Yang Xuan, Lee Ji Hoon, Kattel Shyam, Xu Bingjun, Chen Jingguang G
Department of Chemical Engineering, Columbia University, New York, New York 10027, United States.
Department of Chemical and Biomolecular Engineering, University of Delaware, Newark, Delaware 19716, United States.
Nano Lett. 2022 Jun 8;22(11):4576-4582. doi: 10.1021/acs.nanolett.2c01667. Epub 2022 May 23.
The electrochemical carbon dioxide reduction reaction (CORR) has been studied on Ag, Pd, Ag@Pd nanocubes using a combination of characterization and density functional theory calculations. By manipulating the deposition and diffusion rates of Pd atoms on Ag nanocubes, Ag@Pd core-shell nanocubes with a shell thickness of 1-2 atomic layers have been successfully synthesized for CORR. Pd nanocubes produce CO with high selectivity due to the transformation of Pd to Pd hydride (PdH) during CORR. In contrast, PdH formation becomes more difficult in Ag@Pd core-shell nanocubes, which inhibits CO production from the *HOCO intermediate and thus tunes the reaction pathway toward HCOOH. Ag nanocubes exhibit high selectivity toward H, and there is no phase transition during CORR. The results demonstrate that the CORR reaction pathways can be manipulated through engineering the surface structure of Pd-based catalysts by allowing or preventing the formation of PdH.
采用表征和密度泛函理论计算相结合的方法,对银、钯、银@钯纳米立方体上的电化学二氧化碳还原反应(CORR)进行了研究。通过控制钯原子在银纳米立方体上的沉积和扩散速率,成功合成了壳层厚度为1-2个原子层的银@钯核壳纳米立方体用于CORR。在CORR过程中,由于钯转变为氢化钯(PdH),钯纳米立方体产生CO的选择性很高。相比之下,在银@钯核壳纳米立方体中,PdH的形成变得更加困难,这抑制了*HOCO中间体生成CO,从而使反应路径向HCOOH方向转变。银纳米立方体对H表现出高选择性,并且在CORR过程中没有相变。结果表明,通过允许或阻止PdH的形成来设计钯基催化剂的表面结构,可以调控CORR反应路径。