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学者姓名：詹红兵
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Abstract ：
The ability to rapidly produce large single crystals is crucial for advancing the applications of covalent organic frameworks (COFs). Although the modulation strategy provides a straightforward method for growing high-quality single crystals, the slow crystallization process of COFs often limits their practical use. In this study, we combined the principles of crystallization thermodynamics and kinetics with the modulation strategy to develop a binary solvent-supersaturation method, enabling the growth of single-crystal COFs in a significantly shorter time. By systematically investigating the crystal-growth kinetics across different solvent ratios, we established a diffusion-reaction growth model, highlighting the essential role of supersaturation in controlling COF crystal growth. Especially, under this crystallization guidance, elegant single crystals of COFs built with heteroatom or other functionality can also facilely obtained, which spontaneously validate the universality of the protocol. Importantly, the resulting single-crystal COFs, characterized by high structural symmetry, exhibited notable second harmonic generation (SHG) activity, which could open new avenues for future research in this field.
Keyword ：
Binary solvent-supersaturation Binary solvent-supersaturation Crystal-growth kinetics Crystal-growth kinetics Diffusion-reaction growth model Diffusion-reaction growth model Second harmonic generation Second harmonic generation Single-crystal Single-crystal
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| GB/T 7714 | Jia, Ruiqiang , Ye, Ronglong , Chang, Zhen et al. Supersaturation-Controlled Single-Crystal Growth of Covalent Organic Frameworks with Binary Solvents [J]. | CHEMISTRY-A EUROPEAN JOURNAL , 2025 , 31 (22) . |
| MLA | Jia, Ruiqiang et al. "Supersaturation-Controlled Single-Crystal Growth of Covalent Organic Frameworks with Binary Solvents" . | CHEMISTRY-A EUROPEAN JOURNAL 31 . 22 (2025) . |
| APA | Jia, Ruiqiang , Ye, Ronglong , Chang, Zhen , Yu, Hao , Wang, Ming , Xu, Guohai et al. Supersaturation-Controlled Single-Crystal Growth of Covalent Organic Frameworks with Binary Solvents . | CHEMISTRY-A EUROPEAN JOURNAL , 2025 , 31 (22) . |
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Sodium ion hybrid capacitors (SIHCs) are garnering substantial interest in the energy storage field due to their unique capability to integrate high energy density and power density with the economic advantages of abundant sodium resources. However, the kinetic mismatch between battery-type anodes and capacitor-type cathodes presents a significant obstacle, severely limiting the performance potential of high-performance SIHCs. Herein, we report the development of a favorable pseudocapacitive Na+ storage nanohybrid, featuring VC nanodots confined within an N-doped carbon nanofiber network (VC@N-CNFs), which has been successfully applied to SIHCs. The integration of VC nanodots with a conductive carbon fiber framework significantly enhances electron transport and provides ample interface between the electrolyte and VC active material, thereby effectively improving the reaction kinetics of the anode. Consequently, the VC@N-CNFs demonstrate exceptional sodium storage capability, achieving a high capacity of 160.2 mA h g-1 at 1 A g-1 after 2000 cycles. Thanks to the favorable kinetic matching between the anode and cathode, the assembled SIHCs exhibit high energy and power densities of 97.8 W h kg-1 and 4118.3 W kg-1, respectively, alongside remarkable cycling performance, retaining 73.5% of their capacity after 6000 cycles.
Keyword ：
high conductivity high conductivity interconnected carbon networks interconnected carbon networks nanodots nanodots sodium storage sodium storage vanadium carbide vanadium carbide
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| GB/T 7714 | Yuan, Jun , Pan, Duo , Bo, Zheng et al. Encapsulation of VC Nanodots within N-Doped Carbon Nanofibers as a Robust and Capacitive Anode for Advanced Sodium-Ion Capacitors [J]. | ACS APPLIED ENERGY MATERIALS , 2025 , 8 (7) : 4733-4744 . |
| MLA | Yuan, Jun et al. "Encapsulation of VC Nanodots within N-Doped Carbon Nanofibers as a Robust and Capacitive Anode for Advanced Sodium-Ion Capacitors" . | ACS APPLIED ENERGY MATERIALS 8 . 7 (2025) : 4733-4744 . |
| APA | Yuan, Jun , Pan, Duo , Bo, Zheng , Liu, Yangjie , Yu, Jiaqi , Xu, Lihong et al. Encapsulation of VC Nanodots within N-Doped Carbon Nanofibers as a Robust and Capacitive Anode for Advanced Sodium-Ion Capacitors . | ACS APPLIED ENERGY MATERIALS , 2025 , 8 (7) , 4733-4744 . |
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2D transition metal dichalcogenides (TMDs) have emerged as a novel class of semiconductors with promising applications in optoelectronics, owing to their rich and tunable valley fine structure, known as valleytronics. Strain engineering in TMDs presents opportunities to tailor their valley fine structures and band alignment, which greatly expands the potential to investigate their intrinsic properties and improve device performance, thus opening a new field of straintronics. In this review, recent advances in strain-engineered 2D TMDs are summarized, with a focus on new phenomena and applications enabled by precision tuning of valley physics. The underlying mechanisms and connections are delineated between strain-induced modifications to the valley fine structures based on intravalley, intervalley, and interlayer band alignment in single and heterostructure TMDs. These insights allow targeted strain control strategies to be devised for optimizing optoelectronic characteristics. This review provides perspectives and guidance on the future directions of valley-straintronics and flexible 2D optoelectronics using TMDs, highlighting the substantial promise of valley-strain engineering in TMDs for fundamental valley physics studies as well as practical device applications. Presenting a comprehensive review on recent advancements in strain-engineered 2D transition metal dichalcogenides (TMDs). This review delves into precision tuning of valley physics through strain engineering, elucidating mechanisms and connections between strain-induced modifications and optoelectronic characteristics. It offers insights into future directions of valley-straintronics, underscoring the significant promise of valley-strain engineering in TMDs for fundamental studies and practical applications. image
Keyword ：
2D semiconductors 2D semiconductors straintronics straintronics transition metal dichalcogenides transition metal dichalcogenides valley fine structure valley fine structure valleytronics valleytronics
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| GB/T 7714 | Yang, Shichao , Long, Hanyan , Chen, Wenwei et al. Valleytronics Meets Straintronics: Valley Fine Structure Engineering of 2D Transition Metal Dichalcogenides [J]. | ADVANCED OPTICAL MATERIALS , 2024 , 12 (14) . |
| MLA | Yang, Shichao et al. "Valleytronics Meets Straintronics: Valley Fine Structure Engineering of 2D Transition Metal Dichalcogenides" . | ADVANCED OPTICAL MATERIALS 12 . 14 (2024) . |
| APA | Yang, Shichao , Long, Hanyan , Chen, Wenwei , Sa, Baisheng , Guo, Zhiyong , Zheng, Jingying et al. Valleytronics Meets Straintronics: Valley Fine Structure Engineering of 2D Transition Metal Dichalcogenides . | ADVANCED OPTICAL MATERIALS , 2024 , 12 (14) . |
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The practical applications of lithium-sulfur (Li-S) batteries are severely impeded by the shuttle effect of soluble lithium polysulfides (LiPSs), sluggish redox reaction kinetics, and insulating nature of sulfur and its discharge products (Li2S2/Li2S). Developing sulfur electrocatalysts with high electrocatalytic activity to accelerate the redox kinetics and polysulfide trapping is critical for Li-S batteries but remains a grand challenge. In this contribution, we demonstrate the delicate design and synthesis of oxygen-incorporated heterophase cobalt vanadium selenide nanoplates with dense crystalline/amorphous interfacial sites (denoted as DC/A O-CoVSe NPs) as high-efficiency sulfur electrocatalysts for Li-S batteries. Such DC/A O-CoVSe NPs possess high electronic conductivity and electrocatalytic activity. Besides, the abundant exposed crystalline/amorphous interfacial sites serve as efficient adsorption-catalytic centers to accelerate the conversion kinetics and alleviate the shuttle effect. Moreover, incorporation of oxygen further increases their affinity to LiPSs because of the introduction of more Li-O interactions. Benefiting from the multifarious advantages, Li-S batteries with DC/A O-CoVSe NP modified separators exhibit high discharge capacity (1400.1 mA h g-1 at 0.1C), excellent rate capability (683.8 mA h g-1 at 5C), and good long-term durability (672.4 mA h g-1 at 1C after 500 cycles with a low decay rate of 0.066% per cycle). Even at a high sulfur loading of 5.6 mg cm-2, the battery still delivers a decent reversible capacity of 658.8 mA h g-1 at 0.2C after 100 cycles, indicating its great potential for practical applications. This work could provide a rational viewpoint for developing high-efficiency sulfur electrocatalysts towards future advanced Li-S energy storage systems. Oxygen-incorporated heterophase cobalt vanadium selenide nanoplates with dense crystalline/amorphous interfacial sites (DC/A O-CoVSe NPs) are developed as high-efficiency sulfur electrocatalysts for lithium-sulfur batteries.
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| GB/T 7714 | Tan, Pengcheng , Yin, Yuan , Cai, Daoping et al. Oxygen-incorporated crystalline/amorphous heterophase cobalt vanadium selenide nanoplates with dense interfacial sites for robust lithium-sulfur batteries [J]. | JOURNAL OF MATERIALS CHEMISTRY A , 2024 , 12 (6) : 3711-3721 . |
| MLA | Tan, Pengcheng et al. "Oxygen-incorporated crystalline/amorphous heterophase cobalt vanadium selenide nanoplates with dense interfacial sites for robust lithium-sulfur batteries" . | JOURNAL OF MATERIALS CHEMISTRY A 12 . 6 (2024) : 3711-3721 . |
| APA | Tan, Pengcheng , Yin, Yuan , Cai, Daoping , Fei, Ban , Zhang, Chaoqi , Chen, Qidi et al. Oxygen-incorporated crystalline/amorphous heterophase cobalt vanadium selenide nanoplates with dense interfacial sites for robust lithium-sulfur batteries . | JOURNAL OF MATERIALS CHEMISTRY A , 2024 , 12 (6) , 3711-3721 . |
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van der Waals (vdW) superlattices, comprising different 2D materials aligned alternately by weak interlayer interactions, offer versatile structures for the fabrication of novel semiconductor devices. Despite their potential, the precise control of optoelectronic properties with interlayer interactions remains challenging. Here, we investigate the discrepancies between the SnS/TiS2 superlattice (SnTiS3) and its subsystems by comprehensive characterization and DFT calculations. The disappearance of certain Raman modes suggests that the interactions alter the SnS subsystem structure. Specifically, such structural changes transform the band structure from indirect to direct band gap, causing a strong PL emission (similar to 2.18 eV) in SnTiS3. In addition, the modulation of the optoelectronic properties ultimately leads to the unique phenomenon of thermally activated photoluminescence. This phenomenon is attributed to the inhibition of charge transfer induced by tunable intralayer strains. Our findings extend the understanding of the mechanism of interlayer interactions in van der Waals superlattices and provide insights into the design of high-temperature optoelectronic devices.
Keyword ：
interlayer interactions interlayer interactions photoluminescence photoluminescence SnTiS3 SnTiS3 temperature-dependent temperature-dependent van der Waals heterostructures van der Waals heterostructures
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| GB/T 7714 | Huang, Siting , Bai, Jiahui , Long, Hanyan et al. Thermally Activated Photoluminescence Induced by Tunable Interlayer Interactions in Naturally Occurring van der Waals Superlattice SnS/TiS2 [J]. | NANO LETTERS , 2024 , 24 (20) : 6061-6068 . |
| MLA | Huang, Siting et al. "Thermally Activated Photoluminescence Induced by Tunable Interlayer Interactions in Naturally Occurring van der Waals Superlattice SnS/TiS2" . | NANO LETTERS 24 . 20 (2024) : 6061-6068 . |
| APA | Huang, Siting , Bai, Jiahui , Long, Hanyan , Yang, Shichao , Chen, Wenwei , Wang, Qiuyan et al. Thermally Activated Photoluminescence Induced by Tunable Interlayer Interactions in Naturally Occurring van der Waals Superlattice SnS/TiS2 . | NANO LETTERS , 2024 , 24 (20) , 6061-6068 . |
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Rechargeable lithium-sulfur (Li-S) batteries have received ever-increasing attention owing to their ultrahigh theoretical energy density, low cost, and environmental friendliness. However, their practical application is critically plagued by the sluggish reaction kinetics, shuttling of soluble polysulfide intermediates, and uncontrollable growth of Li dendrites. Herein, a bimetallic telluride electrocatalyst with dense heterointerfaces and rich defects embedded in hollow carbon polyhedron bunches (N subset of CoTe1-x/ZnTe1-y@NC, abbreviated as NCZTC) is rationally designed to simultaneously address the S cathode and Li anode problems. Both experimental and computational results substitute the integration of dense heterointerfaces and rich defects can synergistically modulate the electronic structure, enhance the electrical conductivity, promote the Li+ transportation, strengthen the polysulfides adsorption and improve the catalytic activity, thereby significantly accelerating the redox conversion kinetics and prevent the dendrite growth. Consequently, Li-S batteries with NCZTC-modified separators demonstrate excellent electrochemical performance including high specific discharge capacity, remarkable rate capability, good long-term cycling stability, and competitive areal capacity even at high sulfur loading and lean electrolyte conditions. This study not only provides valuable guidance for designing efficient sulfur electrocatalysts with transition metal tellurides but also emphasizes the importance of heterostructure design and defect engineering for high-performance Li-S batteries. The high-efficiency N subset of CoTe1-x/ZnTe1-y@NC electrocatalyst is rationally designed for Li-S batteries. Both experimental and theoretical results substantiate that the integration of dense heterointerfaces and rich defects (Te vacancy-induced N-doping) can synergistically accelerate the sulfur conversion and protect the lithium anode from corrosion. This study provides an innovative strategy for constructing high-performance sulfur electrocatalysts with transition metal tellurides. image
Keyword ：
bimetallic tellurides bimetallic tellurides defects defects electrocatalysts electrocatalysts heterointerfaces heterointerfaces lithium-sulfur batteries lithium-sulfur batteries
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| GB/T 7714 | Wu, Xiangpeng , Xie, Rongjun , Cai, Daoping et al. Engineering Defect-Rich Bimetallic Telluride with Dense Heterointerfaces for High-Performance Lithium-Sulfur Batteries [J]. | ADVANCED FUNCTIONAL MATERIALS , 2024 , 34 (26) . |
| MLA | Wu, Xiangpeng et al. "Engineering Defect-Rich Bimetallic Telluride with Dense Heterointerfaces for High-Performance Lithium-Sulfur Batteries" . | ADVANCED FUNCTIONAL MATERIALS 34 . 26 (2024) . |
| APA | Wu, Xiangpeng , Xie, Rongjun , Cai, Daoping , Fei, Ban , Zhang, Chaoqi , Chen, Qidi et al. Engineering Defect-Rich Bimetallic Telluride with Dense Heterointerfaces for High-Performance Lithium-Sulfur Batteries . | ADVANCED FUNCTIONAL MATERIALS , 2024 , 34 (26) . |
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Amorphous transition metal oxides have recently received particular research interests in electrochemical energy storage. However, there is still a lack of direct comparisons between amorphous materials and their crystalline counterparts. Here, we demonstrate the rational synthesis of crystalline and amorphous Fe2O3 nanocubes uniformly grown on carbon nanofibers (denoted as CNFs@C-Fe2O3 and CNFs@A-Fe2O3, respectively) for lithiumion batteries (LIBs) and lithium-sulfur batteries (LSBs). In such a structure, the Fe2O3 nanocubes possess strong interfacial bonding with CNFs, which can ensure rapid electron transportation. Besides, these Fe2O3 nanocubes are highly porous, which can effectively alleviate the volume change, enlarge the surface area, increase active sites and facilitate ion diffusion. When employed as freestanding anode for LIBs, the CNFs@C-Fe2O3 electrode delivers much improved lithium ion storage performance compared to that of CNFs@A-Fe2O3. When evaluated as interlayers for LSBs, instead, the batteries with CNFs@A-Fe2O3 exhibit better rate performance cycling stability than that of with CNFs@C-Fe2O3. Moreover, theoretical calculations elucidate the amorphous Fe2O3 has stronger adsorption ability toward the soluble lithium polysulfides. This work would provide new insights into the reasonably development of crystalline and amorphous transition metal oxides toward electrochemical energy storage.
Keyword ：
Amorphous materials Amorphous materials Electrospinning Electrospinning Lithium-ion batteries Lithium-ion batteries Lithium-sulfur batteries Lithium-sulfur batteries Transition metal oxides Transition metal oxides
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| GB/T 7714 | Si, Junhui , Zhao, Mingliang , Cui, Zhixiang et al. Crystalline and amorphous Fe2O3 nanocubes grown on electrospun carbon nanofibers for lithium-ion batteries and lithium-sulfur batteries: A comparative study [J]. | APPLIED SURFACE SCIENCE , 2024 , 657 . |
| MLA | Si, Junhui et al. "Crystalline and amorphous Fe2O3 nanocubes grown on electrospun carbon nanofibers for lithium-ion batteries and lithium-sulfur batteries: A comparative study" . | APPLIED SURFACE SCIENCE 657 (2024) . |
| APA | Si, Junhui , Zhao, Mingliang , Cui, Zhixiang , Cai, Daoping , Zhan, Hongbing , Wang, Qianting . Crystalline and amorphous Fe2O3 nanocubes grown on electrospun carbon nanofibers for lithium-ion batteries and lithium-sulfur batteries: A comparative study . | APPLIED SURFACE SCIENCE , 2024 , 657 . |
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Sodium ion hybrid capacitors (SIHCs) address the high power and energy requirements in energy storage devices but face significant challenges arising from the slow kinetics and cycling instability of the anode side. Introducing atomic disorder and employing structural engineering in anode materials proves to be effective strategies for achieving rapid charge storage. Here, it is demonstrated that N-doped MXene encapsulated amorphous vanadium oxide hollow spheres (VOx@N-MXene HSs) offer multidirectional open pathways and sufficient vacancies, enabling reversible and fast Na+ insertion/extraction. Machine learning potentials, coupled with molecular simulation techniques, confirm the presence of more abundant pores within the amorphous vanadium oxide (VOx) structure. The simulation of the charging/discharging process elucidates the authentic reaction path and structural evolutions of the VOx@N-MXene HSs, providing sufficient insight into the atomic-scale mechanisms associated with these structural superiorities. The full SIHCs devices demonstrate a high energy density of 198.3 Wh kg-1, along with a long-term cycling lifespan of 8000 cycles. This study offers valuable strategies into the intricate design and exploration of amorphous electrodes, contributing to the advancement of next-generation electrochemical energy devices.
Keyword ：
amorphous vanadium oxide amorphous vanadium oxide fast kinetics fast kinetics hollow sphere hollow sphere machine learning machine learning MXene MXene
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| GB/T 7714 | Yuan, Jun , Pan, Duo , Chen, Junxiang et al. Ultrafast Na-Ion Storage in Amorphization Engineered Hollow Vanadium Oxide/MXene Nanohybrids for High-Performance Sodium-Ion Hybrid Capacitors [J]. | ADVANCED MATERIALS , 2024 , 36 (50) . |
| MLA | Yuan, Jun et al. "Ultrafast Na-Ion Storage in Amorphization Engineered Hollow Vanadium Oxide/MXene Nanohybrids for High-Performance Sodium-Ion Hybrid Capacitors" . | ADVANCED MATERIALS 36 . 50 (2024) . |
| APA | Yuan, Jun , Pan, Duo , Chen, Junxiang , Liu, Yangjie , Yu, Jiaqi , Hu, Xiang et al. Ultrafast Na-Ion Storage in Amorphization Engineered Hollow Vanadium Oxide/MXene Nanohybrids for High-Performance Sodium-Ion Hybrid Capacitors . | ADVANCED MATERIALS , 2024 , 36 (50) . |
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Developing alternative two-dimensional (2D) metallic/semiconducting (M/S) van der Waals heterostructures (vdWHs) along with an understanding of interfacial photocarrier behavior is crucial for designing high-performance optoelectronic devices. Here, we comprehensively explored the photophysical model of photocarrier generation and interfacial transfer in as-grown 2D 1T '/2H MoS2 vdWHs using various spectroscopic characterizations. We demonstrated the transitions of activated photocarrier transfer trajectories by tuning the pump photon energies across the 2H MoS2 bandgap. The importance of confined bilayer transfer systems and strong interlayer coupling at vdW interfaces for transfer efficiency was elucidated. Additionally, the fluorophlogopite substrate was found to be an external method for regulating photocarrier generation in individual 2H layers through the p-doping effect at the substrate-2H layer interfaces, and this influence was alleviated after introducing the 2H-1T ' vdW interface. Particularly, 1T ' MoS2 as a broadband hot carrier absorber enabled the ultrafast (similar to 133 fs) injection and extraction of energetic hot carriers into the 2H layer via a photothermionic emission mechanism, achieving a high efficiency of similar to 41% under 900 nm photoexcitation at room temperature. Our work offers fundamental insights into the complex interfacial carrier photophysics in 2D M/S vdWHs, providing a way of constructing advanced multifunctional devices by using these emerging materials as active components and interface engineering.
Keyword ：
1T '/2H MoS2 heterobilayers 1T '/2H MoS2 heterobilayers 2D materials 2D materials fluorophlogopite substrate fluorophlogopite substrate interface engineering interface engineering photocarrier transfer photocarrier transfer
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| GB/T 7714 | Dong, Junhao , Wu, Zhanggui , Huangfu, Changan et al. Interface Engineering for Efficient Photocarrier Generation and Transfer in Strongly Coupled Metallic/Semiconducting 1T′/2H MoS2 Heterobilayers [J]. | ACS NANO , 2024 , 18 (47) : 32868-32877 . |
| MLA | Dong, Junhao et al. "Interface Engineering for Efficient Photocarrier Generation and Transfer in Strongly Coupled Metallic/Semiconducting 1T′/2H MoS2 Heterobilayers" . | ACS NANO 18 . 47 (2024) : 32868-32877 . |
| APA | Dong, Junhao , Wu, Zhanggui , Huangfu, Changan , Su, Yi , Zheng, Xiaoyan , Wu, Wensheng et al. Interface Engineering for Efficient Photocarrier Generation and Transfer in Strongly Coupled Metallic/Semiconducting 1T′/2H MoS2 Heterobilayers . | ACS NANO , 2024 , 18 (47) , 32868-32877 . |
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The intrinsically sluggish sulfur reduction reaction kinetics and serious shuttle effect of soluble lithium polysulfides (LiPSs) severely impede the practical commercialization of lithium-sulfur (Li-S) batteries. Herein, self-supported tungsten nitride and carbide heterostructures with vanadium doping that are directly grown on carbon cloth substrate (CC@V-W2N/WC1-x) are creatively designed for Li-S batteries, which can tandemly catalyze the liquid-liquid conversion and liquid-solid conversion of polysulfide intermediate free of any interference from polymer binders and conductive additives. Noteworthy, the rich heterointerfaces and vanadium doping are beneficial for rapid charge transfer, strong chemical adsorption toward LiPSs, massive exposed catalytically active sites, and remarkable catalytic activities. Consequently, Li-S batteries assembled with the CC@V-W2N/WC1-x/S cathodes exhibit high sulfur utilization, superior rate capability, and decent long-term cycling stability. Furthermore, experimental analyses and theoretical calculations jointly substantiate that the V-W2N component is more effective in catalyzing the conversion of long-chain LiPSs, while the V-WC1-x benefits the favorable Li2S deposition kinetics. More importantly, the Li-S pouch cells are also fabricated to demonstrate their feasibility for practical applications. This work not only highlights the significance of tandem catalysis on the consecutive conversion of LiPSs but also provides a feasible avenue for developing highly efficient electrocatalysts toward high-performance Li-S batteries. A self-supported CC@V-W2N/WC1-x sulfur electrocatalyst with rich heterointerfaces and vanadium doping that is directly grown on carbon cloth substrate is creatively constructed for Li-S batteries. Integrated experimental and theoretical results confirm that the CC@V-W2N/WC1-x can tandemly catalyze the complicated sulfur reduction reaction. This work provides new inspiration for the design of tandem electrocatalysts for Li-S battery system. image
Keyword ：
heterostructure engineering heterostructure engineering lithium-sulfur batteries lithium-sulfur batteries self-supported arrays self-supported arrays sulfur hosts sulfur hosts tandem catalysis tandem catalysis
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| GB/T 7714 | Chen, Yongqing , Zhang, Xudong , Chen, Qidi et al. Self-Supported Tungsten Nitride and Carbide Heterostructures with Vanadium Doping Tandemly Catalyze the Conversion of Polysulfides for Lithium-Sulfur Batteries [J]. | ADVANCED FUNCTIONAL MATERIALS , 2024 , 35 (1) . |
| MLA | Chen, Yongqing et al. "Self-Supported Tungsten Nitride and Carbide Heterostructures with Vanadium Doping Tandemly Catalyze the Conversion of Polysulfides for Lithium-Sulfur Batteries" . | ADVANCED FUNCTIONAL MATERIALS 35 . 1 (2024) . |
| APA | Chen, Yongqing , Zhang, Xudong , Chen, Qidi , Cai, Daoping , Zhang, Chaoqi , Sa, Baisheng et al. Self-Supported Tungsten Nitride and Carbide Heterostructures with Vanadium Doping Tandemly Catalyze the Conversion of Polysulfides for Lithium-Sulfur Batteries . | ADVANCED FUNCTIONAL MATERIALS , 2024 , 35 (1) . |
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