We demonstrate that the inclusion of a small amount of the co-solvent 1,8-diiodooctane in the preparation of a bulk-heterojunction photovoltaic device increases its power conversion efficiency by 20%, through a mechanism of transient plasticisation. We follow the removal of 1,8-diiodooctane directly after spin-coating using ellipsometry and ion beam analysis, while using small angle neutron scattering to characterise the morphological nanostructure evolution of the film. In PffBT4T-2OD/PC71BM devices, the power conversion efficiency increases from 7.2% to above 8.7% as a result of the coarsening of the phase domains. This coarsening process is assisted by thermal annealing and the slow evaporation of 1,8-diiodooctane, which we suggest, acts as a plasticiser to promote molecular mobility. Our results show that 1,8-diiodooctane can be completely removed from the film by a thermal annealing process at temperatures ≤100 °C and that there is an interplay between the evaporation rate of 1,8-diiodooctane and the rate of domain coarsening in the plasticized film which helps elucidate the mechanism by which additives improve device efficiency.

A new fabrication method via sequentially depositing donor and acceptor layers can push the power conversion efficiency of organic solar cells based on non-fullerene acceptors to over 10%.

Superconducting spintronics has emerged in the past decade as a promising new field that seeks to open a new dimension for nanoelectronics by utilizing the internal spin structure of the superconducting Cooper pair as a new degree of freedom 1,2 . Its basic building blocks are spin-triplet Cooper pairs with equally aligned spins, which are promoted by proximity of a conventional superconductor to a ferromagnetic material with inhomogeneous macroscopic magnetization 3 . Using low-energy muon spin-rotation experiments we find an unanticipated e ect, in contradiction with the existing theoretical models of superconductivity and ferromagnetism: the appearance of a magnetization in a thin layer of a non-magnetic metal (gold), separated from a ferromagnetic double layer by a 50-nm-thick superconducting layer of Nb. The e ect can be controlled either by temperature or by using a magnetic field to control the state of the remote ferromagnetic elements, and may act as a basic building block for a new generation of quantum interference devices based on the spin of a Cooper pair.The ability to manipulate the spin degree of freedom of charge carriers is key to realizing future spin-based electronics. Integrating superconductors into spintronic devices can greatly enhance performance 1 and allows the transport of spin over long distances without the dissipation of heat 2 . To achieve the alignment of electron spins, ferromagnetic materials are used. Superconductivity and ferromagnetism are, however, antagonistic states of matter, and the interplay between these two states results in the conversion of conventional spin-singlet into spin-triplet pair correlations 3 . Whereas spin-singlet pairs have spin angular momentum S = 0, spin-triplet pairs have S = 1, with three possible spin projections s z = −1, 0, +1. The realization of such spin-triplet pairs in mesoscopic systems containing interfaces between superconducting (S) and ferromagnetic (F) layers has attracted much interest from both the theoretical and experimental communities. Interaction of spin-singlet superconductivity with collinear ferromagnetism leads to oscillations and suppression of the pair correlation at a short distance ξ f due to the exchange magnetic field in the ferromagnet, which tends to align the spins of electrons parallel 4-7 . However, to create longer-range penetration of spin-triplet superconductivity into the ferromagnet, interaction with a non-collinear magnetism is required [8][9][10] , motivating the discovery of superconducting currents through ferromagnetic metals over distances far longer than the singlet penetration length ξ f (refs 11-13). These long-range triplet components (LRTC) have parallel spin projections (s z = ±1), and are not suppressed by the exchange field. Theory predicts that the conversion into spin-triplet pairs should also give rise to an induced magnetic moment in the superconductor, decaying away from the interface [14][15][16] , often called the inverse or magnetic proximity effect. For diffusive systems this induced m...

Yttrium iron garnet has a very high Verdet constant, is transparent in the infrared and is an insulating ferrimagnet leading to its use in optical and magneto-optical applications. Its high Q-factor has been exploited to make resonators and filters in microwave devices, but it also has the lowest magnetic damping of any known material. In this article we describe the structural and magnetic properties of single crystal thin-film YIG where the temperature dependence of the magnetisation reveals a decrease in the low temperature region. In order to understand this complex material we bring a large number of structural and magnetic techniques to bear on the same samples. Through a comprehensive analysis we show that at the substrate -YIG interface, an interdiffusion zone of only 4–6 nm exists. Due to the interdiffusion of Y from the YIG and Gd from the substrate, an addition magnetic layer is formed at the interface whose properties are crucially important in samples with a thickness of YIG less than 200 nm.