between molecular isomers, a phase transition between inorganic solids, or a change in the crystalline phases of liquid crystals. [8] To date, many thermochromic materials have been reported and commercialized, such as leuco dyes, [9] thermotropic liquid crystals, [10][11][12] titanium and vanadium oxides, [13][14][15] and peptide-based polydiacetylene. [16][17][18] Among these examples, the liquid-based leuco dyes and liquid crystals are unique as they can easily be made to fill various shaped voids, can be deposited onto virtually any substrate, and are straightforward to scale-up in terms of production. However, organic dyes have a tendency to suffer from photodegradation, require longer optical path lengths due to a small absorption coefficient (typically ≈10 4 L mol −1 cm −1 ), and possess limited tunability of the T trans . [19] Liquid crystals require a stringent microencapsulation process to avoid degradation and contamination, [20] and the molecules need to be chemically modified in order to tune the T trans . Instead of addressing these limitations directly, we sought to circumvent them by a different approach to traditional liquid-based thermochromics.Herein, we report a liquid-based thermochromic system based on colloidal antimony selenide (Sb 2 Se 3 ) ultrathin nanowires (NWs) that undergo a reversible growth/dissolution process in a Sn 2+ -added amine-thiol mixture. For brevity, we will refer to this liquid thermochromic system as the amine-thiol nanowire (ATNW) solution. Antimony selenide has an optical bulk bandgap of 1.1-1.2 eV, [21] and therefore absorbs wavelengths across the entire visible and near-infrared (NIR) range. It possesses a high absorption coefficient (>10 5 cm −1 ), [22] has low toxicity, and is composed of relatively earth-abundant constituents. As a material that has in recent times been developed for solar cell and photodetector applications, [23] Sb 2 Se 3 nanostructures are resilient toward photodegradation under hours of continuous irradiation and resistant to oxidation under ambient conditions. We find that ATNWs undergo a continuous color change from transparent pale yellow to dark brown when heated and reverse rapidly to pale yellow when cooled. Different from conventional inorganic pigments whose thermochromic properties are based on changes in crystal structure and/or molecular stoichiometry, the color changes in the ATNW solution are due to rapid crystal growth and dissolution. The Sb 2 Se 3 1806164 (2 of 7) www.advmat.de www.advancedsciencenews.com