Herein, facile room-temperature self-assembly and high-temperature pyrolysis strategy was successively conducted for in situ synthesizing novel TiO2/ TiN@N-C heterostructure by using typical sandwich-like precursors (MXene/ZIF-8). Zerodimensional (0D) TiO2, TiN and N-doped carbon nanoparticles were in situ formed and randomly anchored on the twodimensional (2D) N-doped carbon substrate surface, making TiO2/ TiN@N-C exhibit unique 0D/2D heterostructure. Relative to the extensively studied ZIF-8-derived N-doped carbon nanoparticles, TiO2/ TiN@N-C heterostructure displayed greatly boosted electrochemical active specific surface. Benefiting from the enhanced electrochemical property of TiO2/ TiN@N-C heterostructure, remarkable signal enhancement effect was achieved in terms of the oxidation of multiple hazardous substances, including clozapine, sunset yellow and benomyl. As a result, a novel electrochemical platform was constructed, the linear detection range were 10–1000 nM, 2.5–1250 nM, 10–1000 nM while the detection limits were evaluated to be 3.5 nM, 1.2 nM, 4.5 nM for clozapine, sunset yellow and benomyl, respectively. Besides, the practicability of the newly developed electrochemical method was verified by assessing the content of clozapine, sunset yellow and benomyl in real food samples.

Flexible self-supported laser-induced graphene (LIG) electrode devices were facilely fabricated through laser ablation technique by employing commercial polyimide film as the precursor material. Compared with the widely used traditional glassy carbon electrodes, the resulted LIG electrodes displayed abundant porous structure and surface defects. Notably, the onestep yielded LIG electrode devices were endowed with large electrochemically active surface area and accelerated electron transfer ability. Benefiting from its superior electrochemical property, these unmodified LIG electrodes exhibited remarkable enhanced electrochemical oxidation reactivity toward the food additive molecule Allura Red. Based on the augmented oxidation signal of Allura Red molecules on the LIG electrodes, a novel electrochemical sensor with high sensitivity for the detection of Allura Red was successfully developed. The sensor demonstrated a linear detection range spanning from 5 nM to 1 μM and exhibited a detection limit as low as 2.5 nM. Besides, the sensitivity was calculated to be 240.62 μA μM−1 cm− 2. More importantly, the sensor manifested outstanding stability, reproducibility, and practicality, further emphasizing its potential for real-world application.