Anisotropic Surface Modulation of Pt Catalysts for Highly Reversible Li-O-2 Batteries: High Index Facet as a Critical Descriptor
- Authors
- Song, Kyeongse; Jung, Jaepyeong; Park, Mihui; Park, Hyeokjun; Kim, Hyung-Jin; Choi, Sang-Il; Yang, Junghoon; Kang, Kisuk; Han, Young-Kyu; Kang, Yong-Mook
- Issue Date
- Oct-2018
- Publisher
- AMER CHEMICAL SOC
- Keywords
- oxygen reduction reaction; oxygen evolution reaction; anisotropic surface; high index facet; electrocatalyst; Li-O-2 battery
- Citation
- ACS CATALYSIS, v.8, no.10, pp 9006 - 9015
- Pages
- 10
- Indexed
- SCIE
SCOPUS
- Journal Title
- ACS CATALYSIS
- Volume
- 8
- Number
- 10
- Start Page
- 9006
- End Page
- 9015
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/9035
- DOI
- 10.1021/acscatal.8b02172
- ISSN
- 2155-5435
- 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-O-2 batteries. Here, we succeeded in the preparation of a Pt catalyst with an anisotropic structure and demonstrated its high catalytic activity in nonaqueous Li-O-2 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 g(carbon)(-1), high rate performance, and stable cyclic retention up to 70 cycles with the capacity limited to 1000 mAh g(carbon)(-1) Furthermore, the anisotropic Pt catalyst exhibited high round-trip efficiency of similar to 87% with a low OER potential (3.1 V) at a current density of 200 mA g(carbon)(-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 lown terms of surface energy and O-binding energy.
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Collections - College of Engineering > Department of Energy and Materials Engineering > 1. Journal Articles

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