Query：
学者姓名：张久俊
Refining：
Year
Type
Indexed by
Source
Complex
Co-
Language
Clean All
Abstract ：
Polyether electrolytes (PEs) have attracted significant research and industrial interest for high-performance lithium metal batteries (LMBs). However, traditional PEs are limited by their low lithium-ion (Li+) conductivity primary due to strong Li⁺–polymer interactions (i.e. Li+-oxygen coordination). Current approaches of modifying polymer molecular structures are largely challenged by the inherent molecular structural constraints of specific polymers and the complexity of the required structural engineering processes. Herein, a novel and straightforward strategy i proposed to reduce the Li+−polymer interaction, increase free-Li+ concentration, and introduce ion-channels by regulating the microenvironment of PEs through introducing Ge4+ sites with weak Lewis acidity during in situ polymerization. In this way, the microenvironment regulates PE with a high ionic conductivity of 1.83 mS cm−1 at 25 °C and a Li+ transference number of 0.8 is achieved. Remarkably, the electrolyte exhibits extraordinary cycling stability in Li||Li symmetric cells for over 2000 h, demonstrating dendrite-free Li metal deposition during prolonged cycling. Moreover, the assembled Li||LiFePO4 cells achieve an impressive capacity retention of 92.1% and ≈100% Coulombic efficiency after a long-term stability of 2190 cycles at 5 C. This work provides new insight into the design of polymer electrolytes for high-performance LMBs through microenvironment regulation. © 2025 Wiley-VCH GmbH.
Keyword ：
high ionic conductivity high ionic conductivity long-term stability long-term stability microenvironment regulation microenvironment regulation polyether electrolytes polyether electrolytes quasi-solid-state batteries quasi-solid-state batteries
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Wang, H. , Qian, L. , Zheng, Y. et al. Microenvironment Regulation Unlocks High Li⁺ Conduction in Polyether Electrolytes for High-Performance Quasi-Solid-State Batteries [J]. | Advanced Materials , 2025 . |
| MLA | Wang, H. et al. "Microenvironment Regulation Unlocks High Li⁺ Conduction in Polyether Electrolytes for High-Performance Quasi-Solid-State Batteries" . | Advanced Materials (2025) . |
| APA | Wang, H. , Qian, L. , Zheng, Y. , Duan, S. , Qin, B. , Liu, Z. et al. Microenvironment Regulation Unlocks High Li⁺ Conduction in Polyether Electrolytes for High-Performance Quasi-Solid-State Batteries . | Advanced Materials , 2025 . |
| Export to | NoteExpress RIS BibTex |
Version ：
Abstract ：
Cobalt and iron selenides-based materials with high theoretical capacities, low toxicity and abundant sources have been identified as the promising anode materials for sodium-ion batteries (SIBs). However, they still face the challenges of high volume expansion and slow electrode kinetics, resulting in poor rate performance and fast capacity fading. In this paper, three-dimensional honeycomb-like Co-Fe based selenide composites with different molar ratios are successfully synthesized by one-pot solvothermal, annealing and selenization processes (expressed as Co-FeSe2@C/CNs-fbs, Co-FeSe2@C/CNs-irs and Co-FeSe2@C/CNs-sbs). Benefitted from the design of three-dimensional porous compositing structure, the optimized Co-FeSe2@C/CNs-fbs electrode material possesses more active sites and structural stability, resulting in stable cycling performance and fast electron/ion transport. As a result, Co-FeSe2@C/CNs-fbs anode shows excellent rate capability (353.1 mAh g-1 at 120 A g-1) and long cycling performance (95.7% of capacity retention after 3700 cycles at 60 A g-1), surpassing most previously reported anode materials for SIBs. Meanwhile, a full-cell made up with Na3V2(PO4)3/C cathode and Co-FeSe2@C/CNs-fbs anode shows a high energy density (180.1 Wh kg-1 at a power density 630.5 W kg-1) and capacity retention rate. This study provides a feasible strategy to fabricate selenide-based composites as the anode materials for high-performance SIBs via doping and structure engineering.
Keyword ：
Anode materials Anode materials co doping co doping sodium-ion batteries sodium-ion batteries three-dimensional porous structure three-dimensional porous structure transition metal selenides transition metal selenides
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Ma, Dakai , Qiu, Ruoxue , Zheng, Hui et al. Highly stable cobalt-doped FeSe2 anodes for unexpectedly fast sodium storage enabled by doping and structure engineering [J]. | INTERNATIONAL JOURNAL OF GREEN ENERGY , 2025 . |
| MLA | Ma, Dakai et al. "Highly stable cobalt-doped FeSe2 anodes for unexpectedly fast sodium storage enabled by doping and structure engineering" . | INTERNATIONAL JOURNAL OF GREEN ENERGY (2025) . |
| APA | Ma, Dakai , Qiu, Ruoxue , Zheng, Hui , Luo, Yiyuan , Wang, Kaili , Cai, Junming et al. Highly stable cobalt-doped FeSe2 anodes for unexpectedly fast sodium storage enabled by doping and structure engineering . | INTERNATIONAL JOURNAL OF GREEN ENERGY , 2025 . |
| Export to | NoteExpress RIS BibTex |
Version ：
Abstract ：
Constructing the continuously-distributed and crystalline-NaF-rich solid electrolyte interface (CC-NaF-SEI) is expected to greatly promote the sodium storage performance of hard carbon (HC) anodes. However, such an impressive concept remains extremely intractable to achieve and lacks an efficiently cost-less strategy. Herein, the application of the commercially available LA133 binder is pioneered to engineer such a CC-NaF-SEI. Through comparative analysis of representative binders with distinct functional groups, reveals the critical role of binder chemistry on SEI regulation. Specifically, the LA133 binder demonstrates a dual-regulation mechanism for CC-NaF-SEI formation. The anion-coordination preferred ─CN bonds induce an anion-enriched interfacial solvation structure, and the ─CONH/─CN groups catalytically cleave P─F bond dissociation in PF6−, synergistically promoting anion decomposition kinetics to form crystalline NaF. Furthermore, robust hydrogen bonds between multiple polar groups in LA133 and HC surface create the spatially anion-confined microenvironments to guide orderly anion decomposition and facilitate continuous NaF growth into a mechanically integrated SEI. The optimized CC-NaF-SEI endows HC anodes with exceptional sodium storage performance: an ultrahigh initial Coulombic efficiency (95.9%), remarkable reversible capacity (356.6 mAh g−1), and stable cycling under extreme conditions (−20–60 °C). This work provides fundamental insights into binder-SEI correlations, establishing a novel paradigm for interfacial optimization in sodium-ion batteries. © 2025 Wiley-VCH GmbH.
Keyword ：
anion decomposition anion decomposition binder binder continuously-distributed continuously-distributed crystalline-NaF-rich SEI crystalline-NaF-rich SEI hard carbon hard carbon
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Liu, M. , Cai, J. , Zuo, Y. et al. Constructing Continuously-Distributed and Crystalline-NaF-Rich SEI on Hard Carbon Anode Through Binder Chemistry for High-Performance Sodium-Ion Batteries [J]. | Advanced Materials , 2025 . |
| MLA | Liu, M. et al. "Constructing Continuously-Distributed and Crystalline-NaF-Rich SEI on Hard Carbon Anode Through Binder Chemistry for High-Performance Sodium-Ion Batteries" . | Advanced Materials (2025) . |
| APA | Liu, M. , Cai, J. , Zuo, Y. , Luo, W. , Huang, Y. , Qiu, R. et al. Constructing Continuously-Distributed and Crystalline-NaF-Rich SEI on Hard Carbon Anode Through Binder Chemistry for High-Performance Sodium-Ion Batteries . | Advanced Materials , 2025 . |
| Export to | NoteExpress RIS BibTex |
Version ：
Abstract ：
Anode-free solid-state lithium (Li) metal batteries (AFSSLMBs), with anticipated high energy density and cost-effectiveness, high safety, and simplicity of fabrication, are considered to have great potential in becoming promising alternatives for next-generation electrochemical energy storage devices. Unfortunately, the inefficiency of Li plating/stripping and the rapid capacity decay during cycling have severely hindered the further development of AFSSLMBs. Accordingly, to cope with these faced challenges, enormous efforts have been made in the most recent years. However, a comprehensive review entirely focusing on AFSSLMBs seems not available in terms of the loss and recovery of effective Li. Herein, based on the current understanding of AFSSLMBs, the essential causes of the main challenges faced by AFSSLMBs are attributed to irreversible Li loss and sluggish Li kinetics. Subsequently, five main types of advanced strategies for promoting AFSSLMBs' performance from various critical components are categorized and summarized along with the main line of avoiding effective Li loss, in which the contents from impactful articles published in the most recent one to two years are predominantly comprised. Finally, the challenges and possible future directions of AFSSLMBs are proposed, aiming to accelerate the rapid research and development for practical applications and commercialization of this advanced technology.
Keyword ：
advanced strategies for effective Li recovery advanced strategies for effective Li recovery anode-free solid-state Li-metal batteries anode-free solid-state Li-metal batteries challenges of effective Li loss challenges of effective Li loss irreversible Li loss irreversible Li loss sluggish Li kinetic sluggish Li kinetic
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Zhang, Tianzhu , Huang, Kaixin , Zheng, Yun et al. Loss and Recovery of Effective Lithium in Anode-Free Solid-State Lithium Metal Batteries [J]. | ADVANCED MATERIALS , 2025 . |
| MLA | Zhang, Tianzhu et al. "Loss and Recovery of Effective Lithium in Anode-Free Solid-State Lithium Metal Batteries" . | ADVANCED MATERIALS (2025) . |
| APA | Zhang, Tianzhu , Huang, Kaixin , Zheng, Yun , Luo, Dan , Yan, Wei , Zhang, Jiujun et al. Loss and Recovery of Effective Lithium in Anode-Free Solid-State Lithium Metal Batteries . | ADVANCED MATERIALS , 2025 . |
| Export to | NoteExpress RIS BibTex |
Version ：
Abstract ：
The development of anti-corrosion and anti-poison electrocatalysts for both the hydrogen oxidation reaction (HOR) and oxygen reduction reaction (ORR) is of great importance for effective applications of proton exchange membrane fuel cells (PEMFCs). In this study, a non-carbon supported catalyst, Pt/TiO2-O-v, enriched with oxygen vacancies (O-v), is successfully synthesized using a microwave-assisted method. This catalyst is developed as a bifunctional electrocatalyst with superior contamination tolerance, enabling efficient HOR and ORR performance. The electronic metal-support interaction (EMSI) is leveraged to facilitate electron transfer between Pt and Ti atoms, induced by the formation of oxygen vacancy channels in the small-sized, high surface area TiO2-O-v support. Notably, TiO2-O-v has a lower bandgap than commercial TiO2, enhancing its catalytic properties. In a 0.1 mol/L HClO4 electrolyte, the normalized Pt mass activity (j(k,m)) and specific activity (j(0,s)) of Pt/TiO2-O-v are 1.24 times higher than those of commercial Pt/C. Furthermore, Pt/TiO2-O-v catalyst exhibits minimal current density decay after a prolonged durability testing under hydrogen and oxygen atmospheres. Remarkably, under a H-2/(1000x10(-6)) CO atmosphere, the relative retention rate of Pt/TiO2-O-v significantly exceeds that of Pt/C catalyst, demonstrating its superior CO tolerance and promising potential for practical applications in PEMFCs. This study highlights the critical role of the strong metal-support interaction between the reducible oxide support and the noble metal Pt in improving long-term performance and CO poisoning resistance.
Keyword ：
CO poisoning CO poisoning hydrogen oxidation reaction hydrogen oxidation reaction oxygen reduction reaction oxygen reduction reaction proton exchange membrane fuel cells (PEMFCs) proton exchange membrane fuel cells (PEMFCs) Pt/TiO2 catalyst Pt/TiO2 catalyst
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Lian, Bianyong , Chen, Jinghong , Li, Lingfei et al. Bifunctional Pt/TiO2-Ov catalysts for enhanced electron transfer and CO tolerance in acidic HOR and ORR [J]. | FRONTIERS IN ENERGY , 2025 . |
| MLA | Lian, Bianyong et al. "Bifunctional Pt/TiO2-Ov catalysts for enhanced electron transfer and CO tolerance in acidic HOR and ORR" . | FRONTIERS IN ENERGY (2025) . |
| APA | Lian, Bianyong , Chen, Jinghong , Li, Lingfei , Deng, Shuqi , Wang, Kaili , Yan, Wei et al. Bifunctional Pt/TiO2-Ov catalysts for enhanced electron transfer and CO tolerance in acidic HOR and ORR . | FRONTIERS IN ENERGY , 2025 . |
| Export to | NoteExpress RIS BibTex |
Version ：
Abstract ：
Flexible lithium-ion batteries (FLIBs) have garnered significant research interest as critical energy storage components, driven by rapid advancements in deformable electronic systems. However, it is a challenge to simultaneously realize adequate flexibility, stability, and energy density for FLIBs. Cellulose-based materials demonstrate inherent flexibility, lightweight characteristics, high surface area, and cost-effectiveness, enabling their promising utilization in electrode architectures for high-energy-density flexible battery systems. In this review, we summarize the recent research progress of the application of cellulose-based materials in FLIBs, with special emphasis on roles of cellulose-based materials in electrodes of FLIBs. Firstly, the roles of cellulose-based materials in FLIBs' anodes are categorized into four distinct types: precursor, binder, skeleton, and modification layer, accompanied by an overall review of recent advances. Similarly, their multifunctional contributions in FLIBs cathodes are also systematically classified into three categories: binder, skeleton, and modification layers, with corresponding progress in each domain comprehensively summarized. Finally, the challenges and possible future directions of cellulose-based materials in FLIBs are proposed, aiming to accelerate the rapid research and development for practical applications and commercialization of this advanced technology.
Keyword ：
cellulose-based materials cellulose-based materials electrode modification electrode modification flexible lithium-ion battery flexible lithium-ion battery the roles of cellulose-based materials the roles of cellulose-based materials Wearable electronic devices Wearable electronic devices
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Liu, Xiang , Zhang, Tianzhu , Liu, Zewen et al. Cellulose-based materials enabling high-performance electrodes for flexible lithium-ion batteries: A mini review [J]. | INTERNATIONAL JOURNAL OF GREEN ENERGY , 2025 . |
| MLA | Liu, Xiang et al. "Cellulose-based materials enabling high-performance electrodes for flexible lithium-ion batteries: A mini review" . | INTERNATIONAL JOURNAL OF GREEN ENERGY (2025) . |
| APA | Liu, Xiang , Zhang, Tianzhu , Liu, Zewen , Zheng, Yun , Qin, Bingsen , Lu, Zongtao et al. Cellulose-based materials enabling high-performance electrodes for flexible lithium-ion batteries: A mini review . | INTERNATIONAL JOURNAL OF GREEN ENERGY , 2025 . |
| Export to | NoteExpress RIS BibTex |
Version ：
Abstract ：
Compositing inorganic ceramics and polymer materials to form all-solid-state electrolytes has been recognized as a feasible approach for the development of all-solid-state batteries. However, polymer-based electrolytes such as polyethylene oxide can electrochemically decompose above 3.9 V (vs. Li+/Li), which results in undesirable battery performance. Moreover, dendrite growth can occur on the anode side and further lead to battery short-circuit. This work designs and successfully fabricates stable electrode/electrolyte interfaces on both the composite cathode and anode sides after employing alucone coating layers made through atomic layer deposition. Due to the protection capability of such coating layers, the electrochemical degradation between the composite solid-state electrolytes of Li7La3Zr2O12/polyethylene oxide/lithium bis(trifluoromethane-sulfonyl) imide film and nickel-rich high voltage cathode (LiNi0.8Mn0.1Co0.1O2) has been obviously suppressed through the significantly improved anti- oxidation capability of the electrolyte. Simultaneously, the alucone coating layer can function as the protective barrier for the lithium metal anode, remarkably suppressing the growth of lithium dendrites. As a result, the obtained all-solid-state batteries with dual electrode/electrolyte interfaces show both high capacity retention and long cycle life, whereas the contrasting battery without protection coating layers shows both the fast capacity decay and micro-shorting behavior. This work presents an effective strategy for constructing more stable electrode/electrolyte interfaces for polymers-based all-solid-state batteries, and also provides a design rationale for materials and structure development in the field of energy storage and conversion.
Keyword ：
All-solid-state battery All-solid-state battery alucone alucone atomic layer deposition atomic layer deposition composite solid-state electrolyte composite solid-state electrolyte interface optimization interface optimization lithium metal anode lithium metal anode
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Chen, Guohui , Liu, Xiang , Liu, Zewen et al. Novel "sandwich" configuration with ALD-coating layers on electrode/electrolyte interfaces for durable all-solid-state lithium metal batteries with high voltage cathodes- [J]. | ENERGY MATERIALS , 2025 , 5 (7) . |
| MLA | Chen, Guohui et al. "Novel "sandwich" configuration with ALD-coating layers on electrode/electrolyte interfaces for durable all-solid-state lithium metal batteries with high voltage cathodes-" . | ENERGY MATERIALS 5 . 7 (2025) . |
| APA | Chen, Guohui , Liu, Xiang , Liu, Zewen , Zheng, Yun , Zhang, Tianzhu , Rahmati, Farnood et al. Novel "sandwich" configuration with ALD-coating layers on electrode/electrolyte interfaces for durable all-solid-state lithium metal batteries with high voltage cathodes- . | ENERGY MATERIALS , 2025 , 5 (7) . |
| Export to | NoteExpress RIS BibTex |
Version ：
Abstract ：
Lithium fluoride (LiF)-rich solid electrolyte interface (SEI) is critical for enabling the stable operation of polymer-based all-solid-state lithium-metal batteries (ASSLMBs). Precisely controlling the C & horbar;F dissociation chemistry in fluorine-containing lithium salts to construct a LiF-rich SEI is a logically viable but still challenging approach. Current strategies for constructing LiF-rich SEI primarily focus on designing non-metal polar groups and related structures. In contrast, approaches leveraging metal-based electron donors to facilitate charge transfer for C & horbar;F bond cleavage and LiF formation remain largely unexplored. Herein, a dual-enhanced charge transfer mechanism through prelithiation strategy is proposed in solid polymer electrolyte (SPE) for C & horbar;F bond cleavage. The charge transfer occurs between LiTFSI and the introduced metal sites and further enhanced by lithiation design, thereby achieving a robust LiF-rich SEI. The achieving SPEs enable an excellent cyclability of Li|Li cell over 3800 h at 0.3 mA cm-2. Li||LiFePO4 ASSLMBs demonstrate a high Coulombic efficiency of approximate to 100% and a stability of 1200 cycles with capacity retention of 80% at 2C. The corresponding pouch cell delivers a high average areal capacity of 2.41 mAh cm-2 over 1600 h. This work offers a novel approach for constructing LiF-rich SEI toward durable ASSLMBs.
Keyword ：
dual-enhanced charge transfer mechanism dual-enhanced charge transfer mechanism LiF-rich SEI LiF-rich SEI prelithiation strategy prelithiation strategy solid polymer electrolyte solid polymer electrolyte stable all-solid-state lithium metal batteries stable all-solid-state lithium metal batteries
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Zheng, Yun , Yang, Na , Duan, Song et al. Dual-Enhanced Charge Transfer through Prelithiation Strategy in Polymer Electrolyte Enables Robust LiF-Rich SEI for Ultralong-Life All-Solid-State Batteries [J]. | ADVANCED FUNCTIONAL MATERIALS , 2025 . |
| MLA | Zheng, Yun et al. "Dual-Enhanced Charge Transfer through Prelithiation Strategy in Polymer Electrolyte Enables Robust LiF-Rich SEI for Ultralong-Life All-Solid-State Batteries" . | ADVANCED FUNCTIONAL MATERIALS (2025) . |
| APA | Zheng, Yun , Yang, Na , Duan, Song , Li, Zhenghao , Gao, Rui , Zhu, Yanfei et al. Dual-Enhanced Charge Transfer through Prelithiation Strategy in Polymer Electrolyte Enables Robust LiF-Rich SEI for Ultralong-Life All-Solid-State Batteries . | ADVANCED FUNCTIONAL MATERIALS , 2025 . |
| Export to | NoteExpress RIS BibTex |
Version ：
Abstract ：
Traditional trial-and-error methods are inefficient and costly in discovering novel solvents for next-generation magnesium (Mg) metal-based batteries. Therefore, this work establishes a simple yet efficient screening criterion for solvents by integrating artificial intelligence techniques with a virtual molecular database, potentially revolutionizing the traditional solvent design pathway. A total of 823 solvents are generated using a self-developed algorithm, and LUMO, Delta LUMO, ESPmin, ESPmax , and Eb are identified to establish the screening criterion through the analysis with machine learning (ML) models. Eighteen candidate solvents are successfully identified, and two of which are subsequently selected and experimentally validated, i.e., C1COCOC1 and COCC(C)OC (abbreviated as "DOX" and "DMP"). Notably, neither of these solvents has been previously reported for use in Mg batteries. Experimental results indicate that the DOX solvent, when paired with the Mg boron-based salt, i.e., Mg[B(hfip)4]2, can significantly enhance the electrochemical performance. At a current density of 1.0 mAcm-2, the average coulombic efficiency for Mg plating/stripping reaches 99.54 % after 5200 cycles. Furthermore, the Mg//Cu cell achieves a cumulative capacity exceeding 2000 mAhcm-2, surpassing previously reported results. In summary, this work establishes a virtual molecular database and develops a streamlined screening methodology for Mg battery solvents based on their physicochemical properties, reducing the candidate pool from 823 to 18 and improving efficiency by nearly 50-fold. This research paradigm is not limited to the development of Mg batteries and can be readily extended to the exploration of other battery systems.
Keyword ：
dox dox generative artificial intelligence generative artificial intelligence mg metal batteries mg metal batteries solvent screening solvent screening virtual molecular database virtual molecular database
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Gao, Xiang , Yang, Ao-Qi , Yu, Wen-Bei et al. Generative Artificial Intelligence Navigated Development of Solvents for Next Generation High-Performance Magnesium Batteries [J]. | ADVANCED MATERIALS , 2025 . |
| MLA | Gao, Xiang et al. "Generative Artificial Intelligence Navigated Development of Solvents for Next Generation High-Performance Magnesium Batteries" . | ADVANCED MATERIALS (2025) . |
| APA | Gao, Xiang , Yang, Ao-Qi , Yu, Wen-Bei , Zhou, Jia-Cong , Pei, Mao-Jun , Chen, Jia-Cheng et al. Generative Artificial Intelligence Navigated Development of Solvents for Next Generation High-Performance Magnesium Batteries . | ADVANCED MATERIALS , 2025 . |
| Export to | NoteExpress RIS BibTex |
Version ：
Abstract ：
The electrochemical conversion of small organic molecules to value-added chemicals and hydrogen/electricity without CO2 emissions integrates efficient energy conversions (hydrogen energy or electricity) and value-added chemical productions in one reaction system, which is essentially competitive in the carbon-neutral era. However, the activity, stability, and cost-effectiveness of electrocatalysts, as well as the safety, durability, and scalability of devices, are still challenging for their industrial applications. In addition, a lack of knowledge about relevant and detailed mechanisms restricts the further development of electrocatalysts and devices. A timely review of the electrocatalysts, devices, and mechanisms is essential to shed lights on the correct direction towards further development. In this review, the advances in the design of electrocatalysts, fabrication of devices, and understanding of reaction mechanisms are comprehensively summarized and analyzed. The major challenges are also discussed as well as the potential approaches to overcoming them. The insights for further development are provided to offer a sustainable and environmentally friendly approach to cogeneration of energy and chemicals production.
Keyword ：
Electrocatalytic conversion Electrocatalytic conversion Hydrogen production Hydrogen production Organic molecules Organic molecules Value-added chemicals Value-added chemicals
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Liu, Jianwen , Fu, Guodong , Liao, Yuanfeng et al. Electrochemical conversion of small organic molecules to value-added chemicals and hydrogen/electricity without CO2 emission: Electrocatalysts, devices and mechanisms [J]. | ESCIENCE , 2025 , 5 (1) . |
| MLA | Liu, Jianwen et al. "Electrochemical conversion of small organic molecules to value-added chemicals and hydrogen/electricity without CO2 emission: Electrocatalysts, devices and mechanisms" . | ESCIENCE 5 . 1 (2025) . |
| APA | Liu, Jianwen , Fu, Guodong , Liao, Yuanfeng , Zhang, Wangji , Xi, Xiuan , Si, Fengzhan et al. Electrochemical conversion of small organic molecules to value-added chemicals and hydrogen/electricity without CO2 emission: Electrocatalysts, devices and mechanisms . | ESCIENCE , 2025 , 5 (1) . |
| Export to | NoteExpress RIS BibTex |
Version ：
Export
| Results： |
Selected to |
| Format： |
