Browsing by Author "Su, Huaneng"

Now showing 1 - 6 of 6
  • Thumbnail Image
    Item
    Eliminating micro-porous layer from gas diffusion electrode for use in high temperature polymer electrolyte membrane fuel cell
    (Elsevier, 2017) Su, Huaneng; Xu, Qian; Chong, Junjie
    In this work, we report a simple strategy to improve the performance of high temperature polymer electrolyte membrane fuel cell (HT-PEMFC) by eliminating the micro-porous layer (MPL) from its gas diffusion electrodes (GDEs). Due to the absence of liquid water and the general use of high amount of catalyst, the MPL in a HT-PEMFC system works limitedly. Contrarily, the elimination of the MPL leads to an interlaced micropore/macropore composited structure in the catalyst layer (CL), which favors gas transport and catalyst utilization, resulting in a greatly improved single cell performance. At the normal working voltage (0.6 V), the current density of the GDE eliminated MPL reaches 0.29 A cm2 , and a maximum power density of 0.54 W cm2 at 0.36 V is obtained, which are comparable to the best results yet reported for the HT-PEMFCs with similar Pt loading and operated using air. Furthermore, the MPLfree GDE maintains an excellent durability during a preliminary 1400 h HT-PEMFC operation, owing to its structure advantages, indicating the feasibility of this electrode for practical applications.
  • Thumbnail Image
    Item
    Enhanced performance of polybenzimidazole-based high temperature proton exchange membrane fuel cell with gas diffusion electrodes prepared by automatic catalyst spraying under irradiation technique
    (Elsevier, 2013) Su, Huaneng; Pasupathi, Sivakumar; Bladergroen, Bernard Jan; Linkov, Vladimir; Pollet, Bruno G.
    Gas diffusion electrodes (GDEs) prepared by a novel automatic catalyst spraying under irradiation (ACSUI) technique are investigated for improving the performance of phosphoric acid (PA)-doped polybenzimidazole (PBI) high temperature proton exchange membrane fuel cell (PEMFC). The physical properties of the GDEs are characterized by pore size distribution and scanning electron microscopy (SEM). The electrochemical properties of the membrane electrode assembly (MEA) with the GDEs are evaluated and analyzed by polarization curve, cyclic voltammetry (CV) and electrochemistry impedance spectroscopy (EIS). Effects of PTFE binder content, PA impregnation and heat treatment on the GDEs are investigated to determine the optimum performance of the single cell. At ambient pressure and 160 o C, the maximum power density can reach 0.61 W cm-2, and the current density at 0.6 V is up to 0.38 A cm-2, with H /air and a platinum loading of 0.5 mg cm-2 on both electrodes. The MEA with the GDEs shows good stability for fuel cell operating in a short term durability test.
  • Thumbnail Image
    Item
    Membrane electrode assemblies with low noble metal loadings for hydrogen production from solid polymer electrolyte water electrolysis
    (Elsevier, 2013) Su, Huaneng; Linkov, Vladimir; Bladergroen, Bernard Jan
    High performance membrane electrode assemblies (MEAs) with low noble metal loadings (NMLs) were developed for solid polymer electrolyte (SPE) water electrolysis. The electro- chemical and physical characterization of the MEAs was performed by IeV curves, elec- trochemical impedance spectroscopy (EIS) and scanning electron microscopy (SEM). Even though the total NML was lowered to 0.38 mg cm-2, it still reached a high performance of 1.633 V at 2 A cm-2 and 80 o C, with IrO2 as anode catalyst. The influences of the ionomer content in the anode catalyst layer (CL) and the cell temperature were investigated with the purpose of optimizing the performance. SEM and EIS measurements revealed that the MEA with low NML has very thin porous cathode and anode CLs that get intimate contact with the electrolyte membrane, which makes a reduced mass transport limitation and lower ohmic resistance of the MEA. A short-term water electrolysis operation at 1 A cm-2 showed that the MEA has good stability: the cell voltage maintained at ~1.60 V without distinct degradation after 122 h operation at 80 o C and atmospheric pressure.
  • Thumbnail Image
    Item
    Optimization of gas diffusion electrode for polybenzimidazole-based high temperature proton exchange membrane fuel cell: Evaluation of polymer binders in catalyst layer
    (Elsevier, 2013) Su, Huaneng; Pasupathi, Sivakumar; Bladergroen, Bernard Jan; Linkov, Vladimir; Pollet, Bruno G.
    Gas diffusion electrodes (GDEs) prepared with various polymer binders in their catalyst layers (CLs) were investigated to optimize the performance of phosphoric acid doped polybenzimidazole (PBI)-based high temperature proton exchange membrane fuel cells (HT-PEMFCs). The properties of these binders in the CLs were evaluated by structure characterization, electrochemical analysis, single cell polarization and durability test. The results showed that polytetrafluoroethylene (PTFE) and polyvinylidene difluoride (PVDF) are more attractive as CL binders than conventional PBI or Nafion binder. At ambient pressure and 160 o C, the maximum power density can reach w 0.61 W cm-2 (PTFE GDE), and the current density at 0.6 V is up to ca. 0.52 A cm-2 (PVDF GDE), with H2/air and a platinum loading of 0.5 mg cm-2 on these electrodes. Also, both GDEs showed good stability for fuel cell operation in a short term durability test.
  • Thumbnail Image
    Item
    RuxNb1-xO2 catalyst for the oxygen evolution reaction in proton exchange membrane water electrolysers
    (Elsevier, 2013) Puthiyapura, Vinod Kumar; Pasupathi, Sivakumar; Basu, Suddhasatwa; Wu, Xu; Su, Huaneng; Varagunapandiyan, N.; Pollet, Bruno G.; Scott, Keith
    Bimetallic catalyst system of ruthenium oxide (RuO2) and niobium oxide (Nb2O5) was prepared using the Adams method and the hydrolysis method. Physical and electrochemical characterizations of the catalysts were studied using X-ray diffraction (XRD), Scanning electron microscopy (SEM), cyclic voltammogram (CV) and polarization measurements. Nb2O5 addition to RuO2 was found to increase the stability of RuO2. In Adams method the sodium nitrate was found to be forming complex with Nb2O5 at high temperature reaction. This makes Adams method unsuitable for the synthesis of RuO2eNb2O5 bimetallic system. Hydrolysis method on other hand does not have this problem. But a proper mixture of two oxides was not obtained in hydrolysis method. A lower crystallite size for bimetallic system was obtained with Adams method compared to hydrolysis method. RuO2 prepared by Adams method had higher activity compared to the hydrolysis counterpart in electrolyzer operation with nafion membrane. A cell voltage of 1.62 V was obtained with RuO2 (A) at 1 A/cm2. A higher stability for Ru0.8Nb0.2O2(A) compared to RuO2
  • Thumbnail Image
    Item
    Thermal conductivity and temperature profiles of the micro porous layers used for the polymer electrolyte membrane fuel cell
    (Elsevier, 2013) Burheim, Odne S.; Su, Huaneng; Pasupathi, Sivakumar; Pharoah, Jon G.; Pollet, Bruno G.
    The thermal conductivity and the thickness change with pressure of several different micro porous layers (MPL) used for the polymer electrolyte membrane fuel cell (PEMFC) were measured. The MPL were made with different compositions of carbon and polytetrafluoroethylene (PTFE). A one-dimensional thermal PEMFC model was used to estimate the impact that the MPL has on the temperature profiles though the PEMFC. The thermal conductivity was found to vary from as low as 0.05 up to as high as 0.12 W K 1 m 1 while the compaction pressure was varied from 4 bar and up to around 16 bar resulting in a decrease in thickness of approximately 40%. The PTFE content, which varied between 10 and 25%, did not result in any significant change in the compression or thermal conductivity. Both the thickness and the thermal conductivity changed irreversibly with compaction pressure. Considering a MPL thermal conductivity of 0.1 W K 1 m 1, a MPL thickness of 45 mm, a current density of 10 kAm 2 (1.0 A cm 2), liquid water (production and sorption), and a 30 mm membrane it was found that the MPL is responsible for a temperature increase of up to 2 C. This contribution can be lowered by integrating the MPL into the porous transport layer.