Electrodeposited Cobalt-Phosphorous-Derived Films as Competent Bifunctional Catalysts for Overall Water Splitting

One of the challenges to realize large‐scale water splitting is the lack of active and low‐cost electrocatalysts for its two half reactions: H2 and O2 evolution reactions (HER and OER). Herein, we report that cobalt‐phosphorous‐derived films (Co‐P) can act as bifunctional catalysts for overall water...

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Published in:Angewandte Chemie International Edition Vol. 54; no. 21; pp. 6251 - 6254
Main Authors: Jiang, Nan, You, Bo, Sheng, Meili, Sun, Yujie
Format: Journal Article
Language:English
Published: Weinheim WILEY-VCH Verlag 18-05-2015
WILEY‐VCH Verlag
Wiley Subscription Services, Inc
Edition:International ed. in English
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Summary:One of the challenges to realize large‐scale water splitting is the lack of active and low‐cost electrocatalysts for its two half reactions: H2 and O2 evolution reactions (HER and OER). Herein, we report that cobalt‐phosphorous‐derived films (Co‐P) can act as bifunctional catalysts for overall water splitting. The as‐prepared Co‐P films exhibited remarkable catalytic performance for both HER and OER in alkaline media, with a current density of 10 mA cm−2 at overpotentials of −94 mV for HER and 345 mV for OER and Tafel slopes of 42 and 47 mV/dec, respectively. They can be employed as catalysts on both anode and cathode for overall water splitting with 100 % Faradaic efficiency, rivalling the integrated performance of Pt and IrO2. The major composition of the as‐prepared and post‐HER films are metallic cobalt and cobalt phosphide, which partially evolved to cobalt oxide during OER. Split and polished: Electrodeposited cobalt‐phosphorous‐derived films (Co‐P) can act as superior bifunctional catalysts for overall water splitting. When employed as catalysts on both the anode and cathode for water electrolysis, the Co‐P/Co‐P catalyst couple can rival the integrated performance of IrO2 and Pt in alkaline media. Such a bifunctional Co‐P film is a promising catalyst candidate for overall water‐splitting electrolysis.
Bibliography:ark:/67375/WNG-HN0D036D-9
ArticleID:ANIE201501616
Utah State University
State of Utah
istex:C4D374BD76B2AFF482C39B7B4FDBFB3A309ECAF9
N.J. acknowledges the Governor's Energy Leadership Scholars Grant of the State of Utah. This work was supported by Utah State University and the Principle Energy Issues Program of the State of Utah. We acknowledge the support from the Microscopy Core Facility at Utah State University for the SEM work. A provisional patent application by Y.S., N.J., and B.Y., has been filed for the intellectual property described in this communication. M.S. declares no competing financial interest.
N.J. acknowledges the Governor’s Energy Leadership Scholars Grant of the State of Utah. This work was supported by Utah State University and the Principle Energy Issues Program of the State of Utah. We acknowledge the support from the Microscopy Core Facility at Utah State University for the SEM work. A provisional patent application by Y.S., N.J., and B.Y., has been filed for the intellectual property described in this communication. M.S. declares no competing financial interest.
These authors contributed equally to this work.
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SourceType-Scholarly Journals-1
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ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201501616