In Situ Hyperfine Spectroscopy for Sensing Dihydrogen Isotopologues on the ZIF-8 Framework

IF 3.2 3区 化学 Q2 CHEMISTRY, PHYSICAL The Journal of Physical Chemistry C Pub Date : 2025-02-13 DOI:10.1021/acs.jpcc.4c07894
Muhammad Fernadi Lukman, Stefan Schlayer, Andreas Pöppl
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Abstract

An in situ pulsed electron paramagnetic resonance spectroscopy approach based on three-pulse electron spin echo envelope modulation has been implemented to monitor the adsorption of deuterium (D2) and deuterium hydride (HD) gases into the pores of ZIF-8 on a local microscopic scale within the environment of paramagnetic spin probes such as TEMPO radicals and Cu2+ ions. The desorption of D2 could be followed up to a temperature of 40 K employing the TEMPO probe, where the majority of the gas has left the pores of ZIF-8. In contrast, H2 gas was not detectable at 20 K with this technique due to the predominant para-hydrogen form. The approach utilizing TEMPO radicals can be used as reliable probes to sense weakly coupled D2 or HD adsorbed into the pores of ZIF-8 without interference from the magnetically active 14N nuclei from the organic linker as we observed for HD adsorption on the Cu2+-doped ZIF-8 material.

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在ZIF-8框架上原位超精细光谱检测二氢同位素
采用基于三脉冲电子自旋回波包络调制的原位脉冲电子顺磁共振波谱方法,在顺磁自旋探针如TEMPO自由基和Cu2+离子的环境下,在局部微观尺度上监测了氘(D2)和氢化氘(HD)气体在ZIF-8孔隙中的吸附。使用TEMPO探针可以将D2的解吸持续到40 K,此时大部分气体已经离开了ZIF-8的孔隙。相比之下,由于主要的对氢形式,这种技术在20 K时无法检测到H2气体。利用TEMPO自由基的方法可以作为可靠的探针来检测吸附在ZIF-8孔隙中的弱耦合D2或HD,而不受有机连接体磁性活性14N核的干扰,正如我们在Cu2+掺杂ZIF-8材料上观察到的HD吸附。
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来源期刊
The Journal of Physical Chemistry C
The Journal of Physical Chemistry C 化学-材料科学:综合
CiteScore
6.50
自引率
8.10%
发文量
2047
审稿时长
1.8 months
期刊介绍: The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
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