Ionic liquid based dopant-free band edge shift in BiVO4 particles for photocatalysis under simulated sunlight irradiation. Issue 16 (22nd June 2022)

• Record Type: Journal Article
• Authors: Khan, Niqab; Wolff, Rogério Nunes; Ullah, Hameed; Chacón, Gustavo J.; Rosa, Washington Santa; Dupont, Jairton; Gonçalves, Renato Vitalino; Khan, Sherdil
• Is Part Of: Materials advances. Volume 3:Issue 16(2022)
• Page Start: 6485
• Page End: 6495
• Publication Date: 2022-06-22
• Subjects: 620.11
• DOI: 10.1039/d2ma00259k
• Languages: English
• ISSNs: 2633-5409

Abstract

Abstract : Foreign element dopant-free Ionic liquid-based synthesis can shift the band edges of a semiconductor. Abstract : Foreign elemental doping is a widely utilized strategy to modify the electronic structure of semiconductors. Herein, we present a dopant-free novel synthesis approach to control the electronic structure of a semiconductor. Utilizing butyl methyl imidazolium ([BMIM]Cl) and methoxyethyl methyl imidazolium ([M(MOE)Im][Cl]) chloride ILs, we prepared four different Bi and V based ILs: 3-butyl-1-methyl-1 H -imidazol-3-ium vanadate [BMIm][VO3 ], 3-(2-methoxyethyl)-1-methyl-1 H -imidazol-3-ium vanadate [M(MOE)Im][VO3 ], 3-butyl-1-methyl-1 H -imidazol-3-ium tetrachlorobismate [BMIm][BiCl4 ] and 3-(2-methoxyethyl)-1-methyl-1 H -imidazol-3-ium tetrachlorobismate [M(MOE)Im][BiCl4 ]. Owing to the bimetallic oxide nature of BiVO4, these gels were mixed either with each other or with Bi/V commercial salts and simply heat-treated to obtain monoclinic BiVO4 . Depending on the IL, the bandgap energy of pure BiVO4 will be redshifted (2.44 to 2.25 eV). The IL based synthesis induced oxygen vacancies and uplifted the BiVO4 valence band edge as observed in the X-ray photoelectron spectroscopy (XPS). These effects were profound for IL anchored Bi; however, the side effects of this synthesis were chemisorption of a higher oxygen content and low reactivity of Bi with V to form an additional V2 O5 phase. ILs acted as templates to form smooth spherical particles with improved crystallinity. [M(MOE)Im] based synthesis resulted in lower-order crystallinity and a large V–O bonding length of BiVO4 compared to [BMIm] which may be ascribed to its lower-order cationic–anionic electrostatic attraction associated with the presence of oxygen in the ether-group for [M(MOE)Im]. [BMIm] cation-based synthesis suppressed photogenerated charge-recombination and resulted in a five-fold O2 evolution of ∼30 μmol for 3 h (AM 1.5G illumination) compared to pure BiVO4 which was better compared to the sample prepared by the conventional hydrothermal process. It also improved the photocurrent, and the MS plots have shown that the conduction band was not much affected; however, the defect density was larger for IL based synthesis.