Abstract:In this contribution, we investigate the insertion of sodium into tetracyanoquinodimethane (TCNQ) and its effect on the electronic structure by means of a surface science experiment. We exposed a TCNQ thin film stepwise to sodium vapour and monitored the electronic structure by X-ray photoelectron spectroscopy (XPS) and ultra-violet photoelectron spectroscopy (UPS). During the insertion experiment three stages were observed, which can be related to three different phases, predominantly consisting of TCNQ(0), T… Show more
“…S10b) revealed a peak at 1072.5 eV that is representative of Na + in an ionic salt (viz., NaTFPB). 25 The aforesaid SR-XPS core level chemical states are also consistent with the formation of an electrical double layer of adsorbed/absorbed Na + and TFPB ions within the capacitively charged f-MWCNT SC layer. Figure 2a presents the VB spectra for the PVC/f-MWCNT SC electrode following electrochemical charging of the system to induce an ion-exchange of NaTFPB from the membrane into the f-MWCNT film after removal of the plasticized PVC membrane by sputtering for 8 minutes which correspond to approximately 96 nm in depth (note that the membrane was thinner than in Figure 1).…”
This paper presents the first direct spectroscopic evidence for double layer or capacitive charging of carbon nanomaterial-based solid contacts in all-solid-state polymeric ion-selective electrodes (ISEs). Here, we used synchrotron radiation-X-ray photoelectron spectroscopy (SR-XPS) and SR valence band (VB) spectroscopy in the elucidation of the charging mechanism of the SCs.
“…S10b) revealed a peak at 1072.5 eV that is representative of Na + in an ionic salt (viz., NaTFPB). 25 The aforesaid SR-XPS core level chemical states are also consistent with the formation of an electrical double layer of adsorbed/absorbed Na + and TFPB ions within the capacitively charged f-MWCNT SC layer. Figure 2a presents the VB spectra for the PVC/f-MWCNT SC electrode following electrochemical charging of the system to induce an ion-exchange of NaTFPB from the membrane into the f-MWCNT film after removal of the plasticized PVC membrane by sputtering for 8 minutes which correspond to approximately 96 nm in depth (note that the membrane was thinner than in Figure 1).…”
This paper presents the first direct spectroscopic evidence for double layer or capacitive charging of carbon nanomaterial-based solid contacts in all-solid-state polymeric ion-selective electrodes (ISEs). Here, we used synchrotron radiation-X-ray photoelectron spectroscopy (SR-XPS) and SR valence band (VB) spectroscopy in the elucidation of the charging mechanism of the SCs.
“…[26] Reversible tautomerism is expected to occur on these derivatives. Further In addition to the CN double bonds, tetracyanoethylene [101,102] and tetracyanoquinodimethane (TCNQ) [103] with CN bond have also been investigated as a cathode for SIB. Further In addition to the CN double bonds, tetracyanoethylene [101,102] and tetracyanoquinodimethane (TCNQ) [103] with CN bond have also been investigated as a cathode for SIB.…”
Benefiting from the high abundance and low cost of sodium resource, rechargeable sodium‐ion batteries (SIBs) are regarded as promising candidates for large‐scale electrochemical energy storage and conversion. Due to the heavier mass and larger radius of Na+ than that of Li+, SIBs with inorganic electrode materials are currently plagued with low capacity and insufficient cycling life. In comparison, organic electrode materials display the advantages of structure designability, high capacity and low limitation of cationic radius. However, organic electrode materials also encounter issues such as high‐solubility in electrolyte and low conductivity. Here, recently reported organic electrode materials, which mainly include the reactions based on either carbon‐oxygen double bond or carbon‐nitrogen double bond, and doping reactions, are systematically reviewed. Furthermore, the design strategies of organic electrodes are comprehensively summarized. The working voltage is regulated through controlling the lowest unoccupied molecular orbital energies. The theoretical capacity can be enhanced by increasing the active groups. The dissolution is inhibited with elevating the intermolecular forces with proper molecular weight. The conductivity can be improved with extending conjugated structures. Future research into organic electrodes should focus on the development of full SIBs with aqueous/aprotic electrolytes and long cycling stability.
“…Schiff and pteridine derivatives containing CN bond has an adjustable electrochemical activity, in which plane structure and conjugated structure play an important role in stabilizing their electrochemical activity. [56][57][58][59][60][61] Azo compounds containing NN bonds are newly recognized as electrode materials for OSIBs; the experimental results show that the NN bond acts as an electrochemical activity groups to reversibly bond with Na ions. [62] Through reasonable design of their structures, there is great room for further development.…”
Rechargeable sodium‐ion batteries (SIBs) are considered attractive alternatives to lithium‐ion batteries for next‐generation sustainable and large‐scale electrochemical energy storage. Organic sodium‐ion batteries (OSIBs) using environmentally benign organic materials as electrodes, which demonstrate high energy/power density and good structural designability, have recently attracted great attention. Nevertheless, the practical applications and popularization of OSIBs are generally restricted by the intrinsic disadvantages related to organic electrodes, such as their low conductivity, poor stability, and high solubility in electrolytes. Here, the latest research progress with regard to electrode materials of OSIBs, ranging from small molecules to organic polymers, is systematically reviewed, with the main focus on the molecular structure design/modification, the electrochemical behavior, and the corresponding charge‐storage mechanism. Particularly, the challenges faced by OSIBs and the effective design strategies are comprehensively summarized from three aspects: function‐oriented molecular design, micromorphology regulation, and construction of organic–inorganic composites. Finally, the perspectives and opportunities in the research of organic electrode materials are discussed.
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