In situ TEM probing of crystallization form-dependent sodiation behavior in ZnO nanowires for sodium-ion batteries. (December 2016)
- Record Type:
- Journal Article
- Title:
- In situ TEM probing of crystallization form-dependent sodiation behavior in ZnO nanowires for sodium-ion batteries. (December 2016)
- Main Title:
- In situ TEM probing of crystallization form-dependent sodiation behavior in ZnO nanowires for sodium-ion batteries
- Authors:
- Xu, Feng
Li, Zhengrui
Wu, Lijun
Meng, Qingping
Xin, Huolin L.
Sun, Jun
Ge, Binghui
Sun, Litao
Zhu, Yimei - Abstract:
- Abstract: Development of sodium-ion battery (SIB) electrode materials currently lags behind electrodes in commercial lithium-ion batteries (LIBs). However, in the long term, development of SIB components is a valuable goal. Their similar, but not identical, chemistries require careful identification of the underlying sodiation mechanism in SIBs. Here, we utilize in situ transmission electron microscopy to explore quite different sodiation behaviors even in similar electrode materials through real-time visualization of microstructure and phase evolution. Upon electrochemical sodiation, single-crystalline ZnO nanowires (sc-ZNWs) are found to undergo a step-by-step electrochemical displacement reaction, forming crystalline NaZn13 nanograins dispersed in a Na2 O matrix. This process is characterized by a slowly propagating reaction front and the formation of heterogeneous interfaces inside the ZNWs due to non-uniform sodiation amorphization. In contrast, poly-crystalline ZNWs (pc-ZNWs) exhibited an ultrafast sodiation process, which can partly be ascribed to the availability of unobstructed ionic transport pathways among ZnO nanograins. Thus the reaction front and heterogeneous interfaces disappear. The in situ TEM results, supported by calculation of the ion diffusion coefficient, provide breakthrough insights into the dependence of ion diffusion kinetics on crystallization form. This points toward a goal of optimizing the microstructure of electrode materials in order toAbstract: Development of sodium-ion battery (SIB) electrode materials currently lags behind electrodes in commercial lithium-ion batteries (LIBs). However, in the long term, development of SIB components is a valuable goal. Their similar, but not identical, chemistries require careful identification of the underlying sodiation mechanism in SIBs. Here, we utilize in situ transmission electron microscopy to explore quite different sodiation behaviors even in similar electrode materials through real-time visualization of microstructure and phase evolution. Upon electrochemical sodiation, single-crystalline ZnO nanowires (sc-ZNWs) are found to undergo a step-by-step electrochemical displacement reaction, forming crystalline NaZn13 nanograins dispersed in a Na2 O matrix. This process is characterized by a slowly propagating reaction front and the formation of heterogeneous interfaces inside the ZNWs due to non-uniform sodiation amorphization. In contrast, poly-crystalline ZNWs (pc-ZNWs) exhibited an ultrafast sodiation process, which can partly be ascribed to the availability of unobstructed ionic transport pathways among ZnO nanograins. Thus the reaction front and heterogeneous interfaces disappear. The in situ TEM results, supported by calculation of the ion diffusion coefficient, provide breakthrough insights into the dependence of ion diffusion kinetics on crystallization form. This points toward a goal of optimizing the microstructure of electrode materials in order to develop high performance SIBs. Graphical abstract: Ultrafast sodiation of pc-ZNWs benefiting from abundant ion transport pathways among ZnO grain boundaries. Highlights: Single-crystal ZnO nanowires (sc-ZNWs) undergo a stepwise electrochemical sodiation process. The sodiated sc-ZNWs are characterized by a sluggish reaction front and inner heterogeneous interfaces. Poly-crystal ZNWs (pc-ZNWs) have an ultrafast, uniform sodiation speed. There are abundant ionic transport pathways among ZnO nanograins inside the pc-ZNWs. Chemically identical materials could respond differently during electrochemical sodiation, depending on crystallization form. … (more)
- Is Part Of:
- Nano energy. Volume 30(2016:Dec.)
- Journal:
- Nano energy
- Issue:
- Volume 30(2016:Dec.)
- Issue Display:
- Volume 30 (2016)
- Year:
- 2016
- Volume:
- 30
- Issue Sort Value:
- 2016-0030-0000-0000
- Page Start:
- 771
- Page End:
- 779
- Publication Date:
- 2016-12
- Subjects:
- Sodium-ion batteries -- In situ transmission electron microscopy -- ZnO nanowires -- Electrochemical sodiation -- Microstructure control
Nanoscience -- Periodicals
Nanotechnology -- Periodicals
Nanostructured materials -- Periodicals
Power resources -- Technological innovations -- Periodicals
Nanoscience
Nanostructured materials
Nanotechnology
Power resources -- Technological innovations
Periodicals
621.042 - Journal URLs:
- http://www.sciencedirect.com/science/journal/22112855 ↗
http://www.sciencedirect.com/ ↗ - DOI:
- 10.1016/j.nanoen.2016.09.020 ↗
- Languages:
- English
- ISSNs:
- 2211-2855
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
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