Abstract
Since the discovery of thermochromism in halide perovskites, new perovskite materials with excellent thermochromic properties have been developed. Among them, two-dimensional (2D) layered hybrid perovskites have been extensively explored because of their highly tunable structures and unique thermochromic responses. In this study, the thermochromism in acene alkylamine-spaced 2D perovskite single crystals (PEA)2PbI4 and (NEA)2PbI4 (PEA = 2-phenylethylammonium, NEA = 2-(2-naphthyl)-ethanammonium) is studied. These 2D perovskites undergo a distinct color change between orange and red during heating and cooling cycles, with the corresponding optical bandgap modulation monitored by variable-temperature absorption spectroscopy. The thermochromism in (PEA)2PbI4 and (NEA)2PbI4 is caused by lattice expansion, as confirmed by thermogravimetric–differential scanning calorimetry and variable-temperature powder X-ray diffraction. Compared with the thermochromism caused by structural phase transition, lattice-expansion-modulated thermochromism demonstrates rapid color change and luminescence recovery, and enhanced thermal cycling stability. This study presents a new strategy for developing thermochromic halide perovskites for multifunctional applications.
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