Institute of Chemical Research of Catalonia (ICIQ), The Barcelona Institute of Science and Technology (BIST), Av. Països Catalans 16, E-43007 Tarragona, Spain.
Departament de Química Física i Inorgànica, Universitat Rovira i Virgili, Marcel.lí Domingo 1, E-43007 Tarragona, Spain.
Nat Chem. 2018 Jan;10(1):24-30. doi: 10.1038/nchem.2874. Epub 2017 Oct 30.
Water splitting is a promising approach to the efficient and cost-effective production of renewable fuels, but water oxidation remains a bottleneck in its technological development because it largely relies on noble-metal catalysts. Although inexpensive transition-metal oxides are competitive water oxidation catalysts in alkaline media, they cannot compete with noble metals in acidic media, in which hydrogen production is easier and faster. Here, we report a water oxidation catalyst based on earth-abundant metals that performs well in acidic conditions. Specifically, we report the enhanced catalytic activity of insoluble salts of polyoxometalates with caesium or barium counter-cations for oxygen evolution. In particular, the barium salt of a cobalt-phosphotungstate polyanion outperforms the state-of-the-art IrO catalyst even at pH < 1, with an overpotential of 189 mV at 1 mA cm. In addition, we find that a carbon-paste conducting support with a hydrocarbon binder can improve the stability of metal-oxide catalysts in acidic media by providing a hydrophobic environment.
水分解是一种有前途的方法,可以高效且经济有效地生产可再生燃料,但水氧化仍然是其技术发展的瓶颈,因为它在很大程度上依赖于贵金属催化剂。尽管在碱性介质中,廉价的过渡金属氧化物是有竞争力的水氧化催化剂,但它们在酸性介质中无法与贵金属竞争,因为在酸性介质中,氢气的产生更容易且更快。在这里,我们报告了一种基于丰富地球元素的水氧化催化剂,它在酸性条件下表现良好。具体来说,我们报告了具有铯或钡抗衡阳离子的多金属氧酸盐不溶性盐对氧析出的催化活性增强。特别是,钴-磷钨酸盐多阴离子的钡盐在 pH < 1 时甚至超过了最先进的 IrO 催化剂,在 1 mA cm 时的过电位为 189 mV。此外,我们发现,带有碳氢化合物粘合剂的碳糊导电载体可以通过提供疏水环境来提高金属氧化物催化剂在酸性介质中的稳定性。