A new low-energy pathway is reported for the electrochemical reduction of CO2 to formate and syngas at low overpotentials, utilizing a reactive ionic liquid as the solvent. The superbasic tetraalkyl phosphonium ionic liquid [P66614][124Triz] is able to chemisorb CO2 through equimolar binding of CO2 with the 1,2,4-triazole anion. This chemisorbed CO2 can be reduced at silver electrodes at overpotentials as low as 0.17 V, forming formate. In contrast, physically absorbed CO2 within the same ionic liquid or in ionic liquids where chemisorption is impossible (such as [P66614][NTf2]) undergoes reduction at significantly increased overpotentials, producing only CO as the product.

Solution combustion synthesis (SCS) is shown to be versatile for the rapid-one-pot synthesis of three compounds and four polymorphs in the Cu−V−O ternary family: α-CuV 2 O 6 , αand β-Cu 2 V 2 O 7 , and γ-Cu 3 V 2 O 8. These compounds feature copper/vanadium stoichiometric ratios ranging from 1:1 to 3:1; their structural, electronic, optoelectronic, and photoelectrochemical attributes were comprehensively characterized by a combination of theoretical and experimental techniques. The main contribution of the present study is the demonstration that a range of stoichiometries in this compound family can be derived simply by tuning the precursor mole ratio in the SCS procedure. The Cu−V−O family of samples, derived by SCS, is shown to exemplify the strong effect of compound stoichiometry on the optoelectronic and photoelectrochemical properties. Overall, α-CuV 2 O 6 showed the best performance, rooted in the direct nature of the optical transition in this material. Finally, SCS is very timeefficient and the various compositions can be obtained in a matter of minutes, as opposed to hours or even days in classical solution-based or ceramic synthesis routes.

ESIPT for white-light generation from all-solution-processed OLEDs.

An ultrafast, continuous CO2 capture process driven by moisture gradient and electric field with low energy consumption to capture and concentrate CO2 from dilute sources.

The ionic liquid trihexyltetradecylphosphonium 1,2,4-triazolide, [P66614][124Triz], has been shown to chemisorb CO2 through equimolar binding of the carbon dioxide with the 1,2,4-triazolide anion. This leads to a possible new, low energy pathway for the electrochemical reduction of carbon dioxide to formate and syngas at low overpotentials, utilizing this reactive ionic liquid media. Herein, an electrochemical investigation of water and carbon dioxide addition to the [P66614][124Triz] on gold and platinum working electrodes is reported. Electrolysis measurements have been performed using CO2 saturated [P66614][124Triz] based solutions at −0.9 V and −1.9 V on gold and platinum electrodes. The effects of the electrode material on the formation of formate and syngas using these solutions are presented and discussed.