Advanced Powder Materials最新文献

{"title":"Recent progress in aqueous zinc-ion batteries based on conversion-type cathodes","authors":"Yanan Cao ,&nbsp;Shidi Ju ,&nbsp;Qian Zhang ,&nbsp;Kun Gao ,&nbsp;Augusto Marcelli ,&nbsp;Zhipan Zhang","doi":"10.1016/j.apmate.2025.100278","DOIUrl":"10.1016/j.apmate.2025.100278","url":null,"abstract":"<div><div>Developing advanced secondary batteries with low cost and high safety has attracted increasing research interests across the world. In particular, the aqueous zinc-ion battery (AZIB) has been regarded as a promising candidate owing to the high abundance and capacity of Zn metal. Currently, manganese-based and vanadium-based oxides are most common choices for cathode materials used in AZIBs, but they unfortunately show a moderate cell voltage and limited rate performance induced by slow intercalation-extraction kinetics of Zn²⁺ ions. To address these issues, alternative cathode systems with tunable redox potentials and intrinsic fast kinetics have been exploited. In the past few years, conversion-type cathodes of I₂ and S have become the most illustrative examples to match or even surpass the performance of conventional metal oxide cathodes in AZIBs. Herein, we sum up most recent progress in conversion-type cathodes and focus on novel ideas and concepts in designing/modifying cathodes for AZIBs with high voltage/capacity. Additionally, potential directions and future efforts are tentatively proposed for further development of conversion-type cathodes, aiming to speed up the practical application of AZIBs.</div></div>","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 2","pages":"Article 100278"},"PeriodicalIF":0.0,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143529347","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Electrolyte-independent and sustained inorganic-rich layer with functional anion aggregates for stable lithium metal electrode","authors":"Xiaoyi Wang ,&nbsp;Zhendong Li ,&nbsp;Qinhao Mao ,&nbsp;Shun Wu ,&nbsp;Yifei Cheng ,&nbsp;Yinping Qin ,&nbsp;Zhenlian Chen ,&nbsp;Zhe Peng ,&nbsp;Xiayin Yao ,&nbsp;Deyu Wang","doi":"10.1016/j.apmate.2024.100261","DOIUrl":"10.1016/j.apmate.2024.100261","url":null,"abstract":"<div><div>Lithium (Li) metal batteries (LMBs) featuring ultrahigh energy densities are expected as ones of the most prominent devices for future energy storage applications. Nevertheless, the practical application of LMBs is still plagued by the poor interfacial stability of Li metal anode. Inorganic-rich interlayer derived from anion decomposition in advanced liquid electrolytes is demonstrated as an efficient approach to stabilize the Li metal anode, however, is electrolyte-dependent with limited application conditions due to inappropriate electrolyte properties. Herein, an efficient structuration strategy is proposed to fabricate an electrolyte-independent and sustained inorganic-rich layer, by embedding a type of functional anion aggregates consisting of selected anions ionically bonded to polymerized cation clusters. The anion aggregates can progressively release anions to react with Li⁺ and form key components boosting the structural stability and Li⁺ transfer ability of the artificial layer upon cycling. This self-reinforcing working mechanism endows the artificial layer with a sustained inorganic-rich nature and promising Li protective ability during long-term cycling, while the electrolyte-independent property enables its applications in LMBs using conventional low concentration electrolytes and all-solid-state LMBs with significantly enhanced performances. This strategy establishes an alternative designing route of Li protective layers for reliable LMBs.</div></div>","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 1","pages":"Article 100261"},"PeriodicalIF":0.0,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143165444","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Atomically dispersed Fe boosting elimination performance of g-C3N4 towards refractory sulfonic azo compounds via catalyst-contaminant interaction","authors":"Puying Liang ,&nbsp;Zhouping Wang ,&nbsp;Shiyu Liao ,&nbsp;Yang Lou ,&nbsp;Jiawei Zhang ,&nbsp;Chengsi Pan ,&nbsp;Yongfa Zhu ,&nbsp;Jing Xu","doi":"10.1016/j.apmate.2024.100251","DOIUrl":"10.1016/j.apmate.2024.100251","url":null,"abstract":"<div><div>Herein, an oxygen-doped porous g-C₃N₄ photocatalyst modified with atomically dispersed Fe (Fe₁/OPCN) is successfully prepared and exhibits significant superiority in removing refractory sulfonic azo contaminants from water via catalyst-contaminant interaction. The elimination performance of Fe₁/OPCN towards acid red 9, acid red 13 and amaranth containing similar azonaphthalene structure and increasing sulfonic acid groups increases gradually. The amaranth degradation rate of Fe₁/OPCN is 17.7 and 6.1 times as that of homogeneous Fenton and OPCN, respectively. In addition, Fe₁/OPCN also has more outstanding removal activities towards other contaminants with sulfonic acid and azo groups alone. The considerable enhancement for removing sulfonic azo contaminants of Fe₁/OPCN is mainly ascribed to the following aspects: (1) The modified Fe could enhance the adsorption towards sulfonic azo compounds to accelerate the mass transfer, act as e⁻ acceptor to promote interfacial charge separation, and trigger the self-Fenton reaction to convert in-situ generated H₂O₂ into •OH. (2) Fe(Ⅲ) could coordinate with <strong>—</strong>N=N<strong>—</strong> to form d-π conjugation, which could attract e⁻ transfer to attack <strong>—</strong>N=N<strong>—</strong> bond. Meanwhile, the inhibited charge recombination could release more free h⁺ to oxidize sulfonic acid groups into SO₄⁻•. (3) Under the cooperation of abundant multiple active species (<em>•</em>O₂⁻, h⁺, e⁻, <em>•</em>OH, SO₄⁻•) formed during the degradation reaction, sulfonic azo compounds could be completely mineralized into harmless small molecules (CO₂, H₂O, etc.) by means of <strong>—</strong>N=N<strong>—</strong> cleavage, hydroxyl substitution, and aromatic ring opening. This work offers a novel approach for effectively eliminating refractory sulfonic azo compounds from wastewater.</div></div>","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 1","pages":"Article 100251"},"PeriodicalIF":0.0,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142698806","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Enhanced photoelectric and thermoelectric coupling factor in BiMn2O5 ferroelectric film","authors":"Aohan Xu ,&nbsp;Chong Guo ,&nbsp;Weiqi Qian ,&nbsp;Chris R. Bowen ,&nbsp;Ya Yang","doi":"10.1016/j.apmate.2024.100260","DOIUrl":"10.1016/j.apmate.2024.100260","url":null,"abstract":"<div><div>Ferroelectric film materials have attracted significant interest due to their potential for harvesting various forms of clean energy from natural environmental sources. However, the photoelectric performance of these materials is frequently constrained by heat generation during light absorption, resulting in significant thermal losses. Most of ferroelectric films produce photocurrent and thermocurrent with opposite polarity, thus weakening the coupled photo-thermoelectric output of the devices. Here we report on a LaNiO₃/BiMn₂O₅(BMO)/ITO ferroelectric film to produce photocurrent and thermocurrent with the same polarity. The polarity of the photocurrent generated by the BMO film is shown to be determined solely by the direction of spontaneous polarization, overcoming the detrimental effect of Schottky barrier for energy harvesting in device. We propose a new strategy to enhance the coupling factor, thereby offering valuable new insights for optimizing the utilization of ferroelectric materials in both light and heat energy applications.</div></div>","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 1","pages":"Article 100260"},"PeriodicalIF":0.0,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143165443","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"MA-activated lattice shrinkage and bandgap renormalization advancing the stability of FA1-xMAxPbI3 (x=0–1) perovskites photovoltaic","authors":"Congtan Zhu ,&nbsp;Xueyi Guo ,&nbsp;Si Xiao ,&nbsp;Weihuang Lin ,&nbsp;Zhaozhe Chen ,&nbsp;Lin Zhang ,&nbsp;Hui Zhang ,&nbsp;Xiangming Xiong ,&nbsp;Ying Yang","doi":"10.1016/j.apmate.2024.100264","DOIUrl":"10.1016/j.apmate.2024.100264","url":null,"abstract":"<div><div>Generally, referring to the stability of perovskite, the most studied perovskite material has been MA-free mixed-cation perovskite. The precise role of MA in the light-thermal-humid stability of perovskite solar cells still lacks of a systematically understanding. In this work, the evolution of crystallographic structures, intermediate phase, ultrafast dynamics, and thermal decomposition behavior of MA-mixed perovskite FA_1-<em>x</em>MA_<em>x</em>PbI₃ (<em>x</em>=0–100%) are investigated. The influence of MA on the stability of devices under heat, light, and humidity exposure are revealed. In the investigated compositional space (<em>x</em>=0–100%), device efficiencies vary from 19.5% to 22.8%, and the light, thermal, and humidity exposure stability of the related devices are obviously improved for FA_1-<em>x</em>MA_<em>x</em>PbI₃ (<em>x</em>=20%–30%). Incorporation 20%–30% of MA cations lowers nucleation barrier and causes a significant volume shrinkage, which enhances the interaction between FA and I, thus improving crystallization and stability of the FA_1-<em>x</em>MA_<em>x</em>PbI₃. Thermal behavior analysis reveals that the decomposition temperature of FA_0.8MA_0.2PbI₃ reaches 247 ​°C (FAPbI₃, 233 ​°C) and trace amounts of MA cations enhance the thermal stability of the perovskite. Remarkably, we observe lattice shrinkage using spherical aberration corrected transmission electron microscope (AC-TEM). This work implies that stabilizing perovskites will be realized by incorporating trace amounts of MA, which improve the crystallization and carrier transport, leading to improved stability and performances.</div></div>","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 1","pages":"Article 100264"},"PeriodicalIF":0.0,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143165445","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"3D-printed redox-active polymer electrode with high-mass loading for ultra-low temperature proton pseudocapacitor","authors":"Miaoran Zhang,&nbsp;Tengyu Yao,&nbsp;Tiezhu Xu,&nbsp;Xinji Zhou,&nbsp;Duo Chen,&nbsp;Laifa Shen","doi":"10.1016/j.apmate.2024.100247","DOIUrl":"10.1016/j.apmate.2024.100247","url":null,"abstract":"<div><div>The stable operation of supercapacitors at extremely low temperatures is crucial for applications in harsh environments. Unfortunately, conventional inorganic electrodes suffer from sluggish diffusion kinetics and poor cycling stability for proton pseudocapacitors. Here, a redox-active polymer poly (1,5-diaminonaphthalene) is developed and synthesized as an ultrafast, high-mass loading, and durable pseudocapacitive anode. The charge storage of poly (1,5-diaminonaphthalene) depends on the reversible coordination reaction of the C=N group with H⁺, which enables fast kinetics associated with surface-controlled reactions. The 3D-printed organic electrode delivers a remarkable areal capacitance (8.43 ​F ​cm⁻² at 30.78 ​mg ​cm⁻²) and thickness-independent rate performance. Furthermore, the 3D-printed proton pseudocapacitor exhibits great low-temperature tolerance and delivers a high energy density of 0.44 ​mWh cm⁻² ​at −60 ​°C, as well as operates well even at −80 ​°C. This work signifies that combining organic material design with 3D hierarchical network electrode construction can provide a promising solution for low-temperature-resistant supercapacitors.</div></div>","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 1","pages":"Article 100247"},"PeriodicalIF":0.0,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142699348","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Frustrated lewis pairs regulated solid polymer electrolyte enables ultralong cycles of lithium metal batteries","authors":"Pingping Chang ,&nbsp;Zhenjie Liu ,&nbsp;Murong Xi ,&nbsp;Yong Guo ,&nbsp;Tianlong Wu ,&nbsp;Juan Ding ,&nbsp;Hongtao Liu ,&nbsp;Yudai Huang","doi":"10.1016/j.apmate.2024.100263","DOIUrl":"10.1016/j.apmate.2024.100263","url":null,"abstract":"<div><div>Long-cycling dendrite-free solid-state lithium metal batteries (LMBs) require fast and uniform lithium-ion (Li⁺) transport of solid-state electrolytes (SSEs). However, the SSEs still face the problems of low ionic conductivity, low Li⁺ transference number, and unstable interface with lithium metal. In this work, a novel strategy of frustrated Lewis pairs (FLPs) modulating solid polymer electrolytes (SPEs) has been firstly proposed that enables durable Li reversible cycling. The tunable strength of Lewis acid and base dual-active sites of nickel borate FLPs can synergistically promote both the dissociation of lithium salts and the transfer of Li⁺. As a consequence, the FLPs modulated SPEs (SPE-NiBO-150) exhibit high ionic conductivity of 4.92×10⁻⁴ ​S ​cm⁻¹, high Li⁺ transference number of 0.74, and superior interface compatibility with both lithium anode and LiFePO₄ cathode at room-temperature. The Li//SPE-NiBO-150//Li symmetric cell demonstrates ultralong cycle stability (over 10,000 ​h (417 days) at both current density of 0.2 and 0.5 ​mA ​cm⁻²), and the assembled solid-state LiFePO₄//SPE-NiBO-150//Li battery also shows excellent performance (86% capacity retention for 300 cycles at 0.5C). The present work supplies a new insight into designing high-performance SPEs for solid-state LMB applications.</div></div>","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 1","pages":"Article 100263"},"PeriodicalIF":0.0,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143165288","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Controllable synthesis and heterogeneous tailoring of 1D perovskites, emerging properties and applications","authors":"En Yang ,&nbsp;Mengna Zhang ,&nbsp;Shuaishuai Wei ,&nbsp;Dan Liang ,&nbsp;Mustafa Zeb ,&nbsp;Liping Zhang ,&nbsp;Yoonseob Kim ,&nbsp;Yuan Zhao ,&nbsp;Wei Ma","doi":"10.1016/j.apmate.2024.100250","DOIUrl":"10.1016/j.apmate.2024.100250","url":null,"abstract":"<div><div>One-dimensional perovskites possess unique photoelectric properties that distinguish them from other perovskite types, making them a focal point in photoelectric research. In recent years, there has been a significant surge in interest surrounding the synthesis and application of one-dimensional anisotropic perovskites, spurred by advancements in synthesis techniques and notable breakthroughs in novel methodologies and application properties. This article provides a comprehensive review of the progress made in research on one-dimensional anisotropic perovskites, detailing the synthesis mechanisms and potential pathways for performance enhancement in various applications. We highlight the crucial role of controllable synthesis and heterogeneous effect in tailoring perovskite properties to boost application efficacy. Initially, this review examines the primary synthesis methods and mechanisms for creating heterogeneously induced one-dimensional anisotropic perovskites, categorizing them into two main approaches: the classical wet chemical synthesis, which utilizes selective ligands, and the ligand-free, substrate-assisted method. The precision in controllable synthesis is essential for fabricating heterogeneous structures, where the synthesized precursor, shape, and surface ligand significantly influence the interfacial strength of the heterogenic interface. We also discuss the key features that must be improved for high-performance applications, exploring how heterogeneous effects can enhance performance and drive the development of heterogeneous devices in various applications, such as photodetectors, solar cells, light-emitting diodes, and photocatalysis. Conclusively, by highlighting the emerging potential and promising opportunities offered by strategic heterogeneous construction, we forecast a dynamic and transformative future for their production and application landscapes.</div></div>","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 1","pages":"Article 100250"},"PeriodicalIF":0.0,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142698841","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Promoting homogeneous tungsten doping in LiNiO2 through a grain boundary phase induced by excessive lithium","authors":"Junjie Wang ,&nbsp;Yucen Yan ,&nbsp;Zilan Zhao ,&nbsp;Jiayi Li ,&nbsp;Gui Luo ,&nbsp;Duo Deng ,&nbsp;Wenjie Peng ,&nbsp;Mingxia Dong ,&nbsp;Zhixing Wang ,&nbsp;Guochun Yan ,&nbsp;Huajun Guo ,&nbsp;Hui Duan ,&nbsp;Lingjun Li ,&nbsp;Shihao Feng ,&nbsp;Xing Ou ,&nbsp;Junchao Zheng ,&nbsp;Jiexi Wang","doi":"10.1016/j.apmate.2024.100248","DOIUrl":"10.1016/j.apmate.2024.100248","url":null,"abstract":"<div><div>LiNiO₂ (LNO) is one of the most promising cathode materials for lithium-ion batteries. Tungsten element in enhancing the stability of LNO has been researched extensively. However, the understanding of the specific doping process and existing form of W are still not perfect. This study proposes a lithium-induced grain boundary phase W doping mechanism. The results demonstrate that the introduced W atoms first react with the lithium source to generate a Li–W–O phase at the grain boundary of primary particles. With the increase of lithium ratio, W atoms gradually diffuse from the grain boundary phase to the interior layered structure to achieve W doping. The feasibility of grain boundary phase doping is verified by first principles calculation. Furthermore, it is found that the Li₂WO₄ grain boundary phase is an excellent lithium ion conductor, which can protect the cathode surface and improve the rate performance. The doped W can alleviate the harmful H2↔H3 phase transition, thereby inhibiting the generation of microcracks, and improving the electrochemical performance. Consequently, the 0.3 ​wt% W-doped sample provides a significant improved capacity retention of 88.5 ​% compared with the pristine LNO (80.7 ​%) after 100 cycles at 2.8–4.3 ​V under 1C.</div></div>","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 1","pages":"Article 100248"},"PeriodicalIF":0.0,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142698842","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Multicolor chiral perovskite nanowire films with strong and tailorable circularly polarized luminescence","authors":"Fang Peng ,&nbsp;Dan Liang ,&nbsp;En Yang ,&nbsp;Bongjun Yeom ,&nbsp;Yuan Zhao ,&nbsp;Wei Ma","doi":"10.1016/j.apmate.2024.100262","DOIUrl":"10.1016/j.apmate.2024.100262","url":null,"abstract":"<div><div>Perovskites showcased potential promise for innovative circularly polarized luminescence (CPL)-active multichannel information encryption, owing to the exceptional luminescence brightness. It was still a formidable challenge to fabricate CPL-active perovskites with significant luminescent asymmetry factor (<em>g</em>_lum) and full-colour-tailorable CPL properties. Indeed, compared to isotropic perovskites, anisotropic perovskite nanowires (NWs) were conducive to carrier separation and transport for polarization enhancement. Herein, three types of CsPb(Br/I)₃ NWs with green, orange, red fluorescence (FL) were respectively synthesized and assembled into chiral NW films. The right-handed/left-handed chiral NW films constructed by 4+4 layers and 45° inter-angles exhibits highly symmetric and mirror-like chiral signals. The strongest chiral intensity is more than 3000 medg. CPL signals with wide colour gamut produce ranging from 480 ​nm to 800 ​nm, and tailorable CPL wavelengths are manipulated by the emission wavelength of perovskite NWs. A giant CPL signal with a maximum <em>g</em>_lum of up to 10⁻¹ is achieved. The polarization imaging of chiral NW films produces brilliant differential circularly polarized structural colours, making it more widely used in multilevel anti-counterfeiting systems. A significant breakthrough lies in the development of advanced chiral perovskite materials with remarkable <em>g</em>_lum and tailorable CPL properties, which sheds new light on optical anti-counterfeiting and intelligent information encryption.</div></div>","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 1","pages":"Article 100262"},"PeriodicalIF":0.0,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143165287","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}