Rui Liu , Shuhui Li , Zheng Wang, Huidong Xu, Weihuang Wang, Yixin Jia, Lantian Zhang, Zicheng Xie, Liangbing Wang
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引用次数: 0
Abstract
Reducing size of Na3V2(PO4)3 (NVP) into nanoscale is regarded as an effective way to improve its high-rate performance for sodium-ion storage. However, the current synthetic approaches for nanostructured NVP such as sol-gel, hydrothermal, and electrospinning still possess limitations in terms of long reaction time and complicated operation. Here, we combine high-boiling organic solvent-assisted colloidal synthesis (HOS-CS) and calcination to fabricate carbon-coated NVP nanoparticles (NPs) with the size of about 50 nm distributed in carbon nanotubes scaffolds as the cathode for SIBs. This HOS-CS strategy demonstrates unique merit of short synthetic period, solving the problem of previously-known approaches in the aspect of synthetic efficiency. Impressively, NVP@C@MWCNTs offers up to 108.6 mAh g-1 at 0.5 C, and also achieves 83.67 and 67.6 mAh g-1 of initial capacities nearly 80 % and 76.1 % of retention after 3000 cycles at ultrahigh rates of 30 C and 50 C, respectively. More surprisingly, the NVP@C@MWCNTs cathode is matched with the hard carbon (HC) anode to construct NVP@C@MWCNTs||HC full cell, delivering as high as 71 mAh g-1 of initial capacity with 72.8 % of retention after 500 cycles even at 10 C. This work provides an efficient strategy for synthesizing high-rate-capability NVP-based cathode towards fast chargeable SIBs.
减小Na3V2(PO4)3 (NVP)的纳米尺寸是提高其高速率钠离子存储性能的有效途径。然而,目前纳米结构NVP的合成方法如溶胶-凝胶法、水热法、静电纺丝法等仍存在反应时间长、操作复杂等局限性。本文采用高沸点有机溶剂辅助胶体合成(HOS-CS)和煅烧相结合的方法制备了尺寸约为50 nm的碳包被NVP纳米颗粒(NPs),并将其分布在碳纳米管支架中作为sib的阴极。该HOS-CS策略具有合成周期短的独特优点,解决了现有方法在合成效率方面的问题。令人印象深刻的是,NVP@C@MWCNTs在0.5℃下提供高达108.6 mAh g-1的初始容量,在30℃和50℃的超高倍率下,经过3000次循环后,其初始容量分别达到83.67和67.6 mAh g-1,保留率分别接近80%和76.1%。更令人惊讶的是,NVP@C@MWCNTs阴极与硬碳(HC)阳极相匹配,构建了NVP@C@MWCNTs||HC全电池,即使在10℃下循环500次后,其初始容量高达71 mAh g-1,保留率为72.8%。这项工作为合成高速率容量的基于nvm的快速充电sib阴极提供了一种有效的策略。
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.