Universität Innsbruck, Institut für Ionenphysik und Angewandte Physik, Technikerstraße 25, 6020, Innsbruck, Austria.
Department of Chemistry, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon Tong, Hong Kong SAR, P. R. China.
Chemistry. 2023 May 8;29(26):e202203590. doi: 10.1002/chem.202203590. Epub 2023 Mar 22.
Molecular processes behind hydrogen evolution reactions can be quite complex. In macroscopic electrochemical cells, it is extremely difficult to elucidate and understand their mechanism. Gas phase models, consisting of a metal ion and a small number of water molecules, provide unique opportunities to understand the reaction pathways in great detail. Hydrogen evolution in clusters consisting of a singly charged metal ion and one to on the order of 50 water molecules has been studied extensively for magnesium, aluminum and vanadium. Such clusters with around 10-20 water molecules are known to eliminate atomic or molecular hydrogen upon mild activation by room temperature black-body radiation. Irradiation with ultraviolet light, by contrast, enables hydrogen evolution already with a single water molecule. Here, we analyze and compare the reaction mechanisms for hydrogen evolution on the ground state as well as excited state potential energy surfaces. Five distinct mechanisms for evolution of atomic or molecular hydrogen are identified and characterized.
氢的演化反应背后的分子过程可能非常复杂。在宏观电化学电池中,要阐明和理解其机制极其困难。气相模型由一个金属离子和少量水分子组成,为详细了解反应途径提供了独特的机会。已经对镁、铝和钒组成的带一个正电荷的金属离子和一个到大约 50 个水分子的团簇中的氢的演化进行了广泛的研究。已知这种含有约 10-20 个水分子的团簇在通过室温黑体辐射温和激活时会消除原子或分子氢。相比之下,用紫外线照射可以在仅用一个水分子的情况下实现氢的演化。在这里,我们分析和比较了基态和激发态势能表面上氢的演化反应机制。确定并描述了五种不同的原子或分子氢演化机制。