ADVANCED MATERIALS先进材料
ADVANCED MATERIALS(英文缩写 ADV MATER),ISSN 0935-9648,eISSN 1521-4095,中文译名:先进材料 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。
发文量统计区间：2025-11-01 至 2026-10-31，按本站收录文献的发表日期统计。
期刊介绍
历年影响因子趋势
| JCR 数据年份 | 影响因子 | JCR 分区 |
|---|---|---|
| 2021 | 32.086 | Q1 |
| 2022 | 29.400 | Q1 |
| 2023 | 27.400 | Q1 |
| 2024 | 26.800 | Q1 |
| 2025 | 29.100 | Q1 |
ADVANCED MATERIALS 最新收录文献
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1. Correction to "Short-Wave Infrared Organic Photodetectors With Ultralow Dark Current Density Under Biased Operating Conditions".
1. 对“偏置工作条件下具有超低暗电流密度的短波红外有机光电探测器”的更正PMID:日期:2026-10-05该文献暂无摘要。
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2. {"_":"Accelerated Materials Discovery Through In Situ X-ray Diffraction: Solvothermal Formation of PdM (M═Si, Ge, Sn, Pb) Intermetallic Nanoparticles.","sub":["x","y"]}
2. {"_":"通过原位X射线衍射加速材料发现：PdM（M═Si、Ge、Sn、Pb）金属间化合物纳米颗粒的溶剂热形成。","sub":["x","y"]}PMID:日期:2026-10-05Machine learning and artificial intelligence approaches are expected to accelerate the development of new materials, for example through automated synthesis. Here, we investigate another approach to accelerate materials discovery, namely in situ synchrotron Powder x-ray diffraction (PXRD), which enables efficient exploration of a large range of synthesis parameters to identify optimal synthesis conditions. We study the solvothermal formation of PdM (M═Si, Ge, Sn, Pb) nanoparticles with varying temperature, solvent, and metal precursor. Intermetallic phases are obtained for all systems except for PdSi, and specific conditions are identified for preparing PdGe, PdGe, SnPd, SnPd, SnPd, PbPd, PbPd, PbPd, and PbPd intermetallic phases. A general formation mechanism is suggested, where Pd nanoparticles are formed initially, followed by adsorption and diffusion of the secondary metal to form intermetallic phases. Based on the learnings from the in situ experiments, SnPd, SnPd, and SnPd nanoparticles are synthesized ex situ in a simple solvothermal process. Scanning transmission electron microscopy-energy-dispersive x-ray spectroscopy (STEM-EDS) establishes a gradient of Sn across the nanoparticles with a Pd-rich core and increasing Sn content towards the edges, reflecting the diffusion of Sn into the initial Pd nanoparticles and thereby corroborating the formation mechanism observed from the in situ data.
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3. {"_":"Precise Modulation of CO-to-Ethanol Conversion by Fully-Exposed Cu Clusters Induced by Dangling Bonds in Lacunary Polyoxometalate.","sub":["2","n"]}
3. {"_":"缺位多金属氧酸盐中悬挂键诱导的全暴露铜团簇对一氧化碳到乙醇转化的精确调控。","sub":["2","n"]}PMID:日期:2026-10-05The electrochemical CO reduction toward ethanol under high current density remains challenging. Herein, WO-supported fully exposed Cu clusters (FECCs) confined by hollow mesoporous carbon spheres (HMCS) (Cu-WO@HMCS) are fabricated through the "molecular defect confinement" strategy based on the [PWO]. The [PWO] features a tri-lacunary configuration, single-sided dangling bond characteristics, and excellent liquid-phase stability, enabling precise anchoring of the {Cu } cluster to realize atomic dispersion at the molecular level, while enabling the controllable construction of the geometric size and electronic structure of FECCs via Cu─O─W bonds during pyrolysis. The Cu-WO@HMCS executes exceptional performance for CO-to-ethanol conversion, with Faradaic efficiencies of 80.6% and 75.3% at partial current densities of 322.4 and 677.7 mA cm, respectively. Mechanism studies reveal the synergistic regulation: (1) The FECCs display a higher Fermi level compared to Cu nanoparticles, acting as a superior electron donor to promote CO adsorption and conversion; moreover, the geometric size effect of FECCs increases the CO coverage, favoring the C─C coupling. (2) The WO supplies reactive H, which favors the hydrogenation of CO and CHCOH, steering the asymmetric C─C coupling toward ethanol. This study enables atomic-level design of catalysts by employing polyoxometalates, delivering a crucial method for precisely constructing fully exposed clusters and highly selective CORR-to-ethanol.
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4. Correction to "Silicon-Rivalling Large-Area Flexible Broadband Organic Photodetectors".
PMID:日期:2026-10-05该文献暂无摘要。
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5. Hypoxia-Regulating Nanozymes for Biomedicine.
5. 用于生物医学的缺氧调节纳米酶PMID:日期:2026-10-05Hypoxic microenvironments arise when local oxygen supply fails to meet cellular demand and exert an influence on the progression of cancer, ischemic heart and brain injury, chronic inflammatory disorders, and other diseases. Conventional approaches, including oxygen delivery systems, small-molecule redox drugs, and natural enzymes, can relieve hypoxia but suffer from poor tissue specificity, short duration of action, and limited stability. Nanozymes are engineered nanomaterials with enzyme-like catalytic activity. Through controllable redox reactions, they can regulate oxygen generation or consumption, rebalance reactive oxygen species, and reprogram hypoxic microenvironments at the cellular and tissue levels. In recent years, the field has shifted from empirical trial-and-error to rational nanozyme design, with a focus on defined active sites, disease-responsive activity, and targeted delivery. Herein, we summarize the key design principles governing nanozyme catalytic performance and discuss the catalytic mechanisms involved in hypoxia regulation. We then examine how distinct pathological features of acute and chronic hypoxic microenvironments create different catalytic requirements and how nanozyme functions can be tailored accordingly. Furthermore, we provide an overview of nanozyme applications across hypoxia-associated diseases and discuss emerging opportunities and barriers for clinical translation. This review is expected to provide insights for developing precise and clinically valuable hypoxia-regulating nanozymes.
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6. Engineering Residual Rock-Salt Reconstruction through Near-Surface Fluorine Regulation for Stable 4.6 V Cycling of Regenerated Spent Layered Oxide Cathodes.
6. 通过近表面氟调控工程残余岩盐重构以实现再生废旧层状氧化物正极稳定的PMID:日期:2026-10-05Direct regeneration enables high-value recovery of spent layered oxide cathodes, but their high-voltage reuse requires stabilization of both regenerated surface and lattice oxygen beyond bulk compositional restoration. Here, we report a high-voltage upcycling strategy for spent LiNiCoMnO (NCM) based on near-surface fluorine (F) regulation of residual rock-salt layers. Molten-salt relithiation recovers Li content and layered bulk framework, whereas subsequent fluorine treatment converts the remaining inert surface reconstruction into a thin F-enriched rock-salt interphase. Rather than impeding Li transport, this interphase stabilizes the reconstructed surface, reduces oxygen defects, and mitigates electrolyte-induced interfacial degradation. The resulting cathode with F-enriched rock-salt surface (RFNCM) delivers 208.7 mAh g at 0.1 C within 3.0-4.6 V, and retains 80.28% capacity after 400 cycles at 1 C and 25°C, and 80.93% after 200 cycles at 50°C. In situ X-ray diffraction and gas-evolution measurements reveal more homogeneous high-voltage structural evolution and suppressed oxygen release, respectively. According to analysis results of XPS, in situ Raman and Density functional theory calculations, these improvements can be attributed to strengthened Ni─O interactions and increased oxygen-vacancy formation energies after fluorine incorporation. This work converts an unavoidable reconstruction product into a protective interphase for high-voltage reuse of spent layered oxide cathodes.
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7. Intrinsically Stretchable Neuromorphic Vision Arrays for Conformal Polarization Imaging and Adaptive Perception.
PMID:日期:2026-10-05Micro‑unmanned aerial vehicles urgently require compact, lightweight, and low‑power conformal vision modules capable of wide‑field imaging, polarization perception, and illumination‑adaptive processing. However, the monolithic integration of intrinsic stretchability, polarization sensitivity, and neuromorphic adaptation within a single deformable optoelectronic platform has remained a major challenge. Here, we report an intrinsically stretchable neuromorphic vision transistor array based on a semiconducting composite film consisting of an organic conjugated polymer (TDPP‑Se), CdSe/ZnS quantum dots (QDs), and an elastomeric SEBS matrix. The QDs significantly enhance photoresponsivity and enable gate‑tunable light adaptation, while shear‑aligned polymer chains yield strong polarization sensitivity with a high polarization ratio. The devices integrate sensing, memory, and in‑sensor computing with an ultralow energy consumption of ∼0.56 pJ per synaptic event, and retain stable multimodal performance under tensile strains up to 50%. When conformally laminated onto hemispherical substrates, the system achieves a mechanically tunable FOV from 53° to 149°. When the experimentally measured array responses are computationally mapped onto image preprocessing, the resulting vision framework achieves a classification accuracy of 95.6% under dynamic illumination, strong background interference, and large mechanical deformation. This work establishes a conformal neuromorphic vision platform for robust and energy-efficient artificial vision in micro-autonomous systems.
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8. Electrochemical Solubility Switching Enables Lateral Etching Toward Sub-20 nm Nanopatterning.
8. 电化学溶解度切换实现横向蚀刻以达成亚20纳米级纳米图案化PMID:日期:2026-10-05The miniaturization of patterns to sub-20 nm dimensions remains challenging, owing to the fundamental constraints of optical patterning and the increasing complexity and cost of advanced lithographic technologies such as extreme-ultraviolet lithography. Here, we introduce an electrochemical etching strategy that effectively decouples the final feature size from the optical diffraction limit by leveraging voltage-gated solubility switching in electro-responsive polymers. We discover that the redox-state-dependent solubility of rhodamine-based polymers (Poly-RhNNE-B) can be precisely modulated by applied potentials, enabling programmable electrochemical dissolution. Notably, redox-mediator-facilitated intermolecular charge transfer extends this solubility switching laterally beyond the electrode-contact regions. This electrochemical lateral etching enables electrically controlled post-patterning dimensional refinement, allowing the remaining feature width to be progressively reduced after the initial pattern has been defined and yielding a minimum remaining linewidth of ∼17 nm without requiring the final nanoscale dimension to be directly defined by high-resolution optical exposure. This approach introduces an electrochemical nanofabrication strategy that complements conventional lithographic techniques, potentially reducing process complexity in selected nanoscale pattern-refinement scenarios while enabling high-resolution micro/nano-structuring, thereby expanding the toolbox for next-generation precision nanomanufacturing.
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9. Donor-Selective NiCo-LDH Templating Directs Polymer Assembly for Enhanced Exciton Transport in Efficient Organic Solar Cells.
9. 供体选择性NiCo-LDH模板引导聚合物组装以增强高效有机太阳能电池中的激子传输PMID:日期:2026-10-05Organic solar cells (OSCs) have achieved remarkable progress, yet improving exciton utilization in polymer donors remains challenging due to their intrinsically limited exciton diffusion length (L). Here, we report a donor-selective templating strategy based on few-layer-like nickel-cobalt layered double hydroxide (NiCo-LDH) nanosheets to regulate polymer donor assembly in OSCs. The hydroxyl-rich NiCo-LDH surface exhibits preferential affinity toward polymer donors and promotes ordered donor-chain organization during film formation, while exerting limited influence on the acceptor component. This templating strategy enhances the molecular ordering of the donor phase and increases the L of D18 from 10.7 to 18.9 nm, accompanied by the formation of more ordered donor fibrillar structures. The coordinated improvements in donor organization and exciton transport are further associated with enhanced exciton-to-charge conversion, more balanced carrier transport, and suppressed recombination. Consequently, D18:L8-BO-based OSCs achieve a maximum power conversion efficiency (PCE) of 21.36%, independently certified at 21.09%, together with improved stability under continuous illumination. Analogous donor-biased interactions, enhanced exciton diffusion, regulated fibrillar organization, and improved photovoltaic performance are also observed in PM6 and D18-Cl systems. These results highlight the broader applicability of chemically active 2D templating for coordinating polymer donor assembly and exciton transport toward high-performance OSCs.
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10. Engineering Immunomodulatory Stents Using a Biomimetic Nanozyme System for Vascular Healing.
10. 利用仿生纳米酶系统工程化免疫调节支架促进血管愈合PMID:日期:2026-10-05Delayed endothelialization and inflammatory response are two major obstacles that hinder vascular healing by drug-eluting stents (DES). Here, we report a biomimetic nanozyme strategy to address this issue. We first design and anchor a robust glutathione peroxidase (GPx)-biomimetic nanozyme with diselenide-polyphenol networks on a stent. Then, a thrombin inhibitor, bivalirudin, is efficiently loaded onto the nanozyme utilizing its reversible interactions with polyphenol. The nanozymes exhibit potent GPx activity to controllably generate nitric oxide (NO) and on-demand elution of bivalirudin. The synergistic effects of NO and bivalirudin effectively inhibit thrombin activity, prevent platelet activation, and consequently suppress thrombosis as well as the inflammatory response associated with it. In vitro pathological model cell studies demonstrate that the nanozyme-engineered stents specifically inhibit smooth muscle cell (SMC) proliferation, regulate macrophage polarization, and promote the repair and proliferation of endothelial cells. Thus, it enables rapid endothelialization and vascular healing, preventing restenosis in rabbit and swine models.