Despite the ubiquity of poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) in applications demanding mechanical flexibility, the effect on the mechanical properties of common additives—i.e., dimethylsulfoxide (DMSO), Zonyl fluorosurfactant (Zonyl), and poly(ethyleneimine) (PEI)—has not been reported. This paper describes these effects and uses plasticized films in solar cells and mechanical sensors for the detection of human motion. The tensile moduli of films spin‐coated from solutions containing 0%, 5%, and 10% DMSO and 0.1%, 1%, and 10% Zonyl (nine samples total) are measured using the buckling technique, and the ductility is inferred from measurements of the strain at which cracks form on elastic substrates. Elasticity and ductility are maximized in films deposited from solutions containing 5% DMSO and 10% Zonyl, but the conductivity is greatest for samples containing 0.1% Zonyl. These experiments reveal enlargement of presumably PEDOT‐rich grains, visible by atomic force microscopy, when the amount of DMSO is increased from 0% to 5%. PEI—which is used to lower the work function of PEDOT:PSS—has a detrimental effect on the mechanical properties of the PEDOT:PSS/PEI bilayer films. Wearable electronic sensors employing PEDOT:PSS films containing 5% DMSO and 10% Zonyl are ­fabricated, which exhibit detectable responses at 20% strain and high mechanical robustness through elastic deformation.

In 2 O 3 has recently emerged as a promising catalyst for methanol synthesis from CO 2 . In this work, we present the promotional effect of Pd on this catalyst and investigate structure−performance relationships using in situ X-ray spectroscopy, ex situ characterization, and microkinetic modeling. Catalysts were synthesized with varying In:Pd ratios (1:0, 2:1, 1:1, 1:2, 0:1) and tested for methanol synthesis from CO 2 /H 2 at 40 bar and 300 °C. In:Pd(2:1)/SiO 2 shows the highest activity (5.1 μmol MeOH/g InPd s) and selectivity toward methanol (61%). While all bimetallic catalysts had enhanced catalytic performance, characterization reveals methanol synthesis was maximized when the catalyst contained both In−Pd intermetallic compounds and an indium oxide phase. Experimental results and density functional theory suggest the active phase arises from a synergy between the indium oxide phase and a bimetallic In−Pd particle with a surface enrichment of indium. We show that the promotion observed in the In−Pd system is extendable to non precious metal containing binary systems, in particular In−Ni, which displayed similar composition−activity trends to the In−Pd system. Both palladium and nickel were found to form bimetallic catalysts with enhanced methanol activity and selectivity relative to that of indium oxide.

We demonstrate the translation of a low cost, non-precious metal cobalt phosphide (CoP) catalyst from 1 cm 2 lab-scale experiments to a commercial-scale 86 cm 2 polymer electrolyte membrane (PEM) electrolyser. A 2-step bulk synthesis was adopted to produce CoP on a high surface area carbon support that was readily integrated into an industrial PEM electrolyser fabrication process. The performance of the CoP was compared head-to-head with a platinum-based PEM under the same operating conditions (400 psi, 50 °C). CoP was found to be active and stable, operating at 1.86 A.cm-2 for >1700 hours of continuous hydrogen production while providing substantial material cost savings relative to platinum. This work illustrates a potential pathway for non-precious hydrogen evolution catalysts developed in past decades to translate to commercial applications.