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Extraction of uranium from water: A strategy based on tribocatalysis 从水中提取铀:基于摩擦催化的策略
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-09-28 DOI: 10.1016/j.materresbull.2024.113109
Baoyi Liu , Shuo Zhang , Zihao Ye , Feixue Gao , Peng Zhao , Ming Fang , Bin Ma , Kangle Shang , Xiaoli Tan
Due to most of the U(VI) extraction methods suffering the issues of high cost and low efficiency, finding a new method is still urgent. In this work, we report a way to remove U(VI) from water by tribocatalysis, where a natural mineral of attapulgite is used as the tribocatalyst. By a careful investigation, it is confirmed that the ultrasonic-generated microbubbles rub with the attapulgite to form free radicals of h+, ·O2-, and ·OH, which could then be transformed to H2O2 to react with U(VI) to form UO2O2. The extraction rate of U(VI) from water is up to 87.88% (50 ppm) in 200 min. This work using the natural mineral attapulgite being tribocatalyst has the advantages of low cost and high efficiency, which also provide new insight into the conversion of U(VI) in natural conditions and will have great potential in the treatment of nuclide wastewater and seawater.
由于大多数 U(VI)萃取方法都存在成本高、效率低的问题,因此寻找一种新的方法仍然迫在眉睫。在这项工作中,我们报告了一种通过摩擦催化去除水中六价铀的方法,其中使用了一种天然矿物阿塔蓬石作为摩擦催化剂。通过仔细研究证实,超声波产生的微气泡与阿塔蓬石摩擦形成 h+、-O2- 和 -OH 自由基,然后这些自由基可转化为 H2O2,与 U(VI)反应生成 UO2O2。在 200 分钟内,从水中萃取铀(VI)的比率高达 87.88%(50 ppm)。这项利用天然矿物阿塔波来石作为摩擦催化剂的研究具有成本低、效率高的优点,同时也为自然条件下的铀(VI)转化提供了新的见解,在核素废水和海水处理方面具有巨大的潜力。
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引用次数: 0
NiMoO4@NiSe2 microspheres as electrode materials for high-performance supercapacitor 作为高性能超级电容器电极材料的 NiMoO4@NiSe2 微球
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-09-28 DOI: 10.1016/j.materresbull.2024.113113
Xinyu Huai , Dengke Wang , Xiang Wu , Jinghai Liu
Supercapacitors as novel sustainable energy conversion systems have been a hot spot owing to their high specific capacitance and excellent cycle stabilities. However, the poor electron conductivity limits their further applications. Herein, we synthesize NiMoO4@NiSe2 samples by a controllable hydrothermal route. The heterogeneous structure consists of high conductive nanosheets and high capacitive particles. It can slow down the collapse of electrode materials and enhance the conductivity of material. It also facilitates ion diffusion and faradaic redox reaction, thereby improves the electrochemical performance. The as-synthesized electrode presents a specific capacity of 1193 C g-1 at 1 A g-1 and maintains 82.9 % of the initial capacitance after 10,000 times cycles. A hybrid capacitor is constructed using the composites as the electrode material. It possesses a capacitance of 101 C g-1 at 1 A g-1 and 85.8 % of the retention rate after 10,000 times charging-discharging. This impressive performance of composite could be attributed to their mesoporous surface with high specific surface area (48 m2g-1). Moreover, the supercapacitor shows excellent flexibility after folding, exhibiting a wide application prospect in the field of supercapacitors.
超级电容器作为新型的可持续能源转换系统,因其高比电容和出色的循环稳定性而成为热点。然而,较差的电子传导性限制了它们的进一步应用。在此,我们采用可控的水热法合成了 NiMoO4@NiSe2 样品。这种异质结构由高导电性纳米片和高电容性颗粒组成。它可以减缓电极材料的塌陷,增强材料的导电性。它还能促进离子扩散和法拉第氧化还原反应,从而提高电化学性能。在 1 A g-1 的条件下,合成电极的比容量为 1193 C g-1,循环 10,000 次后仍能保持初始电容的 82.9%。使用这种复合材料作为电极材料构建了一种混合电容器。它在 1 A g-1 时的电容为 101 C g-1,在 10,000 次充放电后的电容保持率为 85.8%。复合材料之所以能取得如此优异的性能,是因为其具有高比表面积(48 m2g-1)的介孔表面。此外,该超级电容器在折叠后具有极佳的柔韧性,在超级电容器领域具有广阔的应用前景。
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引用次数: 0
Facile one-step fabrication of Li4Ti5O12 coatings by suspension plasma spraying 通过悬浮等离子喷涂一步法轻松制备 Li4Ti5O12 涂层
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-09-27 DOI: 10.1016/j.materresbull.2024.113111
Sribalaji Mathiyalagan , Stefan Björklund , Sandra Johansson Storm , Girish Salian , Ronan Le Ruyet , Reza Younesi , Shrikant Joshi
Spinel Li4Ti5O12 (LTO) is a promising anode material for solid state thin film batteries (SSTB) due to its almost-zero volume change and promising Li-ion mobility. However, preparing LTO anodes for SSTB demands tedious vacuum-based processing steps that are not cost effective. In this context, the present study embarks on evaluating the versatile suspension plasma spraying (SPS) approach to fabricate LTO coatings without using any binder. The microstructure and stoichiometry of the fabricated LTO coatings developed through the SPS route reveals retention of ∼76 wt.% of the spinel LTO from the starting feedstock, with minor amounts of rutile and anatase TiO2. The SPS experiments yielded varying thickness build up rates of the LTO coatings depending on the processing parameters adopted. The electrochemical data of the produced LTO based electrode tested in a half-cell through galvanostatic cycling show reversible lithiation and delithiation at expected potential, thereby validating the promise of the SPS technique for potential fabrication of SSTB components once fully optimized.
尖晶石 Li4Ti5O12(LTO)由于其几乎为零的体积变化和良好的锂离子迁移率,是一种很有前途的固态薄膜电池(SSTB)阳极材料。然而,制备用于 SSTB 的 LTO 阳极需要繁琐的真空处理步骤,成本效益不高。在这种情况下,本研究开始评估多功能悬浮等离子喷涂(SPS)方法,以在不使用任何粘合剂的情况下制造 LTO 涂层。通过 SPS 方法制备的 LTO 涂层的微观结构和化学计量显示,起始原料中保留了 76 wt.% 的尖晶石 LTO,以及少量金红石型和锐钛型 TiO2。根据所采用的加工参数,SPS 实验产生了不同厚度的 LTO 涂层。所生产的基于 LTO 的电极在半电池中通过电静力循环测试的电化学数据显示,在预期电位下可发生可逆的锂化和脱锂,从而验证了 SPS 技术在充分优化后用于制造 SSTB 组件的前景。
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引用次数: 0
Size dependence of electrical resistivity caused by stress-induced rejuvenation for metallic glassy microfibers 金属玻璃微纤维应力诱导再生引起的电阻率尺寸依赖性
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-09-27 DOI: 10.1016/j.materresbull.2024.113112
B. Huang, H. Lv, J. Yi, Q. Wang, G. Wang
In this paper, we investigate the electrical transport properties of Zr-, La- and Pd-based metallic glassy fibers (MGFs) with diameters at microscale, which are fabricated by superplastic deformation at high temperatures. It is found that with the decrease of the diameter, the resistivity of the MGF increases with decreasing temperature more quickly. As compared to the thicker one, the structure of the thinner MGF is more strongly rejuvenated with a larger relaxation enthalpy, a larger average short-range atomic distance and less crystal-like structure induced by the larger normal stress during its formation process. Based on the evolution of the heterogeneous structure, the dependence of electrical resistivity on the size for the MGFs is interpreted within the extended Ziman liquid-metal theory. The results might be significant for controlling the electrical properties of MGFs via tunning their glassy states and applying them in micro-electromechanical systems.
本文研究了 Zr-、La- 和 Pd 基金属玻璃纤维(MGF)的电气传输特性,这些纤维是在高温下通过超塑性变形制成的,其直径达到微米级。研究发现,随着直径的减小,MGF 的电阻率随温度的降低而增加。与较厚的 MGF 相比,较薄的 MGF 在其形成过程中由于受到较大的法向应力影响,其结构的年轻化程度更高,弛豫焓更大、平均短程原子间距更大、晶体结构更少。根据异质结构的演变,在扩展的齐曼液态金属理论中解释了 MGF 的电阻率与尺寸的关系。这些结果可能对通过调节玻璃态来控制 MGFs 的电学特性以及将其应用于微机电系统具有重要意义。
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引用次数: 0
Enhanced photocathodic protection performance of Co3S4 nanoparticles modified porous BiVO4 composites for 304 stainless steel 用于 304 不锈钢的 Co3S4 纳米颗粒改性多孔 BiVO4 复合材料的光阴极保护性能得到增强
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-09-26 DOI: 10.1016/j.materresbull.2024.113110
Hong Li , Guidong Li , Zhanyuan Yang , Honggang Liu , Xuan Zhang , Jinke Zhu , Weitao Li , Yanhui Li
A nanoporous Co3S4/BiVO4 composites were successfully fabricated via electrodeposition, immersion and oil-bath heating methods. ZIF-67 was used as a cobalt source and template. Co3S4/BiVO4 obtained by treatment for 6 h displayed the best photocathodic protection (PCP) performance. Under light, Co3S4–6 h/BiVO4 reduced the potential of 304 stainless steel (SS) to −490 mV vs. SCE, which was 200 mV below that of pure BiVO4. In addition, the photocurrent densities of 304 SS coupled with Co3S4–6 h/BiVO4 were up to 13 μA cm−2, which was more than 4 times that of pure BiVO4. Remarkably, the Rct of 304 SS coupled with Co3S4–6h/BiVO4 (142.6 Ω·cm2) was 1/27 of that of pure BiVO4 (3918 Ω·cm2). The outstanding PCP property of Co3S4/BiVO4 can be owed to the synergistic effects of strong visible light absorption, improved charge transfer efficiency, and enhanced electron storage capacity. These advantages make Co3S4/BiVO4 a promising candidate for providing effective PCP effects on metals.
通过电沉积、浸泡和油浴加热方法,成功制备了纳米多孔 Co3S4/BiVO4 复合材料。ZIF-67 被用作钴源和模板。处理 6 小时后得到的 Co3S4/BiVO4 显示出最佳的光阴极保护(PCP)性能。在光照下,Co3S4-6 h/BiVO4 可将 304 不锈钢(SS)的电位降至 -490 mV,比纯 BiVO4 低 200 mV。此外,304 SS 与 Co3S4-6 h/BiVO4 耦合的光电流密度高达 13 μA cm-2,是纯 BiVO4 的 4 倍多。值得注意的是,与 Co3S4-6h/BiVO4 结合的 304 SS 的 Rct(142.6 Ω-cm2)是纯 BiVO4(3918 Ω-cm2)的 1/27。Co3S4/BiVO4 的出色 PCP 特性可归功于强可见光吸收、电荷转移效率提高和电子存储容量增强的协同效应。这些优势使 Co3S4/BiVO4 有希望成为一种能对金属产生有效的 PCP 效应的候选材料。
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引用次数: 0
Polystyrene/Polyacrylonitrile/Polyindole based quasi solid electrolytes for DSSCs: Boosting both efficiency and stability 用于 DSSC 的聚苯乙烯/聚丙烯腈/聚吲哚基准固体电解质:提高效率和稳定性
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-09-26 DOI: 10.1016/j.materresbull.2024.113108
Soner Çakar , Cengiz Soykan , Mahmut Özacar
Recently, the utilization of quasi solid electrolytes has increased to overcome the stability and leakage issues caused by using liquid electrolytes in dye-sensitized solar cells. For this purpose, the novel different amounts of polystyrene/polyacrylonitrile/polyindole based quasi solid electrolytes were prepared and characterized via FTIR, GPC, TGA, DSC and electrochemical procedures. We aimed to develop conductive polymer-based solid electrolytes to be used in DSSCs to improve both solar cell conversion efficiency and stability. The conversion efficiency value of the solar cell using semi-solid electrolyte (PC4) boosted (9.91%) compared to the one using liquid electrolyte (9.74%). Additionally, the solar cells’ stabilities prepared with quasi solid electrolytes are two times higher than solar cells including liquid electrolytes. Therefore, in this study, the potentials of using conductive polymer-based quasi solid electrolytes in DSSCs were investigated and promising results were acquired for future applications.
最近,为了克服在染料敏化太阳能电池中使用液态电解质引起的稳定性和泄漏问题,准固态电解质的使用越来越多。为此,我们制备了不同含量的新型聚苯乙烯/聚丙烯腈/聚吲哚基准固态电解质,并通过傅立叶变换红外光谱(FTIR)、气相色谱-质谱(GPC)、热重分析(TGA)、电化学稳定性测试(DSC)和电化学过程对其进行了表征。我们旨在开发用于 DSSC 的导电聚合物基固体电解质,以提高太阳能电池的转换效率和稳定性。与使用液态电解质的太阳能电池(9.74%)相比,使用半固态电解质(PC4)的太阳能电池转换效率值提高了(9.91%)。此外,使用半固态电解质制备的太阳能电池的稳定性比使用液态电解质的太阳能电池高出两倍。因此,本研究调查了在 DSSC 中使用基于导电聚合物的准固体电解质的潜力,并获得了对未来应用很有帮助的结果。
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引用次数: 0
Microwave, ferroelectric and electromechanical studies of free standing blended electroactive polymer films 独立混合电活性聚合物薄膜的微波、铁电和机电研究
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-09-25 DOI: 10.1016/j.materresbull.2024.113105
P. Nikhil Mohan , C. Thirmal , Andrews Joseph , B. Arun , Karmegam Shanmuga Priya , Pattukkannu Murugavel , K.C. James Raju
This study probes the enhancement of the microwave, ferroelectric and electromechanical properties of electroactive polymer (EAP) blended films made out of P(VDF-TrFE) and Nafion. Blended films are synthesized using the solution casting method, with different Nafion volume percentage (0 % to 30 %), and the phase formation is confirmed using XRD and FTIR spectroscopy. The morphological features are studied using FESEM. The reflection loss of the blended films as a function of thickness has been studied in both X and Ku band using a VNA. The contribution of reflection and absorption to the shielding effectiveness are also explored. 10 % Nafion inclusion effectively minimizes microwave reflection. The P-E hysteresis study reveals that the blended films exhibit high performance in terms of the parameters. The electromechanical coupling factor has been enhanced for 10 % Nafion inclusion. These findings suggest that the blended films have potential applications in flexible piezoelectric sensors, capacitors, memory, and microwave devices.
本研究探讨了如何增强由 P(VDF-TrFE)和 Nafion 制成的电活性聚合物(EAP)共混膜的微波、铁电和机电特性。混合薄膜采用溶液浇铸法合成,Nafion 的体积百分比各不相同(0% 至 30%),并利用 XRD 和傅立叶变换红外光谱确认了相的形成。使用 FESEM 对其形态特征进行了研究。使用 VNA 研究了混合薄膜在 X 和 Ku 波段的反射损耗与厚度的函数关系。此外,还探讨了反射和吸收对屏蔽效果的影响。10 % 的 Nafion 成分能有效地将微波反射降到最低。P-E 滞后研究表明,混合薄膜在参数方面表现出很高的性能。含有 10% Nafion 的薄膜的机电耦合系数有所提高。这些研究结果表明,混合薄膜在柔性压电传感器、电容器、存储器和微波器件方面具有潜在的应用前景。
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引用次数: 0
ZnO/carbon quantum dots nanocomposites derived from Moringa oleifera gum: An improved catalytic vitiation of methylene blue dye 从辣木树胶中提取的氧化锌/碳量子点纳米复合材料:改进亚甲基蓝染料的催化矾化性能
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-09-22 DOI: 10.1016/j.materresbull.2024.113106
Shehla Parveen , Nida Latif , Ghayoor Abbas Chotana , Aqsa Kanwal , Shahid Hussain , Mohamed A. Habila , Amjad Iqbal , Rajesh Kumar Manavalan , Nosheen Farooq
The present study reports on the enhanced photocatalytic and chemocatalytic performance of ZnO/carbon dots (CDs) nanocomposites for the degradation of methylene blue (MB) dye. Carbon quantum dots were prepared by employing Moringa oleifera gum powder as a carbon source through the hydrothermal process. ZnO/CQDs nanocomposites were synthesized by dispersing ZnO nanoparticles into carbon quantum dot solution. The obtained samples were characterized by using techniques like FTIR, UV, and SEM with EDX analysis. When the methylene blue (MB) dye was exposed to visible light at room temperature, the ZnO/CQDs nanocomposites photocatalyst exhibited more photocatalytic and chemocatalytic activity than the pure ZnO nanoparticle photocatalyst. Antibacterial activity and cytotoxic assay of ZnO/CQDs nanocomposites were also investigated. In addition to protecting the environment, the purpose of this research is to create a new visible-light photocatalyst for the effective treatment of organic wastewater.
本研究报告了氧化锌/碳点(CD)纳米复合材料在降解亚甲基蓝(MB)染料方面增强的光催化和化学催化性能。碳量子点是通过水热法采用辣木树胶粉作为碳源制备的。将氧化锌纳米粒子分散到碳量子点溶液中,合成了氧化锌/碳量子点纳米复合材料。利用傅立叶变换红外光谱(FTIR)、紫外光谱(UV)、扫描电子显微镜(SEM)和电子衍射吸收光谱(EDX)分析等技术对得到的样品进行了表征。当亚甲基蓝(MB)染料在室温下暴露于可见光时,ZnO/CQDs 纳米复合材料光催化剂比纯 ZnO 纳米粒子光催化剂表现出更高的光催化活性和化学催化活性。此外,还研究了 ZnO/CQDs 纳米复合材料的抗菌活性和细胞毒性。除了保护环境之外,这项研究的目的还在于创造一种新的可见光光催化剂,用于有效处理有机废水。
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引用次数: 0
Thermal stable NaMgLaTeO6:Dy3+ double perovskite yellow phosphors for w-LEDs and latent fingerprint visualization 热稳定 NaMgLaTeO6:Dy3+ 双包晶黄色荧光粉,用于 w-LED 和潜指纹可视化
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-09-21 DOI: 10.1016/j.materresbull.2024.113098
Xinjing Xie , Yangyang Tuo , Siyu Cheng , Di Gao , Mengkun Zhang , Xiang Liu , Huajuan Deng , Ruijin Yu

The novel Dy3+-doped NaMgLaTeO6 (NaMgLaTeO6:Dy3+) phosphors were produced through a high-temperature solid-state reaction. X-ray diffraction (XRD) analysis and Rietveld refinement manifest that the pure phosphor was committed to the space group (P21/m (11)) and features the double perovskite structure. The band gap (Eg) of the direct semiconductor NaMgLaTeO6 is calculated to be 2.065 eV. Under 388 nm excitation, the 4F9/26H13/2 energy level transition contributes to the maximum emission peak at 572 nm. Other properties of the phosphor include optimal concentration (x = 5 mol %), high thermal stability, activation energy (Ea = 0.31 eV), and internal quantum efficiency (IQE = 31.44 %). The relevant color coordinate of the white light emitting diode (w-LED) prepared by the phosphor is (0.298, 0.311). The features of the latent fingerprint (LFP) created by NaMgLaTeO6:Dy3+ can be clearly reflected on different surfaces. In summary, NaMgLaTeO6:Dy3+ phosphor has proven high potential in w-LEDs production and LFP detection.

新型掺杂 Dy3+ 的 NaMgLaTeO6(NaMgLaTeO6:Dy3+)荧光粉是通过高温固态反应制得的。X 射线衍射(XRD)分析和里特维尔德细化表明,纯荧光粉属于空间群(P21/m (11)),具有双包晶结构。经计算,直接半导体 NaMgLaTeO6 的带隙(Eg)为 2.065 eV。在 388 纳米的激发下,4F9/2→6H13/2 能级跃迁促成了 572 纳米处的最大发射峰。该荧光粉的其他特性包括最佳浓度(x = 5 mol %)、高热稳定性、活化能(Ea = 0.31 eV)和内部量子效率(IQE = 31.44 %)。该荧光粉制备的白光发光二极管(w-LED)的相关色坐标为(0.298,0.311)。由 NaMgLaTeO6:Dy3+ 生成的潜指纹(LFP)的特征可以在不同的表面上清晰地反映出来。总之,NaMgLaTeO6:Dy3+ 荧光粉在 w-LED 生产和 LFP 检测方面具有很大的潜力。
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引用次数: 0
Humidity-enhanced photodegradation mechanism of UiO-66-NH2 metal organic framework UiO-66-NH2 金属有机框架的湿度增强光降解机制
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-09-19 DOI: 10.1016/j.materresbull.2024.113104
Smriti Ranjit , Jennifer R. Soliz , Tecia Grier , Ka Ming Law , Sujan Budhathoki , Adam J. Hauser
The Zr-based metal-organic framework UiO-66-NH2 has been investigated to study the effects of ultraviolet and visible light exposure under dry air and humid environments. Significant impedance and color changes in the material due to ultraviolet and blue light have been observed. These changes happen more rapidly and grow larger in total cumulative magnitude as the atmospheric humidity increases. Samples placed in darkness or in the presence of light with lower energy than blue (450 nm) light showed no discoloration or degradation, regardless of humidity. Impedance data modeling suggests that humidity increases the ionic conductivity of the material and that the degradation occurs at grain boundaries, to a depth that increases with humidity. Nuclear magnetic resonance, X-ray diffraction, and Fourier transform infrared spectroscopy indicate that degradation in samples exposed to light are due to broken linkers between the benzenedicarboxylic acid and Zr clusters. Distribution Statement A. Approved for Public Release. Distribution Unlimited.
研究人员对 Zr 基金属有机框架 UiO-66-NH2 进行了调查,以研究在干燥空气和潮湿环境下紫外线和可见光照射的影响。在紫外线和蓝光的作用下,材料的阻抗和颜色发生了显著变化。随着大气湿度的增加,这些变化发生得更快,总累积幅度也更大。无论湿度如何,将样品放置在黑暗或能量低于蓝光(450 纳米)的环境中,都不会出现变色或降解现象。阻抗数据模型表明,湿度增加了材料的离子传导性,降解发生在晶界,其深度随湿度增加而增加。核磁共振、X 射线衍射和傅立叶变换红外光谱分析表明,暴露在光线下的样品发生降解的原因是苯二甲酸和 Zr 簇之间的连接体断裂。发行声明 A. 批准公开发行。发行无限制。
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引用次数: 0
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