Ye Na, Sheng Wenchao, Zhang Riguang, Yan Binhang, Jiang Zhao, Fang Tao
Department of Chemical Engineering, Shaanxi Key Laboratory of Energy Chemical Process Intensification, Engineering Research Center of New Energy System Engineering and Equipment, Xi'an Jiaotong University, Xi'an, 710049, China.
College of Environmental Science and Engineering, Tongji University, 1239 Siping Road, Shanghai, 200092, China.
Small. 2024 Jan;20(3):e2304990. doi: 10.1002/smll.202304990. Epub 2023 Sep 13.
The splitting of the C-C bonds of ethanol remains a key issue to be addressed, despite tremendous efforts made over the past several decades. This study highlights the enhancement mechanism of inexpensive NbN-modified Pd Sn -NbN/C towards the C-C bonds cleavage for alkaline ethanol oxidation reaction (EOR). The optimal Pd Sn -NbN/C delivers a catalytic activity up to 43.5 times higher than that of commercial Pd/C and high carbonate selectivity (20.5%) toward alkaline EOR. Most impressively, the Pd Sn -NbN/C presents good durability even after 25 200 s of chronoamperometric testing. The enhanced catalytic performance is mainly due to the interfacial interaction between PdSn and NbN, demonstrated by multiple structural characterization results. In addition, in situ ATR-SEIRAS (Attenuated total reflection-surface enhanced infrared absorption spectroscopy) results suggest that NbN facilitates the C-C bonds cleavage towards the alkaline EOR, followed by the enhanced OH adsorption to promote the subsequent oxidation of C1 intermediates after doping Sn. DFT (density functional theory) calculations indicate that the activation barriers of the C-H bond cleavage in CH CH OH, CH CHOH, CH CHO, CH CO, CH CO, and the C-C bond cleavage in CH CO, CH CO, CHCO are evidently reduced and the removal of adsorbed CH CO and CO becomes easier on the PdSn-NbN/C catalyst surface.
尽管在过去几十年里付出了巨大努力,但乙醇中碳 - 碳键的断裂仍然是一个有待解决的关键问题。本研究强调了廉价的氮化铌修饰的钯锡 - 氮化铌/碳对碱性乙醇氧化反应(EOR)中碳 - 碳键断裂的增强机制。优化后的钯锡 - 氮化铌/碳具有高达43.5倍于商业钯/碳的催化活性,以及对碱性EOR的高碳酸盐选择性(20.5%)。最令人印象深刻的是,即使经过25200秒的计时电流测试,钯锡 - 氮化铌/碳仍具有良好的耐久性。多种结构表征结果表明,增强的催化性能主要归因于钯锡和氮化铌之间的界面相互作用。此外,原位衰减全反射 - 表面增强红外吸收光谱(ATR - SEIRAS)结果表明,氮化铌促进了碱性EOR中碳 - 碳键的断裂,随后在掺杂锡后增强了羟基吸附,以促进C1中间体的后续氧化。密度泛函理论(DFT)计算表明,在钯锡 - 氮化铌/碳催化剂表面,乙醇、乙醛、乙酸、乙酸根中的碳 - 氢键断裂以及乙酸、乙酸根、乙酰基中的碳 - 碳键断裂的活化能垒明显降低,吸附的乙酸根和一氧化碳的去除变得更容易。