氧化剂
光催化
降级(电信)
X射线光电子能谱
异质结
催化作用
材料科学
化学工程
吸附
氧气
甲苯
光化学
化学
光电子学
计算机科学
电信
工程类
生物化学
有机化学
作者
Tiantian Ying,Wei Liu,Lixia Yang,Shuqu Zhang,Ziyi Wu,Jinyang Li,Ren‐Jie Song,Weili Dai,Jianping Zou,Shenglian Luo
标识
DOI:10.1016/j.seppur.2023.125272
摘要
Photocatalyst-governing degradation of VOCs emitted from household products is promising due to its high performance and long-term durability. In this study, unique hierarchical CeO2/Cu2O nanowire arrays with S-scheme construction grow on a Cu mesh through a simple wet chemical method. Abundant oxygen vacancies on CeO2 work as adsorption sites, and the effective separation of photogenerated carriers driven by built-in electric field in the S-scheme CeO2/Cu2O heterojunction generates mobile reactive oxygen radicals for oxidizing target VOCs. Spectra of Kelvin probe force microscopy (KPFM) reveal that the potential difference at the CeO2/Cu2O interface grows from 9 mV in dark to 29 mV under irradiation, demonstrating a powerful force for driving the migration of photoelectrons. Therefore, under simulated sunlight exposure, 50 ppm of toluene, xylene and formaldehyde can be completely degraded in 70, 50 and 6 min by 15 cm2 CeO2/Cu2O mesh, respectively. The elimination of actual indoor VOCs confirms the practicability of the self-supporting CeO2/Cu2O catalyst, which figures out new ideas for designing efficient photocatalysts for the removal of VOCs pollutants.
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