化学
电导率
膦酸盐
质子
配体(生物化学)
齿合度
化学稳定性
化学物理
结晶学
理论(学习稳定性)
配位复合体
活化能
纳米技术
同步加速器
金属有机骨架
网状结缔组织
晶体结构
电阻率和电导率
计算化学
物理化学
衍射
化学工程
作者
Fan Yang,Zhiwen Shi,Lipeng Si,Zhengqing Zhang,Jing Ju,Junliang Sun,Xiaoge Wang,Chongli Zhong,Fan Yang,Zhiwen Shi,Lipeng Si,Zhengqing Zhang,Jing Ju,Junliang Sun,Xiaoge Wang,Chongli Zhong
摘要
The sustainable, green, solvent-free synthesis offers new pathways for constructing high-performance metal-organic frameworks (MOFs) that are challenging to access via conventional solution chemistry. Herein, using this approach, we synthesize a highly stable crystalline chromium-phosphonate MOF, TGU-20, while a different counterpart, TGU-30, was obtained in the solution with the same ligand and Cr3+ ion. Interestingly, the three-dimensional electron diffraction technique reveals that TGU-20 adopts a monodeprotonated bidentate phosphonate coordination mode, forming ultranarrow channels densely lined with proton-donating acid P-OH groups. In contrast, TGU-30 features a mixed mono/dideprotonated coordination, resulting in large channels with sparse P-OH sites. As a result, TGU-20 displays exceptional proton conductivity of over 10-2 S cm-1 at 100% RH with a very low activation energy of 0.10 eV, reaching record-high room-temperature proton conductivity among phosphonate MOFs and 2 orders of magnitude higher than that of TGU-30. Additionally, both MOFs exhibit high stability in harsh conditions, including highly concentrated strong acid. The solvent-free synthesis not only directly yields a chromium-phosphonate MOF for the first time but also opens a mild and green avenue for selectively tuning metal-ligand coordination in reticular chemistry.
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