Revealing the synergistic effect of bulk and surface co-doped boron on TiO2 for enhanced photocatalytic H2 evolution

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作者
Li, Bo [1 ]
Zheng, Hongshun [1 ,2 ]
Zhou, Tong [1 ]
Zi, Baoye [1 ]
Lu, Qingjie [1 ]
Li, Dequan [1 ,2 ]
Zhang, Mao [1 ]
Qiu, Zhishi [1 ]
Luo, Zhongge [1 ]
Zhang, Yumin [1 ]
Xiao, Bin [1 ]
Chen, Mingpeng [1 ]
Zhang, Jin [1 ]
Sun, Huachuan [1 ]
Zhao, Jianhong [1 ]
He, Tianwei [1 ]
Zhu, Zhongqi [1 ]
Zhang, Genlin [1 ]
Zhang, Yuxiao [1 ]
Liu, Qingju [1 ,2 ]
机构
[1] Yunnan Key Laboratory for Micro/Nano Materials & Technology, National Center for International Research on Photoelectric and Energy Materials, School of Materials and Energy, Institute of International Rivers and Eco-security, Yunnan University, Kunming,65
[2] Southwest United Graduate School, Kunming,650091, China
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Boron(B) doping is considered as a promising modification method for TiO2 photocatalyst due to the facilitation of separation and migration of photogenerated carriers. However; the modification mechanisms of bulk or surface doping modes on photocatalyst are controversial; and the catalytic activity still needs to be improved. Here; a bulk and surface B co-doped TiO2 (B(B&S)-TiO2) derived from B-containing Ti-MOF (MIL-125(B)) precursor was demonstrated; which achieved a H2 evolution rate of 9.56 mmol∙g−1∙h−1 under 365 nm light without co-catalyst. Detailed investigations reveal the synergistic effect between bulk and surface co-doped B; which optimizes the microstructure; activates the 3-coordinated O (O3C) atoms of B-Ti-O structural units as active sites; enhances the transfer of photoelectrons and inhibits the recombination; balances H* adsorption–desorption during the photocatalytic reactions. This work exhibits a novel strategy of bulk and surface B co-doped photocatalysts and highlights the potential for achieving high photocatalytic H2 evolution rate without co-catalyst. © 2024;
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