199
Views
6
CrossRef citations to date
0
Altmetric
Original Articles

A new In2O3 and NiO co-loaded fly ash-based nanostructural geopolymer for photocatalytic H2 evolution

, , &
Pages 1-9 | Received 14 Sep 2016, Accepted 07 Mar 2017, Published online: 02 Nov 2017
 

ABSTRACT

A nanostructural alkali-activated fly ash-based geopolymer (AFAG) by co-loaded bimetallic oxide semiconductors of In2O3 and NiO were firstly synthesized and used as an excellent nanocatalyst for production of hydrogen by water splitting. XRD results revealed that In2O3 with average particle size of about 14 nm and NiO in the form of amorphous phase dispersed on the surface of AFAG support. UV-vis DRS and photoluminescence spectra showed that the 5In2O3-NiO/AFAG sample has the widest response to sunlight spectrum and the weakest photoluminescence spectrum, respectively. The 5In2O3-NiO/AFAG sample exhibits the excellent photocatalytic activity of H2 evolution of 3180 µmol/g under the irradiation of solar simulation source for 6 h due to its mesoporous structure coupled with In2O3 and NiO.

Funding

This study was financially supported by National Natural Science Foundation of China (No. 21346011 and No. 21676209), the Key Project of Natural Science foundation Research Plan of Shaanxi Province (No. 2013JZ014), and the Key Scientific Research Project of Natural Science in Education Department of Shaanxi Province (No. 16JS055).

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.