NPG Asia MaterialsNPG亚洲材料

NPG Asia Materials(英文缩写 NPG ASIA MATER),ISSN 1884-4049,eISSN 1884-4057,中文译名:NPG亚洲材料 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。

2026 年数据 · 影响因子
9.000
JCR 分区
Q1
CAS 分区
B2
近一年发文量
1
本站 PubMed 收录统计

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。

ISSN: 1884-4049 · eISSN: 1884-4057 · 缩写: NPG ASIA MATER ·中文: NPG亚洲材料

期刊介绍

选择期刊介绍栏目

期刊简介

NPG Asia Materials 是 Nature 出版集团在亚洲地区推出的材料科学期刊,聚焦材料化学、物理与应用交叉研究。内容涵盖能源材料、纳米结构、电子与光子材料、生物材料及可持续材料等方向。读者群包括材料科学、化学、物理及工程领域的研究人员与研究生,尤其关注亚太地区科研群体的高质量成果。

研究方向

主要发表能源转换与存储、纳米材料、二维材料、有机与无机功能材料、生物医用材料及材料表征新方法等方向的研究。论文类型以原创研究论文为主,兼有综述、展望和评论,强调材料设计、性能调控与器件应用之间的关联。

期刊特色

研究取向偏重材料创新性与机理深度,鼓励跨学科方法和实际应用验证。论文通常要求性能数据完整、表征充分,并体现对领域的重要推进。适合材料、化学、物理及工程背景的资深研究者、博士后和博士研究生阅读与投稿。

投稿难度

投稿难度较高,对创新性、数据完整性和机理阐释要求严格。建议在投稿前明确材料体系的新意,补充对照实验与稳定性数据,并针对亚洲及国际同行的工作做充分讨论。若被拒稿,可根据审稿意见转投同领域专业期刊。

历年影响因子趋势

JCR 数据年份影响因子JCR 分区
202110.761Q1
20229.700Q1
20238.600Q1
20248.300Q1
20259.000Q1

NPG Asia Materials 最新收录文献

  1. JCR分区: Q1 CAS分区: B2 影响因子: 9

    1. Aerosol assisted chemical vapor deposition of cobalt-based co-catalysts on bismuth vanadate-based photoelectrodes for solar water splitting systems.

    作者:
    Mengyuan Huang, George Creasey, Zhipeng Lin, Anna Hankin, Brian Tam, Andreas Kafizas
    日期:
    2026-03-18

    Cobalt phosphate (CoPi) is a widely used oxygen evolution reaction (OER) catalyst in photoelectrochemical (PEC) water splitting systems. Traditionally, CoPi is fabricated via photo-assisted electrodeposition (PED) from a cobalt-containing electrolyte solution, a method that is limited in scalability. In this study, we demonstrate a novel and scalable route to CoPi, where cobalt oxide (CoO) is first grown by aerosol-assisted chemical vapour deposition (AACVD) and then surface modified through a dark electrochemical treatment (ET) process. Both fabrication techniques were used to deposit CoPi onto bismuth vanadate (BiVO) photoanodes synthesised by AACVD. CoPi-decorated BiVO fabricated AACVD + ET demonstrated superior charge separation efficiency, stability over four hours of chronoamperometry, and photoelectrochemical performance, achieving an improved half-cell solar-to-hydrogen (HC-STH) efficiency of 1.16% at 1.23 V vs RHE compared to CoPi-decorated BiVO fabricated by PED, which exhibited an HC-STH efficiency of 0.60%. These promising results highlight the potential of AACVD, conducted under atmospheric pressure, to enable the future development of both co-catalysts and scalable photoelectrode fabrication for large-area applications.

  2. JCR分区: Q1 CAS分区: B2 影响因子: 9

    2. Microneedles for controlled and sustained intraocular drug delivery.

    作者:
    Junsang Lee, Jinheon Jeong, Van Phuc Nguyen, Seokkyoon Hong, Yannis M Paulus, Chi Hwan Lee
    日期:
    2025-08-22

    Microneedles (MNs) have emerged as a promising technology for minimally invasive drug delivery, offering significant advantages in the treatment of ocular diseases. These miniaturized needles enable precise, localized drug delivery directly into specific tissues of the eye, such as the cornea, sclera, vitreous, or retina, while minimizing pain and discomfort. MNs can be fabricated from various biocompatible materials, including metals, silicon, and biodegradable polymers, making them highly adaptable to various clinical applications. Recent advancements in MN design include the integration of 3D printing technologies to create highly customized geometries for improved drug delivery precision, the use of smart materials that enable stimuli-responsive and sustained drug release, and the development of hybrid microneedles combining different polymers to enhance both mechanical strength and controlled drug release. These innovations have established MNs as a superior alternative to traditional methods like eye drops or intravitreal injections, which often face issues of limited bioavailability and patient compliance. This review summarizes the current state of research on MN-based ocular drug delivery, focusing on material developments, fabrication methods, drug release mechanisms, and implantation techniques. Future directions for MN technology in ophthalmology are also discussed, highlighting its potential to improve treatment outcomes for complex ocular diseases.

  3. JCR分区: Q1 CAS分区: B2 影响因子: 9

    3. {"_":"Atomic scale determination of magnetism and stoichiometry at the LaSrMnO/SrTiO interface: investigation of inverse hysteresis.","sub":["0.7","0.3","3","3"]}

    作者:
    Gyanendra Panchal, Federico Stramaglia, Pawan Kumar, Enrico Schierle, Klaus Habicht, Carlos A F Vaz, Katharina Fritsch
    日期:
    2025-03-07

    Controlling the correlations and electronic reconstruction at the interface of transition metal oxide heterostructures provides a new pathway for tuning their unique physical properties. Here, we investigate the effects of interfacial nonstoichiometry and vertical phase separation on the magnetic properties and proximity-induced magnetism of epitaxial LaSrMnO (LSMO)/SrTiO(001) oxide heterostructures. We also reinvestigate the recently observed inverse hysteresis behavior reported for this system, which we find emanates from the remanent field of the superconducting solenoid and not from antiferromagnetic intra-layer exchange coupling in low coercivity LSMO thin films. Combined atomically resolved electron energy loss spectroscopy, element-specific X-ray magnetic circular dichroism, and interface-sensitive polarized soft X-ray resonant magnetic reflectivity show the formation of a Mn-enriched interfacial LSMO layer, of a Ti-derived magnetic interface layer coupled ferromagnetically to LaSrMnO, together with a small density of O-vacancies at the interface. These results not only advance the understanding of the magnetism and spin structure of correlated oxide interfaces but also hold promise for practical applications, especially in devices where the performance relies on the control and influence of spin polarization currents by the interfacial spin structure.

  4. JCR分区: Q1 CAS分区: B2 影响因子: 9

    4. Phase stabilization of cesium lead iodide perovskites for use in efficient optoelectronic devices.

    作者:
    Handong Jin, Yu-Jia Zeng, Julian A Steele, Maarten B J Roeffaers, Johan Hofkens, Elke Debroye
    日期:
    2024-05-03

    All-inorganic lead halide perovskites (LHPs) and their use in optoelectronic devices have been widely explored because they are more thermally stable than their hybrid organic‒inorganic counterparts. However, the active perovskite phases of some inorganic LHPs are metastable at room temperature due to the critical structural tolerance factor. For example, black phase CsPbI is easily transformed back to the nonperovskite yellow phase at ambient temperature. Much attention has been paid to improving the phase stabilities of inorganic LHPs, especially those with high solar cell efficiencies. Herein, we discussed the origin of phase stability for CsPbI and the strategies used to stabilize the cubic (α) phase. We also assessed the CsPbI black β/γ phases that are relatively stable at nearly room temperature. Furthermore, we determined the relationship between phase stabilization and defect passivation and reviewed the growing trend in solar cell efficiency based on black phase CsPbI. Finally, we provide perspectives for future research related to the quest for optimum device efficiency and green energy.

  5. JCR分区: Q1 CAS分区: B2 影响因子: 9

    5. Guiding nanomaterials to tumors for breast cancer precision medicine: from tumor-targeting small-molecule discovery to targeted nanodrug delivery.

    作者:
    Xuewei Qu, Penghe Qiu, Ye Zhu, Mingying Yang, Chuanbin Mao
    日期:
    2017-12-08

    Precision medicine emphasizes patient-specific formulation for treatment of diseases, especially cancer. However, in targeted cancer treatment, because the expression level of tumor receptors in each patient varies even for the same type of cancer, the ligand/receptor-mediated approach does not seem promising for precision medicine. In this work, we demonstrated our strategy of using a phage display technique for breast cancer precision medicine. Using biopanning, we first selected an MCF-7 breast tumor-targeting peptide, then tested the effectiveness of the as-selected peptide in tumor homing and finally conjugated the peptide to a model photothermal drug, namely, gold nanorods, to achieve enhanced cancer killing efficacy. The peptides identified by the phage display technique can guide the drug to the tumors without the need to know the exact receptors on the tumor. This approach requires significantly less effort to explore patient-specific targeting molecules for precision medicine.

  6. JCR分区: Q1 CAS分区: B2 影响因子: 9

    6. Spin-wave propagation in cubic anisotropy materials.

    作者:
    Koji Sekiguchi, Seo-Won Lee, Hiroaki Sukegawa, Nana Sato, Se-Hyeok Oh, R D McMichael, Kyung-Jin Lee
    日期:
    2017-06-30

    The information carrier of modern technologies is the electron charge whose transport inevitably generates Joule heating. Spin-waves, the collective precessional motion of electron spins, do not involve moving charges and thus avoid Joule heating [1-3]. In this respect, magnonic devices in which the information is carried by spin-waves attract interest for low-power computing. However implementation of magnonic devices for practical use suffers from low spin-wave signal and on/off ratio. Here we demonstrate that cubic anisotropy materials can enhance spin-wave signals by improving spin-wave amplitude as well as group velocity and attenuation length. Furthermore, cubic anisotropy material shows an enhanced on/off ratio through a laterally localized edge mode, which closely mimics the gate-controlled conducting channel in traditional field-effect transistors. These attractive features of cubic anisotropy materials will invigorate magnonics research towards wave-based functional devices.

  7. JCR分区: Q1 CAS分区: B2 影响因子: 9

    7. Engineering protein nanocages as carriers for biomedical applications.

    作者:
    Sathyamoorthy Bhaskar, Sierin Lim
    日期:
    2017-04-07

    Protein nanocages have been explored as potential carriers in biomedicine. Formed by the self-assembly of protein subunits, the caged structure has three surfaces that can be engineered: the interior, the exterior and the intersubunit. Therapeutic and diagnostic molecules have been loaded in the interior of nanocages, while their external surfaces have been engineered to enhance their biocompatibility and targeting abilities. Modifications of the intersubunit interactions have been shown to modulate the self-assembly profile with implications for tuning the molecular release. We review natural and synthetic protein nanocages that have been modified using chemical and genetic engineering techniques to impart non-natural functions that are responsive to the complex cellular microenvironment of malignant cells while delivering molecular cargos with improved efficiencies and minimal toxicity.

  8. JCR分区: Q1 CAS分区: B2 影响因子: 9

    8. Built-in microscale electrostatic fields induced by anatase-rutile-phase transition in selective areas promote osteogenesis.

    作者:
    Chengyun Ning, Peng Yu, Ye Zhu, Mengyu Yao, Xiaojing Zhu, Xiaolan Wang, Zefeng Lin, Weiping Li, Shuangying Wang, Guoxin Tan, Yu Zhang, Yingjun Wang, Chuanbin Mao
    日期:
    2016-03-04

    Bone has a built-in electric field because of the presence of piezoelectric collagen. To date, only externally applied electric fields have been used to direct cell behavior; however, these fields are not safe or practical for use. In this work, for the first time, we use a periodic microscale electric field (MEF) built into a titanium implant to induce osteogenesis. Such a MEF is generated by the periodic organization of a junction made of two parallel semiconducting TiO zones: anatase and rutile with lower and higher electron densities, respectively. The junctions were formed through anatase-rutile-phase transition in selective areas using laser irradiation on the implants. The and studies confirmed that the built-in MEF was an efficient electrical cue for inducing osteogenic differentiation in the absence of osteogenic supplements and promoted bone regeneration around the implants. Our work opens up a new avenue toward bone repair and regeneration using built-in MEF.

  9. JCR分区: Q1 CAS分区: B2 影响因子: 9

    9. Biological lipid membranes for on-demand, wireless drug delivery from thin, bioresorbable electronic implants.

    9. 用于按需无线药物递送的生物脂质膜,源自薄型生物可吸收电子植入物
    作者:
    Chi Hwan Lee, Hojun Kim, Daniel V Harburg, Gayoung Park, Yinji Ma, Taisong Pan, Jae Soon Kim, Na Yeon Lee, Bong Hoon Kim, Kyung-In Jang, Seung-Kyun Kang, Yonggang Huang, Jeongmin Kim, Kyung-Mi Lee, Cecilia Leal, John A Rogers
    日期:
    2015-11-27

    On-demand, localized release of drugs in precisely controlled, patient-specific time sequences represents an ideal scenario for pharmacological treatment of various forms of hormone imbalances, malignant cancers, osteoporosis, diabetic conditions and others. We present a wirelessly operated, implantable drug delivery system that offers such capabilities in a form that undergoes complete bioresorption after an engineered functional period, thereby obviating the need for surgical extraction. The device architecture combines thermally actuated lipid membranes embedded with multiple types of drugs, configured in spatial arrays and co-located with individually addressable, wireless elements for Joule heating. The result provides the ability for externally triggered, precision dosage of drugs with high levels of control and negligible unwanted leakage, all without the need for surgical removal. and investigations reveal all of the underlying operational and materials aspects, as well as the basic efficacy and biocompatibility of these systems.

  10. JCR分区: Q1 CAS分区: B2 影响因子: 9

    10. Aptamer-conjugated nanomaterials for specific cancer cell recognition and targeted cancer therapy.

    10. 适配体偶联纳米材料用于特异性癌细胞识别与靶向癌症治疗
    作者:
    Qiaoling Liu, Chen Jin, Yanyue Wang, Xiaohong Fang, Xiaobing Zhang, Zhuo Chen, Weihong Tan
    日期:
    2014-04-11

    Based on their unique advantages, increasing interest has been shown in the use of aptamers as target ligands for specific cancer cell recognition and targeted cancer therapy. Recently, the development of aptamer-conjugated nanomaterials has offered new therapeutic opportunities for cancer treatment with better efficacy and lower toxicity. We highlight some of the promising classes of aptamer-conjugated nanomaterials for the specific recognition of cancer cells and targeted cancer therapy. Recent developments in the use of novel strategies that enable sensitive and selective cancer cell recognition are introduced. In addition to targeted drug delivery for chemotherapy, we also review how aptamer-conjugated nanomaterials are being incorporated into emerging technologies with significant improvement in efficiency and selectivity in cancer treatment.

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