eScience最新文献_第4页

A self-damping triboelectric tactile patch for self-powered wearable electronics 一种用于自供电可穿戴电子设备的自阻尼摩擦电触觉贴片

IF 42.9

eScience Pub Date : 2025-03-01 DOI: 10.1016/j.esci.2024.100324

Guoli Du, Jiamin Zhao, Yuzheng Shao, Tao Liu, Bin Luo, Song Zhang, Mingchao Chi, Chenchen Cai, Zhaomeng Liu, Shuangfei Wang, Shuangxi Nie

{"title":"A self-damping triboelectric tactile patch for self-powered wearable electronics","authors":"Guoli Du, Jiamin Zhao, Yuzheng Shao, Tao Liu, Bin Luo, Song Zhang, Mingchao Chi, Chenchen Cai, Zhaomeng Liu, Shuangfei Wang, Shuangxi Nie","doi":"10.1016/j.esci.2024.100324","DOIUrl":"10.1016/j.esci.2024.100324","url":null,"abstract":"<div><div>Wearable tactile sensing systems with bionic designs holds significant promise for environmental interactions and human–machine communication. Triboelectric sensing technology plays a vital role in acquiring and quantifying tactile signals. Conventional elastic sensing materials, however, lack damping performance and are easily damaged by vibrations, leading to sensor failure. To address this challenge, our study proposes a highly damping triboelectric gel based on a hydrogen bonding assisted microphase separation strategy. In microphase separation, the soft phase provides the viscoelasticity needed for the gel, while the hard phase dissipates shock energy. This energy dissipation mechanism enables the gel to achieve excellent damping performance (tan δ = 0.68 at 1Hz), skin-like softness (Young’s modulus of 130 kPa), and stretchability (> 900 %). The resulting self-damping tactile patch effectively absorbs and dissipates external vibrations, ensuring a stable and reliable wearable tactile sensing device. This work provides new insights into the application of triboelectric gels in wearable electronics.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 2","pages":"Article 100324"},"PeriodicalIF":42.9,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143512457","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}

引用次数: 0

Development of noble metal-free electrocatalysts towards acidic water oxidation: From fundamental understanding to state-of-the-art catalysts 开发用于酸性水氧化的无贵金属电催化剂：从基本认识到最先进的催化剂

IF 42.9

eScience Pub Date : 2025-03-01 DOI: 10.1016/j.esci.2024.100295

Jing Ni , Zhaoping Shi , Yibo Wang , Jiahao Yang , Hongxiang Wu , Pengbo Wang , Meiling Xiao , Changpeng Liu , Wei Xing

{"title":"Development of noble metal-free electrocatalysts towards acidic water oxidation: From fundamental understanding to state-of-the-art catalysts","authors":"Jing Ni , Zhaoping Shi , Yibo Wang , Jiahao Yang , Hongxiang Wu , Pengbo Wang , Meiling Xiao , Changpeng Liu , Wei Xing","doi":"10.1016/j.esci.2024.100295","DOIUrl":"10.1016/j.esci.2024.100295","url":null,"abstract":"<div><div>The development of low-cost and efficient electrocatalysts for oxygen evolution reaction (OER) in acid electrolytes is critical to the widespread implementation of proton electrolyte membrane water electrolyzers (PEMWE) towards carbon neutralization. Noble metal Ir- and Ru-based materials are state-of-the-art catalysts but still suffer from prohibitive price and scarcity. In this context, a variety of noble metal-free catalysts have been developed to decrease the cost of PEMWE. In this review, we first summarize the activity expression mechanism and stability issues for non-precious metal catalysts, highlighting the origins of performance degradation and the possible mitigation strategies. Then, we systematically review several recently developed noble metal-free catalysts, focusing on the design rationale and the structure-performance relation. Finally, the development prospects of non-noble metal catalysts are prospected, with the potential challenges for practical applications presented.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 2","pages":"Article 100295"},"PeriodicalIF":42.9,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141696390","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}

引用次数: 0

Selective contact self-assembled molecules for high-performance perovskite solar cells 高性能钙钛矿太阳能电池的选择性接触自组装分子

IF 42.9

eScience Pub Date : 2025-03-01 DOI: 10.1016/j.esci.2024.100329

Huan Bi , Jiaqi Liu , Liang Wang , Tuo Liu , Zheng Zhang , Qing Shen , Shuzi Hayase

引用次数: 0

Quenching-induced atom-stepped bimetallic sulfide heterointerface catalysts for industrial hydrogen generation 淬火诱导原子阶梯双金属硫化物异质界面工业制氢催化剂

IF 42.9

eScience Pub Date : 2025-03-01 DOI: 10.1016/j.esci.2024.100311

Hua Zhang , Nianpeng Li , Sanshuang Gao , Anran Chen , Qihang Qian , Qingquan Kong , Bao Yu Xia , Guangzhi Hu

{"title":"Quenching-induced atom-stepped bimetallic sulfide heterointerface catalysts for industrial hydrogen generation","authors":"Hua Zhang , Nianpeng Li , Sanshuang Gao , Anran Chen , Qihang Qian , Qingquan Kong , Bao Yu Xia , Guangzhi Hu","doi":"10.1016/j.esci.2024.100311","DOIUrl":"10.1016/j.esci.2024.100311","url":null,"abstract":"<div><div>Developing non-noble metal hydrogen evolution reaction (HER) electrocatalysts with high activity and durability at ampere-level current densities is vital for emerging anion exchange membrane (AEM) water electrolysis, but it remains challenging. Here we present an atom-stepped nickel–cobalt bimetallic sulfide (AS-Ni<sub>3</sub>S<sub>2</sub>/Co<sub>3</sub>S<sub>4</sub>) heterostructure that exhibits superior HER performance, with ultra-low overpotentials of 28 and 195 mV at current densities of 10 and 2000 mA cm<sup>−2</sup>, respectively. Experimental analyses and theoretical calculations revealed that the work-function-induced interfacial built-in electric field drives electron transfer from Ni<sub>3</sub>S<sub>2</sub> to Co<sub>3</sub>S<sub>4</sub> via Ni–S–Co interfacial bridging, which effectively accelerates water activation and optimizes hydrogen adsorption and desorption. An AEM electrolyzer using an AS-Ni<sub>3</sub>S<sub>2</sub>/Co<sub>3</sub>S<sub>4</sub> heterostructure as the cathode required cell voltages of only 1.71 and 1.79 V to reach 1.0 and 2.0 A cm<sup>−2</sup>, respectively, and operated stably for 1200 h without activity degradation.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 2","pages":"Article 100311"},"PeriodicalIF":42.9,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143512456","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}

引用次数: 0

Cation-inspired polyhedral distortion boosting moisture/electrolyte stability of iron sulfate cathode for durable high-temperature sodium-ion storage 阳离子激发多面体畸变提高硫酸铁阴极的水分/电解质稳定性，用于持久高温钠离子储存

IF 42.9

eScience Pub Date : 2025-03-01 DOI: 10.1016/j.esci.2024.100313

Longfei Wen , Jiyu Zhang , Jian Zhang , Lingfei Zhao , Xin Wang , Sen Wang , Siyu Ma , Wenbin Li , Jun Luo , Junmin Ge , Weihua Chen

{"title":"Cation-inspired polyhedral distortion boosting moisture/electrolyte stability of iron sulfate cathode for durable high-temperature sodium-ion storage","authors":"Longfei Wen , Jiyu Zhang , Jian Zhang , Lingfei Zhao , Xin Wang , Sen Wang , Siyu Ma , Wenbin Li , Jun Luo , Junmin Ge , Weihua Chen","doi":"10.1016/j.esci.2024.100313","DOIUrl":"10.1016/j.esci.2024.100313","url":null,"abstract":"<div><div>Alluaudite-type iron-based sulfates are prospective positive-electrode active materials for sodium-ion batteries given their low-cost and high operation voltage, yet suffer from poor intrinsic ionic conductivity and (electro) chemical instability at high temperatures. Herein, a cation-modified Na<sub>2.466</sub>Fe<sub>1.724</sub>Mg<sub>0.043</sub>(SO<sub>4</sub>)<sub>3</sub> with micron-sized spherical structure was reported. The substitutive MgO<sub>6</sub> octahedron featured stronger covalent bonding interactions and enriched the ion transfer pathways within the crystals, facilitating the ionic kinetics in bulk. Using <em>in situ</em> mass spectrometry and quartz crystal microbalance techniques, Mg cations were demonstrated to lower the electron density around O atoms and surficial nucleophilicity of materials, which effectively suppressed their side reactions with H<sub>2</sub>O in air and active ester molecule in electrolyte. This interaction enables an inorganic-rich and uniform interphase to stabilize the cathode/electrolyte interface at high voltage (4.5 V vs. Na<sup>+</sup>/Na). The as-prepared cathode exhibits a high discharge capacity of 102.2 mAh g<sup>−1</sup> (voltage platform at 3.74 V), remarkable reaction reversibility (average Coulomb efficiency of 99.3 % over 300 cycles) at high loading (9.0−9.6 mg cm<sup>−2</sup>) and temperature (60 °C), as well as long-lasting cyclability (70.8 %, 5000 cycles). Its application was verified in assembled sodium-ion full cells with a hard carbon negative electrode, showing a long cycling lifetime over 190 cycles.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 2","pages":"Article 100313"},"PeriodicalIF":42.9,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143512455","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}

引用次数: 0

Delithiation-accelerating and self-healing strategies realizes high-capacity and high-rate black phosphorus anode in wide temperature range 加速衰减和自愈策略实现了宽温度范围内高容量、高速率黑磷阳极

IF 42.9

eScience Pub Date : 2025-03-01 DOI: 10.1016/j.esci.2024.100328

Shaojie Zhang , Yanhua Wan , Yu Cao , Yiming Zhang , Haochen Gong , Xu Liang , Baoshan Zhang , Xiaoyi Wang , Siyu Fang , Jiahong Wang , Wei Li , Jie Sun

{"title":"Delithiation-accelerating and self-healing strategies realizes high-capacity and high-rate black phosphorus anode in wide temperature range","authors":"Shaojie Zhang , Yanhua Wan , Yu Cao , Yiming Zhang , Haochen Gong , Xu Liang , Baoshan Zhang , Xiaoyi Wang , Siyu Fang , Jiahong Wang , Wei Li , Jie Sun","doi":"10.1016/j.esci.2024.100328","DOIUrl":"10.1016/j.esci.2024.100328","url":null,"abstract":"<div><div>Black phosphorus (BP) anode with high capacity (2596 mAh g<sup>−1</sup>) and suitable lithiation potential (0.7 V vs. Li<sup>+</sup>/Li) is an ideal candidate for high-energy-density and high-safety lithium-ion batteries, however, the practical implementation is greatly limited by its slow reaction kinetics and huge volume expansion. Here, inspired by nature, liquid metal (LM) is explored as a self-heal agent, which can well stabilize the BP anode through buffering the volumetric expansion and re-activating “dead P and Li<sub>x</sub>P”. Moreover, LM also acts as a good catalyst, which can adjust Li ion concentration and reduce the activation energy of delithiation reaction, thus prolonging the cycling life. Therefore, the LM modified BP/graphite (G) composite delivers an excellent high-rate performance of 1123 mAh g<sup>−1</sup> at 4 C with 80.0 % capacity retention after 200 cycles, a superior wide-temperature performance of 1547.5 mAh g<sup>−1</sup> and 569.0 mAh g<sup>−1</sup> at 50 °C and −20 °C, respectively.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 2","pages":"Article 100328"},"PeriodicalIF":42.9,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143512458","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}

引用次数: 0

Insights into plasmon-assisted chemical reactions: From fabrication to characterization 等离子体辅助化学反应的见解：从制造到表征

IF 42.9

eScience Pub Date : 2025-03-01 DOI: 10.1016/j.esci.2024.100312

Juan Xu , Xinwei Huang , Jing Peng , Shunxing Li , Jian-Feng Li

{"title":"Insights into plasmon-assisted chemical reactions: From fabrication to characterization","authors":"Juan Xu , Xinwei Huang , Jing Peng , Shunxing Li , Jian-Feng Li","doi":"10.1016/j.esci.2024.100312","DOIUrl":"10.1016/j.esci.2024.100312","url":null,"abstract":"<div><div>The integration of surface plasmons with catalysis has opened a new frontier in the field of chemical energy conversion, offering unprecedented opportunities for enhancing reaction activity and selectivity. This review delves into the optical properties of plasmonic materials, the intricate mechanisms of plasmon-assisted chemical reactions (PACRs), and the fabrication of plasmonic catalysts, highlighting the significance of the structure–performance relationship. The mechanisms of PACRs are summarized to understand their synergistic contributions to reactions. The review further examines modern experimental strategies for characterizing surface plasmon resonance properties, including scanning probe microscope, <em>in situ</em> spectroscopy, and ultrafast laser pump-probe techniques, which provide real-time, dynamic insights into molecular interactions and structural changes with high spatial and temporal resolution. We conclude by outlining the challenges and future prospects for PACRs, emphasizing the need for innovative strategies to fully exploit the potential of PACRs for sustainable energy conversion and environmental remediation.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 2","pages":"Article 100312"},"PeriodicalIF":42.9,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143512764","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}

引用次数: 0

Three-dimensional architecture design enables hexaazatriphenylene-based polymers as high-voltage, long-lifespan cathodes for aqueous zinc–organic batteries 三维结构设计使六叠三苯基聚合物成为水锌有机电池的高压、长寿命阴极

IF 42.9

eScience Pub Date : 2025-02-13 DOI: 10.1016/j.esci.2025.100379

Lei Li , Siqi Liu , Jie Luo , Xunan Hou , Junhua Kong , Qichong Zhang , Wenyong Lai , Chaobin He

{"title":"Three-dimensional architecture design enables hexaazatriphenylene-based polymers as high-voltage, long-lifespan cathodes for aqueous zinc–organic batteries","authors":"Lei Li , Siqi Liu , Jie Luo , Xunan Hou , Junhua Kong , Qichong Zhang , Wenyong Lai , Chaobin He","doi":"10.1016/j.esci.2025.100379","DOIUrl":"10.1016/j.esci.2025.100379","url":null,"abstract":"<div><div>Affordable, easily recycled organics with electroactive centers have drawn attention in the pursuit of high-performance aqueous zinc organic batteries (AZOBs). However, intrinsic barriers such as high solubility, undesirable potential, and inferior conductivity hinder their further development. To this end, we have designed an advanced cathode material for AZOBs, comprising an n-type polymer with a three-dimensional (3D) building block (HAT-TP) formed by polymerizing 2,3,6,7,10,11-hexacyano-1,4,5,8,9,12-hexazepenanthrene (HAT-CN) and 3D 2,3,6,7,14,15-hexaaminotriptycene (THA-NH<sub>2</sub>). The introduction of a 3D architecture not only bolsters the insolubility but also exposes redox-active sites for cation coordination, while the material's extended conjugated system promotes electronic delocalization to increase the redox potential and conductivity. As a result, a HAT-TP battery exhibits a notable initial discharge voltage of 1.32 V at 0.1 A g<sup>−1</sup>, followed by a midpoint voltage of 1.17 V. Remarkably, an ultrastable capacity retention ratio of up to 93.4% is achieved, even after 40,000 cycles at 5 A g<sup>−1</sup>. Theoretical simulations reveal that the elevated discharge potential results from the strong electronic delocalization of HAT-TP, which improves the affinity with cations. <em>Ex situ</em> characterizations and theoretical calculations verify that the reversible Zn<sup>2+</sup>/H<sup>+</sup> co-storage mechanism involves only electroactive C=N sites and the best possible coordination paths between them.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 4","pages":"Article 100379"},"PeriodicalIF":42.9,"publicationDate":"2025-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144308024","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}

引用次数: 0

Accelerated commercial battery electrode-level degradation diagnosis via only 11-point charging segments 仅通过11点充电段加速商用电池电极级退化诊断

IF 42.9

eScience Pub Date : 2025-01-01 DOI: 10.1016/j.esci.2024.100325

Yu Tian , Cheng Lin , Xiangfeng Meng , Xiao Yu , Hailong Li , Rui Xiong

{"title":"Accelerated commercial battery electrode-level degradation diagnosis via only 11-point charging segments","authors":"Yu Tian , Cheng Lin , Xiangfeng Meng , Xiao Yu , Hailong Li , Rui Xiong","doi":"10.1016/j.esci.2024.100325","DOIUrl":"10.1016/j.esci.2024.100325","url":null,"abstract":"<div><div>Accelerated and accurate degradation diagnosis is imperative for the management and reutilization of commercial lithium-ion batteries in the upcoming TWh era. Different from traditional methods, this work proposes a hybrid framework for rapid and accurate degradation diagnosis at the electrode level combining both deep learning, which is used to rapidly and robustly predict polarization-free incremental capacity analysis (ICA) curves in minutes, and physical modeling, which is used to quantitatively reveal the electrode-level degradation modes by decoupling them from the ICA curves. Only measured charging current and voltage signals are used. Results demonstrates that 11 points collected at any starting state-of-charge (SOC) in a minimum of 2.5 minutes are sufficient to obtain reliable ICA curves with a mean root mean square error (RMSE) of 0.2774 Ah/V. Accordingly, battery status can be accurately elevated based on their degradation at both macro and electrode levels. Through transfer learning, such a method can also be adapted to different battery chemistries, indicating the enticing potential for wide applications.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 1","pages":"Article 100325"},"PeriodicalIF":42.9,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143145136","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}

引用次数: 0

Atomic Ni-catalyzed cathode and stabilized Li metal anode for high-performance Li–O2 batteries 高性能锂氧电池的原子镍催化阴极和稳定锂金属阳极

IF 42.9

eScience Pub Date : 2025-01-01 DOI: 10.1016/j.esci.2024.100310

Tiansheng Bai , Jiaxian Wang , Hongqiang Zhang , Fengjun Ji , Wei Song , Shenyi Xiao , Dandan Gao , Jingyu Lu , Lijie Ci , Deping Li

{"title":"Atomic Ni-catalyzed cathode and stabilized Li metal anode for high-performance Li–O2 batteries","authors":"Tiansheng Bai , Jiaxian Wang , Hongqiang Zhang , Fengjun Ji , Wei Song , Shenyi Xiao , Dandan Gao , Jingyu Lu , Lijie Ci , Deping Li","doi":"10.1016/j.esci.2024.100310","DOIUrl":"10.1016/j.esci.2024.100310","url":null,"abstract":"<div><div>The Li–O<sub>2</sub> battery (LOB) has attracted growing interest, including for its great potential in next-generation energy storage systems due to its extremely high theoretical specific capacity. However, a series of challenges have seriously hindered LOB development, such as sluggish kinetics during the oxygen reduction and oxygen evolution reactions (ORR/OER) at the cathode, the formation of lithium dendrites, and undesirable corrosion at the lithium metal anode. Herein, we propose a strategy based on the ultra-low loading of atomic Ni catalysts to simultaneously boost the ORR/OER at the cathode while stabilizing the Li metal anode. The resultant LOB delivers a superior discharge capacity (> 16,000 mAh g<sup>−1</sup>), excellent long-term cycling stability (> 200 cycles), and enhanced high rate capability (> 300 cycles @ 500 mA g<sup>−1</sup>). The working mechanisms of these atomic Ni catalysts are revealed through carefully designed <em>in situ</em> experiments and theoretical calculations. This work provides a novel research paradigm for designing high-performance LOBs that are useable in practical applications.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 1","pages":"Article 100310"},"PeriodicalIF":42.9,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143144268","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}

引用次数: 0