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用于增强光催化还原铀酰的氮化碳中P掺杂与结晶度调制的协同作用

Synergy of P doping and crystallinity modulation in carbon nitride for enhancing photocatalytic uranyl reduction.

作者信息

Xie Jin-Qi, Ji Daozhuo, Chang Ziyang, Wu Yuhong, Lv Qiqi, Liu Xiaokang, Shi Lang

机构信息

Hunan Key Laboratory for the Design and Application of Actinide Complexes, College of Chemistry and Chemical Engineering, University of South China, Hengyang, Hunan 421001, China.

School of Chemical Engineering, Beijing University of Chemical Technology, Beijing 100029, China.

出版信息

J Colloid Interface Sci. 2025 Jan 15;678(Pt A):63-76. doi: 10.1016/j.jcis.2024.08.128. Epub 2024 Aug 20.

Abstract

Doping modification is a useful way to promote the catalytic activity of carbon nitride (CN). However, most doped CNs have lower structural symmetry and several edge defects, which hinder the transfer of charge carriers. This work reports a P-doped crystalline carbon nitride (crystalline PCN) for the efficient photoreduction of uranyl. The thermal polymerization and salt post-treatment convert the amorphous PCN into crystalline PCN. Compared to the pristine CN, the crystalline PCN has over 1620 % higher activity for uranyl (U(VI)) reduction, reaching a 97.8 % reduction rate in 60 min. Furthermore, the 2-PCN shows excellent stability and a U(VI) removal efficiency >85.7 % in the pH range of 5-8. Characterization analysis reveal that both the P doping and crystalline modulation do not obviously change their morphology, light absorption property and energy band structure, but markedly promote the delocalization of electrons around the doped P atoms, thereby severely inhibit direct electron-hole recombination. Thus, the more efficient separation of charge carriers generates more reactive specials to participate in the photocatalytic uranyl reduction reaction. This study demonstrates a dual-modification strategy for the rational synthesis of highly active metal-free CN-based photocatalysts for uranyl reduction.

摘要

掺杂改性是提高氮化碳(CN)催化活性的一种有效方法。然而,大多数掺杂的CN具有较低的结构对称性和一些边缘缺陷,这阻碍了电荷载流子的转移。本文报道了一种用于高效光还原铀酰的P掺杂晶态氮化碳(晶态PCN)。热聚合和盐后处理将非晶态PCN转化为晶态PCN。与原始CN相比,晶态PCN对铀酰(U(VI))还原的活性高出1620%以上,在60分钟内还原率达到97.8%。此外,2-PCN在pH值为5-8的范围内表现出优异的稳定性,铀酰去除效率>85.7%。表征分析表明,P掺杂和晶态调制均未明显改变其形貌、光吸收性能和能带结构,但显著促进了掺杂P原子周围电子的离域,从而严重抑制了直接的电子-空穴复合。因此,电荷载流子的更有效分离产生了更多的活性物种参与光催化铀酰还原反应。本研究展示了一种双改性策略,用于合理合成用于铀酰还原的高活性无金属CN基光催化剂。

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