{"title":"解锁高效储能:钒氧化还原液流电池的阴极催化剂——钕铁氧体钙钛矿","authors":"Rui Mu, Wei Zhang, Zhenhe Chang, Chaoyue Zhang, Baohui Wang, Hongjun Wu, Di Gu","doi":"10.1039/d5ta06257h","DOIUrl":null,"url":null,"abstract":"Developing efficient cathode catalysts is pivotal for advancing vanadium redox flow batteries (VRFBs). This study compares hydrothermal (H-NdFeO<small><sub>3</sub></small>@GF) and sol–gel (SG-NdFeO<small><sub>3</sub></small>@GF) synthesis of NdFeO<small><sub>3</sub></small> perovskite-decorated graphite felt, emphasizing structural and catalytic impacts. H-NdFeO<small><sub>3</sub></small>@GF features an ABO<small><sub>3</sub></small> perovskite framework with Nd/Fe occupying A/B-sites, forming a three-dimensional interconnected network-like mesoporous structure that enhances electron/ion transport and vanadium redox kinetics. At 150 mA cm<small><sup>−2</sup></small>, H-NdFeO<small><sub>3</sub></small>@GF exhibits smooth coulombic efficiency (CE) and energy efficiency (EE) profiles over 150 cycles, with a single-cycle capacity of 39.6 Ah L<small><sup>−1</sup></small> (outperforming SG-NdFeO<small><sub>3</sub></small>@GF's 26.2 Ah L<small><sup>−1</sup></small>). In rate capability evaluations across 80–250 mA cm<small><sup>−2</sup></small>, H-NdFeO<small><sub>3</sub></small>@GF retains ∼65.23% EE even at 250 mA cm<small><sup>−2</sup></small>, whereas SG-NdFeO<small><sub>3</sub></small>@GF and traditional GF (TGF) undergo more severe efficiency degradation. For long-cycle stability, H-NdFeO<small><sub>3</sub></small>@GF achieves a high EE of 78.87% (representing a 12.48% enhancement over TGF and a 4.28% improvement over SG-NdFeO<small><sub>3</sub></small>@GF) and sustains 1000 cycles at 150 mA cm<small><sup>−2</sup></small> with a minimal EE decay rate of 0.00352% per cycle. The work demonstrates that hydrothermal synthesis tailors perovskite crystallinity and carbon-matrix integration, which are critical for exposing active sites and improving durability. These findings underscore H-NdFeO<small><sub>3</sub></small>@GF as a high-performance VRFB cathode catalyst, offering a strategic pathway for scalable energy storage through synergistic structural and synthetic engineering.","PeriodicalId":82,"journal":{"name":"Journal of Materials Chemistry A","volume":"22 1","pages":""},"PeriodicalIF":9.5000,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Unlocking high-efficiency energy storage: neodymium ferrite perovskite as a cathode catalyst for vanadium redox flow batteries\",\"authors\":\"Rui Mu, Wei Zhang, Zhenhe Chang, Chaoyue Zhang, Baohui Wang, Hongjun Wu, Di Gu\",\"doi\":\"10.1039/d5ta06257h\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Developing efficient cathode catalysts is pivotal for advancing vanadium redox flow batteries (VRFBs). This study compares hydrothermal (H-NdFeO<small><sub>3</sub></small>@GF) and sol–gel (SG-NdFeO<small><sub>3</sub></small>@GF) synthesis of NdFeO<small><sub>3</sub></small> perovskite-decorated graphite felt, emphasizing structural and catalytic impacts. H-NdFeO<small><sub>3</sub></small>@GF features an ABO<small><sub>3</sub></small> perovskite framework with Nd/Fe occupying A/B-sites, forming a three-dimensional interconnected network-like mesoporous structure that enhances electron/ion transport and vanadium redox kinetics. At 150 mA cm<small><sup>−2</sup></small>, H-NdFeO<small><sub>3</sub></small>@GF exhibits smooth coulombic efficiency (CE) and energy efficiency (EE) profiles over 150 cycles, with a single-cycle capacity of 39.6 Ah L<small><sup>−1</sup></small> (outperforming SG-NdFeO<small><sub>3</sub></small>@GF's 26.2 Ah L<small><sup>−1</sup></small>). In rate capability evaluations across 80–250 mA cm<small><sup>−2</sup></small>, H-NdFeO<small><sub>3</sub></small>@GF retains ∼65.23% EE even at 250 mA cm<small><sup>−2</sup></small>, whereas SG-NdFeO<small><sub>3</sub></small>@GF and traditional GF (TGF) undergo more severe efficiency degradation. For long-cycle stability, H-NdFeO<small><sub>3</sub></small>@GF achieves a high EE of 78.87% (representing a 12.48% enhancement over TGF and a 4.28% improvement over SG-NdFeO<small><sub>3</sub></small>@GF) and sustains 1000 cycles at 150 mA cm<small><sup>−2</sup></small> with a minimal EE decay rate of 0.00352% per cycle. The work demonstrates that hydrothermal synthesis tailors perovskite crystallinity and carbon-matrix integration, which are critical for exposing active sites and improving durability. These findings underscore H-NdFeO<small><sub>3</sub></small>@GF as a high-performance VRFB cathode catalyst, offering a strategic pathway for scalable energy storage through synergistic structural and synthetic engineering.\",\"PeriodicalId\":82,\"journal\":{\"name\":\"Journal of Materials Chemistry A\",\"volume\":\"22 1\",\"pages\":\"\"},\"PeriodicalIF\":9.5000,\"publicationDate\":\"2025-09-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Materials Chemistry A\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1039/d5ta06257h\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Chemistry A","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1039/d5ta06257h","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
开发高效的阴极催化剂是钒氧化还原液流电池发展的关键。本研究比较了水热法(H-NdFeO3@GF)和溶胶-凝胶法(SG-NdFeO3@GF)制备NdFeO3钙钛矿装饰石墨毡的方法,强调了结构和催化影响。H-NdFeO3@GF具有ABO3钙钛矿框架,Nd/Fe占据A/ b位点,形成三维互连的网状介孔结构,增强电子/离子传递和钒氧化还原动力学。在150 mA cm−2时,H-NdFeO3@GF在150次循环中表现出平滑的库仑效率(CE)和能量效率(EE)曲线,单次循环容量为39.6 Ah L−1(优于SG-NdFeO3@GF的26.2 Ah L−1)。在80-250 mA cm - 2的速率能力评估中,H-NdFeO3@GF即使在250 mA cm - 2下也能保持约65.23%的EE,而SG-NdFeO3@GF和传统GF (TGF)的效率下降更为严重。对于长周期稳定性,H-NdFeO3@GF实现78.87%的高EE(比TGF提高12.48%,比SG-NdFeO3@GF提高4.28%),并在150 mA cm - 2下维持1000次循环,每循环的EE衰减率最小为0.00352%。研究表明,水热合成可以调整钙钛矿的结晶度和碳基质整合,这对于暴露活性位点和提高耐久性至关重要。这些发现强调H-NdFeO3@GF是一种高性能的VRFB阴极催化剂,通过协同结构和合成工程为可扩展的储能提供了战略途径。
Unlocking high-efficiency energy storage: neodymium ferrite perovskite as a cathode catalyst for vanadium redox flow batteries
Developing efficient cathode catalysts is pivotal for advancing vanadium redox flow batteries (VRFBs). This study compares hydrothermal (H-NdFeO3@GF) and sol–gel (SG-NdFeO3@GF) synthesis of NdFeO3 perovskite-decorated graphite felt, emphasizing structural and catalytic impacts. H-NdFeO3@GF features an ABO3 perovskite framework with Nd/Fe occupying A/B-sites, forming a three-dimensional interconnected network-like mesoporous structure that enhances electron/ion transport and vanadium redox kinetics. At 150 mA cm−2, H-NdFeO3@GF exhibits smooth coulombic efficiency (CE) and energy efficiency (EE) profiles over 150 cycles, with a single-cycle capacity of 39.6 Ah L−1 (outperforming SG-NdFeO3@GF's 26.2 Ah L−1). In rate capability evaluations across 80–250 mA cm−2, H-NdFeO3@GF retains ∼65.23% EE even at 250 mA cm−2, whereas SG-NdFeO3@GF and traditional GF (TGF) undergo more severe efficiency degradation. For long-cycle stability, H-NdFeO3@GF achieves a high EE of 78.87% (representing a 12.48% enhancement over TGF and a 4.28% improvement over SG-NdFeO3@GF) and sustains 1000 cycles at 150 mA cm−2 with a minimal EE decay rate of 0.00352% per cycle. The work demonstrates that hydrothermal synthesis tailors perovskite crystallinity and carbon-matrix integration, which are critical for exposing active sites and improving durability. These findings underscore H-NdFeO3@GF as a high-performance VRFB cathode catalyst, offering a strategic pathway for scalable energy storage through synergistic structural and synthetic engineering.
期刊介绍:
The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.