An anthraquinone-based bismuth-iron metal-organic framework as an efficient photoanode in photoelectrochemical cells.

Abstract

Metal-organic frameworks (MOFs) are appealing candidate materials to design new photoelectrodes for use in solar energy conversion because of their modular nature and chemical versatility. However, to date there are few examples of MOFs that can be directly used as photoelectrodes, for which they must be able to afford charge separation upon light absorption, and promote the catalytic dissociation of water molecules, while maintaining structural integrity. Here, we have explored the use of the organic linker anthraquinone-2, 6-disulfonate (2, 6-AQDS) for the preparation of MOFs to be used as photoanodes. Thus, the reaction of 2, 6-AQDS with Bi(iii) or a combination of Bi(iii) and Fe(iii) resulted in two new MOFs, BiPF-10 and BiFePF-15, respectively. They display similar structural features, where the metal elements are disposed in inorganic-layer building units, which are pillared by the organic linkers by coordination bonds through the sulfonic acid groups. We show that the introduction of iron in the structure plays a crucial role for the practical use of the MOFs as a robust photoelectrode in a photoelectrochemical cell, producing as much as 1.23 mmol H2 cm-2 with the use of BiFePF-15 as photoanode. By means of time-resolved and electrochemical impedance spectroscopic studies we have been able to unravel the charge transfer mechanism, which involves the formation of a radical intermediate species, exhibiting a longer-lived lifetime by the presence of the iron-oxo clusters in BiFePF-15 to reduce the charge transfer resistance.