Developing novel hybrid negative electrode materials with high specific capacity, rate capacitance, and long-term cycle stability is a key factor for pushing large-scale application of supercapacitors. However, construction of robust interfaces and low-crystalline active materials plays a crucial role in realizing the target. In this paper, a one-step phosphorization approach was employed to make low-crystalline Fe 2 P 2 O 7 nanoplates closely bonded to N/P-co-doped graphene nanotubes (N/ [email protected] 2 P 2 O 7 ) through interfacial chemical bonding. The N and P heteroatoms as substitutions for C in GNT skeletons can introduce rich electronic centers, which induces Fe 2 P 2 O 7 to fix the surface of N/P-GNTs through Fe–N and Fe–P bonds as confirmed by the characterizations. Moreover, the low-crystalline active materials own a disordered internal structure and numerous defects, which not only endows with excellent conductivity but also provides many active sites for redox reactions. Benefiting from the synergistic effects, the prepared N/ [email protected] 2 P 2 O 7 can not only deliver a high capacity of 257 mA h g –1 (927 F g –1 ) at 1 A g –1 but also present an excellent rate capability of 184 mA h g –1 (665 F g –1 ) at 50 A g –1 and outstanding cycle stability (∼90.6% capacity retention over 40,000 cycles). Furthermore, an asymmetric supercapacitor was assembled using the obtained N/ [email protected] 2 P 2 O 7 as electrode materials, which can present the energy density as high as 83.3 W h kg –1 at 791 W kg –1 and long-term durability. Therefore, this strategy not only offers an effective pathway for achieving high-performance negative electrode materials but also lays a foundation for further industrialization.
No takes yet. Share an insight, caveat, or question.
Li et al. (2022) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: