Electrostatic self-assembly of MXene and edge-rich CoAl layered double hydroxide on molecular-scale with superhigh volumetric performances

It is highly desirable to design and synthesize two-dimensional nanostructured electrode materials with high electrical conductivity,large electrolyte-accessible surface area and more exposed active sites for energy storage applications.Herein,MXene/Co Al-LDH heterostructure has been prepared through electrostatic ordered hetero-assembly of monolayer MXene and edge-rich Co Al-LDH nanosheets in a faceto-face manner on molecular-scale for supercapacitor applications.Benefiting from the unique structure,strong interfacial interaction and synergistic effects between MXene and Co Al-LDH nanosheets,the electrical conductivity and exposed electrolyte-accessible active sites are significantly enhanced.The asprepared MXene/Co Al-LDH-80%(ML-80)film exhibits high volumetric capacity of 2472 C cm-3 in 3 M KOH electrolyte with high rate capability of 70.6%at 20 A g-1.Notably,to the best of our knowledge,the high volumetric capacity is the highest among other previously reported values for supercapacitors in aqueous electrolytes.Furthermore,our asymmetric supercapacitor device fabricated with ML-80 and MXene/graphene composite as cathode and anode,respectively,exhibits impressive volumetric energy density of 85.4 Wh L-1 with impressive cycling stability of 94.4%retention ratio after 30,000 continuous charge/discharge cycles.

Fast synthesis of uniform mesoporous titania submicrospheres with high tap densities for high-volumetric performance Li-ion batteries

High-tap density electrode materials are greatly desired for Li-ion batteries with high volumetric capacities to fulfill the growing demands of electric vehicles and portable smart devices. TiOz, which is one of the most attractive an- ode materials, is limited in their application for Li-ion batteries because of its low tap density （usually 〈1 gcm-3） and volumetric capacity. Herein, we report uniform mesoporous TiO2 submicrospheres with a tap density as high as 1.62 gcm-3 as a promising anode material. Even with a high mass load- ing of 24 mg cm-2, the TiO2 submicrospheres have impressive volumetric capacities that are more than double those of their counterparts. Moreover, they can be synthesized with -100% yield and within a reaction time of -6 h by optimizing the experimental conditions and formation mechanism, exhibiting potential for large-scale production for industrial applications. Other mesoporous anode materials, i.e., hightap density mesoporous Li4Ti5O12 submicrospheres, are fabricated using the generalized method. We believe that our work provides a significant reference for the industrial production of mesoporous materials for Li-ion batteries with a high volumetric performance.

Engineering two-dimensional pores in freestanding TiO_2/graphene gel film for high performance lithium ion battery

As the key component of electrochemical energy storage devices, an electrode with superior ions transport pores is the important premise for high electrochemical performance. In this paper, we developed a unique solution process to prepare freestanding TiO_2/graphene hydrogel electrode with tunable density and porous structures. By incorporating room temperature ionic liquids（RTILs）, even upon drying, the non-volatile RTILs that remained in the gel film would preserve the efficient ion transport channels and prevent the electrode from closely stacking, to develop dense yet porous structures. As a result, the dense TiO_2/graphene gel film as an electrode for lithium ion battery displayed a good gravimetric electrochemical performance and more importantly a high volumetric performance.

Nanocellulose/nitrogen and fluorine co-doped graphene composite hydrogels for high-performance supercapacitors

Three-dimensional graphene materials have been studied as typical supercapacitors electrode materials by virtue of their ultrahigh specific surface area and good ion transport capacity.However,improvement of the poor volumetric electrochemical performance of these graphene materials has been required although they have high gravimetric energy density.In this work,nanocellulose/nitrogen and fluorine co-doped graphene composite hydrogels(NC-NFGHs)were prepared through a convenient hydrothermal approach utilizing ammonium fluoride as the heteroatom source.Nanocellulose(NC)and high concentration of graphene oxide(GO)were utilized to adjust the structure of NC-NFGHs and increase their packing density.Subsequently,the aqueous symmetric supercapacitor based on NC-NFGH-80 exhibits remarkable gravimetric(286.6 F·g^(-1))and volumetric(421.3 F·cm^(-3))specific capacitance at 0.3 A·g^(-1),good rate performance,and remarkable cycle stability up to 10,000 cycles.Besides,the all-solid-state flexible symmetric supercapacitors(ASSC)fabricated by NC-NFGH-80 also delivered a large specific capacitance of 117.1 F·g^(-1)at 0.3 A·g^(-1)and long service life over 10,000 cycles at 10 A·g^(-1).This compact porous structure and heteroatom co-doped graphene material supply a favorable strategy for high-performance supercapacitors.