3.2-3.4 活性位点、界面与复合电极
774-777Connects metal redox activity, ligand functionalisation, electrolyte/interface compatibility and conductive polymer or carbon composites to SC behaviour.
Relevance: Peripheral · 776 · 3.4 · Figure 8
LI Zehui, TAN Meijuan, ZHENG Yuanhao, LUO Yuyang, JING Qiushi, JIANG Jingkun, LI Mingjie · Journal of Inorganic Materials · 2020
Review conductive metal-organic frameworks as supercapacitor electrode materials, linking SC storage mechanisms with conductive MOF structure, preparation, charge transport, morphology, active sites, interfaces and composite strategies.
The review’s argument is preserved as a navigable set of section summaries.
Connects metal redox activity, ligand functionalisation, electrolyte/interface compatibility and conductive polymer or carbon composites to SC behaviour.
Relevance: Peripheral · 776 · 3.4 · Figure 8
Introduces the review's four design levers: morphology/nanostructure, composition/active sites, reaction interface optimisation and composite construction.
Relevance: Supporting · 772 · 3 · Figure 2
Frames supercapacitors as high-power, long-life energy-storage devices and introduces conductive MOFs as porous, tunable electrode candidates.
Relevance: Peripheral · 770 · Introduction
Reviews pore size, ligand length, particle size, one-dimensional arrays, two-dimensional pi-conjugated frameworks and three-dimensional hierarchical structures as morphology routes.
Relevance: Supporting · 772 · 3.1 · Figures 3-4
Discusses amorphous MOFs, MOF-derived carbon strategies and four future needs: conductivity, pore/electrolyte matching, stability and non-crystalline/liquid MOFs.
Relevance: Supporting · 778 · 4
Explains why most MOFs are poor conductors, how conjugated or redox-active building blocks improve conduction, and how conductive MOFs can transport charge.
Relevance: Supporting · 771 · 2.2 · Figure 1
Defines electrochemical capacitors and classifies SC storage into electric double-layer capacitance, Faradaic pseudocapacitance and hybrid capacitance.
Relevance: Peripheral · 770 · 1 · Equation 1
Classification systems are attributed to this review and are not treated as a global material registry.
The review maps metal sites to pseudocapacitance, conjugated porous ligands to double-layer behaviour, and their coexistence to hybrid capacitance.
Categories: Metal nodes as redox sites · Organic framework as porous/conjugated double-layer host · Mixed behaviour when both mechanisms operate
772 · 3
Figure 2 and Section 3 organise conductive-MOF SC design around morphology, metal/linker composition, electrode/electrolyte interface and composite construction.
Categories: Microstructure · Active site · Surface interface · Nanocomposite
772 · 3 · Figure 2
Conductive MOFs are interpreted using semiconductor-like mechanisms where carriers move by hopping, spatial transfer between donor/acceptor sites, or delocalised transport through bonds/bands.
Categories: Hopping charge transport · Through-space charge transport · Through-bond or band transport
771 · 2.2 · Figure 1
Morphology is presented as a route to alter ion diffusion length, accessible surface area, active-site exposure, electronic pathways and mechanical buffering.
Categories: Pore-size and surface-area tuning · One-dimensional nanowire or nanotube arrays · Two-dimensional pi-conjugated frameworks · Three-dimensional hierarchical or hollow nanostructures
773 · 3.1 · Figures 3-4
The review organises SC behaviour by whether charge is stored through interfacial double layers, redox/ion-layer pseudocapacitance, or combined electrode mechanisms.
Categories: Electric double-layer capacitance · Faradaic pseudocapacitance · Hybrid capacitance
770 · 1
Review-defined families retain their representative materials and conduction descriptions.
Layered frameworks with extended two-dimensional pi conjugation and graphene-like structures.
Conduction: Electron delocalisation is favoured by extended pi-conjugated sheets or conductive MOF nanowires, giving high electronic conductivity relative to conventional MOFs.
Representative materials: Ni3(HITP)2 · Cu-CAT NWAs
Nodes / linkers: Ni · Cu · Hexaaminotriphenylene-type ligands · Catecholate-type ligands
772 · 3.1 · Figure 4
Co-based MOFs whose pore dimensions, electrolyte compatibility and metal redox activity are linked to SC behaviour.
Conduction: Co redox activity contributes pseudocapacitive behaviour, while pore structure and electrolyte wetting modulate ion access.
Representative materials: Co-BDC · Co-NDC · Co-BPDC · Co-MOF-71 · Co8-MOF-5
Nodes / linkers: Co · Dicarboxylates · Polyethylene glycol · Benzendicarboxylate
772 · 3.1 · Table 1
Electrodes where conductive MOF particles are bridged or interwoven with carbon materials or conducting polymers.
Conduction: Conductive additives can bridge discrete MOF particles and create electron pathways, but excessive composite formation can reduce accessible surface area or increase ion diffusion resistance.
Representative materials: PANI-ZIF-67-CC · PPy/Zn-Ni-MOF · MIL-100(Fe)/carbon · Co-MOF/reduced graphene oxide
Nodes / linkers: Co · Zn/Ni · Fe · ZIF imidazolate frameworks · Pyrrole-derived polymer composites · Carboxylate MOF composites
776 · 3.4 · Figure 8
Ni-centred MOFs, including pillared and Zn-doped variants, used to increase active redox sites and capacitance.
Conduction: Ni sites supply electrochemical activity; ligand functionalisation and Zn doping affect stability, spacing and charge transfer.
Representative materials: Ni-MOF-24 · Ni-DMOF-ADC · Zn-doped Ni-MOF · 1D Ni-MOF
Nodes / linkers: Ni · Zn/Ni · p-Benzenedicarboxylic acid · Anthracenedicarboxylic acid · DABCO-pillared carboxylates
774 · 3.2 · Table 1
MOFs designed to conduct protons through hydrogen-bond networks, cation incorporation or defect-assisted proton carriers.
Conduction: Hydrogen-bond networks, proton carriers and framework defects improve proton conductivity, but this is contextual rather than direct SC electrode evidence.
Representative materials: [Cu2(Htzehp)2(4,4'-bipy)]·3H2O · (NH4)2(adp)-[Zn2(ox)3]·3H2O · Defective UiO-66
Nodes / linkers: Cu · Zn · Zr · Oxalate/adipate systems · Bipyridine-containing systems · Carboxylate ligands
771 · 2.1
Zr(IV) MOFs, especially UiO-66 family and nMOF-867, valued for thermal/solvent stability and nanocrystalline electrode forms.
Conduction: Stability is attributed to strong Zr-O bonding and SBU-based frameworks; capacitance depends on particle size, porosity and interfacial access.
Representative materials: UiO-66 · HP-UiO-66 · nMOF-867 · Amorphous UiO-66
Nodes / linkers: Zr · Terephthalic acid · 2,2'-bipyridine-5,5'-dicarboxylate
774 · 3.2 · Figure 5
Review-level synthesis principles remain separate from primary-study recipes.
Use electrochemically active transition-metal centres or mixed-metal/doped MOFs to increase redox-active sites and pseudocapacitance.
Claimed effects: Metal nodes provide redox sites and can raise pseudocapacitive contribution.
Controlling variables: Metal centre · Metal valence · Mixed-metal composition · Ligand coordination environment
Representative materials: MIL-100(Fe) · Co-MOF · Ni-MOF-24 · Zn-doped Ni-MOF
Caveat: The review explicitly states that further adjustment of activity and Faradaic pseudocapacitance remains unresolved.
774 · 3.2
Connect discrete conductive-MOF particles through carbon cloth, graphene, carbon black, CNTs, PANI or PPy to improve macroscopic charge pathways and device integration.
Claimed effects: Improves electron transport, mechanical flexibility and solid-state device feasibility.
Controlling variables: Composite partner · Polymer loading · Carbon support · MOF-polymer interfacial contact · Ion diffusion resistance
Representative materials: PANI-ZIF-67-CC · PPy/Zn-Ni-MOF · MIL-100(Fe)/carbon · Co-MOF/rGO
Caveat: Composite formation can reduce effective MOF surface area, lower porosity/stability or increase ion diffusion resistance.
776 · 3.4
Select aromatic or pi-conjugated linkers, first/second-row transition metals, redox-active ligands or heterobimetallic structures so charge can move through metal nodes and organic ligands.
Claimed effects: Improves electronic or proton conduction and enables redox/pseudocapacitive behaviour.
Controlling variables: Metal identity · Ligand conjugation · Redox activity · Metal-linker orbital overlap
Representative materials: Cu[Ni(Pdt)2] · MET-1 to MET-6 · Ni3(HITP)2
Caveat: The review notes that most MOFs remain poor conductors because organic ligands are insulating and orbital overlap is often weak.
771 · 2.1
Modify metal-site coordination, ligand functionality, hydrophilicity/hydrophobicity, electrolyte identity or electrode format to improve wetting, ion transport and cycling stability.
Claimed effects: Enhances interface stability, electron/charge transfer and practical SC behaviour.
Controlling variables: Electrolyte composition · Metal-site ligands · Ligand functionalisation · Electrode film architecture · Water stability
Representative materials: Ni-DMOF-ADC · Co-MOF in LiOH · nMOF-867 coin-type SC · STAM-17-OEt
Caveat: Electrode/electrolyte non-wetting can suppress capacitance; aqueous stability remains a major issue.
776 · 3.3 · Figure 7
Tune ligand length, synthesis conditions, templates or hierarchical structures to balance pore access, surface area, diffusion paths and active-site exposure.
Claimed effects: Can improve ion diffusion, capacitance, rate capability and cycling behaviour.
Controlling variables: Ligand length · Pore-size distribution · Particle size · Template pressure or reaction conditions · Mesopore/macropore fraction
Representative materials: Co-BDC/Co-NDC/Co-BPDC · UiO-66 · Zn-doped Ni-MOF · Mesoporous Co-MOF nanospheres
Caveat: Micropores smaller than ion/solvation dimensions can limit electrolyte access.
772 · 3.1
Introduce cations, water/proton carriers, ion substitution or monocarboxylate-induced defects to tune proton conductivity.
Claimed effects: Can increase proton conductivity by improving carrier concentration and mobility.
Controlling variables: Hydrogen-bond network continuity · Cation identity · Defect concentration · Humidity and temperature
Representative materials: (NH4)2(adp)-[Zn2(ox)3]·3H2O · K2(adp)-[Zn2(ox)3]·3H2O · Defective UiO-66
Caveat: These are proton-conduction examples, not direct proof of SC electrode performance.
771 · 2.1
These are the review authors’ synthesis, not newly measured results.
Planar 2D conductive MOFs with extended pi conjugation are presented as among the most conductive framework structures.
Evidence basis: single_reference
Caveat: The review also notes that many 2D conductive MOFs still lack sufficient conductivity or mechanical/chemical stability.
772 · 3.1 · Figure 4
Amorphous MOFs may show useful ion-storage behaviour because gate-opening and unusual spatial structure can enhance electrochemical activity.
Evidence basis: multi_reference
Caveat: The review frames this as an emerging direction needing deeper study.
777 · 3.5
Conductive MOF charge transport can be understood through hopping, through-space transfer and through-bond/band transport.
Evidence basis: single_reference
Caveat: Mechanistic classification is general and not specific to all supercapacitor conditions.
771 · 2.2 · Figure 1
Composite electrodes can improve charge transport and flexibility, but may reduce effective MOF surface area, porosity or stability and can increase ion diffusion resistance.
Evidence basis: multi_reference
Caveat: This is a design tradeoff rather than a settled quantitative rule.
776 · 3.4
Aromatic or pi-conjugated organic linkers are presented as a key route to improve conductive MOF conductivity.
Evidence basis: multi_reference
Caveat: The review does not standardise conductivity measurement conditions across examples.
771 · 2.1
Electrolyte choice can determine whether a MOF electrode exhibits pseudocapacitive behaviour and acceptable capacitance.
Evidence basis: multi_reference
Caveat: The examples are material-specific and should not be generalised without primary-paper checks.
776 · 3.3
Many studies applying conductive MOFs to SCs do not measure or study intrinsic conductivity, leaving the field immature.
Evidence basis: review_reasoning
Caveat: This is an explicit review-level limitation and not tied to one primary study.
778 · 4
The review treats CV, GCD and EIS, plus capacitance, energy density and power density, as the conventional metrics for judging conductive-MOF SC electrodes.
Evidence basis: review_reasoning
Caveat: The review does not discuss cross-paper normalisation problems in depth.
772 · 3
For conductive MOF electrodes, metal sites mainly provide Faradaic redox/pseudocapacitance while the porous conjugated organic framework contributes double-layer behaviour.
Evidence basis: review_reasoning
Caveat: This is the review authors' synthesis of the SC mechanism rather than a single directly cited primary result.
772 · 3
MOFs dominated by micropores below about 2 nm may restrict electrolyte-ion diffusion and limit supercapacitor use.
Evidence basis: single_reference
Caveat: The citation is used for hierarchical-pore MOFs rather than conductive-MOF SC performance directly.
772 · 3.1
Most MOFs are intrinsically poor electronic conductors because organic ligands are insulating and their pi orbitals overlap weakly with metal d orbitals.
Evidence basis: single_reference
Caveat: The review uses this as background for conductive MOF design, not as new evidence.
770 · 2.1
Porous electrode architectures can buffer volume change, shorten ion diffusion paths and expose more electrochemically active sites.
Evidence basis: review_reasoning
Caveat: The claim is a design rationale; primary examples differ in electrolyte, loading and device architecture.
772 · 3.1
Redox-active organic ligands and open-shell metal centres can delocalise charge through conjugation, with self-exchange between redox centres coupled to counter-ion motion.
Evidence basis: single_reference
Caveat: The review presents this as a conceptual transport pathway rather than a quantified SC measurement.
771 · 2.2
Poor stability is a major challenge for conductive MOFs as SC electrodes.
Evidence basis: multi_reference
Caveat: The review discusses both intrinsic material stability and electrode/electrolyte interface stability.
774 · 3.2
Fe, Co, Ni, Cu and Mn are attractive centre metals because they are electrochemically active, abundant and comparatively low-cost.
Evidence basis: review_reasoning
Caveat: Abundance and cost do not by themselves establish high device performance.
774 · 3.2 · Table 1
Every row remains visibly secondary and links to a primary dossier only where the mapping is verified.
| Material | Property | Reported value | Context and quality | Primary evidence | Review source |
|---|---|---|---|---|---|
| SecondaryAmorphous UiO-66 | Specific capacitance | 920 F·g−1 at 10 mV·s−1; crystalline UiO-66 comparator 452 F·g−1 | 10 mV·s−1; amorphous UiO-66 compared with crystalline UiO-66 Text · Exact Reported | No verified corpus mapping | 777 · 3.5 |
| SecondaryMesoporous Co-MOF nanospheres | Specific capacitance and cycling retention | 230.5 F·g−1 at 0.5 A·g−1; 95.2% retention after 10^3 cycles | Co-MOF nanospheres prepared in ionic liquid using supercritical CO2 template Text · Exact Reported | No verified corpus mapping | 774 · 3.1 |
| SecondaryCo-BDC | Specific capacitance | 131.8 F·g−1 | Review Table 1; supercapacitor electrode benchmark Table · Exact Reported | No verified corpus mapping | 775 · 3.2 · Table 1 |
| SecondaryCo-BPDC | Energy and power density | 31.4 Wh·kg−1; 5640 W·kg−1 | Review Table 1; Co-MOF with 4,4-biphenyldicarboxylic acid ligand Table · Exact Reported | No verified corpus mapping | 775 · 3.2 · Table 1 |
| SecondaryCo-MOF | Specific capacitance | 150-200 F·g−1 in 1 mol·L−1 LiOH; capacitance decreased only 1.5% after 10^3 cycles | 1 mol·L−1 LiOH electrolyte Text · Range | No verified corpus mapping | 774 · 3.2 |
| SecondaryCu-CAT NWAs | Areal capacitance | ≈22 μF·cm−2; about 2 times carbon fibre sheet comparator | MOF nanowire arrays grown on carbon fibre paper Text · Approximate | research_0026 | 772 · 3.1 · Figure 3 |
| SecondaryNi3(HITP)2 | Electrical conductivity | >5000 S·m−1 | Review-reported framework conductivity for layered 2D Ni3(HITP)2 Text · Approximate | No verified corpus mapping | 772 · 3.1 · Figure 4 |
| SecondaryNi3(HITP)2 | Specific capacitance and cycling retention | 111 F·g−1 at 0.05 A·g−1; >90% retention after 10^4 cycles | Pressed powder assembled directly into symmetric two-electrode SC; 0.05 A·g−1 Text · Exact Reported | No verified corpus mapping | 772 · 3.1 · Figure 4 |
| SecondaryNi-MOF-24 | Specific capacitance | 1127 F·g−1 at 0.5 A·g−1 | Layered Ni-based MOF using p-benzenedicarboxylic acid ligand; 0.5 A·g−1 Text · Exact Reported | No verified corpus mapping | 774 · 3.2 · Table 1 |
| SecondaryNi-DMOF-ADC | Cycling stability | 2% capacitance loss after 1.6×10^4 cycles | ADC ligand; Ni-DMOF asymmetric SC cycle test Text · Exact Reported | No verified corpus mapping | 775 · 3.3 · Figure 6 |
| SecondarynMOF-867 | Areal capacitance | 5.085 mF·cm−2 areal | Nanocrystalline MOF electrode in SC device; review Table 1/Figure 5 Table · Exact Reported | No verified corpus mapping | 775 · 3.2 · Table 1 |
| SecondaryPPy-coated Zn/Ni-MOF | Specific capacitance and cycling retention | 160.1 F·g−1 at 1 A·g−1; 78.8% retention after 5×10^3 cycles | PPy/Zn-Ni-MOF composite electrode; 1 A·g−1 Text · Exact Reported | No verified corpus mapping | 776 · 3.4 |
| SecondaryZr-MOFs / UiO-66 | Specific capacitance | 1144 F·g−1 at 5 mV·s−1 | Largest surface area (1047 m2·g−1) and smallest particle size (~100 nm); 5 mV·s−1 Text · Exact Reported | No verified corpus mapping | 772 · 3.1 |
| SecondaryZn-doped Ni-MOF | Specific capacity | 237.4 mA·h·g−1 at 1 A·g−1; 88% retention after 4×10^3 cycles | Battery-type supercapacitor electrode; 1 A·g−1 Text · Exact Reported | No verified corpus mapping | 773 · 3.1 |
| SecondaryZn-doped Ni-MOF | Specific capacitance | 1620 F·g−1 at 0.25 A·g−1 | Zn(II)-doped Ni-based MOF; 0.25 A·g−1 Text · Exact Reported | No verified corpus mapping | 774 · 3.2 · Table 1 |
Open questions are presented as review-author priorities, not conclusions from the primary database.
Although performance has been reported, the field is immature and far from commercial application.
Proposed direction: Develop deeper, more systematic studies before claims of industrial readiness.
778 · 4
Effective combination of MOFs with conductive additives remains a key research issue because composites can improve charge transport but reduce surface area or porosity.
Proposed direction: Optimise additive amount and interfacial connectivity to balance electron transport with ion diffusion.
776 · 3.4
The review states that intrinsic electronic conductivity remains a central research focus and is often not measured in SC studies.
Proposed direction: Measure and improve intrinsic electronic conductivity using active inorganic sites and conjugated pi ligands.
778 · 4
The influence of conductive-MOF crystalline state, including amorphous and liquid forms, on capacitance remains underexplored.
Proposed direction: Study how crystal, amorphous and liquid MOF structures affect ion storage and electrochemical activity.
778 · 4
The mechanism by which conductive MOFs interact with electrolytes or electrolyte ions is unclear.
Proposed direction: Clarify how pore-size distribution, solid-liquid or solid-solid contact, and electrolyte identity control accessible area and pore utilisation.
778 · 4
Chemical stability is described as a shortcoming of both conductive MOFs and MOFs more generally.
Proposed direction: Prioritise stability in electrolytes during charge/discharge and relate stability to cycle life and application range.
778 · 4
Mappings show which printed review references have a verified counterpart in the frozen primary corpus.
| Reference | Study | Role and context | Corpus mapping |
|---|---|---|---|
| Ref. 152012 | Conductive metal-organic frameworks and networks: fact or fantasy? | conductivity_context · caveatUsed to support the statement that most MOFs are poor conductors and to frame conductive MOFs as a special subset. | Unmapped |
| Ref. 162010 | Conductivity, doping, and redox chemistry of a microporous dithiolene-based metal-organic framework | conductivity_example · redox_mofExample of an intrinsically conducting porous p-type semiconductor MOF operating through redox chemistry. | research_0203 |
| Ref. 172012 | Porous, conductive metal-triazolates and their structural elucidation by the charge-flipping method | conductivity_example · metal_triazolateUsed as an Fe(II)-containing conductive MOF example with ohmic conductivity. | research_0325 |
| Ref. 192009 | Rational designs for highly proton-conductive metal-organic frameworks | proton_conductivity · hydrogen_bond_networkExample of introducing proton carriers into a layered oxalate-bridged framework. | research_0220 |
| Ref. 202014 | Proton conductivity control by ion substitution in a highly proton-conductive metal–organic framework | proton_conductivity · ion_substitutionUsed for cation substitution control of MOF proton conductivity. | Unmapped |
| Ref. 212015 | Defect control to enhance proton conductivity in a metal–organic framework | defect_engineering · proton_conductivitySupports defect generation as a route to enhance proton conductivity in Zr-MOFs. | Unmapped |
| Ref. 222018 | Conductive two-dimensional metal-organic frameworks as multifunctional materials | transport_mechanism · 2d_conductive_mofsSource for the review's charge-transport taxonomy in conductive MOFs. | research_0050 |
| Ref. 242018 | The role of redox hopping in metal-organic framework electrocatalysis | redox_hopping · transport_mechanismUsed by the review to explain charge transfer via redox-centre self-exchange coupled to counter-ion motion. | Unmapped |
| Ref. 252013 | Supercapacitive property of metal–organic-frameworks with different pore dimensions and morphology | pore_dimension · supercapacitor_benchmarkUsed for Co-MOF pore-size/ligand-length examples and Table 1 benchmarks. | Unmapped |
| Ref. 262015 | An in situ self-assembly template strategy for the preparation of hierarchical-pore metal-organic frameworks | hierarchical_pores · ion_accessSupports the caveat that mostly microporous MOFs can restrict electrolyte-ion diffusion. | Unmapped |
| Ref. 282015 | Facile synthesis and supercapacitive properties of Zr-metal organic frameworks (UiO-66) | morphology_control · supercapacitor_benchmarkUsed for the review's claim that surface area and particle size affect capacitance. | Unmapped |
| Ref. 292017 | Conductive metal-organic framework nanowire array electrodes for high-performance solid-state supercapacitors | solid_state_supercapacitor · nanowire_arrayExample of MOF-based one-dimensional nanowire arrays grown on carbon fibre paper. | research_0026 |
| Ref. 302017 | Conductive MOF electrodes for stable supercapacitors with high areal capacitance | 2d_conductive_mof · supercapacitor_benchmarkKey example of a 2D conductive MOF used directly as a stable supercapacitor electrode. | Unmapped |
| Ref. 322018 | Microwave-assisted synthesis of honeycomblike hierarchical spherical Zn-doped Ni-MOF as a high-performance battery-type supercapacitor electrode material | hierarchical_structure · doped_mofUsed for hierarchical spherical Zn-doped Ni-MOF morphology and capacity benchmark. | Unmapped |
| Ref. 342015 | Dual template effect of supercritical CO2 in ionic liquid to fabricate a highly mesoporous cobalt metal-organic framework | template_synthesis · mesoporous_mofUsed for supercritical CO2 template control of mesoporous Co-MOF nanospheres. | Unmapped |
| Ref. 352014 | A hybrid supercapacitor based on porous carbon and the metal-organic framework MIL-100(Fe) | fe_mof · composite_caveatUsed for Fe-MOF active-site discussion and as a cautionary example where carbon dominated capacitance after cycling. | Unmapped |
| Ref. 362012 | Unusual energy storage and charge retention in Co-based metal–organic-frameworks | co_mof · electrolyte_effectUsed for Co-MOF capacitance in LiOH and electrolyte-dependent pseudocapacitive behaviour. | Unmapped |
| Ref. 392014 | Metal–organic frameworks: a new promising class of material for high performances supercapacitor electrode | ni_mof · supercapacitor_benchmarkUsed for a high-capacitance layered Ni-MOF benchmark. | Unmapped |
| Ref. 412016 | Nickel-based pillared MOFs for high-performance supercapacitors: design, synthesis and stability study | stability · ligand_functionalisationUsed for ADC ligand functionalisation improving cycling stability and preserving interface stability. | Unmapped |
| Ref. 442014 | Supercapacitors of nanocrystalline metal-organic frameworks | nanocrystalline_mof · device_architectureUsed for nMOF-867 and coin-type nanocrystalline MOF SC device examples. | Unmapped |
| Ref. 452014 | Zn-doped Ni-MOF material with a high supercapacitive performance | doped_mof · supercapacitor_benchmarkUsed for high-capacitance Zn(II)-doped Ni-MOF benchmark. | Unmapped |
| Ref. 462012 | Co8-MOF-5 as electrode for supercapacitors | electrolyte_effect · low_capacitance_caveatUsed as an example where non-aqueous electrolyte and poor interfacial wetting may cause low capacitance. | Unmapped |
| Ref. 522015 | Flexible solid-state supercapacitor based on a metal–organic framework interwoven by electrochemically-deposited PANI | composite_electrode · flexible_solid_state_deviceUsed for conductive-polymer interweaving of ZIF-67 crystals on carbon cloth for flexible solid-state SCs. | Unmapped |
| Ref. 532017 | Bimetal–organic framework assisted polymerization of pyrrole involving air oxidant to prepare composite electrodes for portable energy storage | conducting_polymer_composite · tradeoffUsed for PPy-coated Zn/Ni-MOF composite performance and the conductivity/ion-diffusion tradeoff. | Unmapped |
| Ref. 552014 | Amorphous metal-organic frameworks | amorphous_mof · outlookBackground for amorphous MOFs and their potential gate-opening behaviour. | Unmapped |
| Ref. 562018 | Facile synthesis of amorphous UiO-66 (Zr-MOF) for supercapacitor application | amorphous_mof · supercapacitor_benchmarkUsed for amorphous UiO-66 as a supercapacitor benchmark compared with crystalline UiO-66. | Unmapped |
| Ref. 572018 | Hydrolytic stability in hemilabile metal–organic frameworks | hydrolytic_stability · outlookUsed for water-stable MOF strategy and as a reference point for non-crystalline/liquid MOF outlook. | Unmapped |
| Ref. 632017 | Liquid metal–organic frameworks | liquid_mof · outlookCited in the outlook for pore/electrolyte matching and broader non-crystalline MOF structure questions. | Unmapped |