Fu, LuluGuan, ZihaoChen, LuYan, ZhenyiHuang, ZhipengHumphrey, Mark G.Zhang, Chi2026-02-262026-02-260897-4756ORCID:/0000-0002-4433-6783/work/206554210https://hdl.handle.net/1885/733806673Functional materials displaying profound third-order optical nonlinearities across a wide spectral region and a broad temporal domain are required for feasible signal processing and sophisticated laser conditions. Particularly desirable are the materials with convertible nonlinear optical (NLO) activity toward both nanosecond and femtosecond pulses. Herein, for the first time, tunable NLO performance in MXene–porphyrin composite systems is realized through fine control of the configuration. Two D–A-type porphyrin–terpyridine–CdIIBr2complexes with asymmetric, configuration-different structures were designed, synthesized, and subsequently incorporated with MXene (Ti3C2Tx) nanosheets. In these two samples, porphyrin and the CdIIBr2L unit are mutually perpendicular or parallel to each other due to the benzene ring and the resulting steric hindrance. Both samples exhibit remarkably enhanced optical nonlinearity compared with their untreated samples. Notably, Ti3C2Tx–CdCPor (C: coplanar) possesses optimized strong NLO performance with a corresponding nonlinear absorption coefficient (βeff) of 1.06 × 103cm GW–1toward the ultrafast femtosecond lasers at 800 nm, while Ti3C2Tx–CdOPor (O: orthogonal) exhibits strong reverse saturable absorption when it responds to nanosecond laser irradiation at 532 nm and shows no response to femtosecond lasers. These results demonstrate that the two newly developed MXene composites are very promising optical limiting (OL)candidates for practical applications across wide spectral and temporal domains and that covalently functionalizing MXene-based materials with configuration-different chromophores may be a useful and effective approach to engineering adaptable photonic devices with broad-ranging and feasible NLO activity.Financial support from the National Natural Science Foundation of China (51432006), the Ministry of Science and Technology of China for the International Science Linkages Program (2011DFG52970), the Ministry of Education of China for the Changjiang Innovation Research Team (IRT14R23), the Ministry of Education and the State Administration of Foreign Experts Affairs for the 111 Project (B13025), and the Innovation Program of Shanghai Municipal Education Commission is gratefully acknowledged. M.G.H. thanks the Australian Research Council (DP170100411) for support.11en©2025 The authors2025-09-1110.1021/acs.chemmater.5c00892105017228703