Department of Chemistry, Tsinghua University , Beijing 100084, China.
Beijing Guyue New Materials Research Institute, Beijing University of Technology , Beijing 100124, China.
J Am Chem Soc. 2018 Feb 28;140(8):2773-2776. doi: 10.1021/jacs.7b13612. Epub 2018 Feb 16.
Strain engineering has been a powerful strategy to finely tune the catalytic properties of materials. We report a tensile-strained two-to-three atomic-layer Pt on intermetallic PtGa (AL-Pt/PtGa) as an active electrocatalyst for the methanol oxidation reaction (MOR). Atomic-resolution high-angle annular dark-field scanning transmission electron microscopy characterization showed that the AL-Pt possessed a 3.2% tensile strain along the [001] direction while having a negligible strain along the [100]/[010] direction. For MOR, this tensile-strained AL-Pt electrocatalyst showed obviously higher specific activity (7.195 mA cm) and mass activity (1.094 mA/μg) than those of its unstrained counterpart and commercial Pt/C catalysts. Density functional theory calculations demonstrated that the tensile-strained surface was more energetically favorable for MOR than the unstrained one, and the stronger binding of OH* on stretched AL-Pt enabled the easier removal of CO*.
应变工程一直是一种精细调整材料催化性能的强大策略。我们报告了一种受拉伸应变的二维至三维原子层 Pt 负载于金属间化合物 PtGa(AL-Pt/PtGa)上,其作为甲醇氧化反应(MOR)的活性电催化剂。原子分辨率高角度环形暗场扫描透射电子显微镜表征表明,AL-Pt 在[001]方向上具有 3.2%的拉伸应变,而在[100]/[010]方向上应变可以忽略不计。对于 MOR,这种受拉伸应变的 AL-Pt 电催化剂表现出明显更高的比活性(7.195 mA cm)和质量活性(1.094 mA/μg),优于其未受应变的对应物和商业 Pt/C 催化剂。密度泛函理论计算表明,受拉伸应变的表面对于 MOR 比未受应变的表面更有利,并且在拉伸的 AL-Pt 上 OH的更强结合使得 CO更容易去除。