A semiconductor-ionic fuel cell (SIFC) is recognized
as a promising
technology and an alternative approach to reduce the operating temperature
of solid oxide fuel cells. The development of alternative semiconductors
substituting easily reduced transition metal oxide is a great challenge
as high activity and durability should be satisfied simultaneously.
In this study, the B-site Ni-doped La0.2Sr0.7Ti0.9Ni0.1O3−δ (LSTN)
perovskite is synthesized and used as a potential semiconductor for
SIFC. The in situ exsolution and A-site deficiency strategy enable
the homogeneous decoration of Ni/NiO nanoparticles as reactive sites
to improve the electrode reaction kinetics. It also supports the formation
of basic ingredient of the Schottky junction to improve the charge
separation efficiency. Furthermore, additional symmetric Ni0.8Co0.15Al0.05LiO2−δ (NCAL)
electrocatalytic electrode layers significantly enhance the electrode
reaction activity and cells’ charge separation efficiency,
as confirmed by the superior open circuit voltage of 1.13 V (close
to Nernst’s theoretical value) and peak power density of 650
mW cm–2 at 550 °C, where the latter is one
order of magnitude higher than NCAL electrode-free SIFC. Additionally,
a bulk heterojunction effect is proposed to illustrate the electron-blocking
and ion-promoting processes of the semiconductor-ionic composite electrolyte
in SIFCs, based on the energy band values of the applied materials.
Overall, we found that the energy conversion efficiency of novel SIFC
can be remarkably improved through in situ exsolution and intentional
introduction of the catalytic functionality.