电催化剂
析氧
无机化学
微波食品加热
材料科学
离解(化学)
氧化物
分解水
氢
海水
电解水
氢燃料
能量转换
化学工程
制氢
过渡金属
氧气
空位缺陷
电化学能量转换
贵金属
金属
电化学
储能
催化作用
过氧化氢
带隙
化学
光化学
工作(物理)
Pourbaix图
电子供体
光催化分解水
兴奋剂
水溶液
可逆氢电极
作者
Yuanzong Shen,Enze Li,Siyuan Feng,Y Li,Weichen Li,Weiping Xiao,Guangrui Xu,D Chen,F Liu,Lei Wang,Zexing Wu
出处
期刊:Chemsuschem
[Wiley]
日期:2026-04-27
卷期号:19 (9): e70672-e70672
摘要
Metal oxides have emerged as the dominant choice of matrix for the design and synthesis of supported catalysts with high‐performance, because of the tunable surface properties, low cost, and strong interactions with active components. Herein, the nanoflower‐like titanium dioxide (TiO 2 ) is achieved through solvothermal approach. Then, boron (B) doped black TiO 2 loaded with Ru (Ru/B‐TiO 2 ) is achieved through rapid (40 s) microwave quasi‐solid approach. The incorporation of B modulates the energy band structure of the electrocatalyst, creating additional active sites, and then favors the water dissociation and following hydrogen desorption. The presence of oxygen vacancy defects and metal‐support interactions (MSI) lead to satisfactory stabilization of the catalysts. These effects collectively contributed to the superior performance in 1 M KOH and alkaline seawater for the hydrogen evolution reaction (HER) with small overpotentials of 39 and 61 mV, respectively, which also demonstrates excellent activity and stability. This work presents a novel microwave‐assisted strategy for constructing metal oxide supported low‐content noble metals for energy conversion and storage applications.
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