{"title":"Plasma sources and plasma-assisted sputtering (PVD, CVD) for thin film deposition in materials for energy conversion and storage","authors":"Huu Q. Tran , Huy Le-Quoc","doi":"10.1016/j.jpowsour.2025.238609","DOIUrl":"10.1016/j.jpowsour.2025.238609","url":null,"abstract":"<div><div>Plasma–assisted physical and chemical vapor deposition (PVD and CVD) have emerged as transformative approaches for engineering thin films with tailored properties for energy conversion and storage applications. Unlike conventional thermal or chemical methods, plasma-based processes enable precise control of film morphology, defect concentration, and stoichiometry at reduced temperatures. This review provides a comprehensive overview of plasma sources and plasma-assisted sputtering techniques, followed by an in-depth examination of their role in fabricating thin films for thermoelectric, hydrogen storage, and electrochemical energy storage devices. Beyond summarizing existing literature, the article highlights the mechanisms through which plasma processes enhance adhesion, nanostructuring, and electrochemical stability. Comparative analyses with non-plasma methods, supported by schematics and performance data, reveal the unique advantages and limitations of plasma-assisted techniques. Recent advancements such as hybrid plasma systems, machine learning–driven optimization, and sustainable plasma sources are also discussed. The paper concludes by outlining critical insights and future research directions that position plasma-assisted deposition as a key enabler of next-generation energy technologies.</div></div>","PeriodicalId":377,"journal":{"name":"Journal of Power Sources","volume":"661 ","pages":"Article 238609"},"PeriodicalIF":7.9,"publicationDate":"2025-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145360167","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Saman Khademjafari , Alireza Sabour Rouhaghdam , Danial Iravani , Ali Talebi , Ghasem Barati Darband , Sangaraju Shanmugam
{"title":"Binder-free Co-P@Ni-Cu cedar leaf-like hierarchical structure as an efficient and stable electrocatalyst for hydrogen and oxygen evolution reactions","authors":"Saman Khademjafari , Alireza Sabour Rouhaghdam , Danial Iravani , Ali Talebi , Ghasem Barati Darband , Sangaraju Shanmugam","doi":"10.1016/j.jpowsour.2025.238608","DOIUrl":"10.1016/j.jpowsour.2025.238608","url":null,"abstract":"<div><div>The electrochemical water splitting process is one of the most effective methods for hydrogen production. However, its performance and efficiency depend strongly on the use of efficient electrocatalysts to minimize energy loss and material costs. This study introduces a unique hierarchical structure with a high specific surface area to reduce the overpotential of both the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER). In the proposed structure, the Co-P@Ni-Cu nanostructure is synthesized through a two-step electrodeposition process under varying conditions. Under optimal deposition parameters, the Co-P@Ni-Cu electrode requires only 57 mV overpotential for HER and 299 mV for OER to achieve a current density of 10 mA cm<sup>−2</sup>. Additionally, stability tests under industrial-scale hydrogen production conditions demonstrate excellent performance in both HER and OER. The enhanced electrocatalytic activity of the Co-P@Ni-Cu electrode arises from its high surface area, unique porous architecture, and improved charge transfer efficiency. The findings of this study provide valuable insights for designing advanced heterostructure electrodes in electrocatalytic applications.</div></div>","PeriodicalId":377,"journal":{"name":"Journal of Power Sources","volume":"661 ","pages":"Article 238608"},"PeriodicalIF":7.9,"publicationDate":"2025-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145359898","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Construction of polymer/SiO2 nanocomposite proton separators for all-polymer aqueous supercapacitor","authors":"Guangrun Lu, Jiawen Zhang, Aiping Zhu","doi":"10.1016/j.jpowsour.2025.238645","DOIUrl":"10.1016/j.jpowsour.2025.238645","url":null,"abstract":"<div><div>All-polymer aqueous supercapacitor, featuring electrodes and separators made entirely from polymers, which gives them advantages such as the processing ease, inherent safety, and sustainability. Challenges persist with the mechanical properties and high proton transport of separators in aqueous acidic medium. In this study, three types of amphiphilic polymers: polyvinyl alcohol (PVA), polyurethane (PU) latex, and polyacrylate (PA) latex with flexible molecular chains, are used to prepare polymer/SiO<sub>2</sub> nanocomposite proton separators for the polyaniline@Graphene (PANI@GNP) symmetrical supercapacitors. The supercapacitor with PU/SiO<sub>2</sub> nanocomposite proton separator exhibits a high capacity of 706 F/g, and a capacity retention of 83.6 % after 10000 cycles. This excellent electrochemical performance is due to the sufficient mechanical properties of proton separator to stabilize the proton transport channels formed by hydrogen bonds between PU and nanosilicas.</div></div>","PeriodicalId":377,"journal":{"name":"Journal of Power Sources","volume":"661 ","pages":"Article 238645"},"PeriodicalIF":7.9,"publicationDate":"2025-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145360118","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Alexei V. Petrovichev , Irina V. Kutovaya , Gayane A. Kirakosyan , Dmitry A. Cheshkov , Egor M. Pazhetnov , Victoria A. Nikitina , Stanislav S. Fedotov , Olga I. Shmatova
{"title":"Enhancing lithium-ion battery performance through a multi-benefit fluorinated electrolyte","authors":"Alexei V. Petrovichev , Irina V. Kutovaya , Gayane A. Kirakosyan , Dmitry A. Cheshkov , Egor M. Pazhetnov , Victoria A. Nikitina , Stanislav S. Fedotov , Olga I. Shmatova","doi":"10.1016/j.jpowsour.2025.238263","DOIUrl":"10.1016/j.jpowsour.2025.238263","url":null,"abstract":"<div><div>Advanced electrolytes are essential for extending the operational voltage and cycle life of lithium-ion batteries (LIBs) to meet the demands of high-energy applications and enhance safety. Here, we report the design and development of a non-flammable 1M LiPF<sub>6</sub> electrolyte based on methyl 3,3,3-trifluoropropionate (MTFP) and fluoroethylene carbonate (FEC). This electrolyte enables stable cycling of high-voltage graphite||NMC811 LIBs up to 4.5 V, thereby significantly exceeding the voltage limits of conventional carbonate-based electrolytes. Commercial-scale 2.1 Ah pouch cells with a high active material loading (3.8 mA h/cm<sup>2</sup>) retain 72 % of their initial capacity for over 1000 cycles at 0.5C (2.7–4.45 V). This enhanced performance and cycling stability are attributed to the formation of a protective LiF passivation layer on both the cathode and anode surfaces, as revealed by X-ray photoelectron spectroscopy. These findings highlight the viability of MTFP-based electrolytes for next-generation LIBs with higher energy density and extended cycle life.</div></div>","PeriodicalId":377,"journal":{"name":"Journal of Power Sources","volume":"661 ","pages":"Article 238263"},"PeriodicalIF":7.9,"publicationDate":"2025-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145323340","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Sreelakshmi Rajeevan , Sam John , Deepalekshmi Ponnamma , Soney C. George
{"title":"Tuning the electrochemical performance of graphene via covalent surface functionalization using silane coupling agent and incorporation of acid-modified multi-walled carbon nanotube for high energy and high power supercapacitor application","authors":"Sreelakshmi Rajeevan , Sam John , Deepalekshmi Ponnamma , Soney C. George","doi":"10.1016/j.jpowsour.2025.238622","DOIUrl":"10.1016/j.jpowsour.2025.238622","url":null,"abstract":"<div><div>The covalent functionalization of the graphene surface is successfully employed using a silane coupling agent, 3-aminopropyl trimethoxy silane (APTMS). The silane modification increased the interlayer spacing between the rGO layers. The composite electrode loaded with 1.5 g APTMS displayed 97.3 % pseudocapacitance, implying the successful silylation of the oxygenated functional groups on the graphene structure. The silylation imparts a sheet-like internal morphology with sharp edges to rGO's morphology. Among binary electrodes, Si-rGO with 20 wt% loading of acid-treated multi-walled carbon nanotubes (A-CNT) (PSRC20 binary electrodes) show excellent electrochemical properties and the highest specific capacitance. PSRC20 binary electrode displayed 82.6 % pseudocapacitance. A uniform dispersion of A-CNT in the silane-modified rGO matrix is revealed in the TEM micrographs. A specific capacitance of 225.8 F/g is obtained for the aqueous symmetric supercapacitor assembled using the PSRC20 binary electrode. Cycling performance evaluation over 2000 charge-discharge cycles at a current of 0.03 A showed that the device maintained 95 % of its initial capacitance and achieved a coulombic efficiency of 98 %. The perceived specific energy and specific power are 31.4 Wh/kg and 1714 W/kg at a current of 0.03 A. The fabricated pseudocapacitor is highly efficient in high-current applications, providing high energy density.</div></div>","PeriodicalId":377,"journal":{"name":"Journal of Power Sources","volume":"661 ","pages":"Article 238622"},"PeriodicalIF":7.9,"publicationDate":"2025-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145322663","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Production of battery grade power materials from spent lithium iron phosphate (LiFePO4) batteries","authors":"Rukshana Parween , Ankur Sharma , Karina Rani , Apurva Aditi , Balram Ambade , Manis Kumar Jha","doi":"10.1016/j.jpowsour.2025.238615","DOIUrl":"10.1016/j.jpowsour.2025.238615","url":null,"abstract":"<div><div>Lithium iron phosphate (LiFePO<sub>4</sub>) batteries have gained popularity due to their high safety and low cost. Effective recycling processes are needed to sustain indigenous material and economic benefit. In other hand, power materials are imported for the manufacturing of batteries, which compells for the development of process for recovery of the valuable metals (Fe, P, Li, Cu, and Al) from spent LFP batteries. Leaching was carried out at optimized condition using 3 % H<sub>2</sub>SO<sub>4</sub> and 5 % H<sub>2</sub>O<sub>2</sub> maintaining 100 g/L pulp density at 60 °C. 99.99 % Fe, Li, P, Al, and Cu were recovered within 60 min of mixing time. Leaching kinetics of Li followed “Chemical reaction control dense constant size cylindrical particles” model 1−(1−X)<sup>1/2</sup> = k<sub>c</sub>t, while Fe, P, Al, and Cu adhered to a “Chemical reaction control dense constant size or shrinking spheres” model 1−(1−X)<sup>1/3</sup> = k<sub>c</sub>t. Cementation was carried out using scrap iron to recover Cu at room temperature within 40 min. Fe and P were recovered as FePO<sub>4</sub> by precipitation. 99.99 % Al was precipitated using NaOH at pH 7.5, whereas 99.9 % Li was precipitated as Li<sub>2</sub>CO<sub>3</sub> and Li<sub>3</sub>PO<sub>4</sub> at pH 12 and 90 °C using Na<sub>2</sub>CO<sub>3</sub> and Na<sub>3</sub>PO<sub>4</sub>.12H<sub>2</sub>O, respectively. This process is viable for recycling LFP batteries ensuring resource recovery and environmental sustainability.</div></div>","PeriodicalId":377,"journal":{"name":"Journal of Power Sources","volume":"661 ","pages":"Article 238615"},"PeriodicalIF":7.9,"publicationDate":"2025-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145323335","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Meixiu Qu , Lin Peng , Yu Bai , Hang Li , Zhenhua Wang , Kening Sun
{"title":"Expediting reduction kinetics of sulfur species by defect engineering in CoP for high-performance lithium-sulfur battery","authors":"Meixiu Qu , Lin Peng , Yu Bai , Hang Li , Zhenhua Wang , Kening Sun","doi":"10.1016/j.jpowsour.2025.238611","DOIUrl":"10.1016/j.jpowsour.2025.238611","url":null,"abstract":"<div><div>Despite the fact that vacancy and doping engineering have been extensively used to modulate the electronic structures of metal-based compounds and thus develop advanced lithium-sulfur batteries, the intrinsic regulatory essences remain elusive. Herein, we propose a strategy of introducing Co vacancies and Ni-doped atoms into CoP to explore the modulation effect of Co vacancies and Ni-doped atoms on the electronic structure of CoP and reveal the structure-property relationships, thus achieving high-performance Li-S batteries. Systematic experiments and theoretical calculations reveal that introducing Co vacancies and doping with Ni atoms in CoP facilitates the formation of Ni-S and Li-P bonds between polysulfides and Ni-Co<sup>vac</sup>P, thereby significantly enhancing its adsorption ability. At the same time, the electron number of Li atoms near the Fermi level in the Ni-Co<sup>vac</sup>P-Li<sub>2</sub>S<sub>4</sub> system increases, which enhances redox conversion kinetics of polysulfides. Specifically, Ni-Co<sup>vac</sup>P reduces the activity energy for reduction process of sulfur species. The cell with CNT@Ni-Co<sup>vac</sup>P exhibits excellent rate capability (709 mA h g<sup>−1</sup>) and cycling stability over 700 cycles (average capacity decay of 0.04 % per cycle) at 5C. This study develops a sulfur host with exceptional adsorption and catalytic properties through vacancy and doping engineering to facilitate commercial applications of Li-S batteries.</div></div>","PeriodicalId":377,"journal":{"name":"Journal of Power Sources","volume":"661 ","pages":"Article 238611"},"PeriodicalIF":7.9,"publicationDate":"2025-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145324028","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Boran Tao , Zhen Wang , Zhenghua Li , Guilong Jin , Jinzhi Hu , Bingbing Wang , Wei Wu , Fengrui Zhang , Xiaodong Wu
{"title":"Dual modification of single-crystal Ni-rich cathodes for enhanced thermal safety in pouch cells","authors":"Boran Tao , Zhen Wang , Zhenghua Li , Guilong Jin , Jinzhi Hu , Bingbing Wang , Wei Wu , Fengrui Zhang , Xiaodong Wu","doi":"10.1016/j.jpowsour.2025.238631","DOIUrl":"10.1016/j.jpowsour.2025.238631","url":null,"abstract":"<div><div>The trade-off between high energy density and thermal safety in nickel-rich cathodes remains a critical challenge for lithium-ion batteries. This study presents a dual-modification strategy combining fluorine (F<sup>−</sup>) doping with LiCoO<sub>2</sub> (LCO) coating to improve the thermal stability of single-crystalline LiNi<sub>0.83</sub>Co<sub>0.12</sub>Mn<sub>0.05</sub>O<sub>2</sub> (SCNCM). We show that F<sup>−</sup> doping enhances bulk stability by substituting oxygen and forming strong TM–F and Li–F bonds, while the LCO coating suppresses interfacial side reactions. In-situ XRD and DSC-TG-MS analyses indicate that the modified material exhibits delayed phase transitions and reduced oxygen release, due to suppressed cation migration and improved oxygen lattice stability. Accelerating rate calorimetry tests confirm that pouch cells using the modified cathode achieve a 45 °C higher onset thermal runaway temperature (T<sub>2</sub>) and a 70 °C lower peak temperature (T<sub>3</sub>), along with reduced oxygen gas emission. Furthermore, the dual-modified cathode retains 91.5 % capacity after 450 cycles at 0.33C, matching the performance of pristine SCNCM without compromising rate capability. This work demonstrates the synergistic role of bulk doping and surface coating in balancing energy density and thermal safety, providing a viable approach to developing advanced Ni-rich cathodes for high-performance LIBs.</div></div>","PeriodicalId":377,"journal":{"name":"Journal of Power Sources","volume":"661 ","pages":"Article 238631"},"PeriodicalIF":7.9,"publicationDate":"2025-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145324027","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Zhisheng Mei , Tao Jiang , Yiran Teng , Hong Ping , Wenjing Li , Ejigu Alemu Guadie , Fei Teng
{"title":"Effect of gas mass transfer on hydrogen production at ampere-level current densities","authors":"Zhisheng Mei , Tao Jiang , Yiran Teng , Hong Ping , Wenjing Li , Ejigu Alemu Guadie , Fei Teng","doi":"10.1016/j.jpowsour.2025.238616","DOIUrl":"10.1016/j.jpowsour.2025.238616","url":null,"abstract":"<div><div>Water electrolysis driven by renewable energy sources is a green, sustainable hydrogen production method. However, industrial hydrogen production via water electrolysis is challenged by its high cost, high energy consumption and low conversion efficiency. It is urgently necessary to develop efficient, stable, and inexpensive electrocatalysts at ampere-level current densities. In this study, we mainly reveal the gas mass transfer effect under ampere-level current densities during water electrolysis. Typically, we synthesize FeNi-MOF through a simple method. Meanwhile, the Fe<sub>1</sub>Ni<sub>1</sub>P-C electrocatalyst is synthesized through phosphidation of the FeNi-MOF precursor. The Fe<sub>1</sub>Ni<sub>1</sub>P-C electrocatalyst demonstrates an excellent electrocatalytic activity in alkaline electrolyte: for the hydrogen evolution reaction (HER), η<sub>10</sub> = 118.2 mV, η<sub>1000</sub> = 301.2 mV, and Tafel slope = 72.44 mV dec<sup>−1</sup>; for the oxygen evolution reaction (OER), η<sub>10</sub> = 90.8 mV, η<sub>1000</sub> = 332.3 mV, and Tafel slope = 68.69 mV dec<sup>−1</sup>. Moreover, Fe<sub>1</sub>Ni<sub>1</sub>P-C exhibits a high stability at a large current density (110 h @ 1000 mA cm<sup>−2</sup>). Density functional theory (DFT) calculations confirm that the components of Fe<sub>1</sub>Ni<sub>1</sub>P-C exhibit gas-phobic behavior toward H<sub>2</sub> and O<sub>2</sub> molecules, effectively suppressing gas bubble accumulation on electrode surfaces and thereby facilitating continuous and steady reactions. This study presents a material design method that effectively enhances stability under high current density through the presence of a gas-repelling structure.</div></div>","PeriodicalId":377,"journal":{"name":"Journal of Power Sources","volume":"661 ","pages":"Article 238616"},"PeriodicalIF":7.9,"publicationDate":"2025-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145323286","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"N doping promotes the multiplication capability and cycling stability of cobalt-free lithium-rich layered cathode materials","authors":"Yu-Long Cao, Zheng Chen, Peng Liu, Yu-Long Xie","doi":"10.1016/j.jpowsour.2025.238623","DOIUrl":"10.1016/j.jpowsour.2025.238623","url":null,"abstract":"<div><div>Cobalt-free lithium-rich layered oxides (LLOs) become a new hotspot in energy storage science due to their high specific capacity and high voltage. However, challenges such as the dissolution and depletion of transition metals, cycling instability due to irreversible oxygen release, and structural transformations hinder their commercial application. In this study, Li<sub>1.2</sub>Mn<sub>0.6</sub>N<sub>x</sub>Ni<sub>0.2</sub>O<sub>2</sub> (x = 0, 0.01, 0.02, 0.03) is synthesized by de-doping the substrate material with varying amounts of N using carbonate co-precipitation and high-temperature solid-phase methods. The cathode material doped with 2 % N exhibits the best electrochemical performance. This improvement is attributed to the introduction of N, which occupies oxygen sites, enlarges the lattice spacing, mitigates the mixing of Li<sup>+</sup>/Ni<sup>2+</sup> in the material, and enhances lattice oxygen content. This leads to better cycling stability and excellent performance during multiple cycles. The modified sample shows a 27.18 % increase in capacity retention after 0.1C 100-cycle testing, and voltage decay during cycling is limited to only 0.342V. The study introduces a novel approach for anion doping to develop high-performance, cobalt-free, lithium-rich manganese-based cathode materials with enhanced discharge efficiency and cycling stability.</div></div>","PeriodicalId":377,"journal":{"name":"Journal of Power Sources","volume":"661 ","pages":"Article 238623"},"PeriodicalIF":7.9,"publicationDate":"2025-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145323290","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}