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Single-Atom Pt Anchored on Oxygen Vacancy of Monolayer Ti3C2Tx for Superior Hydrogen Evolution.
Zhang, Jiangjiang; Wang, Erqing; Cui, Shiqiang; Yang, Shubin; Zou, Xiaolong; Gong, Yongji.
  • Zhang J; School of Materials Science and Engineering, Beihang University, Beijing 100191, China.
  • Wang E; Shenzhen Geim Graphene Center, Tsinghua-Berkeley Shenzhen Institute and Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China.
  • Cui S; College of Science, Hebei University of Science and Technology, Shijiazhuang 050018, China.
  • Yang S; School of Materials Science and Engineering, Beihang University, Beijing 100191, China.
  • Zou X; Shenzhen Geim Graphene Center, Tsinghua-Berkeley Shenzhen Institute and Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China.
  • Gong Y; School of Materials Science and Engineering, Beihang University, Beijing 100191, China.
Nano Lett ; 22(3): 1398-1405, 2022 Feb 09.
Article en En | MEDLINE | ID: mdl-35041435
Two-dimensional (2D) MXene-loaded single-atom (SA) catalysts have drawn increasing attention. SAs immobilized on oxygen vacancies (OV) of MXene are predicted to have excellent catalytic performance; however, they have not yet been realized experimentally. Here Pt SAs immobilized on the OV of monolayer Ti3C2Tx flakes are constructed by a rapid thermal shock technique under a H2 atmosphere. The resultant Ti3C2Tx-PtSA catalyst exhibits excellent hydrogen evolution reaction (HER) performance, including a small overpotential of 38 mV at 10 mA cm-2, a high mass activity of 23.21 A mgPt-1, and a large turnover frequency of 23.45 s-1 at an overpotential of 100 mV. Furthermore, density functional theory calculations demonstrate that anchoring the Pt SA on the OV of Ti3C2Tx helps to decrease the binding energy and the hybridization strength between H atoms and the supports, contributing to rapid hydrogen adsorption-desorption kinetics and high activity for the HER.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2022 Tipo del documento: Article