Synthesis evidence

Morphologies of thienyl based bimetallic metal-organic frameworks controlled by solvents for high specific capacitance supercapacitor

Song S., Ma X., Zhang B. et al. · Journal of Energy Storage · 2022 · 103627

5 structured synthesis routes

Completeness describes how fully the route could be reconstructed from the main article and supporting information.

Partial recipeSource: Main

Route 1: Solvothermal

3 · 2.2. Materials preparation

Metal precursorsNi(NO3)2.6H2O and Co(NO3)2.6H2O, same molar amounts as E-NCT route
Linker precursorsH2TDC, same molar amount as E-NCT route
SolventsDMF used instead of EtOH
Atmospherenot reported
Temperature150
Time48
Work-upSame procedure as E-NCT; precipitate filtered, washed, and vacuum dried.
ActivationVacuum drying at 80 C for 12 h, inferred from same procedure
Scalability context50 mL autoclave batch synthesis inferred from same procedure.
Show 4 structured reagent records
RoleReagentAmount / concentrationSource
LinkerH2TDCsame as E-NCT route3 · 2.2. Materials preparation
Metal SourceNi(NO3)2.6H2Osame as E-NCT route3 · 2.2. Materials preparation
Metal SourceCo(NO3)2.6H2Osame as E-NCT route3 · 2.2. Materials preparation
SolventDMFnot restated3 · 2.2. Materials preparation
Complete recipeSource: Main

Route 2: Solvothermal

3 · 2.2. Materials preparation

Metal precursors0.25 mM Ni(NO3)2.6H2O and 0.25 mM Co(NO3)2.6H2O
Linker precursors0.25 mM H2TDC
SolventsEtOH: 20 mL for linker solution A; 15 mL for metal solution B
Atmospherenot reported
Temperature150
Time48
Work-upNaturally cooled, precipitate separated by suction filtration and washed with EtOH several times.
ActivationVacuum drying at 80 C for 12 h
Scalability context50 mL autoclave batch synthesis.
Show 4 structured reagent records
RoleReagentAmount / concentrationSource
LinkerH2TDC0.25 mM3 · 2.2. Materials preparation
Metal SourceNi(NO3)2.6H2O0.25 mM3 · 2.2. Materials preparation
Metal SourceCo(NO3)2.6H2O0.25 mM3 · 2.2. Materials preparation
SolventEtOH20 mL + 15 mL3 · 2.2. Materials preparation
Partial recipeSource: Main

Route 3: Solvothermal

3 · 2.2. Materials preparation

Metal precursorsNi(NO3)2.6H2O and Co(NO3)2.6H2O, same molar amounts as E-NCT route
Linker precursorsH2TDC, same molar amount as E-NCT route
SolventsMeOH used instead of EtOH
Atmospherenot reported
Temperature150
Time48
Work-upSame procedure as E-NCT; precipitate filtered, washed, and vacuum dried.
ActivationVacuum drying at 80 C for 12 h, inferred from same procedure
Scalability context50 mL autoclave batch synthesis inferred from same procedure.
Show 4 structured reagent records
RoleReagentAmount / concentrationSource
LinkerH2TDCsame as E-NCT route3 · 2.2. Materials preparation
Metal SourceNi(NO3)2.6H2Osame as E-NCT route3 · 2.2. Materials preparation
Metal SourceCo(NO3)2.6H2Osame as E-NCT route3 · 2.2. Materials preparation
SolventMeOHnot restated3 · 2.2. Materials preparation
Vague recipeSource: Main

Route 4: Solvothermal

3 · 2.2. Materials preparation

Metal precursorsNi(NO3)2.6H2O and Co(NO3)2.6H2O, inferred from same procedure
Linker precursorsterephthalic acid (PTA)
Solventsnot explicitly restated; same procedure as NCT MOF
Atmospherenot reported
Temperature150
Time48
Work-upSame procedure as NCT MOF, not fully restated.
ActivationVacuum drying at 80 C for 12 h, inferred from same procedure
Show 3 structured reagent records
RoleReagentAmount / concentrationSource
Linkerterephthalic acid (PTA)not reported3 · 2.2. Materials preparation
Metal SourceNi(NO3)2.6H2Oinferred same as NCT route3 · 2.2. Materials preparation
Metal SourceCo(NO3)2.6H2Oinferred same as NCT route3 · 2.2. Materials preparation
Partial recipeSource: Main

Route 5: Drop Cast

3 · 2.4. Electrochemical measurements

SolventsEtOH
Additivesacetylene black and PTFE
Atmospherenot reported
Substrate orientationfoamed nickel current collector
Work-upSlurry coated on foamed nickel and dried.
Activationdried after coating; conditions not reported
Show 4 structured reagent records
RoleReagentAmount / concentrationSource
OtherNi/Co MOF8 parts by mass ratio3 · 2.4. Electrochemical measurements
Additiveacetylene black1.5 parts by mass ratio3 · 2.4. Electrochemical measurements
AdditivePTFE0.5 parts by mass ratio3 · 2.4. Electrochemical measurements
SolventEtOHNot specified3 · 2.4. Electrochemical measurements