IF 39.8 1区材料科学

Joule Pub Date : 2026-08-20 DOI: 10.1016/j.joule.2026.102634

Long Chen,Haikuo Zhang,Junyi Hua,Ruhong Li,Tao Zhou,Sen Jiang,Shuoqing Zhang,Jinze Wang,Long Li,Haotian Zhu,Yong Li,Rui Guo,Feng Guo,Chao Le,Lixin Chen,Tao Deng,Zhongtao Li,Xiulin Fan

{"title":"Molecular charge-topology electrolytes enable >630 Wh kg−1 lithium-metal batteries","authors":"Long Chen,Haikuo Zhang,Junyi Hua,Ruhong Li,Tao Zhou,Sen Jiang,Shuoqing Zhang,Jinze Wang,Long Li,Haotian Zhu,Yong Li,Rui Guo,Feng Guo,Chao Le,Lixin Chen,Tao Deng,Zhongtao Li,Xiulin Fan","doi":"10.1016/j.joule.2026.102634","DOIUrl":"https://doi.org/10.1016/j.joule.2026.102634","url":null,"abstract":"The reductive stability of electrolyte solvents fundamentally governs interfacial chemistry and cycling reversibility in lithium-metal batteries. However, molecular design remains largely empirical because a unified physical model linking electronic structure with reduction dynamics is lacking. Here, we establish a molecular charge-topology framework that identifies intramolecular charge distribution as a key determinant of electrochemical stability. Two descriptors, charge asymmetry degree (CAD) and balance of charges (BOC), correlate with electron affinity and reorganization energy, respectively, thereby connecting reduction thermodynamics and kinetics. Guided by this framework, a molecular charge-topology electrolyte enables Li||Cu cycling for over 5,600 h with an average Coulombic efficiency above 99.5%. Under ultra-lean conditions (electrolyte-to-capacity [E/C] = 0.75 g Ah−1), 13.0 Ah NCM955||Li pouch cells deliver over 630 Wh kg−1, while 5.0 Ah anode-free cells sustain cycling at a 5 A discharge rate. This work provides a bottom-up paradigm for rational electrolyte design.","PeriodicalId":343,"journal":{"name":"Joule","volume":"34 1","pages":""},"PeriodicalIF":39.8,"publicationDate":"2026-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148769085","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}

引用次数: 0

Scalable dual-step deposition of cascaded nickel oxide enables high-efficiency inverted perovskite solar cells and mini-modules 级联氧化镍的可扩展双步沉积使高效的倒钙钛矿太阳能电池和迷你模块成为可能

IF 39.8 1区材料科学

Joule Pub Date : 2026-08-20 DOI: 10.1016/j.joule.2026.102635

Jiani Liu,Ping Xu,Xin Chen,Qi Wang,Wei Hui,Ben Fan,Lin Song,Xiaopeng Xu,Yihui Wu,Qiang Peng

{"title":"Scalable dual-step deposition of cascaded nickel oxide enables high-efficiency inverted perovskite solar cells and mini-modules","authors":"Jiani Liu,Ping Xu,Xin Chen,Qi Wang,Wei Hui,Ben Fan,Lin Song,Xiaopeng Xu,Yihui Wu,Qiang Peng","doi":"10.1016/j.joule.2026.102635","DOIUrl":"https://doi.org/10.1016/j.joule.2026.102635","url":null,"abstract":"Inverted perovskite solar cells (PSCs) face efficiency and stability bottlenecks at the hole transport layer (HTL)/perovskite interface. This study addresses these issues by developing a synergistic, cascaded NiOx architecture via a robust dual-step chemical-bath deposition strategy. By identifying the rubidium ion (Rb+) as an optimal dopant, we construct a favorable interfacial energetic alignment that promotes hole extraction and reduces interfacial recombination. Beyond its electronic benefits, this cascaded HTL acts as a versatile template to regulate subsequent perovskite crystallization, facilitating strain-relaxed growth of the perovskite and suppressing non-radiative recombination at the buried interface. Consequently, small-area (0.09 cm2) PSCs achieve a high power conversion efficiency (PCE) of 27.05% (certified at 26.82%) with a fill factor of 86.96%. Industrial viability is demonstrated through 12.96 cm2 mini-modules yielding a 23.63% PCE. Furthermore, unencapsulated devices retain over 93% of their initial performance after 1,160 h of operation. This work establishes a facile and effective cascade design protocol for scalable, high-performance perovskite manufacturing.","PeriodicalId":343,"journal":{"name":"Joule","volume":"49 1","pages":""},"PeriodicalIF":39.8,"publicationDate":"2026-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148769086","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}

引用次数: 0

Rapid epitaxial growth of perovskite homojunctions via thermal shock for air-processed photovoltaics 空气处理光伏电池中钙钛矿同质结的热冲击快速外延生长

IF 37.1 1区材料科学

Joule Pub Date : 2026-08-19 Epub Date: 2026-04-22 DOI: 10.1016/j.joule.2026.102433

Bowen Jin, Yifei Kang, Hanming Li, Xiaonan Shen, Yecheng Ju, Hong Tian, Yanxiang Li, Yilong Song, Qingfeng Dong

{"title":"Rapid epitaxial growth of perovskite homojunctions via thermal shock for air-processed photovoltaics","authors":"Bowen Jin, Yifei Kang, Hanming Li, Xiaonan Shen, Yecheng Ju, Hong Tian, Yanxiang Li, Yilong Song, Qingfeng Dong","doi":"10.1016/j.joule.2026.102433","DOIUrl":"10.1016/j.joule.2026.102433","url":null,"abstract":"<div><div>The construction of high-quality crystalline junctions is pivotal for unlocking the full potential of perovskite optoelectronics, yet it remains challenging, especially via solution processing in ambient air. Here, we demonstrate a rapid epitaxial growth strategy for fabricating orientation-controlled perovskite homojunctions using a solvent-mediated thermal-shock process. This air-based epitaxy leverages the synergy between thermal-shock-induced flash crystallization and the inverse temperature solubility of 2-methoxyethanol, which maintains interfacial stability while enabling directional growth, thus combining solution-processing simplicity with epitaxial precision. The resultant 3D/3D perovskite homojunction exhibits a highly consistent (001) orientation (Hermans’ orientation factor of −0.3643) and a low trap-state density. Consequently, the corresponding homojunction perovskite solar cell (PSC) achieves a remarkable power conversion efficiency of 25.58% with outstanding operational stability, maintaining 93%, 97%, and 94% of its initial efficiency under International Summit on Organic Photovoltaic Stability (ISOS)-D-1, ISOS-L-1I, and ISOS-D-2I protocols, respectively.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"10 8","pages":"Article 102433"},"PeriodicalIF":37.1,"publicationDate":"2026-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148774960","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}

引用次数: 0

Tunable ions leaching drives active-site self-replenishment in high-entropy alloy for ultra-stable hydrogen evolution electrode 可调离子浸出驱动高熵合金超稳定析氢电极活性位点自补

IF 37.1 1区材料科学

Joule Pub Date : 2026-08-19 Epub Date: 2026-04-28 DOI: 10.1016/j.joule.2026.102436

Rongrong Shi, Bing Li, Jinshuo Pang, Yimin Zhang, Feng Gao, Enzuo Liu, Liying Ma, Biao Chen, Fang He, Chunsheng Shi, Chunnian He, Naiqin Zhao, Jianli Kang

{"title":"Tunable ions leaching drives active-site self-replenishment in high-entropy alloy for ultra-stable hydrogen evolution electrode","authors":"Rongrong Shi, Bing Li, Jinshuo Pang, Yimin Zhang, Feng Gao, Enzuo Liu, Liying Ma, Biao Chen, Fang He, Chunsheng Shi, Chunnian He, Naiqin Zhao, Jianli Kang","doi":"10.1016/j.joule.2026.102436","DOIUrl":"10.1016/j.joule.2026.102436","url":null,"abstract":"<div><div>Developing cost-effective electrodes with high activity and sustained stability under harsh conditions is crucial for advancing industrial alkaline water electrolysis. Nanostructured high-entropy alloys (HEAs) have emerged as promising hydrogen evolution reaction (HER) catalysts, yet effective methodologies for modulating their stability remain unavailable. Here, we present a “self-replenishment of active sites” strategy to resolve this challenge. We establish novel leaching criteria based on standard electrode potentials to rationally select sacrificial vs. stable components, coupled with precise modulation of the leaching kinetics of the sacrificial element, manganese. This continuous replenishment of active sites enables the MnFeCoNiMo HEA to achieve record-breaking HER stability, operating for 10,000 h at 1 A cm<sup>−2</sup>. Furthermore, industrial feasibility is demonstrated in a commercial alkaline water electrolyzer with 110-mm-diameter electrodes. Our strategy, focusing on ion-leaching kinetics, provides a comprehensive design framework for developing long-lasting electrodes through integrated composition and structure engineering.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"10 8","pages":"Article 102436"},"PeriodicalIF":37.1,"publicationDate":"2026-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148774948","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}

引用次数: 0

A constricted potassium evaporation strategy promoting ordered segregation for superior air electrodes in protonic ceramic fuel cells 在质子陶瓷燃料电池中，一种收缩的钾蒸发策略促进了优越空气电极的有序分离

IF 37.1 1区材料科学

Joule Pub Date : 2026-08-19 Epub Date: 2026-04-28 DOI: 10.1016/j.joule.2026.102435

Shuo Zhai, Senran Hao, Rubao Zhao, Yufei Song, Xi Chen, Jianhui Shen, Geng Xue, Idris Temitope Bello, Na Yu, Yifei Sun, Meidan Ye, Yuming Shu, Di Chen, Xingke Cai, Bin Chen, Daqin Guan, Guangming Yang, Zongping Shao, Meng Ni, Heping Xie

{"title":"A constricted potassium evaporation strategy promoting ordered segregation for superior air electrodes in protonic ceramic fuel cells","authors":"Shuo Zhai, Senran Hao, Rubao Zhao, Yufei Song, Xi Chen, Jianhui Shen, Geng Xue, Idris Temitope Bello, Na Yu, Yifei Sun, Meidan Ye, Yuming Shu, Di Chen, Xingke Cai, Bin Chen, Daqin Guan, Guangming Yang, Zongping Shao, Meng Ni, Heping Xie","doi":"10.1016/j.joule.2026.102435","DOIUrl":"10.1016/j.joule.2026.102435","url":null,"abstract":"<div><div>Understanding and controlling air-electrode structural evolution at elevated temperatures is crucial for efficient and durable protonic ceramic fuel cells (PCFCs). Here, a constricted potassium evaporation strategy is developed to induce ordered segregation in SrCo<sub>0.9</sub>Nb<sub>0.1</sub>O<sub>3−δ</sub> (SNC), transforming an otherwise inactive material into a highly active and stable cathode. The induced structural reconstruction generates uniformly distributed shell-core nanoparticles and an Sr/O-deficient perovskite phase, which greatly enhances oxygen reduction reaction (ORR) activity by promoting hydration kinetics and proton diffusion while suppressing detrimental SrO surface segregation. As a result, the reconstructed cathode delivers a peak power density of 744 mW cm⁻<sup>2</sup> at 550°C, around 75% higher than that of pristine SNC, along with a low polarization resistance of 0.28 Ω cm<sup>2</sup> and stable operation for over 500 h. Moreover, it functions as a robust bifunctional air electrode for reversible protonic ceramic electrolysis cells (PCECs) and oxygen-ion-conducting fuel cells, demonstrating broad applicability.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"10 8","pages":"Article 102435"},"PeriodicalIF":37.1,"publicationDate":"2026-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148774949","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}

引用次数: 0

Rethinking the green power grid for stability, not just for climate 重新思考绿色电网的稳定性，而不仅仅是气候

IF 37.1 1区材料科学

Joule Pub Date : 2026-08-19 Epub Date: 2026-06-15 DOI: 10.1016/j.joule.2026.102522

Yiming Wang, Arthur N. Montanari, Adilson E. Motter

引用次数: 0

In situ optical techniques for perovskite crystallization 钙钛矿结晶的原位光学技术

IF 37.1 1区材料科学

Joule Pub Date : 2026-08-19 Epub Date: 2026-07-07 DOI: 10.1016/j.joule.2026.102546

Yunfan Wang, Ziyao Yue, Zixin Zeng, Yuanhang Cheng, Zhuoqiong Zhang, Sai-Wing Tsang

{"title":"In situ optical techniques for perovskite crystallization","authors":"Yunfan Wang, Ziyao Yue, Zixin Zeng, Yuanhang Cheng, Zhuoqiong Zhang, Sai-Wing Tsang","doi":"10.1016/j.joule.2026.102546","DOIUrl":"10.1016/j.joule.2026.102546","url":null,"abstract":"<div><div>Solution-processed perovskites have garnered significant attention in photovoltaics owing to their rapid improvement in power conversion efficiency. These advances are largely driven by enhanced film quality enabled by crystallization regulation. However, the roles of various optimization strategies during crystallization remain actively debated, in part because of the lack of reliable approaches to probe the complex, rapid crystallization process. Recently, an increasing number of studies have employed <em>in situ</em> optical techniques to monitor perovskite crystallization. In this review, we provide a systematic overview of the development and application of <em>in situ</em> optical techniques for studying perovskite crystallization. We focus on experimental design considerations, analytical frameworks for correlating time-resolved optical signals with crystallization processes, and representative applications ranging from mechanistic understanding to process optimization. This work aims to offer a comprehensive technical guide for researchers seeking to employ <em>in situ</em> optical methods to investigate perovskite crystallization.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"10 8","pages":"Article 102546"},"PeriodicalIF":37.1,"publicationDate":"2026-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148624287","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}

引用次数: 0

Hydrogels as interfacial materials for the water-energy nexus 水凝胶作为水-能联系的界面材料

IF 37.1 1区材料科学

Joule Pub Date : 2026-08-19 Epub Date: 2026-06-08 DOI: 10.1016/j.joule.2026.102499

Weixin Guan, Chuxin Lei, An Hoai Vu, Tianrui Zheng, Xiaomeng Liu, Yaxuan Zhao, Guihua Yu

{"title":"Hydrogels as interfacial materials for the water-energy nexus","authors":"Weixin Guan, Chuxin Lei, An Hoai Vu, Tianrui Zheng, Xiaomeng Liu, Yaxuan Zhao, Guihua Yu","doi":"10.1016/j.joule.2026.102499","DOIUrl":"10.1016/j.joule.2026.102499","url":null,"abstract":"<div><div>Hydrogels are crosslinked polymer networks swollen with water that combine a percolated aqueous phase for transport with a solid-like scaffold that can be processed into films, fibers, and porous monoliths. This review positions hydrogels as interfacial materials for the water-energy nexus, emphasizing that coupled water, heat, and charge fluxes are governed by gradients in water chemical potential and ion electrochemical potential. We summarize how hydrogel chemistry and architecture tune both driving-force strength and response kinetics. Key variables include hygroscopic additives, functional groups, crosslinking, thermoresponsive transitions, porosity, architectures, and structural gradients. Together, these features enable control of water activity, ion partitioning, and interfacial resistances. These principles underpin hydrogel-enabled technologies, including interfacial solar water generation and atmospheric water harvesting, moisture- and evaporation-driven hydrovoltaic generators, and hydrogel electrolytes for aqueous batteries that suppress water splitting and direct ion flux for metal deposition. Finally, we discuss translational challenges related to environmental resilience, scalable manufacturing and system integration, safety-by-design, and life cycle sustainability, and we outline opportunities in programmable synthesis and AI-enabled closed-loop discovery to accelerate deployable hydrogel interfaces.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"10 8","pages":"Article 102499"},"PeriodicalIF":37.1,"publicationDate":"2026-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148624274","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}

引用次数: 0

Energy use of AI inference, efficiency pathways, and test-time scaling 人工智能推理的能量使用、效率路径和测试时间缩放

IF 37.1 1区材料科学

Joule Pub Date : 2026-08-19 Epub Date: 2026-04-22 DOI: 10.1016/j.joule.2026.102430

Felipe Oviedo, Fiodar Kazhamiaka, Esha Choukse, Allen Kim, Amy Luers, Melanie Nakagawa, Ricardo Bianchini, Juan M. Lavista Ferres

{"title":"Energy use of AI inference, efficiency pathways, and test-time scaling","authors":"Felipe Oviedo, Fiodar Kazhamiaka, Esha Choukse, Allen Kim, Amy Luers, Melanie Nakagawa, Ricardo Bianchini, Juan M. Lavista Ferres","doi":"10.1016/j.joule.2026.102430","DOIUrl":"10.1016/j.joule.2026.102430","url":null,"abstract":"<div><div>As artificial intelligence (AI) inference scales to billions of queries, estimates of per-query energy use are increasingly important for capacity planning, efficiency interventions, and policy. Yet many public estimates assume non-production settings, leading to systematic overestimation. We introduce a bottom-up framework estimating inference energy from token throughput, node power, and overhead under large-scale deployment assumptions. For frontier-scale models (>200B parameters) on H100 nodes, we estimate a median energy of 0.31 Wh/query (interquartile range [IQR] 0.16–0.60), indicating that widely cited estimates are overstated by 4–20×. In test-time scaling scenarios 15× longer than typical queries, the median energy rises 13× to 3.91 Wh (IQR 2.15–7.05). Across models, serving systems, and hardware, we estimate 8–20× line-of-sight energy reductions. At data-center scale, serving 1 billion queries/day requires 0.7 GWh; if 10% are long queries, demand rises to 1.7 GWh/day. With efficiency interventions, it falls to 0.8 GWh/day, mitigating the energy impact of test-time scaling.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"10 8","pages":"Article 102430"},"PeriodicalIF":37.1,"publicationDate":"2026-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147736005","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}

引用次数: 0

Reactive capture and electro-conversion of triethylamine-captured CO2 to high-concentration formic acid 三乙胺捕获二氧化碳的反应捕集和电转化为高浓度甲酸

IF 37.1 1区材料科学

Joule Pub Date : 2026-08-19 Epub Date: 2026-04-29 DOI: 10.1016/j.joule.2026.102437

Kezia Langie, Changsoo Kim, Andi Haryanto, Kwangho Park, Dong Ki Lee, Seunggyun Shin, Chan Woo Lee, Ung Lee, Da Hye Won

{"title":"Reactive capture and electro-conversion of triethylamine-captured CO2 to high-concentration formic acid","authors":"Kezia Langie, Changsoo Kim, Andi Haryanto, Kwangho Park, Dong Ki Lee, Seunggyun Shin, Chan Woo Lee, Ung Lee, Da Hye Won","doi":"10.1016/j.joule.2026.102437","DOIUrl":"10.1016/j.joule.2026.102437","url":null,"abstract":"<div><div>Among advanced carbon capture and utilization strategies, the reactive capture and conversion (RCC) strategy offers significant advantages by directly converting CO<sub>2</sub> in its captured state, eliminating the need for high-purity CO<sub>2</sub> and separation processes. Herein, we developed an electrochemical RCC system that efficiently converts the captured CO<sub>2</sub> into high-purity formic acid by integrating CO<sub>2</sub> capture, electrochemical conversion, and formic acid purification. Triethylamine (TREA) was selected as the CO<sub>2</sub> absorbent because it captures CO<sub>2</sub> as bicarbonate. The TREA-captured CO<sub>2</sub> was converted to formate with a 60% Faradaic efficiency and a 94% CO<sub>2</sub>-to-formate yield through an electrochemical RCC system equipped with a Sn-Cu catalyst in a membrane electrode assembly electrolyzer. Purification was completed via a two-step process involving amine exchange for TREA regeneration and distillation. <em>In situ</em> Raman spectroscopy elucidated the key intermediates and demonstrated the roles of the catalyst and CO<sub>2</sub> absorbent. Techno-economic analysis and life cycle analysis highlighted this system’s promising profitability and environmental sustainability.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"10 8","pages":"Article 102437"},"PeriodicalIF":37.1,"publicationDate":"2026-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148774947","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}

引用次数: 0

Joule最新文献