DOI: 10.1038/s43246-025-00886-0
Mairi McCauley, Lida Ansari, Farzan Gity, Matthew Rogers, Joel Burton, Satoshi Sasaki, Quentin Ramasse, Craig Knox, Paul K Hurley, Donald MacLaren, Timothy Moorsom

Topological Insulators (TIs) present an interesting materials platform for nanoscale, high frequency devices because they support high mobility, low scattering electronic transport within confined surface states. However, a robust methodology to control the properties of surface plasmons in TIs has yet to be developed. Surface doping of TIs with molecules may provide tunable control of the two-dimensional plasmons in Bi2Se3, but exploration of such heterostructures is still at an early stage and usually confined to monolayers. We have grown heterostructures of Bi2Se3/C60 with exceptional crystallinity. Electron energy loss spectroscopy (EELS) reveals significant hybridisation of π states at the interface, despite the expectation for only weak van der Waals interactions, including quenching of 2D plasmons. Momentum-resolved EELS measurements are used to probe the plasmon dispersion, with Density Functional Theory predictions providing an interpretation of results based on interfacial charge dipoles. This work provides growth methodology and characterization of highly crystalline TI/molecular interfaces that can be engineered for plasmonic applications in energy, communications and sensing.

拓扑绝缘体(TIs)为纳米级高频器件提供了一个有趣的材料平台,因为它们支持高迁移率,在受限表面状态下的低散射电子输运。然而,一种强有力的方法来控制表面等离子体在ti中的性质尚未开发。分子表面掺杂ti可以提供对Bi2Se3中二维等离子体激元的可调控制,但对这种异质结构的探索仍处于早期阶段,通常仅限于单层。我们已经培养出具有优异结晶度的Bi2Se3/C60异质结构。电子能量损失谱(EELS)揭示了界面上π态的显著杂化,尽管预期只有弱范德华相互作用,包括二维等离子体的猝灭。动量分辨EELS测量用于探测等离子体色散,密度泛函理论预测提供了基于界面电荷偶极子的结果解释。这项工作提供了高结晶TI/分子界面的生长方法和表征,可用于能源,通信和传感领域的等离子体应用。
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引用次数: 0
Evaluation of radiochromic formulations for dosimetry in high-energy photon and proton beams. 高能光子和质子束剂量测定用放射致色配方的评价。
IF 9.6 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-01-01 Epub Date: 2025-11-19 DOI: 10.1038/s43246-025-00978-x
Rohith Kaiyum, Cornelia Hoehr, Sebastian Tattenberg, Rachel L Shum, Ozzy Mermut, Alexandra Rink

Radiochromic crystals have many suitable features for dosimetry across a broad range of radiotherapy modalities, yet the study of these materials within the medical physics community has been limited. Here, we study three types of radiochromic pentacosa-10,12-diynoic acid-based formulations: two analogues of commercially available materials and one newly developed. Formulations coated on polyethylene are irradiated with photon (6 and 10 MV) and proton (74 MeV) beams (0-25 Gy) using custom fibre-optic setups that enable real-time transmission measurements at 1.5-2 cm depth to maintain dosimetric accuracy. The dose response to ionizing radiation is compared between the formulations and all formulations were characterized using a variety of analytical methods. The response of radiochromic crystals to ionizing radiation is complex and influenced by factors such as monomer composition and resulting macroscopic crystal morphology. By optimizing these parameters, it could be possible to develop dosimeters suitable for a variety of clinical applications.

放射性致色晶体具有许多适用于多种放射治疗方式的剂量学特征,但医学物理学界对这些材料的研究一直受到限制。在这里,我们研究了三种类型的放射性变色五甲酸-10,12-二甲酸基配方:两种市售材料的类似物和一种新开发的。涂层在聚乙烯上的配方使用定制的光纤装置,用光子(6和10 MV)和质子(74 MeV)光束(0-25 Gy)照射,实现1.5-2厘米深度的实时传输测量,以保持剂量学精度。比较了各剂型对电离辐射的剂量响应,并用各种分析方法对各剂型进行了表征。放射性致色晶体对电离辐射的响应是复杂的,受单体组成和由此产生的宏观晶体形态等因素的影响。通过优化这些参数,有可能开发出适合各种临床应用的剂量计。
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引用次数: 0
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