Mechanism of visible light photocatalytic NOx oxidation with plasmonic Bi cocatalyst-enhanced (BiO)2CO3 hierarchical microspheres

文献情報

出版日 2015-02-27
DOI 10.1039/C4CP06045H
インパクトファクター 3.676
著者

Yanjuan Sun, Zaiwang Zhao, Fan Dong, Wei Zhang


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要旨

Semimetal bismuth (Bi), as an emerging non-noble metal-based cocatalyst and plasmonic photocatalyst, has attracted significant attention. In this work, a one-pot solvent-controlled synthesis strategy was utilized for the in situ-deposition of plasmonic Bi nanoparticles onto the surfaces of (BiO)2CO3 microspheres (BOC-WE) using bismuth citrate, sodium carbonate, and ethylene glycol as precursors. The introduction of the Bi nanoparticles has a pivotal effect on the morphology, optical and photocatalytic performance of the pristine (BiO)2CO3. The results indicated that the Bi nanoparticles were generated on the surface of (BiO)2CO3 microspheres via the in situ reduction of Bi3+ by ethylene glycol. The Bi-deposited (BiO)2CO3 microspheres were used for the photocatalytic purification of NOx in air under visible light irradiation. Significantly, the BOC-WE samples exhibited a drastically promoted photocatalytic performance with a NOx removal ratio (η) of 37.2%, superior to pristine (BiO)2CO3 (η = 19.1%), outperforming other well-known visible light photocatalysts, such as C-doped TiO2 (η = 21.8%), BiOBr (η = 21.3%), BiOI (η = 14.9%) and C3N4 (η = 25.5%). The conspicuously enhanced photocatalytic capability can be attributed to the synergistic effects of the surface plasmon resonance (SPR) effect, increased visible light absorption and the efficient separation of electron–hole pairs induced by the Bi nanoparticles. The Bi nanoparticles can act as a non-noble metal-based cocatalyst for strengthening photocatalytic performance, which is similar to the behavior of noble metals (Au, Ag) in enhancing photocatalysis. The mechanism of visible light photocatalytic NOx oxidation was investigated. DMPO-ESR spin-trapping results demonstrated that hydroxyl radicals were confirmed to be the main active species for NOx photo-oxidation. Due to the SPR effect of Bi, the BOC-WE could produce more hydroxyl radicals than BOC, which was responsible for the enhanced NO photo-oxidation ability. Moreover, the BOC-WE photocatalysts showed high photochemical stability under repeated irradiation. This work demonstrates the feasibility of utilizing low cost Bi cocatalysts as a substitute for noble metals to enhance the performance of other photocatalysts. This work could not only provide new insights into the in situ fabrication of Bi/semiconductor nanocomposites, but also pave a new way for the modification of photocatalysts with non-noble metals as cocatalysts to achieve an enhanced performance for environmental and energetic applications.

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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
自己引用率: 10.3%
年間論文数: 3036

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

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