“…The deconvolution of C 1 s spectrum revealed the nature of these functionalities, denoting the existence of C–C (284.5 eV), C–O (285.8 eV), C=O (287.0 eV), and O–C=O (288.3 eV) groups, and π−π* transitions (290.0 eV). Here, C–O groups (phenols and ethers [ 2 , 28 , 46 ]) are predominant, followed by C=O (carbonyls, quinones [ 2 , 28 , 44 ]), O–C=O (carboxylic [ 2 , 28 , 46 ]), and π−π* transitions (HOMO−LUMO transitions coming from the ring excited by the exciting photoelectrons for unsaturated carbon in aromatic rings [ 47 ]). Furthermore, the deconvolution of O 1 s spectrum showed the presence of peaks at 530.5, 532.1 and 533.7 eV, which can be related to O 2- in nickel oxide [ 48 ], O=C in carbonyl and carboxylic groups [ 46 ], and O–C in phenols, ethers, and lactones [ 46 ], respectively.…”