Chemical doping is widely used to manipulate the electrical and thermoelectric properties of organic semiconductors, yet intelligent design of polymer–dopant systems remains elusive. It is challenging to predict the electrical and thermoelectric properties of doped organic semiconductors due to the large number of variables impacting these properties, including film morphology, dopant and polymer energetics, dopant size, and degree of polaron delocalization. Herein, a series of dopants with varying sizes and electron affinities (EAs) are combined with polymers of differing ionization energies (IEs) to investigate how the difference between polymer IE and dopant EA influences the doping efficiency and electrical conductivity, and how the dopant size influences the thermoelectric properties. Our experiments demonstrate that at low doping levels the doping efficiency strongly depends on the difference between the polymer IE and dopant EA; the effectiveness of doping on increasing electrical conductivity drastically decreases at high loadings for the molybdenum dithiolene complexes, while FeCl₃ remains effective at high loadings; and the large molybdenum complexes lead to more delocalized polarons as compared to FeCl₃. To take advantage of the complementary doping characteristics of the molybdenum complexes and FeCl₃, both dopants are employed simultaneously to reach high power factors at relatively low dopant concentrations.

Mesoporous titania (mp-TiO₂) has drawn tremendous attention for a diverse set of applications due to its high surface area, interfacial structure, and tunable combination of pore size, pore orientation, wall thickness, and pore connectivity. Its pore structure facilitates rapid diffusion of reactants and charge carriers to the photocatalytically active interface of TiO₂. However, because the large band gap of TiO₂ limits its ability to utilize visible light, non-metal doping has been extensively studied to tune the energy levels of TiO₂. While first-principles calculations support the efficacy of this approach, it is challenging to efficiently introduce active non-metal dopants into the lattice of TiO₂. This review surveys recent advances in the preparation of mp-TiO₂ and their doping with non-metal atoms. Different doping strategies and dopant sources are discussed. Further, co-doping with combinations of non-metal dopants are discussed as strategies to reduce the band gap, improve photogenerated charge separation, and enhance visible light absorption. The improvements resulting from each doping strategy are discussed in light of potential changes in mesoporous architecture, dopant composition and chemical state, extent of band gap reduction, and improvement in photocatalytic activities. Finally, potential applications of non-metal-doped mp-TiO₂ are explored in water splitting, CO₂ reduction, and environmental remediation with visible light.

UV- and blue-emitting graphene quantum dots (GQDs) were synthesized from carbon nano-onions and compared for metal ion sensing.