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用于药物降解和析氧的宏观自发压电极化与氧空位耦合的稳健NaNbO₃/FeOOH异质结:实验与理论相结合的研究

Macroscopic Spontaneous Piezopolarization and Oxygen-Vacancy Coupled Robust NaNbO/FeOOH Heterojunction for Pharmaceutical Drug Degradation and O Evolution: Combined Experimental and Theoretical Study.

作者信息

Priyadarshini Newmoon, Mansingh Sriram, Das Kundan Kumar, Garg Romy, Parida Kaushik, Parida Kulamani

机构信息

Centre for Nanoscience and Nanotechnology, Siksha 'O' Anusandhan (Deemed to be University), Bhubaneswar, Odisha 751030, India.

Quantum Materials and Devices Unit, Institute of Nano Science and Technology, Mohali, Punjab 140306, India.

出版信息

Inorg Chem. 2024 Jan 8;63(1):256-271. doi: 10.1021/acs.inorgchem.3c03085. Epub 2023 Dec 19.

Abstract

Prompt recombination of photoproduced charges in bulk and surface of a photocatalyst significantly impedes catalytic efficiency. To address these challenges, FeOOH nanorods (NRs) anchored NaNbO (NNO) piezoelectric microcubes (MCs) have been fabricated for ciprofloxacin (CIP) degradation and oxygen evolution through water splitting by coupling macroscopic spontaneous piezoelectric polarization and a built-in electric field. The local electric field induced by surface oxygen vacancies (Ovs) and orientation of FeOOH NRs over NNO MCs afford the polarization electric field a significant boost, driving the quick separation/migration of charge carriers from bulk to the surface. The polarized NNO/FeOOH composite with ample Ovs demonstrates an outstanding piezophotocatalytic CIP degradation of 93% in 1 h, higher than pristine materials (NNO and FeOOH), and a high O evolution rate of 1155 μmol h. The effect of piezoelectric polarization on the catalytic activity is supplemented by theoretical simulations. This work offers an avenue for selective pollutant remediation and water splitting through the rational design of piezoelectric polarization-mediated heterostructure systems with surface Ovs.

摘要

光催化剂体相和表面光生电荷的快速复合显著阻碍了催化效率。为应对这些挑战,通过耦合宏观自发压电极化和内建电场,制备了锚定在铌酸钠(NNO)压电微立方块(MCs)上的氢氧化铁(FeOOH)纳米棒(NRs),用于通过水分解降解环丙沙星(CIP)和析氧。表面氧空位(Ovs)诱导的局部电场以及FeOOH NRs在NNO MCs上的取向显著增强了极化电场,驱动载流子从体相快速分离/迁移到表面。具有大量Ovs的极化NNO/FeOOH复合材料在1小时内展现出93%的出色压电光催化CIP降解率,高于原始材料(NNO和FeOOH),并且析氧速率高达1155 μmol h。理论模拟补充了压电极化对催化活性的影响。这项工作通过合理设计具有表面Ovs的压电极化介导异质结构系统,为选择性污染物修复和水分解提供了一条途径。

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