“…To study the surface chemistry of the CQDs, X-ray photoelectron spectroscopy (XPS) and Fourier-transform infrared (FTIR) spectroscopy were carried out. The three representative peaks at 284.7, 531.6, and 399.6 eV in the XPS full spectrum of N-CQDs-1 (Figure A) correspond to C 1s, O 1s, and N 1s, respectively; the high-resolution XPS spectrum of C 1s (Figure B) exhibits four peaks at 284.7, 286.0, 288.0, and 288.9 eV, corresponding to the CC/C–C, C–N, C–O/C–O–C, and CO groups, respectively; , the O 1s spectrum of N-CQDs-1 (Figure C) presents two peaks at 530.6 and 531.8 eV assigned to the CO and the C–OH/C–O–C groups; , and the N 1s spectrum of N-CQDs-1 (Figure D) depicts two peaks at 399.6 and 401.1 eV, attributed to C–N–C and N–H, respectively. , The full spectrum of N-CQDs-2 presented in Figure A is similar to that of N-CQDs-1, showing three typical peaks: C 1s (284.8 eV), N 1s (399.5 eV), and O 1s (531.3 eV); the high-resolution XPS spectrum of C 1s (Figure B) indicates that CC/C–C (284.7 eV), C–N (286.0 eV), C–O/C–O–C (288.0 eV), and CO (288.9 eV) groups exist in N-CQDs-2; the O 1s spectrum (Figure C) of N-CQDs-2 shows the presence of CO (529.6 eV) and C–OH/C–O–C (531.3 eV) groups in N-CQDs-2; and the high-resolution N 1s spectra (Figure D) of N-CQDs-2 shows that N exists in the form of C–N–C (399.5 eV) and N–H (401.2 eV) in N-CQDs-2. ,− Comparing the XPS results of the two CQDs, most of the functional groups are similar. The above results indicate that N has been successfully doped into the structure of CDs, and the CQDs were coated with oxygen-containing functional groups, such as carboxylic, hydroxyl, carbonyl, and epoxy groups, which facilitate their hydrophilicity and dispersity in water.…”