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ACS Omega. 2017 Jul 14;2(7):3647-3657. doi: 10.1021/acsomega.7b00548. eCollection 2017 Jul 31.
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Nanostructuring one-dimensional and amorphous lithium peroxide for high round-trip efficiency in lithium-oxygen batteries.用于锂氧电池中实现高往返效率的一维及非晶态过氧化锂纳米结构构建
Nat Commun. 2018 Feb 14;9(1):680. doi: 10.1038/s41467-017-02727-2.
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Macroscale and Nanoscale Morphology Evolution during in Situ Spray Coating of Titania Films for Perovskite Solar Cells.用于钙钛矿太阳能电池的原位喷涂 TiO2 薄膜的宏观和纳米形貌演变。
ACS Appl Mater Interfaces. 2017 Dec 20;9(50):43724-43732. doi: 10.1021/acsami.7b14850. Epub 2017 Dec 11.
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Diffusion and nucleation in multilayer growth of PTCDI-C studied with in situ X-ray growth oscillations and real-time small angle X-ray scattering.利用原位 X 射线生长动力学和实时小角 X 射线散射研究 PTCDI-C 多层生长中的扩散和成核。
J Chem Phys. 2017 Feb 7;146(5):052803. doi: 10.1063/1.4961460.
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Manipulating the Assembly of Spray-Deposited Nanocolloids: In Situ Study and Monolayer Film Preparation.喷雾沉积纳米胶体组装的调控:原位研究与单层膜制备。
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Sorption of Water and Initial Stages of Swelling of Thin PNIPAM Films Using in Situ GISAXS Microfluidics.利用原位GISAXS微流体技术研究PNIPAM薄膜对水的吸附及溶胀初期阶段
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The Crystallization of PEDOT:PSS Polymeric Electrodes Probed In Situ during Printing.印刷过程中原位探测的聚(3,4-乙撑二氧噻吩):聚苯乙烯磺酸聚合物电极的结晶
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Colloidal Nanoparticle Interaction Transition during Solvent Evaporation Investigated by in-Situ Small-Angle X-ray Scattering.通过原位小角X射线散射研究溶剂蒸发过程中的胶体纳米颗粒相互作用转变
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Hydrodynamic alignment and assembly of nanofibrils resulting in strong cellulose filaments.纳米纤维的流体动力学排列与组装形成了坚固的纤维素细丝。
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在钠离子电池中对TiO纳米颗粒进行纳米级形态演变的原位监测。

Operando monitoring the nanometric morphological evolution of TiO nanoparticles in a Na-ion battery.

作者信息

Santoro Gonzalo, Amarilla José Manuel, Tartaj Pedro, Vázquez-Santos María Beatriz

机构信息

Institute of Materials Science of Madrid, ICMM-CSIC, c/ Sor Juana Inés de la Cruz 3, Cantoblanco, E-28049, Madrid, Spain.

出版信息

Mater Today Energy. 2018 Dec 1;10:23-27. doi: 10.1016/j.mtener.2018.08.005. Epub 2018 Aug 24.

DOI:10.1016/j.mtener.2018.08.005
PMID:30854498
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6404958/
Abstract

Na-ion batteries are nowadays receiving renewed attention because of its propitiousness for large-scale stationary applications. Although the Na storage mechanism is still not completely understood, TiO nanoparticles are very promising active anode materials in Na-ion batteries provided that a correct dispersion is achieved within the battery electrode. Whilst the structural changes, either in crystallinity or crystalline phase, that occur during operation are receiving much recent attention, the nanometric morphological evolution of the TiO nanoparticles within the electrode is yet to be thoroughly addressed, despite its implication in battery efficiency. In the present work, small-angle x-ray scattering studies on TiO/Na-ion batteries show that whereas the nanoparticle size is preserved during the discharge-charge cycles, the mean distance between nanoparticles increases. The observed morphological changes are consistent with electrode swelling and nanoparticle aggregation during operation, being one phenomenon dominant over the other depending on the applied density current; thus, depending on the differences in ion diffusion within the electrode.

摘要

由于钠离子电池在大规模固定应用方面具有优势,如今正重新受到关注。尽管钠存储机制仍未完全理解,但只要在电池电极内实现正确的分散,TiO纳米颗粒在钠离子电池中是非常有前景的活性负极材料。虽然运行过程中发生的结晶度或晶相的结构变化最近受到了很多关注,但电极内TiO纳米颗粒的纳米级形态演变尚未得到充分研究,尽管其对电池效率有影响。在本工作中,对TiO/钠离子电池的小角X射线散射研究表明,虽然纳米颗粒尺寸在充放电循环中保持不变,但纳米颗粒之间的平均距离增加。观察到的形态变化与运行过程中的电极膨胀和纳米颗粒聚集一致,根据施加的密度电流,一种现象比另一种现象更占主导;因此,取决于电极内离子扩散的差异。