An analysis of degradation phenomena in polymer electrolyte membrane water electrolysis

被引:215
|
作者
Rakousky, Christoph [1 ]
Reimer, Uwe [1 ]
Wippermann, Klaus [1 ]
Carmo, Marcelo [1 ]
Lueke, Wiebke [1 ]
Stolten, Detlef [1 ,2 ]
机构
[1] Forschungszentrum Julich GmbH, Electrochem Proc Engn IEK 3, D-52425 Julich, Germany
[2] Rhein Westfal TH Aachen, Chair Fuel Cells, Aachen, Germany
关键词
PEM electrolyzer; Water electrolysis; Durability; Degradation; Porous transport layer; PTL; DYNAMIC HYDROGEN ELECTRODE; ION CONTAMINATION; BIPOLAR PLATES; ELECTROCATALYSIS; PERFORMANCE; TITANIUM; POLARIZATION; STABILITY;
D O I
10.1016/j.jpowsour.2016.06.082
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The durability of a polymer electrolyte membrane (PEM) water electrolysis single cell, assembled with regular porous transport layers (PTLs) is investigated for just over 1000 h. We observe a significant degradation rate of 194 mu V h(-1) and conclude that 78% of the detectable degradation can be explained by an increase in ohmic resistance, arising from the anodic Ti-PTL. Analysis of the polarization curves also indicates a decrease in the anodic exchange current density, j(0), that results from the over-time contamination of the anode with Ti species. Furthermore, the average Pt-cathode particle size increases during the test, but we do not believe this phenomenon makes a significant contribution to increased cell voltages. To validate the anode Ti-PTL as a crucial source of increasing resistance, a second cell is assembled using Pt-coated Ti-PTLs. This yields a substantially reduced degradation rate of only 12 mu V h(-1), indicating that a non-corroding anode PTI. is vital for PEM electrolyzers. It is our hope that forthcoming tailored PTLs will not only contribute to fast progress on cost-efficient stacks, but also to its long-term application of PEM electrolyzers involved in industrial processes. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:120 / 128
页数:9
相关论文
共 50 条
  • [31] Advances in study of solid polymer electrolyte water electrolysis
    Wan, NF
    Pang, ZC
    HYDROGEN ENERGY PROGRESS XIII, VOLS 1 AND 2, PROCEEDINGS, 2000, : 266 - 268
  • [32] Polymer Electrolyte Membranes for Water Photo-Electrolysis
    Arico, Antonino S.
    Girolamo, Mariarita
    Siracusano, Stefania
    Sebastian, David
    Baglio, Vincenzo
    Schuster, Michael
    MEMBRANES, 2017, 7 (02)
  • [33] Developments of water electrolysis technology by solid polymer electrolyte
    Han, SD
    Park, KB
    Rana, R
    Singh, KC
    INDIAN JOURNAL OF CHEMISTRY SECTION A-INORGANIC BIO-INORGANIC PHYSICAL THEORETICAL & ANALYTICAL CHEMISTRY, 2002, 41 (02): : 245 - 253
  • [34] NEW SOLID POLYMER ELECTROLYTE COMPOSITES FOR WATER ELECTROLYSIS
    MILLET, P
    PINERI, M
    DURAND, R
    JOURNAL OF APPLIED ELECTROCHEMISTRY, 1989, 19 (02) : 162 - 166
  • [35] HYDROGEN GENERATION BY SOLID POLYMER ELECTROLYTE WATER ELECTROLYSIS
    RUSSELL, JH
    NUTTAL, LJ
    FICKETT, AP
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1973, (AUG26): : 2 - 2
  • [37] SOLID POLYMER ELECTROLYTE WATER ELECTROLYSIS - DEVELOPMENT STATUS
    NUTTALL, LJ
    RUSSELL, JH
    INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 1980, 5 (01) : 75 - 84
  • [38] On the influence of porous transport layers parameters on the performances of polymer electrolyte membrane water electrolysis cells
    Pushkarev, A. S.
    Pushkareva, I., V
    Solovyev, M. A.
    Prokop, M.
    Bystron, T.
    Rajagopalan, S. K.
    Bouzek, K.
    Grigoriev, S. A.
    ELECTROCHIMICA ACTA, 2021, 399
  • [39] Insight into elevated temperature and thin membrane application for high efficiency in polymer electrolyte water electrolysis
    Garbe, Steffen
    Futter, Jonas
    Schmidt, Thomas J.
    Gubler, Lorenz
    ELECTROCHIMICA ACTA, 2021, 377
  • [40] Influences of Nanostructures of Sn and Ir for the Oxygen Evolution Reaction in Polymer Electrolyte Membrane Water Electrolysis
    Bunea, Sorin
    Li, Min
    Demiroz, Ezgi
    Zeng, Peng
    Willinger, Marc Georg
    Urakawa, Atsushi
    ENERGY & FUELS, 2023, 38 (01) : 637 - 646