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Amorphous FePO4/Carbon Nanotube Cathode Preparation via in Situ Nanoprecipitation and Coagulation in a Microreactor

机译:通过在微反应器中原位纳米沉淀和混凝制备非晶态FePO4 /碳纳米管阴极

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摘要

In this article, nanostructured amorphous FePO4 (a-FePO4)–carbon nanotube (CNT) composites, with high purity of FePO4 and a controllable FePO4/C ratio, were directly synthesized by a fast nanoprecipitation process in a microreactor, using Fe(NO3)3 and (NH4)3PO4 as precursors. Oxidized CNTs are well dispersed via strong electrostatic repulsion in a high pH solution system. Subsequently, a-FePO4 nanoparticles are adhered onto CNTs just following the fast nanoprecipitation process; then, the precipitated composites are compacted by ball-milling, forming a compact conductive network with well dispersed and highly loaded active materials. As cathode materials for lithium-ion batteries, the composites exhibit a capacity of 175.8 mAh g–1 at 0.1 C, close to the theoretical capacity (178 mAh g–1), and a good cycle performance with a reversible capacity of 137.0 mAh g–1 after 500 cycles at 5 C. Importantly, the enhanced micromixing enables fast nanoprecipitation in suspension and opens a shortcut for constructing nanostructured composites that have potential in functionalization and are easy to handle.
机译:在本文中,使用Fe(NO3)在微反应器中通过快速纳米沉淀工艺直接合成了具有高FePO4纯度和可控FePO4 / C比的纳米结构非晶态FePO4(a-FePO4)-碳纳米管(CNT)复合材料。 3和(NH4)3PO4作为前体。氧化的CNT通过强静电排斥力在高pH溶液系统中很好地分散。随后,就在快速纳米沉淀过程之后,将a-FePO4纳米颗粒粘附到CNT上。然后,将沉淀的复合材料通过球磨机压实,形成具有良好分散和高负载活性材料的致密导电网络。作为锂离子电池的正极材料,复合材料在0.1 C下的容量为175.8 mAh g–1,接近理论容量(178 mAh g–1),并且具有良好的循环性能,可逆容量为137.0 mAh g在5 C下经过500次循环后,结果为–1。重要的是,增强的微混合可实现悬浮液中快速纳米沉淀,并为构建具有功能化潜力且易于处理的纳米结构复合材料提供了捷径。

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