4.8 Article

Tailoring 3D-Printed Electrodes for Enhanced Water Splitting

期刊

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c12579

关键词

3D printing; water splitting; gas bubbles; electrocatalyst; electrodeposition

资金

  1. National Science Foundation (NSF) [CHE-1664941, CHE-2102307]
  2. Welch Foundation [F-1436]

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This study investigates the impact of electrode and surface design on the performance of water electrolysis by modifying extrinsic electrode properties and studying bubble release effects. Robust and cost-effective electrodes are fabricated through 3D printing and metal deposition. The results demonstrate that modifying electrode geometry, size, and electrolyte flow rate can decrease overpotential and result in different bubble diameters and lifetimes. The suitability and stability of ordered, Ni-coated 3D porous structures are also confirmed. Additionally, this study demonstrates the effectiveness of 3D-printed electrodes for testing electrocatalytic materials while extrinsic properties are controlled.
Alkaline water electrolysis, a promising technology for clean energy storage, is constrained by extrinsic factors in addition to intrinsic electrocatalytic activity. To begin to compare between catalytic materials for electrolysis applications, these extrinsic factors must first be understood and controlled. Here, we modify extrinsic electrode properties and study the effects of bubble release to examine how the electrode and surface design impact the performance of water electrolysis. We fabricate robust and cost-effective electrodes through a sequential three-dimensional (3D) printing and metal deposition procedure. Through a systematic assessment of the deposition procedure, we confirm the close relationship between extrinsic electrode properties (i.e., wettability, surface roughness, and electrochemically active surface area) and electrochemical performance. Modifying the electrode geometry, size, and electrolyte flow rate results in an overpotential decrease and different bubble diameters and lifetimes for the hydrogen (HER) and oxygen evolution reactions (OER). Hence, we demonstrate the essential role of the electrode architecture and forced electrolyte convection on bubble release. Additionally, we confirm the suitability of ordered, Ni-coated 3D porous structures by evaluating the HER/OER performance, bubble dissipation, and long-term stability. Finally, we utilize the 3D porous electrode as a support for studying a benchmark NiFe electrocatalyst, confirming the robustness and effectiveness of 3D-printed electrodes for testing electrocatalytic materials while extrinsic properties are precisely controlled. Overall, we demonstrate that tailoring electrode architectures and surface properties result in precise tuning of extrinsic electrode properties, providing more reproducible and comparable conditions for testing the efficiency of electrode materials for water electrolysis.

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