Kim Dae Won, Kang Dong Won, Kang Minjung, Choi Doo San, Yun Hongryeol, Kim Sun Young, Lee Su Min, Lee Jung-Hoon, Hong Chang Seop
Department of Chemistry, Korea University, Seoul 02841, Republic of Korea.
Computational Science Research Center, Korea Institute of Science and Technology (KIST), Seoul 02792, Republic of Korea.
J Am Chem Soc. 2022 Jun 8;144(22):9672-9683. doi: 10.1021/jacs.2c01117. Epub 2022 May 24.
Ammonia is a promising energy vector that can store the high energy density of hydrogen. For this reason, numerous adsorbents have been investigated as ammonia storage materials, but ammonia adsorbents with a high gravimetric/volumetric ammonia capacity that can be simultaneously regenerated in an energy-efficient manner remain underdeveloped, which hampers their practical implementation. Herein, we report Ni_acryl_TMA (TMA = thiomallic acid), an acidic group-functionalized metal-organic framework prepared via successive postsynthetic modifications of mesoporous NiClBTDD (BTDD = bis(1-1,2,3,-triazolo [4,5-],-[4',5'-]) dibenzo[1,4]dioxin). By virtue of the densely located acid groups, Ni_acryl_TMA exhibited a top-tier gravimetric ammonia capacity of 23.5 mmol g and the highest ammonia storage of 0.39 g cm at 1 bar and 298 K. The structural integrity and ammonia storage capacity of Ni_acryl_TMA were maintained after ammonia adsorption-desorption tests over five cycles. Temperature-programmed desorption analysis revealed that the moderate strength of the interaction between the functional groups and ammonia significantly reduced the desorption temperature compared to that of the pristine framework with open metal sites. The structures of the postsynthetic modified analogues were elucidated based on Pawley/Rietveld refinement of the synchrotron powder X-ray diffraction patterns and van der Waals (vdW)-corrected density functional theory (DFT) calculations. Furthermore, the ammonia adsorption mechanism was investigated via in situ infrared and vdW-corrected DFT calculations, revealing an atypical guest-induced binding mode transformation of the integrated carboxylate. Dynamic breakthrough tests showed that Ni_acryl_TMA can selectively capture traces of ammonia under both dry and wet conditions (80% relative humidity). These results demonstrate that Ni_acryl_TMA is a superior ammonia storage/capture material.
氨是一种很有前景的能量载体,能够储存高能量密度的氢。因此,人们已经研究了许多吸附剂作为氨储存材料,但具有高重量/体积氨容量且能以节能方式同时再生的氨吸附剂仍未得到充分发展,这阻碍了它们的实际应用。在此,我们报道了Ni_acryl_TMA(TMA = 硫代苹果酸),一种通过对介孔NiClBTDD(BTDD = 双(1-1,2,3,-三唑并[4,5-],-[4',5'-])二苯并[1,4]二恶英)进行连续的后合成修饰制备的酸性基团功能化金属有机框架。凭借密集分布的酸性基团,Ni_acryl_TMA在1巴和298 K下表现出高达23.5 mmol/g的顶级重量氨容量和0.39 g/cm³的最高氨储存量。经过五个循环的氨吸附 - 解吸测试后,Ni_acryl_TMA的结构完整性和氨储存容量得以保持。程序升温脱附分析表明,与具有开放金属位点的原始框架相比,功能基团与氨之间相互作用的适度强度显著降低了解吸温度。基于同步加速器粉末X射线衍射图谱的Pawley/Rietveld精修和范德华(vdW)校正密度泛函理论(DFT)计算,阐明了后合成修饰类似物的结构。此外,通过原位红外和vdW校正DFT计算研究了氨吸附机制,揭示了整合羧酸盐的非典型客体诱导结合模式转变。动态突破测试表明,Ni_acryl_TMA在干燥和潮湿条件(80%相对湿度)下都能选择性捕获痕量氨。这些结果表明Ni_acryl_TMA是一种优异的氨储存/捕获材料。