Department of Physics and Astronomy, University of New Mexico , Albuquerque, New Mexico 87131, United States.
Johannes Gutenberg University Mainz , D 55099 Mainz, Germany.
Nano Lett. 2016 Feb 10;16(2):1478-84. doi: 10.1021/acs.nanolett.5b05149. Epub 2016 Jan 29.
Hydrogen dissociation is a critical step in many hydrogenation reactions central to industrial chemical production and pollutant removal. This step typically utilizes the favorable band structure of precious metal catalysts like platinum and palladium to achieve high efficiency under mild conditions. Here we demonstrate that aluminum nanocrystals (Al NCs), when illuminated, can be used as a photocatalyst for hydrogen dissociation at room temperature and atmospheric pressure, despite the high activation barrier toward hydrogen adsorption and dissociation. We show that hot electron transfer from Al NCs to the antibonding orbitals of hydrogen molecules facilitates their dissociation. Hot electrons generated from surface plasmon decay and from direct photoexcitation of the interband transitions of Al both contribute to this process. Our results pave the way for the use of aluminum, an earth-abundant, nonprecious metal, for photocatalysis.
氢解是许多氢化反应的关键步骤,这些反应对于工业化学生产和污染物去除至关重要。这一步骤通常利用铂和钯等贵金属催化剂的有利能带结构,在温和条件下实现高效率。在这里,我们证明了在室温常压下,即使对于氢气吸附和离解的高活化能垒,当受到光照时,铝纳米晶体 (Al NCs) 可以用作光催化剂来实现氢的离解。我们表明,从 Al NCs 到氢分子反键轨道的热电子转移促进了它们的离解。表面等离子体衰减和 Al 带间跃迁的直接光激发产生的热电子都有助于这一过程。我们的结果为使用铝——一种丰富的、非贵金属——进行光催化铺平了道路。