Add like
Add dislike
Add to saved papers

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.

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)3 ]AgPb2 I7 [TM = Ni (1), Co (2) and Zn (3)], [Co(2,2'-bipy)3 ]CuPb2 Br7 (4) and [TM(2,2'-bipy)3 ]AgPb2 Br7 [TM = Ni (5) and Fe (6)], have been solvothermally prepared and structurally characterized. Compounds 1-3 feature 1D [AgPb2 I7 ]2- chains built from the condensation of [Ag2 I6 ] dimers and [Pb4 I14 ] tetramers, and compounds 4, 5 and 6 contain similar 1D [CuPb2 Br7 ]2- and [AgPb2 Br7 ]2- 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.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app