纳米线
电解质
铂金
电催化剂
催化作用
材料科学
化学工程
电解
电解水
电流密度
密度泛函理论
分解水
氢
纳米技术
化学
电极
电化学
计算化学
有机化学
物理化学
工程类
物理
光催化
量子力学
作者
Wen Xin Li,Zhi Yong Liu,Sheng Chao Yang,Jian Ning Wu,Liang Sun,En Guang,Hua Gui Yang,Xuhong Guo
标识
DOI:10.1007/s40843-022-2258-3
摘要
Platinum-based material is the most efficient and durable electrocatalyst for motivating the hydrogen evolution reaction (HER) in an acidic electrolyte; however, its low abundance and high cost limit its further application in proton-exchange membrane water electrolysis (PEMWE) technology. Therefore, minimizing the Pt amount while retaining high activity would be desirable. Herein, we use defect-rich W18O49 nanowires to anchor well-dispersed, ultrafine Pt species (Pt−W18O49) via a freeze-drying method to avoid aggregation, further mediating an efficient and durable HER in acidic water. Density functional theory analyses also demonstrate that the strong electronic interaction between the Pt species and W18O49 support greatly improves the HER performance. With a 1/10 Pt loading amount of the commercial 20 wt% Pt/C, the Pt−W18O49 catalyst requires the over-potentials of 116 and 743 mV to achieve high current densities of 100 and 1000 mA cm−2 in 0.5 mol L−1 H2SO4, outperforming those of the 20 wt% Pt/C benchmark. More importantly, the Pt−W18O49 catalyst can sustain a high-current-density HER at 500 mA cm−2 for more than 38 h without obvious degradation. This work paves a new avenue for synergistically reducing the Pt amount and retaining high activity for real-world PEMWE.
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