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Synergistically Tuning Graphene Layer and Active Sites for Flexible Zn–Air Batteries
Fewer layer graphene principally has a higher surface area to support more catalytic sites for energy conversion, but it is still challenging to synthesize monolayer graphene without oxidation from graphite at a low cost. Here, a method for synergistically thinning graphene layers and constructing c...
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Published in: | Advanced functional materials 2024-07 |
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Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Fewer layer graphene principally has a higher surface area to support more catalytic sites for energy conversion, but it is still challenging to synthesize monolayer graphene without oxidation from graphite at a low cost. Here, a method for synergistically thinning graphene layers and constructing catalytic sites to create a superior bifunctional oxygen catalyst through vapor intercalation of multi‐layer graphene or its derivatives is described. The synthesized small sheet sizes of 1–2 layer graphene‐supported FeN 4 and FeCo active sites exhibit superior reversible activity of oxygen reduction and evolution reactions with a low overall overpotential of 0.648 V. The sheet‐shaped catalyst is further used to fabricate flexible soft‐packed and wearable cable‐type quasi‐solid‐state zinc–air batteries, achieving high performances (>188 mW cm −2 , >450 cycles) and enabling smartphone charging. DFT calculations reveal that fewer layer graphene coupled with atomic FeN 4 and alloy FeCo sites enables lower Gibbs free energy for favorable OOH* intermediate adsorption/desorption benefiting superior oxygen redox process. This study introduces a strategy for scalable synthesis of 1–2 layer graphene from cheap microcrystalline graphite minerals for wearable and durable energy devices. |
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ISSN: | 1616-301X 1616-3028 |
DOI: | 10.1002/adfm.202411935 |