Abstract

The unique atomic monolayer structure of graphene gives rise to a broad range of remarkable mechanical folding properties. However, significant challenges remain in effectively harnessing them in a controllable and scalable manner. In this study, we introduce an innovative approach that employs micron-scale cavities, fabricated through ultrafast laser patterning, in a stretchable polymer substrate to locally modulate adhesion and strain transfer to a graphene monolayer. This technique enables the deterministic induction of single folds in graphene with fold dimensions, width and height in the hundreds of nanometers, tunable through the geometry of the polymer cavities and the applied strain. Importantly, these folds are reversible, returning to a flat morphology with minimal structural damage, as confirmed by Raman spectroscopy. Additionally, our method allows for the creation of fields of folds with reproducible periodicity, defining clear potential for practical applications. These findings pave the way for the development of advanced devices that would leverage the strain and morphology-sensitive properties of graphene.

Abstract

The unique atomic monolayer structure of graphene gives rise to a broad range of remarkable mechanical folding properties. However, significant challenges remain in effectively harnessing them in a controllable and scalable manner. In this study, we introduce an innovative approach that employs micron-scale cavities, fabricated through ultrafast laser patterning, in a stretchable polymer substrate to locally modulate adhesion and strain transfer to a graphene monolayer. This technique enables the deterministic induction of single folds in graphene with fold dimensions, width and height in the hundreds of nanometers, tunable through the geometry of the polymer cavities and the applied strain. Importantly, these folds are reversible, returning to a flat morphology with minimal structural damage, as confirmed by Raman spectroscopy. Additionally, our method allows for the creation of fields of folds with reproducible periodicity, defining clear potential for practical applications. These findings pave the way for the development of advanced devices that would leverage the strain and morphology-sensitive properties of graphene.

Abstract

The unique atomic monolayer structure of graphene gives rise to a broad range of remarkable mechanical folding properties. However, significant challenges remain in effectively harnessing them in a controllable and scalable manner. In this study, we introduce an innovative approach that employs micron-scale cavities, fabricated through ultrafast laser patterning, in a stretchable polymer substrate to locally modulate adhesion and strain transfer to a graphene monolayer. This technique enables the deterministic induction of single folds in graphene with fold dimensions, width and height in the hundreds of nanometers, tunable through the geometry of the polymer cavities and the applied strain. Importantly, these folds are reversible, returning to a flat morphology with minimal structural damage, as confirmed by Raman spectroscopy. Additionally, our method allows for the creation of fields of folds with reproducible periodicity, defining clear potential for practical applications. These findings pave the way for the development of advanced devices that would leverage the strain and morphology-sensitive properties of graphene.

Abstract

The unique atomic monolayer structure of graphene gives rise to a broad range of remarkable mechanical folding properties. However, significant challenges remain in effectively harnessing them in a controllable and scalable manner. In this study, we introduce an innovative approach that employs micron-scale cavities, fabricated through ultrafast laser patterning, in a stretchable polymer substrate to locally modulate adhesion and strain transfer to a graphene monolayer. This technique enables the deterministic induction of single folds in graphene with fold dimensions, width and height in the hundreds of nanometers, tunable through the geometry of the polymer cavities and the applied strain. Importantly, these folds are reversible, returning to a flat morphology with minimal structural damage, as confirmed by Raman spectroscopy. Additionally, our method allows for the creation of fields of folds with reproducible periodicity, defining clear potential for practical applications. These findings pave the way for the development of advanced devices that would leverage the strain and morphology-sensitive properties of graphene.