Energy Storage material status and challenges for KSA and practical application of 3D holey-graphene structure. Imran Shakir

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Energy Storage material status and challenges for KSA and practical application of 3D holey-graphene structure Imran Shakir

Specific Power (W/kg) Energy Storage Research Group Objective Development of low-cost, high-performance functional materials for large-scale, affordable storage devices for portable electronics, vehicle electrification, smart grid as well as the broad-scale deployment of alternative energy resources such as solar and wind. Portable electronics 20-30% CO 2 emission Specific Energy (Wh/kg) Energy storage is one of the key challenges we face in the 21 st century 2

ELECTROCHEMICAL ENERGY TECHNOLOGIES Alternative Energy Technologies Solar, wind, nuclear, hydro, geothermal, fuel cells, batteries, supercapacitors Fuel cells, batteries, supercapacitors: Only viable option for automobiles (~ 30%) Batteries: Critical for storing and efficiently utilizing solar and wind energies Fuel Cell Battery Supercapacitor Heat H 2 e - 2e - + H 2 2H + H + conductor 2e - H 2 O e - 1 / 2 O 2 Anode Cathode Electrolyte Conversion Device Portable, transportation, & stationary Air H 2 O e - Anode Load Charge Li + Discharge Li + Electrolyte e - Cathode Storage Device Portable, transportation, & stationary Electrode + + + + + + - - - - - - o o Electrolyte - - - - - - + + + + + + Electrode Storage Device Portable & transportation Chemical energy directly into electrical energy clean energy technologies Challenges: high cost, safety, durability, & operability problems

Current Energy Storage Devices Power density Capacitors Very limited energy storage capacity Bulky Heavy Gap in capabilities Insufficient power Cannot provide burst power Safety and durability issues Batteries/ Fuel Cells Energy density

Current Energy Storage Devices Supercapacitors have a unique ability to provide a solution that is small, lightweight and has the power to fill the gap in capabilities Supercapacitor Applications Power density Capacitors Capacitor replacements Battery complements Battery replacements Batteries / Fuel Cells Energy density

Energy Storage Devices Capacitor Supercapacitor C α 1/thickness Electrolyte solution E= ½ CV 2

Energy Storage Devices Batteries Electrolyte solution Capacitors and Super-capacitors are surface Storage Batteries are bulk Storage

Materials Challenges Reactions occur at the electrode surfaces We want to get as high a surface area as possible Need to have ions and electrons together for reactions to occur However e.g. Nanoparticles behave differently than bulk materials Energy of the reactions also depend on the surface properties Electrons must still be able to get outside the cell 1. Electron resistance cannot be too high 2. Separator must be robust and allow rapid transfer of ions 3. Fundamental materials properties need to be understood

Materials Requirements Large reversible capacity Small irreversible capacity Desirable charge profile Desirable kinetics (rate capability) Long cycle and calendar life Ease of processing Safety Compatibility with electrolyte and binder systems Low cost

Nanotechnology For Energy Storage Bulk Nanoparticles Nanowires NATURE MATERIALS, VOL 9, FEBRUARY 2010 Chem. Commun., 2010, 46, 4324 4326

Background on graphene 0D 1D 2D 1985 1991 2004 Electronic properties (ballistic transport, high carrier mobility) Mechanical properties (~1.1 TPa modulus, ~130 Gpa fracture strength) Thermal conductivity (~5300 W m 1 K 1 in plane, highly anistropic) Optical transmittance (97.7%) Specific surface area (theoretical: 2630 m 2 g 1 ) Specific Capacitance (theoretical: 550 Fg 1 )

Potential Applications Energy Storage Materials Volume 2, January 2016, Pages 107 138

Preparation of graphene Schematic of the most common graphene production methods. Each method has been evaluated in terms of graphene quality (G), cost aspect (C; a low value corresponds to high cost of production), scalability (S), purity (P) and yield (Y) of the overall production process. NATURE MATERIALS, VOL 14, 271-279 (2015)

Preparation of Graphene Based Composites The most common synthetic pathways for producing graphene-based materials (GO, RGO, GO- and RGO-based compounds) for use as electrode active materials in EESDs. NATURE MATERIALS, VOL 14, 271-279 (2015)

Preparation of Graphene Based Composites Structural models and a possible drawback of graphene composites. NATURE MATERIALS, VOL 14, 271-279 (2015)

Potential Applications of 3D Graphene Composites ACS Nano 2016, 10, 7231 7247.

Solution Processable Holey Graphene Oxide and Its Derived Macrostructures for High-Performance Supercapacitors GO was prepared by oxidation of natural graphite powder according to the modified Hummers method. HGO was prepared according to the following procedure: Typically, 5 ml 30% H 2 O 2 aqueous solution was mixed with 50 ml 2 mg/ml GO aqueous dispersion and then heated at 100 C for 4 h under stirring. HGHs were prepared according to the following procedure: 0.5 ml 1 M sodium ascorbate aqueous solution was added into 10 ml 2 mg/ml HGO aqueous dispersion and then the homogeneous mixture was heated at 100 C for 2 h without stirring Nano Lett. 2015, 15, 4605.

Solution Processable Holey Graphene Oxide and Its Derived Macrostructures for High-Performance Supercapacitors With the flexible processability of HGO dispersion, the sizes and shapes of HGH can be easily tailored by changing the type of reactors. The freeze-dried HGH showed an interconnected 3D porous network with the pore size ranging from submicrometers to several micrometers. The HGH showed a very high accessible SSA of 1330 m 2 /g, 34% higher than that of GH ( 990 m 2 /g), With the flexible processability of HGO dispersion, the sizes and shapes of HGH can be easily tailored by changing the type of reactors. Nano Lett. 2015, 15, 4605.

Solution Processable Holey Graphene Oxide and Its Derived Macrostructures for High-Performance Supercapacitors The HGH exhibited a specific capacitance of 283 F/g at a current density of 1 A/g, 38% higher than that of GH (205 F/g) Nano Lett. 2015, 15, 4605.

Solution Processable Holey Graphene Oxide and Its Derived Macrostructures for High-Performance Supercapacitors By chemical reduction of the HGO dispersion, we can also obtain welldispersed solution processable HG which can be further assembled into large-area flexible HGP with a compact layered structure via a flow-directed self assembly strategy. Nano Lett. 2015, 15, 4605.

Solution Processable Holey Graphene Oxide and Its Derived Macrostructures for High-Performance Supercapacitors The HGP exhibited a specific capacitance of 209 F/g at 1 A/g, respectively, considerably higher than those of GP (116 F/g). With a high packing density of 1.12 g/cm 3, the HGP could deliver an ultrahigh volumetric capacitance of 234 F/cm 3. Nano Lett. 2015, 15, 4605.

Solution Processable Holey Graphene Oxide and Its Derived Macrostructures for High-Performance Supercapacitors The entire flexible solid-state supercapacitor based on HGP showed a superior volumetric capacitance of 34 F/cm 3, which outperform most of previous reported results. Nano Lett. 2015, 15, 4605.

Solution Processable Holey Graphene Oxide and Its Derived Macrostructures for High-Performance Supercapacitors With EMIMBF 4 /AN as organic electrolyte, a high energy density of 116 and 77 Wh/kg can be achieved for HGH and HGP, respectively. Moreover, the HGP could show a high volumetric capacitance of 203 F/cm 3 and a high volumetric energy density of 86 Wh/L. Nano Lett. 2015, 15, 4605.

Three-Dimensional Graphene/Polyimide Composites Schematic of the preparation process of GF-PI; (b) Photographs of precursor solution of GO, naphthalenetetracarboxylic dianhydride (NTCDA) and ethanediamine (EDA), the resultant GF-PI gel in N-Methyl-2-pyrrolidone (NMP) solution, the GH-PI with interior NMP exchanged by water, and the final GF-PI monolith after freeze-drying and annealing; (c) Synthetic route to PI; (d) Electrochemical redox mechanism of PI. J. Mater. Chem. A, 2017,5, 2710-2716

Three-Dimensional Graphene/Polyimide Composites Low- and (b) high-magnification SEM images and (c) TEM image of GF-PI; (d) Low- and (e) high-magnification SEM images of pure PI; (f-i) Elemental mapping images of GF-PI (by SEM): Carbon (g), N (h), and O (i) distribution in the selected area. J. Mater. Chem. A, 2017,5, 2710-2716

Three-Dimensional Graphene/Polyimide Composites Preparation of a flexible binder-free GF-PI electrode. A piece of GF-PI (above) was mechanically pressed into a film electrode (down); SEM image of the side-view (b, c) and top-view (d, e) of the pressed GF-PI film. J. Mater. Chem. A, 2017,5, 2710-2716

Three-Dimensional Graphene/Polyimide Composites Electrochemical characterization of GF-PI as LIB cathode. J. Mater. Chem. A, 2017,5, 2710-2716

Three-Dimensional Graphene/Polyimide Composites Nyquist plots for GF-PI, G-PI and C-PI electrodes; (b) Nyquist plots for GF-PI electrode before and after cycling test; (c) SEM and (d) TEM image of the GF-PI after 600 cycles. J. Mater. Chem. A, 2017,5, 2710-2716

Three-Dimensional Graphene/Polyimide Composites Electrochemical characterization of GF-PI as SIB cathode. J. Mater. Chem. A, 2017,5, 2710-2716

Three-Dimensional Graphene/Poly (anthraquinonyl sulfide) (PAQS) Composites Schematic process of GPA. (b) Homogenous mixture of GO and poly (anthraquinonyl sulfide) PAQS in NMP and reduction and self-assembly of GO to form 3D graphene framework with encapsulated PAQS particles. (c) Freezedried aerogel of graphene/paqs composite. (d) Preparation of a flexible binder-free GPA film electrode by mechanical pressing. (e) Synthetic route to PAQS. (f) Reversible redox mechanisms of PAQS in LIBs and SIBs. ACS Appl. Mater. Interfaces 2017, 9, 15549 15556 30

Porous Fe 2 O 3 Nanoframeworks Encapsulated within Three-Dimensional Graphene Schematic illustration of the preparation procedure of 3DG/Fe 2 O 3. (a) Excessive metal ions induced combination, (b) self-assembly and spatially confined Ostwald ripening, and (c) thermal treatment under air condition. ACS Nano: 2017, 11, 5140 5147 31

Porous Fe 2 O 3 Nanoframeworks Encapsulated within Three-Dimensional Graphene SEM and (c) TEM images of the microstructure of 3DG/Fe 2 O 3 prepared by annealing of 3DG/PB at 250 C for 2h. (d) HR-TEM image of 3DG/Fe 2 O 3 and (e) the SAED pattern showing the poor crystallinity of Fe 2 O 3. Elemental mapping images of C (f), Fe (g), and O (h) of 3DG/Fe 2 O 3 composite shown in (d). ACS Nano: 2017, 11, 5140 5147 32

Porous Fe 2 O 3 Nanoframeworks Encapsulated within Three-Dimensional Graphene Discharge/charge profiles of 3DG/Fe 2 O 3 at a current density of 0.2 A/g. The cycling performance at 0.2 A/g (b) and rate performance (c) of 3DG/Fe 2 O 3 and Fe 2 O 3, respectively. (d) Cycling performance of 3DG/Fe 2 O 3 at 5 A/g. ACS Nano: 2017, 11, 5140 5147 33

Porous Fe 2 O 3 Nanoframeworks Encapsulated within Three-Dimensional Graphene The Nyquist plots of 3DG/Fe 2 O 3 before and after cycling test. (b) The Nyquist plots of 3DG/Fe 2 O 3 and Fe 2 O 3 after cycling test. (c) TEM image of 3DG/Fe 2 O 3 and (d) higher magnification image of a single Fe 2 O 3 nanoframework under delithiation state after cycling test. (e) The schematic of delithiation/lithiation reactions of 3DG/Fe2O3 ACS Nano: 2017, 11, 5140 5147 34

Three-Dimensional Holey-Graphene/Niobia Composite Architectures Science 356, 599 604 (2017) 35

Three-Dimensional Holey-Graphene/Niobia Composite Architectures TEM images of graphene sheets with tailored pores obtained by etching in H 2 O 2 for 0, 0.5, 1.0, and 2.0 hours, respectively, (E) Cross-sectional image of Nb 2 O 5 /HGF composite shows 3D hierarchically porous structure, (F) XRD patterns, (G) TEM image of graphene sheets with uniformly decorated T-Nb 2 O 5 nanoparticles, (H) HR-TEM image of T-Nb 2 O 5 nanoparticles, (I) Raman spectra of Nb 2 O 5 /G powder after thermal annealing, and freestanding Nb 2 O 5 /GF and Nb 2 O 5 /HGF electrodes. The D and G bands are characteristic of RGO; The Raman bands at 120, 230, 310, and 690 cm 1 further confirm the orthorhombic phase of T-Nb 2 O 5. (J) Comparison of DFT pore size distributions. The prominent pore size shifts from micropores (~1.5 nm) to mesopores (2.7 nm) for the composite prepared from HGO with increasing etching time. Science 356, 599 604 (2017) 36

Three-Dimensional Holey-Graphene/Niobia Composite Architectures Comparison of Nyquist plots obtained from potentiostatic EIS of a symmetric cell using two identical electrodes (11 mg cm 2 ) at a SOC 0%. The projection of the 45 slope in the high-frequency region is used to determine the ionic resistance for the electrolyte-filled porous architectures in a nonfaradaic process.the open symbols and solid lines represent the experimental and simulation results, respectively. (B) The ionic resistance (Rion) as a function of the porosity of the electrode materials. With increasing porosity, the ionic resistance is reduced substantially. (C) Galvanostatic chargedischarge curves of electrodes with tunable nanoporosity at a rate of 10C in the voltage window 1.1 to 3.0 V (versus Li/Li+). (D) Comparison of specific capacities (normalized by the total mass of the electrodes) at various rates (1 to 100C) for composite electrodes with tunable nanoporosity. Science 356, 599 604 (2017) 37

Three-Dimensional Holey-Graphene/Niobia Composite Architectures Effects of mass loading on electrochemical characteristics. (A and B) Galvanostaticcharge-discharge curves for (A) the Nb2O5/G control electrode and (B) the Nb2O5/HGF-2.0 electrode at a rate of 10C for the mass loadings of 1, 6, and 11 mg cm 2. (C) Comparison of the rate performance between 1C and 100C for Nb2O5/HGF-2.0 (open) and Nb2O5/G (solid) electrodes under different mass loadings (1, 6, and 11 mg cm 2). (D and E) Retention of specific capacity at (D) 10C and (E) 50C as a function of mass loading for three different electrodes. The properties of Nb2O5/HGF-2.0 and Nb2O5/GF electrodes were normalized by the total mass of the electrode materials (free of conductive additives and binders); the control Nb2O5/G electrodes were normalized by the total mass of the electrode materials (including binders and conductive additives). Science 356, 599 604 (2017) 38

Conclusions The first direction is to integrate active/synergetic nanomaterials The second direction is to improve the overall electrical conductivity of metal oxide films/arrays to the largest extent by integrating with diverse conducting agents The third direction is the innovation in electrode structure design. For some future applications, good electrodes are expected to be lightweight, full of porosity, mechanically flexible but still robust enough to maintain the power supply.

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