Abstract:The capacitor performance of newly synthesized crystalline POMOFs was higher than those of the majority of reported POMOF-, state-of-the-art MOF- and POM-based materials.
“…In sharp contrast to the inorganic electrode materials, their diverse topology structure, tunable porosity, and abundant metal ions allow them to be a promising energy storage material . However, the poor conductivity and lack of structural stability of pristine MOFs remain the critical limitations for practical applications in energy storage devices . Except for MOFs‐derived nanocarbons or metal compounds, hybridizing MOFs with conductive polymers or carbon substrates is an additional productive tactic to improve the conductivity and stability, which can accelerate the electron transfer and reduce the inner resistance during the electrochemical reactions, even though the loading of active MOF species is lowered by the existence of conducting materials in a hybrid composition .…”
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confidence: 99%
“…The Co‐Ni‐B‐S presents the highest capacitance with two pairs of redox peaks at the scan rate of 20 mV s −1 , whereas only one pair for the other materials (Co‐Ni MOF, Co‐Ni‐B, Co‐Ni‐S, and Co‐Ni‐S‐B) is resulted from the Co/Ni multivalences and amorphous structure after the redox treatment . The electrochemically active surface area (ECSA) of Co‐Ni MOF and its derivatives are also evaluated through the CV measurements at the potential window (0–0.1 V versus Hg/HgO) (Figure S10, Supporting Information) . The specific electrical double layer capacitance ( C dl ) of Co‐Ni MOF, Co‐Ni‐B, Co‐Ni‐B‐S, Co‐Ni‐S, and Co‐Ni‐S‐B is 110.66, 45.8, 145.4, 48, and 2.5 F g −1 , respectively.…”
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confidence: 99%
“…[16,17] However, the poor conductivity and lack of structural stability of pristine MOFs remain the critical limitations for practical applications in energy storage devices. [18,19] Except for MOFs-derived nanocarbons or metal compounds, [15,20,21] hybridizing MOFs with conductive polymers or carbon substrates is an additional productive tactic to improve the conductivity and stability, which can accelerate the electron transfer and reduce the inner resistance during the electrochemical reactions, even though the loading of active MOF species is lowered by the existence of conducting materials in a hybrid composition. [22][23][24][25] Nevertheless, the charge storage behaviors of these MOFs materials are mainly based on the surface area-dependent and non-faradaic electrical double-layer capacitance (EDLC), while there is a poor utilization of abundant redox-active metal ion sites at the higher rates.…”
The development of efficient electrode materials is a cutting‐edge approach for high‐performance energy storage devices. Herein, an effective chemical redox approach is reported for tuning the crystalline and electronic structures of bimetallic cobalt/nickel–organic frameworks (Co‐Ni MOFs) to boost faradaic redox reaction for high energy density. The as‐obtained cobalt/nickel boride/sulfide exhibits a high specific capacitance (1281 F g−1 at 1 A g−1), remarkable rate performance (802.9 F g−1 at 20 A g−1), and outstanding cycling stability (92.1% retention after 10 000 cycles). An energy storage device fabricated with a cobalt/nickel boride/sulfide electrode exhibits a high energy density of 50.0 Wh kg−1 at a power density of 857.7 W kg−1, and capacity retention of 87.7% (up to 5000 cycles at 12 A g−1). Such an effective redox approach realizes the systematic electronic tuning that activates the fast faradaic reactions of the metal species in cobalt/nickel boride/sulfide which may shed substantial light on inspiring MOFs and their derivatives for energy storage devices.
“…In sharp contrast to the inorganic electrode materials, their diverse topology structure, tunable porosity, and abundant metal ions allow them to be a promising energy storage material . However, the poor conductivity and lack of structural stability of pristine MOFs remain the critical limitations for practical applications in energy storage devices . Except for MOFs‐derived nanocarbons or metal compounds, hybridizing MOFs with conductive polymers or carbon substrates is an additional productive tactic to improve the conductivity and stability, which can accelerate the electron transfer and reduce the inner resistance during the electrochemical reactions, even though the loading of active MOF species is lowered by the existence of conducting materials in a hybrid composition .…”
mentioning
confidence: 99%
“…The Co‐Ni‐B‐S presents the highest capacitance with two pairs of redox peaks at the scan rate of 20 mV s −1 , whereas only one pair for the other materials (Co‐Ni MOF, Co‐Ni‐B, Co‐Ni‐S, and Co‐Ni‐S‐B) is resulted from the Co/Ni multivalences and amorphous structure after the redox treatment . The electrochemically active surface area (ECSA) of Co‐Ni MOF and its derivatives are also evaluated through the CV measurements at the potential window (0–0.1 V versus Hg/HgO) (Figure S10, Supporting Information) . The specific electrical double layer capacitance ( C dl ) of Co‐Ni MOF, Co‐Ni‐B, Co‐Ni‐B‐S, Co‐Ni‐S, and Co‐Ni‐S‐B is 110.66, 45.8, 145.4, 48, and 2.5 F g −1 , respectively.…”
mentioning
confidence: 99%
“…[16,17] However, the poor conductivity and lack of structural stability of pristine MOFs remain the critical limitations for practical applications in energy storage devices. [18,19] Except for MOFs-derived nanocarbons or metal compounds, [15,20,21] hybridizing MOFs with conductive polymers or carbon substrates is an additional productive tactic to improve the conductivity and stability, which can accelerate the electron transfer and reduce the inner resistance during the electrochemical reactions, even though the loading of active MOF species is lowered by the existence of conducting materials in a hybrid composition. [22][23][24][25] Nevertheless, the charge storage behaviors of these MOFs materials are mainly based on the surface area-dependent and non-faradaic electrical double-layer capacitance (EDLC), while there is a poor utilization of abundant redox-active metal ion sites at the higher rates.…”
The development of efficient electrode materials is a cutting‐edge approach for high‐performance energy storage devices. Herein, an effective chemical redox approach is reported for tuning the crystalline and electronic structures of bimetallic cobalt/nickel–organic frameworks (Co‐Ni MOFs) to boost faradaic redox reaction for high energy density. The as‐obtained cobalt/nickel boride/sulfide exhibits a high specific capacitance (1281 F g−1 at 1 A g−1), remarkable rate performance (802.9 F g−1 at 20 A g−1), and outstanding cycling stability (92.1% retention after 10 000 cycles). An energy storage device fabricated with a cobalt/nickel boride/sulfide electrode exhibits a high energy density of 50.0 Wh kg−1 at a power density of 857.7 W kg−1, and capacity retention of 87.7% (up to 5000 cycles at 12 A g−1). Such an effective redox approach realizes the systematic electronic tuning that activates the fast faradaic reactions of the metal species in cobalt/nickel boride/sulfide which may shed substantial light on inspiring MOFs and their derivatives for energy storage devices.
“…reported that the NENU‐5/PPy nanocomposite has 5147 mF cm −2 and a symmetric supercapacitor device was developed in 2018. In 2019, Li et al . studied Mo‐based POMOFs, the highest specific capacitance of which was 249.0 F g −1 .…”
Section: Introductionmentioning
confidence: 99%
“…[31] reported that the NENU-5/PPy nanocomposite has5 147 mF cm À2 and as ymmetric supercapacitor device was developed in 2018. In 2019, Li et al [32] studied Mo-based POMOFs, the highest specific capacitance of which was 249.0 Fg À1 .I nP OMOFs, the silver ion with d 10 configuration is as oft Lewis acid metal ion, and the multifunctional coordination number and the adjustable coordination shell can be adopted to increase the chance of coordination with the POMs andt he organic ligands. Meanwhile, Ag-MOF and Ag-POMOFs [33,34] have been little researched for SCs, mainly because these substances are synthesized by hydrothermal methods, which have the disadvantages of tedious experiments, long reaction times, low yields, and poor stability of repeated synthesis.…”
Successful synthesis of three kinds of dynamically stable compounds by a simple grinding method is reported, giving Ag6Mo7O24, Ag‐BTC (Ag‐MOF, BTC=benzene‐1,3,5‐tricarboxylic acid), and {Ag6Mo7O24}@Ag‐MOF metal–organic frameworks (MOFs). According to the electrochemical dynamic analysis, these materials have pseudocapacitor behavior and high capacitance. The unique nanorod structure of {Ag6Mo7O24}@Ag‐MOF provides more active sites, faster ion/electron transfer, and electrolyte diffusion pathways, resulting in excellent specific capacitance (971 F g−1) higher than the other compounds. {Ag6Mo7O24}@Ag‐MOF (glassy carbon electrode) also has an excellent rate ability (60.1 %) and long cycle stability (98 % retention after 5000 cycles). In addition, the fully symmetrical button battery (with nickel foam as the current collector) fabricated with {Ag6Mo7O24}@Ag‐MOF delivers an energy density of 11.1 Wh kg−1 at 600.1 Wh kg−1 coupled with excellent cycling stability (86.4 %) at 1.2 V. These results demonstrate a new simple grinding method to prepare polyoxometalate‐based metal–organic frameworks (POMOFs) for high‐performance materials.
Metal‐organic compounds, including molecular complexes and coordination polymers, have attracted much attention as electrode materials in supercapacitors owing to their large surface area, high porosity, tailorable pore size, controllable structure, good electrochemical reversibility, and abundant active sites. Among the variety of metal‐organic compounds exhibiting desired supercapacitor performances (high specific capacitance, long cycling life, high energy density, and power density), those with metals in the first transition metal series are the most studied due to their rich covalent states, light atom weight, environmental‐friendliness, non‐toxicity, and low cost. In this review, the recent reports on the metal‐organic compounds of the first transition metal series as electrode materials in supercapacitors are summarized and their electrode and device performances are discussed in terms of different metal elements and typical multidentate ligands. Moreover, the current challenges, design strategies, future opportunities and further research directions are also highlighted for metal‐organic compounds in the field of supercapacitors.
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