材料导报:能源(英文)Pub Date : 2025-05-01DOI: 10.1016/j.matre.2025.100325
Yanqi Tang , Jiehui Hao , Jiafu Qu , Yahui Cai , Xiaogang Yang , Chang Ming Li , Jundie Hu
{"title":"Robust synergistic effects of doping and defect engineering in photocatalytic H2O2 production","authors":"Yanqi Tang , Jiehui Hao , Jiafu Qu , Yahui Cai , Xiaogang Yang , Chang Ming Li , Jundie Hu","doi":"10.1016/j.matre.2025.100325","DOIUrl":"10.1016/j.matre.2025.100325","url":null,"abstract":"<div><div>Hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) photosynthesis represents an advanced on-site production method with significant potential for on-demand supply. However, various challenges hinder the efficiency of H<sub>2</sub>O<sub>2</sub> yield, including weak oxygen adsorption capacity, reliance on sacrificial agents, low charge separation and transfer efficiency. In this regard, doping design and defect engineering have emerged as robust and effective strategies for catalyst modification, particularly through their synergistic effects. Additionally, advanced in situ characterization techniques for investigating reaction mechanisms are gaining momentum. Herein, this review provides a comprehensive analysis of the fundamentals and challenges associated with photocatalytic H<sub>2</sub>O<sub>2</sub> production, and highlights the advantages of doping and defect engineering. Subsequently, it outlines preparation methods and applications of these strategies. More importantly, it emphasizes the advanced characterization techniques utilized to validate doping and defects, as well as to investigate underlying mechanisms. Finally, the potential prospects and challenges of this reaction are anticipated. This review aims to offer valuable insights for researchers from both experimental and theoretical perspectives.</div></div>","PeriodicalId":61638,"journal":{"name":"材料导报:能源(英文)","volume":"5 2","pages":"Article 100325"},"PeriodicalIF":0.0,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144185106","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}
材料导报:能源(英文)Pub Date : 2025-05-01DOI: 10.1016/j.matre.2025.100331
Long Cheng , Yuanyi Luo , Hao Wang , Zhiyue Zhou , Mengkai Yang , Chen Li , Yujie Zheng , Meng Li , Lei Wang , Kuan Sun
{"title":"Optimized synthesis and electrochemical behaviors of Prussian blue analogues cathodes for potassium-ion batteries","authors":"Long Cheng , Yuanyi Luo , Hao Wang , Zhiyue Zhou , Mengkai Yang , Chen Li , Yujie Zheng , Meng Li , Lei Wang , Kuan Sun","doi":"10.1016/j.matre.2025.100331","DOIUrl":"10.1016/j.matre.2025.100331","url":null,"abstract":"<div><div>The superior adaptability of Prussian blue analogues (PBAs) in interacting with potassium ions has shifted research focus toward their potential application as cathodes of potassium-ion batteries (PIBs). The large interstitial space formed between metal ions and –C≡N– in PBAs can accommodate large-radius K<sup>+</sup>. However, the rapid nucleation in the co-precipitation synthesis process of PBAs induces many lattice defects of [M(CN)<sub>6</sub>]<sup>4−</sup> vacancies (V<sub>[M–C</sub><sub>≡</sub><sub>N]</sub>), interstitial and coordinated H<sub>2</sub>O molecules, which will directly lead to performance degradation. Moreover, originating from various transition metal elements in low/high-spin electron configuration states, PBAs exhibit diverse electrochemical behaviors, such as low reaction kinetics of low-spin iron (II), Jahn-Teller distortion and dissolution of manganese (III), and electrochemical inertness of nickel (II) and copper (II). Here, we summarize recently reported structures and properties of PBAs, classifying them based on the types of transition metals (iron, cobalt, manganese, copper, nickel) employed. Advanced synthesis strategies, including control engineering of crystallinity based on H<sub>2</sub>O molecules and V<sub>[M–C</sub><sub>≡</sub><sub>N]</sub>, were discussed. Also, the approaches for enhancing the electrochemical performance of PBAs were highlighted. Finally, the challenges and prospects towards the future development of PBAs are put forward. The review is expected to provide technical and theoretical support for the design of high-performance PBAs.</div></div>","PeriodicalId":61638,"journal":{"name":"材料导报:能源(英文)","volume":"5 2","pages":"Article 100331"},"PeriodicalIF":0.0,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144185107","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}
材料导报:能源(英文)Pub Date : 2025-05-01DOI: 10.1016/j.matre.2025.100328
Georgios Charalampopoulos , Maria K. Daletou
{"title":"Comparative development and evaluation of Fe–N–C electrocatalysts for the oxygen reduction reaction: The effect of pyrolysis and iron-bipyridine structures","authors":"Georgios Charalampopoulos , Maria K. Daletou","doi":"10.1016/j.matre.2025.100328","DOIUrl":"10.1016/j.matre.2025.100328","url":null,"abstract":"<div><div>Proton exchange membrane fuel cells (PEMFCs) constitute a promising avenue for environmentally friendly power generation. However, the reliance on unsustainable platinum-based electrocatalysts used at the electrodes poses challenges to the commercial viability of PEMFCs. Non-platinum group metal (non-PGM) alternatives, like nitrogen-coordinated transition metals in atomic dispersion (M–N–C catalysts), show significant potential. This work presents a comparative study of two distinct sets of Fe–N–C materials, prepared by pyrolyzing hybrid composites of polyaniline (PANI) and iron (II) chloride on a hard template. One set uses bipyridine (BPy) as an additional nitrogen source and iron ligand, offering an innovative approach. The findings reveal that the choice of pyrolysis temperature and atmosphere influences the catalyst properties. The use of ammonia in pyrolysis emerges as a crucial parameter for promoting atomic dispersion of iron, as well as increasing surface area and porosity. The optimal catalyst, prepared using BPy and ammonia, exhibits a half-wave potential of 0.834 V in 0.5 M H<sub>2</sub>SO<sub>4</sub> (catalyst loading of 0.6 mg cm<sup>−</sup><sup>2</sup>), a mass activity exceeding 3 A g<sup>−</sup><sup>1</sup> and high stability in acidic electrolyte, positioning it as a promising non-PGM structure in the field.</div></div>","PeriodicalId":61638,"journal":{"name":"材料导报:能源(英文)","volume":"5 2","pages":"Article 100328"},"PeriodicalIF":0.0,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144185649","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}
材料导报:能源(英文)Pub Date : 2025-05-01DOI: 10.1016/j.matre.2025.100332
Yu Zou , Yang Lyu , Hanxin Wei , Baohui Chen , Xiansi Wang , Ming Zhang
{"title":"A green route based on π-π interactions to coat graphite for high-rate and long-life anodes in lithium-ion batteries","authors":"Yu Zou , Yang Lyu , Hanxin Wei , Baohui Chen , Xiansi Wang , Ming Zhang","doi":"10.1016/j.matre.2025.100332","DOIUrl":"10.1016/j.matre.2025.100332","url":null,"abstract":"<div><div>Although graphite (G) materials dominate the commercial lithium-ion battery (LIBs) anode market due to their excellent overall performance, their limited rate performance and cycle life hinder applications in high-performance fields. To improve the cycling and rate performance of graphite anodes, this study first employed economical and eco-friendly tannic acid (TA) as a carbon coating precursor to coat graphite surfaces via π-π stacking interactions. In an oxygen-rich alkaline environment, tannic acid undergoes oxidation polymerization and crosslinks with formaldehyde to form a polymer matrix that coats the graphite surface. After subsequent carbonization, carbon-coated graphite material (G@C) was successfully synthesized. Carbon coatings on graphite effectively lower LIB resistance, enhance lithium-ion diffusion, and prevent exfoliation during cycling, thereby significantly boosting rate performance and prolonging the cycle life of graphite. After 500 cycles at 2C, the specific capacity of G@C was 103.7 mAh g<sup>−</sup><sup>1</sup>, with a retention of 89%. However, G exhibited only 68.7 mAh g<sup>−</sup><sup>1</sup> and 85% retention under identical conditions. This carbon-coated graphite modification strategy offers a novel, green, and economical approach for designing and tailoring graphite anode materials for lithium-ion batteries with long cycle life and high rate.</div></div>","PeriodicalId":61638,"journal":{"name":"材料导报:能源(英文)","volume":"5 2","pages":"Article 100332"},"PeriodicalIF":0.0,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144185650","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}
材料导报:能源(英文)Pub Date : 2025-05-01DOI: 10.1016/j.matre.2025.100333
Shiyao Sun , Jialin Zhao , Yijia Lei , Jingyi Wu , Jian Gao , Na Li , Jiayao Yang , Jiahao Lu , Liying Yin , Zhe Wang
{"title":"Constructing main/side chain dual-cation poly(mequitazine-terphenyl piperidinium) anion exchange membranes for high-performance fuel cells","authors":"Shiyao Sun , Jialin Zhao , Yijia Lei , Jingyi Wu , Jian Gao , Na Li , Jiayao Yang , Jiahao Lu , Liying Yin , Zhe Wang","doi":"10.1016/j.matre.2025.100333","DOIUrl":"10.1016/j.matre.2025.100333","url":null,"abstract":"<div><div>Anion exchange membranes (AEMs) combining high hydroxide conductivity and alkali-resistant stability have become a major challenge for the long-term development of anion exchange membrane fuel cells (AEMFCs). Here, we designed a series of poly(mequitazine-terphenyl piperidinium) (QPMTP-<em>X</em>) AEMs with dual-functionalized quaternary ammonium cations by introducing a certain proportion of large steric hindrance mequitazine (MEQ) molecular building unit into the poly(aryl piperidinium) backbone. QPMTP-<em>X</em> retains the excellent mechanical properties of the poly(aryl piperidinium), while also combining the alkaline stability and high ionic conductivity exhibited by MEQ with flexible quinuclidinium side chains, achieving an overall improvement of membrane performance. Notably, QPMTP-30 exhibits an ultra-high conductivity of up to 206.83 mS cm<sup>−</sup><sup>1</sup> and excellent alkaline stability (over 95% conductivity is maintained after 1000 h of conditioning in 2 M NaOH at 80 °C). In fuel cell performance test, QPMTP-30 achieves a peak power density (PPD) of 974.5 mW cm<sup>−</sup><sup>2</sup> and operates stably at 80 °C for more than 60 h (0.1 A cm<sup>−</sup><sup>2</sup>). Incorporating large steric hindrance building blocks and multi-cations into the poly(aryl piperidinium) backbone not only synergizes the development of high-performance AEMs but also opens up new ideas for the structural design of future AEMs.</div></div>","PeriodicalId":61638,"journal":{"name":"材料导报:能源(英文)","volume":"5 2","pages":"Article 100333"},"PeriodicalIF":0.0,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144185647","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}
材料导报:能源(英文)Pub Date : 2025-05-01DOI: 10.1016/j.matre.2025.100327
Jian Luo , Junjie Zheng , Mingjie Wu , Fang Dong , Yuyu Liu , Jinli Qiao , Yingkui Yang
{"title":"Local microenvironment reactive zone engineering promotes water activation","authors":"Jian Luo , Junjie Zheng , Mingjie Wu , Fang Dong , Yuyu Liu , Jinli Qiao , Yingkui Yang","doi":"10.1016/j.matre.2025.100327","DOIUrl":"10.1016/j.matre.2025.100327","url":null,"abstract":"<div><div>Beyond conventional electrocatalyst engineering, recent studies have demonstrated the effectiveness of manipulating the local reaction environment to enhance the performance of electrocatalytic reactions. The general principles and strategies of local environmental engineering for different electrocatalytic processes have been extensively investigated. This perspective critically appraises the recent advancements in local reaction environment engineering for water activation, aiming to provide a comprehensive assessment of this emerging field.</div></div>","PeriodicalId":61638,"journal":{"name":"材料导报:能源(英文)","volume":"5 2","pages":"Article 100327"},"PeriodicalIF":0.0,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144185105","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}
材料导报:能源(英文)Pub Date : 2025-05-01DOI: 10.1016/j.matre.2025.100329
Jiankai Liu , Xiaoping Dong , Duolong Jin , Qianran Pang , Liying Yang , Cuibiao Wang
{"title":"Comparative study on the electrochemical performance of β-manganese dioxide-3D graphene mixtures with (without) carbon nanotubes","authors":"Jiankai Liu , Xiaoping Dong , Duolong Jin , Qianran Pang , Liying Yang , Cuibiao Wang","doi":"10.1016/j.matre.2025.100329","DOIUrl":"10.1016/j.matre.2025.100329","url":null,"abstract":"<div><div>Manganese dioxide is widely used as a cathode material in aqueous zinc-ion batteries, and the cathode material is a key factor limiting the performance of these batteries. In this study, β-manganese dioxide was used as the base material to synthesize two hybrid materials, i.e. manganese dioxide-3D graphene carbon nanotube hybrids (MnO<sub>2</sub>@3D-GPE/CNT) and manganese dioxide-3D-graphene hybrids (MnO<sub>2</sub>@3D-GPE), via intermittent high-energy vibration ball milling. Electrochemical tests revealed that the CNT-containing hybrid materials exhibited a higher specific capacity of 480 mAh g<sup>−1</sup> and superior cycling stability, maintaining over 80% of its initial capacity after 1000 cycles at 500 mA g<sup>−1</sup> with a Coulombic efficiency close to 100%. MnO<sub>2</sub>@3D-GPE/CNT had a smaller particle size distribution and a larger specific surface area than MnO<sub>2</sub>@3D-GPE, explaining its enhanced electrochemical performance. Additionally, MnO<sub>2</sub>@3D-GPE/CNT exhibited lower electrode impedance, further supporting its efficacy as a cathode material.</div></div>","PeriodicalId":61638,"journal":{"name":"材料导报:能源(英文)","volume":"5 2","pages":"Article 100329"},"PeriodicalIF":0.0,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144185651","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}
{"title":"Tunable properties of WSe2 nanosheets and nano-dispersion via energy dependent exfoliation","authors":"Panwad Chavalekvirat , Thanit Saisopa , Nichakarn Sornnoei , Wisit Hirunpinyopas , Weekit Sirisaksoontorn , Wutthikrai Busayaporn , Pawin Iamprasertkun","doi":"10.1016/j.matre.2025.100326","DOIUrl":"10.1016/j.matre.2025.100326","url":null,"abstract":"<div><div>Transition metal dichalcogenides (TMDs) have emerged as promising electrocatalysts for various electrocatalytic processes. Molybdenum disulfide has been widely used, but a single electrocatalyst can hardly be applied to all reactions, making it essential to understand the electrochemistry of selected TMDs. Tungsten diselenide (WSe<sub>2</sub>) is reactive in gas evolution processes, similar to molybdenum, yet has received limited attention. This work explores how different exfoliation powers affect WSe<sub>2</sub> structural configurations and their impact on catalytic performance in hydrogen evolution, oxygen evolution, and capacitive behaviour. The study investigates the structural properties of WSe<sub>2</sub> nanosheets in both liquid (dispersion) and solid (electrode) phases. Low exfoliation power (90.4 W) contributes to well-defined WSe<sub>2</sub>, while higher power (814 W) leads to an increased number of selenium vacancies. These modifications influence key properties such as thickness, band gaps (1.518 to 1.578 eV), exfoliation yield (0.27 to 0.12 mg mL<sup>−</sup><sup>1</sup>), and oxide content (44.3% to 53.9%), resulting in distinct electrochemical behaviours in different electrolytes. WSe<sub>2</sub> nanosheets exfoliated at higher power exhibit reduced activity in the hydrogen evolution reaction (HER) due to the loss of W–Se bonds and the formation of an amorphous structure, but they show enhanced oxygen evolution reaction (OER) performance, particularly in alkaline media. Additionally, a higher concentration of selenium vacancies improves capacitive performance in acidic conditions due to proton contributions but are less favourable in neutral and basic electrolytes. This study highlights the importance of exfoliation power in tuning the structural properties of WSe<sub>2</sub> for specific electrochemical applications, advancing the understanding of its synthesis and performance.</div></div>","PeriodicalId":61638,"journal":{"name":"材料导报:能源(英文)","volume":"5 2","pages":"Article 100326"},"PeriodicalIF":0.0,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144185108","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}
材料导报:能源(英文)Pub Date : 2025-05-01DOI: 10.1016/j.matre.2025.100330
Dong Sun , Lu Zhao , Yin Yang , Changbo Lu , Chunming Xu , Zhihua Xiao , Xinlong Ma
{"title":"Thiophene-S doping assisted constructing high-performance pitch-based hard carbon anode for sodium-ion batteries","authors":"Dong Sun , Lu Zhao , Yin Yang , Changbo Lu , Chunming Xu , Zhihua Xiao , Xinlong Ma","doi":"10.1016/j.matre.2025.100330","DOIUrl":"10.1016/j.matre.2025.100330","url":null,"abstract":"<div><div>Hard carbon has emerged as a promising anode material for sodium-ion batteries (SIBs) due to its exceptional chemical stability and abundant resources. However, its application in energy storage is limited by the poor fast-charging performance caused by the slow Na<sup>+</sup> reaction kinetics. Herein, thiophene-S doped oxidized pitch (SOP-600) with outstanding fast-charging performance has been fabricated via a facile ball milling and carbonization procedure. Benefiting from the high thiophene-S doping content, the optimized SOP samples (SOP-600) exhibit plentiful active sites and a rich micro-mesoporous structure with rapid ion transport channels, significantly enhancing the Na<sup>+</sup> reaction kinetics and improving the fast-charging performance. When employed as SIBs anode, SOP-600 delivers an impressive specific capacity of 690.3 mAh g<sup>−</sup><sup>1</sup> at 0.05 A g<sup>−1</sup>. In addition, it maintains a significant reversible capacity of 373.5 mAh g<sup>−1</sup> at 7 A g<sup>−1</sup> with a capacity retention rate of 54.1%, demonstrating excellent fast-charging performance. Moreover, SOP-600 anode exhibits a remarkable cycling capacity of 490.7 mAh g<sup>−1</sup> under 1 A g<sup>−1</sup>, with 92.5% capacity retention after 1000 cycles, highlighting its robust structural stability. Furthermore, sodium ion hybrid capacitors (SICs) assembled with SOP-600 anode and activated carbon cathode achieve a high reversible capacity of 53.5 mAh g<sup>−1</sup> at 1 A g<sup>−1</sup>. This work provides theoretical insights into how thiophene-S doping enhances the fast-charging performance of hard carbon in SIBs.</div></div>","PeriodicalId":61638,"journal":{"name":"材料导报:能源(英文)","volume":"5 2","pages":"Article 100330"},"PeriodicalIF":0.0,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144185109","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}