化学
电解
金属间化合物
碱性水电解
氢
无机化学
化学工程
合金
物理化学
有机化学
电解质
电极
工程类
作者
Kai Wei,Liwen Cao,Ziqing Li,Yuanyuan Sun,Nian‐Tzu Suen
标识
DOI:10.1021/acs.inorgchem.4c04664
摘要
In this work, we have demonstrated a double-boosting strategy that can significantly enhance the stability of hydrogen evolution reaction (HER) for non-noble-metal-based electrocatalysts operating in harsh industrial conditions (6.0 M KOH, 343 K). With the incorporation of early-transition-metal and main-group elements in Ni metal, ternary TiAlNi2 and TiNi2Sn both exhibit higher robust durability for HER than binary AlNi and metal Ni due to the strong bonding states of Ti-Ni and Al/Sn-Ni below the Fermi level. Additionally, they display remarkable HER efficiency, for which only overpotentials of ca. -22 and -67 mV are required for TiAlNi2 and TiNi2Sn to reach a current density of 10 mA/cm2 (η10) in 1.0 M KOH. Theoretical calculation revealed that their outstanding HER activities (outperforming commercial Pt/C, Pt = 5 wt %, η10 = -76 mV) can be attributed to a synergistic teamwork among Ti, Ni, and Al/Sn elements. The overpotentials at 500 mA/cm2 of TiAlNi2 and TiNi2Sn are much smaller than that of commercial Ni foam. More importantly, they show steady HER performances over a period of 400 h at a high current density (400 mA/cm2) in harsh industrial conditions.
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