Acta Phys. -Chim. Sin. ›› 2024, Vol. 40 ›› Issue (2): 2303060.doi: 10.3866/PKU.WHXB202303060
• REVIEW • Previous Articles Next Articles
Yan Xin1,2,*(
), Yunnian Ge2, Zezhong Li2, Qiaobao Zhang3,*(
), Huajun Tian1,2,*(
)
Received:2023-03-31
Revised:2023-05-10
Accepted:2023-05-17
Published:2023-05-29
Contact:
Email: xinyan@ncepu.edu.cn (Yan Xin)zhangqiaobao@xmu.edu.cn (Qiaobao Zhang)huajun.tian@ncepu.edu.cn (Huajun Tian)
Supported by:Yan Xin, Yunnian Ge, Zezhong Li, Qiaobao Zhang, Huajun Tian. Research Progress on Modification Strategies of Organic Electrode Materials for Energy Storage Batteries[J]. Acta Phys. -Chim. Sin. 2024, 40(2), 2303060. doi: 10.3866/PKU.WHXB202303060
Table 1
Characteristics and applications of organic electrode materials."
| OEMs species | Advantages | Disadvantages | Applications |
| Carbonyl compounds (C=O) | High specific capacity Fast kinetics Flexible structure design | High solubility Poor electrical conductivity | LIB PIB MIB |
| Conductive polymers | High conductivity | Limited doping level Finite energy density | LIB PIB MIB |
| Nitrile compounds (C≡N) | High discharge potential | High solubility | LIB |
| Organosulfur compounds (S―S) | High specific capacity Wide operating temperature range | High solubility Shuttle effect Sluggish kinetics Poor electrical conductivity | LIB MIB |
| Organic free radical compounds (N―O) | High discharge potential Fast kinetics Multiplier performance | Low specific capacity Poor electrical conductivity Self-discharge | LIB ZIB |
| Imine compounds (C=N) | High specific capacity Fast kinetics | High solubility Poor electrical conductivity | LIB ZIB AIB |
| Compounds with superlitigation ability | High specific capacity Fast kinetics | High solubility Poor electrical conductivity | LIB PIB |
| Azo compounds (N=N) | High specific capacity Stable cycle performance | High solubility Poor electrical conductivity | LIB PIB |
| Conjugated sulfonamides (R―S(=O)2−) | High discharge potential Stable cycle performance High energy density | Still uncertain | LIB |
Table 2
Effects of different substituents and representative organic molecular structures."
| Substituents | Functions | Molecular structure illustrations |
| O | Increase the potential | |
| S | Increase the potential Heighten conductivity | |
| N | Increase the potential | |
| ―X (= F, Cl, Br) | Increase the potential | |
| ―OH | Reduce solubility Improve cycle performance Increase the potential | |
| ―C≡N | Higher energy density Increase the potential | |
| ―NH2 | Formation of hydrogen bonds Reduce solubility | |
| XCOO― (X = Li, Na, K) | Reduce solubility Improve cycle performance Reduce the potential | |
| XSO3― (X = Li, Na, K) | Reduce solubility Improve cycle performance Increase the potential |
Fig 5
(a) Structural formula, redox process and electrochemical performance of conjugated system extension (−)-NDI-Δ and monomer derivative NDI-Ref. 106; (b) synthetic routes of BBQ, BBQB, TBQB and corresponding electrochemical properties107; (c) the chemical structure of SBDC and three possible extended π-conjugated structures and molecular packing diagram of SSDC108."
Fig 6
(a) The optimized geometries of the four materials: AQ, PAQS, P14AQ, and P15AQ and cycle profiles at a current density of 0.2C and long cycle profiles of P14AQ at a current density of 1C and 2C112; (b) The synthesis scheme of polymers EDP, HP and UP113; (c) Structures of polymers containing BQ and NQ, synthetic routes of poly(NBE-BQ) and poly(NBE-NQ)114."
Fig 7
(a) Synthesis, energy storage mechanism and electrochemical performance of 2D-PAI@CNT135; (b) graphical representation of COF@CNTs with few COF layers covered on the exterior surface of CNTs141; (c) the synthesis strategy, morphological characterization and cycle performance of PMTA/SWCNT142."
Fig 8
(a) Scheme of the synthesis process of PC/G composites and the corresponding cycle performance151; (b) schematic illustration of the synthesis of VG 8/G composite and the corresponding cycle performance153; (c) schematic illustration of the formation of Na2TP@GE and the corresponding cycle performance154; (d) schematic diagram of in situ braided GDY nanocoatings and the corresponding cycle performance156."
Fig 12
(a) Schematic diagram of layer-by-layer stacking of 2D-COF with different thicknesses and corresponding electrochemical performance170; (b) schematic illustration for the exfoliation of 2D redox-Active COF into exfoliated COF as cathodes for lithium ion battery122; (c) exfoliation of COF-43 yields a suspension of few-layer 2D polymers171."
Fig 13
(a) The physical and chemical properties of different electrolytes and the electrochemical performance of PI-1/CNT as electrode materials174; (b) HOMO and LUMO energy levels of different solvents and salts175; (c) interaction and cycle performance of PBALS in liquid and solid electrolytes176."
Table 3
Representative OEM with excellent long cycle performance."
| Materials | Electrolyte | Current density/initial specific capacity (mAh∙g−1) | Range of voltage (V) | Cycle number/capacity retention rate (%) | Ref. |
| HATN(3Q)//Li | LiPF6/EC + DEC | 0.5 A∙g−1/152 | 1.5–4.0 | 2000/80 | |
| HATN(3Q)//Li | 1 mol∙L−1 LiTFSI in DME/DOL | 8 A∙g−1/215 | 1.2–3.9 | 6000/80 | |
| 2Q//Li | 1 mol∙L−1 LiTFSI in DME/DOL | 8 A∙g−1/229 | 1.2–3.9 | 6000/81 | |
| BAQIT//Li | 1 mol∙L−1 LiTFSI in DOL/DME = 1 : 1 v/v | 0.5 A∙g−1/155 | 1.5–3.5 | 2200/86 | |
| PBQS//Li | 1 mol∙L−1 LiTFSI in DOL/DME = 1 : 1 v/v | 0.5 A∙g−1/231 | 1.5–4.0 | 1000/86 | |
| P14AQ//Li | 1 mol∙L−1 LiTFSI in DOL/DME = 2 : 1 v/v | 0.52 A∙g−1/235 | 1.5–3.0 | 1000/96 | |
| PI2//Li | 1 mol∙L−1 LiTFSI in DOL/DME = 1 : 1 v/v | 0.37 A∙g−1/170 | 1.5–3.0 | 1000/81.3 | |
| PPTS//Na | 1 mol∙L−1 NaPF6 in DME | 1 A∙g−1/271 | 0.8–3.2 | 2000/84.8 | |
| BQ1-COF//Li | 1 mol∙L−1 LiTFSI in DOL/DME = 1 : 1 v/v | 1.55 A∙g−1/245 | 1.2–3.5 | 1000/81 | |
| HATNPF1//Li | 1 mol∙L−1 LiTFSI in G4 | 0.5 A∙g−1/180 | 1.5–4.0 | 1200/92 | |
| NSHATN//Li | 1 mol∙L−1 LiTFSI in G4 | 0.5 A∙g−1/183 | 1.5–4.0 | 1500/83 | |
| TQBG-COF//Na | 1 mol∙L−1 NaPF6 in DEGDME | 1 A∙g−1/221 | 1.0–3.6 | 1000/96.4 | |
| HATN//Zn | 2 mol∙L−1 ZnSO4 aqueous | 5 A∙g−1/150 | 0.3–1.1 | 5000/93.3 | |
| HFHATN//Zn | 2 mol∙L−1 ZnSO4 aqueous | 5 A∙g−1/196 | 0.1–1.46 | 1000/97.4 | |
| CLPy//Zn | 30 mol∙L−1 ZnCl2 aqueous | 3 A∙g−1/205 | 0.6–1.8 | 38000/96.4 | |
| Tp-PTO-COF//Zn | 2 mol∙L−1 ZnSO4 aqueous | 2 A∙g−1/230 | 0.4–1.5 | 1000/95 |
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