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Facile synthesis of TiO 2 /Ag 3 PO 4 composites with co-exposed high-energy facets for efficient photodegradation of rhodamine B solution under visible light irradiation.

Authors :
Du YE
Li W
Bai Y
Huangfu Z
Wang W
Chai R
Chen C
Yang X
Feng Q
Source :
RSC advances [RSC Adv] 2020 Jun 26; Vol. 10 (41), pp. 24555-24569. Date of Electronic Publication: 2020 Jun 26 (Print Publication: 2020).
Publication Year :
2020

Abstract

In this study, TiO <subscript>2</subscript> /Ag <subscript>3</subscript> PO <subscript>4</subscript> composites based on anatase TiO <subscript>2</subscript> nanocrystals with co-exposed {101}, {010}/{100}, {001} and [111]-facets and Ag <subscript>3</subscript> PO <subscript>4</subscript> microcrystals with irregular and cubic-like polyhedron morphologies were successfully synthesized by combining hydrothermal and ion-exchange methods. The anatase TiO <subscript>2</subscript> nanocrystals with different high-energy facets were controllably prepared via hydrothermal treatment of the exfoliated [Ti <subscript>4</subscript> O <subscript>9</subscript> ] <superscript>2-</superscript> /[Ti <subscript>2</subscript> O <subscript>5</subscript> ] <superscript>2-</superscript> nanosheet solutions at desired pH values. The Ag <subscript>3</subscript> PO <subscript>4</subscript> microcrystal with different morphologies was prepared via the ion-exchange method in the presence of AgNO <subscript>3</subscript> and NH <subscript>4</subscript> H <subscript>2</subscript> PO <subscript>4</subscript> at room temperature, which was used as a substrate to load the as-prepared anatase TiO <subscript>2</subscript> nanocrystals on its surface and to form TiO <subscript>2</subscript> /Ag <subscript>3</subscript> PO <subscript>4</subscript> heterostructures. The apparent rate constant of the pH 3.5-TiO <subscript>2</subscript> /Ag <subscript>3</subscript> PO <subscript>4</subscript> composite was the highest at 12.0 × 10 <superscript>-3</superscript> min <superscript>-1</superscript> , which was approximately 1.1, 1.2, 1.4, 1.6, 13.3, and 24.0 fold higher than that of pH 0.5-TiO <subscript>2</subscript> /Ag <subscript>3</subscript> PO <subscript>4</subscript> (10.5 × 10 <superscript>-3</superscript> min <superscript>-1</superscript> ), pH 7.5-TiO <subscript>2</subscript> /Ag <subscript>3</subscript> PO <subscript>4</subscript> (10.2 × 10 <superscript>-3</superscript> min <superscript>-1</superscript> ), pH 11.5-TiO <subscript>2</subscript> (8.8 × 10 <superscript>-3</superscript> min <superscript>-1</superscript> ), Ag <subscript>3</subscript> PO <subscript>4</subscript> (7.7 × 10 <superscript>-3</superscript> min <superscript>-1</superscript> ), blank sample (0.9 × 10 <superscript>-3</superscript> min <superscript>-1</superscript> ), and the commercial TiO <subscript>2</subscript> (0.5 × 10 <superscript>-3</superscript> min <superscript>-1</superscript> ), respectively. The pH 3.5-TiO <subscript>2</subscript> /Ag <subscript>3</subscript> PO <subscript>4</subscript> composite exhibited the highest visible-light photocatalytic activity which can be attributed to the synergistic effects of its heterostructure, relatively small crystal size, large specific surface area, good crystallinity, and co-exposed high-energy {001} and [111]-facets. The as-prepared TiO <subscript>2</subscript> /Ag <subscript>3</subscript> PO <subscript>4</subscript> composites still exhibited good photocatalytic activity after three successive experimental runs, indicating that they had remarkable stability. This study provides a new way for the preparation of TiO <subscript>2</subscript> /Ag <subscript>3</subscript> PO <subscript>4</subscript> composite semiconductor photocatalysts with high energy crystal surfaces and high photocatalytic activity.<br />Competing Interests: The authors declare no conflict of interest.<br /> (This journal is © The Royal Society of Chemistry.)

Details

Language :
English
ISSN :
2046-2069
Volume :
10
Issue :
41
Database :
MEDLINE
Journal :
RSC advances
Publication Type :
Academic Journal
Accession number :
35516206
Full Text :
https://doi.org/10.1039/d0ra04183a