Anisotropic phenanthroline-based ruthenium polymers grafted on a titanium metal-organic framework for efficient photocatalytic hydrogen evolution

Conjugated polymers and titanium-based metal-organic framework (Ti-MOF) photocatalysts have demonstrated promising features for visible-light-driven hydrogen production. We report herein a strategy of anisotropic phenanthroline-based ruthenium polymers (PPDARs) over Ti-MOF, a tunable platform for efficient visible-light-driven photocatalytic hydrogen evolution reaction (HER). Several analytical methods including X-ray absorption spectroscopy (XAS) revealed the judicious integration of the surface-active polymer over the Ti-MOF reinforcing the catalytic activity over the broad chemical space. PPDAR-4 polyacrylate achitecture led to a substantial increase in the H(2) evolution rate of 2438 µmolg(−1)h(−1) (AQY: 5.33%) compared to pristine Ti-MOF (238 µmol g(−1) h(−1)). The separation of photogenerated charge carriers at the PPDAR-4/Ti-MOF interface was confirmed by the optical and electrochemical investigations. The experimental, as well as theoretical data, revealed their physical and chemical properties which are positively correlated with the H(2) generation rate. This offers a new avenue in creating polymer-based MOF robust photocatalysts for sustainable energy.