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Probing a solid electrolyte interphase layer with sub-nanometer pores using redox mediators 利用氧化还原介质探测具有亚纳米孔的固体电解质间相层
IF 42.9
eScience Pub Date : 2025-05-01 Epub Date: 2024-12-03 DOI: 10.1016/j.esci.2024.100351
Ximei Lv , Jie Liu , Chenkun Li , Fengjiao Yu , Dengji Xiao , Shulin Zhao , Yuping Wu , Yuhui Chen
{"title":"Probing a solid electrolyte interphase layer with sub-nanometer pores using redox mediators","authors":"Ximei Lv ,&nbsp;Jie Liu ,&nbsp;Chenkun Li ,&nbsp;Fengjiao Yu ,&nbsp;Dengji Xiao ,&nbsp;Shulin Zhao ,&nbsp;Yuping Wu ,&nbsp;Yuhui Chen","doi":"10.1016/j.esci.2024.100351","DOIUrl":"10.1016/j.esci.2024.100351","url":null,"abstract":"<div><div>The solid electrolyte interphase (SEI) layer is crucial for lithium-ion batteries and has a significant impact on the electrochemical performance of negative electrodes, particularly for conversion-type materials with large volume changes and metallic lithium anode. However, the SEI layer has not yet been well understood. In this work, we used redox mediators of various sizes to probe the SEI layer that formed in carbonate-based electrolytes. The SEI layer has diffusion channels that allow the mediators smaller than benzoquinone (5.7 ​Å) to pass, suggesting that lithium ions have to partially de-solvate to pass through. Additionally, due to partial desolvation, the diffusion coefficient in the diffusion channels was higher than that in the bulk electrolytes. Both lithium salts and solvents influenced the size and areal density of channels. Herein, we aim to enhance comprehension of SEI structure and provide a method to study porous SEI layers using mediators, which can be extended to other electrochemical systems.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 3","pages":"Article 100351"},"PeriodicalIF":42.9,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143931611","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Organic–inorganic S-scheme heterojunction photocatalysts: Design, synthesis, applications, and challenges 有机-无机s型异质结光催化剂:设计、合成、应用和挑战
IF 42.9
eScience Pub Date : 2025-05-01 Epub Date: 2024-12-14 DOI: 10.1016/j.esci.2024.100354
Jingzhao Cheng , Bei Cheng , Jingsan Xu , Jiaguo Yu , Shaowen Cao
{"title":"Organic–inorganic S-scheme heterojunction photocatalysts: Design, synthesis, applications, and challenges","authors":"Jingzhao Cheng ,&nbsp;Bei Cheng ,&nbsp;Jingsan Xu ,&nbsp;Jiaguo Yu ,&nbsp;Shaowen Cao","doi":"10.1016/j.esci.2024.100354","DOIUrl":"10.1016/j.esci.2024.100354","url":null,"abstract":"<div><div>Since the concept was introduced in 2019, step-scheme (S-scheme) heterojunctions have emerged as an important subclass of heterojunction technology and attracted much attention for solar energy conversion. S-scheme heterojunctions are capable of maximizing redox ability through conferring enhanced photocatalytic performance by addressing the problem of rapid electron–hole recombination. In particular, the organic–inorganic S-scheme heterojunction (OI-SHJ) can integrate atomic long-range ordered inorganic semiconductors with tailored organic materials using diverse organic molecular building blocks and integration methods, offering brilliant prospects for innovation. Here, we review the state-of-the-art progress in OI-SHJ photocatalysts by introducing their charge transfer mechanism, design criteria, preparation approaches, and applications. We also highlight the synergistic role of organic and inorganic materials in S-scheme heterojunctions and what is understood so far about their structure–activity relationship. We conclude by summarizing the existing challenges and emphasizing the current outlook for the future development of OI-SHJ photocatalysts.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 3","pages":"Article 100354"},"PeriodicalIF":42.9,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143931607","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Bio-inspired and programmable Marangoni motor for highly maneuverable and adaptable S-aquabots 生物启发和可编程的Marangoni电机,用于高度机动和适应性强的S-aquabots
IF 42.9
eScience Pub Date : 2025-05-01 Epub Date: 2024-11-15 DOI: 10.1016/j.esci.2024.100335
Yexi Zhou , Xiao Guan , Dazhe Zhao , Kaijun Zhang , YongAn Huang , Junwen Zhong
{"title":"Bio-inspired and programmable Marangoni motor for highly maneuverable and adaptable S-aquabots","authors":"Yexi Zhou ,&nbsp;Xiao Guan ,&nbsp;Dazhe Zhao ,&nbsp;Kaijun Zhang ,&nbsp;YongAn Huang ,&nbsp;Junwen Zhong","doi":"10.1016/j.esci.2024.100335","DOIUrl":"10.1016/j.esci.2024.100335","url":null,"abstract":"<div><div>Mobility, environmental adaptability, and functionality are essential attributes of robots, but these become challenging for small-scale on-water robots, also referred to as S-aquabots. Herein, we propose a programmable Marangoni motor (PM-motor) to propel centimeter-scale S-aquabots with high maneuverability and adaptability. Lightweight, compact, flexible hybrid electronics are used to precisely release ethanol to achieve controllable propulsion, smart sensing, and wireless communication functions. The PM-motor utilizes the surface tension gradient generated by the ethanol, which is released from leaf-inspired veins and improves fuel efficiency by 3.5 times when compared with traditional Marangoni effect-propelled robots. As a result, the device’s endurance is up to ∼226 ​s for a navigation distance of ∼5 ​m with just 1.2 ​mL ethanol. Benefiting from the leaf-like shape and negligible noise production, the S-aquabots can also blend well with their surroundings. Autonomous response capability is demonstrated by guiding an S-aquabot with laser spots to complete a butterfly-shaped trajectory. Equipped with a mini-camera or digital sensors, untethered S-aquabots deployed on an outdoor pool can capture real-time videos or monitor long-term environmental conditions. This work is beneficial for inspiring insightful design strategies to develop S-aquabots with high practical potential.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 3","pages":"Article 100335"},"PeriodicalIF":42.9,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143931615","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synergetic energy coupled thermal catalytic systems for CO2 reduction 二氧化碳还原的协同能量耦合热催化系统
IF 42.9
eScience Pub Date : 2025-05-01 Epub Date: 2024-08-20 DOI: 10.1016/j.esci.2024.100306
Juxia Xiong , Jiapeng Ji , Qiong Lei , Xinchun Yang , Yang Bai , Xiaolong Zhang , Hui-Ming Cheng
{"title":"Synergetic energy coupled thermal catalytic systems for CO2 reduction","authors":"Juxia Xiong ,&nbsp;Jiapeng Ji ,&nbsp;Qiong Lei ,&nbsp;Xinchun Yang ,&nbsp;Yang Bai ,&nbsp;Xiaolong Zhang ,&nbsp;Hui-Ming Cheng","doi":"10.1016/j.esci.2024.100306","DOIUrl":"10.1016/j.esci.2024.100306","url":null,"abstract":"<div><div>Converting CO<sub>2</sub> into fuel or chemicals using renewable energy is a promising strategy for closing the anthropogenic carbon cycle. However, due to the highly stable C=O bond, CO<sub>2</sub> activation requires a significant energy input to elevate the reactant to a higher energy state, plus an efficient catalyst to surmount the activation energy barrier. Despite significant advancements in catalytic methods using a single energy input for CO<sub>2</sub> reduction, the catalytic efficiency and economic viability have yet to be improved. However, integrating multiple energy sources in catalysis has shown significant potential for improving catalytic efficiency. These energy-coupled systems demonstrate a synergistic effect, stemming from the multiple excitation modes of the reactants, the reaction intermediates, or even the catalysts. To our knowledge, there has not been a systematic review addressing synergetic energy-coupled catalysis for CO<sub>2</sub> reduction. Herein, we aim to offer a comprehensive overview of recent advances in CO<sub>2</sub> reduction driven by synergetic energy-coupled catalysis. Furthermore, we explore the technological challenges and prospects associated with the synergistic effect in energy-coupled catalytic systems, presenting our insights on potential breakthrough directions.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 3","pages":"Article 100306"},"PeriodicalIF":42.9,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143931606","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Unraveling the dipole field in ultrathin, porous, and defective carbon nitride nanosheets for record-high piezo-photocatalytic H2O2 production 超薄、多孔和有缺陷的氮化碳纳米片中的偶极子场,用于创纪录的高压电光催化H2O2生产
IF 42.9
eScience Pub Date : 2025-05-01 Epub Date: 2024-12-27 DOI: 10.1016/j.esci.2024.100370
Zhaoqiang Wang , Guixiang Ding , Hongwei Huang , Juntao Zhang , Qi Lv , Li Shuai , Yonghao Ni , Guangfu Liao
{"title":"Unraveling the dipole field in ultrathin, porous, and defective carbon nitride nanosheets for record-high piezo-photocatalytic H2O2 production","authors":"Zhaoqiang Wang ,&nbsp;Guixiang Ding ,&nbsp;Hongwei Huang ,&nbsp;Juntao Zhang ,&nbsp;Qi Lv ,&nbsp;Li Shuai ,&nbsp;Yonghao Ni ,&nbsp;Guangfu Liao","doi":"10.1016/j.esci.2024.100370","DOIUrl":"10.1016/j.esci.2024.100370","url":null,"abstract":"<div><div>Piezo-photocatalysis is capable of concerting mechanical vibration into chemical energy, portraying a promising alternative technology for H<sub>2</sub>O<sub>2</sub> production. However, low mechanical energy conversion efficiency and constrained surface active sites hinder its practical application. Herein, ultrathin porous carbon nitride nanosheets with controlled carbon vacancies and oxygen doping (OCN-X, where X represents the calcination temperature) are synthesized by thermal oxidation etching to achieve unprecedented piezo-photocatalytic H<sub>2</sub>O<sub>2</sub> production. The carbon vacancies and oxygen doping cause the formation of asymmetric structure of triazine unit with a strong dipole field, which creates spontaneous polarization field to speed up directional electron transfer to the nitrogen active sites for effective piezo-photocatalysis. Meanwhile, the ultrathin and porous structure formed by hot-oxygen etching enhances the mechanical energy conversion efficiency and collaboratively induces adsorbed oxygen via indirect two-electron oxygen reduction reaction (ORR) transfer pathway to effectively produce H<sub>2</sub>O<sub>2</sub>. Consequently, without any co-catalysts, the as-prepared OCN-460 displays record-high piezo-photocatalytic H<sub>2</sub>O<sub>2</sub> production rate of 19.30 ​mmol ​g<sup>−1</sup> ​h<sup>−1</sup>, far outdistancing those previously reported for piezo-photocatalysts. Furthermore, it also still maintains a notable piezo-photocatalytic activity of 2.87 ​mmol ​g<sup>−1</sup> ​h<sup>−1</sup> in the pure water system. This work offers some new insights for the future design of an effective piezo-photocatalytic H<sub>2</sub>O<sub>2</sub> production system.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 3","pages":"Article 100370"},"PeriodicalIF":42.9,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143931614","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cutting-edge advances in pressurized electrocatalytic reactors 加压电催化反应器的最新进展
IF 42.9
eScience Pub Date : 2025-05-01 Epub Date: 2024-12-27 DOI: 10.1016/j.esci.2024.100369
Yang Li , Guining Shao , Xinyu Zheng , Yansong Jia , Yanghong Xia , Yuhai Dou , Ming Huang , Chaohua Gu , Jianfeng Shi , Jinyang Zheng , Shixue Dou
{"title":"Cutting-edge advances in pressurized electrocatalytic reactors","authors":"Yang Li ,&nbsp;Guining Shao ,&nbsp;Xinyu Zheng ,&nbsp;Yansong Jia ,&nbsp;Yanghong Xia ,&nbsp;Yuhai Dou ,&nbsp;Ming Huang ,&nbsp;Chaohua Gu ,&nbsp;Jianfeng Shi ,&nbsp;Jinyang Zheng ,&nbsp;Shixue Dou","doi":"10.1016/j.esci.2024.100369","DOIUrl":"10.1016/j.esci.2024.100369","url":null,"abstract":"<div><div>As an important component in electrochemical energy conversion and storage systems, electrochemical reactors (ECRs) are widely used for commodity chemical synthesis, including electrolytic H<sub>2</sub> production, NH<sub>3</sub> synthesis, and high-value CO<sub>2</sub> utilization. However, ECRs pose challenges related to low energy efficiency and selectivity due to the low solubility of their gaseous reactants, slow kinetics, and limitations in mass transfer. It is thus imperative to develop advanced high-pressure (HP) ECRs to address these issues. In this review, we start by presenting a comprehensive analysis of the fundamental mechanisms of HP ECRs. Then, we summarize the state-of-the-art HP ECR applications for water electrolysis, the N<sub>2</sub> reduction reaction, and the CO<sub>2</sub> reduction reaction. We also demonstrate that mathematical simulations are valuable tools for digital validation and guidance to accelerate the design of better reactors. Finally, we make recommendations on developing relevant specifications and standards for the industrial application of HP ECRs.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 3","pages":"Article 100369"},"PeriodicalIF":42.9,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143931608","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Facet-orientation-enhanced thermal transfer for temperature-insensitive and stable p-i-n perovskite solar cells 温度不敏感和稳定的p-i-n钙钛矿太阳能电池的面取向增强热传递
IF 42.9
eScience Pub Date : 2025-05-01 Epub Date: 2025-01-11 DOI: 10.1016/j.esci.2025.100372
Jiabao Li , Jialong Duan , Chenlong Zhang , Ziting Qi , Ya Liu , Xingxing Duan , Yueji Liu , Jie Dou , Qiyao Guo , Benlin He , Yuanyuan Zhao , Peizhi Yang , Qunwei Tang
{"title":"Facet-orientation-enhanced thermal transfer for temperature-insensitive and stable p-i-n perovskite solar cells","authors":"Jiabao Li ,&nbsp;Jialong Duan ,&nbsp;Chenlong Zhang ,&nbsp;Ziting Qi ,&nbsp;Ya Liu ,&nbsp;Xingxing Duan ,&nbsp;Yueji Liu ,&nbsp;Jie Dou ,&nbsp;Qiyao Guo ,&nbsp;Benlin He ,&nbsp;Yuanyuan Zhao ,&nbsp;Peizhi Yang ,&nbsp;Qunwei Tang","doi":"10.1016/j.esci.2025.100372","DOIUrl":"10.1016/j.esci.2025.100372","url":null,"abstract":"<div><div>Persistent operation inevitably elevates the temperature of perovskite solar cells (PSCs), posing a challenge for maximizing their power output and stability even after effective defect passivation and encapsulation techniques have been implemented. Regulating the thermal conductivity of halide perovskites by additive engineering is now a mainstream strategy for achieving self-cooling devices, but our fundamental understanding of how perovskites with atomic disorder function remains insufficient. This theoretical study unveils the underlying mechanism of facet-dependent thermodynamic properties in mixed-cation perovskites. The results demonstrate that the (100) facet has higher thermal conductivity than the (110) and (111) facets. By carefully controlling the (100) crystallographic orientation through buried and bulk modification, the thermal conductivity of the target perovskite film can be increased from 1.005 to 1.068 ​W ​m<sup>−1</sup> ​K<sup>−1</sup>, which lowers the PSC's equilibrium temperature 5.25 ​°C by accelerating heat transport and dissipation. Consequently, we achieve an inverted PSC with an excellent efficiency of 25.12%, accompanied by a significantly reduced temperature coefficient and better long-term stability: a conservation rate exceeding 90% after aging at 85 ​°C and exposure to persistent light irradiation for 1100 ​h. This work elucidates a previously unidentified outcome of crystal facet engineering: the achievement of thermal management in high-performance PSCs.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 3","pages":"Article 100372"},"PeriodicalIF":42.9,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143931612","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Influence of active hydrogen on pathway selection in electrochemical nitrate reduction 活性氢对硝酸电化学还原途径选择的影响
IF 42.9
eScience Pub Date : 2025-05-01 Epub Date: 2024-11-30 DOI: 10.1016/j.esci.2024.100350
Junchao Yu , Zichao Xi , Jinhui Su , Peng Jing , Xuan Xu , Baocang Liu , Yu Wang , Jun Zhang
{"title":"Influence of active hydrogen on pathway selection in electrochemical nitrate reduction","authors":"Junchao Yu ,&nbsp;Zichao Xi ,&nbsp;Jinhui Su ,&nbsp;Peng Jing ,&nbsp;Xuan Xu ,&nbsp;Baocang Liu ,&nbsp;Yu Wang ,&nbsp;Jun Zhang","doi":"10.1016/j.esci.2024.100350","DOIUrl":"10.1016/j.esci.2024.100350","url":null,"abstract":"<div><div>Electrochemical nitrate reduction reaction in alkaline condition involves two reactants, the nitrate (<span><math><mrow><msup><msub><mtext>NO</mtext><mn>3</mn></msub><mo>−</mo></msup></mrow></math></span>) and the water (H<sub>2</sub>O). Although the significance of the active ∗H species produced from the dissociation of H<sub>2</sub>O has been proved, the correlation between the reaction pathways and the ∗H species is often overlooked. Herein, Co(OH)<sub>2</sub>–CoP supported Ru nanoclusters is designed for electrocatalytic nitrate reduction and shows a record-high faradaic efficiency of 99.7% at an ultralow potential of 0.1 ​V versus reversible hydrogen electrode. Experiments and theoretical calculations reveal that in addition to the faster proton transfer kinetics, the reaction pathway is strongly correlated with ∗H supply with the aid of CoP, that is, the direct hydrogenation of ∗NOH instead of deprotonation over Ru sites with the lowest energy barrier is promoted with the moderate production of ∗H species. This work provides new insights into the impact of ∗H species on the thermodynamics and kinetics of electrocatalytic nitrate reduction.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 3","pages":"Article 100350"},"PeriodicalIF":42.9,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143931610","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Revisiting the critical role of metallic ash elements in the development of hard carbon for advancing sodium-ion battery applications 回顾了金属灰分元素在硬碳发展中的关键作用,以推进钠离子电池的应用
IF 42.9
eScience Pub Date : 2025-05-01 Epub Date: 2025-01-13 DOI: 10.1016/j.esci.2025.100371
Chun Wu , Wenjie Huang , Yinghao Zhang , Qinghang Chen , Li Li , Yajun Zhang , Xingqiao Wu , Shu-Lei Chou
{"title":"Revisiting the critical role of metallic ash elements in the development of hard carbon for advancing sodium-ion battery applications","authors":"Chun Wu ,&nbsp;Wenjie Huang ,&nbsp;Yinghao Zhang ,&nbsp;Qinghang Chen ,&nbsp;Li Li ,&nbsp;Yajun Zhang ,&nbsp;Xingqiao Wu ,&nbsp;Shu-Lei Chou","doi":"10.1016/j.esci.2025.100371","DOIUrl":"10.1016/j.esci.2025.100371","url":null,"abstract":"<div><div>Hard carbon (HC) anodes in sodium-ion batteries (SIBs) are prized for their high capacity, durability, cost-efficiency, environmental sustainability, and safety. The metallic ash elements in HCs inevitably affect the overall performance of SIBs, however, the unclear role of metallic ash elements during carbonization and the electrochemical sodium storage process presents challenges for advancing HC design concepts. In this review, the traditional role of metallic ash element realized in the past and the deep understanding by a new sight from the view of intrinsic types in precursor matrix are initially introduced. Subsequently, the effect of catalyzing graphitization degree, constructing pore structure, tuning SEI formation and tailoring defects of the HCs regulated by extrinsic factors introduced through experimental conditions in recent years are comprehensively summarized. Additionally, future development prospects and perspectives on the research about metallic ash element in HC are also briefly outlined. It is believed that this review can deliver noteworthy viewpoints by introducing metallic ash elements, for the continued development of adjusting the microstructure of HCs at the nanoscale to actualize high-performance SIBs.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 3","pages":"Article 100371"},"PeriodicalIF":42.9,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143931432","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Orbital modulation in platinum-group-metal (PGM) electrocatalysts: An effective approach to boost catalytic performance 铂族金属(PGM)电催化剂中的轨道调制:提高催化性能的有效方法
IF 42.9
eScience Pub Date : 2025-03-01 Epub Date: 2024-04-15 DOI: 10.1016/j.esci.2024.100270
Xuan Liu , Gang Wu , Qing Li
{"title":"Orbital modulation in platinum-group-metal (PGM) electrocatalysts: An effective approach to boost catalytic performance","authors":"Xuan Liu ,&nbsp;Gang Wu ,&nbsp;Qing Li","doi":"10.1016/j.esci.2024.100270","DOIUrl":"10.1016/j.esci.2024.100270","url":null,"abstract":"<div><div>Platinum group metal (PGM) electrocatalysts play an irreplaceable role in many electrochemical reactions for sustainable energy conversion. In the past few decades, the electronic orbital modulation methods have emerged as an important way to produce high-performance electrocatalysts, often by adjusting surface reactivity and enhancing structural stability. In this review, we first systematically elaborate on the basic principles and strategies of orbital modulation for PGM-based catalysts, mainly from the perspective of improving activity and stability, in which we highlight some exploratory theoretical studies over the past few decades. Then we describe a series of representative works to elucidate the specific approaches used to realize precise orbital modulation in PGM catalysts. Finally, we clarify the existing challenges and propose some perspectives for the development of related theories and practical applications.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 2","pages":"Article 100270"},"PeriodicalIF":42.9,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140795924","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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