选择性
催化作用
钯
化学
氧气
氧原子
Atom(片上系统)
有机化学
生物化学
分子
计算机科学
嵌入式系统
作者
Shi-Ming Yu,Xing Cheng,Yueshuai Wang,Bo Xiao,Yiran Xing,Junfeng Ren,Yue Lu,Hongyi Li,Chunqiang Zhuang,Ge Chen
标识
DOI:10.1038/s41467-022-32450-6
摘要
Abstract Nanosized palladium (Pd)-based catalysts are widely used in the direct hydrogen peroxide (H2O2) synthesis from H2 and O2, while its selectivity and yield remain inferior because of the O-O bond cleavage from both the reactant O2 and the produced H2O2, which is assumed to have originated from various O2 adsorption configurations on the Pd nanoparticles. Herein, single Pd atom catalyst with high activity and selectivity is reported. Density functional theory calculations certify that the O-O bond breaking is significantly inhibited on the single Pd atom and the O2 is easier to be activated to form *OOH, which is a key intermediate for H2O2 synthesis; in addition, H2O2 degradation is shut down. Here, we show single Pd atom catalyst displays a remarkable H2O2 yield of 115 mol/gPd/h and H2O2 selectivity higher than 99%; while the concentration of H2O2 reaches 1.07 wt.% in a batch.
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