Framework Cu-doped boron nitride nanobelts with enhanced internal electric field for effective Fenton-like removal of organic pollutants. Issue 12 (6th March 2019)
- Record Type:
- Journal Article
- Title:
- Framework Cu-doped boron nitride nanobelts with enhanced internal electric field for effective Fenton-like removal of organic pollutants. Issue 12 (6th March 2019)
- Main Title:
- Framework Cu-doped boron nitride nanobelts with enhanced internal electric field for effective Fenton-like removal of organic pollutants
- Authors:
- Li, Lingfei
Hu, Chun
Zhang, Lili
Yu, Guangfei
Lyu, Lai
Li, Fan
Jiang, Ning - Abstract:
- Abstract : The internal electric field in Cu-BN promotes the reduction of H2 O2 and the oxidation of H2 O to generate aggressive ·OH. Abstract : Framework Cu-doped boron nitride nanobelts (Cu-BN) were synthesized via a facile pyrolysis method. XPS and EXAFS fitting results demonstrated that Cu existed in the form of Cu–N bonds in the Cu-BN framework, in a raised position on the plane network of the bulk BN. Experimental and theoretical studies verified that the framework incorporation of Cu led to the formation of an internal electric field due to the nonuniform electron distribution with electropositive Cu sites and electronegative N sites. This unique structure promoted the reduction of H2 O2 on the electronegative N sites and the oxidation of H2 O on the electropositive Cu sites to generate highly aggressive ˙OH, accelerating the degradation of pollutants adsorbed on Cu-BN. On the other hand, organic pollutants can donate electrons to Cu by the π → Cu(ii ) interaction in the σ–Cu–ligand complexes between phenolic groups and surface Cu, accompanied by the oxidation of pollutants, as confirmed by solid EPR. As a result, various refractory pollutants could be efficiently degraded and mineralized in the Cu-BN/H2 O2 system over a wide pH range of 3–11. Moreover, high H2 O2 utilization efficiency was obtained, with the production of 1.46 mol ˙OH radicals from per mol H2 O2 in the first 15 min, much higher than that (0.1–0.6 mol) in traditional systems. This study indicates thatAbstract : The internal electric field in Cu-BN promotes the reduction of H2 O2 and the oxidation of H2 O to generate aggressive ·OH. Abstract : Framework Cu-doped boron nitride nanobelts (Cu-BN) were synthesized via a facile pyrolysis method. XPS and EXAFS fitting results demonstrated that Cu existed in the form of Cu–N bonds in the Cu-BN framework, in a raised position on the plane network of the bulk BN. Experimental and theoretical studies verified that the framework incorporation of Cu led to the formation of an internal electric field due to the nonuniform electron distribution with electropositive Cu sites and electronegative N sites. This unique structure promoted the reduction of H2 O2 on the electronegative N sites and the oxidation of H2 O on the electropositive Cu sites to generate highly aggressive ˙OH, accelerating the degradation of pollutants adsorbed on Cu-BN. On the other hand, organic pollutants can donate electrons to Cu by the π → Cu(ii ) interaction in the σ–Cu–ligand complexes between phenolic groups and surface Cu, accompanied by the oxidation of pollutants, as confirmed by solid EPR. As a result, various refractory pollutants could be efficiently degraded and mineralized in the Cu-BN/H2 O2 system over a wide pH range of 3–11. Moreover, high H2 O2 utilization efficiency was obtained, with the production of 1.46 mol ˙OH radicals from per mol H2 O2 in the first 15 min, much higher than that (0.1–0.6 mol) in traditional systems. This study indicates that the construction of an internal electric field through tuning the electron distribution of catalysts is feasible and effective in Fenton-like reactions for water environmental remediation. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 7:Issue 12(2019)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 7:Issue 12(2019)
- Issue Display:
- Volume 7, Issue 12 (2019)
- Year:
- 2019
- Volume:
- 7
- Issue:
- 12
- Issue Sort Value:
- 2019-0007-0012-0000
- Page Start:
- 6946
- Page End:
- 6956
- Publication Date:
- 2019-03-06
- Subjects:
- Materials -- Research -- Periodicals
Chemistry, Analytic -- Periodicals
Environmental sciences -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/ta ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9ta00255c ↗
- Languages:
- English
- ISSNs:
- 2050-7488
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205100
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9678.xml