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Time-Resolved ESR Study of Chromium(III) Complexes in the Ground State

机译:基态铬(III)配合物的时间分辨ESR研究

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摘要

The time-resolved ESR (TR-ESR) signals of ground-state (~4A_(2g)) of Cr(III) ion were observed in ruby and of Cr(acac)_3 doped in Al(acac)_3 single crystals after irradiation with the second harmonic of a Nd : YAG laser at 77 K. At room temperature, TR-ESR signal was observed in ruby, but not in Cr(acac)_3. Both spectra at 77 K were of the emissive type; however, the intensity of the Cr(acac)_3 signal was very weak. The observed TR-ESR signal in ruby was changed from emissive polarity to an absorptive one at 700 μs. The results of ruby and Cr(acac)_3 doped in Al(acac)_3 were explained by the initial emissive polarization and the recovery absorptive polarization from the excited state ~2E. The spin polarization in the sublevels of the ground state was very long (about 500 μs).
机译:在红宝石中观察到Cr(III)离子的基态(〜4A_(2g))的时间分辨ESR(TR-ESR)信号,在辐照后观察到Al(acac)_3单晶中掺杂的Cr(acac)_3 Nd:YAG激光的二次谐波在77K。在室温下,在红宝石中观察到TR-ESR信号,但在Cr(acac)_3中未观察到。 77 K处的两个光谱均为发射型。但是,Cr(acac)_3信号的强度非常弱。红宝石中观察到的TR-ESR信号在700μs时从发射极性变为吸收性极性。掺杂在Al(acac)_3中的红宝石和Cr(acac)_3的结果由初始发射极化和从激发态〜2E恢复的吸收极化解释。基态子级的自旋极化非常长(约500μs)。

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