覆盖层
催化作用
甲醛
煅烧
氧化物
氮气
金属
化学
部分氧化
无机化学
图层(电子)
贵金属
材料科学
化学工程
过渡金属
纳米颗粒
电子结构
多相催化
光化学
氧化还原
一氧化碳中毒
氮氧化物
亚氧化物
还原(数学)
格式化
还原剂
选择性催化还原
电子效应
作者
Jingyi Wang,Chunying Wang,Jinpeng Du,Qiao-Chu Wang,Xudong Chen,Wen Wei,Yaobin Li,Wenpo Shan
标识
DOI:10.1021/acs.est.5c05945
摘要
Creating vacancies and modulating the strong metal-support interaction (SMSI) are crucial strategies for enhancing catalytic activity in heterogeneous catalysis, widely explored for noble metals and oxide supports. In this work, these regulating strategies were extended to nonoxide supports. Specifically, CN supports were calcined at different temperatures to control N-vacancies, while the SMSI effect was tuned via varying the reduction temperature. Characterization and DFT calculations demonstrated that N-vacancies are capable of donating electrons to Pd nanoparticles, promoting the activation of O2 and thus promoting catalytic performance. Nevertheless, SMSI overlayer forms during reduction and may inhibit activity once Pd is fully encapsulated. As the reduction temperature reaches 300 °C, partial de-encapsulation leaves a residual ultrathin layer. This defective SMSI layer resembles support defects, enhancing the electronic activity of the metal surface and further improving catalytic activity. By optimizing N-vacancies and SMSI, the Pd/CN650 catalyst reduced at 300 °C exhibited excellent HCHO oxidation performance at room temperature, highlighting the potential of nonoxide supports for sustainable catalysis.
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