Márquez Raúl A, Kawashima Kenta, Son Yoon Jun, Rose Roger, Smith Lettie A, Miller Nathaniel, Carrasco Jaim Omar Ali, Celio Hugo, Mullins C Buddie
Department of Chemistry, The University of Texas at Austin, Austin, Texas 78712, United States.
McKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, Texas 78712, United States.
ACS Appl Mater Interfaces. 2022 Sep 21;14(37):42153-42170. doi: 10.1021/acsami.2c12579. Epub 2022 Sep 9.
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 (, 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.
碱性水电解是一种很有前景的清洁能源存储技术,除了内在的电催化活性外,还受到外在因素的制约。为了开始比较用于电解应用的催化材料,必须首先了解并控制这些外在因素。在此,我们改变外在电极特性并研究气泡释放的影响,以考察电极和表面设计如何影响水电解性能。我们通过连续的三维(3D)打印和金属沉积工艺制造出坚固且经济高效的电极。通过对沉积工艺的系统评估,我们证实了外在电极特性(润湿性、表面粗糙度和电化学活性表面积)与电化学性能之间的密切关系。改变电极几何形状、尺寸和电解液流速会导致过电位降低,并且对于析氢反应(HER)和析氧反应(OER)会产生不同的气泡直径和寿命。因此,我们证明了电极结构和强制电解液对流对气泡释放的重要作用。此外,我们通过评估HER/OER性能、气泡消散和长期稳定性,证实了有序的、镀镍3D多孔结构的适用性。最后,我们将3D多孔电极用作研究基准NiFe电催化剂的载体,证实了在精确控制外在特性的同时,3D打印电极用于测试电催化材料的稳健性和有效性。总体而言,我们证明了定制电极结构和表面性质可实现对外在电极特性的精确调节,为测试水电解电极材料的效率提供更具可重复性和可比性的条件。