Huang Xin, Bian Yuan, Wu Bo, Duan Xiaohui, Xiao Zhongliang, Duan Xikai, Li Zhaoqian, Liu Xun, Zhou Yong, Pei Chonghua
State Key Laboratory of Environment-Friendly Energy Materials, Southwest University of Science and Technology, Mianyang 621010, P. R. China.
Key Laboratory of Special Energy Materials (Nanjing University of Science and Technology), Ministry of Education, Nanjing 210094, P. R. China.
Inorg Chem. 2025 Jul 7;64(26):13069-13081. doi: 10.1021/acs.inorgchem.5c01215. Epub 2025 Jun 24.
To date, the catalytic mechanism of metal oxides in the thermal decomposition of ammonium perchlorate (AP) remains unclear and hinders the design and manufacture of efficient AP catalysts. Herein, a catalytic mechanism of the superoxide promotion (SOP) effect is reported, and the more oxygen vacancies and the lower band gaps of the catalysts allow deep decomposition of AP by •O. With the addition of 2 wt % δ-MnO, the HTD temperature of AP decreases from 419.4 to 298.8 °C, and the Δ increases from 585.5 to 1446.0 J g. The SOP effect accelerates the thermal decomposition of AP at low temperatures. Moreover, density functional theory (DFT) calculations confirm that the elongation of the O-O bond (1.34 Å) facilitates the activation of the O adsorbed on these vacancies. δ-MnO shows the most powerful SOP effect; thus, it is one of the best catalysts for AP thermal decomposition. In addition, Δ and the ratio of NO/NO are highly correlated with •O; these results indicate that the diverse catalytic activity exhibited by the different crystal phases of MnO on AP is caused by the differences in the SOP effect.
迄今为止,金属氧化物在高氯酸铵(AP)热分解中的催化机理仍不明确,这阻碍了高效AP催化剂的设计与制造。在此,报道了一种超氧化物促进(SOP)效应的催化机理,催化剂中更多的氧空位和更低的带隙使得AP能被•O深度分解。添加2 wt%的δ-MnO后,AP的高温分解(HTD)温度从419.4℃降至298.8℃,Δ从585.5 J g增加到1446.0 J g。SOP效应加速了AP在低温下的热分解。此外,密度泛函理论(DFT)计算证实,O−O键(1.34 Å)的伸长促进了吸附在这些空位上的O的活化。δ-MnO表现出最强的SOP效应;因此,它是AP热分解的最佳催化剂之一。此外,Δ以及NO/NO的比率与•O高度相关;这些结果表明,MnO不同晶相对AP表现出的不同催化活性是由SOP效应的差异引起的。