催化作用
退火(玻璃)
材料科学
可扩展性
纳米技术
纳米颗粒
Atom(片上系统)
金属
化学工程
组合化学
计算机科学
化学
有机化学
嵌入式系统
数据库
工程类
冶金
复合材料
作者
Jiong Lu,Xiao Hai,Shibo Xi,Sharon Mitchell,Karim Harrath,Haomin Xu,Dario Faust Akl,Debin Kong,Jing Li,Zejun Li,Tao Sun,Huimin Yang,Yige Cui,Chenliang Su,Xiaoxu Zhao,Jun Li,Javier Pérez‐Ramírez
出处
期刊:Research Square - Research Square
日期:2021-04-14
被引量:11
标识
DOI:10.21203/rs.3.rs-394916/v1
摘要
Abstract The stabilization of transition metals as isolated centres on suitably tailored carriers with high density is crucial to exploit the technical potential of single-atom heterogeneous catalysts, enabling their maximized productivity in industrial reactors. Wet-chemical methods are best suited for practical applications due to their amenability to scale up. However, achieving single-atom dispersions at metal contents above 2 wt.% remains challenging. We introduce a versatile approach combining impregnation and two-step annealing to synthesize ultra-high-density single-atom catalysts (UHD-SACs) with unprecedented metal contents up to 23 wt.% for 15 metals on chemically-distinct carriers. Translation to an automated protocol demonstrates its robustness and provides a path to explore virtually unlimited libraries of mono or multimetallic catalysts. At the molecular level, characterization of the synthesis mechanism through experiments and simulations shows that controlling the bonding of metal precursors with the carrier via stepwise ligand removal prevents their thermally-induced aggregation into nanoparticles, ensuring atomic dispersion in the resulting UHD‑SACs. The catalytic benefits of UHD-SACs are demonstrated for the electrochemical reduction of CO 2 to CO over NiN 4 motifs on carbon.
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