TY - JOUR
T1 - Overcoming Defect Limitations in Photocatalysis
T2 - Boron-Incorporation Engineered Crystalline Red Phosphorus for Enhanced Hydrogen Production
AU - Pei, Xinya
AU - Bian, Junwei
AU - Zhang, Wei
AU - Hu, Zhuofeng
AU - Ng, Yun Hau
AU - Dong, Yi
AU - Zhai, Xinhui
AU - Wei, Zhen
AU - Liu, Yuxi
AU - Deng, Jiguang
AU - Dai, Hongxing
AU - Jing, Lin
PY - 2024/7/17
Y1 - 2024/7/17
N2 - Photocatalytic hydrogen evolution (PHE) from water splitting is a promising technology for clean and renewable energy production. Elemental crystalline red phosphorus (CRP) is purposefully designed and developed for PHE reaction. However, the photocatalytic activity of CRP is limited by its intrinsic P vacancy (VP) defects, which lead to detrimental charge trapping at deep states and hence its severe recombination. To address this issue, a boron (B) incorporated CRP (B-CRP) photocatalyst is tailored, synthesized via a simple and mild boric acid-assisted hydrothermal strategy. The incorporation of B effectively fills the VP defects, reducing deep trap states (DTS) and introducing beneficial shallow trap states (STS) within the band structure of CRP. This defect engineering approach leads to enhanced photocatalytic activity, with B-CRP achieving a PHE rate of 1392 µmol g−1 h−1, significantly outperforming most reported elemental photocatalysts in the literature. Density functional theory (DFT) simulations and ultrafast spectroscopy support the constructive role of B-dopant-induced STS in prolonging active charge carrier lifetimes, promoting more efficient photocatalytic reactions. The findings not only demonstrate the effectiveness of B-CRP as a photocatalyst but also highlight the usefulness of dopant-induced STS in advancing PHE technologies. © 2024 Wiley-VCH GmbH.
AB - Photocatalytic hydrogen evolution (PHE) from water splitting is a promising technology for clean and renewable energy production. Elemental crystalline red phosphorus (CRP) is purposefully designed and developed for PHE reaction. However, the photocatalytic activity of CRP is limited by its intrinsic P vacancy (VP) defects, which lead to detrimental charge trapping at deep states and hence its severe recombination. To address this issue, a boron (B) incorporated CRP (B-CRP) photocatalyst is tailored, synthesized via a simple and mild boric acid-assisted hydrothermal strategy. The incorporation of B effectively fills the VP defects, reducing deep trap states (DTS) and introducing beneficial shallow trap states (STS) within the band structure of CRP. This defect engineering approach leads to enhanced photocatalytic activity, with B-CRP achieving a PHE rate of 1392 µmol g−1 h−1, significantly outperforming most reported elemental photocatalysts in the literature. Density functional theory (DFT) simulations and ultrafast spectroscopy support the constructive role of B-dopant-induced STS in prolonging active charge carrier lifetimes, promoting more efficient photocatalytic reactions. The findings not only demonstrate the effectiveness of B-CRP as a photocatalyst but also highlight the usefulness of dopant-induced STS in advancing PHE technologies. © 2024 Wiley-VCH GmbH.
KW - boron incorporation
KW - charge trapping
KW - photocatalytic hydrogen evolution
KW - red phosphorus
KW - vacancy defects
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U2 - 10.1002/adfm.202400542
DO - 10.1002/adfm.202400542
M3 - RGC 21 - Publication in refereed journal
SN - 1616-301X
VL - 34
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 29
M1 - 2400542
ER -