Abstract-Gibbs free energies of formation for the ideal gas, liquid phase, and species in solution were estimated for 75 polychlorinated dibenzo-p-dioxins (PCDDs) at 298.15 K and 100,000 Pa. These values were used to calculate standard redox potentials, with H 2 as the electron donor. Owing to the lack of experimental thermodynamic data for the involved chemical species, the standard-state ideal gas enthalpies of formation were evaluated by several semiempirical methods including the Modified Neglect of Diatomic Differential Overlap (MNDO), Austin Model 1 (AM1), and MNDO-Parametric Method 3 (PM3). Three different implementations of Benson's group additivity method for estimation of ideal gas enthalpies of formation were also evaluated. As a result of the evaluation, the CHETAH program based on Benson's group additive method was chosen for ideal gas enthalpy of formation calculations. Entropies, vapor pressure, and aqueous solubility were calculated by existing methods in order to complete the thermodynamic cycle. Calculated redox potentials indicate that chlorodioxins, including 2,3,7,8-tetrachlorodioxin, can serve as electron acceptors in anaerobic environments, at least from a thermodynamic perspective.

Naphthalenediimide (NDI) and its pi-extended derivatives have been one of the most important building blocks to constitute n-type organic semiconductors. To further explore new materials in the NDI family, an...

Conjugated polymers (CPs) have been actively utilized as photocatalysts for hydrogen evolution due to their easy synthetic tunability to endow specific functionalities, including visible-light absorption, higher-lying LUMO energy for proton reduction, and sufficient photochemical stability. Enhancing interfacial surface and compatibility of hydrophobic CPs with hydrophilic water is the central focus to improve the hydrogen evolution rate (HER). Although a number of successful approaches have been developed in recent years, tedious chemical modifications or post-treatment of CPs make reproducibility of the materials difficult. In this work, a solution processable PBDB-T polymer is directly deposited on a glass substrate to form a thin film that is immersed in an aqueous solution to photochemically catalyze H 2 generation. The PBDB-T thin film showed a much higher hydrogen evolution rate (HER) than the typical method of using PBDB-T suspended solids due to the enhanced interfacial area with a more suitable solid-state morphology. When the thickness of the thin film is reduced to dramatically improve the utilization of the photocatalytic material, the 0.1 mg-based PBDB-T thin film exhibited an unprecedentedly high HER of 120.90 mmol h −1 g −1 .

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