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Effects of the at pi-electrons in fused polycyclic aromatic hydrocarbons on positron annihilation

机译:PI-电子在熔融多环芳烃上对正电子湮没的影响

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摘要

The mesoporous phenol-formaldehyde resins (PFR) were synthesized using formaldehyde, phenol, F127 template as raw materials by high temperature hydrothermal method under different temperatures. Nitrogen doped mesoporous PFR were synthesized in the same way with another additional raw material HMTA. Two series of carbon materials PCs and PCNs were obtained after calcinating PFR at 700, 800, 900 degrees C. N-2 adsorption analysis indicates that both the two kind of carbon materials have relatively large specific surface area (325-619 cm(2)/g for PCs and 431-580 cm(2)/g for PCNs). TEM and XRD analyses prove highly ordered mesoporous structure of the samples. Both the elemental analysis and IR results suggest a high carbon content and the abundant fused-ring structure of the test materials. The positron annihilation spectra show that the corresponding intensity I-3 of the longest lifetime component tau(3) is less than 2%, indicating that the pi electrons in the fused rings with low ionization energy are capable of trapping positrons and inhibiting the formation of o-Ps.
机译:通过在不同温度下,使用高温水热法,使用甲醛,苯酚,F127模板作为原料合成了介孔酚醛 - 甲醛树脂(PFR)。以与另一种额外的原料HMTA相同的方式合成氮掺杂介孔PFR。在700,800,900℃下煅烧PFR后获得两种系列碳材料PC和PCNS .N-2吸附分析表明两种碳材料两种具有相对大的比表面积(325-619厘米(2) / g对于PCS和331-580cm(2)/ g的PCN)。 TEM和XRD分析证明了样品的高度有序的介孔结构。元素分析和红外结果都表明了高碳含量和测试材料的丰富融合环结构。正电子湮没光谱表明,最长寿命部件TAU(3)的相应强度I-3小于2%,表明熔融环中具有低电离能量的PI电子能够捕获正弦并抑制形成o-ps。

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