Pub Date : 2023-11-24DOI: 10.1038/s41427-023-00509-5
Daniel Şopu, Florian Spieckermann, Xilei Bian, Simon Fellner, Jonathan Wright, Megan Cordill, Christoph Gammer, Gang Wang, Mihai Stoica, Jürgen Eckert
Residual stress engineering is widely used in the design of new advanced lightweight materials. For metallic glasses, attention has been given to structural changes and rejuvenation processes. High-energy scanning X-ray diffraction strain mapping reveals large elastic fluctuations in notched metallic glasses after deformation under triaxial compression. Microindentation hardness mapping hints at a competing hardening–softening mechanism after compression and reveals the complementary effects of stress and structure modulation. Transmission electron microscopy proves that structure modulation and elastic heterogeneity distribution under room temperature deformation are related to shear band formation. Molecular dynamics simulations provide an atomistic understanding of the confined deformation mechanism in notched metallic glasses and the related fluctuations in the elastic and plastic strains. Thus, future focus should be given to stress modulation and elastic heterogeneity, which, together with structure modulation, may allow the design of metallic glasses with enhanced ductility and strain-hardening ability.
{"title":"Rejuvenation engineering in metallic glasses by complementary stress and structure modulation","authors":"Daniel Şopu, Florian Spieckermann, Xilei Bian, Simon Fellner, Jonathan Wright, Megan Cordill, Christoph Gammer, Gang Wang, Mihai Stoica, Jürgen Eckert","doi":"10.1038/s41427-023-00509-5","DOIUrl":"https://doi.org/10.1038/s41427-023-00509-5","url":null,"abstract":"<p>Residual stress engineering is widely used in the design of new advanced lightweight materials. For metallic glasses, attention has been given to structural changes and rejuvenation processes. High-energy scanning X-ray diffraction strain mapping reveals large elastic fluctuations in notched metallic glasses after deformation under triaxial compression. Microindentation hardness mapping hints at a competing hardening–softening mechanism after compression and reveals the complementary effects of stress and structure modulation. Transmission electron microscopy proves that structure modulation and elastic heterogeneity distribution under room temperature deformation are related to shear band formation. Molecular dynamics simulations provide an atomistic understanding of the confined deformation mechanism in notched metallic glasses and the related fluctuations in the elastic and plastic strains. Thus, future focus should be given to stress modulation and elastic heterogeneity, which, together with structure modulation, may allow the design of metallic glasses with enhanced ductility and strain-hardening ability.</p>","PeriodicalId":19382,"journal":{"name":"Npg Asia Materials","volume":"103 ","pages":""},"PeriodicalIF":9.7,"publicationDate":"2023-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138506402","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-11-24DOI: 10.1038/s41427-023-00508-6
Lizhi Guan, Weixiang Peng, Rachel Ng Jing Wen, Jingbo Fan, Hortense Le Ferrand
The Bouligand structure found in the dactyl club of mantis shrimps is known for its impact resistance. However, Bouligand-inspired reinforced composites with 3D shapes and impact resistance characteristics have not yet been demonstrated. Herein, direct ink writing was used to 3D print composites reinforced with glass microfibers assembled into Bouligand structures with controllable pitch angles. The energy absorption levels of the Bouligand composites under impact were found to surpass those of composites with unidirectional microfiber alignment. Additionally, the Bouligand composites with a pitch angle of 40° exhibited a maximum energy absorption of 2.4 kJ/m2, which was 140% higher than that of the unidirectional composites. Furthermore, the characterization of the topography of the fractured surface, supplemented with numerical simulations, revealed a combination of crack twisting and crack bridging mechanisms. Flexural tests conducted on the composites with a pitch angle of 40° revealed that these composites had the strongest properties, including a flexural strength of 36.9 MPa, a stiffness of 2.26 GPa, and energy absorption of 8 kJ/m2. These findings are promising for the microstructural design of engineered composites using direct ink writing for applications in aerospace, transportation, and defense.
{"title":"Izod impact resistance of 3D printed discontinuous fibrous composites with Bouligand structure","authors":"Lizhi Guan, Weixiang Peng, Rachel Ng Jing Wen, Jingbo Fan, Hortense Le Ferrand","doi":"10.1038/s41427-023-00508-6","DOIUrl":"https://doi.org/10.1038/s41427-023-00508-6","url":null,"abstract":"<p>The Bouligand structure found in the dactyl club of mantis shrimps is known for its impact resistance. However, Bouligand-inspired reinforced composites with 3D shapes and impact resistance characteristics have not yet been demonstrated. Herein, direct ink writing was used to 3D print composites reinforced with glass microfibers assembled into Bouligand structures with controllable pitch angles. The energy absorption levels of the Bouligand composites under impact were found to surpass those of composites with unidirectional microfiber alignment. Additionally, the Bouligand composites with a pitch angle of 40° exhibited a maximum energy absorption of 2.4 kJ/m<sup>2</sup>, which was 140% higher than that of the unidirectional composites. Furthermore, the characterization of the topography of the fractured surface, supplemented with numerical simulations, revealed a combination of crack twisting and crack bridging mechanisms. Flexural tests conducted on the composites with a pitch angle of 40° revealed that these composites had the strongest properties, including a flexural strength of 36.9 MPa, a stiffness of 2.26 GPa, and energy absorption of 8 kJ/m<sup>2</sup>. These findings are promising for the microstructural design of engineered composites using direct ink writing for applications in aerospace, transportation, and defense.</p>","PeriodicalId":19382,"journal":{"name":"Npg Asia Materials","volume":"492 ","pages":""},"PeriodicalIF":9.7,"publicationDate":"2023-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138506378","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-11-10DOI: 10.1038/s41427-023-00506-8
Nixian Qian, Chunhua Chen, Yonghui Zhou, Shuyang Wang, Liangyu Li, Ranran Zhang, Xiangde Zhu, Yifang Yuan, Xuliang Chen, Chao An, Ying Zhou, Min Zhang, Xiaoping Yang, Zhaorong Yang
Abstract Pressure engineering in semiconductors leads to a variety of novel physical phenomena and has recently received considerable attention. Here, we report on pressure-induced superconductivity in III–V gallium phosphide (GaP), a commercially important semiconductor that exhibits excellent optical performance. We show that the emergence of superconductivity is accompanied by the concurrence of piezochromic transition and metallization and can be correlated to a structural transition from the cubic to orthorhombic phase. In line with the structural origin of superconductivity, the critical temperature T c monotonically decreases with increasing pressure up to ~50 GPa. Moreover, the superconductivity could be preserved toward ambient pressure because of the irreversibility of the structural transition. Nevertheless, the superconducting transition displays evident broadening associated with the presence of amorphization in the depressurized sample. The synchronous evolution of the structural and electronic properties not only shows a vivid structure-property relationship but also could facilitate the exploration of novel functionalities by means of pressure treatment.
{"title":"Two high-pressure superconducting phases in pressurized optical semiconductor GaP","authors":"Nixian Qian, Chunhua Chen, Yonghui Zhou, Shuyang Wang, Liangyu Li, Ranran Zhang, Xiangde Zhu, Yifang Yuan, Xuliang Chen, Chao An, Ying Zhou, Min Zhang, Xiaoping Yang, Zhaorong Yang","doi":"10.1038/s41427-023-00506-8","DOIUrl":"https://doi.org/10.1038/s41427-023-00506-8","url":null,"abstract":"Abstract Pressure engineering in semiconductors leads to a variety of novel physical phenomena and has recently received considerable attention. Here, we report on pressure-induced superconductivity in III–V gallium phosphide (GaP), a commercially important semiconductor that exhibits excellent optical performance. We show that the emergence of superconductivity is accompanied by the concurrence of piezochromic transition and metallization and can be correlated to a structural transition from the cubic to orthorhombic phase. In line with the structural origin of superconductivity, the critical temperature T c monotonically decreases with increasing pressure up to ~50 GPa. Moreover, the superconductivity could be preserved toward ambient pressure because of the irreversibility of the structural transition. Nevertheless, the superconducting transition displays evident broadening associated with the presence of amorphization in the depressurized sample. The synchronous evolution of the structural and electronic properties not only shows a vivid structure-property relationship but also could facilitate the exploration of novel functionalities by means of pressure treatment.","PeriodicalId":19382,"journal":{"name":"Npg Asia Materials","volume":"16 6","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135092377","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-10-27DOI: 10.1038/s41427-023-00505-9
Peisen Zhang, Jiaoqiong Guan, Ni Zhang, Lichong Zhu, Yu Wang, Wenyue Li, Zhe Shi, Xueyuan Liu, Xue Li, Meng Qin, Yi Hou, Yue Lan
Abstract Depression is a prevalent mental illness that imposes a substantial public health burden. However, the diverse clinical phenotypes observed in patients make it difficult to realize precise diagnosis. Recently, accumulating preclinical and clinical evidence has suggested that inflammation is involved in the pathophysiology of depression. Herein, a molecular imaging–based strategy was proposed as a means to diagnose depression precisely by specifically visualizing the inflammation status associated with depression. Inflammation-targeting MRI nanoprobes were constructed by attaching an intercellular cell adhesion molecule-1 (ICAM-1)-targeting peptide to biocompatible Fe 3 O 4 nanoparticles. Systematic studies demonstrated that the nanoprobes could specifically target inflamed vascular endothelial cells and visualize the spatial distribution of inflammation in the depressed brain in vivo through susceptibility-weighted imaging (SWI), which was further confirmed by histological analysis. Additionally, these inflammatory brain regions identified by nanoprobe-based imaging are consistent with the focal regions closely associated with the symptoms of depression as reported in previous behavioral studies. Overall, this is the first study to directly visualize the distribution of inflammation in the depressed brain in vivo through a molecular imaging strategy, which may not only facilitate insight into the biological mechanism underlying depression but also provide a potential target within the depressed brain for the further development of anti-inflammatory therapies.
{"title":"Visualizing the spatial distribution of inflammation in the depressed brain with a targeted MRI nanoprobe in vivo","authors":"Peisen Zhang, Jiaoqiong Guan, Ni Zhang, Lichong Zhu, Yu Wang, Wenyue Li, Zhe Shi, Xueyuan Liu, Xue Li, Meng Qin, Yi Hou, Yue Lan","doi":"10.1038/s41427-023-00505-9","DOIUrl":"https://doi.org/10.1038/s41427-023-00505-9","url":null,"abstract":"Abstract Depression is a prevalent mental illness that imposes a substantial public health burden. However, the diverse clinical phenotypes observed in patients make it difficult to realize precise diagnosis. Recently, accumulating preclinical and clinical evidence has suggested that inflammation is involved in the pathophysiology of depression. Herein, a molecular imaging–based strategy was proposed as a means to diagnose depression precisely by specifically visualizing the inflammation status associated with depression. Inflammation-targeting MRI nanoprobes were constructed by attaching an intercellular cell adhesion molecule-1 (ICAM-1)-targeting peptide to biocompatible Fe 3 O 4 nanoparticles. Systematic studies demonstrated that the nanoprobes could specifically target inflamed vascular endothelial cells and visualize the spatial distribution of inflammation in the depressed brain in vivo through susceptibility-weighted imaging (SWI), which was further confirmed by histological analysis. Additionally, these inflammatory brain regions identified by nanoprobe-based imaging are consistent with the focal regions closely associated with the symptoms of depression as reported in previous behavioral studies. Overall, this is the first study to directly visualize the distribution of inflammation in the depressed brain in vivo through a molecular imaging strategy, which may not only facilitate insight into the biological mechanism underlying depression but also provide a potential target within the depressed brain for the further development of anti-inflammatory therapies.","PeriodicalId":19382,"journal":{"name":"Npg Asia Materials","volume":"24 3","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136317994","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Abstract The rise of three-dimensional topological insulators as an attractive playground for the observation and control of various spin-orbit effects has ushered in the field of topological spintronics. To fully exploit their potential as efficient spin-orbit torque generators, it is crucial to investigate the efficiency of spin injection and transport at various topological insulator/ferromagnet interfaces, as characterized by their spin-mixing conductances and interfacial spin transparencies. Here, we use all-optical time-resolved magneto-optical Kerr effect magnetometry to demonstrate efficient room-temperature spin pumping in Sub/BiSbTe 1.5 Se 1.5 (BSTS)/Co 20 Fe 60 B 20 (CoFeB)/SiO 2 thin films. From the modulation of Gilbert damping with BSTS and CoFeB thicknesses, the spin-mixing conductances of the BSTS/CoFeB interface and the spin diffusion length in BSTS are determined. For BSTS thicknesses far exceeding the spin diffusion length, in the so-called “perfect spin sink” regime, we obtain an interfacial spin transparency as high as 0.9, promoting such systems as scintillating candidates for spin-orbitronic devices.
三维拓扑绝缘体的兴起为观察和控制各种自旋轨道效应提供了一个有吸引力的平台，从而迎来了拓扑自旋电子学领域的发展。为了充分发挥其作为高效自旋轨道转矩发生器的潜力，研究自旋注入和输运在不同拓扑绝缘体/铁磁体界面上的效率是至关重要的，其特征是自旋混合电导和界面自旋透明度。在这里，我们使用全光时间分辨磁光克尔效应磁强计来证明在Sub/BiSbTe 1.5 Se 1.5 (BSTS)/Co 20 Fe 60 b20 (CoFeB)/ sio2薄膜中有效的室温自旋泵浦。通过BSTS和CoFeB厚度对Gilbert阻尼的调制，确定了BSTS/CoFeB界面的自旋混合电导和BSTS中的自旋扩散长度。当BSTS厚度远远超过自旋扩散长度时，在所谓的“完美自旋汇”机制下，我们获得了高达0.9的界面自旋透明度，促进了该系统成为自旋轨道电子器件的闪烁候点。
{"title":"All-optical observation of giant spin transparency at the topological insulator BiSbTe1.5Se1.5/Co20Fe60B20 interface","authors":"Suchetana Mukhopadhyay, Pratap Kumar Pal, Subhadeep Manna, Chiranjib Mitra, Anjan Barman","doi":"10.1038/s41427-023-00504-w","DOIUrl":"https://doi.org/10.1038/s41427-023-00504-w","url":null,"abstract":"Abstract The rise of three-dimensional topological insulators as an attractive playground for the observation and control of various spin-orbit effects has ushered in the field of topological spintronics. To fully exploit their potential as efficient spin-orbit torque generators, it is crucial to investigate the efficiency of spin injection and transport at various topological insulator/ferromagnet interfaces, as characterized by their spin-mixing conductances and interfacial spin transparencies. Here, we use all-optical time-resolved magneto-optical Kerr effect magnetometry to demonstrate efficient room-temperature spin pumping in Sub/BiSbTe 1.5 Se 1.5 (BSTS)/Co 20 Fe 60 B 20 (CoFeB)/SiO 2 thin films. From the modulation of Gilbert damping with BSTS and CoFeB thicknesses, the spin-mixing conductances of the BSTS/CoFeB interface and the spin diffusion length in BSTS are determined. For BSTS thicknesses far exceeding the spin diffusion length, in the so-called “perfect spin sink” regime, we obtain an interfacial spin transparency as high as 0.9, promoting such systems as scintillating candidates for spin-orbitronic devices.","PeriodicalId":19382,"journal":{"name":"Npg Asia Materials","volume":"74 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135566618","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Abstract Highly efficient electrocatalysts for the hydrogen evolution reaction (HER) are essential for sustainable hydrogen energy. The controllable production of hydrogen energy by water decomposition depends heavily on the catalyst, and it is extremely important to seek sustainable and highly efficient water-splitting electrocatalysts for energy applications. Herein, bimetallic RuYO 2 − x nanoparticles (Ru: 8.84 at.% and Y: 13 at.%) with high densities and low loadings were synthesized and anchored on graphene through a simple solvothermal strategy by synthesizing hydrogen yttrium ketone (H x YO 2 − x ) serving as an inserted medium. Electron microscopy demonstrated that the RuYO 2 − x /C was composed of densely arranged particles and graphene flakes. Electrochemical results showed that the RuYO 2 − x /C had a remarkably low overpotential of η 10 = 56 mV at a current density of 10 mA cm −2 in alkaline media, a Tafel slope of 63.18 mV dec −1 , and 24 h of stability. The oxygen vacancies of RuYO 2 − x /C provided a large proton storage capacity and a strong tendency to bind hydrogen atoms. DFT calculations showed that RuYO 2 − x/ C catalysts with more Ru-O-Y bonds and V O dramatically decreased the energy barrier for breaking H-OH bonds. Moreover, the robust metal-support interactions provided optimized energies for hydrogen adsorption and desorption, which explained the high activity and favorable kinetics for RuYO 2 − x /C catalytic hydrogen precipitation in alkaline electrolyte reactions. This work presents a hydrogen insertion method for the preparation of low-loading, high-density, high-performance and stable water decomposition catalysts for hydrogen production.
{"title":"Implanting HxYO2−x sites into Ru-doped graphene and oxygen vacancies for low-overpotential alkaline hydrogen evolution","authors":"Xiang Li, Wei Deng, Yun Weng, Jingjing Zhang, Haifang Mao, Tiandong Lu, Wenqian Zhang, Renqiang Yang, Fei Jiang","doi":"10.1038/s41427-023-00501-z","DOIUrl":"https://doi.org/10.1038/s41427-023-00501-z","url":null,"abstract":"Abstract Highly efficient electrocatalysts for the hydrogen evolution reaction (HER) are essential for sustainable hydrogen energy. The controllable production of hydrogen energy by water decomposition depends heavily on the catalyst, and it is extremely important to seek sustainable and highly efficient water-splitting electrocatalysts for energy applications. Herein, bimetallic RuYO 2 − x nanoparticles (Ru: 8.84 at.% and Y: 13 at.%) with high densities and low loadings were synthesized and anchored on graphene through a simple solvothermal strategy by synthesizing hydrogen yttrium ketone (H x YO 2 − x ) serving as an inserted medium. Electron microscopy demonstrated that the RuYO 2 − x /C was composed of densely arranged particles and graphene flakes. Electrochemical results showed that the RuYO 2 − x /C had a remarkably low overpotential of η 10 = 56 mV at a current density of 10 mA cm −2 in alkaline media, a Tafel slope of 63.18 mV dec −1 , and 24 h of stability. The oxygen vacancies of RuYO 2 − x /C provided a large proton storage capacity and a strong tendency to bind hydrogen atoms. DFT calculations showed that RuYO 2 − x/ C catalysts with more Ru-O-Y bonds and V O dramatically decreased the energy barrier for breaking H-OH bonds. Moreover, the robust metal-support interactions provided optimized energies for hydrogen adsorption and desorption, which explained the high activity and favorable kinetics for RuYO 2 − x /C catalytic hydrogen precipitation in alkaline electrolyte reactions. This work presents a hydrogen insertion method for the preparation of low-loading, high-density, high-performance and stable water decomposition catalysts for hydrogen production.","PeriodicalId":19382,"journal":{"name":"Npg Asia Materials","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135566807","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-10-13DOI: 10.1038/s41427-023-00502-y
Dongjoon Shin, Seunghoon Chae, Seonghyun Park, Byungseok Seo, Wonjoon Choi
Abstract High-entropy oxides (HEOs) are promising conversion-type anode materials for Li-ion batteries (LIBs) owing to their excellent cycling stabilities and rate capabilities. However, the conventional syntheses and screening processes are time-consuming and complex and require phase and interfacial segregation of individual elements. Herein, we report a rational screening strategy for LIB anodes using precisely tunable HEOs fabricated by one-step combustion syntheses with different fuel-to-oxidizer ratios (φ). A slightly lean fuel mixture (φ-0.95) enabled a suitable temperature and non-reducing atmosphere for optimal HEO syntheses. This provided high crystallinity, perfectly homogeneous elemental distributions, and adequate pore structures without selective precipitation, whereas lower or higher fuel-to-oxidizer ratios resulted in excessively porous morphologies or elemental segregation. HEO-based anodes with φ-0.95 exhibited outstanding specific capacities (1165 mAh g −1 , 80.9% retention at 0.1 A g −1 , and 791 mAh g −1 even at 3 A g −1 ), excellent rate capabilities, and stable cycling lifetimes (1252 mAh g −1 , 80.9% retention after 100 cycles at 0.2 A g −1 ). This design strategy will provide fascinating HEO electrodes that cannot be prepared with conventional fabrication methods.
摘要:高熵氧化物(HEOs)具有良好的循环稳定性和倍率性能，是锂离子电池(LIBs)极有前途的转换型负极材料。然而，传统的合成和筛选过程耗时且复杂，并且需要对单个元素进行相分离和界面分离。在此，我们报告了一种合理的筛选策略，使用一步燃烧合成的具有不同燃料-氧化剂比(φ)的精确可调谐HEOs来筛选锂离子电池阳极。稍稀薄的燃料混合物(φ-0.95)为最佳的HEO合成提供了合适的温度和非还原气氛。这提供了高结晶度、完全均匀的元素分布和足够的孔隙结构，没有选择性沉淀，而较低或较高的燃料与氧化剂比会导致过度多孔形态或元素偏析。φ-0.95的heo基阳极具有出色的比容量(1165 mAh g−1，在0.1 A g−1下保持80.9%，在3 A g−1下保持791 mAh g−1)，优异的倍率能力和稳定的循环寿命(1252 mAh g−1，在0.2 A g−1下循环100次后保持80.9%)。这种设计策略将提供传统制造方法无法制备的令人着迷的HEO电极。
{"title":"Rational engineering of high-entropy oxides for Li-ion battery anodes with finely tuned combustion syntheses","authors":"Dongjoon Shin, Seunghoon Chae, Seonghyun Park, Byungseok Seo, Wonjoon Choi","doi":"10.1038/s41427-023-00502-y","DOIUrl":"https://doi.org/10.1038/s41427-023-00502-y","url":null,"abstract":"Abstract High-entropy oxides (HEOs) are promising conversion-type anode materials for Li-ion batteries (LIBs) owing to their excellent cycling stabilities and rate capabilities. However, the conventional syntheses and screening processes are time-consuming and complex and require phase and interfacial segregation of individual elements. Herein, we report a rational screening strategy for LIB anodes using precisely tunable HEOs fabricated by one-step combustion syntheses with different fuel-to-oxidizer ratios (φ). A slightly lean fuel mixture (φ-0.95) enabled a suitable temperature and non-reducing atmosphere for optimal HEO syntheses. This provided high crystallinity, perfectly homogeneous elemental distributions, and adequate pore structures without selective precipitation, whereas lower or higher fuel-to-oxidizer ratios resulted in excessively porous morphologies or elemental segregation. HEO-based anodes with φ-0.95 exhibited outstanding specific capacities (1165 mAh g −1 , 80.9% retention at 0.1 A g −1 , and 791 mAh g −1 even at 3 A g −1 ), excellent rate capabilities, and stable cycling lifetimes (1252 mAh g −1 , 80.9% retention after 100 cycles at 0.2 A g −1 ). This design strategy will provide fascinating HEO electrodes that cannot be prepared with conventional fabrication methods.","PeriodicalId":19382,"journal":{"name":"Npg Asia Materials","volume":"25 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135805511","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-10-13DOI: 10.1038/s41427-023-00500-0
Yangbo Dong, Danyang Feng, Wei Li, Rui Zhang, Shuzhen Dou, Luoqi Wang, Yan Yang, Li Wang, Yang Yang, Feng Wei, Zhen-An Qiao
Abstract Gradient porous structures enable the fast capillary-directed mass transport and enhance the chemical reaction rate with optimal efficiency and minimal energy consumption. Rational design and facile synthesis of functional mesoporous materials with sheet structure and gradient mesopores still face challenges of stacked structures and unadjustable pore sizes. Herein, an interfacial co-assembly strategy for gradient mesoporous hollow silica sheets is reported. The modulated oil-water interface allows the assembly of gradient mesoporous silica layers on the water-removable ammonium sulfate crystals. The obtained mesoporous silica layers possess narrow pore size distributions (~2.2 nm and ~6.6 nm). Owing to the good mono-dispersity, sheet structure and proper pore size, the designed gradient mesoporous hollow silica sheets can serve as flexible building blocks for fabricating nanoscale molecule filtration device. Experiments reveal that the obtained nanofiltration device shows remarkable gradient rejection rates (range from 23.5 to 99.9%) for molecules with different sizes (range from 1.2 to 4.4 nm).
{"title":"Interfacial co-assembly strategy towards gradient mesoporous hollow sheet for molecule filtration","authors":"Yangbo Dong, Danyang Feng, Wei Li, Rui Zhang, Shuzhen Dou, Luoqi Wang, Yan Yang, Li Wang, Yang Yang, Feng Wei, Zhen-An Qiao","doi":"10.1038/s41427-023-00500-0","DOIUrl":"https://doi.org/10.1038/s41427-023-00500-0","url":null,"abstract":"Abstract Gradient porous structures enable the fast capillary-directed mass transport and enhance the chemical reaction rate with optimal efficiency and minimal energy consumption. Rational design and facile synthesis of functional mesoporous materials with sheet structure and gradient mesopores still face challenges of stacked structures and unadjustable pore sizes. Herein, an interfacial co-assembly strategy for gradient mesoporous hollow silica sheets is reported. The modulated oil-water interface allows the assembly of gradient mesoporous silica layers on the water-removable ammonium sulfate crystals. The obtained mesoporous silica layers possess narrow pore size distributions (~2.2 nm and ~6.6 nm). Owing to the good mono-dispersity, sheet structure and proper pore size, the designed gradient mesoporous hollow silica sheets can serve as flexible building blocks for fabricating nanoscale molecule filtration device. Experiments reveal that the obtained nanofiltration device shows remarkable gradient rejection rates (range from 23.5 to 99.9%) for molecules with different sizes (range from 1.2 to 4.4 nm).","PeriodicalId":19382,"journal":{"name":"Npg Asia Materials","volume":"235 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135806023","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-10-06DOI: 10.1038/s41427-023-00496-7
Guangyang Dai, Yating Jia, Bo Gao, Yi Peng, Jianfa Zhao, Yanming Ma, Changfeng Chen, Jinlong Zhu, Quan Li, Runze Yu, Changqing Jin
Abstract Recently, topological insulators (TIs) KHgX (X = As, Sb, Bi) with hourglass-shaped dispersion have attracted great interest. Different from the TIs protected by either time-reversal or mirror crystal symmorphic symmetry tested in previous experiments, these materials were proposed as the first material class whose band topology relies on nonsymmorphic symmetries. As a result, KHgX shows many exotic properties, such as hourglass-shaped electronic channels and three-dimensional doubled quantum spin Hall effects. To date, high-pressure experimental studies on these nonsymmorphic TIs are minimal. Here, we carried out high-pressure electrical measurements up to 55 GPa, together with high-pressure X-ray diffraction measurements and high-pressure structure prediction on KHgAs. We found a pressure-induced semiconductor-metal transition between ~16 and 20 GPa, followed by the appearance of superconductivity with a T c of ~3.5 K at approximately 21 GPa. The superconducting transition temperature was enhanced to a maximum of ~6.6 K at 31.8 GPa and then slowly decreased until 55 GPa. Furthermore, three high-pressure phases within 55 GPa were observed, and their crystal structures were established. Our results showed the high-pressure phase diagram of KHgAs and determined the pressure-induced superconductivity in nonsymmorphic TIs. Thus, our study can be used to facilitate further research on superconductivity and topologically nontrivial features protected by nonsymmorphic symmetries.
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