Boron-Functionalized Graphitic Carbon Nitride Materials for Photocatalytic Applications: Effects on Chemical, Adsorptive, Optoelectronic, and Photocatalytic Properties

IF 6.5 Q2 CHEMISTRY, PHYSICAL
Ioanna Itskou, Sharminaz C. Sageer, Daniel M. Dawson, Andreas Kafizas, Irena Nevjestic, Catriona M. McGilvery, Matyas Daboczi, Gwilherm Kerherve, Salvador Eslava, Sandrine Heutz, Sharon E. Ashbrook* and Camille Petit*, 
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引用次数: 0

Abstract

Graphitic carbon nitride (gC3N4, or CN herein) is widely studied as a photocatalyst owing to its ease of synthesis, high stability, and optoelectronic properties. However, its photocatalytic performance often remains limited, and a common approach to tune its function and enhance its performance is by doping. Boron (B) functionalization of CN has showed a potential benefit on photocatalytic performance for several reactions. However, the reason for this improvement and the links between synthesis method, exact B chemical environment, and performance remain unclear. Here, we present a fundamental study that elucidates the influence of (i) B functionalization, (ii) B content, and (iii) choice of B precursor on the physicochemical, adsorptive, optoelectronic, and photocatalytic properties of bulk B-CN. We synthesized two sets of B-CN materials (0.5–11 at% B), using either elemental boron or boric acid as precursors. The samples were characterized using several imaging and spectroscopic techniques, which confirm the integration of B into the material through B–O bonding and the creation of B clusters in the case of the boron precursor, with density functional theory (DFT) calculations supporting our analyses. The distribution of B atoms within B-CN particles remained heterogeneous. Compared to CN, B-functionalized materials show enhanced porosity and CO2 uptake, with similar degrees of light absorption and deeper energy band positions. Transient absorption spectroscopy (TAS) measurements showed that charge carrier populations, lifetimes, and kinetics were not significantly affected by B functionalization; however, at 5 at% B doping, an increase in the concentration of charge carriers was seen. Higher B content enhances the photocatalytic NOx removal under UVA irradiation (almost two-fold) and the selectivity to NO3 from NOx photooxidation, but has no significant effect on CO2 photoreduction, compared to pristine CN. Overall, this study provides fundamental insights to build on and more rationally produce better-performing B-CN photocatalysts.

光催化用硼功能化石墨化氮化碳材料:化学、吸附、光电和光催化性能的影响。
石墨化氮化碳(gC3N4,本文简称CN)由于其易于合成、高稳定性和光电性能而被广泛研究作为光催化剂。然而,它的光催化性能往往仍然有限,而调整其功能和提高其性能的常用方法是掺杂。CN的硼(B)功能化对若干反应的光催化性能有潜在的好处。然而,这种改进的原因以及合成方法、确切的化学环境和性能之间的联系尚不清楚。在这里,我们提出了一项基础研究,阐明了(i) B功能化,(ii) B含量,以及(iii) B前驱体的选择对本体B- cn的物理化学,吸附,光电和光催化性能的影响。我们以单质硼或硼酸为前体,合成了两组B- cn材料(0.5-11,% B)。使用多种成像和光谱技术对样品进行了表征,这些技术证实了硼通过B- o键结合到材料中,并且在硼前驱体的情况下形成了B簇,密度泛函理论(DFT)计算支持了我们的分析。B原子在B- cn粒子中的分布是不均匀的。与CN相比,b功能化材料的孔隙率和CO2吸收率提高,光吸收程度相似,能带位置更深。瞬态吸收光谱(TAS)测量表明,B功能化对载流子数量、寿命和动力学没有显著影响;然而,当掺杂率为5%时,载流子的浓度有所增加。与原始CN相比,较高的B含量提高了UVA照射下光催化nox的去除率(几乎提高了两倍)和NO x光氧化对NO3 -的选择性,但对CO2光还原没有显著影响。总的来说,这项研究为构建和更合理地生产性能更好的B-CN光催化剂提供了基础见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Materials Au
ACS Materials Au 材料科学-
CiteScore
5.00
自引率
0.00%
发文量
0
期刊介绍: ACS Materials Au is an open access journal publishing letters articles reviews and perspectives describing high-quality research at the forefront of fundamental and applied research and at the interface between materials and other disciplines such as chemistry engineering and biology. Papers that showcase multidisciplinary and innovative materials research addressing global challenges are especially welcome. Areas of interest include but are not limited to:Design synthesis characterization and evaluation of forefront and emerging materialsUnderstanding structure property performance relationships and their underlying mechanismsDevelopment of materials for energy environmental biomedical electronic and catalytic applications
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