Bridging N-doped graphene and carbon rich C3N4 layers for photo-promoted multi-functional electrocatalysts. (10th September 2019)
- Record Type:
- Journal Article
- Title:
- Bridging N-doped graphene and carbon rich C3N4 layers for photo-promoted multi-functional electrocatalysts. (10th September 2019)
- Main Title:
- Bridging N-doped graphene and carbon rich C3N4 layers for photo-promoted multi-functional electrocatalysts
- Authors:
- Yang, Yimei
Hu, Baoshan
Zhao, Wenbin
Yang, Qian
Yang, Feng
Ren, Juncong
Li, Xiaogang
Jin, Yan
Fang, Liang
Pan, Qingjiang - Abstract:
- Abstract: Distinctive electronegativity and similar atomic radius for elements of C and N afford their allotropic substances composed of these two elements with excellent photo- and electro-chemical performance for energy conversion. To explore the synergetic roles of allotropic substances, carbon-rich C3 N4 (CCN) is in - situ hydrothermally synthesized with the N-doped graphene (NG) grown by chemical vapor deposition (CVD) as the template to prepare the N-doped graphene/carbon-rich C3 N4 composite. Compared to the N-doped graphene and carbon-rich C3 N4, N-doped graphene/carbon-rich C3 N4 composite exhibits the remarkable enhancement of catalytic activities toward hydrogen evolution reaction (HER), oxygen evolution reaction (OER) and oxygen reduction reaction (ORR). Particularly, visible light irradiation can significantly improve the catalytic performance of N-doped graphene/carbon-rich C3 N4 toward the above three reactions. Further results confirm that N-doped graphene/carbon-rich C3 N4 exhibits the improved electrochemically active surface area (ECSA), light-harvesting ability, effective separation of electron-hole pairs, and interfacial charge transfer as compared to the N-doped graphene and carbon-rich C3 N4 which should be originated from the efficient bridging between N-doped graphene and carbon-rich C3 N4 layers. Our elucidation facilitates to pave their promising applications in microelectronic devices, wearable devices, photoelectrochemical batteries, sensors andAbstract: Distinctive electronegativity and similar atomic radius for elements of C and N afford their allotropic substances composed of these two elements with excellent photo- and electro-chemical performance for energy conversion. To explore the synergetic roles of allotropic substances, carbon-rich C3 N4 (CCN) is in - situ hydrothermally synthesized with the N-doped graphene (NG) grown by chemical vapor deposition (CVD) as the template to prepare the N-doped graphene/carbon-rich C3 N4 composite. Compared to the N-doped graphene and carbon-rich C3 N4, N-doped graphene/carbon-rich C3 N4 composite exhibits the remarkable enhancement of catalytic activities toward hydrogen evolution reaction (HER), oxygen evolution reaction (OER) and oxygen reduction reaction (ORR). Particularly, visible light irradiation can significantly improve the catalytic performance of N-doped graphene/carbon-rich C3 N4 toward the above three reactions. Further results confirm that N-doped graphene/carbon-rich C3 N4 exhibits the improved electrochemically active surface area (ECSA), light-harvesting ability, effective separation of electron-hole pairs, and interfacial charge transfer as compared to the N-doped graphene and carbon-rich C3 N4 which should be originated from the efficient bridging between N-doped graphene and carbon-rich C3 N4 layers. Our elucidation facilitates to pave their promising applications in microelectronic devices, wearable devices, photoelectrochemical batteries, sensors and other fields. Graphical abstract: Image 1 … (more)
- Is Part Of:
- Electrochimica acta. Volume 317(2019)
- Journal:
- Electrochimica acta
- Issue:
- Volume 317(2019)
- Issue Display:
- Volume 317, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 317
- Issue:
- 2019
- Issue Sort Value:
- 2019-0317-2019-0000
- Page Start:
- 25
- Page End:
- 33
- Publication Date:
- 2019-09-10
- Subjects:
- N-doped graphene -- Carbon-rich C3N4 -- Photo-electrochemical catalysis -- Synergism -- Separation and transfer of charges
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.2019.05.140 ↗
- 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:
- 11309.xml