Tailoring the active surface sites of ZnO nanorods on the glass substrate for photocatalytic activity enhancement

Liszulfah Roza, Vivi Fauzia, Mohd Yusri Abd Rahman

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

The urgent need for inexpensive, efficient, ease in use and reusable photocatalyst has attracted the attention of many researchers. Here, the photocatalyst ZnO nanorods were synthesized with a simple, low cost and rapid ultrasonic spray pyrolysis method and then grown with a hydrothermal method for 2, 4, 6 and 8 h. The ZnO nanorods grown for 6 h shows the highest photocatalytic efficiency although do not have the largest surface area. This is probably due to its surface is dominated by (002) facets as indicated by the highest texture coefficient (TC) value. The (002) polar facets consisting of a positive Zn-terminated (002) facets and a negative O-terminated (00-2) facets may play an important role in more efficient UV absorption and photogenerated charges separation. Moreover, the highest crystallite size as shown in XRD result provide pathways for electrons and holes for redox reactions on the surface of ZnO nanorods. The synthesized ZnO nanorods also contain high concentration of oxygen interstitial as a source of holes that react with the OH− ions that easily adsorbed on (002) facets.

Original languageEnglish
Pages (from-to)117-124
Number of pages8
JournalSurfaces and Interfaces
Volume15
DOIs
Publication statusPublished - 1 Jun 2019

Fingerprint

Nanorods
Glass
Substrates
Photocatalysts
Spray pyrolysis
Redox reactions
Crystallite size
Textures
Ultrasonics
Ions
Oxygen
Electrons
Costs

Keywords

  • Facets
  • Nanorods
  • Photocatalysts
  • Ultrasonic spray pyrolysis
  • ZnO

ASJC Scopus subject areas

  • Surfaces, Coatings and Films

Cite this

Tailoring the active surface sites of ZnO nanorods on the glass substrate for photocatalytic activity enhancement. / Roza, Liszulfah; Fauzia, Vivi; Abd Rahman, Mohd Yusri.

In: Surfaces and Interfaces, Vol. 15, 01.06.2019, p. 117-124.

Research output: Contribution to journalArticle

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