Abstract A hydrothermal approach was used to prepare B-doped graphene with B 2 O 3 as reductant and boron source. Results reveal that the boron atoms have been successfully embedded… Click to show full abstract
Abstract A hydrothermal approach was used to prepare B-doped graphene with B 2 O 3 as reductant and boron source. Results reveal that the boron atoms have been successfully embedded into graphene with a high content of a total B species (2.85 at.%). Then, B-doped graphene was exfoliated further into monolayer nanosheet by impregnating Au@AuPt core-shell nanoparticles (Au@AuPt NPs) because boron atom creates a net positive charge, which facilitates Au@AuPt NPs adsorption to form Au@AuPt NPs/B-doped graphene hybrid nanocatalysts. After that, the Au@AuPt NPs/B-doped hybrid suspension was dropped on glassy carbon electrode for sensing rutin. In this way, the dispersed carboxyl units of B-doped graphene can form hydrogen bonding with the phenolic hydroxyl groups of rutin, making rutin enrich easily on modified electrode surface to enhance the electrochemical response. At the same time, its electrochemical mechanism on the modified electrode was elucidated using cyclic voltammetry. It was found that its electrochemical behavior on modified electrode surface was a surface-controlled quasi-reversible process, and the charge transfer coefficient (α) and electron transfer number (n) were 0.296 and 2, respectively. This electrochemical sensor for rutin provided a wide linear response range of 2.00 × 10 −9 –4.00 × 10 −6 M with the detection limit (S/N = 3) of 2.84 × 10 −10 M. The proposed method was applied successfully to selective determination of rutin in Tablets with acceptable recovery range (97.23–101.65%).
               
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