Piqué Oriol, Koleva Iskra Z, Viñes Francesc, Aleksandrov Hristiyan A, Vayssilov Georgi N, Illas Francesc
Departament de Ciència de Materials i Química Física & Institut de Química Teòrica i Computacional (IQTCUB), Universitat de Barcelona, c/ Martí i Franquès 1, Barcelona, 08028, Spain.
Faculty of Chemistry and Pharmacy, University of Sofia, 1126, Sofia, Bulgaria.
Angew Chem Int Ed Engl. 2019 Feb 4;58(6):1744-1748. doi: 10.1002/anie.201813037. Epub 2019 Jan 4.
Carbon moieties on late transition metals are regarded as poisoning agents in heterogeneous catalysis. Recent studies show the promoting catalytic role of subsurface C atoms in Pd surfaces and their existence in Ni and Pt surfaces. Here energetic and kinetic evidence obtained by accurate simulations on surface and nanoparticle models shows that such subsurface C species are a general issue to consider even in coinage noble-metal systems. Subsurface C is the most stable situation in densely packed (111) surfaces of Cu and Ag, with sinking barriers low enough to be overcome at catalytic working temperatures. Low-coordinated sites at nanoparticle edges and corners further stabilize them, even in Au, with negligible subsurface sinking barriers. The malleability of low-coordinated sites is key in the subsurface C accommodation. The incorporation of C species decreases the electron density of the surrounding metal atoms, thus affecting their chemical and catalytic activity.
在多相催化中,晚期过渡金属上的碳部分被视为中毒剂。最近的研究表明,表面下的碳原子在钯表面具有促进催化作用,并且它们也存在于镍和铂表面。在此,通过对表面和纳米颗粒模型进行精确模拟获得的能量和动力学证据表明,即使在贵金属体系中,这种表面下的碳物种也是一个需要考虑的普遍问题。在铜和银的密集堆积(111)表面中,表面下的碳是最稳定的情况,其下沉势垒足够低,在催化工作温度下能够被克服。纳米颗粒边缘和角落处的低配位位点进一步使它们稳定,即使在金中也是如此,其表面下沉势垒可忽略不计。低配位位点的延展性是表面下碳容纳的关键。碳物种的掺入降低了周围金属原子的电子密度,从而影响它们的化学和催化活性。