过电位
材料科学
纳米颗粒
催化作用
化学工程
三元运算
合金
纳米技术
可逆氢电极
纳米结构
反键分子轨道
电极
冶金
物理化学
电化学
化学
工作电极
有机化学
电子
工程类
物理
原子轨道
量子力学
程序设计语言
计算机科学
作者
Zhenxing Li,Chengzhong Yu,Yikun Kang,Xin Zhang,Yangyang Wen,Zhao‐Kui Wang,Chang Ma,Cong Wang,Kaiwen Wang,Xianlin Qu,Miao He,Ya‐Wen Zhang,Weiyu Song
摘要
Hollow nanoparticles with large specific surface area and high atom utilization are promising catalysts for the hydrogen evolution reaction (HER). We describe herein the design and synthesis of a series of ultra-small hollow ternary alloy nanostructures using a simple one-pot strategy. The same technique was demonstrated for hollow PtNiCu nanoparticles, hollow PtCoCu nanoparticles and hollow CuNiCo nanoparticles. During synthesis, the displacement reaction and oxidative etching played important roles in the formation of hollow structures. Moreover, our hollow PtNiCu and PtCoCu nanoparticles were single crystalline, with an average diameter of 5 nm. Impressively, ultra-small hollow PtNiCu nanoparticles, containing only 10% Pt, exhibited greater electrocatalytic HER activity and stability than a commercial Pt/C catalyst. The overpotential of hollow PtNiCu nanoparticles at 10 mA cm-2 was 28 mV versus reversible hydrogen electrode (RHE). The mass activity was 4.54 A mgPt-1 at -70 mV versus RHE, which is 5.62-fold greater than that of a commercial Pt/C system (0.81 A mgPt-1). Through analyses of bonding and antibonding orbital filling, density functional theory calculations demonstrated that the bonding strength of different metals to the hydrogen intermediate (H*) was in the order of Pt > Co > Ni > Cu. The excellent HER performance of our hollow PtNiCu nanoparticles derives from moderately synergistic interactions between the three metals and H*. This work demonstrates a new strategy for the design of low-cost and high-activity HER catalysts.
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