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Preferential oxidation of carbon monoxide in hydrogen using zinc oxide photocatalysts promoted and tuned by adsorbed copper ions

机译:使用吸附的铜离子促进和调节的氧化锌光催化剂在氢气中优先氧化一氧化碳

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摘要

Preferential oxidation of CO (63 Pa) and O _2 (76 Pa) in H _2 (6.3 kPa) using spheroidal ZnO nanoparticles (22 nm × 47 nm) converted 52% of CO into CO _2, and selectivity to CO _2 was 92 mol% under UV-visible light for 5 h. When 0.5 wt.% of Cu ~(2+) was adsorbed on ZnO, 91% of CO was converted into CO _2 with a selectivity of 99 mol% under UV-visible light for 3 h. CO (63 Pa) was photocatalytically decreased to 2.3 mPa (0.35 ppm) in O _2 (150 Pa) and H _2 (6.3 kPa) for 5 h with a selectivity of 94 mol%. As evident from a XANES peak at 8983.1 eV, the surface Cu ~(II) sites trapped photogenerated electrons. Furthermore, O _2-derived species were reduced by accepting electrons from Cu ~I and protons from the neighboring formate species, as indicated by the FT-IR peaks at 2985, 2879, 1627, 1587, and 1297 cm ~(-1).
机译:使用球形ZnO纳米粒子(22 nm×47 nm)在H _2(6.3 kPa)中优先氧化CO(63 Pa)和O _2(76 Pa),将52%的CO转化为CO _2,对CO _2的选择性为92 mol %在紫外线可见光下持续5小时。当0.5wt。%的Cu〜(2+)吸附在ZnO上时,91%的CO在紫外可见光下3小时以99 mol%的选择性转化为CO _2。在O _2(150 Pa)和H _2(6.3 kPa)中将CO(63 Pa)光催化还原至2.3 mPa(0.35 ppm)5小时,选择性为94 mol%。从在8983.1 eV处的XANES峰可以明显看出,表面Cu〜(II)位点捕获了光生电子。此外,O _2衍生的物种通过接受来自Cu〜I的电子和来自邻近甲酸盐物种的质子而还原,如2985、2879、1627、1587和1297 cm〜(-1)的FT-IR峰所示。

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