材料科学
合金
选择性
跷跷板分子几何学
格子(音乐)
Atom(片上系统)
凝聚态物理
纳米技术
化学物理
催化作用
冶金
粒子物理学
嵌入式系统
生物化学
化学
物理
计算机科学
声学
中微子
作者
Fengyu Zhang,Yanping Yang,Qian Wang,Xiaomeng Chen,Lulu Xie,Xintao Li,Dianqing Li,Junting Feng,Xue Duan
标识
DOI:10.1021/acsami.5c02716
摘要
When single-atom catalysts are oriented toward practical applications, in addition to balancing the seesaw between activity and selectivity, the capability of thermal management also merits attention. Herein, we proposed a facility approach that, based on active Pd in the state of a single atom, tunes the guest Cu size to simultaneously enhance the effect of d-electron domination and the heat transfer behavior in microregions. Along with the Cu size in an order of magnitude increase, more delocalized electrons were generated and transferred to isolated Pd sites, with the d band center shifting from 1.438 to 1.052 eV, closer to the Fermi level. Simultaneously, more long-range ordered lattices are much favorable for transferring in situ generated thermally phonons with the diffusivity surging from 12.36 to 103.49 mm2/s. The optimized Pd1Cu-SAA catalyst exhibited state-of-the-art performance in acetylene hydrogenation, achieving full conversion at 140 °C, with 95.3% selectivity and good stability in the test period.
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