Sunset yellow (SY) is a synthetic azo dye widely used in food and cosmetics. However, concerns have been raised about its potential health risks, including its nephrotoxicity and genotoxicity, when used in excessive amounts. Illegal addition of SY may cause allergic reactions or genetic damage. Therefore, a rapid method for detecting SY is needed. To develop a rapid detection method for sunset yellow (SY) with the aim of preventing its illegal addition in food, this study utilized agricultural waste asparagus peel (AP) as a carbon source and synthesized amino-functionalized carbon quantum dots (AP-CDs) via a green hydrothermal method. A highly sensitive detection platform was established based on the fluorescence quenching mechanism of AP-CDs in the presence of SY. The microstructure of AP-CDs was characterized using transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). Their optical properties were assessed via ultraviolet–visible absorption spectroscopy (UV-vis) and fluorescence spectroscopy (FS). Furthermore, key experimental parameters affecting SY detection were systematically optimized. Results revealed that the synthesized AP-CDs possessed surface hydrophilic functional groups, including hydroxyl, amide, and carboxyl groups, and were composed of carbon (C), oxygen (O), and nitrogen (N) elements. Optical performance studies demonstrated that AP-CDs exhibited a strong fluorescence emission at 470 nm under 380 nm excitation, with a quantum yield (Φ) of 15.9%. Under the optimized conditions (pH 7.0, 0.5 mg/mL AP-CDs), the fluorescence intensity showed a linear response to the concentration of SY over the range of 0.1 to 100 μM (R² = 0.9929), achieving a detection limit of 0.92 μM. This strategy not only enables sustainable resource utilization but also provides a sensitive and practical approach for food safety monitoring, demonstrating significant potential for real-world applications.

In recent years, various devices utilizing surface acoustic waves (SAW) have emerged as powerful tools for manipulating particles and fluids in microchannels. Although they demonstrate a wide range of functionalities across diverse applications, existing devices still face limitations in flexibility, manipulation efficiency, and spatial resolution. In this study, we developed a dual-sided standing surface acoustic wave (SSAW) device that simultaneously excites acoustic waves through two piezoelectric substrates positioned at the top and bottom of a microchannel. By fully exploiting the degrees of freedom offered by two pairs of interdigital transducers (IDTs) on each substrate, the system enables highly flexible control of microparticles. To explore its capability on particle aggregation, we developed a two-dimensional numerical model to investigate the influence of the SAW phase modulation on the established acoustic fields within the microchannel. Single-particle motion was first examined under the influence of the phase-modulated acoustic fields to form a reference for identifying effective phase modulation strategies. Key parameters, such as the phase changes and the duration of each phase modulation step, were determined to maximize the lateral motion while minimizing undesired vertical motion of the particle. Our dual-sided SSAW configuration, combined with novel dynamic phase modulation strategy, leads to rapid and precise aggregation of microparticles towards a single focal point. This study sheds new light on the design of acoustofluidic devices for efficient spatiotemporal particle concentration.