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Silicon (100) surface passivation-driven tuning of Ag film crystallinity and its impact on the performance of Ag/n-Si mid-infrared Schottky photodetector 硅 (100) 表面钝化驱动的银膜结晶度调整及其对 Ag/n-Si 中红外肖特基光电探测器性能的影响
IF 6.1 2区 材料科学 Q1 Engineering Pub Date : 2024-06-01 DOI: 10.1063/5.0214341
Krishna Hari Sharma, Yao-Han Dong, Po-Hsien Chiang, Zih-Chun Su, Ching-Fuh Lin
The utilization of metal/semiconductor Schottky devices for plasmonic harvesting of hot carriers holds immense potential in the field of sub-bandgap photodetection. In this work, we explore a surface passivation scheme using air plasma exposure to modify the Si (100) surface and subsequently the crystal orientation of the deposited Ag film for photon detection in the mid-infrared (MIR) regime. This tailoring was achieved by varying the plasma exposure duration (0, 150, 300, 450, and 600 s). As a result, we could tune the crystal orientation of Ag from the (200) to the (210) crystal plane, with the Ag (111) orientation present in all devices. Furthermore, the photo-response behavior under MIR exposure at λ = 4.2 µm was studied both experimentally and using COMSOL simulations. It was observed that both photoelectric (PE) and photothermal (PT) effects contributed to the photo-response behavior of all devices. The Ag/Si device exposed to air plasma for 300 s exhibited the maximum PE-driven response (2.73 µA/W), while the device exposed to air plasma for 600 s showed a significant PT-driven response (13.01 µA/W). In addition, this strategy helped reduce the reverse leakage current by up to 99.5%. This study demonstrates that MIR detection at longer wavelengths can be optimized by tailoring the crystal orientation of the metal film.
利用金属/半导体肖特基器件进行热载流子的等离子收集,在亚带隙光子探测领域具有巨大的潜力。在这项工作中,我们探索了一种表面钝化方案,利用空气等离子体曝光来改变硅(100)表面,进而改变沉积银薄膜的晶体取向,以实现中红外(MIR)波段的光子探测。这种定制是通过改变等离子体曝光持续时间(0、150、300、450 和 600 秒)来实现的。因此,我们可以调整银的晶体取向,从(200)晶面到(210)晶面,所有器件中的银取向均为(111)。此外,我们还通过实验和 COMSOL 仿真研究了在 λ = 4.2 µm 的中红外光照射下的光响应行为。结果表明,光电(PE)和光热(PT)效应对所有器件的光反应行为都有影响。暴露在空气等离子体中 300 秒的 Ag/Si 器件表现出最大的 PE 驱动响应(2.73 µA/W),而暴露在空气等离子体中 600 秒的器件则表现出显著的 PT 驱动响应(13.01 µA/W)。此外,这种策略还有助于减少高达 99.5% 的反向漏电流。这项研究表明,可以通过调整金属膜的晶体取向来优化较长波长的近红外检测。
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引用次数: 0
Relationship between structure and charge/orbital order in epitaxial single layer Ruddlesden–Popper manganite thin films 外延单层 Ruddlesden-Popper 锰矿薄膜的结构与电荷/轨道之间的关系
IF 6.1 2区 材料科学 Q1 Engineering Pub Date : 2024-06-01 DOI: 10.1063/5.0208123
Christoph Flathmann, Tobias Meyer, U. Ross, Annika Dehning, Christian Jooss, M. Seibt
Ruddlesden–Popper manganites are strongly correlated, quasi two-dimensional systems with highly tunable functional properties, which can, for example, be controlled by composition, strain, and defects. Praseodymium calcium manganite is a particularly interesting Ruddlesden–Popper system due to its remarkably high temperature at which ordering phenomena set in, enabling correlation physics above room temperature. However, in order to utilize the correlation phenomena and the quasi-two-dimensionality of the Ruddlesden–Popper systems for applications, one needs to grow thin film junctions, making it necessary to control the structure–property relation of Ruddlesden–Popper thin films. Here, we present a cryogenic transmission electron microscopy study of praseodymium calcium manganite thin films, deposited on niobium doped strontium titanate substrates, where we analyze the structure of the manganite thin film, as well as the effect of the epitaxial strain and defects on the charge/orbital order of the system. We identify a structural phase transition above the onset of charge/orbital order, frequently occurring extended defects and the temperature dependence and spatial distribution of charge/orbital ordering in the film. Our results show in detail the relationships between strain/defects and properties of the ordered phases and thus give important insights into how to tailor the functional properties of thin film junctions of strongly correlated materials.
Ruddlesden-Popper 锰矿是强相关的准二维系统,具有高度可调的功能特性,例如,可以通过成分、应变和缺陷来控制。镨锰钙锰矿是一种特别有趣的 Ruddlesden-Popper 系统,因为它的有序现象是在极高的温度下产生的,从而实现了室温以上的相关物理学。然而,为了利用相关现象和 Ruddlesden-Popper 系统的准二维性进行应用,我们需要生长薄膜结,因此有必要控制 Ruddlesden-Popper 薄膜的结构-性能关系。在此,我们介绍了在掺铌钛酸锶基底上沉积的镨钙锰矿薄膜的低温透射电子显微镜研究,分析了锰矿薄膜的结构,以及外延应变和缺陷对系统电荷/轨道的影响。我们确定了电荷/轨道有序开始时的结构相变、经常出现的扩展缺陷以及薄膜中电荷/轨道有序的温度依赖性和空间分布。我们的研究结果详细显示了应变/缺陷与有序相特性之间的关系,从而为如何定制强相关材料薄膜结的功能特性提供了重要启示。
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引用次数: 0
Flexible water-resistant bamboo-like perovskite-embedded polymer nano/microfibers exhibiting Fabry–Pérot lasing 显示法布里-佩罗激光的柔性防水竹节状包覆过氧化物聚合物纳米/微纤维
IF 6.1 2区 材料科学 Q1 Engineering Pub Date : 2024-06-01 DOI: 10.1063/5.0200465
Hsin-Ming Cheng, You-Jia Pang, Chia-Kai Lin, Sheng‐Chan Wu, Bo-Zhu You, Jung‐Yao Chen, Hsu-Cheng Hsu
Methylammonium lead bromide perovskite (MAPbBr3)-embedded nano- and micro-fibers are successfully fabricated by using the uniaxial electrospinning technique. Through the study of solidification and coordination between perovskite with hybrid polymers, polymethyl methacrylate, and polyacrylonitrile, the bamboo-like perovskite-embedded polymer nano/microfibers are unpredictably formed. Encapsulated in polymer, the passive perovskite-embedded polymer fibers exhibit a long-term fluorescence performance when simultaneously exposed to both water immersion and short-wavelength laser irradiation. Notably, due to the efficient gain media, the perovskite-rich region of the electrospun fiber can act as an optical microcavity. Multi-mode and single-mode lasing behaviors can be achieved via different cavity lengths. The mechanism of a microlaser within this perovskite fiber is confirmed through a Fabry–Pérot cavity, which provides an opportunity for optical components in lasers.
利用单轴电纺丝技术,成功制备出了包埋甲基溴化铅闪长岩(MAPbBr3)的纳米和微纤维。通过对包晶石与混合聚合物、聚甲基丙烯酸甲酯和聚丙烯腈的凝固和配位的研究,不可预知地形成了竹节状的包埋包晶石聚合物纳米/微纤维。被聚合物包裹的无源包埋闪长岩聚合物纤维在同时暴露于水浸泡和短波长激光照射的情况下具有长期荧光性能。值得注意的是,由于存在高效增益介质,电纺光纤中富含透辉石的区域可以充当光学微腔。通过不同的腔长可以实现多模和单模激光行为。通过法布里-佩罗腔,证实了该包晶光纤中的微激光机制,这为激光器中的光学元件提供了机会。
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引用次数: 0
Duality of a coiled phononic crystal enables reflectionless interfaces 盘绕声子晶体的双重性实现了无反射界面
IF 6.1 2区 材料科学 Q1 Engineering Pub Date : 2024-06-01 DOI: 10.1063/5.0200887
C. L. Willey, V. Chen, A. Juhl
Recently, it has been demonstrated that one-dimensional bar-based phononic crystals can exhibit subwavelength Bragg bandgaps by coiling the bars and locking the nodal rotational degrees of freedom to create what is termed a coiled phononic crystal (CPnC) [C. L. Willey et al., Phys. Rev. Appl. 18, 014035 (2022)]. Here, it is shown that the CPnC exhibits duality of its dispersion curves relative to its coiling/twist angle, meaning that the dispersion curves are symmetric about a particular coiling/twist angle defined configuration. An exciting implication of this finding is that under a certain set of constraints, segments of dual unit cells with perpendicular wave propagation directions can be connected such that their wave transmission is equivalent to a finite CPnC entirely composed of identical unit cells with parallel wave propagation directions. The ability to link unit cells with different wave propagation orientations, but the same dispersion/dynamic stiffness, is used to create an elastic hierarchically coiled phononic crystal based on a fractal space-filling curve design. The novelty of this work is that it numerically demonstrates reflectionless wave propagation in large fractal architectures (created from specific combinations of dual unit cells) such that regular phononic properties (i.e., passbands and bandgaps) are preserved, allowing for propagation of broadband signals and filtering.
最近,有研究表明,一维棒状声子晶体可以通过卷绕棒状物并锁定节点旋转自由度来产生所谓的卷绕声子晶体(CPnC),从而表现出亚波长布拉格带隙[C. L. Willey 等人,Phys.这里的研究表明,CPnC 的色散曲线相对于其卷曲/扭转角度具有二重性,这意味着色散曲线对于特定卷曲/扭转角度定义的构型是对称的。这一发现的一个令人兴奋的含义是,在一定的约束条件下,可以将波传播方向垂直的双单元单元连接起来,使它们的波传输等同于一个完全由波传播方向平行的相同单元单元组成的有限 CPnC。利用连接波传播方向不同但色散/动态刚度相同的单元格的能力,可以在分形空间填充曲线设计的基础上创建弹性分层盘绕声子晶体。这项研究的新颖之处在于,它以数值方式证明了波在大型分形结构(由特定的双单元格组合而成)中的无反射传播,从而保留了规则的声波特性(即通带和带隙),使宽带信号的传播和滤波成为可能。
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引用次数: 0
High-temperature insulating ferromagnetic state in charge-disproportionated and spin-state-disproportionated strained SrCoO2.5 thin film 电荷不成比例和自旋态不成比例应变 SrCoO2.5 薄膜中的高温绝缘铁磁态
IF 6.1 2区 材料科学 Q1 Engineering Pub Date : 2024-05-30 DOI: 10.1063/5.0188767
Sourav Chowdhury, Anupam Jana, Ritu Rawat, Priyanka Yadav, Rajibul Islam, Fei Xue, A. K. Mandal, Sumit Sarkar, Rajan Mishra, R. Venkatesh, D. M. Phase, R. J. Choudhary
Ferromagnetic insulators (FMIs) have widespread applications in microwave devices, magnetic tunneling junctions, and dissipationless electronic and quantum-spintronic devices. However, the sparsity of the available high-temperature FMIs has led to the quest for a robust and controllable insulating ferromagnetic state. Here, we present compelling evidence of modulation of the magnetic ground state in a SrCoO2.5 (SCO) thin film via strain engineering. The SCO system is an antiferromagnetic insulator with a Neel temperature, TN, of ∼550 K. Applying in-plane compressive strain, the SCO thin film reveals an insulating ferromagnetic state with an extraordinarily high Curie temperature, TC, of ∼750 K. The emerged ferromagnetic state is associated with charge-disproportionation (CD) and spin-state-disproportionation (SSD), involving high-spin Co2+ and low-spin Co4+ ions. The density functional theory calculation also produces an insulating ferromagnetic state in the strained SCO system, consistent with the CD and SSD, which is associated with the structural ordering in the system. Transpiring the insulating ferromagnetic state through modulating the electronic correlation parameters via strain engineering in the SCO thin film will have a significant impact in large areas of modern electronic and spintronic applications.
铁磁绝缘体(FMIs)在微波设备、磁隧道结、无耗散电子设备和量子自旋电子设备中有着广泛的应用。然而,由于现有高温铁磁绝缘体的稀缺性,人们开始寻求一种稳健、可控的绝缘铁磁态。在这里,我们提出了通过应变工程调制 SrCoO2.5 (SCO) 薄膜磁基态的有力证据。SCO 系统是一种反铁磁绝缘体,其 Neel 温度(TN)为 ∼550 K。施加面内压应变后,SCO 薄膜显示出一种绝缘铁磁态,其居里温度(TC)超高,达到 ∼750 K。密度泛函理论计算还得出了应变 SCO 系统中的绝缘铁磁态,与 CD 和 SSD 相一致,这与系统中的结构有序性有关。通过应变工程调控 SCO 薄膜中的电子相关参数来激发绝缘铁磁态,将对现代电子和自旋电子应用领域产生重大影响。
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引用次数: 0
Reciprocal space x-ray computed tomography 对等空间 X 射线计算机断层扫描
IF 6.1 2区 材料科学 Q1 Engineering Pub Date : 2024-05-30 DOI: 10.1063/5.0203995
Arturas Vailionis, Liyan Wu, Jonathan E. Spanier
Three-dimensional reciprocal space mapping (3D-RSM) offers crucial insights into the intricate microstructural properties of materials, including spatial domain distribution, directional long-range ordering, multilayer-substrate mismatch, layer tilting, and defect structure. Traditionally, 3D-RSMs are conducted at synchrotron facilities where instrumental resolution is constrained in all three directions. Lab-based sources have often been considered suboptimal for 3D-RSM measurements due to poor instrumental resolution along the axial direction. However, we demonstrate that, by employing three-dimensional reciprocal space x-ray computed tomography (RS-XCT), the same perceived limitation in resolution can be effectively leveraged to acquire high quality 3D-RSMs. Through a combination of ultrafast reciprocal space mapping and computed tomography reconstruction routines, lab-based 3D-RSMs achieve resolutions comparable to those obtained with synchrotron-based techniques. RS-XCT introduces a practical modality for lab-based x-ray diffractometers, enabling high-resolution 3D-RSM measurements on a variety of materials exhibiting complex three-dimensional scattering landscapes in reciprocal space.
三维倒易空间制图(3D-RSM)可帮助人们深入了解材料错综复杂的微观结构特性,包括空间畴分布、定向长程有序、多层衬底错配、层倾斜和缺陷结构。传统上,3D-RSM 是在同步辐射设施中进行的,在同步辐射设施中,仪器在所有三个方向上的分辨率都受到限制。由于沿轴向的仪器分辨率较低,基于实验室的光源通常被认为是 3D-RSM 测量的次优选择。然而,我们证明,通过采用三维往复空间 X 射线计算机断层扫描 (RS-XCT),可以有效地利用同样的分辨率限制来获取高质量的三维 RSM。通过结合超快倒易空间映射和计算机断层扫描重建程序,基于实验室的三维 RSM 可达到与同步加速器技术相媲美的分辨率。RS-XCT 为基于实验室的 X 射线衍射仪引入了一种实用模式,可对在倒易空间呈现复杂三维散射景观的各种材料进行高分辨率 3D-RSM 测量。
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引用次数: 0
Impact of sulfur addition on the structure and dynamics of Ni–Nb alloy melts 加硫对 Ni-Nb 合金熔体结构和动力学的影响
IF 6.1 2区 材料科学 Q1 Engineering Pub Date : 2024-05-29 DOI: 10.1063/5.0205058
Nicolai Grund, Dirk Holland-Moritz, Saba Khademorezaian, Lucas P. Kreuzer, Nico Neuber, Lucas M. Ruschel, Hendrik Voigt, Johanna Wilden, Fan Yang, Soham Banerjee, Malte Blankenburg, Ann-Christin Dippel, Jan Peter Embs, Sergiy Divinski, Ralf Busch, Andreas Meyer, Gerhard Wilde
We investigated the change in the structure and dynamics of a Ni–Nb bulk metallic glass upon sulfur addition on both microscopic and macroscopic scales. With the sulfur concentration of 3 at. %, where the composition Ni58Nb39S3 exhibits the best glass forming ability in the investigated sulfur concentration range, both the equilibrium and undercooled melt dynamics remain almost unchanged. Only in the glassy state does sulfur seem to result in mass transport less decoupled to the viscosity of the undercooled liquid, where the measured Ag tracer diffusion coefficient is slower in the ternary alloy. With the structural disorder introduced by the alloying sulfur, the improved glass forming ability is attributed to geometrical frustration, where crystal nucleation requires a depletion of sulfur and hence long range diffusion, as long as no primary sulfur-containing crystalline phase is involved.
我们从微观和宏观两个尺度研究了 Ni-Nb 块状金属玻璃在添加硫后的结构和动力学变化。硫浓度为 3 at.%时,平衡和欠冷熔体动力学几乎保持不变。只有在玻璃态时,硫似乎才会导致质量传输与过冷液体粘度的脱钩程度降低,在三元合金中测量到的银示踪剂扩散系数较慢。由于合金中的硫造成了结构紊乱,玻璃形成能力的提高归因于几何挫折,在这种情况下,只要不涉及原生含硫结晶相,晶体成核就需要硫的耗竭,从而导致长程扩散。
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引用次数: 0
Development of one-step roll-to-roll system with incorporated vacuum sputtering for large-scale production of plasmonic sensing chips 开发用于大规模生产等离子传感芯片的一步式卷对卷系统,其中包含真空溅射技术
IF 6.1 2区 材料科学 Q1 Engineering Pub Date : 2024-05-29 DOI: 10.1063/5.0211084
Tae Eon Kim, Sunghoon Jung, Soo Hyun Lee, ChaeWon Mun, Eun-Yeon Byeon, Jun-Yeong Yang, Jucheol Park, Seunghun Lee, Heemin Kang, Sung-Gyu Park
The trade-off relationship between cost and performance is a major challenge in the development of surface-enhanced Raman spectroscopy (SERS) sensors for practical applications. We propose a roll-to-roll system with incorporated vacuum sputtering to manufacture Ag-coated nanodimples (Ag/NDs) on A4-scale films in a single step. The Ag/ND SERS platforms were prepared via O2 ion beam sputtering and Ag sputtering deposition. The concave three-dimensional spaces in the Ag/NDs functioned as hotspots, and their optimal fabrication conditions were investigated with two variables: moving speed and Ag thickness. The entire process was automated, which resulted in highly consistent optical responses (i.e., relative standard deviation of ∼10%). The activation of plasmonic hotspots was demonstrated by electric-field profiles calculated via the finite-difference time-domain method. The wavelength dependency of the Ag/ND platforms was also examined by dark-field microscopy. The results indicate that the developed engineering technique for the large-scale production of Ag/ND plasmonic chips would likely be competitive in the commercial market.
在开发实际应用的表面增强拉曼光谱(SERS)传感器时,成本与性能之间的权衡关系是一大挑战。我们提出了一种结合真空溅射的辊对辊系统,可在 A4 级薄膜上一步制备 Ag 涂层纳米微粒(Ag/ND)。Ag/ND SERS 平台是通过 O2 离子束溅射和 Ag 溅射沉积制备的。Ag/ND 中的凹面三维空间起到了热点的作用,通过两个变量:移动速度和 Ag 厚度,研究了其最佳制备条件。整个过程都是自动化的,因此产生了高度一致的光学响应(即相对标准偏差∼10%)。通过有限差分时域法计算的电场曲线证明了等离子热点的激活。此外,还通过暗场显微镜检查了 Ag/ND 平台的波长依赖性。结果表明,所开发的大规模生产 Ag/ND 等离子芯片的工程技术很可能在商业市场上具有竞争力。
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引用次数: 0
Speed limits of the laser-induced phase transition in FeRh 激光诱导 FeRh 相变的速度极限
IF 6.1 2区 材料科学 Q1 Engineering Pub Date : 2024-05-28 DOI: 10.1063/5.0206095
M. Mattern, J. Jarecki, J. A. Arregi, V. Uhlíř, M. Rössle, M. Bargheer
We use ultrafast x-ray diffraction and the polar time-resolved magneto-optical Kerr effect to study the laser-induced metamagnetic phase transition in two FeRh films with thicknesses below and above the optical penetration depth. In the thin film, we identify an intrinsic timescale for the light-induced nucleation of ferromagnetic (FM) domains in the antiferromagnetic material of 8ps, which is substantially longer than the time it takes for strain waves to traverse the film. For the inhomogeneously excited thicker film, only the optically excited near-surface part transforms within 8ps. For strong excitations, we observe an additional slow rise of the FM phase, which we experimentally relate to a growth of the FM phase into the depth of the layer by comparing the transient magnetization in frontside and backside excitation geometry. In the lower lying parts of the film, which are only excited via near-equilibrium heat transport, the FM phase emerges significantly slower than 8ps after heating above the transition temperature.
我们利用超快 X 射线衍射和极地时间分辨磁光克尔效应,研究了厚度低于和高于光学穿透深度的两层 FeRh 薄膜中激光诱导的元磁相变。在薄膜中,我们确定了反铁磁材料中铁磁(FM)畴的光诱导成核的固有时间尺度为 8ps,大大长于应变波穿过薄膜所需的时间。对于不均匀激发的较厚薄膜,只有光学激发的近表面部分会在 8ps 内发生转变。对于强激励,我们观察到调频相的额外缓慢上升,通过比较正面和背面激励几何形状下的瞬态磁化,我们在实验中将其与调频相向膜层深处的增长联系起来。在薄膜的低层部分,仅通过近平衡热传导激发,调频相在加热到转变温度以上后出现的速度明显慢于 8ps。
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引用次数: 0
Effective polysulfide control in lithium–sulfur batteries utilizing BiFeO3 nanoparticles 利用 BiFeO3 纳米粒子有效控制锂硫电池中的多硫化物
IF 6.1 2区 材料科学 Q1 Engineering Pub Date : 2024-05-28 DOI: 10.1063/5.0209845
Mohan K. Bhattarai, Balram Tripathi, Shweta Shweta, Satyam Kumar, Claudia C. Zuluaga-Gómez, Rajesh K. Katiyar, Brad R. Weiner, Ram S. Katiyar, Gerardo Morell
Lithium–sulfur batteries (LiSBs) offer high energy density, cost-effectiveness, and eco-friendliness, making them promising for future energy storage. This study explores using BiFeO3 (BFO) nanoparticles (NPs) to tackle challenges such as lithium polysulfides (LiPs) and shuttle issues in LiSBs. It employs a solid-state melt diffusion technique, encapsulates sulfur in single-walled carbon nanotubes (SCNTs), and utilizes BFO for effective polysulfide control. Herein, composite cathodes of sulfur (S)/SCNTs (abbr. SCNT) were fabricated, and cells were designed using a BFO-coated separator (SCNT-BFS). In addition, a cathode modification was performed with composite S/SCNTs/BFO (SCNT-BF), and a comparative analysis was conducted to assess the effectiveness of the BFO in the separator and the cathode. Cyclic voltammetry measurements revealed that the increased current peak intensity at lower reduction potential in SCNT-BF and SCNT-BFS indicated control of higher-order LiPs (Li2Sx, where 4 ≤ x ≤ 8), resulting in the generation of more stable lower-order products (Li2S2/Li2S). The charge/discharge analysis revealed controlled LiPs, resulting in high-capacity retention in SCNT-BF (∼75%) and SCNT-BFS (∼88%) over 200 cycles, which yielded capacities of 526 and 700 mAh/g at C/8 (1C = 1675 mA/g). These promising results suggest that incorporating BFO into the cathode and separator can advance the commercialization of durable LiSBs.
锂硫电池(LiSBs)具有能量密度高、成本效益高和生态友好的特点,因此在未来的能源存储中大有可为。本研究探讨了如何利用 BiFeO3(BFO)纳米粒子(NPs)来应对锂多硫化物(LiPs)和锂硫电池中的穿梭问题等挑战。该研究采用固态熔融扩散技术,将硫封装在单壁碳纳米管(SCNT)中,并利用 BFO 有效控制多硫化物。本文制备了硫(S)/单壁碳纳米管(SCNT)复合阴极,并设计了使用 BFO 涂层隔膜(SCNT-BFS)的电池。此外,还使用 S/SCNTs/BFO 复合材料(SCNT-BF)对阴极进行了改性,并进行了对比分析,以评估 BFO 在隔膜和阴极中的有效性。循环伏安法测量结果表明,SCNT-BF 和 SCNT-BFS 在较低还原电位下的电流峰值强度增加,表明高阶锂聚合物(Li2Sx,其中 4 ≤ x ≤ 8)受到控制,从而生成了更稳定的低阶产物(Li2S2/Li2S)。充电/放电分析表明,受控的 LiPs 使 SCNT-BF(∼75%)和 SCNT-BFS(∼88%)在 200 次循环中保持高容量,在 C/8 条件下(1C = 1675 mA/g),容量分别为 526 和 700 mAh/g。这些充满希望的结果表明,在阴极和分离器中加入 BFO 可以推动耐用锂电池的商业化。
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引用次数: 0
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