| Literature DB >> 32015530 |
Jan Kosco1, Matthew Bidwell2, Hyojung Cha2, Tyler Martin3, Calvyn T Howells4, Michael Sachs2, Dalaver H Anjum4, Sandra Gonzalez Lopez4, Lingyu Zou2, Andrew Wadsworth2, Weimin Zhang4, Lisheng Zhang4, James Tellam5, Rachid Sougrat4, Frédéric Laquai4, Dean M DeLongchamp3, James R Durrant2, Iain McCulloch6,7.
Abstract
Photocatalysts formed from a single organic semiconductor typically suffer from inefficient intrinsic charge generation, which leads to low photocatalytic activities. We demonstrate that incorporating a heterojunction between a donor polymer (PTB7-Th) and non-fullerene acceptor (EH-IDTBR) in organic nanoparticles (NPs) can result in hydrogen evolution photocatalysts with greatly enhanced photocatalytic activity. Control of the nanomorphology of these NPs was achieved by varying the stabilizing surfactant employed during NP fabrication, converting it from a core-shell structure to an intermixed donor/acceptor blend and increasing H2 evolution by an order of magnitude. The resulting photocatalysts display an unprecedentedly high H2 evolution rate of over 60,000 µmol h-1 g-1 under 350 to 800 nm illumination, and external quantum efficiencies over 6% in the region of maximum solar photon flux.Entities:
Year: 2020 PMID: 32015530 PMCID: PMC7558859 DOI: 10.1038/s41563-019-0591-1
Source DB: PubMed Journal: Nat Mater ISSN: 1476-1122 Impact factor: 47.656