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Comparison studies of hybrid lead halide [MPb 2 X 7 ] 2- (M = Cu, Ag; X = Br, I) chains: band structures and visible light driven photocatalytic properties.

Authors :
Yue CY
Lei XW
Lu XX
Li Y
Wei JC
Wang W
Yin YD
Wang N
Source :
Dalton transactions (Cambridge, England : 2003) [Dalton Trans] 2017 Jul 18; Vol. 46 (28), pp. 9235-9244.
Publication Year :
2017

Abstract

By using transition-metal (TM) complex cationic dyes as structure-directing agents and photosensitizers, a series of inorganic-organic hybrid metal halides, namely, [TM(2,2'-bipy) <subscript>3</subscript> ]AgPb <subscript>2</subscript> I <subscript>7</subscript> [TM = Ni (1), Co (2) and Zn (3)], [Co(2,2'-bipy) <subscript>3</subscript> ]CuPb <subscript>2</subscript> Br <subscript>7</subscript> (4) and [TM(2,2'-bipy) <subscript>3</subscript> ]AgPb <subscript>2</subscript> Br <subscript>7</subscript> [TM = Ni (5) and Fe (6)], have been solvothermally prepared and structurally characterized. Compounds 1-3 feature 1D [AgPb <subscript>2</subscript> I <subscript>7</subscript> ] <superscript>2-</superscript> chains built from the condensation of [Ag <subscript>2</subscript> I <subscript>6</subscript> ] dimers and [Pb <subscript>4</subscript> I <subscript>14</subscript> ] tetramers, and compounds 4, 5 and 6 contain similar 1D [CuPb <subscript>2</subscript> Br <subscript>7</subscript> ] <superscript>2-</superscript> and [AgPb <subscript>2</subscript> Br <subscript>7</subscript> ] <superscript>2-</superscript> chains, respectively. UV-Vis diffuse reflectance measurements reveal narrow band gaps of 1.75-2.18 eV for compounds 1-6, which lead to efficient and stable photocatalytic degradation activities over organic pollutants under visible light irradiation. Among the title compounds, sample 5 shows the highest photocatalytic degradation activity. The possible mechanism for their stable photocatalytic activities is proposed based on the experimental and theoretical studies.

Details

Language :
English
ISSN :
1477-9234
Volume :
46
Issue :
28
Database :
MEDLINE
Journal :
Dalton transactions (Cambridge, England : 2003)
Publication Type :
Academic Journal
Accession number :
28682377
Full Text :
https://doi.org/10.1039/c7dt00820a