The effect of B-site alloying on the electronic and opto-electronic properties of RbPbI3: A DFT study

Abstract

Divalent cations mixed lead halide perovskites with enhanced performances, high stabilities, and reduced toxicity are requisite to make persistent progress in perovskite solar cells. However, the mixing strategy is not reported extensively in search of a lead reduced structure. Herein, we report the structural, electronic and optical properties of RbPb1-xMxI3 (where, M = {Sn,Ge} and x = {0.25, 0.50, 0.75}) by alloying the B-site with Sn and Ge, using the density functional theory. The formation enthalpy is estimated for all RbPb1-xMxI3 (with x = 0.25, 0.50, 0.75), which confirms stability for all the structures. The energy bandgap and density of states (DOS) have been thoroughly investigated. The energy bandgap decreases with the increasing Sn/Ge contents, the lowest bandgap of 1.850eV is observed at x=0.50 in the case of RbPb1-xGexI3 systems. Further, the effective masses and the binding energy of excitons and spectroscopic limited maximum efficiency (SLME) are also estimated for all the mixed systems. The exciton type is observed to change from Mott–Wannier to Frenkel type with increasing the contents of both Sn and Ge at the B-site. The maximum efficiency of 23% is achieved using an active layer containing an equal admixture of Sn/Ge and Pb. The estimated parameters of both the mixed systems are consistent with the available literature of similar types.