Highly Stable and Reversible Coloration of Oxide Nanoparticles Film by Ultrafast‐CW Laser Induced Band Engineering

Abstract

Coloration in oxides meets the challenge in achieving high stability and repeatability simultaneously. In this work, reversible coloration of TiO2 nanoparticles (NPs) film is demonstrated by alternate ultrafast (UF) laser and continuous wave (CW) laser irradiation. Under UF laser irradiation, oxygen vacancies are introduced in the TiO2 lattice, which lead to the bandgap reduction (2.73 to 1.50 eV) and surface blackening. The blackened area can achieve high resolution with size down to ≈1.1 µm. This coloration in TiO2 also shows excellent thermal stability that color fading is negligible even after thermal annealing at 700 K for 2 h in air. The generated high temperature by CW irradiation is known to be beneficial for the O2 dissociation on defected TiO2, thus promoting the internal oxygen diffusion to eliminate the vacancies. The energy band structure of TiO2 can be recovered accordingly, and decoloration is achieved. TiO2‐NPs film shows stable microstructures with barely changed optical properties after 12 cycles of coloration–decoloration process. This band engineering‐induced reversible coloration can also be applicable for broad oxides, e.g., ZnO, HfO2, and Ga2O3. Such highly stable and reversible coloration is promising in high‐performance micro/nano‐devices development for color display and optical encryption.