4.8 Article

In Situ Transformation of Hydrogen-Evolving CoP Nanoparticles: Toward Efficient Oxygen Evolution Catalysts Bearing Dispersed Morphologies with Co-oxo/hydroxo Molecular Units

期刊

ACS CATALYSIS
卷 5, 期 7, 页码 4066-4074

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.5b00349

关键词

water splitting; oxygen evolution; hydrogen evolution; cobalt phosphide nanoparticle; in situ transformation

资金

  1. Global Frontier R Program on Center for Multiscale Energy System [NRF-2012M3A6A7054283]
  2. NRF grant - MSIP [2014R1A2A2A04003865]
  3. KIST Institutional Program of Korea Institute of Science and Technology (KIST)
  4. New and Renewable Energy Core Technology Program of KETEP grant - MOTIE [20133030011320]
  5. KCRC grant - MSIP [2014M1A8A1049349]
  6. Korea Evaluation Institute of Industrial Technology (KEIT) [20133030011320] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  7. National Research Foundation of Korea [2011-0031571, 2014R1A2A2A04003865] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Reported herein is elucidation of a novel Co-based oxygen evolution catalyst generated in situ from cobalt phosphide (CoP) nanoparticles. The present CoP nanoparticles, efficient alkaline hydrogen-evolving materials at the cathode, are revealed to experience unique metamorphosis upon anodic potential cycling in an alkaline electrolyte, engendering efficient and robust catalytic environments toward the oxygen evolution reaction (OER). Our extensive ex situ characterization shows that the transformed catalyst bears porous and nanoweb-like dispersed morphologies along with unique microscopic environments mainly consisting of discrete cobalt-oxo/hydroxo molecular units within a phosphate-enriched amorphous network. Outstanding OER efficiency is achievable with the activated catalyst, which is favorably comparable to even a precious iridium catalyst. A more remarkable feature is its outstanding long-term stability, superior to iridium and conventional cobalt oxide-based materials. Twelve-hour bulk electrolysis continuously operating at high current density is completely tolerable with the present catalyst.

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