It is of great significance to synthesize carbon dots (CDs) with desirable hydrophilicity for the ever-growing application of CDs in different fields. In this study, the hydrophilic and hydrophobic CDs were facilely prepared by solvothermal treatment of o-dihydroxybenzene and urea in N,N-dimethylformamide (DMF). Optimization experiments revealed that the solvothermal temperature has a great impact on the surface states of the CDs. The hydrophobic CDs with a contact angle of 110.7° was obtained at 200 °C. The structural and optical characterizations, along with theoretical calculations elucidated that the lipophilic nature of the CDs was resulting from the formation of polymer chains. The presence of extended conjugated sp²-domains and amino groups contributed to the red emission of the CDs synthesized at low reaction temperatures (160–200 °C). With the further increase of solvothermal temperature, the hydrophobic CDs were gradually transformed to the hydrophilic state accompanying the blue shift of the fluorescence of the CDs. The highly hydrophilic CDs with a contact angle of 25.9° were obtained at 240 °C due to the increased formation of hydrophilic functional groups on the surface of CDs. The red emissive CDs exhibited a sensitive color and fluorescence response to ethanol content while the fluorescence of the blue emissive CDs remained constant. By combining the two kinds of CDs, a dual-emission sensor was constructed, which was successfully applied for the evaluation of the alcoholic strength in commercial Baijiu commodities in both fluorometric and colorimetric modes.

Diatomic site catalysts (DACs) with two adjacent atomic metal species can provide synergistic interactions and more sophisticated functionalities to break the bottleneck of intrinsic drawbacks of single atom catalysts (SACs). Herein, we have designed a CuZn diatomic site (CuZn-DAS) electrocatalyst with unique coordination structure (CuN₄–ZnN₄) by anchoring and ordering the spatial distance between the metal precursors on the carbon nitride (C₃N₄) derived N-doped carbon (NC) substrate. The CuZn-DAS/NC shows high activity and selectivity for electroreduction CO₂ into CO. The Faradaic efficiency for CO of CuZn-DAS/NC (98.4%) is higher than that of Cu single atomic site on NC (Cu-SAS/NC) (36.4%) and Zn single atomic site on NC (Zn-SAS/NC) (66.8%) at −0.6 V versus reversible hydrogen electrode (vs. RHE). In situ characterizations reveal that the CuZn-DAS is more favorable for the formation and adsorption of *COOH than those of the electrocatalysts with single atomic site. Theorical calculations show that the charge redistribution of Zn site in CuZn-DAS/NC caused by the considerable electron transfers from Zn atoms to the adjacent Cu atoms can reduce the adsorption energy barriers for *COOH and *CO production, improving the activity and CO selectivity.