Direct detection of ethyl carbamate in baijiu by molecularly imprinted electrochemical sensors based on perovskite and graphene oxide.

Ethyl carbamate (EC), a carcinogen commonly found in Baijiu, requires an efficient detection method for quality control and monitoring. This study introduces a novel molecularly imprinted electrochemical sensor for sensitive and selective EC detection. We proposed a simple sol-gel method for the growth of perovskite-structured lanthanum manganate (LaMnO3) on graphene oxide (GO). A non-enzymatic electrochemical sensor was developed by coating a molecularly imprinted polymer synthesized via precipitation polymerization onto the surface of LaMnO3@GO. LaMnO3, with its superior three-dimensional nanocube structure, demonstrated excellent electrocatalytic activity, while the addition of GO provided a large specific surface area. The results indicate that the developed sensor exhibits exceptional recognition ability and electrochemical activity, which is attributed to the high affinity of LaMnO3@GO@MIP for EC. The sensor displays a broad linear range from 10 to 2000 µM, with a detection limit as low as 2.18 µM and long-term durability of 28 days. Notably, it demonstrates excellent selectivity, reproducibility, and stability even under different interference conditions. The sensor was successfully used to determine EC in real Baijiu samples. Overall, the sensor has broad application prospects for detecting trace contaminants in the field of food safety.

A sensitive enzyme-free electrochemical sensor based on ZnWO4@co-MNPC@MIP for specific recognition and determination of chloramphenicol in milk sample.

We have carefully built a new chloramphenicol (CAP) electrochemical sensor, which takes the zinc tungstate @ cobalt magnetic nanoporous carbon @ molecularly imprinted polymer (ZnWO4@Co-MNPC@MIP) as the core. First, we successfully prepared Co-MNPC nanomaterials using an efficient one-step hydrothermal method and a direct carbonization method. Next, we recombined ZnWO4 with Co-MNPC and synthesized the completely new ZnWO4@Co-MNPC complex by using the hydrothermal method. To further improve its performance, we combined ZnWO4@Co-MNPC with a molecular imprinted polymer and coated a molecular imprinted (MIP) shell on the surface of ZnWO4@Co-MNPC by precipitation polymerization. This shell not only gives the sensor a new performance but also gives it a stronger peak current, resulting in a more accurate detection of CAP. Under optimal conditions, the ZnWO4@Co-MNPC@MIP (MMIP) electrode has a stronger CAP detection peak current than the one-component electrode, with a fairly wide linear range: 0.007-200 µM and 200-1400 µM. Even more surprisingly, the detection limit is as low as 0.0027 µM, which allows the sensor to maintain excellent selectivity and stability in the face of various interferences, making it an excellent electrochemically modified electrode. Compared to magnetic non-molecular imprint sensors (MNIPs), MMIP sensors have higher detection efficiency. After practical application, we found that the ZnWO4@Co-MNPC@MIP modified electrode was satisfactory in milk samples.

Carrier Tuning in ZnSnN2 by Forming Amorphous and Microcrystalline Phases.

ZnSnN2 (ZTN), an earth-abundant element semiconductor, is a potential candidate for photovoltaic applications. However, the excessively high n-type carrier concentration caused by intrinsic defects hinders its progress. In this work, a series of Zn1± xSnN2 thin films are fabricated by RF-magnetron sputtering deposition. The zinc-rich composition is found to promote the crystallization of ZTN. As a main source of n-type carriers in the zinc-rich thin films, the interstitial Zn dominates the change of carrier concentration with an increase in the Zn/Sn ratio. Near the stoichiometric ratio, amorphous ZTN (a-ZTN) thin films are fabricated, and the n-type carrier concentration is suppressed to 1016 cm-3. With an increase in the Zn/Sn ratio from 0.9 to 1.3, the n-type carrier concentration can be tuned in the range 1016-1019 cm-3, accompanied by the phase-transition from a-ZTN to microcrystalline ZTN (µc-ZTN). For the a-ZTN thin film, the carrier mobility reaches up to 7 cm2 V-1 s-1, and the photoresponse covers almost the whole visible band. The above properties demonstrate that a-ZTN and µc-ZTN are potential candidates for photovoltaic applications.