Uneven phosphoric acid interfaces with enhanced electrochemical performance for high-temperature polymer electrolyte fuel cells.

Ultrahigh mass transport resistance and excessive coverage of the active sites introduced by phosphoric acid (PA) are among the major obstacles that limit the performance of high-temperature polymer fuel cells, especially compared to their low-temperature counterparts. Here, an alternative strategy of electrode design with fibrous networks is developed to optimize the redistribution of acid within the electrode. Via structural tailoring with varied electrospinning parameters, uneven migration of PA with dispersed droplets is observed, subverting the immersion model of conventional porous electrode. Combining with experimental and calculation results, the microscaled uneven PA interfaces could not only provide extra diffusion pathways for oxygen but also minimize the thickness of PA layers. This electrode architecture demonstrates enhanced electrochemical performance of oxygen reduction within the PA phase, resulting in a 28% enhancement of the maximum power density for the optimally designed electrode as cathode compared to that of a conventional one.

Efficient Design for a High-Energy and High-Power Capability Hybrid Electric Power Device with Enhanced Electrochemical Interfaces.

Fabrication of novel electrode architectures with tailored electrochemical interfaces (EI) is an effective strategy for enhancing charge and mass transport processes within electrochemical devices. Here, we design and fabricate a well-hybrid electrode based on the coupling of polyaniline (PANI) nanowires and Pt-based electrocatalysts to manufacture a hybrid electric power device (HEPD) combining the advantages of supercapacitors and fuel cells. Because of the boosted charge transfer between PANI nanowires and Pt-based materials via enhanced EIs, the HEPD assembled with hybrid electrodes shows remarkable performance with a peak power density of 222 mW cm-2, a specific power of 3810 W kg-1, and a specific energy of 2100 Wh kg-1, normalized to the mass of membrane electrode assemblies. The in situ Raman spectra and extended electrochemical studies demonstrate the intrinsic mechanism of charge transfer processes within hybrid electrodes, shedding light on the alternative progress of electrochemical energy conversion systems and storage devices.