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Synergistic structural integrity and remarkable structural stability of NC@Si anodes for lithium-ion batteries 用于锂离子电池的 NC@Si 阳极的协同结构完整性和显著的结构稳定性
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-22 DOI: 10.1016/j.materresbull.2024.113162
Shuaibo Zeng , Zheng Lin , Jing Peng , Zixing He , Xinghua Liang , Yongyi Li , Yang Lv , Liangbin Xiong
The silicon-based anode has attracted wide attention because of its high theoretical specific capacity, which is expected to greatly improve the batteries’ energy density. However, during the charge-discharge cycles, the great volume expansion of the anode active silicon seriously restricts its electrochemical stability. Herein, N-doping carbon-coated silicon microsphere was prepared for lithium-ion batteries. Benefit from the core-shell structure formed from silicon carbon, the volume change of silicon anode during the cycle is well coordinated. What's more, N-doping carbon reduces the reaction energy barrier between silicon and lithium and accelerates the electrochemical reaction, which improves the cycling performance of the battery. The specific capacity of the prepared button battery is as high as 2913.13 mAh g−1 at the current density of 0.21 mA g−1, and the average coulomb efficiency is higher than 99.84 % during the cycling. And the capacity of NC@SiO2 anode gradually stabilizes after 500 cycles.
硅基负极因其理论比容量高,有望大大提高电池的能量密度而受到广泛关注。然而,在充放电循环过程中,阳极活性硅的巨大体积膨胀严重制约了其电化学稳定性。本文制备了用于锂离子电池的 N 掺杂碳包覆硅微球。得益于硅碳形成的核壳结构,硅负极在循环过程中的体积变化得到了很好的协调。此外,掺杂 N 的碳降低了硅与锂之间的反应能垒,加速了电化学反应,从而提高了电池的循环性能。在 0.21 mA g-1 的电流密度下,制备的纽扣电池的比容量高达 2913.13 mAh g-1,循环过程中的平均库仑效率高于 99.84%。NC@SiO2 阳极的容量在循环 500 次后逐渐趋于稳定。
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引用次数: 0
Hollow N doped carbon/SiCN hierarchical structures for thermostable electromagnetic absorptions 用于恒温电磁吸收的掺 N 空心碳/SiCN 分层结构
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-22 DOI: 10.1016/j.materresbull.2024.113161
Shaoxi Zhang , Xiangnan Chen , Leilei Jiang , Haina Wang , Xin Tian , Ruohao Li , Jingyi Fan , Guangjun Gou
Electromagnetic absorption materials present widespread application prospects. The thermal oxidative aging issues for electromagnetic absorption materials have received little attention. In this paper, N-doped carbon tubes, and the SiCN ceramics are combined to realize thermostable electromagnetic absorptions. The hierarchical structures show significantly enhanced broadband electromagnetic absorption with an optimal RL of -53.61 dB at 14 GHz under a thickness of 2 mm. The effective electromagnetic absorption bandwidth reaches 5.53 GHz, and the coverage range is 11.88–17.41 GHz. More importantly, after 1 h calcination at 300 °C, the optimum RL of NCT/SiCN-1 h is still -45.67 dB under the thickness of 2.5 mm. The effective electromagnetic absorption bandwidth increases to 5.95 GHz, and the coverage range is 10.69–16.64 GHz. Our work proves the possibility for improving the thermostable electromagnetic absorptions of carbon materials, and provides referencing ways for the design of thermostable electromagnetic absorption materials.
电磁吸收材料具有广泛的应用前景。但电磁吸收材料的热氧化老化问题却鲜有人关注。本文将掺杂 N 的碳管和 SiCN 陶瓷结合起来,实现了热稳定性电磁吸收。在厚度为 2 mm 的情况下,分层结构的宽带电磁吸收能力明显增强,在 14 GHz 频率下的最佳 RL 为 -53.61 dB。有效电磁吸收带宽达到 5.53 GHz,覆盖范围为 11.88-17.41 GHz。更重要的是,在 300 °C 煅烧 1 h 后,厚度为 2.5 mm 的 NCT/SiCN-1 h 的最佳 RL 仍为 -45.67 dB。有效电磁吸收带宽增至 5.95 GHz,覆盖范围为 10.69-16.64 GHz。我们的工作证明了提高碳材料恒温电磁吸收性能的可能性,并为恒温电磁吸收材料的设计提供了参考方法。
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引用次数: 0
Zr and Y co-doped SrFe0.8Zr0.1Y0.1O3-δ perovskite oxide as a stable, high-performance symmetrical electrode for solid oxide cells 掺杂 Zr 和 Y 的 SrFe0.8Zr0.1Y0.1O3-δ 包晶氧化物作为一种稳定、高性能的对称电极用于固体氧化物电池
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-22 DOI: 10.1016/j.materresbull.2024.113157
Qian Zhai , Dong Guo , Enyi Zhou , Chunling Lu , Dongchao Qiu , Gaobin Liu , Bingbing Niu , Biao Wang
Symmetrical solid oxide cells (SSOCs), which use the same material for both anode and cathode, simplify the cell fabrication process and effectively resist carbon deposition and sulfur poisoning. In this study, Zr, Y co-doped SrFe0.8Zr0.1Y0.1O3-δ (SFZY) perovskite oxide is synthesized and evaluated its properties as an SSOFCs electrode. Density functional theory (DFT) indicates that the local state density of SFZY is lower than that of SrFeO3-δ (SFO). SFZY has good chemical compatibility with La0.8Sr0.2Ga0.83Mg0.17O3−δ (LSGM) electrolyte below cell operating temperature. Zr, Y co-doped SrFe0.8Zr0.1Y0.1O3-δ maintains structural stability in H2 atmosphere. At 750 ℃, the polarization resistance (Rp) of SFZY is 0.11 and 1.06 Ω cm2 in air and hydrogen atmosphere, respectively. During the Rp stability test, SFZY exhibits better stability than that of SrFeO3-δ in air and hydrogen atmosphere. At 750 ℃, the maximum power density of SFZY/LSGM/SFZY fuel cell reaches 420.1 and 258.31 mWcm−2 using H2 and wet C3H8 as fuel, respectively. In electrolytic mode, the current density of SFZY/LSGM/SFZY electrolysis cell reaches -0.55 A cm−2 at 1.3 V for electrolysis of pure CO2 at 750 ℃. In summary, SFZY has a great potential as SSOCs electrode.
对称固体氧化物电池(SSOC)的阳极和阴极使用相同的材料,简化了电池制造工艺,并能有效防止碳沉积和硫中毒。本研究合成了 Zr、Y 共掺杂的 SrFe0.8Zr0.1Y0.1O3-δ(SFZY)包晶氧化物,并评估了其作为 SSOFCs 电极的性能。密度泛函理论(DFT)表明,SFZY 的局域态密度低于 SrFeO3-δ (SFO)。在电池工作温度以下,SFZY 与 La0.8Sr0.2Ga0.83Mg0.17O3-δ (LSGM)电解质具有良好的化学相容性。Zr、Y共掺杂的SrFe0.8Zr0.1Y0.1O3-δ在H2气氛中保持结构稳定。在 750 ℃ 时,SFZY 在空气和氢气环境中的极化电阻(Rp)分别为 0.11 和 1.06 Ω cm2。在 Rp 稳定性测试中,SFZY 在空气和氢气环境中比 SrFeO3-δ 表现出更好的稳定性。在 750 ℃ 下,以 H2 和湿 C3H8 为燃料,SFZY/LSGM/SFZY 燃料电池的最大功率密度分别达到 420.1 和 258.31 mWcm-2。在电解模式下,SFZY/LSGM/SFZY 电解池在 750 ℃ 下电解纯 CO2 时的电流密度在 1.3 V 时达到 -0.55 A cm-2。总之,SFZY 具有作为 SSOCs 电极的巨大潜力。
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引用次数: 0
Doped NaMnOx cathodes for Zn-MnO2 batteries for improved capacity and rechargeability 用于 Zn-MnO2 电池的掺杂 NaMnOx 阴极可提高容量和充电性能
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-22 DOI: 10.1016/j.materresbull.2024.113159
Yiğit Akbaş , Necdet Özgür Darıcıoğlu , Tayfur Öztürk
Zn-MnO2 batteries are safe, low cost, and have a high energy density comparable to Li-ion batteries. This study focuses on finding a new MnO2-based cathode composition for rechargeable mildly acidic Zn-MnO2 battery. For this purpose, a combinatorial approach was used, and thick film cathodes were deposited on nickel substrates using sputter targets MnO2, Na0.7MnO2, NiO and Bi2O3. A total of 36 cathodes were produced over a wide compositional range. The study has shown two regions of high rechargeable capacity, one centered on Bi0.02Na0.63Ni0.02Mn0.33Ox and the other on Bi0.04Na0.37Ni0.06Mn0.53Ox to be developed as cathodes using conventional slurry method.
Zn-MnO2 电池安全、成本低、能量密度高,可与锂离子电池媲美。本研究的重点是为可充电的弱酸性 Zn-MnO2 电池寻找一种新的基于 MnO2 的阴极成分。为此,我们采用了组合方法,使用溅射靶 MnO2、Na0.7MnO2、NiO 和 Bi2O3 在镍基底上沉积了厚膜阴极。在广泛的成分范围内,共生产出 36 种阴极。研究结果表明,采用传统的浆料法开发的阴极具有两个高充电容量区域,一个以 Bi0.02Na0.63Ni0.02Mn0.33Ox 为中心,另一个以 Bi0.04Na0.37Ni0.06Mn0.53Ox 为中心。
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引用次数: 0
Effects of tree species pore structure characteristics and CO2 activation on the performance of their derived carbon electrode for supercapacitors 树种孔隙结构特征和二氧化碳活化对超级电容器用衍生碳电极性能的影响
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-22 DOI: 10.1016/j.materresbull.2024.113158
Qi Wang , Luwen Fan , Jingru Sun , Zhenglin Tan , Jiajia Mu , Xiaoming Zhou , Lizhi Sheng
Herein, we investigated the effects of tree species selection on the specific surface area and electrochemical properties of wood-derived carbon electrodes. The SEM, Raman spectra and aperture distribution test results showed that compared with BCW and ZCW, CW had a more complex hierarchical porous structure and more defects. The N2 adsorption/desorption isotherms and electrochemical test results showed that CW had the largest specific surface area and the best electrochemical performance, with a specific surface area of 495.3 m2 g−1 and an areal capacitance of 3079 mF cm−2 at 5 mA cm−2. The specific surface area and electrochemical properties of ACW, ABCW and AZCW electrodes obtained by CO2 activation were significantly improved compared with CW, BCW and ZCW electrodes. Among the activated electrodes, the ACW electrode had the highest specific surface area (558.4 m2 g−1) and the highest areal capacitance (3727 mF cm−2 at 5 mA cm−2).
在此,我们研究了树种选择对木质碳电极比表面积和电化学性能的影响。扫描电镜、拉曼光谱和孔径分布测试结果表明,与 BCW 和 ZCW 相比,CW 具有更复杂的分层多孔结构和更多缺陷。N2 吸附/解吸等温线和电化学测试结果表明,CW 的比表面积最大,电化学性能最好,比表面积为 495.3 m2 g-1,在 5 mA cm-2 时的等效电容为 3079 mF cm-2。与 CW、BCW 和 ZCW 电极相比,通过二氧化碳活化获得的 ACW、ABCW 和 AZCW 电极的比表面积和电化学性能都有显著提高。在活化电极中,ACW 电极的比表面积最大(558.4 m2 g-1),电容值最高(5 mA cm-2 时为 3727 mF cm-2)。
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引用次数: 0
Passivator materials based on the benzothiazole-sulfonamide hybrid: Synthesis, optical, electrochemical properties, and molecular modeling for perovskite solar cells 基于苯并噻唑-磺酰胺杂化物的钝化剂材料:用于过氧化物太阳能电池的合成、光学、电化学特性和分子建模
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-22 DOI: 10.1016/j.materresbull.2024.113151
Ahmed M․ M․ Fadl , Ahmed Mourtada Elseman , Abu-Bakr A․ A․ M․ El-Adasy , M․ M․ Rashad , M․ S․ A․ El-Gaby
This study presents the synthesis of N-(4-(N-carbamimidoylsulfamoyl)phenyl)benzo[d]thiazole-2-carbohydrazonoyl cyanide (NCSBC), a novel passivator material for perovskite solar cells (PSCs). The structure was confirmed by FTIR, ¹H NMR, and ¹³C NMR, while Hall-effect measurements revealed a hole mobility of 1.15 × 10³ cm²/Vs. UV–Vis analysis showed absorption peaks at 295 and 422 nm, corresponding to transitions related to azo groups and aromatic rings in NCSBC. The compound exhibited an optical energy gap of 2.47 eV, consistent with DFT-based molecular modeling. Thermal stability and electrochemical properties further validated its suitability for photovoltaic applications. Incorporating NCSBC into PSCs with an FTO/c-TiO2/MAPbI3/NCSBC/spiroMeOTAD/Ag device configuration resulted in a power conversion efficiency (PCE) of 16.21 %, compared to 14.47 % for the control. This work highlights NCSBC's potential for cost-effective, high-efficiency defect passivation in PSCs.
本研究介绍了 N-(4-(N-氨基甲酰亚胺基磺酰基)苯基)苯并[d]噻唑-2-羧酰肼氰化物(NCSBC)的合成,这是一种用于过氧化物太阳能电池(PSC)的新型钝化剂材料。傅立叶变换红外光谱、¹H NMR 和 ¹³C NMR 证实了其结构,霍尔效应测量显示其空穴迁移率为 1.15 × 10³ cm²/Vs。紫外可见光分析表明,在 295 纳米和 422 纳米处出现了吸收峰,这些吸收峰与 NCSBC 中的偶氮基团和芳香环的跃迁有关。该化合物的光学能隙为 2.47 eV,与基于 DFT 的分子建模一致。热稳定性和电化学特性进一步验证了其在光伏应用中的适用性。将 NCSBC 纳入 FTO/c-TiO2/MAPbI3/NCSBC/spiroMeOTAD/Ag 器件配置的 PSC 中,功率转换效率 (PCE) 为 16.21%,而对照组为 14.47%。这项工作凸显了 NCSBC 在 PSC 中进行低成本、高效率缺陷钝化的潜力。
{"title":"Passivator materials based on the benzothiazole-sulfonamide hybrid: Synthesis, optical, electrochemical properties, and molecular modeling for perovskite solar cells","authors":"Ahmed M․ M․ Fadl ,&nbsp;Ahmed Mourtada Elseman ,&nbsp;Abu-Bakr A․ A․ M․ El-Adasy ,&nbsp;M․ M․ Rashad ,&nbsp;M․ S․ A․ El-Gaby","doi":"10.1016/j.materresbull.2024.113151","DOIUrl":"10.1016/j.materresbull.2024.113151","url":null,"abstract":"<div><div>This study presents the synthesis of <em>N</em>-(4-(<em>N</em>-carbamimidoylsulfamoyl)phenyl)benzo[d]thiazole-2-carbohydrazonoyl cyanide (<em>N<img></em>CSBC), a novel passivator material for perovskite solar cells (PSCs). The structure was confirmed by FTIR, ¹H NMR, and ¹³C NMR, while Hall-effect measurements revealed a hole mobility of 1.15 × 10³ cm²/Vs. UV–Vis analysis showed absorption peaks at 295 and 422 nm, corresponding to transitions related to azo groups and aromatic rings in <em>N<img></em>CSBC. The compound exhibited an optical energy gap of 2.47 eV, consistent with DFT-based molecular modeling. Thermal stability and electrochemical properties further validated its suitability for photovoltaic applications. Incorporating <em>N<img></em>CSBC into PSCs with an FTO/c-TiO<sub>2</sub>/MAPbI<sub>3</sub>/<em>N</em><img>CSBC/spiroMeOTAD/Ag device configuration resulted in a power conversion efficiency (PCE) of 16.21 %, compared to 14.47 % for the control. This work highlights <em>N<img></em>CSBC's potential for cost-effective, high-efficiency defect passivation in PSCs.</div></div>","PeriodicalId":18265,"journal":{"name":"Materials Research Bulletin","volume":"182 ","pages":"Article 113151"},"PeriodicalIF":5.3,"publicationDate":"2024-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142553502","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
The catalytic effect of Pt0 species on Pt/ZnO nanorods for robust triethylamine sensing detection Pt/ZnO 纳米棒上的 Pt0 物种对三乙胺传感检测的催化作用
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-22 DOI: 10.1016/j.materresbull.2024.113156
Li-Juan Yue , Su-Mei Shen , Wen-Jie Zhang , Fei-Long Gong, Xuan-Yu Yang, Yong-Hui Zhang
The noble metal Pt modified ZnO nanomaterials are widely used to improve their gas sensing performance. However, the relationship between the catalytic effect of Ptx+ species on the oxygen vacancies formation and gas-sensing performance is still unclear. Herein, the Pt/ZnO nanorods are successfully synthesized by using hydrothermal method, and the content of Pt0 species are finely tuned through treating in different atmospheres. Notably, Pt modified ZnO calcined under Ar/H2 (Pt/ZnO-3) exhibits excellent sensing response (Ra/Rg = 2196, 81 times higher than pure ZnO) to 50 ppm triethylamine at 140 °C, with fast response/recovery behavior, low limit of detection, and superior selectivity. Detailed structural characterization indicates that Pt nanoparticle modification reduces the band gap of the samples. In addition, the high content of Pt0 species promotes the generation of adsorbed oxygen, which significantly enhances the gas-sensitive performance of the sensor. This work demonstrates that the concentration of Pt0 species greatly affects gas-sensing performance.
贵金属铂修饰的 ZnO 纳米材料被广泛用于提高其气体传感性能。然而,Ptx+物种对氧空位形成的催化作用与气体传感性能之间的关系尚不清楚。本文采用水热法成功合成了 Pt/ZnO 纳米棒,并通过在不同气氛中的处理对 Pt0 物种的含量进行了微调。值得注意的是,在 Ar/H2 条件下煅烧的铂修饰氧化锌(Pt/ZnO-3)在 140 °C 下对 50 ppm 的三乙胺具有极佳的传感响应(Ra/Rg = 2196,是纯氧化锌的 81 倍)、快速响应/恢复行为、低检测限和卓越的选择性。详细的结构表征表明,铂纳米粒子修饰降低了样品的带隙。此外,高含量的 Pt0 物种促进了吸附氧的生成,从而显著提高了传感器的气敏性能。这项工作表明,Pt0 物种的浓度会极大地影响气敏性能。
{"title":"The catalytic effect of Pt0 species on Pt/ZnO nanorods for robust triethylamine sensing detection","authors":"Li-Juan Yue ,&nbsp;Su-Mei Shen ,&nbsp;Wen-Jie Zhang ,&nbsp;Fei-Long Gong,&nbsp;Xuan-Yu Yang,&nbsp;Yong-Hui Zhang","doi":"10.1016/j.materresbull.2024.113156","DOIUrl":"10.1016/j.materresbull.2024.113156","url":null,"abstract":"<div><div>The noble metal Pt modified ZnO nanomaterials are widely used to improve their gas sensing performance. However, the relationship between the catalytic effect of Pt<sup>x+</sup> species on the oxygen vacancies formation and gas-sensing performance is still unclear. Herein, the Pt/ZnO nanorods are successfully synthesized by using hydrothermal method, and the content of Pt<sup>0</sup> species are finely tuned through treating in different atmospheres. Notably, Pt modified ZnO calcined under Ar/H<sub>2</sub> (Pt/ZnO-3) exhibits excellent sensing response (R<sub>a</sub>/R<sub>g</sub> = 2196, 81 times higher than pure ZnO) to 50 ppm triethylamine at 140 °C, with fast response/recovery behavior, low limit of detection, and superior selectivity. Detailed structural characterization indicates that Pt nanoparticle modification reduces the band gap of the samples. In addition, the high content of Pt<sup>0</sup> species promotes the generation of adsorbed oxygen, which significantly enhances the gas-sensitive performance of the sensor. This work demonstrates that the concentration of Pt<sup>0</sup> species greatly affects gas-sensing performance.</div></div>","PeriodicalId":18265,"journal":{"name":"Materials Research Bulletin","volume":"182 ","pages":"Article 113156"},"PeriodicalIF":5.3,"publicationDate":"2024-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142561512","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
Evaluating the synergistic effect of co-sputtered W-TiN and W-CrN electrodes for superior capacitance in hybrid supercapacitors 评估共溅镀 W-TiN 和 W-CrN 电极的协同效应,以提高混合超级电容器的电容量
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-21 DOI: 10.1016/j.materresbull.2024.113155
Muhammad Zahir Iqbal , Hamid Ali , Rashid Ali , Abhinav Kumar , Md Rezaul Karim , Mohammad Abul Farah
Bimetallic transition metal nitrides have gained significant attention as battery-grade electrode materials for the application of energy storage. This study investigates the electrochemical performance of co-sputtered tungsten (W) with titanium nitride (TiN) and chromium nitride (CrN), where the electrode fabrication is carried out using an RF/DC magnetron sputtering unit. The structural properties, surface morphology, and elemental content of the sample are analyzed with X-ray diffraction, SEM, and EDX, respectively. The battery-grade nature of the electrode materials is revealed by the electrochemical performance in half-cell configuration. In half-cell assembly specific capacity (Qs) of 1408 C/ g is achieved with W-TiN and 583.8 C/ g with W-CrN electrode, respectively. The device (W-TiN//AC) delivers a specific capacity of 347.2 C/g, with energy and power densities of 88 Wh/kg and 1700 W/kg. Linear and quadratic models are employed to deconvolute the capacitive and diffusive impact on the total capacity of the device.
双金属过渡金属氮化物作为电池级电极材料在储能领域的应用备受关注。本研究调查了氮化钛(TiN)和氮化铬(CrN)共溅射钨(W)的电化学性能。样品的结构特性、表面形貌和元素含量分别通过 X 射线衍射、扫描电镜和电离辐射显微镜进行了分析。半电池配置的电化学性能揭示了电极材料的电池级性质。在半电池组件中,W-TiN 和 W-CrN 电极的比容量(Qs)分别达到了 1408 C/g 和 583.8 C/g。装置(W-TiN//AC)的比容量为 347.2 C/g,能量密度和功率密度分别为 88 Wh/kg 和 1700 W/kg。采用线性和二次模型来解构电容和扩散对装置总容量的影响。
{"title":"Evaluating the synergistic effect of co-sputtered W-TiN and W-CrN electrodes for superior capacitance in hybrid supercapacitors","authors":"Muhammad Zahir Iqbal ,&nbsp;Hamid Ali ,&nbsp;Rashid Ali ,&nbsp;Abhinav Kumar ,&nbsp;Md Rezaul Karim ,&nbsp;Mohammad Abul Farah","doi":"10.1016/j.materresbull.2024.113155","DOIUrl":"10.1016/j.materresbull.2024.113155","url":null,"abstract":"<div><div>Bimetallic transition metal nitrides have gained significant attention as battery-grade electrode materials for the application of energy storage. This study investigates the electrochemical performance of co-sputtered tungsten (W) with titanium nitride (TiN) and chromium nitride (CrN), where the electrode fabrication is carried out using an RF/DC magnetron sputtering unit. The structural properties, surface morphology, and elemental content of the sample are analyzed with X-ray diffraction, SEM, and EDX, respectively. The battery-grade nature of the electrode materials is revealed by the electrochemical performance in half-cell configuration. In half-cell assembly specific capacity (Q<sub>s</sub>) of 1408 C/ g is achieved with W-TiN and 583.8 C/ g with W-CrN electrode, respectively. The device (W-TiN//AC) delivers a specific capacity of 347.2 C/g, with energy and power densities of 88 Wh/kg and 1700 W/kg. Linear and quadratic models are employed to deconvolute the capacitive and diffusive impact on the total capacity of the device.</div></div>","PeriodicalId":18265,"journal":{"name":"Materials Research Bulletin","volume":"182 ","pages":"Article 113155"},"PeriodicalIF":5.3,"publicationDate":"2024-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142561478","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
Temperature responsive behaviour of SrAl2O4(Eu, Dy):ZnGa2O4(Cr) phosphor-glass composite SrAl2O4(Eu, Dy):ZnGa2O4(Cr)荧光粉-玻璃复合材料的温度响应特性
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-19 DOI: 10.1016/j.materresbull.2024.113154
Kiran, Y. Dwivedi
The current investigation reports on laser spectroscopy and temperature-sensitive optical response of composite consisting of phosphors (ZnGa2O4:Cr3+ and SrAl2O4:Eu2+, Dy3+) coated on a tellurite glass layer. Based on this composite, a temperature sensor, sensitve in the range of 298 K to 423 K, demonstrates a remarkable temperature sensitivity. Various analytical techniques, such as X-ray Diffraction, Scanning Electron Microscopy, High-Resolution Transmission Electron Microscopy, laser spectroscopy, etc., were employed to analyze the prepared composite. The investigation reveals the presence of ZGO and SrAl phosphors with crystalline sizes of approximately 36 nm and 25 nm, respectively, while the particle size ranges from 400 nm to 600 nm. A dip coating method was utilized to deposit tellurite-phosphor layers on the glass substrate to create a temperature sensor. SEM analysis indicates a layer thickness of around 93 µm. The existence of Eu2+ and Cr3+ ions was confirmed through photoexcitation and emission spectra on a 405 nm laser excitation. The temperature-dependent luminescence was studied using a ratiometric technique, showing a linear variation with temperature, resulting in an excellent temperature sensitivity of about 1.41 % K−1 at 298 K. Our preliminary study of the phosphor-tellurite composite suggests significant potential for extensive use in the field of dual-mode highly sensitive optical thermometry.
目前的研究报告介绍了涂覆在碲玻璃层上的荧光粉(ZnGa2O4:Cr3+ 和 SrAl2O4:Eu2+、Dy3+)复合材料的激光光谱和温敏光学响应。基于这种复合材料,温度传感器的灵敏度范围为 298 K 至 423 K,具有极高的温度灵敏度。在分析制备的复合材料时,采用了多种分析技术,如 X 射线衍射、扫描电子显微镜、高分辨率透射电子显微镜、激光光谱等。研究表明,ZGO 和 SrAl 荧光粉的结晶尺寸分别约为 36 纳米和 25 纳米,粒径范围为 400 纳米至 600 纳米。利用浸涂法在玻璃基板上沉积碲荧光粉层,以制造温度传感器。扫描电子显微镜分析表明,层厚度约为 93 微米。通过 405 纳米激光激发下的光激发和发射光谱,证实了 Eu2+ 和 Cr3+ 离子的存在。我们对荧光粉-碲酸盐复合材料的初步研究表明,它在双模高灵敏度光学温度测量领域具有广泛应用的巨大潜力。
{"title":"Temperature responsive behaviour of SrAl2O4(Eu, Dy):ZnGa2O4(Cr) phosphor-glass composite","authors":"Kiran,&nbsp;Y. Dwivedi","doi":"10.1016/j.materresbull.2024.113154","DOIUrl":"10.1016/j.materresbull.2024.113154","url":null,"abstract":"<div><div>The current investigation reports on laser spectroscopy and temperature-sensitive optical response of composite consisting of phosphors (ZnGa<sub>2</sub>O<sub>4</sub>:Cr<sup>3+</sup> and SrAl<sub>2</sub>O<sub>4</sub>:Eu<sup>2+</sup>, Dy<sup>3+</sup>) coated on a tellurite glass layer. Based on this composite, a temperature sensor, sensitve in the range of 298 K to 423 K, demonstrates a remarkable temperature sensitivity. Various analytical techniques, such as X-ray Diffraction, Scanning Electron Microscopy, High-Resolution Transmission Electron Microscopy, laser spectroscopy, etc., were employed to analyze the prepared composite. The investigation reveals the presence of ZGO and SrAl phosphors with crystalline sizes of approximately 36 nm and 25 nm, respectively, while the particle size ranges from 400 nm to 600 nm. A dip coating method was utilized to deposit tellurite-phosphor layers on the glass substrate to create a temperature sensor. SEM analysis indicates a layer thickness of around 93 µm. The existence of Eu<sup>2+</sup> and Cr<sup>3+</sup> ions was confirmed through photoexcitation and emission spectra on a 405 nm laser excitation. The temperature-dependent luminescence was studied using a ratiometric technique, showing a linear variation with temperature, resulting in an excellent temperature sensitivity of about 1.41 % <em>K</em><sup>−1</sup> at 298 K. Our preliminary study of the phosphor-tellurite composite suggests significant potential for extensive use in the field of dual-mode highly sensitive optical thermometry.</div></div>","PeriodicalId":18265,"journal":{"name":"Materials Research Bulletin","volume":"182 ","pages":"Article 113154"},"PeriodicalIF":5.3,"publicationDate":"2024-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142553497","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
Photoluminescence and Raman spectroscopy of Ce3+ doped Y3Al5O12 single crystalline films grown onto Y3Al5O12 and Lu3Al5O12 substrates 在 Y3Al5O12 和 Lu3Al5O12 基底上生长的掺杂 Ce3+ 的 Y3Al5O12 单晶薄膜的光致发光和拉曼光谱
IF 5.3 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-10-18 DOI: 10.1016/j.materresbull.2024.113141
Anton Markovskyi , Piotr Radomski , Wioletta Dewo , Vitalii Gorbenko , Alexander Fedorov , Tomasz Runka , Yuriy Zorenko
Raman spectroscopy, high spectral resolution luminescence, and X-ray diffraction techniques were employed to study two Ce3+ doped Y3Al5O12 single crystalline films grown by liquid phase epitaxy method onto Y3Al5O12 and Lu3Al5O12 single crystal substrates. Optical spectra were obtained with a micrometer step along the cross-sections of epitaxial structures, allowing excellent differentiation of the film, the transition layer, and the substrate of each sample. X-ray measurements demonstrate the mismatch between the lattice constants of the Y3Al5O12:Ce3+ film and its Lu3Al5O12 substrate, an effect related to different compositions. Consequently, the film grown onto Lu3Al5O12 exhibits higher residual stresses than its counterpart grown onto Y3Al5O12. This was confirmed by a mutual comparison of the Raman bands positions of the films. The luminescence spectra of both samples consist mainly of cerium 5d-4f emission, the intensity of which allows for additional study of epitaxial cross section and estimation of the size of transition layer.
采用拉曼光谱、高光谱分辨率发光和 X 射线衍射技术,研究了通过液相外延方法在 Y3Al5O12 和 Lu3Al5O12 单晶基底上生长的两种掺杂 Ce3+ 的 Y3Al5O12 单晶薄膜。沿着外延结构的横截面以微米为单位获得了光学光谱,从而很好地区分了每个样品的薄膜、过渡层和基底。X 射线测量结果表明,Y3Al5O12:Ce3+ 薄膜及其 Lu3Al5O12 基底的晶格常数不匹配,这种效应与不同的成分有关。因此,与生长在 Y3Al5O12 上的薄膜相比,生长在 Lu3Al5O12 上的薄膜表现出更高的残余应力。这一点通过相互比较薄膜的拉曼带位置得到了证实。这两种样品的发光光谱主要由铈 5d-4f 发射组成,其强度有助于进一步研究外延截面和估计过渡层的大小。
{"title":"Photoluminescence and Raman spectroscopy of Ce3+ doped Y3Al5O12 single crystalline films grown onto Y3Al5O12 and Lu3Al5O12 substrates","authors":"Anton Markovskyi ,&nbsp;Piotr Radomski ,&nbsp;Wioletta Dewo ,&nbsp;Vitalii Gorbenko ,&nbsp;Alexander Fedorov ,&nbsp;Tomasz Runka ,&nbsp;Yuriy Zorenko","doi":"10.1016/j.materresbull.2024.113141","DOIUrl":"10.1016/j.materresbull.2024.113141","url":null,"abstract":"<div><div>Raman spectroscopy, high spectral resolution luminescence, and X-ray diffraction techniques were employed to study two Ce<sup>3+</sup> doped Y<sub>3</sub>Al<sub>5</sub>O<sub>12</sub> single crystalline films grown by liquid phase epitaxy method onto Y<sub>3</sub>Al<sub>5</sub>O<sub>12</sub> and Lu<sub>3</sub>Al<sub>5</sub>O<sub>12</sub> single crystal substrates. Optical spectra were obtained with a micrometer step along the cross-sections of epitaxial structures, allowing excellent differentiation of the film, the transition layer, and the substrate of each sample. X-ray measurements demonstrate the mismatch between the lattice constants of the Y<sub>3</sub>Al<sub>5</sub>O<sub>12</sub>:Ce<sup>3+</sup> film and its Lu<sub>3</sub>Al<sub>5</sub>O<sub>12</sub> substrate, an effect related to different compositions. Consequently, the film grown onto Lu<sub>3</sub>Al<sub>5</sub>O<sub>12</sub> exhibits higher residual stresses than its counterpart grown onto Y<sub>3</sub>Al<sub>5</sub>O<sub>12</sub>. This was confirmed by a mutual comparison of the Raman bands positions of the films. The luminescence spectra of both samples consist mainly of cerium 5d-4f emission, the intensity of which allows for additional study of epitaxial cross section and estimation of the size of transition layer.</div></div>","PeriodicalId":18265,"journal":{"name":"Materials Research Bulletin","volume":"182 ","pages":"Article 113141"},"PeriodicalIF":5.3,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142532275","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
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