摘要
Abstract Multimode luminescence relates to how charge carriers are transported and recombined in response to various physical excitations. It shows promising applications in many fields like advanced anti‐counterfeiting, information storage and encryption. Enabling a stable single compound with multimode luminescence is a unique technology but still remains a challenge. Herein, a versatile and high‐performance energy storage LiTaO 3 :0.01Tb 3+ ,xGd 3+ perovskite is discovered by utilizing the interplay of electron‐trapping defect levels and hole‐trapping Tb 3+ . It combines an excellent charge carrier storage capacity (≈7 and 12 times higher than state‐of‐the‐art BaFBr(I):Eu 2+ and Al 2 O 3 :C), >1200 h storage duration, >40 h afterglow, efficient optically stimulated luminescence, persistent mechanoluminescence, and force‐induced charge carrier storage features. Particularly, it well responds to various stimuli channels, i.e., wide‐range X‐rays to 850 nm infrared photons, thermal activation, mechanical force grinding, or compression. To elucidate this multimode luminescence, charge carrier trapping and release processes in LiTaO 3 :0.01Tb 3+ ,xGd 3+ with various physical stimulations will be unraveled by combining the vacuum‐referred binding diagram construction, spectroscopy, thermoluminescence, and mechanoluminescence techniques. The versatile and high‐performance LiTaO 3 :0.01Tb 3+ ,xGd 3+ enables promising proof‐of‐concept multimode luminescence applications in advanced anti‐counterfeiting, flexible X‐ray imaging, continuous compression force sensing, and non‐real‐time recording.