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Abstract The structural defects on graphene grown on a metal substrate via chemical vapor deposition can readily stimulate severe galvanic corrosion phenomena. For any defect passivation method that can be technologically promising for superior corrosion‐resistant graphene coatings, efficiency and accuracy are two critical but still challenging requirements. In this work, the authors design a rapid processing method (within just 15 min) that can accurately heal various structural defects of different types and sizes on graphene coating, where the hydrophobic 1 H ,1 H ,2 H ,2 H ‐perfluorooctanethiol (PFOT) molecules are self‐assembled onto the defect sites. The surface morphologies, atomic bonding states, and defect‐healing mechanism are deeply understood by comprehensive experimental characterizations and first‐principles calculations. Both weak physical PFOT‐pristine graphene bonding and strong covalent PFOT‐defect bonding are two microscopic factors that enhance defect healing efficiency and accuracy. Spatially resolved electronic and electrochemical measurements show that the defect‐healing not only effectively suppresses galvanic corrosion phenomena during both short‐term and long‐term tests, but also well preserves the superior electronic conductivity of pristine graphene. The defect healing strategy proposed here can find its wide potential applications in the fields like electro‐industry, coating, and sensors that require the graphene coatings having both superior corrosion resistance and electronic property.
Wu et al. (Mon,) studied this question.