Atomically Dispersed Indium Sites for Selective CO2 Electroreduction to Formic Acid.
Peilong LuXin TanHaitao ZhaoQian XiangKaili LiuXiaoxu ZhaoXinmao YinXinzhe LiXiao HaiShibo XiAndrew Thye Shen WeeStephen John PennycookXue-Feng YuMenglei YuanJian-Bo WuGuangjin ZhangSean C SmithZongyou YinPublished in: ACS nano (2021)
An atomically dispersed structure is attractive for electrochemically converting carbon dioxide (CO2) to fuels and feedstock due to its unique properties and activity. Most single-atom electrocatalysts are reported to reduce CO2 to carbon monoxide (CO). Herein, we develop atomically dispersed indium (In) on a nitrogen-doped carbon skeleton (In-N-C) as an efficient catalyst to produce formic acid/formate in aqueous media, reaching a turnover frequency as high as 26771 h-1 at -0.99 V relative to a reversible hydrogen electrode (RHE). Electrochemical measurements show that trace amounts of In loaded on the carbon matrix significantly improve the electrocatalytic behavior for the CO2 reduction reaction, outperforming conventional metallic In catalysts. Further experiments and density functional theory (DFT) calculations reveal that the formation of intermediate *OCHO on isolated In sites plays a pivotal role in the efficiency of the CO2-to-formate process, which has a lower energy barrier than that on metallic In.
Keyphrases
- density functional theory
- carbon dioxide
- molecular dynamics
- ionic liquid
- metal organic framework
- highly efficient
- reduced graphene oxide
- gold nanoparticles
- drug delivery
- electron transfer
- genome wide
- heavy metals
- single cell
- room temperature
- mass spectrometry
- dna methylation
- high resolution
- risk assessment
- cancer therapy
- molecularly imprinted
- molecular dynamics simulations
- molecular docking
- transition metal