The evolution of grain size and shape as well as type and frequency of grain boundary structures during thermal annealing of lamellar diblock copolymer microstructures is established using large area image reconstruction and analysis. Grain coarsening is found to proceed via an initial transient stage that is characterized by the rapid relaxation of unstable "frozen-in" defects such as kink boundaries and the subsequent quasi-stationary coarsening that is dominated by the continuous relaxation of low-angle symmetric tilt boundaries. The particular relevance of low-angle symmetric tilt boundaries to grain coarsening is interpreted as the consequence of both the associated decrease of boundary energy as well as the availability of favorable kinetic pathwayssuch as grain boundary splittingto facilitate the coarsening process. The inverse relation between grain boundary energy and frequency suggests that the reduction of boundary energy is a relevant governing parameter for the evolution of grain boundary structuresas it is in inorganic materials. The existence of "inert" boundary types (such as asymmetric tilt and twist) thatwithin the experimental windowdo not participate in the coarsening process is expected to have dominant influence on the final morphology that can be attained by thermal annealing of the microstructure. The reduction of the density of inert boundaries during the film preparation process should therefore provide a strategy for increasing the coarsening kinetics in block copolymer films during thermal annealing and thus a path toward a higher degree of order in block copolymer microstructures.

The characterization of microstructures in three dimensions is reviewed, with an emphasis on the use of automated electron back-scatter diffraction techniques. Both statistical reconstruction of polycrystalline structures from multiple cross sections and reconstruction from parallel, serial sections are discussed. In addition, statistical reconstruction of second-phase particle microstructures from multiple cross sections is reviewed.

Output power of thermoelectric generators depends on device engineering minimizing heat loss as well as inherent material properties. However, the device engineering has been largely neglected due to the limited flat or angular shape of devices. Considering that the surface of most heat sources where these planar devices are attached is curved, a considerable amount of heat loss is inevitable. To address this issue, here, we present the shape-engineerable thermoelectric painting, geometrically compatible to surfaces of any shape. We prepared Bi2Te3-based inorganic paints using the molecular Sb2Te3 chalcogenidometalate as a sintering aid for thermoelectric particles, with ZT values of 0.67 for n-type and 1.21 for p-type painted materials that compete the bulk values. Devices directly brush-painted onto curved surfaces produced the high output power of 4.0 mW cm−2. This approach paves the way to designing materials and devices that can be easily transferred to other applications.

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The beneficial use of a hole transport layer (HTL) as a substitution for poly(3,4-ethlyenedioxythiophene): polystyrene sulfonate (PEDOT:PSS) is regarded as one of the most important approaches for improving the stability and efficiency of inverted perovskite solar cells. Here, we demonstrate highly efficient and stable inverted perovskite solar cells by applying a GO-doped PEDOT:PSS (PEDOT:GO) film as an HTL. The high performance of this solar cell stems from the excellent optical and electrical properties of the PEDOT:GO film, including a higher electrical conductivity, a higher work function related to the reduced contact barrier between the perovskite layer and the PEDOT:GO layer, enhanced crystallinity of the perovskite crystal, and suppressed leakage current. Moreover, the device with the PEDOT:GO layer showed excellent long-term stability in ambient air conditions. Thus, the enhancement in the efficiency and the excellent stability of inverted perovskite solar cells are promising for the eventual commercialization of perovskite optoelectronic devices.