4.6 Article

Triple phase boundary and power density enhancement in PEMFCs of a Pt/C electrode with double catalyst layers

Journal

RSC ADVANCES
Volume 9, Issue 27, Pages 15635-15641

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9ra01741k

Keywords

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Funding

  1. BK21 plus program from the Ministry of Education and Human-Resource Development, South of Korea
  2. National Research Foundation of Korea (NRF) - Korean government (MSIP) [2015042417, 2016R1A2B4014090, 2017R1A2B3006141]
  3. LINC Plus Research Project [2018-C-G022-010102]
  4. National Research Foundation of Korea [2017R1A2B3006141, 2016R1A2B4014090] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Exploring efficient approaches to design electrodes for proton exchange membrane fuel cells (PEMFCs) is of great advantage to overcome the current limitations of the standard platinum supported carbon (Pt/C) catalyst. Herein, a Pt/C electrode consisting of double catalyst layers (DCL) with low Pt loading of around 0.130 mg(Pt) cm(-2) is prepared using spray and electrophoresis (EPD) methods. The DCL electrode demonstrated a higher electrochemical surface area (ECSA-52.5 m(2) g(Pt)(-1)) and smaller internal resistance (133 ) as compared to single catalyst layer (SCL) sprayed (37.1 m(2) g(Pt)(-1) and 184 ) or EPD (42.4 m(2) g(Pt)(-1) and 170 ) electrodes. In addition, the corresponding DCL membrane electrode assembly (MEA), which consists of a Pt/C DCL electrode at the anode side and a Pt/C sprayed electrode at the cathode side, also showed improved PEMFC performance as compared to others. Specifically, the DCL MEA generated the highest power density of 4.9 W mg(Pt)(-1), whereas, the SCL MEAs only produced 3.1 and 3.8 W mg(Pt)(-1), respectively. The superior utilization of the Pt catalysts into the DCL MEA can originate from the enrichment of the triple phase boundary (TPB) presented on the Pt/C DCL electrode, which can strongly promote the adsorbed hydrogen intermediates' removal from the anode side, thus improving the overall PEMFC performance.

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