Scalable Synthesis of N–Doped Graphene–Oxide–Supported FeCo(OH)x Nanosheets for Efficient Co–Doped Fe3O4 Nanoparticle-Based Oxygen Reduction Reaction Electrocatalysis

IF 10.7 2区 材料科学 Q1 CHEMISTRY, PHYSICAL Journal of Materials Chemistry A Pub Date : 2024-11-12 DOI:10.1039/d4ta06684g
Sunglun Kwon, Jong Hyeon Lee
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Abstract

Developing efficient and cost-effective materials is crucial for advancing electrochemical oxygen reduction reaction (ORR). This study presents a synthesis route for high-performance spinel Fe and Co oxide nanoparticles on N-doped reduced graphene oxide (NRGO). This solvothermal synthesis in formamide yields well-dispersed, ultrafine FeCo(OH)x nanoparticles (∼5 nm) anchored on NRGO. These nanoparticles can be employed for the formation of spinel FexCo3-xO4 oxide nanoparticles, potentially because of their high surface area and intense interaction with the NRGO support. By introducing Co2+ ions into formamide, our method prevents rapid Fe2+ oxidation to Fe3+, promoting the formation of well-defined Fe3O4 nanoparticles, not Fe2O3. This, in turn, facilitates the successful decoration of highly dispersed spinel FexCo3-xO4 oxide nanoparticles (∼30 nm) onto the NRGO support, even after calcination at 900°C, which represents the critical temperature for conventional graphitization. This unique approach results in significantly reduced particle aggregation compared with that of conventional methods. The (Co)Fe3O4–NRGO nanocomposite exhibits remarkable ORR activity, achieving an electron number of ∼3.7 and a current density of 5.01 mA·cm−2 at E = 0.75 VRHE, comparable to those of commercial Pt/C catalysts. Furthermore, the catalyst exhibits remarkable stability, maintaining a reducing current density that is 42% lower after 40,000 s of uninterrupted operation at 0.75 VRHE compared with a 75% reduction observed with Pt/C. This exceptional performance is attributed to the strong interaction between the (Co)Fe3O4 nanoparticles and NRGO, facilitated by the Co ion precursor during annealing.
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可扩展地合成 N 掺杂氧化石墨烯支撑的 FeCo(OH)x 纳米片,用于基于共掺 Fe3O4 纳米粒子的高效氧还原反应电催化
开发高效且具有成本效益的材料对于推进电化学氧还原反应(ORR)至关重要。本研究提出了在掺杂 N 的还原氧化石墨烯 (NRGO) 上合成高性能尖晶石氧化铁和氧化钴纳米粒子的路线。这种在甲酰胺中进行的溶热合成可以在 NRGO 上锚定出分散良好的超细 FeCo(OH)x 纳米粒子(∼5 nm)。这些纳米颗粒可用于形成尖晶石 FexCo3-xO4 氧化物纳米颗粒,这可能是因为它们具有高比表面积并与 NRGO 支持物有强烈的相互作用。通过在甲酰胺中引入 Co2+ 离子,我们的方法可以防止 Fe2+ 快速氧化为 Fe3+,从而促进形成定义明确的 Fe3O4 纳米粒子,而不是 Fe2O3。这反过来又促进了高度分散的尖晶石 FexCo3-xO4 氧化物纳米颗粒(∼30 nm)在 NRGO 支持物上的成功装饰,即使在 900°C 煅烧之后也是如此,而这正是传统石墨化的临界温度。与传统方法相比,这种独特的方法大大减少了颗粒的聚集。(Co)Fe3O4-NRGO 纳米复合材料表现出显著的 ORR 活性,在 E = 0.75 VRHE 时电子数达到 3.7,电流密度达到 5.01 mA-cm-2,与商用 Pt/C 催化剂相当。此外,该催化剂还表现出显著的稳定性,在 0.75 VRHE 下不间断运行 40,000 秒后,其还原电流密度降低了 42%,而 Pt/C 催化剂的还原电流密度降低了 75%。这种优异的性能归功于(Co)Fe3O4 纳米颗粒与 NRGO 之间强烈的相互作用,而退火过程中 Co 离子前驱体又促进了这种相互作用。
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来源期刊
Journal of Materials Chemistry A
Journal of Materials Chemistry A CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
19.50
自引率
5.00%
发文量
1892
审稿时长
1.5 months
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.
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