4.6 Article

CVD Synthesis of 3D-Shaped 3D Graphene Using a 3D-Printed Nickel-PLGA Catalyst Precursor

Journal

ACS OMEGA
Volume 6, Issue 43, Pages 29009-29021

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.1c04072

Keywords

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Funding

  1. National Institute for Occupational Safety and Health through the Pilot Research Project Training Program of the University of Cincinnati Education and Research Center Grant [T42OH008432]
  2. NSF MRIR2 award [0959511]
  3. Graduate Student Government (GSG) at the University of Cincinnati
  4. Department of Engineering Education at the University of Cincinnati

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This study successfully synthesized high-quality 3D graphene structures through the combination of 3D printing and CVD processes, without the need for binders, showcasing unique advantages and characteristics.
Earlier, various attempts to develop graphene structures using chemical and nonchemical routes were reported. Being efficient, scalable, and repeatable, 3D printing of graphene-based polymer inks and aerogels seems attractive; however, the produced structures highly rely on a binder or an ice support to stay intact. The presence of a binder or graphene oxide hinders the translation of the excellent graphene properties to the 3D structure. In this communication, we report our efforts to synthesize a 3D-shaped 3D graphene (3D(2)G) with good quality, desirable shape, and structure control by combining 3D printing with the atmospheric pressure chemical vapor deposition (CVD) process. Direct ink writing has been used in this work as a 3D-printing technique to print nickel powder-PLGA slurry into various shapes. The latter has been employed as a catalyst for graphene growth via CVD. Porous 3D(2)G with high purity was obtained after etching out the nickel substrate. The conducted micro CT and 2D Raman study of pristine 3D(2)G revealed important features of this new material. The interconnected porous nature of the obtained 3D(2)G combined with its good electrical conductivity (about 17 S/cm) and promising electrochemical properties invites applications for energy storage electrodes, where fast electron transfer and intimate contact with the active material and with the electrolyte are critically important. By changing the printing design, one can manipulate the electrical, electrochemical, and mechanical properties, including the structural porosity, without any requirement for additional doping or chemical postprocessing. The obtained binderfree 3D(2)G showed a very good thermal stability, tested by thermo-gravimetric analysis in air up to 500 degrees C. This work brings together two advanced manufacturing approaches, CVD and 3D printing, thus enabling the synthesis of high-quality, binder-free 3D(2)G structures with a tailored design that appeared to be suitable for multiple applications.

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