Hannah Faye M. Austria
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Hannah Faye M. Austria has a total of 9 co-authors. Here are the top co-authors by number of shared publications:
- Anawati Anawati
Department of Physics Faculty of Mathematics and Natural Sciences Universitas Indonesia 16424 Depok Indonesia
1 shared publication - Januar Widakdo
Universitas Indonesia
1 shared publication - Ming-Hua Ho
Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei, Taiwan
1 shared publication - Owen Setiawan
Graduate Institute of Applied Science and Technology Advanced Membrane Materials Research Center National Taiwan University of Science and Technology Taipei 10607 Taiwan
1 shared publication - Subrahmanya Thagare Manjunatha
Advanced Membrane Materials Research Center, Graduate Institute of Applied Science and Technology, National Taiwan University of Science and Technology, Taipei 106335, Taiwan
1 shared publication - Tsung-Han Huang
Graduate Institute of Applied Science and Technology, Advanced Membrane Research Center, National Taiwan University of Science and Technology, Taipei 10607, Taiwan
1 shared publication
Latest Publications
- Open Access
Effects of Co-Solvent-Induced Self-Assembled Graphene-PVDF Composite Film on Piezoelectric Application
A persistent purpose for self-powered and wearable electronic devices is the fabrication of graphene-PVDF piezoelectric nanogenerators with various co-solvents that could provide enhanced levels of durability and stability while generating a higher output. This study resulted in a piezoelectric nanogenerator based on a composite film composed of graphene, and poly (vinylidene fluoride) (PVDF) as a flexible polymer matrix that delivers high performance, flexibility, and cost-effectiveness. By adjusting the co-solvent in the solution, a graphene-PVDF piezoelectric nanogenerator can be created (acetone, THF, water, and EtOH). The solution becomes less viscous and is more diluted the more significant the concentration of co-solvents, such as acetone, THF, and EtOH. Additionally, when the density is low, the thickness will be thinner. The final film thickness for all is ~25 µm. Furthermore, the- crystal phase becomes more apparent when graphene is added and combined with the four co-solvents. Based on the XRD results, the peak changes to the right, which can be inferred to be more dominant with the β-phase. THF is the co-solvent with the highest piezoelectric output among other co-solvents. Most of the output voltages produced are 0.071 V and are more significant than the rest.
Open AccessEffects of Co-Solvent-Induced Self-Assembled Graphene-PVDF Composite Film on Piezoelectric Application
A persistent purpose for self-powered and wearable electronic devices is the fabrication of graphene-PVDF piezoelectric nanogenerators with various co-solvents that could provide enhanced levels of durability and stability while generating a higher output. This study resulted in a piezoelectric nanogenerator based on a composite film composed of graphene, and poly (vinylidene fluoride) (PVDF) as a flexible polymer matrix that delivers high performance, flexibility, and cost-effectiveness. By adjusting the co-solvent in the solution, a graphene-PVDF piezoelectric nanogenerator can be created (acetone, THF, water, and EtOH). The solution becomes less viscous and is more diluted the more significant the concentration of co-solvents, such as acetone, THF, and EtOH. Additionally, when the density is low, the thickness will be thinner. The final film thickness for all is ~25 µm. Furthermore, the- crystal phase becomes more apparent when graphene is added and combined with the four co-solvents. Based on the XRD results, the peak changes to the right, which can be inferred to be more dominant with the β-phase. THF is the co-solvent with the highest piezoelectric output among other co-solvents. Most of the output voltages produced are 0.071 V and are more significant than the rest.