“…The remarkable strides achieved in perovskite application development over a short period stem from the realization of high-quality perovskites in the form of crystals and thins films. The perovskite formation entails the synthesis of their parent precursors, which was found long before. , The first metal-halide perovskites, reported in 1893, employed cesium as A-site cations to form CsPbX 3 , which was later identified to follow the perovskite structure in 1958. , In 1978, methylammonium ions (MA + ) were introduced, leading to organic–inorganic metal halide perovskites based on either Pb or Sn. , A range of options for ions to occupy in their corresponding sites in the ABX 3 structure is possible, and each chemical composition determines their own distinct optoelectronic properties such as their band gap, absorption coefficients, and photoluminescence. , Perovskite dimensions can also be manipulated to form nanoparticles, 2D, or quasi-2D structures through appropriate precursor and synthesis choices. − The chemical reaction governing the perovskite synthesis is seemingly straightforward, for example, simply by mixing precursors in solution followed by casting films or growing free-standing particles, as described by the following chemical equation: AX + BX 2 → ABX 3 Here, A represents organic or inorganic monovalent cations occupying A-sites, surrounded by corner-sharing BX 6 octahedra to maintain a charge balance. B symbolizes divalent transition metal cations, while halide ions such as Cl – , Br – , and I – occupy X-sites. , …”