Tailoring 3D-Printed Electrodes for Enhanced Water Splitting

材料科学 电极 过电位 电解质 电解水 电解 分解水 析氧 电催化剂 纳米技术 化学工程 表面粗糙度 多孔性 润湿 电化学 复合材料 催化作用 光催化 化学 物理化学 工程类 生物化学
作者
Raúl A. Márquez,Kenta Kawashima,Yoon Jun Son,Roger G. Rose,Lettie A. Smith,Nathan Miller,Omar A. Carrasco-Jaim,Hugo Celio,C. Buddie Mullins
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:14 (37): 42153-42170 被引量:29
标识
DOI:10.1021/acsami.2c12579
摘要

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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