| Literature DB >> 26235276 |
Liang Liang1, Hao Cheng2, Fengcai Lei1, Jun Han3, Shan Gao1, Chengming Wang1, Yongfu Sun4, Shaista Qamar1, Shiqiang Wei5, Yi Xie6.
Abstract
The bottleneck in water electrolysis lies in the kinetically sluggish oxygen evolution reaction (OER). Herein, conceptually new metallic non-metal atomic layers are proposed to overcome this drawback. Metallic single-unit-cell CoSe2 sheets with an orthorhombic phase are synthesized by thermally exfoliating a lamellar CoSe2 -DETA hybrid. The metallic character of orthorhombic CoSe2 atomic layers, verified by DFT calculations and temperature-dependent resistivities, allows fast oxygen evolution kinetics with a lowered overpotential of 0.27 V. The single-unit-cell thickness means 66.7 % of the Co(2+) ions are exposed on the surface and serve as the catalytically active sites. The lowered Co(2+) coordination number down to 1.3 and 2.6, gives a lower Tafel slope of 64 mV dec(-1) and higher turnover frequency of 745 h(-1) . Thus, the single-unit-cell CoSe2 sheets have around 2 and 4.5 times higher catalytic activity compared with the lamellar CoSe2 -DETA hybrid and bulk CoSe2 .Entities:
Keywords: atomic layers; cobalt diselenide; electrocatalysis; water splitting
Year: 2015 PMID: 26235276 DOI: 10.1002/anie.201505245
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336