Pub Date : 2026-03-04DOI: 10.1038/s41563-026-02510-z
Hidekazu Kurebayashi, Joseph Barker, Takumi Yamazaki, Varun K. Kushwaha, Kilian D. Stenning, Harry Youel, Xueyao Hou, Troy Dion, Daniel Prestwood, Gerrit E. W. Bauer, Kei Yamamoto, Takeshi Seki
Spin transfer torques (STTs) control magnetization by electric currents, enabling a range of nano-scale spintronic applications. They can destabilize the equilibrium magnetization state by counteracting magnetic relaxation. Here we maximize the STT effect through a dedicated growth-annealing protocol for CoFeB thin films, such that magnetic anisotropies originating from the interface and shape almost cancel each other. The nearly isotropic magnets enable low-current dynamical stabilization of the magnetization in the direction opposite to an applied magnetic field, thereby realizing a spintronic analogue of the Kapitza pendulum. In an intermediate current regime, the STT drives large magnetization vector fluctuations that cover the entire Bloch sphere. The continuous variable associated with the stochastic magnetization direction may serve as a resource for probabilistic computing and neuromorphic hardware. Our results establish isotropic magnets as a platform to study as-yet-uncharted, far-from-equilibrium spin dynamics including anti-magnonics, with promising implications for unconventional computing paradigms.
{"title":"Dynamical stability by spin transfer in nearly isotropic magnets","authors":"Hidekazu Kurebayashi, Joseph Barker, Takumi Yamazaki, Varun K. Kushwaha, Kilian D. Stenning, Harry Youel, Xueyao Hou, Troy Dion, Daniel Prestwood, Gerrit E. W. Bauer, Kei Yamamoto, Takeshi Seki","doi":"10.1038/s41563-026-02510-z","DOIUrl":"https://doi.org/10.1038/s41563-026-02510-z","url":null,"abstract":"Spin transfer torques (STTs) control magnetization by electric currents, enabling a range of nano-scale spintronic applications. They can destabilize the equilibrium magnetization state by counteracting magnetic relaxation. Here we maximize the STT effect through a dedicated growth-annealing protocol for CoFeB thin films, such that magnetic anisotropies originating from the interface and shape almost cancel each other. The nearly isotropic magnets enable low-current dynamical stabilization of the magnetization in the direction opposite to an applied magnetic field, thereby realizing a spintronic analogue of the Kapitza pendulum. In an intermediate current regime, the STT drives large magnetization vector fluctuations that cover the entire Bloch sphere. The continuous variable associated with the stochastic magnetization direction may serve as a resource for probabilistic computing and neuromorphic hardware. Our results establish isotropic magnets as a platform to study as-yet-uncharted, far-from-equilibrium spin dynamics including anti-magnonics, with promising implications for unconventional computing paradigms.","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":"54 1","pages":""},"PeriodicalIF":41.2,"publicationDate":"2026-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147346886","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 : 2026-03-04DOI: 10.1038/s41563-026-02545-2
Heterogeneous microstructure engineering has become a powerful strategy for optimizing properties and performance of metallic alloys.
非均相组织工程已成为优化金属合金性能的有力手段。
{"title":"Heterogeneity by design","authors":"","doi":"10.1038/s41563-026-02545-2","DOIUrl":"10.1038/s41563-026-02545-2","url":null,"abstract":"Heterogeneous microstructure engineering has become a powerful strategy for optimizing properties and performance of metallic alloys.","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":"25 3","pages":"335-335"},"PeriodicalIF":38.5,"publicationDate":"2026-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.comhttps://www.nature.com/articles/s41563-026-02545-2.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147352898","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The efficacy of in situ cancer vaccination has been hampered by a poor spatiotemporal orchestration of multiple key steps of the cancer-immunity cycle in most tumours and systemic toxicity related to therapeutic strategies. Here we report a systemic injectable and pyroptosis-enabled nanoadjuvant that evokes the secretion of a vaccine-like pyroptosome in the tumour area for robust antitumour immunity. This systemic injectable and pyroptosis-enabled nanoadjuvant induces vigorous immunogenic pyroptosis, triggering the efficient release of tumour antigen-rich pyroptosomes, damage-associated molecular patterns and proinflammatory cytokines. Photoactivatable release of a TLR7/8 agonist into the pyroptosome generates an in situ cancer vaccine platform that cooperatively activates the cancer-immunity cycle and avoids systemic toxicity. The vaccine boosts both innate and adaptive immune responses, facilitating the eradication of primary tumours and metastatic nodules, thereby providing long-lasting cancer prevention. Overall, the rational design of pyroptosis-inducing nanomedicines for boosting the cancer-immunity cycle reported here might aid in the development of more efficient personalized cancer immunotherapy approaches.
{"title":"In situ-generated vaccine-like pyroptosome for personalized cancer immunotherapy","authors":"Binlong Chen, Fangjie Wan, Heming Xia, Xingquan Pan, Letong Wang, Yaoqi Wang, Yue Yan, Jianxiong Liu, Mingmei Tang, Ye Yang, Mengmeng Qin, Jiaona Ren, Bushu Zhou, Lijun Zhong, Wei Chen, Chuanhui Han, Mi Deng, Qiang Zhang, Yiguang Wang","doi":"10.1038/s41563-026-02506-9","DOIUrl":"https://doi.org/10.1038/s41563-026-02506-9","url":null,"abstract":"The efficacy of in situ cancer vaccination has been hampered by a poor spatiotemporal orchestration of multiple key steps of the cancer-immunity cycle in most tumours and systemic toxicity related to therapeutic strategies. Here we report a systemic injectable and pyroptosis-enabled nanoadjuvant that evokes the secretion of a vaccine-like pyroptosome in the tumour area for robust antitumour immunity. This systemic injectable and pyroptosis-enabled nanoadjuvant induces vigorous immunogenic pyroptosis, triggering the efficient release of tumour antigen-rich pyroptosomes, damage-associated molecular patterns and proinflammatory cytokines. Photoactivatable release of a TLR7/8 agonist into the pyroptosome generates an in situ cancer vaccine platform that cooperatively activates the cancer-immunity cycle and avoids systemic toxicity. The vaccine boosts both innate and adaptive immune responses, facilitating the eradication of primary tumours and metastatic nodules, thereby providing long-lasting cancer prevention. Overall, the rational design of pyroptosis-inducing nanomedicines for boosting the cancer-immunity cycle reported here might aid in the development of more efficient personalized cancer immunotherapy approaches.","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":"130 1","pages":""},"PeriodicalIF":41.2,"publicationDate":"2026-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147346797","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 : 2026-03-03DOI: 10.1038/s41563-026-02515-8
Dinar Khusyainov,Rein Liefferink,MengXing Na,Fabian Kammerbauer,Robert Frömter,Mathias Kläui,Dmitry Kozodaev,Nikolay Vovk,Rostislav V Mikhaylovskiy,Dmytro Afanasiev,Alexey V Kimel,Johan H Mentink,Theo Rasing
Controlling magnetic textures at ever smaller length scales and timescales is of fundamental and technological interest. External stimuli capable of acting at the nanoscale pose a challenge, motivating alternative approaches that exploit the intrinsic inhomogeneity of magnetic textures. Here we use a Pt/Co/Pt ferromagnetic thin film to investigate magnetization reversal with circularly polarized picosecond laser pulses. Magnetic force microscopy reveals stochastic nucleation of complex nanotextured domains from an initial monodomain state. Subsequent illumination of these domains with laser pulses induces deterministic and homogeneous magnetization switching. We find that the domain growth depends on the complexity of the texture, revealing a helicity- and texture-dependent mechanism that contrasts with temperature-gradient-driven domain expansion. We complement our observations with a stochastic model in which domain nucleation is governed by light helicity and the local magnetic environment. These results provide an insight into the mechanism of multipulse helicity-dependent all-optical switching.
{"title":"Texture-dependent all-optical switching in ferromagnetic films via stochastic nucleation of nanoscale domains.","authors":"Dinar Khusyainov,Rein Liefferink,MengXing Na,Fabian Kammerbauer,Robert Frömter,Mathias Kläui,Dmitry Kozodaev,Nikolay Vovk,Rostislav V Mikhaylovskiy,Dmytro Afanasiev,Alexey V Kimel,Johan H Mentink,Theo Rasing","doi":"10.1038/s41563-026-02515-8","DOIUrl":"https://doi.org/10.1038/s41563-026-02515-8","url":null,"abstract":"Controlling magnetic textures at ever smaller length scales and timescales is of fundamental and technological interest. External stimuli capable of acting at the nanoscale pose a challenge, motivating alternative approaches that exploit the intrinsic inhomogeneity of magnetic textures. Here we use a Pt/Co/Pt ferromagnetic thin film to investigate magnetization reversal with circularly polarized picosecond laser pulses. Magnetic force microscopy reveals stochastic nucleation of complex nanotextured domains from an initial monodomain state. Subsequent illumination of these domains with laser pulses induces deterministic and homogeneous magnetization switching. We find that the domain growth depends on the complexity of the texture, revealing a helicity- and texture-dependent mechanism that contrasts with temperature-gradient-driven domain expansion. We complement our observations with a stochastic model in which domain nucleation is governed by light helicity and the local magnetic environment. These results provide an insight into the mechanism of multipulse helicity-dependent all-optical switching.","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":"40 1","pages":""},"PeriodicalIF":41.2,"publicationDate":"2026-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147346538","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}
The rapid growth of artificial intelligence models has outpaced the capabilities of current dynamic random-access memory/flash storage systems in speed, density and energy efficiency. Three-dimensional phase-change memory offers a scalable solution, yet cross-point integration is limited by selector performance. Here, by reverse-tracing previously reported ovonic threshold switch (OTS) materials, we identify amorphous elemental selenium as a highly effective OTS selector. It exhibits an ultralow leakage current (4 × 10-12 A), an on/off current ratio exceeding 108, high drive current density (21.2 MA cm-2), fast switching speed (~20 ns) and endurance up to 2 × 109 cycles. Photoexcitation spectroscopy and density functional theory calculations reveal a charge-triggered mechanism: dense trap pairs in amorphous selenium strongly pin the Fermi level and suppress leakage, while full carrier excitation in these traps near threshold, together with impact-ionization-induced avalanche multiplication, enables abrupt switching and high on-current. Integrated selenium-selector/phase-change memory arrays demonstrate reliable write/erase operations with a 0.75-V read margin. These results clarify the OTS mechanism and establish amorphous selenium as a leading selector material for three-dimensional memory.
人工智能模型的快速发展在速度、密度和能效方面已经超过了当前动态随机存取存储器/闪存存储系统的能力。三维相变存储器提供了一种可扩展的解决方案，但交叉点集成受到选择器性能的限制。在这里，通过反向追踪以前报道的卵泡阈值开关（OTS）材料，我们确定了无定形元素硒作为一个非常有效的OTS选择器。它具有超低漏电流（4 × 10-12 A），开/关电流比超过108，高驱动电流密度（21.2 MA cm-2），快速开关速度（~20 ns）和长达2 × 109次循环的寿命。光激发光谱和密度泛函理论计算揭示了电荷触发机制：无定形硒中的密集陷阱对强烈地钉住费米能级并抑制泄漏，而这些陷阱中接近阈值的全载流子激发以及撞击电离诱导的雪崩倍增可以实现突然开关和高导通电流。集成的硒选择器/相变存储器阵列具有0.75 v的读裕量，具有可靠的写/擦除操作。这些结果阐明了OTS机理，并确立了无定形硒作为三维记忆的首选选择材料的地位。
{"title":"Charge-triggered switching mechanism in selenium selector enabling ultralow leakage current.","authors":"Yuting Sun,Tamihiro Gotoh,Jiayi Zhao,Mengfei Zhang,Shucheng Shi,Hui Zhang,Zhi Liu,Jiabin Shen,Richard Dronskowski,Zhitang Song,Stephen R Elliott,Min Zhu","doi":"10.1038/s41563-026-02499-5","DOIUrl":"https://doi.org/10.1038/s41563-026-02499-5","url":null,"abstract":"The rapid growth of artificial intelligence models has outpaced the capabilities of current dynamic random-access memory/flash storage systems in speed, density and energy efficiency. Three-dimensional phase-change memory offers a scalable solution, yet cross-point integration is limited by selector performance. Here, by reverse-tracing previously reported ovonic threshold switch (OTS) materials, we identify amorphous elemental selenium as a highly effective OTS selector. It exhibits an ultralow leakage current (4 × 10-12 A), an on/off current ratio exceeding 108, high drive current density (21.2 MA cm-2), fast switching speed (~20 ns) and endurance up to 2 × 109 cycles. Photoexcitation spectroscopy and density functional theory calculations reveal a charge-triggered mechanism: dense trap pairs in amorphous selenium strongly pin the Fermi level and suppress leakage, while full carrier excitation in these traps near threshold, together with impact-ionization-induced avalanche multiplication, enables abrupt switching and high on-current. Integrated selenium-selector/phase-change memory arrays demonstrate reliable write/erase operations with a 0.75-V read margin. These results clarify the OTS mechanism and establish amorphous selenium as a leading selector material for three-dimensional memory.","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":"63 1","pages":""},"PeriodicalIF":41.2,"publicationDate":"2026-03-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147329345","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 : 2026-03-02DOI: 10.1038/s41563-026-02522-9
Bang Wu,Li Liu,Hanqing Liu,Xinrui Mao,Xu-Jie Wang,Haiqiao Ni,Zhichuan Niu,Zhiliang Yuan
Generating light in well-defined photon-number states is central to photonic quantum technologies. While deterministic single-photon sources are well established, producing efficient two-photon states from individual emitters remains challenging. Here we demonstrate a high-efficiency two-photon emitter using the degenerate biexciton-exciton cascade in a Purcell-enhanced quantum dot-micropillar system. Leveraging polarization-selective p-shell excitation, we achieve effective biexciton loading and identify stimulated emission as a key mechanism enhancing two-photon temporal correlation. The emitter exhibits a two-photon correlation of g(2)(0) = 3,966(324), with a two-photon fraction of 0.983(1), and operates in a hybrid, predominantly cascade-dominated regime where cavity-stimulated two-photon emission coexists with the conventional biexciton-exciton cascade. These findings represent progress towards developing practical, on-demand, solid-state two-photon sources.
{"title":"Purcell-enhanced two-photon emission from a quantum dot via dark-state biexciton loading.","authors":"Bang Wu,Li Liu,Hanqing Liu,Xinrui Mao,Xu-Jie Wang,Haiqiao Ni,Zhichuan Niu,Zhiliang Yuan","doi":"10.1038/s41563-026-02522-9","DOIUrl":"https://doi.org/10.1038/s41563-026-02522-9","url":null,"abstract":"Generating light in well-defined photon-number states is central to photonic quantum technologies. While deterministic single-photon sources are well established, producing efficient two-photon states from individual emitters remains challenging. Here we demonstrate a high-efficiency two-photon emitter using the degenerate biexciton-exciton cascade in a Purcell-enhanced quantum dot-micropillar system. Leveraging polarization-selective p-shell excitation, we achieve effective biexciton loading and identify stimulated emission as a key mechanism enhancing two-photon temporal correlation. The emitter exhibits a two-photon correlation of g(2)(0) = 3,966(324), with a two-photon fraction of 0.983(1), and operates in a hybrid, predominantly cascade-dominated regime where cavity-stimulated two-photon emission coexists with the conventional biexciton-exciton cascade. These findings represent progress towards developing practical, on-demand, solid-state two-photon sources.","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":"50 1","pages":""},"PeriodicalIF":41.2,"publicationDate":"2026-03-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147329347","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 : 2026-03-02DOI: 10.1038/s41563-026-02523-8
{"title":"Efficient two-photon emission from a quantum dot.","authors":"","doi":"10.1038/s41563-026-02523-8","DOIUrl":"https://doi.org/10.1038/s41563-026-02523-8","url":null,"abstract":"","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":"47 1","pages":""},"PeriodicalIF":41.2,"publicationDate":"2026-03-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147329359","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 : 2026-03-02DOI: 10.1038/s41563-026-02527-4
Haisong Feng, Xin Zhang, Min Wei
{"title":"Stability in the dilute limit.","authors":"Haisong Feng, Xin Zhang, Min Wei","doi":"10.1038/s41563-026-02527-4","DOIUrl":"https://doi.org/10.1038/s41563-026-02527-4","url":null,"abstract":"","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":" ","pages":""},"PeriodicalIF":38.5,"publicationDate":"2026-03-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147344690","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 : 2026-03-02DOI: 10.1038/s41563-026-02489-7
Jordan Finzel,Audrey Dannar,Shoutian Sun,Adam S Hoffman,Yogita Soni,Bin Wang,Simon R Bare,E Charles H Sykes,Phillip Christopher
Dilute-metal-alloy nanoparticles exhibit enhanced catalytic performance compared with monometallic nanoparticles for many reactions. Anecdotal reports indicate that very dilute alloying can also slow the sintering rates of supported nanoparticles, although this has not been rigorously assessed and cannot be explained using bulk descriptors such as metal melting temperature. Here we utilize methanol synthesis reactivity, microscopy and in situ spectroscopy measurements to demonstrate that 1 atom% Pt addition to ~1-2-nm-diameter Cu (Pt1Cu100) nanoparticles supported on SiO2 dramatically decreases their sintering rates. Minimal sintering of Pt1Cu100 nanoparticles is observed during aging in H2 up to 700 °C versus 500 °C for Cu nanoparticles. Scanning tunnelling microscopy reveals that the addition of 0.01 monolayer of Pt to a Cu(110) surface decreases the detachment rate of undercoordinated atoms, demonstrating that dilute dopants can locally decrease the rate of the first step in nanoparticle sintering. Density functional theory calculations quantify the stabilization and predict other sinter-resistant dilute alloys. We find that the degree of host-dopant d-state hybridization correlates with decreased surface mobility, providing a mechanistic framework for designing sinter-resistant catalysts.
{"title":"Metal hybridization in dilute-alloy catalysts promotes sintering resistance by decreasing surface mobility.","authors":"Jordan Finzel,Audrey Dannar,Shoutian Sun,Adam S Hoffman,Yogita Soni,Bin Wang,Simon R Bare,E Charles H Sykes,Phillip Christopher","doi":"10.1038/s41563-026-02489-7","DOIUrl":"https://doi.org/10.1038/s41563-026-02489-7","url":null,"abstract":"Dilute-metal-alloy nanoparticles exhibit enhanced catalytic performance compared with monometallic nanoparticles for many reactions. Anecdotal reports indicate that very dilute alloying can also slow the sintering rates of supported nanoparticles, although this has not been rigorously assessed and cannot be explained using bulk descriptors such as metal melting temperature. Here we utilize methanol synthesis reactivity, microscopy and in situ spectroscopy measurements to demonstrate that 1 atom% Pt addition to ~1-2-nm-diameter Cu (Pt1Cu100) nanoparticles supported on SiO2 dramatically decreases their sintering rates. Minimal sintering of Pt1Cu100 nanoparticles is observed during aging in H2 up to 700 °C versus 500 °C for Cu nanoparticles. Scanning tunnelling microscopy reveals that the addition of 0.01 monolayer of Pt to a Cu(110) surface decreases the detachment rate of undercoordinated atoms, demonstrating that dilute dopants can locally decrease the rate of the first step in nanoparticle sintering. Density functional theory calculations quantify the stabilization and predict other sinter-resistant dilute alloys. We find that the degree of host-dopant d-state hybridization correlates with decreased surface mobility, providing a mechanistic framework for designing sinter-resistant catalysts.","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":"22 1","pages":""},"PeriodicalIF":41.2,"publicationDate":"2026-03-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147329346","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 : 2026-02-27DOI: 10.1038/s41563-026-02500-1
Carsten Deibel
{"title":"Deeper insights into charge photogeneration in organic solar cells.","authors":"Carsten Deibel","doi":"10.1038/s41563-026-02500-1","DOIUrl":"https://doi.org/10.1038/s41563-026-02500-1","url":null,"abstract":"","PeriodicalId":19058,"journal":{"name":"Nature Materials","volume":" ","pages":""},"PeriodicalIF":38.5,"publicationDate":"2026-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147317747","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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