Add like
Add dislike
Add to saved papers

Al-Doped CoP nanoarray: a durable water-splitting electrocatalyst with superhigh activity.

Nanoscale 2017 April 7
The scalable production of hydrogen fuel through electrochemical water reduction needs efficient Earth-abundant electrocatalysts to make the whole water-splitting process more energy efficient. In this Article, we report that an Al-doped CoP nanoarray on carbon cloth (Al-CoP/CC) behaves as a durable hydrogen evolution electrocatalyst with superhigh activity in 0.5 M H2 SO4 . It demands a pretty low overpotential of 23 mV to drive a geometrical catalytic current density of 10 mA cm-2 , outperforming all reported non-precious metal catalysts. Density functional theory calculations reveal that Al-CoP has a more thermo-neutral hydrogen adsorption free energy than CoP. Notably, this Al-CoP/CC is also superior in activity and durability as a bifunctional catalyst for alkaline water electrolysis, and its two-electrode water electrolyser delivers 10 mA cm-2 water-splitting current at a cell voltage of 1.56 V in 1.0 M KOH. This work offers us an attractive cost-effective catalyst electrode in water-splitting devices for large-scale production of hydrogen fuels.

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