Jingxuan Chen, Gangwen Fu, Yu Tian, Xingchuan Li, Mengqi Luo, Xiaoyu Wei, Ting Zhang, Tian Gao, Cheng Chen, Somboon Chaemchuen, Xi Xu, Xing Sun, Tongle Bu, Francis Verpoort, John Wang, Zongkui Kou
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引用次数: 0
摘要
用于可扩展制氢的碱性氢进化反应(HER)在很大程度上取决于能否解决传统镍基电极上迟缓的气泡动力学问题,尤其是在安培级电流密度及以上的情况下。本文设计并制造了具有不同支架的三维打印镍基硫化物(3DPNS)电极。微观层面的现场观察表明,气泡逸出速度随支架中孔边(HS)数量的增加而增加。随后,我们进行了多物理场模拟,以说明当孔的形状从正方形、五边形和六边形过渡到圆形时,气泡附着的 HS 长度和气泡周围的压力平衡时间明显减少,从而导致气泡尺寸减小,气泡逸出速度加快。最终,具有圆形孔构型的 3DPNS 电极表现出了最有利的 HER 性能,在电流密度高达 1000 mA cm-2 的情况下,过电位为 297 mV,持续 120 小时。
Alkaline hydrogen evolution reaction (HER) for scalable hydrogen production largely hinges on addressing the sluggish bubble-involved kinetics on the traditional Ni-based electrode, especially for ampere-level current densities and beyond. Herein, 3D-printed Ni-based sulfide (3DPNS) electrodes with varying scaffolds are designed and fabricated. In situ observations at microscopic levels demonstrate that the bubble escape velocity increases with the number of hole sides (HS) in the scaffolds. Subsequently, we conduct multiphysics field simulations to illustrate that as the hole shapes transition from square, pentagon, and hexagon to circle, where a noticeable reduction in the bubble-attached HS length and the pressure balance time around the bubbles results in a decrease in bubble size and an acceleration in the rate of bubble escape. Ultimately, the 3DPNS electrode with circular hole configurations exhibits the most favorable HER performance with an overpotential of 297 mV at the current density of up to 1000 mA cm−2 for 120 h. The present study highlights a scalable and effective electrode scaffold design that promotes low-cost and low-energy green hydrogen production through the ampere-level alkaline HER.