Inverse conductance signal outputs of solid-state AgCl electrochemistry dependent on counteranions of Ag-MOFs

被引:4
作者
Yan, Tingting [1 ]
Xie, Chen-Fei [1 ]
Xu, Zou-Hong [1 ]
Lu, Yi [1 ]
Sun, Wei-Yin [1 ]
机构
[1] Nanjing Univ, Coordinat Chem Inst, Collaborat Innovat Ctr Adv Microstruct,Nanjing Nat, Sch Chem & Chem Engn,State Key Lab Coordinat Chem, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
solid-state AgCl electrochemistry; Ag-MOF; Counteranions; Sensing; METAL-ORGANIC FRAMEWORKS; ELECTRODE; FOAM;
D O I
10.1016/j.electacta.2022.140688
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Metal-organic frameworks (MOFs) as crystalline materials have been extensively applied in the electrochemical sensing. However, the influence of the counteranion of MOFs on electrochemical analysis was rarely reported. In this work, three Ag-MOFs [Ag3(L)3](NO3)3 (A1), [Ag3(L)3](CF3SO3)3 (A2) and [Ag2(L)(NO3)2] (A3) with the same ligand of 1,1,2,2-tetrakis(4-(1H-pyrazol-1-yl)phenyl)ethene (L) but different counteranions were utilized to explore their electrochemical detection performance for chloride (Cl & xe213; ) ions based on the electrochemical redox of solid-state AgCl. It is interesting to find that the solid-state AgCl derived from A2 with CF3SO3 & xe213; counteranions exhibits inverse conductance signal output compared with that derived from A1 with counteranions of noncoordinated NO3 & xe213; or by A3 with coordinated NO3 & xe213; . Besides, the signals of peak potentials for the solid-state AgCl derived from these Ag-MOFs are stable, which showed excellent linear relationship and high sensitivity, favorable for the further applications. This is the first example of the counteranions of MOFs determined electrochemical sensing of chloride, and revealed the importance of the counteranions of MOFs in the field of the electrochemical sensing.
引用
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页数:6
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