Moore Colin E, Gyenge Előd L
Department of Chemical and Biological Engineering, Clean Energy Research Centre, University of British Columbia, 2360 East Mall, Vancouver, BC, V6T 1Z3, Canada.
ChemSusChem. 2017 Sep 11;10(17):3512-3519. doi: 10.1002/cssc.201700761. Epub 2017 Aug 10.
Bimetallic Sn-Pb catalysts with five different Sn/Pb atomic ratios were electrodeposited on Teflonated carbon paper and non-Teflonated carbon cloth using both fluoroborate- and oxide-containing deposition media to produce catalysts for the electrochemical reduction of CO (ERC) to formate (HCOO ). The interaction between catalyst composition, morphology, substrate, and deposition media was investigated by using cyclic voltammetry and constant potential electrolysis at -2.0 V versus Ag/AgCl for 2 h in 0.5 m KHCO . The catalysts were analyzed before and after electrolysis by using SEM and XRD to determine the mechanisms of Faradaic efficiency loss and degradation. Catalysts that are mainly Sn with 15-35 at % Pb generated Faradaic efficiencies up to 95 % with a stable performance. However, pure Sn catalysts showed high initial stage formate production rates but experienced an extensive (up to 30 %) decrease of the Faradaic efficiency. The XRD results demonstrated the presence of polycrystalline SnO after electrolysis using Sn-Pb catalysts with 35 at % Pb and its absence in the case of pure Sn. It is proposed that the presence of Pb (15-35 at %) in mainly Sn catalysts stabilized SnO , which is responsible for the enhanced Faradaic efficiency and catalytic durability in the ERC.
采用含氟硼酸盐和氧化物的沉积介质,在聚四氟乙烯化碳纸和非聚四氟乙烯化碳布上电沉积了五种不同锡/铅原子比的双金属锡-铅催化剂,以制备用于将CO电化学还原(ERC)为甲酸盐(HCOO)的催化剂。通过循环伏安法以及在0.5m KHCO中相对于Ag/AgCl在-2.0V下进行2h的恒电位电解,研究了催化剂组成、形态、基底和沉积介质之间的相互作用。在电解前后,使用扫描电子显微镜(SEM)和X射线衍射(XRD)对催化剂进行分析,以确定法拉第效率损失和降解的机制。主要为含15-35at%铅的锡的催化剂产生的法拉第效率高达95%,性能稳定。然而,纯锡催化剂在初始阶段显示出较高的甲酸盐生成速率,但法拉第效率大幅下降(高达30%)。XRD结果表明,使用含35at%铅的锡-铅催化剂电解后存在多晶SnO,而纯锡的情况下不存在。有人提出,主要为锡的催化剂中铅(15-35at%)的存在稳定了SnO,这是导致ERC中法拉第效率提高和催化耐久性增强的原因。