Repository logo
  • English
  • 中文
Log In
Have you forgotten your password?
  1. Home
  2. College of Engineering / 工學院
  3. Chemical Engineering / 化學工程學系
  4. Reconstructed vanadium carbide MXene supported cerium based trimetallic phosphide as an efficient electrocatalyst for alkaline water splitting
 
  • Details

Reconstructed vanadium carbide MXene supported cerium based trimetallic phosphide as an efficient electrocatalyst for alkaline water splitting

Journal
Chemical Engineering Journal
Journal Volume
515
Start Page
163888
ISSN
1385-8947
Date Issued
2025-07-01
Author(s)
Pan, Yu-Han
Perumal, Sakthivel
Sakthivel, Mani
Lin, Shan-Ni
Yeh, Min-Hsin
Wen-Yueh Yu  
KUO-CHUAN HO  
DOI
10.1016/j.cej.2025.163888
URI
https://www.scopus.com/record/display.uri?eid=2-s2.0-105005398006&origin=resultslist
https://scholars.lib.ntu.edu.tw/handle/123456789/730044
Abstract
Developing cost-effective bifunctional electrocatalysts with high activity and durability for alkaline water splitting is vital for scalable green hydrogen production. One promising approach involves designing effective catalyst supports that can strongly anchor active particles and tune their electronic properties and oxidation states. Among various candidates, the ease of modulating cerium oxidation states and the unique conductivity and surface chemistry of V2C MXene have drawn our attention. In this work, we present a simple strategy to prepare a novel cerium-based trimetallic phosphide combined with V2C MXene heterostructure electrocatalyst (CeCoFeP@MXene) for efficient alkaline water splitting. We systematically studied the influence of MXene content on the activity of CeCoFeP. The optimal catalyst required only 91 mV and 266 mV overpotential to achieve 10 mA cm−2 for HER and OER, respectively. The assembled electrolyzer needed just 1.63 V to deliver 10 mA cm−2 and exhibited excellent durability over 120 h. The in-situ grown CeCo-layered double hydroxide and Prussian blue on MXene offered good conductivity, structural stability, and a porous, high-surface-area architecture. The multiple oxidation states of vanadium facilitated electron transfer, while the Ce3+/Ce4+ redox pair and transition metals optimized intermediate adsorption. Phosphorus doping further tuned the metal sites’ electronic structure, promoting an ensemble effect and enhanced charge transfer. Notably, in-situ generated phosphate-containing metal hydroxides and oxyhydroxides acted as the true active sites for HER and OER. This study highlights the synergistic effects of Ce–Co–Fe trimetallic phosphides, phosphate stabilization, and a conductive MXene framework, laying the foundation for next-generation MXene-based electrocatalyst designs.
Subjects
Cerium cobalt iron phosphide
Electrocatalytic water splitting
Hydrogen evolution reaction
Layered double hydroxides
MXene
Oxygen evolution reaction
Prussian blue analogues
SDGs

[SDGs]SDG6

[SDGs]SDG7

Publisher
Elsevier BV
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