Chiral inorganic polar BaTiO3/BaCO3 nanohybrids with spin selection for asymmetric photocatalysis

Chirality-dependent photocatalysis is an emerging domain that leverages unique chiral light-matter interactions for enabling asymmetric catalysis driven by spin polarization induced by circularly polarized light selection. Herein, we synthesize chiral inorganic polar BaTiO3/BaCO3 nanohybrids for asy...

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Main Authors: Sun, Yemeng, Zhang, Yan, Ni, Jingren, Shen, Yihui, Yu, Hongjian, Lee, Hiang Kwee, Hu, Jun, Zhan, Xiuqin, Zhou, Chuanqiang, Han, Jie
Other Authors: School of Chemistry, Chemical Engineering and Biotechnology
Format: Journal Article
Language:English
Published: 2025
Subjects:
Online Access:https://hdl.handle.net/10356/182322
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author Sun, Yemeng
Zhang, Yan
Ni, Jingren
Shen, Yihui
Yu, Hongjian
Lee, Hiang Kwee
Hu, Jun
Zhan, Xiuqin
Zhou, Chuanqiang
Han, Jie
author2 School of Chemistry, Chemical Engineering and Biotechnology
author_facet School of Chemistry, Chemical Engineering and Biotechnology
Sun, Yemeng
Zhang, Yan
Ni, Jingren
Shen, Yihui
Yu, Hongjian
Lee, Hiang Kwee
Hu, Jun
Zhan, Xiuqin
Zhou, Chuanqiang
Han, Jie
author_sort Sun, Yemeng
collection NTU
description Chirality-dependent photocatalysis is an emerging domain that leverages unique chiral light-matter interactions for enabling asymmetric catalysis driven by spin polarization induced by circularly polarized light selection. Herein, we synthesize chiral inorganic polar BaTiO3/BaCO3 nanohybrids for asymmetric photocatalysis via a hydrothermal method employing chiral glucose as a structural inducer. When excited by opposite circularly polarized light, the same material exhibits significant asymmetric catalysis, while enantiomers present an opposite polarization preference. More importantly, the preferred circularly polarized light undergoes reversal with reversal of the CD signal. Systematic experimental results demonstrate that more photogenerated carriers are generated in chiral semiconductors under suitable circularly polarized light irradiation, including more spin-polarized electrons, which inhibits the recombination of electron-hole pairs and promotes the activation of oxygen molecules into reactive oxygen species, thus inducing this asymmetric photocatalytic feature. This study provides valuable insights for the development of highly efficient polarization-sensitive chiral perovskite nanostructures as promising candidates for next-generation, multifunctional chiral device applications.
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spelling ntu-10356/1823222025-01-22T01:54:25Z Chiral inorganic polar BaTiO3/BaCO3 nanohybrids with spin selection for asymmetric photocatalysis Sun, Yemeng Zhang, Yan Ni, Jingren Shen, Yihui Yu, Hongjian Lee, Hiang Kwee Hu, Jun Zhan, Xiuqin Zhou, Chuanqiang Han, Jie School of Chemistry, Chemical Engineering and Biotechnology Chemistry Asymmetric photocatalysis Chirality Chirality-dependent photocatalysis is an emerging domain that leverages unique chiral light-matter interactions for enabling asymmetric catalysis driven by spin polarization induced by circularly polarized light selection. Herein, we synthesize chiral inorganic polar BaTiO3/BaCO3 nanohybrids for asymmetric photocatalysis via a hydrothermal method employing chiral glucose as a structural inducer. When excited by opposite circularly polarized light, the same material exhibits significant asymmetric catalysis, while enantiomers present an opposite polarization preference. More importantly, the preferred circularly polarized light undergoes reversal with reversal of the CD signal. Systematic experimental results demonstrate that more photogenerated carriers are generated in chiral semiconductors under suitable circularly polarized light irradiation, including more spin-polarized electrons, which inhibits the recombination of electron-hole pairs and promotes the activation of oxygen molecules into reactive oxygen species, thus inducing this asymmetric photocatalytic feature. This study provides valuable insights for the development of highly efficient polarization-sensitive chiral perovskite nanostructures as promising candidates for next-generation, multifunctional chiral device applications. The authors gratefully acknowledge financial support from the Natural Science Foundation of Jiangsu Province (BK20220596), Innovative science and technology platform project of cooperation between Yangzhou City and Yangzhou University, China (No. YZ202026305), Natural Science Foundation of China (21922202, 21673202, 22272146, and 22272147), and the Priority Academic Program Development of Jiangsu Higher Education Institutions. 2025-01-22T01:54:25Z 2025-01-22T01:54:25Z 2024 Journal Article Sun, Y., Zhang, Y., Ni, J., Shen, Y., Yu, H., Lee, H. K., Hu, J., Zhan, X., Zhou, C. & Han, J. (2024). Chiral inorganic polar BaTiO3/BaCO3 nanohybrids with spin selection for asymmetric photocatalysis. Nano Letters, 24(48), 15316-15323. https://dx.doi.org/10.1021/acs.nanolett.4c04295 1530-6984 https://hdl.handle.net/10356/182322 10.1021/acs.nanolett.4c04295 39561320 2-s2.0-85209705861 48 24 15316 15323 en Nano Letters © 2024 American Chemical Society. All rights reserved.
spellingShingle Chemistry
Asymmetric photocatalysis
Chirality
Sun, Yemeng
Zhang, Yan
Ni, Jingren
Shen, Yihui
Yu, Hongjian
Lee, Hiang Kwee
Hu, Jun
Zhan, Xiuqin
Zhou, Chuanqiang
Han, Jie
Chiral inorganic polar BaTiO3/BaCO3 nanohybrids with spin selection for asymmetric photocatalysis
title Chiral inorganic polar BaTiO3/BaCO3 nanohybrids with spin selection for asymmetric photocatalysis
title_full Chiral inorganic polar BaTiO3/BaCO3 nanohybrids with spin selection for asymmetric photocatalysis
title_fullStr Chiral inorganic polar BaTiO3/BaCO3 nanohybrids with spin selection for asymmetric photocatalysis
title_full_unstemmed Chiral inorganic polar BaTiO3/BaCO3 nanohybrids with spin selection for asymmetric photocatalysis
title_short Chiral inorganic polar BaTiO3/BaCO3 nanohybrids with spin selection for asymmetric photocatalysis
title_sort chiral inorganic polar batio3 baco3 nanohybrids with spin selection for asymmetric photocatalysis
topic Chemistry
Asymmetric photocatalysis
Chirality
url https://hdl.handle.net/10356/182322
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