Hung Ting-Chieh, Liao Ting-Wei, Liao Guan-Jr, Liao Zhen-He, Hsu Po-Wei, Lai Yu-Ling, Hsu Yao-Jane, Wang Chia-Hsin, Yang Yaw-Wen, Wang Jeng-Han, Luo Meng-Fan
Department of Physics, National Central University 300 Jhongda Road, Jhongli District Taoyuan 32001 Taiwan
National Synchrotron Radiation Research Center 101 Hsin-Ann Road, Hsinchu Science Park Hsinchu 30076 Taiwan.
RSC Adv. 2021 Jul 15;11(40):24762-24771. doi: 10.1039/d1ra04066a. eCollection 2021 Jul 13.
Annealed Rh nanoclusters on an ordered thin film of AlO/NiAl(100) were shown to exhibit a promoted reactivity toward the decomposition of methanol-d, under both ultrahigh vacuum and near-ambient-pressure conditions. The Rh clusters were grown with vapor deposition onto the AlO/NiAl(100) surface at 300 K and annealed to 700 K. The decomposition of methanol-d proceeded only through dehydrogenation, with CO and deuterium as products, on Rh clusters both as prepared and annealed. Nevertheless, the catalytic reactivity of the annealed clusters, measured with the production of either CO or deuterium per surface Rh site from the reaction, became at least 2-3 times that of the as-prepared ones. The promoted reactivity results from an altered support effect associated with an annealing-induced mass transport at the surface. Our results demonstrate a possibility to practically prepare reactive Rh clusters, regardless of the cluster size, that can tolerate an elevated reaction temperature, with no decreased reactivity.
研究表明,在超高真空和近常压条件下,有序AlO/NiAl(100)薄膜上的退火Rh纳米团簇对甲醇-d的分解表现出增强的反应活性。Rh团簇在300 K下通过气相沉积生长在AlO/NiAl(100)表面,并退火至700 K。甲醇-d的分解仅通过脱氢进行,产物为CO和氘,无论是制备态还是退火态的Rh团簇均如此。然而,通过反应中每个表面Rh位点产生CO或氘来衡量,退火团簇的催化反应活性至少是制备态团簇的2至3倍。反应活性的提高源于与退火诱导的表面质量传输相关的载体效应改变。我们的结果表明,有可能实际制备出具有反应活性的Rh团簇,无论团簇大小如何,都能耐受升高的反应温度,且反应活性不会降低。