Graphene oxide membrane (GOM) shows promise as an alternative
for
proton exchange membrane fuel cells (PEMFCs) due to its hydrophilic
nature, which promotes attractive proton conductivity under wet conditions.
However, GOM-based fuel cells (GOMFCs) exhibit lower maximum power
density than Nafion(R) due to issues such as fuel crossover,
membrane degradation, and loss of oxygen surface functional groups.
In this study, amorphous double-layer Ni64Zr36/Ni36Zr64 thin films demonstrate superior hydrogen
permeability compared to double-layer Ni64Zr36/Ni36Zr64 (crystalline), single-layer Ni64Zr36 (amorphous/crystalline), and Pd77Ag23 thin films at low temperatures, particularly near
room temperature. Two types of amorphous and crystalline Ni–Zr
metal films, with double or single layers, were characterized, and
their hydrogen purification performance was reported. For hydrogen
membrane fuel cell (HMFC) applications, a silanization process was
employed by reacting a 50 wt % (5 mg/mL) solution of graphene oxide
(GO) with an equimolar ratio of (3-mercaptopropyl)trimethoxysilane
[MPTS, HS(CH2)3Si(OCH3)3] (0.790 g/mL) to form a MPTS-modified GO composite electrolyte (MGC-50).
In the HMFCs, double-layer membranes composed of GOM or MGC-50 and
the hydrogen-permeable Ni–Zr thin film developed in this study
were investigated as an electrolyte membrane. A hydrogen-permeable
metal thin film, around 40 nm in thickness, was deposited onto GOM
or MGC-50 using a Pd or Ni–Zr target via DC magnetron sputtering,
resulting in a double-layer graphene oxide-hydrogen membrane (GOHM)
electrolyte. The fuel cell performance of the fabricated Pd- and Ni–Zr-based
GOHMFCs was compared with conventional PEMFCs.