Chen Peng, Lei Ben, Dong Xing'an, Wang Hong, Sheng Jianping, Cui Wen, Li Jieyuan, Sun Yanjuan, Wang Zhiming, Dong Fan
Research Center for Environmental and Energy Catalysis, Institute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu 611731, China.
The Center of New Energy Materials and Technology, School of New Energy and Materials, Southwest Petroleum University, Chengdu 610500, China.
ACS Nano. 2020 Nov 24;14(11):15841-15852. doi: 10.1021/acsnano.0c07083. Epub 2020 Nov 3.
Photocatalytic CO conversion into valuable solar fuels is highly appealing, but lack of directional charge-transfer channel and insufficient active sites resulted in limited CO reduction efficiency and selectivity for most photocatalytic systems. Herein, we designed and fabricated rare-earth La single-atoms on carbon nitride with La-N charge-transfer bridge as the active center for photocatalytic CO reaction. The formation of La single-atoms was certified by spherical aberration-corrected HAADF-STEM, STEM-EELS, EXAFS, and theoretical calculations. The electronic structure of the La-N bridge enables a high CO-yielding rate of 92 μmol·g·h and CO selectivity of 80.3%, which is superior to most g-CN-based photocatalytic CO reductions. The CO production rate remained nearly constant under light irradiation for five cycles of 20 h, indicating its stability. The closely combined experimental and DFT calculations clearly elucidated that the variety of electronic states induced by 4f and 5d orbitals of the La single atom and the p-d orbital hybridization of La-N atoms enabled the formation of charge-transfer channel. The La-N charge bridges are found to function as the key active center for CO activation, rapid COOH* formation, and CO desorption. The present work would provide a mechanistic understanding into the utilization of rare-earth single-atoms in photocatalysis for solar energy conversion.
光催化将CO转化为有价值的太阳能燃料极具吸引力,但对于大多数光催化体系而言,缺乏定向电荷转移通道以及活性位点不足导致CO还原效率和选择性受限。在此,我们设计并制备了以La-N电荷转移桥为光催化CO反应活性中心的氮化碳负载稀土La单原子。通过球差校正的高角度环形暗场扫描透射电子显微镜(HAADF-STEM)、扫描透射电子显微镜能量损失谱(STEM-EELS)、扩展X射线吸收精细结构谱(EXAFS)以及理论计算证实了La单原子的形成。La-N桥的电子结构实现了92 μmol·g·h的高CO产率以及80.3%的CO选择性,优于大多数基于g-CN的光催化CO还原反应。在光照下经过五个20小时的循环,CO生成速率几乎保持恒定,表明其稳定性。紧密结合的实验和密度泛函理论(DFT)计算清楚地阐明,La单原子的4f和5d轨道诱导的电子态变化以及La-N原子的p-d轨道杂化使得电荷转移通道得以形成。发现La-N电荷桥作为CO活化、快速形成COOH*以及CO脱附的关键活性中心。本工作将为稀土单原子在光催化太阳能转化中的应用提供机理理解。