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首页> 外文期刊>Journal of Applied Physics >Site selective substitution Pt for Ti in KTiOPO4:Ga crystals revealed by electron paramagnetic resonance
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Site selective substitution Pt for Ti in KTiOPO4:Ga crystals revealed by electron paramagnetic resonance

机译:电子顺磁共振显示KTiOPO 4 :Ga晶体中Ti的位置选择性取代Pt

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摘要

Electron Paramagnetic Resonance at low temperatures has been used to characterize potassium titanyl phosphate (KTiOPO4) single crystals grown by different techniques. Irradiation with 20 MeV electrons performed at room temperature and liquid nitrogen temperature caused an appearance of electrons and holes. Platinum impurities act as electron traps in KTiOPO4 creating Pt3+ centers. Two different Pt3+ centers were observed, Pt(A) and Pt(D). The Pt(A) centers are dominant in undoped samples, whereas Pt(D)—in Ga-doped KTP crystals. Superhyperfine structure registered for Pt(D) centers was attributed to interactions of platinum electrons with 39K and two 31P nuclei in their surroundings. In both Pt(A) and Pt(D) centers, Pt3+ ions substitute for Ti4+ ions, but with a preference to one of two electrically distinct crystallographic positions. The site selective substitution can be controlled by the Ga-doping.
机译:低温电子顺磁共振已被用来表征通过不同技术生长的磷酸钛氧钾(KTiOPO 4 )单晶。在室温和液氮温度下用20 MeV电子照射会出现电子和空穴。铂杂质充当KTiOPO 4 中的电子陷阱,从而形成Pt 3 + 中心。观察到两个不同的Pt 3 + 中心,Pt(A)和Pt(D)。在未掺杂样品中,Pt(A)中心占主导地位,而在Ga掺杂KTP晶体中,Pt(D)中心占据主导地位。 Pt(D)中心注册的超超细结构归因于铂电子与周围环境中 39 K和两个 31 P核的相互作用。在Pt(A)和Pt(D)中心,Pt 3 + 离子替代Ti 4 + 离子,但优先选择两个电学不同的晶体位置之一。可以通过Ga掺杂来控制位点选择性取代。

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