Reduction of carbon dioxide to methane and ethanol on the surface of graphyne-like boron nitride (BNyen) monolayer: A DFT study

IF 4.3 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Journal of Physics and Chemistry of Solids Pub Date : 2024-10-11 DOI:10.1016/j.jpcs.2024.112380
Mohamed J. Saadh , Ahmed Mahal , Maha Mohammed Tawfiq , Abbas Hameed Abdul Hussein , Aseel Salah Mansoor , Usama Kadem Radi , Ahmad J. Obaidullah , Parminder Singh , Ahmed Elawady
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Abstract

Recently, scientists have created a novel type of boron nitride material known as BNyen. This material is similar in structure to Graphyne and has a higher N:B ratio than traditional boron nitride due to the addition of boron and nitrogen connecting segments within its units. This material has been studied for its potential as a photocatalyst for reduction of CO2 using DFT approaches. Optical and electronic attributes of BNyen suggest that it has a wider visible-light range and a band gap of 5.69 eV. By adding boron to BNyen, patial distributions of LUMO and HOMO indicate that π network has been extended, resulting in significantly greater photocatalytic efficiency. Upon the adsorption of CO2 on BNyen monolayer, the band gap significantly decreases, indicating a strong interaction between the BNyen and CO2. DFT computations were employed to explore the mechanism of CO2 reduction to a single carbon product catalyzed by BNyen. Based on the ΔG values, the optimized pathway for this reduction is from CO2 to CH4. Additionally, the potential formation of di-carbon products was considered, and based on the free energy values, CH3CH2OH is identified as the final di-carbon product. The Gibbs free energies for potential CO2 reaction pathways on BNyen were calculated, revealing that CO2 can be reduced to CH4 with a low limiting potential of −0.37 V and to CH3CH2OH with a low limiting potential of −0.57 V, both processes being powered by solar energy. In CO2RR, the competing hydrogen evolution reaction (HER) must be considered. The free energy of HER (ΔG = 0.96 eV) is significantly higher than the ΔG of the rate-determining steps for the mono-carbon product (0.37 eV) and the di-carbon product (0.57 eV) on BNyen. Therefore, BNyen effectively suppresses HER during the CO2RR process. This research can serve as a valuable guide for developing novel types of BNyen as appropriate photocatalysts for CO2 reduction reactions (CO2RR).
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在类石墨氮化硼(BNyen)单层表面将二氧化碳还原成甲烷和乙醇:DFT 研究
最近,科学家们创造出了一种新型氮化硼材料--BNyen。这种材料的结构与石墨烯相似,但由于在其单元中添加了硼和氮连接段,其氮硼比高于传统的氮化硼。利用 DFT 方法研究了这种材料作为光催化剂还原二氧化碳的潜力。BNyen 的光学和电子特性表明,它具有更宽的可见光范围和 5.69 eV 的带隙。通过在 BNyen 中添加硼,LUMO 和 HOMO 的拍面分布表明,π 网络得到了扩展,从而显著提高了光催化效率。在 BNyen 单层上吸附二氧化碳后,带隙显著减小,这表明 BNyen 与二氧化碳之间存在很强的相互作用。利用 DFT 计算探讨了 BNyen 催化二氧化碳还原成单碳产物的机理。根据 ΔG 值,这种还原的优化途径是从 CO2 还原到 CH4。此外,还考虑了可能形成的二碳产物,根据自由能值,CH3CH2OH 被确定为最终的二碳产物。计算了 BNyen 上潜在的 CO2 反应途径的吉布斯自由能,结果表明 CO2 可还原成 CH4,极限电位低至 -0.37 V,还原成 CH3CH2OH 的极限电位低至 -0.57 V,这两个过程都由太阳能驱动。在 CO2RR 中,必须考虑竞争性氢进化反应 (HER)。在 BNyen 上,HER 的自由能(ΔG = 0.96 eV)明显高于一碳产物(0.37 eV)和二碳产物(0.57 eV)的速率决定步骤的ΔG。因此,在 CO2RR 过程中,BNyen 能有效抑制 HER。这项研究可为开发新型 BNyen 作为二氧化碳还原反应 (CO2RR) 的适当光催化剂提供有价值的指导。
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来源期刊
Journal of Physics and Chemistry of Solids
Journal of Physics and Chemistry of Solids 工程技术-化学综合
CiteScore
7.80
自引率
2.50%
发文量
605
审稿时长
40 days
期刊介绍: The Journal of Physics and Chemistry of Solids is a well-established international medium for publication of archival research in condensed matter and materials sciences. Areas of interest broadly include experimental and theoretical research on electronic, magnetic, spectroscopic and structural properties as well as the statistical mechanics and thermodynamics of materials. The focus is on gaining physical and chemical insight into the properties and potential applications of condensed matter systems. Within the broad scope of the journal, beyond regular contributions, the editors have identified submissions in the following areas of physics and chemistry of solids to be of special current interest to the journal: Low-dimensional systems Exotic states of quantum electron matter including topological phases Energy conversion and storage Interfaces, nanoparticles and catalysts.
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