Light harvesting articles from across Nature Portfolio

Controlling molecular motion at nanoscale is important for the design of nanomachines. Here the authors use ultrafast vibrational and electronic spectroscopy to characterize the mechanism of motion of a light driven molecular motor designed to support translational movement.

Noble metals dominate the field of photosensitizers and luminophores. Now, an approach incorporating cyclometalating and carbene functions into Fe^III complexes has been shown to enable dual emission from the opposing ligand-to-metal and metal-to-ligand charge-transfer states. The latter shows an exceptionally long lifetime of 4.6 ns and is quenched by oxygen and other quenchers.

A class of inexpensive aminoanthraquinone organic dyes are shown to facilitate visible-light-driven CO₂ reduction. Overall reaction efficiencies were found to be optimal when both electron donating and accepting groups were on a single dye molecule.

Circularly polarized luminescent materials with large dissymmetry and efficiency are in demand. Here, the authors investigate chirality-induced spin polarization in achiral gold nanorods decorated with chiral dye-loaded micelles to enhance chiroptic activity.

Principles of quantum interference can guide the design of chromophores that undergo singlet fission. Now, ‘pencil and paper’ graphical models can be used to understand and predict the dynamics of triplet pairs generated through singlet fission in bridged dimers.

Photoinduced isomerization reactions can be used to efficiently dissipate absorbed energy in photosystems such as molecular motors, but the ultrafast processes are challenging to characterize. Here, the authors track the formation of the E and Z isomers of ethyl sinapate in real time via transient vibrational absorption spectroscopy and find that photoinduced internal conversion occurs at multiple points along the potential energy surface.