Dual electric fields in Ni-CdS@Ni(OH)2 heterojunction: A synergistic spatial charge separation approach for enhanced coupled CO2 photoreduction and selective toluene oxidation

异质结 甲苯 对偶(语法数字) 材料科学 电场 电荷(物理) 分离(统计) 光化学 光电子学 化学工程 化学 物理 有机化学 计算机科学 工程类 艺术 文学类 机器学习 量子力学
作者
Khakemin Khan,Ahmed Mahmoud Idris,Haseebul Hassan,Sajjad Haider,Salah Ud-Din Khan,A. Miotello,Ihsanullah Khan
出处
期刊:Advanced powder materials [Elsevier BV]
卷期号:4 (3): 100284-100284 被引量:20
标识
DOI:10.1016/j.apmate.2025.100284
摘要

Simultaneously inducing dual built-in electric fields (EFs) both within a single component and at the heterojunction interface creates a dual-driving force that is crucial for promoting spatial charge separation. This is particularly significant in challenging coupled systems, such as CO 2 photoreduction integrated with selective oxidation of toluene to benzaldehyde. However, developing such a system is quite challenging and often requires a precise design and engineering. Herein, we demonstrate a unique Ni-CdS@Ni(OH) 2 heterojunction synthesized via an in-situ self-assembly method. Comprehensive mechanistic and theoretical investigations reveal that the Ni-CdS@Ni(OH) 2 heterojunction induces dual electric fields (EFs): an intrinsic polarized electric-field within the CdS lattice from Ni doping and an interfacial electric-field from the growth of ultrathin nanosheets of Ni(OH) 2 on Ni-CdS nanorods, enabling efficient spatial charge separation and enhanced redox potential. As proof of concept, the Ni-CdS@Ni(OH) 2 heterojunction simultaneously exhibits outstanding bifunctional photocatalytic performance, producing CO at a rate of 427 ​μmol ​g −1 ​h −1 and selectively oxidizing toluene to benzaldehyde at a rate of 1476 ​μmol ​g −1 ​h −1 with a selectivity exceeding 85%. This work offers a promising strategy to optimize the utilization of photogenerated carriers in heterojunction photocatalysts, advancing synergistic photocatalytic redox systems. A novel Ni-CdS@Ni(OH) 2 heterojunction with dual intrinsic and interfacial electric fields was developed. This unique design leads to efficient charge separation and enhanced redox potentials, enabling simultaneous CO 2 photoreduction and selective toluene oxidation with exceptional performance . • A novel Ni-CdS@Ni(OH) 2 heterojunction photocatalyst is synthesized via an in-situ self-assembly method. • The heterojunction induces dual electric fields: an intrinsic polarized field within CdS due to Ni doping and an interfacial field from Ni(OH) 2 nanosheets, promoting efficient spatial charge separation. • Innovative hierarchical photocatalyst with dual-function activity: high CO production and selective toluene oxidation. Highlights its potential for synergistic redox systems.
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