The regulation of water content in polymeric membranes is important in a number of applications, such as reverse electrodialysis and proton-exchange fuel-cell membranes. External thermal and water management systems add both mass and size to systems, and so intrinsic mechanisms of retaining water and maintaining ionic transport in such membranes are particularly important for applications where small system size is important. For example, in proton-exchange membrane fuel cells, where water retention in the membrane is crucial for efficient transport of hydrated ions, by operating the cells at higher temperatures without external humidification, the membrane is self-humidified with water generated by electrochemical reactions. Here we report an alternative solution that does not rely on external regulation of water supply or high temperatures. Water content in hydrocarbon polymer membranes is regulated through nanometre-scale cracks ('nanocracks') in a hydrophobic surface coating. These cracks work as nanoscale valves to retard water desorption and to maintain ion conductivity in the membrane on dehumidification. Hydrocarbon fuel-cell membranes with surface nanocrack coatings operated at intermediate temperatures show improved electrochemical performance, and coated reverse-electrodialysis membranes show enhanced ionic selectivity with low bulk resistance.

A novel end-group crosslinked anion exchange membrane showed the connecting ionic-clustered morphology that improved electrochemical performances and durability for alkaline fuel cell operation.

Two series of random sulfonated poly-(benzothiazole-co-benzimidazole) polymers (sPBT-BI) with 70% and 60% degree of sulfonation were evaluated as proton exchange membranes. sPBT was also prepared for a comparative study. The mechanical properties of sPBT-BI were greatly enhanced by incorporation of benzimidazole (BI); sPBT-BI70-10 showed a tensile strength of 125 MPa and elongation at break of 38.9%, an increase of 56.5% and 145%, respectively, compared with sPBT. The solubility, dimensional stability, thermal properties, and oxidative stability of sPBT-BI were also improved. The ionic clusters of sPBT-BI membranes in both AFM phase images and TEM images became narrower with increasing amounts of BI while containing the same molar amount of sulfonic acid groups. This resulted in lower dimensional swelling and higher mechanical strength, but the proton conductivity decreased. However, high proton conductivity was achieved by incorporating an appropriate content of BI. PEMFC H 2 /air single cell performances and durabilities were improved by incorporation of 5% of BI units in sPBT.

We propose and fabricate a random light scattering layer for light extraction in organic light-emitting diodes (OLEDs) with silver nanodots, which were obtained by melting silver nanowires. The OLED with the light scattering layer as an internal light extraction structure was enhanced by 49.1% for the integrated external quantum efficiency (EQE). When a wrinkle structure is simultaneously used for an external light extraction structure, the total enhancement of the integrated EQE was 65.3%. The EQE is maximized to 65.3% at a current level of 2.0 mA/cm(2). By applying an internal light scattering layer and wrinkle structure to an OLED, the variance in the emission spectra was negligible over a broad viewing angle. Power mode analyses with finite difference time domain (FDTD) simulations revealed that the use of a scattering layer effectively reduced the waveguiding mode while introducing non-negligible absorption. Our method offers an effective yet simple approach to achieve both efficiency enhancement and spectral stability for a wide range of OLED applications.

In this work, three functional groups were introduced in poly(arylene ether sulfone) membranes to investigate the effects of cationic functional groups in the membranes on reverse electrodialysis performance. Our results showed that controlling the swelling behaviour of the membranes was an important factor for increasing the permselectivity while maintaining their high conductivity.

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Since the first demonstration of oxide TFT driving AM‐OLED, oxide TFT technology has attracted explosive interesting and has been developed for the mass production. The performance of oxide TFT has been verified and the remained issue is bias temperature stability. In this paper, we report the effect of interface process including channel and back channel on the oxide TFT performance in a top gate and a bottom gate structure. We also demonstrate transparent AM‐OLED driven by highly stable Al doped ZTO TFT.