2017
DOI: 10.1039/c7ra04041e
|View full text |Cite
|
Sign up to set email alerts
|

Controlled synthesis of Sn-based oxides via a hydrothermal method and their visible light photocatalytic performances

Abstract: Controlled synthesize of Sn-oxides was achieved via a facile hydrothermal method with SnCl2 as precursor. A visible light photocatalytic activity of SnO2 can be induced by doping with Sn2+ or coupling with SnO.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

4
44
0

Year Published

2018
2018
2024
2024

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 72 publications
(49 citation statements)
references
References 61 publications
4
44
0
Order By: Relevance
“…Figure 5 b reports the DR spectra of SnO 2 _C with respect to a commercial SnO 2 powder: both of the samples exhibit absorption curves that are characteristic of semiconductor materials; however, the position of the absorption edge varies greatly between the two samples. While the commercial oxide shows a light absorption only in the UV region, in good agreement with literature band gap values for SnO 2 [ 18 , 19 ], the SnO 2 _C sample presents a red-shifted absorption edge that leads to a marked visible light absorption up to ca. 500 nm.…”
Section: Resultssupporting
confidence: 88%
See 1 more Smart Citation
“…Figure 5 b reports the DR spectra of SnO 2 _C with respect to a commercial SnO 2 powder: both of the samples exhibit absorption curves that are characteristic of semiconductor materials; however, the position of the absorption edge varies greatly between the two samples. While the commercial oxide shows a light absorption only in the UV region, in good agreement with literature band gap values for SnO 2 [ 18 , 19 ], the SnO 2 _C sample presents a red-shifted absorption edge that leads to a marked visible light absorption up to ca. 500 nm.…”
Section: Resultssupporting
confidence: 88%
“…However, the doping of SnO 2 by Sn 2+ has been recently reported to induce visible light activity in the semiconductor. Additionally, in this case, reducing conditions are required during the synthesis, leading to yellowish powders [ 18 , 19 ].…”
Section: Introductionmentioning
confidence: 99%
“…These molecules are possibly regarded to the surface hydroxylation of SnO 2 , coordinated as Sn(OH) 4 , as a remnant of polycondensation step during coprecitation [21] . These OH groups undergo oxidation by the holes ( h + ) formed in the catalyst valence band when under UV, leading to the formation of hydroxyl radicals (⋅OH) with high oxidizing power (−SnOH+ h + ↔−Sn 2+ +⋅OH) [22] .…”
Section: Figurementioning
confidence: 99%
“…Adsorbed OH‐ groups on the catalyst surface this potential to 1.6 V vs NHE, favoring the radical formation [3] . Therefore, the attack of these radicals leads to oxidation reactions, indicating that the indirect photodegradation mechanism plays an important role in the photoactivity of the synthesized SnO 2 samples [21,23] …”
Section: Figurementioning
confidence: 99%
“…The maximal photocurrent density of Sn-2 is over 200 μA cm −2 , about four times larger than that of sample Sn-1. This value is much larger than ever reported self-powered photodetectors (SPPDs) [28], 75 μA cm −2 in SnO x [29] and 60 μA cm −2 in Sn 2+ -SnO 2 composites [30]. To investigate the changes of the electrochemical specific surface area, the difference in current density variation plotted against scan rate is shown in figure 4(b).…”
Section: Resultsmentioning
confidence: 77%