of more than 20% in the last few years. [1,2] Hybrid lead halide perov skites typically have a 3D ABX 3 (where, A = CH 3 NH 3 + (MA), B = Pb, and X = Cl, Br, and I) crystal structure con sisting of [PbI 6 ] and MA + units in their lattice framework and their band gaps can be tuned by halide engineering. [3][4][5] However, the key challenge in commer cializing 3D organic-inorganic hybrid perovskite photovoltaics is related to well known issues with longterm instability of devices under ambient conditions. [6,7] Recently, another class of 2D organicinorganic hybrid perovskite counterparts have attracted attention owing to their superior ambient stability and prom ising optoelectronic properties. [8][9][10][11][12][13][14] There is now considerable interest in 2D hybrid perovskite compounds, typi cally represented by the generic for mula (Aʹ) 2 (MA) n−1 M n X 3n+1 , where Aʹ is a longchain organic spacer, MA is small organic cation, M is a divalent metal, and n is the number of perovskite layers per unit cell. [15,16] These 2D hybrid halide perovskites exhibit a characteristic quantum well (QW)like structure owing to the selfassembled periodic array of perovskite [PbI 6 ] This work reveals the intrinsic carrier transport behavior of 2D organolead halide perovskites based on phase-pure homologous (n = 1, 2, and 3) Ruddelsden-Popper perovskite (RPP) (BA) 2 (MA) n−1 Pb n I 3n+1 single crystals. The 2D perovskite field effect transistors with high-quality exfoliated 2D perovskite bulk crystals are fabricated, and characteristic output and transfer curves are measured from individual single-crystal flakes with various n values under different temperatures. Unipolar n-type transport dominated the electrical properties of all these 2D RPP single crystals. The transport behavior of the 2D organolead halide hybrid perovskites exhibits a strong dependence on the n value and the mobility substantially increases as the ratio of the number of inorganic perovskite slabs per organic spacer increases. By extracting the effect of contact resistances, the corrected mobility values for n = 1, 2, and 3 are 2 × 10 −3 , 8.3 × 10 −2 , and 1.25 cm 2 V −1 s −1 at 77 K, respectively. Furthermore, by combining temperature-dependent electrical transport and optical measurements, it is found that the origin of the carrier mobility dependence on the phase transition for 2D organolead halide perovskites is very different from that of their 3D counterparts. Our findings offer insight into fundamental carrier transport behavior of 2D organic-inorganic hybrid perovskites based on phase-pure homologous single crystals.
Field Effect Transistors