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Surface engineering improving selective hydrogenation of p-chloronitrobenzene over AuPt alloy/SnNb2O6 ultrathin nanosheets under visible light
Surface Engineering Improving Selective Hydrogenation of p-Chloronitrobenzene over AuPt alloy/SnNb2O6 ultrathin nanosheets under Visible light. [Display omitted] •Bimetallic alloy AuPt decorated SnNb2O6 nanosheet (AuPt/SN) as a photocatalyst has been constructed successfully.•The catalyst (Au0.5Pt0....
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Published in: | Chemical engineering science 2022-11, Vol.262, p.117936, Article 117936 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Surface Engineering Improving Selective Hydrogenation of p-Chloronitrobenzene over AuPt alloy/SnNb2O6 ultrathin nanosheets under Visible light.
[Display omitted]
•Bimetallic alloy AuPt decorated SnNb2O6 nanosheet (AuPt/SN) as a photocatalyst has been constructed successfully.•The catalyst (Au0.5Pt0.5/SN) exhibits a high catalytic conversion efficiency for p-chloronitrobenzene (99.8%) with a selectivity of p-chloroaniline (99.1%).•SN could activate p-chloronitrobenzene via a Sn2+···–NO2 coordination.•A synergetic effect among Lewis base sites (Sn2+), AuPt alloy and photogenerated electrons is proposed.•A photocatalytic mechanism is determined at molecule scale.
AuPt alloy/SnNb2O6 ultrathin nanosheet (AuPt/SN) as a photocatalyst is constructed for selective hydrogenation of p-chloronitrobenzene (p-CNB) under visible light irradiation. A typical catalyst (Au0.5Pt0.5/SN) exhibits a high conversion of halonitrobenzenes (99.8%) and selectivity of haloaniline (99.1%). The results of in situ ATR-IR, XPS and Raman indicate a preferential chemoselective adsorption of –NO2 that Lewis base sites (Sn2+) on the catalyst could selectively coordinate with –NO2 whereas C-Cl bond is not be bonded, improving the catalytic selectivity. Atom Pt in alloy is responsible for the formation of ·H, while Au inhabits the dissociation of C-Cl via repressing the generation of Pt-H. The photogenerated electrons can accelerate the ·H formation. ·H could be transferred to Sn2+ sites for the hydrogenation of –NO2 by hydrogen spillover. Therefore, the high performance of the catalyst can be attributed to a surface synergetic effect among Lewis base sites (Sn2+), AuPt alloy and photogenerated electrons. |
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ISSN: | 0009-2509 1873-4405 |
DOI: | 10.1016/j.ces.2022.117936 |