光催化
异质结
生物炭
水溶液
材料科学
X射线光电子能谱
化学工程
可见光谱
吸附
兴奋剂
无机化学
化学
催化作用
光电子学
有机化学
热解
工程类
作者
Vatika Soni,Sonu Sonu,Pardeep Singh,Sourbh Thakur,Pankaj Thakur,Tansir Ahamad,Van‐Huy Nguyen,Quyet Van Le,Chaudhery Mustansar Hussain,Pankaj Raizada
标识
DOI:10.1016/j.jece.2023.110856
摘要
The photoactive O-ZnO/Cu2O/NCDB heterojunction was fabricated by co-precipitation route to illustrate the advantage of utilizing photoinduced e--h+ pair in degrading Doxycycline hydrochloride and reducing Cr(VI) ions. Herein, we have engineered the electronic structure by generating Ov in ZnO that acts as an interface e- transfer mediator to promote heterojunction formation with Cu2O, supported by NCDB. The content of graphitic N in CDB was positively correlated with the photoactivity owing to the enhanced conductivity and facilitated e- migration. From XRD, XPS, and FTIR results, it was identified that pyridinic/pyrrolic/graphitic N in NCDB and generated Ov in ZnO lattice as dual active sites significantly courage the photocatalytic adsorption and degradation/reduction. The optimized S-scheme based O-ZnO/Cu2O/NCDB heterojunction displayed overall 88.9% Cr(VI) reduction (0.0105 min−1) and 92.9% DCHCl oxidation (0.0128 min−1) within 90 min. Overall, stable O-ZnO/Cu2O/NCDB exhibited the good efficacy of 86% and 89% over four consecutive cycles for Cr(VI) and DCHCl, respectively. This research work provides a neoteric idea for fabricating N-doped CDB along with visible active photocatalysts and deepens the mechanistic understanding for forming biochar-supported visible active S-scheme heterojunction.
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