An Fe-doped Co-oxide electrocatalyst synthesized through a post-modification method toward advanced water oxidation. Issue 8 (3rd February 2022)
- Record Type:
- Journal Article
- Title:
- An Fe-doped Co-oxide electrocatalyst synthesized through a post-modification method toward advanced water oxidation. Issue 8 (3rd February 2022)
- Main Title:
- An Fe-doped Co-oxide electrocatalyst synthesized through a post-modification method toward advanced water oxidation
- Authors:
- Xu, Zhenhang
Zuo, Wei
Shi, Tianyu
Liu, Xinghai
Li, Houbin
Zhao, Pingping
Cheng, Gongzhen - Abstract:
- Abstract : A new type of Fe-doped Co-oxide electrocatalyst Co3− x Fe x O4 -0.01 exhibited excellent OER activity at a current density of 10 mA cm −2 . The introduction of Fe not only successfully achieved the synergistic effect of CoFe, but also promoted the formation of oxygen bridges. Abstract : In the context of the ever-increasing energy crisis, electrocatalytic water splitting has attracted widespread attention as an effective means to provide clean energy. However, the oxygen evolution reaction (OER), which is an important anodic half reaction, shows very slow kinetics due to the multi-step electron transfer process, which severely restricts the efficiency of energy conversion. Herein, we used a simple solvothermal method to dope iron into the cobalt-containing hydroxide precursor, and successfully prepared the Fe-doped Co-oxide electrocatalyst Co3− x Fe x O4 -0.01. It only needs an overpotential of 294 mV to perform the OER at a current density of 10 mA cm −2, and has a low Tafel slope of 47.3 mV dec −1 . Moreover, Co3− x Fe x O4 -0.01 has excellent stability. There is no significant increase in the overpotential for oxygen evolution at a current density of 10 mA cm −2 after nearly 20 h. BET surface area test and XPS spectroscopy results show that Fe doping provides more mesopores and oxygen bridges, which is conducive to the construction of active sites and electronic regulation during the OER. This work can help design more bimetallic based highly active OERAbstract : A new type of Fe-doped Co-oxide electrocatalyst Co3− x Fe x O4 -0.01 exhibited excellent OER activity at a current density of 10 mA cm −2 . The introduction of Fe not only successfully achieved the synergistic effect of CoFe, but also promoted the formation of oxygen bridges. Abstract : In the context of the ever-increasing energy crisis, electrocatalytic water splitting has attracted widespread attention as an effective means to provide clean energy. However, the oxygen evolution reaction (OER), which is an important anodic half reaction, shows very slow kinetics due to the multi-step electron transfer process, which severely restricts the efficiency of energy conversion. Herein, we used a simple solvothermal method to dope iron into the cobalt-containing hydroxide precursor, and successfully prepared the Fe-doped Co-oxide electrocatalyst Co3− x Fe x O4 -0.01. It only needs an overpotential of 294 mV to perform the OER at a current density of 10 mA cm −2, and has a low Tafel slope of 47.3 mV dec −1 . Moreover, Co3− x Fe x O4 -0.01 has excellent stability. There is no significant increase in the overpotential for oxygen evolution at a current density of 10 mA cm −2 after nearly 20 h. BET surface area test and XPS spectroscopy results show that Fe doping provides more mesopores and oxygen bridges, which is conducive to the construction of active sites and electronic regulation during the OER. This work can help design more bimetallic based highly active OER materials. … (more)
- Is Part Of:
- Dalton transactions. Volume 51:Issue 8(2022)
- Journal:
- Dalton transactions
- Issue:
- Volume 51:Issue 8(2022)
- Issue Display:
- Volume 51, Issue 8 (2022)
- Year:
- 2022
- Volume:
- 51
- Issue:
- 8
- Issue Sort Value:
- 2022-0051-0008-0000
- Page Start:
- 3137
- Page End:
- 3145
- Publication Date:
- 2022-02-03
- Subjects:
- Chemistry, Inorganic -- Periodicals
Chemistry, Physical and theoretical -- Periodicals
Chemistry, Inorganic -- Periodicals
546.05 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/dt#!issueid=dt043040&type=current&issnprint=1477-9226 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d1dt03936a ↗
- Languages:
- English
- ISSNs:
- 1477-9226
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3517.830000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 21164.xml