能源化学最新文献

{"title":"In-situ interfacial passivation and self-adaptability synergistically stabilizing all-solid-state lithium metal batteries","authors":"Huanhui Chen ,&nbsp;Xing Cao ,&nbsp;Moujie Huang ,&nbsp;Xiangzhong Ren ,&nbsp;Yubin Zhao ,&nbsp;Liang Yu ,&nbsp;Ya Liu ,&nbsp;Liubiao Zhong ,&nbsp;Yejun Qiu","doi":"10.1016/j.jechem.2023.09.020","DOIUrl":"10.1016/j.jechem.2023.09.020","url":null,"abstract":"<div><p>The function of solid electrolytes and the composition of solid electrolyte interphase (SEI) are highly significant for inhibiting the growth of Li dendrites. Herein, we report an in-situ interfacial passivation combined with self-adaptability strategy to reinforce Li_0.33La_0.557TiO₃ (LLTO)-based solid-state batteries. Specifically, a functional SEI enriched with LiF/Li₃PO₄ is formed by in-situ electrochemical conversion, which is greatly beneficial to improving interface compatibility and enhancing ion transport. While the polarized dielectric BaTiO₃-polyamic acid (BTO-PAA, BP) film greatly improves the Li-ion transport kinetics and homogenizes the Li deposition. As expected, the resulting electrolyte offers considerable ionic conductivity at room temperature (4.3 × 10⁻⁴ S cm⁻¹) and appreciable electrochemical decomposition voltage (5.23 V) after electrochemical passivation. For Li-LiFePO₄ batteries, it shows a high specific capacity of 153 mA h g⁻¹ at 0.2 C after 100 cycles and a long-term durability of 115 mA h g⁻¹ at 1.0 C after 800 cycles. Additionally, a stable Li plating/stripping can be achieved for more than 900 h at 0.5 mA cm⁻². The stabilization mechanisms are elucidated by ex-situ XRD, ex-situ XPS, and ex-situ FTIR techniques, and the corresponding results reveal that the interfacial passivation combined with polarization effect is an effective strategy for improving the electrochemical performance. The present study provides a deeper insight into the dynamic adjustment of electrode-electrolyte interfacial for solid-state lithium batteries.</p></div>","PeriodicalId":67498,"journal":{"name":"能源化学","volume":"88 ","pages":"Pages 282-292"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135889879","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"High-silica faujasite zeolite-tailored metal encapsulation for the low-temperature production of pentanoic biofuels","authors":"Wenhao Cui ,&nbsp;Yuanshuai Liu ,&nbsp;Pengfei Guo ,&nbsp;Zhijie Wu ,&nbsp;Liqun Kang ,&nbsp;Huawei Geng ,&nbsp;Shengqi Chu ,&nbsp;Linying Wang ,&nbsp;Dong Fan ,&nbsp;Zhenghao Jia ,&nbsp;Haifeng Qi ,&nbsp;Wenhao Luo ,&nbsp;Peng Tian ,&nbsp;Zhongmin Liu","doi":"10.1016/j.jechem.2023.10.009","DOIUrl":"https://doi.org/10.1016/j.jechem.2023.10.009","url":null,"abstract":"<div><p>Zeolite-encapsulated metal nanoclusters are at the heart of bifunctional catalysts, which hold great potential for petrochemical conversion and the emerging sustainable biorefineries. Nevertheless, efficient encapsulation of metal nanoclusters into a high-silica zeolite Y in particular with good structural integrity still remains a significant challenge. Herein, we have constructed Ru nanoclusters (∼1 nm) encapsulated inside a high-silica zeolite Y (SY) with a SiO₂/Al₂O₃ ratio (SAR) of 10 via a cooperative strategy for direct zeolite synthesis and a consecutive impregnation for metal encapsulation. Compared with the benchmark Ru/H-USY and other analogues, the as-prepared Ru/H-SY markedly boosts the yields of pentanoic biofuels and stability in the direct hydrodeoxygenation of biomass-derived levulinate even at a mild temperature of 180 °C, which are attributed to the notable stabilization of transition states by the enhanced acid accessibility and properly sized constraints of zeolite cavities owing to the good structural integrity.</p></div>","PeriodicalId":67498,"journal":{"name":"能源化学","volume":"88 ","pages":"Pages 552-560"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137116357","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Understanding the oxidation chemistry of Ti3C2Tx (MXene) sheets and their catalytic performances","authors":"Suvdanchimeg Sunderiya ,&nbsp;Selengesuren Suragtkhuu ,&nbsp;Solongo Purevdorj ,&nbsp;Tumentsereg Ochirkhuyag ,&nbsp;Munkhjargal Bat-Erdene ,&nbsp;Purevlkham Myagmarsereejid ,&nbsp;Ashley D. Slattery ,&nbsp;Abdulaziz S.R. Bati ,&nbsp;Joseph G. Shapter ,&nbsp;Dorj Odkhuu ,&nbsp;Sarangerel Davaasambuu ,&nbsp;Munkhbayar Batmunkh","doi":"10.1016/j.jechem.2023.09.037","DOIUrl":"https://doi.org/10.1016/j.jechem.2023.09.037","url":null,"abstract":"<div><p>Transition metal carbides and nitrides (MXenes) nanosheets are attractive two-dimensional (2D) materials, but they suffer from oxidation/degradation issues during storage and/or applications due to their sensitivity to water and oxygen. Despite the great research progress, the exact oxidation kinetics of Ti₃C₂T<em>_x</em> (MXene) and their final products after oxidation are not fully understood. Herein, we systematically tracked the oxidation process of few-layer Ti₃C₂T<em>_x</em> nanosheets in an aqueous solution at room temperature over several weeks. We also studied the oxidation effects on the electrocatalytic properties of Ti₃C₂T<em>_x</em> for hydrogen evolution reaction and found that the overpotential to achieve a current density of 10 mA cm⁻² increases from 0.435 to 0.877 V after three weeks of degradation, followed by improvement to stabilized values of around 0.40 V after eight weeks. These results suggest that severely oxidized MXene could be a promising candidate for designing efficient catalysts. According to our detailed experimental characterization and theoretical calculations, unlike previous studies, black titanium oxide is formed as the final product in addition to white Ti (IV) oxide and disordered carbons after the complete oxidation of Ti₃C₂T<em>_x</em>. This work presents significant advancements in better understanding of 2D Ti₃C₂T<em>_x</em> (MXene) oxidation and enhances the prospects of this material for various applications.</p></div>","PeriodicalId":67498,"journal":{"name":"能源化学","volume":"88 ","pages":"Pages 437-445"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2095495623005533/pdfft?md5=7c1985dbb614f42bf6e8ab6dc22baf44&pid=1-s2.0-S2095495623005533-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137116359","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Porous metal oxides in the role of electrochemical CO2 reduction reaction","authors":"Ziqi Zhang ,&nbsp;Jinyun Xu ,&nbsp;Yu Zhang ,&nbsp;Liping Zhao ,&nbsp;Ming Li ,&nbsp;Guoqiang Zhong ,&nbsp;Di Zhao ,&nbsp;Minjing Li ,&nbsp;Xudong Hu ,&nbsp;Wenju Zhu ,&nbsp;Chunming Zheng ,&nbsp;Xiaohong Sun","doi":"10.1016/j.jechem.2023.09.018","DOIUrl":"https://doi.org/10.1016/j.jechem.2023.09.018","url":null,"abstract":"<div><p>The global energy-related CO₂ emissions have rapidly increased as the world economy heavily relied on fossil fuels. This paper explores the pressing challenge of CO₂ emissions and highlights the role of porous metal oxide materials in the electrocatalytic reduction of CO₂ (CO₂RR). The focus is on the development of robust and selective catalysts, particularly metal and metal-oxide-based materials. Porous metal oxides offer high surface area, enhancing the accessibility to active sites and improving reaction kinetics. The tunability of these materials allows for tailored catalytic behavior, targeting optimized reaction mechanisms for CO₂RR. The work also discusses the various synthesis strategies and identifies key structural and compositional features, addressing challenges like high overpotential, poor selectivity, and low stability. Based on these insights, we suggest avenues for future research on porous metal oxide materials for electrochemical CO₂ reduction.</p></div>","PeriodicalId":67498,"journal":{"name":"能源化学","volume":"88 ","pages":"Pages 373-398"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137116361","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Atomic-level coupled RuO2/BaRuO3 heterostructure for efficient alkaline hydrogen evolution reaction","authors":"Yueying Yan ,&nbsp;Tian Meng ,&nbsp;Yuting Chen ,&nbsp;Yang Yang ,&nbsp;Dewen Wang ,&nbsp;Zhicai Xing ,&nbsp;Xiurong Yang","doi":"10.1016/j.jechem.2023.09.028","DOIUrl":"https://doi.org/10.1016/j.jechem.2023.09.028","url":null,"abstract":"<div><p>The slow water dissociation is the rate-determining step that slows down the reaction rate in alkaline hydrogen evolution reaction (HER). Optimizing the surface electronic structure of the catalyst to lower the energy barrier of water dissociation and regulating the binding strength of adsorption intermediates are crucial strategy for boosting the catalytic performance of HER. In this study, RuO₂/BaRuO₃ (RBRO) heterostructures with abundant oxygen vacancies and lattice distortion were in-situ constructed under a low temperature via the thermal decomposition of gel-precursor. The RBRO heterostructures obtained at 550 °C exhibited the highest HER activity in 1 M KOH, showing an ultra-low overpotential of 16 mV at 10 mA cm⁻² and a Tafel slope of 33.37 mV dec⁻¹. Additionally, the material demonstrated remarkable durability, with only 25 mV of degradation in overpotential after 200 h of stability testing at 10 mA cm⁻². Density functional theory calculations revealed that the redistribution of charges at the heterojunction interface can optimize the binding energies of H* and OH* and effectively lower the energy barrier of water dissociation. This research offers novel perspectives on surpassing the water dissociation threshold of alkaline HER catalysts by means of a systematic design of heterogeneous interfaces.</p></div>","PeriodicalId":67498,"journal":{"name":"能源化学","volume":"88 ","pages":"Pages 356-362"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137116337","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Self-assembly of perovskite nanocrystals: From driving forces to applications","authors":"Yi Li,&nbsp;Fei Zhang","doi":"10.1016/j.jechem.2023.09.048","DOIUrl":"https://doi.org/10.1016/j.jechem.2023.09.048","url":null,"abstract":"<div><p>Self-assembly of metal halide perovskite nanocrystals (NCs) into superlattices can exhibit unique collective properties, which have significant application values in the display, detector, and solar cell field. This review discusses the driving forces behind the self-assembly process of perovskite NCs, and the commonly used self-assembly methods and different self-assembly structures are detailed. Subsequently, we summarize the collective optoelectronic properties and application areas of perovskite superlattice structures. Finally, we conclude with an outlook on the potential issues and future challenges in developing perovskite NCs.</p></div>","PeriodicalId":67498,"journal":{"name":"能源化学","volume":"88 ","pages":"Pages 561-578"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"92230959","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The initial stages of Li2O2 formation during oxygen reduction reaction in Li-O2 batteries: The significance of Li2O2 in charge-transfer reactions within devices","authors":"Daniela M. Josepetti ,&nbsp;Bianca P. Sousa ,&nbsp;Simone A.J. Rodrigues ,&nbsp;Renato G. Freitas ,&nbsp;Gustavo Doubek","doi":"10.1016/j.jechem.2023.09.034","DOIUrl":"https://doi.org/10.1016/j.jechem.2023.09.034","url":null,"abstract":"<div><p>Lithium-oxygen batteries are a promising technology because they can greatly surpass the energy density of lithium-ion batteries. However, this theoretical characteristic has not yet been converted into a real device with high cyclability. Problems with air contamination, metallic lithium reactivity, and complex discharge and charge reactions are the main issues for this technology. A fast and reversible oxygen reduction reaction (ORR) is crucial for good performance of secondary batteries’, but the partial knowledge of its mechanisms, especially when devices are concerned, hinders further development. From this perspective, the present work uses operando Raman experiments and electrochemical impedance spectroscopy (EIS) to assess the first stages of the discharge processes in porous carbon electrodes, following their changes cycle by cycle at initial operation. A growth kinetic formation of the discharge product signal (Li₂O₂) was observed with operando Raman, indicating a first-order reaction and enabling an analysis by a microkinetic model. The solution mechanism in the evaluated system was ascribed for an equivalent circuit with three time constants. While the time constant for the anode interface reveals to remain relatively constant after the first discharge, its surface seemed to be more non-uniform. The model indicated that the reaction occurs at the Li₂O₂ surface, decreasing the associated resistance during the initial discharge phase. Furthermore, the growth of Li₂O₂ forms a hetero-phase between Li₂O₂/electrolyte, while creating a more compact and homogeneous on the Li₂O₂/cathode surface. The methodology here described thus offers a way of directly probing changes in surface chemistry evolution during cycling from a device through EIS analysis.</p></div>","PeriodicalId":67498,"journal":{"name":"能源化学","volume":"88 ","pages":"Pages 223-231"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137116008","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"A cascade of in situ conversion of bicarbonate to CO2 and CO2 electroreduction in a flow cell with a Ni-N-S catalyst","authors":"Linghui Kong ,&nbsp;Min Wang ,&nbsp;Yongxiao Tuo ,&nbsp;Shanshan Zhou ,&nbsp;Jinxiu Wang ,&nbsp;Guangbo Liu ,&nbsp;Xuejing Cui ,&nbsp;Jiali Wang ,&nbsp;Luhua Jiang","doi":"10.1016/j.jechem.2023.09.024","DOIUrl":"https://doi.org/10.1016/j.jechem.2023.09.024","url":null,"abstract":"<div><p>Combination of CO₂ capture using inorganic alkali with subsequently electrochemical conversion of the resultant <span><math><msubsup><mtext>HCO</mtext><mrow><mtext>3</mtext></mrow><mtext>-</mtext></msubsup></math></span> to high-value chemicals is a promising route of low cost and high efficiency. The electrochemical reduction of <span><math><msubsup><mtext>HCO</mtext><mrow><mtext>3</mtext></mrow><mtext>-</mtext></msubsup></math></span> is challenging due to the inaccessible of negatively charged molecular groups to the electrode surface. Herein, we adopt a comprehensive strategy to tackle this challenge, i.e., cascade of in situ chemical conversion of <span><math><msubsup><mtext>HCO</mtext><mrow><mtext>3</mtext></mrow><mtext>-</mtext></msubsup></math></span> to CO₂ and CO₂ electrochemical reduction in a flow cell. With a tailored Ni-N-S single atom catalyst (SACs), where sulfur (S) atoms located in the second shell of Ni center, the CO₂ electroreduction (CO₂ER) to CO is boosted. The experimental results and density functional theory (DFT) calculations reveal that the introduction of S increases the <em>p</em> electron density of N atoms near Ni atom, thereby stabilizing *H over N and boosting the first proton coupled electron transfer process of CO₂ER, i.e., *+e^–+*H+*CO₂→*COOH. As a result, the obtained catalyst exhibits a high faradaic efficiency (FE_CO ∼ 98%) and a low overpotential of 425 mV for CO production as well as a superior turnover frequency (TOF) of 47397 h⁻¹, outcompeting most of the reported Ni SACs. More importantly, an extremely high FE_CO of 90% is achieved at 50 mA cm⁻² in the designed membrane electrode assembly (MEA) cascade electrolyzer fed with liquid bicarbonate. This work not only highlights the significant role of the second coordination on the first coordination shell of the central metal for CO₂ER, but also provides an alternative and feasible strategy to realize the electrochemical conversion of <span><math><msubsup><mtext>HCO</mtext><mrow><mtext>3</mtext></mrow><mtext>-</mtext></msubsup></math></span> to high-value chemicals.</p></div>","PeriodicalId":67498,"journal":{"name":"能源化学","volume":"88 ","pages":"Pages 183-193"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67740104","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Recent progress on copper catalysts with different surface states for CO2 electroreduction","authors":"Wenjun Zhang ,&nbsp;Yang Yang ,&nbsp;Donggang Guo ,&nbsp;Lu Liu","doi":"10.1016/j.jechem.2023.09.002","DOIUrl":"https://doi.org/10.1016/j.jechem.2023.09.002","url":null,"abstract":"<div><p>The electrochemical carbon dioxide reduction reaction (eCO₂RR), which converts CO₂ into various hydrocarbons or alcohols, has been extensively researched because it promises a sustainable energy economy. However, only copper (Cu) can currently achieve stable and efficient hydrocarbon conversion in the eCO₂RR. Therefore, understanding the catalytic mechanisms and summarizing the research progress on synthesis strategies of Cu catalysts are essential for the eCO₂RR. This paper reviews Cu catalysts with different surface states of Cu catalysts: oxide-derived Cu, Cu nanoparticles, Cu single atoms, and Cu nanoclusters. It then reviews the development and progress of different Cu-catalyst preparation methods in recent years, focusing on the activity and selectivity of materials. Besides revealing the tendencies of catalytic selection and deep reactive mechanisms of Cu catalysts with four different surface states, this review can guide the subsequent construction of catalysts and provides an understanding of catalytic mechanisms.</p></div>","PeriodicalId":67498,"journal":{"name":"能源化学","volume":"88 ","pages":"Pages 10-27"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67740082","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Advanced preparation and application of bimetallic materials in lithium-sulfur batteries: A review","authors":"Yongbing Jin,&nbsp;Nanping Deng,&nbsp;Yanan Li,&nbsp;Hao Wang,&nbsp;Meiling Zhang,&nbsp;Weimin Kang,&nbsp;Bowen Cheng","doi":"10.1016/j.jechem.2023.09.031","DOIUrl":"https://doi.org/10.1016/j.jechem.2023.09.031","url":null,"abstract":"<div><p>Lithium-sulfur (Li-S) batteries are considered highly promising as next-generation energy storage systems due to high theoretical capacity (2600 W h kg⁻¹) and energy density (1675 mA h g⁻¹) as well as the abundant natural reserves, low cost of elemental sulfur, and environmentally friendly properties. However, several challenges impede its commercialization including low conductivity of sulfur itself, the severe “shuttle effect” caused by lithium polysulfides (LiPSs) during charge–discharge processes, volume expansion effects and sluggish reaction kinetics. As a solution, polar metal particles and their compounds have been introduced as the main hosts for sulfur cathode due to their robust catalytic activity and adsorption capability, effectively suppressing the “shuttle effect” of LiPSs. Bimetallic alloys and their compounds with multi-functional properties exhibit remarkable electrochemical performance more readily when compared to single-metal materials. Well-designed bimetallic materials demonstrate larger specific surface areas and richer active sites, enabling simultaneous high adsorption capability and strong catalytic properties. The synergistic effect of the “adsorption-catalysis” sites accelerates the adsorption-diffusion-conversion process of LiPSs, ultimately achieving a long-lasting Li-S battery. Herein, the latest progress and performance of bimetallic materials in cathodes, separators, and interlayers of Li-S batteries are systematically reviewed. Firstly, the principles and challenges of Li-S batteries are briefly analyzed. Then, various mechanisms for suppressing “shuttle effects” of LiPSs are emphasized at the microscale. Subsequently, the performance parameters of various bimetallic materials are comprehensively summarized, and some improvement strategies are proposed based on these findings. Finally, the future prospects of bimetallic materials are discussed, with the hope of providing profound insights for the rational design and manufacturing of high-performance bimetallic materials for LSBs.</p></div>","PeriodicalId":67498,"journal":{"name":"能源化学","volume":"88 ","pages":"Pages 469-512"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"92282716","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}