4.6 Article

Partial Dehydration in Hydrated Tungsten Oxide Nanoplates Leads to Excellent and Robust Bifunctional Oxygen Reduction and Hydrogen Evolution Reactions in Acidic Media

期刊

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 8, 期 25, 页码 9507-9518

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.0c02502

关键词

electrocatalysts; bifunctional catalysts; hydrogen evolution reaction; oxygen reduction reaction; hydrated tungsten oxide

资金

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Science, ICT & Future Planning [2018R1D1A1A02085938]
  2. Human Resources Program in Energy Technology of the Korea Institute of Energy Technology Evaluation and Planning (KETEP) from Ministry of Trade, Industry & Energy, Republic of Korea [20194010201890]
  3. Ministry of Trade, Industry & Energy, Republic of Korea [20194010201890]
  4. National Research Foundation of Korea [2018R1D1A1A02085938] 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

The development of efficient, low-cost, and stable bifunctional catalysts is necessary for renewable energy storage and conversion, but it remains a challenge. Herein, we first report a novel strategy to develop WO3 center dot nH(2)O (n = 0.33, 1.00, or 2.00) as a highly active and durable bifunctional catalyst for the oxygen reduction reaction (ORR) and hydrogen evolution reaction (HER) in acidic media by controlling the degree of hydration. The content of solvated water molecules in WO3 center dot nH(2)O can be precisely controlled by selectively using ethylenediaminetetraacetic acid or DL-malic acid for room-temperature precipitation synthesis. Structural flexibility associated with water solvation in WO3 center dot nH(2)O leads to excellent bifunctional catalytic activity as well as durability in acidic media. The bifunctional catalytic mechanism of WO3 center dot nH(2)O is mainly attributed to spontaneous partial dehydration during electrolysis, resulting in simultaneous formation of active phases for HER and ORR, respectively.

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