Add like
Add dislike
Add to saved papers

Water Oxidation Electrocatalysis with a Cobalt-Borate-Based Hybrid System under Neutral Conditions.

The development of new water oxidation electrocatalysts that are both stable and efficient, particularly in neutral conditions, holds great promise for overall water splitting. In this study, the electrocatalytic water oxidation performance of a new cobalt-based catalyst, Co3 (BO3 )2 , with a Kotoite-type crystal structure is investigated under neutral conditions. The catalyst is also hybridized with CNTs to enhance its electrocatalytic properties. A remarkable increase in catalytic current along with a significant shift in the onset overpotential is observed in Co3 (BO3 )2 @CNT. Additionally, CNT addition also greatly influences the surface concentration of the catalyst: 12.7 nmol cm-2 for Co3 (BO3 )2 @CNT compared with 3.9 nmol cm-2 for Co3 (BO3 )2 . Co3 (BO3 )2 @CNT demands overpotentials of 303 and 487 mV to attain current densities of 1 and 10 mA cm-2 , respectively, at pH 7. Electrochemical and characterization studies performed over varying pH conditions reveal that the catalyst retains its stability over a pH range of 3-14. Multi-reference quantum chemical calculations are performed to study the nature of the active cobalt sites and the effect of boron atoms on the activity of the cobalt ions.

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