Escuela Superior de Ingeniería Química e Industrias Extractivas (ESIQIE)-Instituto Politécnico Nacional, Col. Zacatenco, 07738, Ciudad de México, México.
Laboratorio de catálisis, Departamento de Química, División de Ciencias Básicas e Ingeniería, Universidad Autónoma Metropolitana-Iztapalapa, Av. San Rafael Atlixco No. 186, 09340, Ciudad de México, México.
Environ Sci Pollut Res Int. 2023 Apr;30(18):54119-54129. doi: 10.1007/s11356-023-26155-6. Epub 2023 Mar 4.
The photocatalytic reduction of carbon dioxide (CO) to produce methanol (CHOH) is a promising strategy for producing clean energy. The catalyst, the aqueous medium, and the UV light are key parameters for the formation of the most relevant pair (e/h) and the specific selectivity towards the desired product (methanol). The use of GaO and VO in the photocatalytic reduction of CO to produce methanol has been little studied. However, the combination of these oxides is important to generate synergies and decrease the band energy, enhancing the photocatalytic activity in CO reduction. In this work, VO-GaO combined photocatalysts have been prepared and investigated for the photocatalytic reduction of CO. These photocatalysts were characterized by spectroscopic and microscopic techniques. The results showed that textural properties such as surface area and morphology do not influence the photocatalytic activity. However, species such as Ga2p and Ga2p identified by XPS enhanced the photocatalytic activity, most likely due to the formation of vacancies and the reduction of the bandgap in the combined oxides, as compared to single oxides. The contribution of these factors in pair interactions (e/h) with CO to generate methanol is demonstrated.
二氧化碳(CO)光催化还原为甲醇(CHOH)是生产清洁能源的一种很有前途的策略。催化剂、水介质和紫外光都是形成最相关电子对(e/h)和特定选择性目标产物(甲醇)的关键参数。GaO 和 VO 在 CO 光催化还原为甲醇中的应用研究较少。然而,这些氧化物的结合对于产生协同作用和降低能带能量以提高 CO 还原的光催化活性很重要。在这项工作中,制备了 VO-GaO 复合光催化剂并对其进行了 CO 光催化还原研究。这些光催化剂通过光谱和显微镜技术进行了表征。结果表明,表面面积和形态等结构特性不会影响光催化活性。然而,XPS 鉴定的 Ga2p 和 Ga2p 等物种增强了光催化活性,这很可能是由于形成了空位和复合氧化物带隙的减少,与单一氧化物相比。证明了这些因素在与 CO 生成甲醇的电子对(e/h)相互作用中的贡献。