JoulePub Date : 2025-02-19DOI: 10.1016/j.joule.2024.12.004
Joris Bücker , R. Maria del Rio-Chanona , Anton Pichler , Matthew C. Ives , J. Doyne Farmer
{"title":"Employment dynamics in a rapid decarbonization of the US power sector","authors":"Joris Bücker , R. Maria del Rio-Chanona , Anton Pichler , Matthew C. Ives , J. Doyne Farmer","doi":"10.1016/j.joule.2024.12.004","DOIUrl":"10.1016/j.joule.2024.12.004","url":null,"abstract":"<div><div>We analyze the employment dynamics of a rapid decarbonization of the US power sector, reducing emissions by 95% before 2035. We couple an input-output model with an occupational mobility network and identify three labor market phases: “scale-up,” “scale-down,” and a long-term, low-carbon, “steady state.” During the scale-up (2023–2034), for every job lost in an industry, 12 new jobs are created elsewhere. However, few occupations see sustained growth throughout the transition. We predict that skill mismatches will create frictions during the transition, especially in the scale-down phase. Compared with the size and fluctuations of the US labor market, the impact of this transition is modest, particularly if the US increases exports of clean energy technologies to counteract the domestic scale-down phase. However, without proper planning, rapidly growing industries will struggle to find skilled labor during the scale-up phase, while displaced workers might struggle finding jobs during the scale-down phase.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 2","pages":"Article 101803"},"PeriodicalIF":38.6,"publicationDate":"2025-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142987413","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
JoulePub Date : 2025-02-19DOI: 10.1016/j.joule.2024.11.004
Feng Gao , Hang Li , Boxin Jiao , Liguo Tan , Chengtang Deng , Xianjin Wang , Chao Luo , Changling Zhan , Elke Debroye , Yingchen Peng , Ye Yang , Chenyi Yi , Qing Zhao
{"title":"Perovskite facet heterojunction solar cells","authors":"Feng Gao , Hang Li , Boxin Jiao , Liguo Tan , Chengtang Deng , Xianjin Wang , Chao Luo , Changling Zhan , Elke Debroye , Yingchen Peng , Ye Yang , Chenyi Yi , Qing Zhao","doi":"10.1016/j.joule.2024.11.004","DOIUrl":"10.1016/j.joule.2024.11.004","url":null,"abstract":"<div><div>Polycrystalline perovskite films feature distinct facet orientations on the surface, which give rise to diverse chemical and electronic landscapes. These facet variations manifest in differences in optoelectronic characteristics, including energy level alignment and carrier mobility. Heterojunction structures, a staple in traditional photovoltaic devices, involve the strategic combination of two distinct components with unique optoelectronic properties. The heterogeneity of optoelectronic properties across the facets offers opportunities to create junctions that can enhance device performance. Here, we engineer a bilayer facet heterojunction (FHJ) in a perovskite-based photovoltaic device through integrating two films expressing distinct crystal facets (001)/(111). The buried interface of the FHJ devices demonstrates effective type II band alignment. The FHJ has propelled the power conversion efficiency (PCE) of evaporated perovskite solar cells (PSCs) to 24.92%. The operational stability of the target device has been significantly improved by retaining 91.7% of its initial performance after 2,000 h of operation at maximum power output.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 2","pages":"Article 101787"},"PeriodicalIF":38.6,"publicationDate":"2025-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142760634","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
JoulePub Date : 2025-02-19DOI: 10.1016/j.joule.2024.101809
Aliakbar Hassanpouryouzband , Moein Jahanbani Veshareh , Mark Wilkinson , Hamidreza M. Nick , Bryne T. Ngwenya , R. Stuart Haszeldine
{"title":"In situ hydrogen generation from underground fossil hydrocarbons","authors":"Aliakbar Hassanpouryouzband , Moein Jahanbani Veshareh , Mark Wilkinson , Hamidreza M. Nick , Bryne T. Ngwenya , R. Stuart Haszeldine","doi":"10.1016/j.joule.2024.101809","DOIUrl":"10.1016/j.joule.2024.101809","url":null,"abstract":"<div><div>Hydrogen is essential for achieving net-zero emissions by 2050, acting as both an energy carrier and source. It can store renewable energy, decarbonize difficult sectors, and serve as a zero-carbon feedstock. Conventional hydrogen production methods, such as natural gas reforming, inherently produce CO<sub>2.</sub> Electrolysis, though CO<sub>2</sub> free during operation, can still contribute to emissions through the construction of the energy source and electrolyzer; however, using surplus renewable energy that would otherwise be wasted can offset this. <em>In situ</em> hydrogen generation from underground fossil hydrocarbons presents a compelling alternative. This method produces hydrogen directly within geological formations, using existing fossil fuel resources and infrastructure while keeping CO<sub>2</sub> sequestered underground, thus minimizing environmental impact and reducing the need for extensive surface processing. Our research examines various <em>in situ</em> techniques, including thermochemical and biological processes, showcasing their potential to enhance current hydrogen production methods. Despite its promise, this approach faces significant challenges and requires extensive research to overcome these hurdles. Addressing these challenges is crucial for integrating this method into the global energy transition, potentially reducing the carbon footprint of hydrogen production and advancing toward cleaner energy systems. This paper highlights the necessary steps and the long path ahead to make <em>in situ</em> hydrogen generation a viable and sustainable solution.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 2","pages":"Article 101809"},"PeriodicalIF":38.6,"publicationDate":"2025-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142992515","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
JoulePub Date : 2025-02-19DOI: 10.1016/j.joule.2024.12.005
Magda Moner-Girona , Fernando Fahl , Georgia Kakoulaki , Do-Hyung Kim , Iyke Maduako , Sándor Szabó , Godwell Nhamo , Benjamin K. Sovacool , Daniel J. Weiss
{"title":"Empowering quality education through sustainable and equitable electricity access in African schools","authors":"Magda Moner-Girona , Fernando Fahl , Georgia Kakoulaki , Do-Hyung Kim , Iyke Maduako , Sándor Szabó , Godwell Nhamo , Benjamin K. Sovacool , Daniel J. Weiss","doi":"10.1016/j.joule.2024.12.005","DOIUrl":"10.1016/j.joule.2024.12.005","url":null,"abstract":"<div><div>Africa’s schools will educate the majority of the 21st century’s working population, influencing the global economy. Through combined spatial analysis techniques on over 500,000 schools, we estimate a 2 billion EUR cost to power unelectrified schools with decentralized solar photovoltaic systems. Given the positive effect on children’s food security and the growing need for digitalization, ensuring clean electricity access includes both electricity demand for internet connectivity and electric cooking. Our analysis reveals that 32% of African school-aged children live near unelectrified schools, with the nearest electrified school often too far away. The electrification of these facilities would reduce education-seeking trips by an average 45 min by motorized transport or 6 h on foot. This significant time savings, combined with the broader benefits of decentralized energy, can significantly enhance educational access, economic development, and environmental sustainability in Africa.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 2","pages":"Article 101804"},"PeriodicalIF":38.6,"publicationDate":"2025-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142939520","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
JoulePub Date : 2025-02-19DOI: 10.1016/j.joule.2024.11.007
Chang Li , Rishabh D. Guha , Stephen D. House , J. David Bazak , Yue Yu , Laidong Zhou , Kevin Zavadil , Kristin A. Persson , Linda F. Nazar
{"title":"A dynamically bare metal interface enables reversible magnesium electrodeposition at 50 mAh cm−2","authors":"Chang Li , Rishabh D. Guha , Stephen D. House , J. David Bazak , Yue Yu , Laidong Zhou , Kevin Zavadil , Kristin A. Persson , Linda F. Nazar","doi":"10.1016/j.joule.2024.11.007","DOIUrl":"10.1016/j.joule.2024.11.007","url":null,"abstract":"<div><div>Understanding and facilitating pure magnesium nucleation/growth electrodeposition behavior with ultrahigh Coulombic efficiency is complicated by the phenomenon of solid electrolyte interphase (SEI) formation in state-of-the-art, halogen-free magnesium electrolytes. Defining the electrolyte properties necessary to achieve ideal electrodeposition/stripping (E/S) thus remains elusive. Here, we reveal for the first time, rapid magnesium electrodeposition behavior that forms densely aligned, micron-sized thin platelets by establishing a dynamic bare magnesium/electrolyte interface during high-rate net plating. This effectively “SEI-free” interface allows facile magnesium diffusion and migration in stripping with near-unity E/S efficiency under demanding conditions over long-term cycling. The intrinsic electrolyte stability of the salt/solvent at the molecular level is the key to forming such an interface. The efficacy of the dynamic bare interface and an electrodeposited, free-standing magnesium anode is demonstrated in a high-areal-capacity full cell. These findings provide new design principles and fundamental understanding of interfacial chemistry in multivalent metal batteries.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 2","pages":"Article 101790"},"PeriodicalIF":38.6,"publicationDate":"2025-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142782966","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
JoulePub Date : 2025-02-19DOI: 10.1016/j.joule.2024.11.010
Fumeng Ren , Xiaoxuan Liu , Rui Chen , Zhaoyi Jiang , Zhenxing Sun , Qisen Zhou , Xueqing Cai , Jing Zhou , Jianan Wang , Sanwan Liu , Guanhaojie Zheng , Wenxi Liang , Zonghao Liu , Pavel A. Troshin , Yabing Qi , Wei Chen
{"title":"Crosslinker-stabilized quasi-two-dimensional perovskite for solar modules with certified stability","authors":"Fumeng Ren , Xiaoxuan Liu , Rui Chen , Zhaoyi Jiang , Zhenxing Sun , Qisen Zhou , Xueqing Cai , Jing Zhou , Jianan Wang , Sanwan Liu , Guanhaojie Zheng , Wenxi Liang , Zonghao Liu , Pavel A. Troshin , Yabing Qi , Wei Chen","doi":"10.1016/j.joule.2024.11.010","DOIUrl":"10.1016/j.joule.2024.11.010","url":null,"abstract":"<div><div>Upscaling perovskite solar cells to the module level while ensuring long-term stability is crucial for their commercialization. Here, we report a bottom-up crosslinking strategy utilizing 4-(aminomethyl)benzoic acid as a dual-anchor linker integrated into quasi-two-dimensional (2D) perovskite to reduce the weak van der Waals gap between individual 3D perovskite layers and to functionalize the NiO<sub>x</sub>/perovskite interface. This approach not only enhances the coupling of the perovskite slabs within the quasi-2D structure, leading to enhanced stability, but it also promotes the vertical growth of highly ordered, phase-pure low-dimensional perovskite films with improved carrier transport. The quasi-2D perovskite solar modules (PSMs) fabricated using this method have demonstrated an optimal efficiency of 16.05% over an aperture area of 9.66 cm<sup>2</sup>, utilizing a blade-coating technique in ambient air. Meanwhile, the PSMs have passed the standard damp-heat and operational stability tests for 1,000 h with negligible degradation, as verified by the VDE Prüfund Zertifizierungsinstitut GmbH (VDE Institute).</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 2","pages":"Article 101793"},"PeriodicalIF":38.6,"publicationDate":"2025-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142804968","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
JoulePub Date : 2025-02-19DOI: 10.1016/j.joule.2024.101813
Felix Zaussinger , Tobias S. Schmidt , Florian Egli
{"title":"Skills-based and regionally explicit labor market exposure to the low-carbon transition in Europe","authors":"Felix Zaussinger , Tobias S. Schmidt , Florian Egli","doi":"10.1016/j.joule.2024.101813","DOIUrl":"10.1016/j.joule.2024.101813","url":null,"abstract":"<div><div>Transitioning to a low-carbon economy leads to shifts in the labor market. Yet, an effective policy response to such shifts is currently limited by knowledge gaps on the occupations at risk, their skill profiles, and their regional and sectoral distributions. Here, based on a novel classification of occupational exposure covering 3,008 occupations and 13,500 skills, we map the labor market exposure to the low-carbon transition across European regions and sectors using granular labor force surveys. We find that workers in high-carbon jobs lacking industry decarbonization options (at-risk jobs) have significantly fewer skills and that their skills are less transversal compared with low-carbon or neutral jobs, which may inhibit switching to in-demand occupations. Moreover, large variations between regions and sectors can be expected. For example, while at-risk jobs are most frequent in the mining sector in relative terms (11%), the manufacturing sector is most affected in absolute terms (0.9 M). Crucially, our approach shows that effective deployment of industry decarbonization options helps reduce the number of at-risk workers from 6.2 to 2.3 M. Finally, we show that, among European countries with available data, Germany and Hungary face a particular challenge with a disproportionately high share of their workforce at risk, combined with low public support via the EU Just Transition Fund. Responding to these national and regional labor market impacts is critical to avoid policy backlash.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 2","pages":"Article 101813"},"PeriodicalIF":38.6,"publicationDate":"2025-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143192699","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
JoulePub Date : 2025-02-10DOI: 10.1016/j.joule.2025.101847
Minghao Zhang, Karnpiwat Tantratian, So-Yeon Ham, Zhuo Wang, Mehdi Chouchane, Ryosuke Shimizu, Shuang Bai, Hedi Yang, Zhao Liu, Letian Li, Amir Avishai, Lei Chen, Ying Shirley Meng
{"title":"Grain selection growth of soft metal in electrochemical processes","authors":"Minghao Zhang, Karnpiwat Tantratian, So-Yeon Ham, Zhuo Wang, Mehdi Chouchane, Ryosuke Shimizu, Shuang Bai, Hedi Yang, Zhao Liu, Letian Li, Amir Avishai, Lei Chen, Ying Shirley Meng","doi":"10.1016/j.joule.2025.101847","DOIUrl":"https://doi.org/10.1016/j.joule.2025.101847","url":null,"abstract":"Soft metals like lithium and sodium play a critical role in battery technology owing to their high-energy density. Texture formation by grain selection growth of soft metals during electrochemical processes is a crucial factor affecting power and safety. Here, a general thermodynamic theory and phase-field model are formulated to study the grain selection growth of soft metals. Our study focuses on the interplay between surface energy and atomic mobility-related intrinsic strain energy in grain selection growth. Differences in grain selection growth arise from the anisotropy in surface energy and the diffusion barrier of soft metal atoms. Our findings highlight the kinetic limitations of solid-state Li metal batteries, which originate from load stress-induced surface energy anisotropy. These insights lead to the development of an amorphous Li<sub>x</sub>Si<sub>1−x</sub> (0.50 < x < 0.79) seed layer, improving the critical current density at room temperature for anode-free Li solid-state batteries through the control of grain selection growth.","PeriodicalId":343,"journal":{"name":"Joule","volume":"59 1","pages":""},"PeriodicalIF":39.8,"publicationDate":"2025-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143375525","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
JoulePub Date : 2025-02-10DOI: 10.1016/j.joule.2025.101846
Ling Lv, Haikuo Zhang, Di Lu, Ruhong Li, Haotian Zhu, Baochen Ma, Shuoqing Zhang, Yiqiang Huang, Tao Zhou, Zunhao Fan, Jing Zhang, Lixin Chen, Xiayin Yao, Tao Deng, Xiulin Fan
{"title":"Additive engineering enables aggressive high-voltage LiCoO2 lithium-ion batteries","authors":"Ling Lv, Haikuo Zhang, Di Lu, Ruhong Li, Haotian Zhu, Baochen Ma, Shuoqing Zhang, Yiqiang Huang, Tao Zhou, Zunhao Fan, Jing Zhang, Lixin Chen, Xiayin Yao, Tao Deng, Xiulin Fan","doi":"10.1016/j.joule.2025.101846","DOIUrl":"https://doi.org/10.1016/j.joule.2025.101846","url":null,"abstract":"The advancement of additive engineering in high-voltage LiCoO<sub>2</sub> (LCO)-based lithium-ion batteries (LIBs) is limited by the lack of effective guiding principles. Here, we report a lattice coupling mechanism for designing nitrile additives, systematically evaluating 20 candidates to quantify their enhancement effects on LCO performance. Key to this mechanism are two motif descriptors: the O 2<em>p</em> band center energy and the energy gap (<em>Δ</em><em>E</em>) between the O 2<em>p</em> band center and the Co <em>3d</em> band center, which significantly improve the structural and interfacial stability of the LCO cathode. Guided by this principle, we developed 1,2,2,3-propanetetracarbonitrile (PCN) as a representative additive, achieving 80% capacity retention in 4.55 V 1.0 Ah artificial graphite (AG)||LCO pouch cells after over 770 and 380 cycles at 25°C and 45°C, respectively. This work provides new insights into the exploration and evaluation of additive chemistry for high-voltage LCO cathode.","PeriodicalId":343,"journal":{"name":"Joule","volume":"53 1","pages":""},"PeriodicalIF":39.8,"publicationDate":"2025-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143375526","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
JoulePub Date : 2025-02-05DOI: 10.1016/j.joule.2024.101817
Zhou Xing, Suxiang Ma, Bin-Wen Chen, Mingwei An, Ajuan Fan, Xinqiong Hu, Yang Wang, Lin-Long Deng, Qiufeng Huang, Hiroyuki Kanda, Fahad Gallab Al-Amri, Gainluca Pozzi, Yi Zhang, Jianxing Xia, Jiazhen Wu, Xugang Guo, Mohammad Khaja Nazeeruddin
{"title":"Solubilizing and stabilizing C60 with n-type polymer enables efficient inverted perovskite solar cells","authors":"Zhou Xing, Suxiang Ma, Bin-Wen Chen, Mingwei An, Ajuan Fan, Xinqiong Hu, Yang Wang, Lin-Long Deng, Qiufeng Huang, Hiroyuki Kanda, Fahad Gallab Al-Amri, Gainluca Pozzi, Yi Zhang, Jianxing Xia, Jiazhen Wu, Xugang Guo, Mohammad Khaja Nazeeruddin","doi":"10.1016/j.joule.2024.101817","DOIUrl":"https://doi.org/10.1016/j.joule.2024.101817","url":null,"abstract":"Pristine fullerene C<sub>60</sub> is currently the best-performing electron transport layer (ETL) for perovskite solar cells (PSCs) but suffers from significant aggregation in solution. Consequently, the high-cost and complex thermal evaporation method is typically used to deposit high-quality C<sub>60</sub> ETLs. To address this challenge, we introduce an n-type polymeric additive that can solubilize and stabilize C<sub>60</sub> molecules for solution processing, leading to efficient and stable solution-processed-C<sub>60</sub> (SP-C<sub>60</sub>) ETLs. The achievement is attributed to the well-matched properties of the n-type polymer and the precisely controlled intermolecular interactions between the polymer and C<sub>60</sub>. As a result, the SP-C<sub>60</sub> ETL with 5-wt % polymer addition afforded a champion power conversion efficiency of 25.60% (certified 25.09%). This is not only the highest performance among the current SP-C<sub>60</sub> devices but also highly competitive to the state-of-the-art thermally evaporated C<sub>60</sub> devices. Importantly, the champion device showed significantly enhanced stability (<em>T</em><sub>95, light</sub> > 1,800 h; <em>T</em><sub>80, heat</sub> = 700 h).","PeriodicalId":343,"journal":{"name":"Joule","volume":"61 1","pages":""},"PeriodicalIF":39.8,"publicationDate":"2025-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143124950","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}