A first report on orientationally ordered room-temperature discotic nematic phases having ambipolar charge carrier mobility (of the order of up to 10⁻³ cm² V⁻¹ s⁻¹).

π-Conjugated pyrene–thiophene-based room-temperature discotic liquid crystals armed with four peripheral aliphatic chains are reported to study their potential use in a hole-transporting organic semiconductor. The charge carrier mobility studies using the ToF method revealed room temperature hole mobility in the order of 10⁻⁴ cm² V⁻¹ s⁻¹ for both mesogens. However, the mobility values for compound 1a were observed in the order of 10⁻³ cm² V⁻¹ s⁻¹ at high temperatures. Such molecular systems can potentially be used in nonlinear organic electronic applications.

The development of substantial, environment-friendly and low-cost electrocatalysts for an efficient oxygen reduction reaction (ORR) is essentially important for the production and storage of green energy which has sparked the curiosity of researchers for scalable production of metal-free electrocatalysts from biowaste. We report an easy transformation of chestnut-derived biowaste into reduced graphene oxide (rGO) and pyridinic-N-dominated nitrogen-doped rGO (NCS-rGO). The synthesized catalyst exhibits better ORR activity with an onset and half-wave potential of 0.93 V and 0.86 V, respectively, along with a high diffusion-limiting current density of 5.05 mA cm⁻². Under alkaline conditions, we found that NCS-rGO shows an unusually high electrocatalytic activity that is superior to that of the commercial 20% Pt/C catalyst. More notably, the NCS-rGO-based ORR electrocatalyst manifests higher methanol tolerance, without deterioration in catalytic activity even in the presence of significant amount of methanol, outperforming the current state-of-the-art Pt electrocatalyst. Density functional theory (DFT) studies illustrate that pyridinic N is a decisive part of NCS-rGO to achieve the best ORR performance.

An uncommon approach to the synthesis of ambipolar semiconductors based on di- and tri-nuclear gold isocyano–triphenylene complexes of the formula [(AuX) _n (CN–C ₆ H ₄ –O–(CH ₂ ) ₆ ) _n –TriPh] ( n = 2, 3; X = Cl, CC–Ph) is described.