4.7 Article

Favorable morphology and electronic conductivity of functional sublayers for highly efficient water splitting electrodes

Journal

JOURNAL OF ENERGY STORAGE
Volume 36, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.est.2021.102342

Keywords

Water splitting; Nanoporous morphology; Conductivity; Functional sublayers; Visualization; Ohmic resistance

Categories

Funding

  1. U.S. Department of Energy's Office of Energy Efficiency and Renewable Energy (EERE) under the Fuel Cell Technologies Office [DE-EE0008426, DE-EE0008423]
  2. U.S. Department of Energy's Office of Energy Efficiency and Renewable Energy (EERE) under National Renewable Energy Laboratory [DE-AC36-08GO28308]
  3. U.S. Department of Energy's Office of Energy Efficiency and Renewable Energy (EERE) under National Energy Technology Laboratory [DE-FE0011585]

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The study revealed that introducing conductive sublayers with different conductivities and morphologies into membrane-based water electrolyzers can significantly improve the sheet conductivity of anode electrodes, reduce the ohmic resistance of water electrolyzers, and increase the current density of water splitting. Carbon nanotube (CNT) film provided a higher electrochemical active area than Au mesh, leading to improved water electrolysis performance.
Low electronic conductivities and improper morphologies of anode electrodes greatly limit the reaction area, catalyst utilization and efficiency in proton exchange membrane water electrolyzers. In this study, conductive sublayers with different conductivities and morphologies were introduced into anode electrodes in membrane-based water electrolyzers. In-situ and ex-situ investigation results showed that conductive sublayers (Au mesh and carbon nanotube (CNT) film) augmented the sheet conductivity of anode electrodes by up to 4000 times (from 2000 to 0.5 ohm square(-1)), and the ohmic resistance of water electrolyzers was reduced to 1/3 when inserting conductive sublayers. In addition, CNT film provided a higher electrochemical active area than Au mesh, because of favorable morphologies (large porosity and surface area) of CNT fibers on CNT films. Therefore, the current density of water splitting was increased by 3 times (from 4.55 mA cm(-2) to 14.83 mA cm(-2)) at 2.5 V compared to a conventional anode electrode. Visualizations on bubble dynamics showed improved performances with conductive sublayers; this was mainly due to greatly increased number of reaction sites, highly spread reaction area (from 50 to 1000 um), and reduced activation overpotential. Thus, a balance between high electronic conductivity and nanoporous morphology is essential to the anode electrode for larger reaction sites and areas in highly efficient water electrolyzers.

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