Calcined Co(II)-Triethylenetetramine, Co(II)- Polyaniline-Thiourea as the Cathode Catalyst of Proton Exchanged Membrane Fuel Cell.
Lin-Chia HoLi-Cheng JhengTar-Hwa HsiehWen-Yao HuangYen-Zen WangYi-Jhun GaoPo-Hao TsengPublished in: Polymers (2020)
Triethylenetetramine (TETA) and thiourea complexed Cobalt(II) (Co(II)) ions are used as cathode catalysts for proton exchanged membrane fuel cells (PEMFCs) under the protection of polyaniline (PANI) which can become a conducting medium after calcination. Fourier-transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) spectra clearly reveal the presence of typical carbon nitride and sulfide bonds of the calcined Nitrogen (N)- or Sulfur (S)-doped co-catalysts. Clear (002) and (100) planes of carbon-related X-ray diffraction patterns are found for co-catalysts after calcination, related to the formation of a conducting medium after the calcination of PANI. An increasing intensity ratio of the D to G band of the Raman spectra reveal the doping of N and S elements. More porous surfaces of co-catalysts are found in scanning electronic microscopy (SEM) micropictures when prepared in the presence of both TETA and thiourea (CoNxSyC). Linear sweep voltammetry (LSV) curves show the highest reducing current to be 4 mAcm-2 at 1600 rpm for CoNxSyC, indicating the necessity for both N- and S-doping. The membrane electrode assemblies (MEA) prepared with the cathode made of CoNxSyC produces the highest maximum power density, close to 180 mW cm-2.
Keyphrases
- reduced graphene oxide
- highly efficient
- metal organic framework
- transition metal
- high resolution
- gold nanoparticles
- quantum dots
- single cell
- electron microscopy
- carbon nanotubes
- single molecule
- density functional theory
- ion batteries
- cell therapy
- high speed
- solar cells
- cystic fibrosis
- cell cycle arrest
- dna methylation
- mesenchymal stem cells
- mass spectrometry
- solid state
- escherichia coli
- oxidative stress
- cell death