Advanced Powder Materials最新文献

{"title":"Electronic structure regulation inducing robust solid electrolyte interphase for stable anode-free sodium metal batteries","authors":"Peng Xu ,&nbsp;Yinghan Liu ,&nbsp;Mulan Qin ,&nbsp;Fei Huang ,&nbsp;Shuquan Liang ,&nbsp;Guozhao Fang","doi":"10.1016/j.apmate.2025.100303","DOIUrl":"10.1016/j.apmate.2025.100303","url":null,"abstract":"<div><div>Anode-free sodium metal batteries (AFSMBs) have gained attention as next-generation storage systems with high energy density and cost-effectiveness. However, non-uniform sodium (Na) deposition and an unsteady solid electrolyte interphase (SEI) lead to dendrite-related issues and severe irreversible Na⁺ plating/stripping, greatly aggravating their cycle deterioration. In this study, we effectively modified the 3D current collector's electronic structure by introducing Zn-N_<em>x</em> active sites (Zn-CNF), which enhances lateral Na⁺ diffusion and the Na planar growth, enabling uniform deep Na deposition at an exceptionally high capacity of 10 ​mA ​h ​cm⁻². Furthermore, the Zn-N_<em>x</em> bonds enhance the adsorption capacity of PF₆⁻ and contribute to forming a stable inorganic-rich SEI layer. Consequently, Zn-CNF with the electronic structure regulation endows an ultra-low nucleation overpotential (8 ​mV) and ultra-high Coulombic efficiency of 99.94% over 1,600 cycles. Symmetric cells demonstrate stable Na⁺ plating/stripping behavior for more than 4,400 ​h at 1 ​mA ​cm⁻². Moreover, under high cathode loading (7.97 ​mg ​cm⁻²), the AFSMBs achieve a high energy density of 374 ​W h kg⁻¹ and retain a high discharge capacity of 82.49 ​mA ​h ​g⁻¹ with a capacity retention of 80.4% after 120 cycles. This work proposes a viable strategy to achieving high-energy-density AFSMBs.</div></div>","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 4","pages":"Article 100303"},"PeriodicalIF":0.0,"publicationDate":"2025-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144167033","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Enhancing dipole polarization loss in conjugated metal-organic frameworks via coordination symmetry breaking under electromagnetic field","authors":"Weize Wang ,&nbsp;Rong Liu ,&nbsp;Jiaqi Tao ,&nbsp;Tinglei Yu ,&nbsp;Yijie Liu ,&nbsp;Lvtong Duan ,&nbsp;Zifu Zhang ,&nbsp;Zhihao He ,&nbsp;Shuang Chen ,&nbsp;Jintang Zhou ,&nbsp;Ping Chen ,&nbsp;Peijiang Liu ,&nbsp;Zhengjun Yao","doi":"10.1016/j.apmate.2025.100302","DOIUrl":"10.1016/j.apmate.2025.100302","url":null,"abstract":"<div><div>Modulating the dipole polarization loss in the single-atom region and establishing its direct relationship with the electromagnetic wave absorption (EWA) performance remain an unmet challenge. Here, a dual-ligand modulation strategy, i.e., partially changing coordination atoms in the single-metal region (sMr), is introduced to effectively break the coordination symmetry of conjugated metal-organic frameworks (cMOFs), finally enhancing EWA property of cMOFs materials. Further, the asymmetrical sMr is experimentally found to elicit the dipole polarization loss, overcoming the handicaps of other electromagnetic wave loss mechanisms, which directly contribution to enhance EWA performance of this series of cMOFs. This strategy is further confirmed by replacing metal centers. Among studied series of cMOFs, Cu_2.25/Co_0.75(HHTP_1.67HITP_0.33) achieves excellent EWA performance with an effective absorption bandwidth of 5.00 ​GHz and a reflection loss of −66.03 ​dB. We introduce a dual-ligand modulation strategy targeting single-metal regions within cMOFs here, aiming to achieve superior EWA performance through atomic-scale dipole polarization loss modulation. We hope our study can inspire more exploration to realize high-performance EWA materials.</div></div>","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 4","pages":"Article 100302"},"PeriodicalIF":0.0,"publicationDate":"2025-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144254406","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Recent progress on high-precision construction of nanoarchitectured SERS substrates for ultrasensitive bio-medical sensors","authors":"Heguang Liu ,&nbsp;Ben Mou ,&nbsp;Jinxin Li ,&nbsp;Na Tian ,&nbsp;Yiming Feng ,&nbsp;Xiaodong Cui ,&nbsp;Yury Kapitonov ,&nbsp;Huageng Liang ,&nbsp;Caiyin You ,&nbsp;Yuan Li ,&nbsp;Tianyou Zhai","doi":"10.1016/j.apmate.2025.100300","DOIUrl":"10.1016/j.apmate.2025.100300","url":null,"abstract":"<div><div>Surface-enhanced Raman spectroscopy (SERS) has evolved from a laboratory technique to a practical tool for ultra-sensitive detection, particularly in the biomedical field, where precise molecular identification is crucial. Despite significant advancements, a gap remains in the literature, as no comprehensive review systematically addresses the high-precision construction of SERS substrates for ultrasensitive biomedical detection. This review fills that gap by exploring recent progress in fabricating high-precision SERS substrates, emphasizing their role in enabling ultrasensitive bio-medical sensors. We carefully examine the key to these advancements is the precision engineering of substrates, including noble metals, semiconductors, carbon-based materials, and two-dimensional materials, which is essential for achieving the high sensitivity required for ultrasensitive detection. Applications in biomedical diagnostics and molecular analysis are highlighted. Finally, we address the challenges in SERS substrate preparation and outline future directions, focusing on improvement strategies, design concepts, and expanding applications for these advanced materials.</div></div>","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 4","pages":"Article 100300"},"PeriodicalIF":0.0,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144190126","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Integrating luminescence with triboelectricity: Meticulously designed hybrid nanogenerator for multipurpose applications","authors":"Mandar Vasant Paranjape ,&nbsp;Punnarao Manchi ,&nbsp;Harishkumarreddy Patnam ,&nbsp;Anand Kurakula ,&nbsp;Venkata Siva Kavarthapu ,&nbsp;Jae Su Yu","doi":"10.1016/j.apmate.2025.100301","DOIUrl":"10.1016/j.apmate.2025.100301","url":null,"abstract":"<div><div>A seamless combination of mechanical energy-harvesting triboelectric nanogenerators with other technologies is the key to widening their applicability. Combining luminescent and triboelectric materials can develop hybrid nanogenerators (HNGs) which can be utilized for energy-harvesting, optical thermometry, and lighting applications. In this study, we designed an Er³⁺ and Eu³⁺ co-doped Sr_1.85Ca_0.15NaNb₅O₁₅ (SCNNO:EE) green-yellow-emitting phosphor with excellent temperature-sensing capabilities. SCNNO:EE possessed a high dielectric constant and was thus utilized as a filler inside the polydimethylsiloxane polymer to fabricate composite films. The composite films were employed to fabricate various HNG devices and the filler concentration was optimized to attain the highest electrical output of 170 ​V, 5.05 ​μA, and 75 ​μC/m². The piezoelectric-structured energy-harvesting device (PSEHD) was fabricated and further modified to fabricate a self-activated PSEHD (SAPSEHD) for solid-state lighting applications. Different engraved aluminum electrodes were attached to the composite films to obtain different glowing words and patterns. The electrical signals generated by the PSEHD, when the pressure was applied, were fed into the processing unit, which further flowing into the SAPSEHD. The SAPSEHD can generate electrical signals when pressure is applied and automatically produce light by activating the phosphor in the composite film. This type of devices could attract attention at the places where pressure-activated automatic lighting is required. Also, owing to the promising properties of the proposed devices, they can be utilized for various applications on a large scale.</div></div>","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 4","pages":"Article 100301"},"PeriodicalIF":0.0,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144190127","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Single bond regulated 1O2 and ‧O2− selective generation of heptazine-based conjugated polymers for high-selectivity photocatalysis","authors":"Guobang Li ,&nbsp;Mengkai Wang ,&nbsp;Dan Yang ,&nbsp;Ziwen Yu ,&nbsp;Tianyu Qiu ,&nbsp;Tonghui Wang ,&nbsp;Qing Jiang ,&nbsp;Yangguang Li ,&nbsp;Huaqiao Tan","doi":"10.1016/j.apmate.2025.100299","DOIUrl":"10.1016/j.apmate.2025.100299","url":null,"abstract":"<div><div>In conjugated polymers (CPs) photocatalytic system, the generation of reactive oxygen species (ROS) is regulated by cross-scale factors involving active site, excitonic behavior, and O₂ activation process on the surface. However, research on exploring the domino effect of “structure → excitonic behavior → O₂ activation → photocatalytic reaction” through structural modification at the atomic scale remains at its early stages. Herein, two heptazine-based CPs, CP-DPA, and CP-CZ were successfully prepared by polymerization of precursors formed by reacting diphenylamine (DPA) and carbazole (CZ) with cyameluric chloride, respectively. The minute difference in single bond between DPA and CZ endows the polymers with distinct physicochemical properties. Owing to the rotation between benzene rings, CP-DPA exhibits relatively lower conjugation, resulting in increased exciton binding energy (<em>E</em>_b) and inhibited exciton dissociation. Meanwhile, its more triplet state excitons facilitate energy transfer to generate singlet oxygen. Therefore, CP-DPA shows excellent activity for phenylboronic acid oxidation. Conversely, CP-CZ possesses relatively higher conjugation, minimal <em>E</em>_b and intensified exciton dissociation, which promotes charge transfer to produce superoxide radical. Consequently, CP-CZ displays optimal activity for phenylacetylene oxidation and [3 ​+ ​2] cycloaddition. This work provides new insights into regulating ROS generation by modulating the composition and structure of photocatalysts at the atomic scale.</div></div>","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 4","pages":"Article 100299"},"PeriodicalIF":0.0,"publicationDate":"2025-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144154984","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Honeycomb-like single-atom catalysts with FeN3Cl sites for high-performance oxygen reduction","authors":"Jinfeng Xu ,&nbsp;Yu Meng ,&nbsp;Xiaoyi Qiu ,&nbsp;Hong Zhong ,&nbsp;Shaokang Liu ,&nbsp;Lili Zhang ,&nbsp;Jiayang Zhang ,&nbsp;Pengxiang Hou ,&nbsp;Scott P. Beckman ,&nbsp;Feng Wu ,&nbsp;Chang Liu ,&nbsp;Minhua Shao ,&nbsp;Jincheng Li","doi":"10.1016/j.apmate.2025.100298","DOIUrl":"10.1016/j.apmate.2025.100298","url":null,"abstract":"<div><div>The great interest of Fe-N/C based Zn-air batteries and fuel cells intrigues large numbers of studies on modulating the pore structure for fast mass transport and the electronic structure of atomic Fe centers for enhancing intrinsic activity for oxygen reduction reaction (ORR). A Zn-assisted strategy herein is developed to synthesize a honeycomb-like micro-nanoscale porous Fe-N/C catalyst with atomic FeN₃Cl active sites. Specifically, Zn-guided synthesis of honeycomb-like porous carbon supported ZnO, ZnO-templated assembly of hemin modified ZIF-8 on honeycomb-like carbon and Zn/ZnO-assisted pyrolysis of the ZIF-8 precursor are involved. The synthetic mechanism is revealed by <em>in-situ</em> transmission electron microscopy imaging and <em>in-situ</em> X-ray diffraction analysis. Density functional theory calculations demonstrate FeN₃Cl can prominently lower the ORR energy barrier on the Fe centers, greatly facilitating catalytic kinetics. Hence, high ORR performance, including half-wave potentials of 0.81 ​V in acidic conditions and 0.91 ​V under alkaline media, is achieved. Besides, Zn-air batteries and H₂-O₂ fuel cells base on the resulting catalyst are investigated, also exhibiting excellent battery/cell performances. This study provides a novel strategy for the preparation of honeycomb-like micro-nanoscale porous single-atom catalysts as well as a significant new insight on the catalytic mechanisms, helping to advance in energy devices.</div></div>","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 4","pages":"Article 100298"},"PeriodicalIF":0.0,"publicationDate":"2025-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144155021","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"High-throughput theoretical exploration of multifunctional planar MBenes: Magnetism, topology, superconductivity, and anode applications","authors":"Xiaodong Lv ,&nbsp;Ting Han ,&nbsp;Rong Liu ,&nbsp;Fengyu Li ,&nbsp;Jian Gong ,&nbsp;Zhongfang Chen","doi":"10.1016/j.apmate.2025.100297","DOIUrl":"10.1016/j.apmate.2025.100297","url":null,"abstract":"<div><div>Pursuing new two-dimensional (2D) materials has been a hot topic in materials science, driven by their potential for diverse applications. Recent research has unveiled stable planar hypercoordinate motifs with unconventional geometric arrangements and bonding patterns that facilitate the synthesis of new 2D materials with diverse applications. Among these, yet the design of 2D transition metal systems featuring planar pentacoordinate boron (ppB) is particularly intriguing. Here we address this gap by proposing a novel family of transition metal boride monolayers (MBenes) composed of ppB and heptacoordinate M motifs. The novelty of our MBenes stems from their distinct atomic arrangements and bonding configurations, setting them apart from traditional 2D materials. High-throughput calculations identified 10 stable MBenes (with the stoichiometry of MB, M ​= ​Cr, Fe, Co, Ni, Cu, Mo, Pd, Ag, Pt, Au) with exceptional thermodynamic, dynamic, thermal, and mechanical stabilities attributed to strong B−B covalent bonds and M−B ionic interactions. Notably, five of these MBenes (M ​= ​Ni, Pd, Pt, Ag, Au) hold high promise as topological superconducting materials with superconducting transition temperatures of 2.4–5.2 ​K. This discovery not only enriches the family of topological superconducting materials but also opens new avenues for quantum device development. Meanwhile, FeB monolayer exhibits robust ferromagnetic properties with a high Curie temperature of ∼750 ​K, which is particularly significant for spintronics applications. In addition, NiB and CuB MBenes demonstrate extremely low sodium diffusion barriers (about 30 and 90 ​meV) and high sodium storage capacities (788 and 734 mAh g⁻¹, respectively), making them promising anode materials for sodium-ion batteries (SIBs). This study expands the selection of electrode materials for SIBs and mitigates some existing limitations in battery technology. Overall, these findings underscore the multifunctional potential of MBenes, positioning them as transformative materials for quantum computing, spintronics, and energy storage applications.</div></div>","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 3","pages":"Article 100297"},"PeriodicalIF":0.0,"publicationDate":"2025-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143885946","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Regulating electric double layer in non-fluorinated ether electrolyte enables high-voltage and low-temperature lithium metal batteries","authors":"Renfei Zhao ,&nbsp;Yuanhang Gao ,&nbsp;Zuosu Qin ,&nbsp;Yuelin Li ,&nbsp;Tao Zhang ,&nbsp;Anqiang Pan ,&nbsp;Ning Zhang ,&nbsp;Renzhi Ma ,&nbsp;Xiaohe Liu ,&nbsp;Gen Chen","doi":"10.1016/j.apmate.2025.100296","DOIUrl":"10.1016/j.apmate.2025.100296","url":null,"abstract":"<div><div>The poor oxidation stability of ether-based solvents has long been a major challenge limiting their practical application. To enhance the oxidative stability of ether-based electrolytes, the physicochemical properties of various glycol dimethyl ethers are screened, and diglyme (G2) is selected as the sole solvent for the electrolyte. Lithium bis(fluorosulfonyl)imide (LiFSI), a highly dissociative salt, is used as the primary salt; while lithium nitrate (LiNO₃) and lithium difluorophosphate (LiDFP), which have small ionic sizes and strong binding energies, are added as secondary salts. The resulting electrolyte can modulate the electric double layer structure by NO₃⁻ and DFP⁻ on the cathode side, leading to an increased Li⁺ concentration that is originally repelled by the cathode. Additionally, the oxidation stability of the electrolyte is improved and the formed electrode-electrolyte interphase is more uniform and stable, thereby enhancing the electrochemical performance of the cells. As a result, cells assembled with a total of 1 M ternary lithium salts in G2 solvent can operate at high voltage of 4.4 ​V. The Li||NCM811 ​cells maintain 80.2% capacity retention after 270 cycles at room temperature, with an average Coulombic efficiency of 99.5%, and exhibit 88.4% capacity retention after 200 cycles at −30 ​°C.</div></div>","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 3","pages":"Article 100296"},"PeriodicalIF":0.0,"publicationDate":"2025-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143899386","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Exploring the potential of low-dimensional materials from cigarette butts for energy applications: A comprehensive review","authors":"Ye Chen ,&nbsp;Shilong Li ,&nbsp;Congxin Xia ,&nbsp;Miao Tian ,&nbsp;Yaxin Guo ,&nbsp;Xupo Liu ,&nbsp;Mingjin Cui ,&nbsp;Shixue Dou ,&nbsp;Hanleem Lee ,&nbsp;Vadivel Subramaniam ,&nbsp;Krishnamoorthy Ramachandran ,&nbsp;Xinghui Liu","doi":"10.1016/j.apmate.2025.100295","DOIUrl":"10.1016/j.apmate.2025.100295","url":null,"abstract":"<div><div>Carbon-based low-dimensional materials (CLDM) with elemental carbon as the main component have unique physical and chemical properties, and become the focus of research in many fields including energy, environmental protection, and information technology. Notably, cellulose acetate, the main component of cigarette butts (CBs), is a one-dimensional precursor with a large specific surface area and aspect ratio. Still, their usefulness as building fillers has often been underestimated before. This review summarizes recent advances in CBs recycling and provides suggested guidelines for its use as a CLDM material in renewable energy. Specifically, we first describe the harmful effects of CBs as pollutants in our lives to emphasize the importance of proper recycling. We then summarize previous methods of recycling CBs waste, including clay bricks, asphalt concrete pavement, gypsum, acoustic materials, chemisorption, vector control, and corrosion control. The potential applications of CBs include triboelectric nanogenerator applications, flexible batteries, enhanced metal-organic framework material energy storage devices, and carbon-based hydrogen storage. Finally, the advantages of utilizing CBs-derived CLDM materials over conventional solutions in the energy field are discussed. This review will provide new avenues for solving the intractable problem of CBs and reducing the manufacturing costs of renewable materials.</div></div>","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 3","pages":"Article 100295"},"PeriodicalIF":0.0,"publicationDate":"2025-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143894883","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Erratum to “Electrolyte-independent and sustained inorganic-rich layer with functional anion aggregates for stable lithium metal electrode” [Adv. Powder Mater. 4 (1) (2025) 100261]","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.2025.100285","DOIUrl":"10.1016/j.apmate.2025.100285","url":null,"abstract":"","PeriodicalId":7283,"journal":{"name":"Advanced Powder Materials","volume":"4 3","pages":"Article 100285"},"PeriodicalIF":0.0,"publicationDate":"2025-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143785775","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}