Journal Article
Research Support, Non-U.S. Gov't
Add like
Add dislike
Add to saved papers

Spontaneous formation of Cu2O-g-C3N4 core-shell nanowires for photocurrent and humidity responses.

Nanoscale 2015 June 8
The assembly of low dimensional g-C3N4 structures in a geometrically well-defined fashion and the complexation of g-C3N4 with other materials are the main approaches to construct fancy structures for special functions. While high temperature was often indispensable for the preparation process, the realization of room temperature assembly of the low dimensional g-C3N4 and the preparation of g-C3N4-based semiconductor composites will provide many additional advantages for new functional materials and applications. Herein, the unique cuprous oxide (Cu2O)-graphitic carbon nitrides (g-C3N4) core-shell nanowires with highly hierarchical sharp edges on the surface have been prepared by a spontaneous reduction and assembly approach based on oxygen-functional g-C3N4 (O-functional g-C3N4) at room temperature. Combined with the hybrid effect of Cu2O with g-C3N4, such hierarchical Cu2O-g-C3N4 core-shell nanowires possess sensitivity to humidity and photocurrent response.

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