Pluntke Y, Kibler L A, Kolb D M
Institute of Electrochemistry, University of Ulm, 89069, Ulm, Germany.
Phys Chem Chem Phys. 2008 Jul 7;10(25):3684-8. doi: 10.1039/b802915f. Epub 2008 May 12.
Well-defined Au/Pd(111) alloy films have been prepared on a Ru(0001) substrate by electrochemical metal deposition and subsequent heating up to 700 degrees C. The electrochemical behaviour of the 20 monolayers thick epitaxially-grown films is in excellent agreement with both equilibrium surface composition and distribution for Au/Pd alloys on Mo(110) as previously reported (D. W. Goodman et al., J. Phys. Chem., 2005, B109, 18535). The electrocatalytic activity of the AuPd(111) surface alloys was studied for the hydrogen evolution in 0.1 M H(2)SO(4) as a function of surface composition. Maximum activities were found for Pd fractions of 0.2 +/- 0.1, where the population of Pd atoms surrounded by Au has its maximum. These Pd monomers are found to be about 20 times more active than Pd atoms in the Pd overlayer.
通过电化学金属沉积并随后加热至700摄氏度,在Ru(0001)衬底上制备了定义明确的Au/Pd(111)合金薄膜。如先前报道(D. W. Goodman等人,《物理化学杂志》,2005年,B109,18535),20个单层厚的外延生长薄膜的电化学行为与Mo(110)上Au/Pd合金的平衡表面组成和分布非常吻合。研究了AuPd(111)表面合金在0.1 M H(2)SO(4)中作为表面组成函数的析氢电催化活性。发现当Pd分数为0.2 +/- 0.1时活性最大,此时被Au包围的Pd原子数量最多。发现这些Pd单体的活性比Pd覆盖层中的Pd原子高约20倍。