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基于硒化铁的异质结构建及缺陷工程用于快速钾/钠离子存储

Iron Selenide-Based Heterojunction Construction and Defect Engineering for Fast Potassium/Sodium-Ion Storage.

作者信息

Kong Zhen, Wang Lu, Iqbal Sikandar, Zhang Bo, Wang Bin, Dou Jianmin, Wang Fengbo, Qian Yitai, Zhang Meng, Xu Liqiang

机构信息

Key Laboratory of Colloid and Interface Chemistry, School of Chemistry and Chemical Engineering, State Key Laboratory of Crystal Materials, Shandong University, Shandong, 250100, China.

Key Laboratory/Collaborative Innovation Center of Chemical Energy Storage & Novel Cell Technology, School of Chemistry and Chemical Engineering, Liaocheng University, Shandong, 252000, China.

出版信息

Small. 2022 Apr;18(15):e2107252. doi: 10.1002/smll.202107252. Epub 2022 Feb 27.

Abstract

Suitable anode materials with high capacity and long cycling stability, especially capability at high current densities, are urgently needed to advance the development of potassium ion batteries (PIBs) and sodium ion batteries (SIBs). Herein, a porous Ni-doped FeSe /Fe Se heterojunction encapsulated in Se-doped carbon (NF S/C) is designed through selenization of MOFs precursor. The porous composite possesses enriched active sites and facilitates transport for both ion and electron. Ni-doping is adopted to enrich the lattice defects and active sites. The Se-C bond and carbon framework endow integrity of the composite and hamper aggregation of selenide nano-particles during potassiation/de-potassiation. The NF S/C exhibits exceptional rate performance and ultra-long cycling stability (177.3 mA h g after 3050 cycles at 2 A g for PIBs and 208.8 mA h g after 2000 cycles at 8 A g for SIBs). The potassiation/de-potassiation mechanism is investigated via ex-situ X-ray powder diffraction, high-resolution transmission electron microscopy, X-ray photoelectron spectrocopy and Raman analysis. PTCDA//NF S/C full cell stably cycles for 1200 cycles at 200 mA g with a capacity of 103.7 mA h g , indicating the high application potential of the electrode for highly stable rechargeable batteries.

摘要

为推动钾离子电池(PIBs)和钠离子电池(SIBs)的发展,迫切需要具有高容量和长循环稳定性的合适阳极材料,尤其是在高电流密度下的性能。在此,通过对MOF前驱体进行硒化,设计了一种封装在硒掺杂碳中的多孔镍掺杂FeSe/FeSe异质结(NF S/C)。这种多孔复合材料具有丰富的活性位点,有利于离子和电子的传输。采用镍掺杂来富集晶格缺陷和活性位点。Se-C键和碳骨架赋予了复合材料的完整性,并在钾化/脱钾过程中阻碍了硒化物纳米颗粒的聚集。NF S/C表现出优异的倍率性能和超长的循环稳定性(PIBs在2 A g下3050次循环后为177.3 mA h g,SIBs在8 A g下2000次循环后为208.8 mA h g)。通过非原位X射线粉末衍射、高分辨率透射电子显微镜、X射线光电子能谱和拉曼分析研究了钾化/脱钾机制。PTCDA//NF S/C全电池在200 mA g下稳定循环1200次,容量为103.7 mA h g,表明该电极在高稳定性可充电电池中具有很高的应用潜力。

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