催化作用
光化学
离解(化学)
氧气
分解
辐照
材料科学
电子转移
吸附
结晶度
化学
光热治疗
物理化学
纳米技术
结晶学
有机化学
核物理学
物理
作者
Xuanyu Yue,Duojia Zheng,Ming Gao,Ke Wang,Zizhong Zhang,Wenxin Dai,Xianzhi Fu
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2023-11-27
卷期号:13 (24): 15841-15850
被引量:12
标识
DOI:10.1021/acscatal.3c04590
摘要
The direct decomposition of CO2 to produce CO and O2 requires extremely high temperatures in catalysis. Here, we proposed the photoassisted oxygen vacancy active sites for CO2 dissociation to lower the reaction temperature. The designed low-crystalline Nb2O5 nanoribbons (LC-Nb2O5 NRs) showed a good CO production rate under mild conditions (≤250 °C) with Xe lamp irradiation. Under light irradiation, the rate of CO yields of LC-Nb2O5 NRs increased to 68 μmol g–1 h–1 at 250 °C, with no activity at all under light conditions. The high activity arose from unsaturated coordination with low crystallinity and CO2 reactants as an electron donor for forming an electron cycle with the Nb2O5 NRs, which played a key role in the generation of oxygen vacancies for the subsequent photoexcited electron transfer process at mild temperatures. The feasibility of this approach is further verified over Nb2O5/C nanofibers that make full use of photothermal and photoelectric effects to achieve long-term stable CO2 decomposition.
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