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Tracking Charge Transfer to Residual Metal Clusters in Conjugated Polymers for Photocatalytic Hydrogen Evolution

preprint
submitted on 09.05.2020, 20:00 and posted on 12.05.2020, 09:23 by Michael Sachs, Hyojung Cha, Jan Kosco, Catherine M. Aitchison, Laia Francàs, Sacha Corby, Chao-Lung Chiang, Anna A. Wilson, Robert Godin, Alexander Fahey-Williams, Andrew I. Cooper, Seb Sprick, Iain McCulloch, James R Durrant
Semiconducting polymers are versatile materials for solar energy conversion and have gained popularity as photocatalysts for sunlight-driven hydrogen production. Organic polymers often contain residual metal impurities such as palladium (Pd) clusters that are formed during the polymerization reaction, and there is increasing evidence for a catalytic role of such metal clusters in polymer photocatalysts. Using transient optical spectroscopies on nanoparticles of F8BT, P3HT, and the dibenzo[b,d]thiophene sulfone homopolymer, P10, we demonstrate how differences in the timescale of electron transfer to Pd clusters translate into hydrogen evolution activity optima at extremely different residual Pd concentrations. For F8BT nanoparticles with common Pd concentrations of >1000 ppm (>0.1 wt. %), we find that residual Pd clusters quench photogenerated excitons via energy and electron transfer on the fs – ns timescale, thus outcompeting reductive quenching via the electron donor diethylamine in the solution phase. We spectroscopically identify reduced Pd clusters in our F8BT nanoparticles from the µs timescale onwards and show that the predominant location of long-lived electrons gradually shifts to the F8BT polymer when the Pd content is lowered. However, a low yield of long-lived electrons limits the hydrogen evolution activity of F8BT. P10, on the other hand, exhibits a substantially higher hydrogen evolution activity, which we demonstrate results from higher yields of long-lived electrons compared to F8BT due to more efficient reductive quenching. Surprisingly, and despite the higher performance of P10, long-lived electrons reside on the P10 polymer rather than on the Pd clusters in P10 particles, even at very high Pd concentrations of 27,000 ppm (2.7 wt. %). We show that these long-lived electrons in P10 react orders of magnitude slower at lower Pd levels, which suggests that their transfer to Pd sites constitutes a kinetic bottleneck and thus reveals a direction towards further improvements for this already very performant material. In contrast, long-lived electrons in F8BT already reside on Pd clusters before the typical timescale of hydrogen evolution. This comparison illustrates that P10 exhibits efficient reductive quenching but slow electron transfer to residual Pd clusters, whereas the opposite is the case for F8BT. We discuss possible reasons for this pronounced difference in the predominant location of long-lived electrons in F8BT and P10. Our results suggest that the development of even more efficient polymer photocatalysts should target materials that combine both rapid reductive quenching and rapid charge transfer to a metal-based co-catalyst.

Funding

Imperial College London President's PhD Scholarship

EPSRC Doctoral Prize Fellowship

KAUST OSR-2015-CRG4-2572

KAUST OSR-2018-CRG7-3749.2

EPSRC EP/N004884/1

Marie Curie Fellowship (658270)

Imperial College London Schrödinger Scholarship

FRQNT postdoctoral award

NSERC Discovery Grant

History

Email Address of Submitting Author

michael.sachs14@imperial.ac.uk

Institution

Imperial College London

Country

United Kingdom

ORCID For Submitting Author

0000-0001-9775-9336

Declaration of Conflict of Interest

The authors declare no conflicts of interest.

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