Pub Date : 2024-10-02DOI: 10.1016/j.matt.2024.08.012
Yunjie Xu , Jungryun Kim , Hyeonji Rha , Jong Seung Kim
The advent of photon-controlled pyroptosis activation (PhotoPyro) has attracted great interest in photoimmunotherapy. Recently in Nature Communication, Seo, Min, Kwon, and co-workers reported an amphiphilic photocatalyst that induces non-canonical pyroptosis through the oxidative photocatalysis of water molecules into highly reactive hydroxyl radicals, triggering intracellular membrane-focused oxidative stress, a maladaptive unfolded protein response, and cation mobilization. This elegant work represents a new strategy for elucidating the cellular response to intracellular membrane oxidation.
{"title":"Oxidative photocatalysis on intracellular membranes lights up PhotoPyro","authors":"Yunjie Xu , Jungryun Kim , Hyeonji Rha , Jong Seung Kim","doi":"10.1016/j.matt.2024.08.012","DOIUrl":"10.1016/j.matt.2024.08.012","url":null,"abstract":"<div><div>The advent of photon-controlled pyroptosis activation (PhotoPyro) has attracted great interest in photoimmunotherapy. Recently in <em>Nature Communication</em>, Seo, Min, Kwon, and co-workers reported an amphiphilic photocatalyst that induces non-canonical pyroptosis through the oxidative photocatalysis of water molecules into highly reactive hydroxyl radicals, triggering intracellular membrane-focused oxidative stress, a maladaptive unfolded protein response, and cation mobilization. This elegant work represents a new strategy for elucidating the cellular response to intracellular membrane oxidation.</div></div>","PeriodicalId":388,"journal":{"name":"Matter","volume":"7 10","pages":"Pages 3253-3255"},"PeriodicalIF":17.3,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142363175","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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 : 2024-10-02DOI: 10.1016/j.matt.2024.07.005
Geoffrey Ozin
The heat is on, the temperature is rising, and the urgency of global warming means we’ve got to get cracking with the transition of the world’s energy supply from burning nature’s unsustainable legacy resources to the sustainable power gifted to humanity in earth’s unlimited sunlight, wind, tidal and geothermal, and dare I say, nuclear energy supplies.
{"title":"Let’s get cracking – Solar ethene and hydrogen","authors":"Geoffrey Ozin","doi":"10.1016/j.matt.2024.07.005","DOIUrl":"10.1016/j.matt.2024.07.005","url":null,"abstract":"<div><div>The heat is on, the temperature is rising, and the urgency of global warming means we’ve got to get cracking with the transition of the world’s energy supply from burning nature’s unsustainable legacy resources to the sustainable power gifted to humanity in earth’s unlimited sunlight, wind, tidal and geothermal, and dare I say, nuclear energy supplies.</div></div>","PeriodicalId":388,"journal":{"name":"Matter","volume":"7 10","pages":"Pages 3224-3225"},"PeriodicalIF":17.3,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142363168","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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 : 2024-10-02DOI: 10.1016/j.matt.2024.08.025
Steve Cranford
As editor-in-chief, I frequently travel to conferences and universities to meet researchers, discuss science, and promote the Cell Press portfolio. A crucial geographical region for Matter’s success has been China—a key player in the world of materials science. Here, I recount my most recent August 2024 visit to give a glimpse of what it’s like to be an editor far from home.
{"title":"The editor-in-chief in China, or there and back again","authors":"Steve Cranford","doi":"10.1016/j.matt.2024.08.025","DOIUrl":"10.1016/j.matt.2024.08.025","url":null,"abstract":"<div><div>As editor-in-chief, I frequently travel to conferences and universities to meet researchers, discuss science, and promote the Cell Press portfolio. A crucial geographical region for <em>Matter</em>’s success has been China—a key player in the world of materials science. Here, I recount my most recent August 2024 visit to give a glimpse of what it’s like to be an editor far from home.</div></div>","PeriodicalId":388,"journal":{"name":"Matter","volume":"7 10","pages":"Pages 3226-3233"},"PeriodicalIF":17.3,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142363169","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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 : 2024-10-02DOI: 10.1016/j.matt.2024.09.003
Alazne Moreno-Lanceta , Elazer R. Edelman , João Conde , Pedro Melgar-Lesmes
The incidence of chronic liver disease is increasing worldwide. Inflammation is a driving force in this disease; however, there is a need to further define the centrality of macrophages. With advances in nanotechnology, the therapeutic landscape of modulating macrophages against liver inflammation, fibrosis, and cancer can be considered using nanotherapeutics.
{"title":"Nano-navigated macrophages: Piercing liver inflammation, fibrosis, and cancer","authors":"Alazne Moreno-Lanceta , Elazer R. Edelman , João Conde , Pedro Melgar-Lesmes","doi":"10.1016/j.matt.2024.09.003","DOIUrl":"10.1016/j.matt.2024.09.003","url":null,"abstract":"<div><div>The incidence of chronic liver disease is increasing worldwide. Inflammation is a driving force in this disease; however, there is a need to further define the centrality of macrophages. With advances in nanotechnology, the therapeutic landscape of modulating macrophages against liver inflammation, fibrosis, and cancer can be considered using nanotherapeutics.</div></div>","PeriodicalId":388,"journal":{"name":"Matter","volume":"7 10","pages":"Pages 3234-3237"},"PeriodicalIF":17.3,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142363170","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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 : 2024-10-02DOI: 10.1016/j.matt.2024.05.042
Recent advancements in property-directed generative design of inorganic materials account for periodicity and global Euclidian symmetry through translations, rotations, and reflections; however, they do not account for symmetry constraints within allowed space groups. To address this, we introduce a generative design framework (WyCryst) composed of three components: (1) a Wyckoff position-based inorganic crystal representation, (2) a property-directed variational autoencoder (VAE) model, and (3) an automated density functional theory (DFT) workflow for structure refinement. Our framework selectively generates materials by encoding the Wyckoff representation for each space group. As validation, we reproduce a variety of existing materials, CaTiO3, CsPbI3, BaTiO3, and CuInS2, for both ground-state and polymorphic crystal structure predictions. We also generate several ternary materials not found in the training database, which are proven to retain their symmetry and are phononically stable using our automated DFT workflow. We believe our symmetry-aware WyCryst takes a vital step toward AI-driven inorganic materials discovery.
{"title":"WyCryst: Wyckoff inorganic crystal generator framework","authors":"","doi":"10.1016/j.matt.2024.05.042","DOIUrl":"10.1016/j.matt.2024.05.042","url":null,"abstract":"<div><div><span><span>Recent advancements in property-directed generative design of inorganic materials account for periodicity and global Euclidian symmetry through translations, rotations, and reflections; however, they do not account for symmetry constraints within allowed space groups. To address this, we introduce a generative design framework (WyCryst) composed of three components: (1) a Wyckoff position-based inorganic crystal representation, (2) a property-directed variational </span>autoencoder<span> (VAE) model, and (3) an automated density functional theory (DFT) workflow for structure refinement. Our framework selectively generates materials by encoding the Wyckoff representation for each space group. As validation, we reproduce a variety of existing materials, CaTiO</span></span><sub>3</sub>, CsPbI<sub>3</sub>, BaTiO<sub>3</sub>, and CuInS<sub>2</sub>, for both ground-state and polymorphic crystal structure predictions. We also generate several ternary materials not found in the training database, which are proven to retain their symmetry and are phononically stable using our automated DFT workflow. We believe our symmetry-aware WyCryst takes a vital step toward AI-driven inorganic materials discovery.</div></div>","PeriodicalId":388,"journal":{"name":"Matter","volume":"7 10","pages":"Pages 3469-3488"},"PeriodicalIF":17.3,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141448845","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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 : 2024-10-02DOI: 10.1016/j.matt.2024.05.047
Multiphase formations within quasi-two-dimensional (quasi-2D) perovskite films have been shown to impede efficient charge transfer, reducing device performance. To address this issue, we propose using acetic acid (AcOH) as an additive to achieve a narrow phase distribution in quasi-2D perovskite films. In situ UV-visible light absorption spectra show an effective reduction in phase polydispersity in the early stage of film crystallization. First-principles calculations confirm that the AcOH coordination alters the reaction path, lowering the enthalpy of formation for a concentrated phase distribution. This configuration leads to carrier diffusion length exceeding 1 μm, and the mobility is up to 7.18 cm2 V−1 s−1 in the quasi-2D perovskite film. The resultant solar cells exhibit a champion power conversion efficiency (PCE) of 19.05% and demonstrate exceptional long-term stability, retaining over 90% of their initial PCEs over 10,000 h and maintaining over 80% efficiency after 500 h under continuous illumination tracking at the maximum power point.
{"title":"Governing the dispersion of quasi-2D perovskite phases toward efficient and stable perovskite solar cells","authors":"","doi":"10.1016/j.matt.2024.05.047","DOIUrl":"10.1016/j.matt.2024.05.047","url":null,"abstract":"<div><div>Multiphase formations within quasi-two-dimensional (quasi-2D) perovskite films have been shown to impede efficient charge transfer, reducing device performance. To address this issue, we propose using acetic acid (AcOH) as an additive to achieve a narrow phase distribution in quasi-2D perovskite films. <em>In situ</em> UV-visible light absorption spectra show an effective reduction in phase polydispersity in the early stage of film crystallization. First-principles calculations confirm that the AcOH coordination alters the reaction path, lowering the enthalpy of formation for a concentrated phase distribution. This configuration leads to carrier diffusion length exceeding 1 μm, and the mobility is up to 7.18 cm<sup>2</sup> V<sup>−1</sup> s<sup>−1</sup> in the quasi-2D perovskite film. The resultant solar cells exhibit a champion power conversion efficiency (PCE) of 19.05% and demonstrate exceptional long-term stability, retaining over 90% of their initial PCEs over 10,000 h and maintaining over 80% efficiency after 500 h under continuous illumination tracking at the maximum power point.</div></div>","PeriodicalId":388,"journal":{"name":"Matter","volume":"7 10","pages":"Pages 3500-3517"},"PeriodicalIF":17.3,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141453243","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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 : 2024-10-02DOI: 10.1016/j.matt.2024.05.045
Field-free switching of perpendicular magnetization driven by magnons is a promising technology that can significantly reduce energy dissipation and potential damage to spintronic devices. However, achieving such switching experimentally often demands an additional in-plane magnetic field or other complex measures, severely limiting its prospects. Here, we have successfully demonstrated field-free switching of perpendicular magnetization through a magnon current with tilted polarization in specially designed all-oxide heterostructures of SrRuO3/LaMnO3/SrIrO3. The ferromagnetic interface, resulting from charge reconstruction between the LaMnO3 and SrIrO3 layers, generates a tilted-polarized magnon current. This magnon current effectively breaks the mirror symmetry that traditionally hinders deterministic switching in spin-orbit torque setups and realizes field-free switching of perpendicular magnetization. In addition, the critical switching current density is significantly lower than that in conventional metallic systems. These findings open a promising avenue for developing highly efficient all-oxide spintronic devices that can be operated by magnon current.
{"title":"Manipulation of perpendicular magnetization via magnon current with tilted polarization","authors":"","doi":"10.1016/j.matt.2024.05.045","DOIUrl":"10.1016/j.matt.2024.05.045","url":null,"abstract":"<div><div><span><span>Field-free switching of perpendicular magnetization driven by magnons is a promising technology that can significantly reduce energy dissipation and potential damage to </span>spintronic<span> devices. However, achieving such switching experimentally often demands an additional in-plane magnetic field or other complex measures, severely limiting its prospects. Here, we have successfully demonstrated field-free switching of perpendicular magnetization through a magnon current with tilted polarization in specially designed all-oxide heterostructures of SrRuO</span></span><sub>3</sub>/LaMnO<sub>3</sub>/SrIrO<sub>3</sub>. The ferromagnetic interface, resulting from charge reconstruction between the LaMnO<sub>3</sub> and SrIrO<sub>3</sub> layers, generates a tilted-polarized magnon current. This magnon current effectively breaks the mirror symmetry that traditionally hinders deterministic switching in spin-orbit torque setups and realizes field-free switching of perpendicular magnetization. In addition, the critical switching current density is significantly lower than that in conventional metallic systems. These findings open a promising avenue for developing highly efficient all-oxide spintronic devices that can be operated by magnon current.</div></div>","PeriodicalId":388,"journal":{"name":"Matter","volume":"7 10","pages":"Pages 3489-3499"},"PeriodicalIF":17.3,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141448912","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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 : 2024-10-02DOI: 10.1016/j.matt.2024.08.004
Zhen Yu , Ting Xiong , Yaoxin Zhang
Interfacial solar evaporators have attracted increasing attention recently. Traditional photothermal absorbers typically rely on capillary wicking for continuous water supply, often resulting in water filling the entire porous structure and thus causing unnecessary parasitic heat loss. The formation of the micro-nano water films in the evaporation materials enabled rapid solar-driven water evaporation owing to the reduced evaporation entropy, larger evaporation area, and minimized heat loss.
{"title":"Dynamic water gating facilitated the formation of micro-nano water films for rapid solar-driven evaporation","authors":"Zhen Yu , Ting Xiong , Yaoxin Zhang","doi":"10.1016/j.matt.2024.08.004","DOIUrl":"10.1016/j.matt.2024.08.004","url":null,"abstract":"<div><div>Interfacial solar evaporators have attracted increasing attention recently. Traditional photothermal absorbers typically rely on capillary wicking for continuous water supply, often resulting in water filling the entire porous structure and thus causing unnecessary parasitic heat loss. The formation of the micro-nano water films in the evaporation materials enabled rapid solar-driven water evaporation owing to the reduced evaporation entropy, larger evaporation area, and minimized heat loss.</div></div>","PeriodicalId":388,"journal":{"name":"Matter","volume":"7 10","pages":"Pages 3250-3252"},"PeriodicalIF":17.3,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142363178","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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 : 2024-10-02DOI: 10.1016/j.matt.2024.06.012
Noncovalent organic frameworks (NCOFs) are porous materials constructed by diverse intermolecular interactions. It is challenging to obtain polymorphic NCOFs with adjustable pores and high-performance polarized luminescence. Here, two polymorphic organometallic NCOFs, 1-α and 1-β, are presented from an iridium complex 1 based on the intralayer F···H hydrogen bonding and interlayer cation-anion electrostatic interactions. These metalloligand-anion frameworks display linearly polarized blue phosphorescence with a polarization degree of up to 0.91 and optical waveguide properties. The 1-α microcrystals doped with a ruthenium acceptor manifest a reversible response to Et2O vapor, showing modulated energy transfer and polarized luminescence. The 1-α and 1-β microcrystals are transformed into another polymorphic 1-γ crystal by incorporating chiral (R/S)-carvone guests, affording tunable circularly polarized luminescence with a dissymmetry factor of around 0.1. This work provides a unique concept to obtain polymorphic NCOFs, demonstrating prominent potential in multifunctional optical and chiroptical applications.
{"title":"Metalloligand-anion frameworks: Tunable polarized luminescence and crystal-to-crystal transformation","authors":"","doi":"10.1016/j.matt.2024.06.012","DOIUrl":"10.1016/j.matt.2024.06.012","url":null,"abstract":"<div><div><span><span>Noncovalent organic frameworks (NCOFs) are porous materials constructed by diverse intermolecular interactions. It is challenging to obtain polymorphic NCOFs with adjustable pores and high-performance </span>polarized luminescence<span>. Here, two polymorphic organometallic NCOFs, </span></span><strong>1</strong>-<em>α</em> and <strong>1</strong>-<em>β</em><span>, are presented from an iridium complex </span><strong>1</strong><span><span> based on the intralayer F···H hydrogen bonding and interlayer cation-anion </span>electrostatic interactions<span>. These metalloligand-anion frameworks display linearly polarized blue phosphorescence with a polarization degree of up to 0.91 and optical waveguide properties. The </span></span><strong>1</strong>-<em>α</em><span> microcrystals<span> doped with a ruthenium acceptor manifest a reversible response to Et</span></span><sub>2</sub>O vapor, showing modulated energy transfer and polarized luminescence. The <strong>1</strong>-<em>α</em> and <strong>1</strong>-<em>β</em><span> microcrystals are transformed into another polymorphic </span><strong>1</strong>-<em>γ</em> crystal by incorporating chiral (<em>R</em>/<em>S</em><span>)-carvone guests, affording tunable circularly polarized luminescence with a dissymmetry factor of around 0.1. This work provides a unique concept to obtain polymorphic NCOFs, demonstrating prominent potential in multifunctional optical and chiroptical applications.</span></div></div>","PeriodicalId":388,"journal":{"name":"Matter","volume":"7 10","pages":"Pages 3537-3553"},"PeriodicalIF":17.3,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141561824","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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 : 2024-10-02DOI: 10.1016/j.matt.2024.06.023
Supreeth Nagendran , Amoghavarsha Mahadevegowda , Sundeep Vema , Mohsen Danaie , Weixin Song , Bo Wen , Caterina Ducati , Clare P. Grey
Niobium tungsten oxides are gaining attention as anodes for lithium-ion batteries due to their high volumetric energy storage densities obtained at high cycling rates. Two new niobium tungsten bronze structures, NbWO5.5 and β-Nb2WO8, were prepared with microwave-assisted solution-based methods at 800°C. These adopt a simple tetragonal tungsten bronze (TTB) and a √2 × √2 TTB superstructure, respectively. Nb3WO10.5 with a structure closely related to β-Nb2WO8 was formed at higher Nb:W ratios. Nb:W ≥ 4 compositions result in two-phase behavior forming Nb2O5 and Nb3WO10.5, while W-rich bronzes (Nb:W < 1) exhibited local domains of WO3 within the NbWO5.5 lattice. Diffraction and electron microscopy analysis revealed cation ordering in the bronzes at different length scales. The microwave synthesis method produced microporous spheres, with the high-Nb-content phases showing promising high-rate capabilities and long cycle lives, making them suitable for energy-storage applications. The microwave-assisted solution method holds potential for synthesizing complex oxide materials across diverse applications.
{"title":"Cation ordering in low-temperature niobium-rich NbWO bronzes: New anodes for high-rate Li-ion batteries","authors":"Supreeth Nagendran , Amoghavarsha Mahadevegowda , Sundeep Vema , Mohsen Danaie , Weixin Song , Bo Wen , Caterina Ducati , Clare P. Grey","doi":"10.1016/j.matt.2024.06.023","DOIUrl":"10.1016/j.matt.2024.06.023","url":null,"abstract":"<div><div>Niobium tungsten oxides are gaining attention as anodes for lithium-ion batteries due to their high volumetric energy storage densities obtained at high cycling rates. Two new niobium tungsten bronze structures, NbWO<sub>5.5</sub> and β-Nb<sub>2</sub>WO<sub>8</sub>, were prepared with microwave-assisted solution-based methods at 800°C. These adopt a simple tetragonal tungsten bronze (TTB) and a √2 × √2 TTB superstructure, respectively. Nb<sub>3</sub>WO<sub>10.5</sub> with a structure closely related to β-Nb<sub>2</sub>WO<sub>8</sub> was formed at higher Nb:W ratios. Nb:W ≥ 4 compositions result in two-phase behavior forming Nb<sub>2</sub>O<sub>5</sub> and Nb<sub>3</sub>WO<sub>10.5</sub>, while W-rich bronzes (Nb:W < 1) exhibited local domains of WO<sub>3</sub> within the NbWO<sub>5.5</sub> lattice. Diffraction and electron microscopy analysis revealed cation ordering in the bronzes at different length scales. The microwave synthesis method produced microporous spheres, with the high-Nb-content phases showing promising high-rate capabilities and long cycle lives, making them suitable for energy-storage applications. The microwave-assisted solution method holds potential for synthesizing complex oxide materials across diverse applications.</div></div>","PeriodicalId":388,"journal":{"name":"Matter","volume":"7 10","pages":"Pages 3567-3586"},"PeriodicalIF":17.3,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141732702","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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