Rapid Activation of Platinum with Black Phosphorus for Efficient Hydrogen Evolution
Research output: Journal Publications and Reviews (RGC: 21, 22, 62) › 21_Publication in refereed journal › peer-review
Author(s)
Related Research Unit(s)
Detail(s)
Original language | English |
---|---|
Pages (from-to) | 19060-19066 |
Journal / Publication | Angewandte Chemie (International Edition) |
Volume | 58 |
Issue number | 52 |
Online published | 7 Oct 2019 |
Publication status | Published - 19 Dec 2019 |
Link(s)
Abstract
Modulation of the electronic structure of metal catalysts is an effective approach to optimize the electrocatalytic activity. Herein, we show a surprisingly strong activation effect of black phosphorus (BP) on platinum (Pt) catalysts to give greatly enhanced catalytic activity in the hydrogen evolution reaction (HER). The unique and negative binding energy between BP and Pt leads to spontaneous formation of Pt-P bonds producing strong synergistic ligand effects on the Pt nanoparticles. No Pt-P bonds are formed with red phosphorus which is another allotrope of P. By controlling the number of Pt-P bonds, 3.5-fold enhancement in the HER activity can be achieved from the BP-activated Pt catalyst and the activity is 6.1 times higher than that of the state-of-the-art commercial Pt/C catalyst. The BP-activated Pt catalyst exhibits a current density of 82.89 mA cm-2 with only 1 μg of Pt in 1 M KOH at an overpotential of 70 mV.
Research Area(s)
- activation effects, black phosphorus, electronic structure, hydrogen evolution reaction, platinum catalysts, OXYGEN REDUCTION REACTION, ACTIVE EDGE SITES, CATALYTIC-ACTIVITY, PARTICLE-SIZE, ENERGY, ELECTROCATALYSTS, SINGLE, NANOCLUSTERS
Citation Format(s)
Rapid Activation of Platinum with Black Phosphorus for Efficient Hydrogen Evolution. / Wang, Xin; Bai, Licheng; Lu, Jiang et al.
In: Angewandte Chemie (International Edition), Vol. 58, No. 52, 19.12.2019, p. 19060-19066.Research output: Journal Publications and Reviews (RGC: 21, 22, 62) › 21_Publication in refereed journal › peer-review