Abstract
Ultrathin two-dimensional (2D) materials have attracted considerable attention for their unique physicochemical properties and promising applications; however, preparation of freestanding ultrathin 2D noble metal remains a significant challenge. Here, for the first time, we report use of a wet-chemical method to synthesize partially hydroxylated ultrathin Ir nanosheets (Ir-NSs) of only five to six atomic layers' thickness. Detailed analysis indicates that the growth confinement effect of carbon monoxide and the partially hydroxylated surface play a critical role in formation of the ultrathin structure. The ultrathin Ir-NSs exhibit excellent performance for both the hydrogen evolution reaction and oxygen evolution reaction in a wide pH range, outperforming the state-of-the-art Pt/C and IrO2, respectively. Density-functional theory calculations reveal that the partial hydroxylation not only enhances the surface electron transfer between Ir-sites and intermediate O-species, but also guarantees efficient initial activation of bond cleavage of H-O-H for first-step H2O splitting.This, ultimately, breaks through barriers to full water splitting, with efficient electron transfer essentially maintained.
Original language | English |
---|---|
Pages (from-to) | 1340-1348 |
Number of pages | 9 |
Journal | National Science Review |
Volume | 7 |
Issue number | 8 |
DOIs | |
Publication status | Published - 1 Aug 2020 |
Keywords
- 2D material
- Hydroxylation
- Iridium
- Nanosheet
- Overall water splitting
ASJC Scopus subject areas
- General