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.