Repository logo
  • English
  • 中文
Log In
Have you forgotten your password?
  1. Home
  2. College of Science / 理學院
  3. Chemistry / 化學系
  4. Strong Catalyst-Support Interactions in Electrochemical Oxygen Evolution on Ni-Fe Layered Double Hydroxide
 
  • Details

Strong Catalyst-Support Interactions in Electrochemical Oxygen Evolution on Ni-Fe Layered Double Hydroxide

Journal
ACS Energy Letters
Journal Volume
5
Journal Issue
10
Pages
3185-3194
Date Issued
2020
Author(s)
Gu, Haoyang et al.
HAO MING CHEN  
DOI
10.1021/acsenergylett.0c01584
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85094903453&doi=10.1021%2facsenergylett.0c01584&partnerID=40&md5=9d6c6a6fe234c459bb70ef6e1eafba88
https://scholars.lib.ntu.edu.tw/handle/123456789/575722
Abstract
Strong catalyst-support interaction plays a key role in heterogeneous catalysis, as has been well-documented in high-temperature gas-phase chemistry, such as the water gas shift reaction. Insight into how catalyst-support interactions can be exploited to optimize the catalytic activity in aqueous electrochemistry, however, is still lacking. In this work, we show the rationally designed electrocatalyst/support interface can greatly impact the overall electrocatalytic activity of Ni-Fe layered double hydroxide (NiFeLDH) in water oxidation. In particular, the use of Co as a non-noble metal support greatly improves the activity of NiFeLDH 10-fold compared to the traditional electrocatalytic supports such as fluorine-/indium-doped tin oxide (FTO/ITO) and glassy carbon. We attribute the activity enhancement of NiFeLDH/Co to the in situ formation of a porous NiFeCoOxHy layer via Co incorporation, which dramatically promotes the redox chemistry of metal centers on the outer surface and enhances the electrical conductivity of the catalyst over 2 orders of magnitude. This new discovery highlights the importance of a rationally designed electrocatalyst/support interface and offers a new paradigm for designing and developing highly active electrocatalytic systems via marrying catalyst and support and creating synergy. Copyright ? 2020 American Chemical Society.
Subjects
Binary alloys; Catalysis; Catalyst activity; Chemical shift; Cobalt; Electrocatalysts; Iron compounds; Nickel compounds; Oxygen; Phase interfaces; Precious metals; Tin oxides; Water gas shift; Activity enhancement; Aqueous electrochemistry; Electrical conductivity; Electrocatalytic activity; Electrocatalytic system; Electrochemical oxygen; Layered double hydroxides; Water gas shift (WGS) reaction; Catalyst supports
SDGs

[SDGs]SDG6

[SDGs]SDG7

Type
journal article

臺大位居世界頂尖大學之列,為永久珍藏及向國際展現本校豐碩的研究成果及學術能量,圖書館整合機構典藏(NTUR)與學術庫(AH)不同功能平台,成為臺大學術典藏NTU scholars。期能整合研究能量、促進交流合作、保存學術產出、推廣研究成果。

To permanently archive and promote researcher profiles and scholarly works, Library integrates the services of “NTU Repository” with “Academic Hub” to form NTU Scholars.

總館學科館員 (Main Library)
醫學圖書館學科館員 (Medical Library)
社會科學院辜振甫紀念圖書館學科館員 (Social Sciences Library)

開放取用是從使用者角度提升資訊取用性的社會運動,應用在學術研究上是透過將研究著作公開供使用者自由取閱,以促進學術傳播及因應期刊訂購費用逐年攀升。同時可加速研究發展、提升研究影響力,NTU Scholars即為本校的開放取用典藏(OA Archive)平台。(點選深入了解OA)

  • 請確認所上傳的全文是原創的內容,若該文件包含部分內容的版權非匯入者所有,或由第三方贊助與合作完成,請確認該版權所有者及第三方同意提供此授權。
    Please represent that the submission is your original work, and that you have the right to grant the rights to upload.
  • 若欲上傳已出版的全文電子檔,可使用Open policy finder網站查詢,以確認出版單位之版權政策。
    Please use Open policy finder to find a summary of permissions that are normally given as part of each publisher's copyright transfer agreement.
  • 網站簡介 (Quickstart Guide)
  • 使用手冊 (Instruction Manual)
  • 線上預約服務 (Booking Service)
  • 方案一:臺灣大學計算機中心帳號登入
    (With C&INC Email Account)
  • 方案二:ORCID帳號登入 (With ORCID)
  • 方案一:定期更新ORCID者,以ID匯入 (Search for identifier (ORCID))
  • 方案二:自行建檔 (Default mode Submission)
  • 方案三:學科館員協助匯入 (Email worklist to subject librarians)

Built with DSpace-CRIS software - Extension maintained and optimized by 4Science