Sulfur-Bridged Asymmetric CuNi Bimetallic Atom Sites for CO 2 Reduction with High Efficiency.
Zhiyi SunChen LiZihao WeiFang ZhangZiwei DengKejia ZhouYong WangJinhong GuoJiayi YangZequn XiangPeijie MaHuazhang ZhaiShenghua LiWenxing ChenPublished in: Advanced materials (Deerfield Beach, Fla.) (2024)
Double-atom catalysts (DACs) with asymmetric coordination are crucial for enhancing the benefits of electrochemical carbon dioxide reduction and advancing sustainable development, however, the rational design of DACs is still challenging. Herein, this work synthesizes atomically dispersed catalysts with novel sulfur-bridged Cu-S-Ni sites (named Cu-S-Ni/SNC), utilizing biomass wool keratin as precursor. The plentiful disulfide bonds in wool keratin overcome the limitations of traditional gas-phase S ligand etching process and enable the one-step formation of S-bridged sites. X-ray absorption spectroscopy (XAS) confirms the existence of bimetallic sites with N 2 Cu-S-NiN 2 moiety. In H-cell, Cu-S-Ni/SNC shows high CO Faraday efficiency of 98.1% at -0.65 V versus RHE. Benefiting from the charge tuning effect between the metal site and bridged sulfur atoms, a large current density of 550 mA cm -2 can be achieved at -1.00 V in flow cell. Additionally, in situ XAS, attenuated total reflection surface-enhanced infrared absorption spectroscopy (ATR-SEIRAS), and density functional theory (DFT) calculations show Cu as the main adsorption site is dual-regulated by Ni and S atoms, which enhances CO 2 activation and accelerates the formation of *COOH intermediates. This kind of asymmetric bimetallic atom catalysts may open new pathways for precision preparation and performance regulation of atomic materials toward energy applications.
Keyphrases
- metal organic framework
- density functional theory
- molecular dynamics
- carbon dioxide
- solid state
- high efficiency
- high resolution
- single cell
- transition metal
- aqueous solution
- cell therapy
- single molecule
- gold nanoparticles
- stem cells
- minimally invasive
- magnetic resonance imaging
- ionic liquid
- electron transfer
- oxidative stress
- dna damage
- molecular dynamics simulations
- computed tomography