Alkaline anion exchange membrane water electrolysis: Effects of electrolyte feed method and electrode binder content

Authors
Cho, Min KyungPark, Hee-YoungLee, Hye JinKim, Hyoung-JuhnLim, AhyounHenkensmeier, DirkYoo, Sung JongKim, Jin YoungLee, So YoungPark, Hyun S.Jang, Jong Hyun
Issue Date
2018-04
Publisher
ELSEVIER SCIENCE BV
Citation
JOURNAL OF POWER SOURCES, v.382, pp.22 - 29
Abstract
Herein, we investigate the effects of catholyte feed method and anode binder content on the characteristics of anion exchange membrane water electrolysis (AEMWE) to construct a high-performance electrolyzer, revealing that the initial AEMWE performance is significantly improved by pre-feeding 0.5 M aqueous KOH to the cathode. The highest long-term activity during repeated voltage cycling is observed for AEMWE operation in the dry cathode mode, for which the best long-term performance among membrane electrode assemblies (MEAs) featuring polytetrafluoroethylene (PTFE) binder-impregnated (5-20 wt%) anodes is detected for a PTFE content of 20 wt%. MEAs with low PTFE content (5 and 9 wt%) demonstrate high initial performance, rapid performance decay, and significant catalyst loss from the electrode during long-term operation, whereas the MEA with 20 wt % PTFE allows stable water electrolysis for over 1600 voltage cycles. Optimization of cell operating conditions (i.e., operation in dry cathode mode at an optimum anode binder content following an initial solution feed) achieves an enhanced water splitting current density (1.07 A cm(-2) at 1.8 V) and stable long-term AEMWE performance (0.01% current density reduction per voltage cycle).
Keywords
HYDROGEN-PRODUCTION; IONOMER CONTENT; CARBON NANOTUBES; CATALYST LAYER; PERFORMANCE; POLYMER; CELL; ELECTROCATALYSTS; OPTIMIZATION; TECHNOLOGIES; Alkaline anion exchange membrane water electrolysis; Electrolyte feed method; Membrane electrode assembly; Binder content
ISSN
0378-7753
URI
https://pubs.kist.re.kr/handle/201004/121566
DOI
10.1016/j.jpowsour.2018.02.025
Appears in Collections:
KIST Article > 2018
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