Organic molecule electrode with high capacitive performance originating from efficient collaboration between caffeic acid and graphene & graphene nanomesh hydrogel. (5th December 2019)
- Record Type:
- Journal Article
- Title:
- Organic molecule electrode with high capacitive performance originating from efficient collaboration between caffeic acid and graphene & graphene nanomesh hydrogel. (5th December 2019)
- Main Title:
- Organic molecule electrode with high capacitive performance originating from efficient collaboration between caffeic acid and graphene & graphene nanomesh hydrogel
- Authors:
- Wang, Xiaotong
Hou, Lijie
Chen, Wenlian
Xie, Yandong
Xie, Kefeng
An, Ning
Hu, Zhongai - Abstract:
- Abstract: The present work reports an organic molecule electrode (OME) based on the graphene and graphene nanomesh (GNM) hydrogel non-covalently functionalized by caffeic acid (CFA) molecules (denoted as G&GMH-CFA). In such electrode system, the three-dimensional conductive network has a cross-linking channel constructed by means of the in-plane pores on the graphene nanomesh, which is benefit for exposing more active sites accessible to electrolyte and accordingly enhancing supercapacitive behaviors of the OME. The G&GMH-CFA delivers a specific capacitance of 482.6 F g −1 at current density of 1 A g −1 . And it is noted that the Faraday current response peaks are located in the positive potential range of 0.6 V, which is superior to the organic molecules electrode reported in the correlative works. In addition, the density functional theory (DFT) calculations are used to illuminate the core issue of charge storage mechanism and binding interactions between CFA and graphene. To match with the resultant positive electrode, AQ functionalize graphene-like nanoflower (CNF-AQ) was prepared as counterpart (negative) electrode. The assembled asymmetric supercapacitors (ASC) CNF-AQ//G&GMH-CFA2 could exhaustively release the supercapacitive performance due to match and self-coordination based on the reasonable matching of two electrodes in structure, charge quantity and kinetics during the electrochemical energy storage process. The CNF-AQ//G&GMH-CFA2 delivered energy density ofAbstract: The present work reports an organic molecule electrode (OME) based on the graphene and graphene nanomesh (GNM) hydrogel non-covalently functionalized by caffeic acid (CFA) molecules (denoted as G&GMH-CFA). In such electrode system, the three-dimensional conductive network has a cross-linking channel constructed by means of the in-plane pores on the graphene nanomesh, which is benefit for exposing more active sites accessible to electrolyte and accordingly enhancing supercapacitive behaviors of the OME. The G&GMH-CFA delivers a specific capacitance of 482.6 F g −1 at current density of 1 A g −1 . And it is noted that the Faraday current response peaks are located in the positive potential range of 0.6 V, which is superior to the organic molecules electrode reported in the correlative works. In addition, the density functional theory (DFT) calculations are used to illuminate the core issue of charge storage mechanism and binding interactions between CFA and graphene. To match with the resultant positive electrode, AQ functionalize graphene-like nanoflower (CNF-AQ) was prepared as counterpart (negative) electrode. The assembled asymmetric supercapacitors (ASC) CNF-AQ//G&GMH-CFA2 could exhaustively release the supercapacitive performance due to match and self-coordination based on the reasonable matching of two electrodes in structure, charge quantity and kinetics during the electrochemical energy storage process. The CNF-AQ//G&GMH-CFA2 delivered energy density of 26.4 Wh kg −1 at the power density of 0.7 kW kg −1 . Two tandem CNF-AQ//G&GMH-CFA2 devices could easily light 88 LEDs. Graphical abstract: The organic molecule electrode is fabricated by the CFA functionalized graphene hydrogel with plentiful transport channels inside of the conductive skeleton, matching with CNF-AQ to assemble full-carbon ASC could easily light 88 LEDs.Image 1 … (more)
- Is Part Of:
- Electrochimica acta. Volume 326(2019)
- Journal:
- Electrochimica acta
- Issue:
- Volume 326(2019)
- Issue Display:
- Volume 326, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 326
- Issue:
- 2019
- Issue Sort Value:
- 2019-0326-2019-0000
- Page Start:
- Page End:
- Publication Date:
- 2019-12-05
- Subjects:
- Organic molecule electrode -- Caffeic acid -- Non-covalently functionalize -- Graphene nanomesh -- Asymmetric supercapacitors
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.2019.134953 ↗
- 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:
- 11975.xml