4.8 Article

Graphitization with Suppressed Carbon Loss for High-Quality Reduced Graphene Oxide

Journal

ACS NANO
Volume 15, Issue 7, Pages 11655-11666

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.1c02178

Keywords

reduced graphene oxide; Fischer-Tropsch reaction; delafossite; carbon loss; graphitization

Funding

  1. NRF [NRF-2019M1A2A2065612, NRF-2020R1A2C2014050]
  2. Samsung Electronics Co., Ltd.
  3. Ministry of Science & ICT (MSIT), Republic of Korea [IBS-R019-D1-2021-A00] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The in situ deoxidation and graphitization mechanism using a Fischer-Tropsch reaction catalyst allowed for high-quality reduced graphene oxide sheets under low temperature conditions. The process suppressed carbon loss in graphene oxide sheets, resulting in near-perfect graphene with lower electrical resistance and acting as an efficient catalyst for hydrogen and oxygen evolution reactions.
An efficient reduction method to obtain high-quality graphene sheets from mass-producible graphene oxide is highly desirable for practical applications. Here, we report an in situ deoxidation and graphitization mechanism for graphene oxide that allows for high-quality reduced graphene oxide sheets under the low temperature condition (<300 degrees C) by utilizing a well-known Fischer-Tropsch reaction catalyst (CuFeO2). By applying modified FTR conditions, where graphene oxide was reduced on the catalyst surface under the hydrogen-poor condition, deoxidation with much suppressed carbon loss was possible, resulting in high-quality graphene sheets. Our experimental data and density functional theory calculations proved that reduction which occurred on the CuFeO2 surface preferentially removed adsorbed oxygen atoms in graphene oxide sheets, leaving dissociated carbon structures to be restored to a near-perfect few-layer graphene sheet. TGA-mass data revealed that GO with catalysts released 92.8% less carbon-containing gases than GO without catalysts during the reduction process, which suggests that this process suppressed carbon loss in graphene oxide sheets, leading to near-perfect graphene. The amount of oxygen related to the epoxide group in the basal plane of GO significantly decreased to near zero (from 43.84 to 0.48 at. %) in catalyst-assisted reduced graphene oxide (CA-rGO). The average domain size and the density of defects of CA-rGO were 4 times larger and 0.1 times lower than those for thermally reduced graphene oxide (TrGO), respectively. As a result, CA-rGO had a 246 and 8 times lower electrical resistance than TrGO and CVD-graphene. With these performances, CA-rGO coated paper connected to a coin-cell battery successfully lit an LED bulb, and CA-rGO itself acted as an efficient catalyst for both the hydrogen evolution reaction and the oxygen evolution reaction.

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