Abstract
The surface structure of solid catalysts has been regarded as a critical descriptor for determining the catalytic activities in various applications. However, structure-dependent catalytic activities have been rarely understood for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) within Li-O2 batteries. Here, we succeeded in the preparation of a Pt catalyst with an anisotropic structure and demonstrated its high catalytic activity in nonaqueous Li-O2 batteries. The cathode incorporating Pt exposed with high-index {411} facets showed greatly enhanced ORR and OER performance in comparison to commercial Pt/C cathode. The anisotropic Pt catalyst improved ORR activity with a large capacity of 12 985 mAh gcarbon -1, high rate performance, and stable cyclic retention up to 70 cycles with the capacity limited to 1000 mAh gcarbon -1. Furthermore, the anisotropic Pt catalyst exhibited high round-trip efficiency of ∼87% with a low OER potential (3.1 V) at a current density of 200 mA gcarbon -1. Our first-principles calculations revealed that the high-index facets, which contain step edge, kink, and ledge sites, are significantly more reactive than the low-index facets in terms of surface energy and O-binding energy.
Original language | English |
---|---|
Pages (from-to) | 9006-9015 |
Number of pages | 10 |
Journal | ACS Catalysis |
Volume | 8 |
Issue number | 10 |
DOIs | |
State | Published - 5 Oct 2018 |