Add like
Add dislike
Add to saved papers

Dual Z-scheme TCN/ZnS/ ZnIn 2 S 4 with efficient separation for photocatalytic nitrogen fixation.

The development of an efficient catalyst that can use solar energy for NH3 production is of great significance in solving the environmental and energy crisis caused by the traditional ammonia synthesis process. In this work, a dual Z-scheme tubular carbon nitride/zinc sulfide/zinc indium sulfide ternary composited photocatalyst (TCN/ZnS/ZnIn2 S4 ) with excellent nitrogen photofixation performance under visible light was prepared by self-assembly and hydrothermal methods. The crystal structure studies confirmed that tubular carbon nitride (TCN) had more active sites that could promote N2 adsorption. The photochemical studies proved that the double charge transfer channel provided by the dual Z-scheme heterojunction could improve the efficiency of electron-hole separation and achieve excellent photocatalytic nitrogen fixation. The ammonia production rate of the TCN/ZnS/ZnIn2 S4 catalyst was up to 136.56 μmol/L, and it also has good stability and reusability. This work provides new insight into the development of Z-scheme heterojunction photocatalysts with green and efficient nitrogen fixation.

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