Boosting the charge storage of layered double hydroxides derived from carbon nanotube-tailored metal organic frameworks. (1st April 2019)
- Record Type:
- Journal Article
- Title:
- Boosting the charge storage of layered double hydroxides derived from carbon nanotube-tailored metal organic frameworks. (1st April 2019)
- Main Title:
- Boosting the charge storage of layered double hydroxides derived from carbon nanotube-tailored metal organic frameworks
- Authors:
- Ran, Feitian
Yang, Xiaobin
Xu, Xueqing
Bai, Yongping
Shao, Lu - Abstract:
- Abstract: Metal-organic frameworks derived nanoarchitectures attract considerable interests especially in electrochemical energy storage. However, controllably tuning crystal size with synchronously improving conductivity of metal-organic frameworks derived nanostructure is still the challenge for further capacity enhancement. Herein, we first conceive a strategy for the controllable synthesis of carboxylated carbon nanotubes connected hollow layered double hydroxides via sequential ion exchange of carboxylated carbon nanotubes-tailored metal-organic framework nanoarchitectures. By introducing the carboxylated carbon nanotubes, the derived hollow nanohybrids appear much smaller size and higher specific surface area, which is crucial to electrochemical reactions between electrolyte ions and electrodes. Owing to its well-designed structure and improved conductivity, the as-synthesized nanohybrids exhibit a significantly boosted specific capacity (855C g −1 at 1 A g −1 ) and unprecedented rate capability (91% capacity retention at 15 A g −1 ). When compared with the literature data by the "Ragone plots", the hybrid supercapacitor assembled by as-synthesized nanaohybrids and active carbon demonstrates the extraordinary performance with a high energy density of 49.9 Wh kg −1 at a power density of 895 W kg −1 . This novel strategy can stimulate the controllable synthesis of diverse metal-organic frameworks derived nanoarchitectures for energy storage, molecular adsorption,Abstract: Metal-organic frameworks derived nanoarchitectures attract considerable interests especially in electrochemical energy storage. However, controllably tuning crystal size with synchronously improving conductivity of metal-organic frameworks derived nanostructure is still the challenge for further capacity enhancement. Herein, we first conceive a strategy for the controllable synthesis of carboxylated carbon nanotubes connected hollow layered double hydroxides via sequential ion exchange of carboxylated carbon nanotubes-tailored metal-organic framework nanoarchitectures. By introducing the carboxylated carbon nanotubes, the derived hollow nanohybrids appear much smaller size and higher specific surface area, which is crucial to electrochemical reactions between electrolyte ions and electrodes. Owing to its well-designed structure and improved conductivity, the as-synthesized nanohybrids exhibit a significantly boosted specific capacity (855C g −1 at 1 A g −1 ) and unprecedented rate capability (91% capacity retention at 15 A g −1 ). When compared with the literature data by the "Ragone plots", the hybrid supercapacitor assembled by as-synthesized nanaohybrids and active carbon demonstrates the extraordinary performance with a high energy density of 49.9 Wh kg −1 at a power density of 895 W kg −1 . This novel strategy can stimulate the controllable synthesis of diverse metal-organic frameworks derived nanoarchitectures for energy storage, molecular adsorption, catalysis, drug delivery and separation towards sustainability. … (more)
- Is Part Of:
- Electrochimica acta. Volume 301(2019)
- Journal:
- Electrochimica acta
- Issue:
- Volume 301(2019)
- Issue Display:
- Volume 301, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 301
- Issue:
- 2019
- Issue Sort Value:
- 2019-0301-2019-0000
- Page Start:
- 117
- Page End:
- 125
- Publication Date:
- 2019-04-01
- Subjects:
- Metal-organic frameworks -- Layered double hydroxides -- Hybrid supercapacitor -- Rate capability
Electrochemistry -- Periodicals
Electrochemistry, Industrial -- Periodicals
541.37 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00134686 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.electacta.2019.01.142 ↗
- Languages:
- English
- ISSNs:
- 0013-4686
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3698.950000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 10516.xml