Lu Peilong, Tan Xin, Zhao Haitao, Xiang Qian, Liu Kaili, Zhao Xiaoxu, Yin Xinmao, Li Xinzhe, Hai Xiao, Xi Shibo, Wee Andrew T S, Pennycook Stephen J, Yu Xuefeng, Yuan Menglei, Wu Jianbo, Zhang Guangjin, Smith Sean C, Yin Zongyou
Research School of Chemistry, College of Science, Australian National University, Canberra, ATC 2601, Australia.
Key Laboratory of Green Process and Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China.
ACS Nano. 2021 Mar 23;15(3):5671-5678. doi: 10.1021/acsnano.1c00858. Epub 2021 Feb 15.
An atomically dispersed structure is attractive for electrochemically converting carbon dioxide (CO) to fuels and feedstock due to its unique properties and activity. Most single-atom electrocatalysts are reported to reduce CO 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 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 CO 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 CO-to-formate process, which has a lower energy barrier than that on metallic In.
原子分散结构因其独特的性质和活性,在将二氧化碳(CO₂)电化学转化为燃料和原料方面具有吸引力。据报道,大多数单原子电催化剂可将CO₂还原为一氧化碳(CO)。在此,我们开发了一种负载在氮掺杂碳骨架(In-N-C)上的原子分散铟(In)作为高效催化剂,用于在水性介质中生产甲酸/甲酸盐,相对于可逆氢电极(RHE),在-0.99 V时的周转频率高达26771 h⁻¹。电化学测量表明,负载在碳基质上的痕量In显著改善了CO₂还原反应的电催化行为,优于传统的金属In催化剂。进一步的实验和密度泛函理论(DFT)计算表明,孤立In位点上中间体*OCHO的形成在CO₂转化为甲酸盐的过程效率中起关键作用,其能垒低于金属In上的能垒。