All-inorganic perovskite
solar cells (IPSCs) have gained massive
attention due to their less instability against common degradation
factors (light, heat, and moisture) than their organic–inorganic
hybrid counterparts. Inorganic perovskites bear a general formula
of CsPbX3 (X = Cl, I, Br). The mixed halide CsPbIBr2 perovskite possesses an intermediate band gap of 2.03 eV
with enhanced stability, which is still available for photovoltaic
applications and the research focus of this work. We present a synergistic
approach of pre-heated solution dropping with inorganic additive inclusion
to deposit the organic-free triple anion CsPbIBr2 PSC.
Erbium (Er)-passivated triple-anion CsI(PbBr2)0.97(ErCl3)0.03 IPSCs with inorganic carrier selective
layers (CTLs), that is, organic-free, are fabricated with enhanced
carrier diffusion length and crystalline grain size while lessening
the grain boundaries near perovskite active layer (PAL)-bulk/carrier
selective interfaces. As a result, the trap-state densities within
the perovskite bulk were suppressed with stabilized CTL/PAL interfaces
for smooth and enhanced carrier transportation. Therefore, for the
first time, we contradict the common belief of V
OC loss due to halide segregation, as a nice V
OC of about 1.34 V is achieved for an organic-free IPSC
through enriching initial radiative efficiency, even when halide segregation
is present. The optimized organic-free IPSC yielded a power conversion
efficiency of 11.61% and a stabilized power output of 10.72%, which
provides the potential opportunity to integrate into agrivoltaics
(AgV) projects.