Specific Energy Storage Research Articles

Sulfur-doped porous carbon as high-capacity anodes for lithium and sodium ions batteries

S-doped porous carbon (S/C) has been successfully fabricated from biomass waste (drug residue). The S/C not only has a unique porous structure and channel, but porous structures are interconnected to form a sponge-like structures. The unique structure not only increases the specific surface area and energy storage sites, but also shortens the path of ion transmission and charge transfer. When S/C-1 is used as lithium ion batteries (LIBs) anode, the capacity of 710 mAh g−1 can be achieved after 50 cycles at 0.1 A g−1. The capacity still has 364 mAh g−1 at 5 A g−1 for long-life-cycle. For sodium ion batteries (SIBs), a capacity of 518 mAh g−1 can be delivered at 0.1 A g−1 for 50 cycles, and a capacity of long-life-cycle at 5 A g−1 still maintains 230 mAh g−1. The improving rate capacities of S/C-1 can be attributed to the short diffusion lengths of Li+ and Na+ ions for uniform sponge-like structure, large specific surface area (SSA) and additional active sites. This work has an important opportunity to change the current energy situation.

Aqueous Diels-Alder reactions for thermochemical storage and heat transfer fluids identified using density functional theory.

Thermal storage and transfer fluids have important applications in industrial, transportation, and domestic settings. Current thermal fluids have relatively low specific heats, often significantly below that of water. However, by introducing a thermochemical reaction to a base fluid, it is possible to enhance the fluid's thermal properties. In this work, density functional theory (DFT) is used to screen Diels-Alder reactions for use in aqueous thermal fluids. From an initial set of 52 reactions, four are identified with moderate aqueous solubility and predicted turning temperature near the liquid region of water. These reactions are selectively modified through 60 total functional group substitutions to produce novel reactions with improved solubility and thermal properties. Among the reactions generated by functional group substitution, seven have promising predicted thermal properties, significantly improving specific heat (by as much as 30.5%) and energy storage density (by as much as 4.9%) compared to pure water.

Graphene quantum dots synthesis and energy application: a review

Graphene Quantum Dots (GQDs), zero-dimensional nanoparticles which are derived from carbon-based sources owned the new pavement for the energy storage applications. With the varying synthesis routes, the in-built properties of GQDs are enhanced in different categories like quantum efficiency, nominal size range, and irradiation wavelength which could be applied for the several of energy and optoelectronics applications. GQDs are especially applicable in the specific energy storage devices such as super capacitors, solar cells, and lithium-ion batteries which were demonstrated in this work. This paper critically reviews about the synthesis techniques used for the GQDs involving energy storage applications with increased capacitance, energy conversion, retention capability, and stability.

Potential Sites for Underground Energy and CO2 Storage in Greece: A Geological and Petrological Approach

Underground geological energy and CO2 storage contribute to mitigation of anthropogenic greenhouse-gas emissions and climate change effects. The present study aims to present specific underground energy and CO2 storage sites in Greece. Thermal capacity calculations from twenty-two studied aquifers (4 × 10−4–25 × 10−3 MJ) indicate that those of Mesohellenic Trough (Northwest Greece), Western Thessaloniki basin and Botsara flysch (Northwestern Greece) exhibit the best performance. Heat capacity was investigated in fourteen aquifers (throughout North and South Greece) and three abandoned mines of Central Greece. Results indicate that aquifers present higher average total heat energy values (up to ~6.05 × 106 MWh(th)), whereas abandoned mines present significantly higher average area heat energy contents (up to ~5.44 × 106 MWh(th)). Estimations indicate that the Sappes, Serres and Komotini aquifers could cover the space heating energy consumption of East Macedonia-Thrace region. Underground gas storage was investigated in eight aquifers, four gas fields and three evaporite sites. Results indicate that Prinos and South Kavala gas fields (North Greece) could cover the electricity needs of households in East Macedonia and Thrace regions. Hydrogen storage capacity of Corfu and Kefalonia islands is 53,200 MWh(e). These values could cover the electricity needs of 6770 households in the Ionian islands. Petrographical and mineralogical studies of sandstone samples from the Mesohellenic Trough and Volos basalts (Central Greece) indicate that they could serve as potential sites for CO2 storage.

Pristine NiCo2O4 nanorods loaded rGO electrode as a remarkable electrode material for asymmetric supercapacitors

In this work, NiCo2O4 nanorods and rGO supported NiCo2O4 (NiCo2O4/rGO) are synthesized. The samples are evaluated by XRD, Raman, XPS, SEM, TEM, CV, EIS, and galvanostatic charge/discharge. The charge transfer resistance of NiCo2O4/rGO obtains 7.59 Ω, which is 7.6 times lower than that of NiCo2O4 (57.5 Ω). Also, the specific capacity of NiCo2O4/rGO hybrid found to be 63.2 mAh g−1 at discharge current density of 0.5 mA cm−2. The high specific surface area of rGO and the electrostatic interactions between rGO and NiCo2O4 enhance the electroactive sites of material and increase the specific capacitive and energy storage. NiCo2O4/rGO exhibits excellent charge storage and high rate capability with 55% capacitive retention at 4 mA cm−2. Both specific surface area of rGO and specific nanorod morphology of NiCo2O4 contribute significantly to the high electrochemical performance of NiCo2O4/rGO for energy storage.

Alternative storage options for solar thermal systems

The efficient implementation of solar systems in buildings depends on the storage of energy yielded, as it can both increase the solar system's autonomy and make it a feasible solution for zero energy buildings, and make storage vessels more compact, reducing precious space requirements. This is of particular important in places with reduced time of sunshine, where solar systems are less effective, because of the deviation between solar radiation and the demand. The traditional storage options use water, which is practical, safe and low-cost, especially when the storage requirements are small. However, when larger storage is needed, limits concerning the use of water exist, mainly due to the need for larger installation space and the increased thermal losses. The use of phase change materials (PCM) for thermal energy storage seems an upcoming technology. The main idea is the substitution of water with PCM, which feature larger specific energy storage capacity compared to other conventional materials. In the context of the specific paper, a combined solar thermal system used for the preparation of domestic hot water (DHW) and space heating (Solar Combi System) with two different types of storage is studied, for two Greek cities. The aim is to find out which is the most efficient way of storing energy with respect to the autonomy of the system, for a solar combi system. This is being achieved by determining the comparative autonomy of PCM and water storage system for various climates. It was proven that using PCM is advantageous, as it can extend the autonomy duration of the solar system for 2 to 8 hours, depending on the season and the climatic conditions. However, it was also seen that in solar combi systems used throughout the whole year, PCM are inefficient during summer period.

A Fast Charge/Discharge and Wide-Temperature Battery with a Germanium Oxide Layer on a Ti3C2 MXene Matrix as Anode.

A rapid charge/discharge secondary battery is critical in portable electronic devices and electric vehicles. Germanium, due to the metallic property and facile alloying reaction with lithium, displays great potential in fast charge/discharge batteries in contrast to other intercalation batteries. In order to accommodate the over 300% volume change, a 2D hybrid composite electrode consisting of a homogeneous, amorphous GeOx(x=1.57) layer bonded on Ti3C2 MXenes was successfully developed via an industry available method. The expanded interlayer space inside the MXene matrix accommodates the restricted isotropic expansion from the stress-released, ultrathin GeOx layer. Owing to the improved e-/Li+ conductivity from both metallic reduced Ge and MXene, the battery showed an excellent charge/discharge performance as fast as 3 min (20.0 C). A high-capacity retention of ∼1048.1 mAh/g along with a Coulombic efficiency (CE) of 99.8% at 0.5 C after 500 cycles was achieved. Under 1.0 C, the capacity was still up to 929.6 mAh/g with a CE of 99.6% (<0.02% capacity decay per cycle) after ultralong (1000) cycling. An almost doubled capacity of 671.6 mAh/g compared to graphite (372 mAh/g at 0.1 C) under 5.0 C and a capacity of 300.5 mAh/g under 10.0 C after 1000 cycles were respectively received. Under cold conditions, due to the low interface energy barrier, an efficient alloying reaction happens which prevents the Li plating on the electrode surface. High capacities of 631.6, 333.9, and 841.7 mAh/g under -20, -40, and 60 °C after 100 cycles demonstrate a wide temperature tolerance of the battery. In addition, a full-cell battery paired with LiNi0.8Mn0.1Co0.1O2 (NMC811) displayed a high capacity of 536.8 mAh/g after 200 cycles. A high capacity retention of a full pouch cell after 50 cycles was also obtained. The superhigh rate capability along with long cycling, wide temperature range, scalable production, and relatively low cost of this hybrid composite display promising potential in specific energy storage applications.

Carbon fiber micron film guided uniform plating/stripping of metals: A universal approach for highly stable metal batteries

Rechargeable metal batteries are desirable for next-generation high specific energy electrochemical energy storage systems. However, low coulombic efficiency and severe dendrite growth during the stripping/plating of metals (e.g. Li, Na, Zn and etc.) considerably hinder their practical applications. To address the above issues, in this work, a facile, versatile, and scalable approach by means of spray depositing carbon fiber micron film (CFMF) onto metals is developed. The porous, uniform, and highly conductive CFMF firmly attached to metal surface with a scaffold structure is found to effectively guide the uniform plating/stripping of both the Zn metal in aqueous electrolytes and the Li metal in organic electrolytes, thus enabling much higher efficiencies of Zn (98.4%) and Li (99.7%) for the 100th cycle on the CFMF-modified current collectors than those of bare current collectors. And the so far record high cycling stability for the symmetric cells using CFMF/Zn (2500 h) and CFMF/Li (1000 h) electrodes is achieved at 1 mA cm−2 and 4 mA cm−2, respectively. Benefiting from the delicately designed CFMF-modified Zn or Li metal anodes, the full cells of Zn–MnO2 and Li–LiMn2O4 are rendered excellent rate capability and significantly extended cycle life.

Day-Ahead Optimal Battery Operation in Islanded Hybrid Energy Systems and Its Impact on Greenhouse Gas Emissions

This paper proposes a management strategy for the daily operation of an isolated hybrid energy system (HES) using heuristic techniques. Incorporation of heuristic techniques to the optimal scheduling in day-head basis allows us to consider the complex characteristics of a specific battery energy storage system (BESS) and the associated electronic converter efficiency. The proposed approach can determine the discharging time to perform the load peak-shaving in an appropriate manner. A recently proposed version of binary particle swarm optimization (BPSO), which incorporates a time-varying mirrored S-shaped (TVMS) transfer function, is proposed for day-ahead scheduling determination. Day-ahead operation and greenhouse gas (GHG) emissions are studied through different operating conditions. The complexity of the optimization problem depends on the available wind resource and its relationship with load profile. In this regard, TVMS-BPSO has important capabilities for global exploration and local exploitation, which makes it a powerful technique able to provide a high-quality solution comparable to that obtained from a genetic algorithm.

Morphology Reshaping Enabling Self‐Densification of Manganese Oxide Hybrid Materials for High‐Density Lithium Storage Anodes

AbstractMorphology reshaping or reconfiguration, a concept widely used in plastic surgery, energy harvesting, and reconfigurable robots, is introduced for the first time to construct densified electrodes and realize compact Li‐ion storage desirable for high specific energy storage field. Hausmannite‐based hybrid materials, as a proof‐of‐concept prototype, engineered by 1‐methyl‐2‐pyrrolidinone‐soluble surface/interface organic encapsulation, which is crucial in reshaping, exhibit a remarkable increase in the volumetric capacity of more than five times after this process (≈1889 Ah L−1 vs ≈322 Ah L−1). With the simultaneous maintenance of the intrinsic nature, good contact, and no collapsed/agglomerated unit structures of the materials in electrodes, the design affords a maximal increase in the packing compactness and manifests no sacrifice of the reversible ion storage capability (1150 mAh g−1 at 40 mA g−1), stable cycling (≈100% capacity retention), high rate performance (185 mAh g−1 at 10 A g−1), and long lifespan (1000 cycles with 108% capacity retention, ≈455 mAh g−1 at 3 A g−1) for relatively highly loaded electrodes (active materials: 1.20–5.34 mg cm−2). The concept may not only shed new light on fabricating advanced Si‐based and other high capacity–related densified Li storage electrodes but also inject fresh vitality into the field of high‐density power sources.

Development and evaluation of a new hybrid ammonia fuel cell system with solar energy

In this study, a novel hybrid thermal energy storage and ammonia fuel cell system is developed and investigated for a solar tower based power plant. An annual analysis of the developed system is performed by considering the monthly average days. Also, the actual power demands as well as the solar intensity changes are taken into account. Thermodynamic approaches of energy and exergy analyses are utilized for system analysis. The energetic efficiency of the proposed power plant varies between 5.3% and 37% while the exergy efficiency ranges between 5.7% and 39%, depending on the corresponding power demands as well as available solar energy. The system simulation results for each month are also described in terms of the specific exergies and enthalpies at the turbine inlets. Furthermore, energy efficiency of the direct ammonia fuel cell is evaluated to be 37% and the exergy efficiency is found to be 34% at the peak power density. At a temperature of 500 °C, a specific thermal energy storage capacity of 266 kJ kg−1 is determined for the hybrid system.

A novel multiwalled LiF@GO@SiO2 microcapsule with high phase change temperature

High temperature phase change materials (PCMs)-encapsulated microcapsules with large heat exchange area for addressing specific energy storage have increasing application potentials in many fields. Herein, a novel hybrid multiwalled microcapsule LiF@GO@SiO2 with high phase change temperature was designed and fabricated, which could overcome strong corrosion and volume expansion of lithium fluoride (LiF) during heat storage process. The multiwalled structure of microcapsule contained three layers, consisting of volume expansion buffer layer polydopamine (PDA), anti-corrosion leakage-proof layer (GO) and heat-resist strength layer (SiO2), respectively. Volume expansion buffer layer would be vanished during thermal cycling, and GO as well as SiO2 layers played important roles in protecting molten LiF from leakage. A series of tests including SEM, SEM-EDS, FTIR, XPS, XRD and TGA revealed that three-layer shells were sequentially coated on the surface of core material LiF successfully. Besides, DSC results via quantitatively analyzing, indicated that LiF@GO@SiO2 microcapsules had high phase change temperature of 848 °C, encapsulation ratio of 82.0% and latent melting heat of 894.5 J/g. In addition, encapsulation ratio of the microcapsule had a minor deflection within 5% after 10 times loops by calculating and comparing corresponding enthalpies, which displayed prepared microcapsule could be used repeatedly in high temperature energy storage. Overall, our results opened new avenues for the utilization of high temperature PCMs and their packaging technique.

Recent developments in thermo-physical property enhancement and applications of solid solid phase change materials

Phase change materials (PCM) have a potential role in thermal energy storage applications. Recent progress has shown notable work on solid solid phase change materials (SS-PCM) which possess unique advantages of low subcooling, limited volume expansion due to a solid solid phase transition, high thermal stability and also had significant latent heat and thermal conductivity values. This review addresses current research on SS-PCM with the focus on solid solid phase transition mechanisms, properties, thermo-physical property enhancement, and experimental case studies for specific energy storage applications. The mechanism of solid solid phase transition for different classifications of SS-PCM with regards to a phase transition temperature and latent heat has provided in detail. This review also includes information regarding fundamental properties of SS-PCM along with methods for property enhancement, details on binary/ternary mixtures of SS-PCM and hybrid SS-PCMs, which allow altering phase transition temperature and increase thermal conductivity. Finally, the potential use of enhanced SS-PCM are discussed in detail, guiding researchers to select, customize, future scope, and addresses research gap of the SS-PCM for different energy storage applications.

A Self-Doped Polyaniline Cathode for Rechargeable Aqueous Zinc Batteries

Rechargeable batteries offer promising solutions to the energy shortage issue.[1] In comparison to non-aqueous Li-ion batteries, aqueous rechargeable batteries possess the merits of using low-cost and high-safety water-based electrolytes. Aqueous electrolytes also provide higher ionic conductivities than non-aqueous ones, which promotes better rate performance of the cell.[2] These superiorities make the system suitable for stationary grid-level energy storages. The zinc metal is a convenient anode for aqueous batteries due to its low redox potential (-0.76 V vs. standard hydrogen electrode), high theoretical capacity (5845 mAh cm-3, 819 mAh g-1) and good compatibility with water.[3]-[5] Its abundant earth storage, non-toxicity and stability in air furthermore benefits large-scale productions. Using neutral or slightly acidic solutions to replace the alkaline electrolytes can suppress the dendritic growth of Zn anode.[4] One urgent requirement of zinc battery research is to find a suitable cathode. Benefiting from the long π-electron conjugated systems, conducting polymers hold higher conductivities compared to metal oxides and organic materials.[6] The highly conductive polyaniline (PANI) is a potential cathode, but it tends to deactivate in low acidic electrolytes (i.e. pH > 1) due to the de-protonation of the polymer. Herein, we synthesized a sulfo self-doped PANI electrode by a facile electrochemical copolymerization process. The -SO3 - self-dopant functions as an internal proton reservoir to ensure locally high acidic environment and facilitate the redox process in the weak acidic ZnSO4 electrolyte. In a full zinc cell, the self-doped PANI cathode delivers a high capacity of 180 mAh g-1, excellent rate performance of 70% capacity retention at 50 times current density increase, and long cycle life of over 2000 cycles with coulombic efficiency close to 100%. The detailed charge storage processes were investigated by X-ray photoelectron spectroscopy and X-ray diffraction. They suggest partial proton insertion into self-doped PANI during discharge, which leads to the internal protonation of -N= units and facilitates further reduction. This helps the polymer to maintain high electrochemical activity and stable capacity retention over cycling, in direct contrast to the fast capacity decay with the non-self-doped PANI cathode. Overall, our work utilizes the smart pH adjustment ability of self-dopants to overcome the discrepancy of active conditions between PANI cathode and Zn anode. More importantly, it demonstrates the potential applications of conducting polymers as cathode materials for rechargeable zinc batteries, with the specific energy storage behavior tunable thanks to the rich chemistry of their family.

Effect of alkali and halide ion doping on the energy storage characteristics of ionic liquid based supercapacitors

The electrochemical properties of supercapacitors based on carbide-derived carbon electrodes doped with up to 5 wt% mixture of halide or alkali ion salts in 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl) imide (EMImTFSI) have been studied to exploit their specific energy storage mechanism. To separately highlight the effect of redox active mixture doped electrodes, neat EMImTFSI is applied as the electrolyte for all studied supercapacitor systems. A noticeable increase of capacitance for carbon electrodes doped with halide ions has been observed, as measured by three different electrochemical analysis techniques. Compared with neat EMImTFSI based system, carbon electrodes doped with alkali ion salt mixtures do not show a noticeable improvement of energy storage characteristics. Interestingly, both 5 wt% alkali and halide ion salt mixture doped system exhibit a stable high capacitance up to 124 F/g at 3 V. It is shown that this enhancement of capacitance is due to reversible faradaic processes and the specific adsorption of halide ions within the micro- and mesoporous electrode material and does not limit the bulk electrolyte properties. It is seen that the alkali and halide ion doped systems display greater electrochemical stability compared with neat EMImTFSI based system within constant voltage floating tests.

Enhanced Thermochemical Heat Capacity of Liquids: Molecular to Macroscale Modeling

ABSTRACTThermal fluids have many applications in the storage and transfer of thermal energy, playing a key role in heating, cooling, refrigeration, and power generation. However, the specific heat capacity of conventional thermal fluids, which is directly linked to energy density, has remained relatively low. To tackle this challenge, we explore a thermochemical energy storage mechanism that can greatly enhance the heat capacity of base fluids (by up to threefold based on simulation) by creating a solution with reactive species that can absorb and release additional thermal energy. Based on the classical theory of equilibrium thermodynamics, we developed a macroscale theoretical model that connects fundamental properties of the underlying reaction to the thermophysical properties of the liquids. This framework allows us to employ state-of-the-art molecular scale computational tools such as density functional theory calculations to identify and refine the most suitable molecular systems for subsequent experimental studies. Our approach opens up a new avenue for developing next-generation heat transfer fluids that may break traditional barriers to achieve high specific heat and energy storage capacity.

Inert and Reactive Oxide Particles for High-Temperature Thermal Energy Capture and Storage for Concentrating Solar Power

Oxide particles have potential as robust heat transfer and thermal energy storage (TES) media for concentrating solar power (CSP). Particles of low-cost, inert oxides such as alumina and/or silica offer an effective, noncorrosive means of storing sensible energy at temperatures above 1000 °C. However, for TES subsystems coupled to high-efficiency, supercritical-CO2 cycles with low temperature differences for heat addition, the limited specific TES (in kJ kg−1) of inert oxides requires large mass flow rates for capture and total mass for storage. Alternatively, reactive oxides may provide higher specific energy storage (approaching 2 or more times the inert oxides) through adding endothermic reduction. Chemical energy storage through reduction can benefit from low oxygen partial pressures (PO2) sweep-gas flows that add complexity, cost, and balance of plant loads to the TES subsystem. This paper compares reactive oxides, with a focus on Sr-doped CaMnO3–δ perovskites, to low-cost alumina-silica particles for energy capture and storage media in CSP applications. For solar energy capture, an indirect particle receiver based on a narrow-channel, counterflow fluidized bed provides a framework for comparing the inert and reactive particles as a heat transfer media. Low-PO2 sweep gas flows for promoting reduction impact the techno-economic viability of TES subsystems based on reactive perovskites relative to those using inert oxide particles. This paper provides insights as to when reactive perovskites may be advantageous for TES subsystems in next-generation CSP plants.

Untying thioether bond structures enabled by "voltage-scissors" for stable room temperature sodium-sulfur batteries.

A steady sulfur cathode is central to realizing stable room temperature sodium-sulfur (RT Na-S) batteries. Here, sulfur atoms are incorporated into carbon to form thioether bond functionalized carbon (SC) as a cathode material for sodium storage, which is capable of the complete elimination or great suppression of the shuttle effect of soluble poly-sulfides by the generation of insoluble sulfides in RT Na-S batteries using an ordinary carbonate electrolyte. This thioether bond structure (C-S-C) in sulfur-doped carbon can be disassembled by the assistance of "voltage-scissors" in the low voltage range of 0.01-0.50 V vs. Na/Na+. The small sulfur species derived from the thioether bond structure react with the sodium anode to form insoluble sulfides. Moreover, the insoluble sulfides Na2S2 and Na2S are confined in the carbon defects induced by the cleaved sulfur to prevent them from degrading the long-chain poly-sulfides. The distinctive electrochemical performance of SC enriches our understanding of the sulfur cathode, and could provide novel insights for constructing stable sulfur cathode materials for specific energy storage devices.

VC2 and V1/2Mn1/2C2 nanosheets with robust mechanical and thermal properties as promising materials for Li-ion batteries.

In this paper, vanadium carbides VC2 and bi-transition-metal carbides V1/2Mn1/2C2 are predicted to be stable metallic nanosheets showing promising mechanical properties and their Young's moduli are 70.8 N m-1 and 83.7 N m-1, respectively. Ab initio molecular dynamics results showed that both VC2 and V1/2Mn1/2C2 can tolerate temperatures up to 1000 K showing favorable thermal properties. The excellent Li-ion specific energy storage capacity and low diffusion barrier also make them promising candidates as anode materials. In addition, nonmagnetic-ferromagnetic (-ferrimagnetic) transitions in VC2 and V1/2Mn1/2C2 can be tuned easily by oxygen or fluorine passivation.

Grafting Benzenediazonium Tetrafluoroborate onto LiNixCoyMnzO2 Materials Achieves Subzero‐Temperature High‐Capacity Lithium‐Ion Storage via a Diazonium Soft‐Chemistry Method

AbstractSubzero‐temperature Li‐ion batteries (LIBs) are highly important for specific energy storage applications. Although the nickel‐rich layered lithium transition metal oxides(LiNixCoyMnzO2) (LNCM) (x &gt; 0.5, x + y +z = 1) are promising cathode materials for LIBs, their very slow Li‐ion diffusion is a main hurdle on the way to achieve high‐performance subzero‐temperature LIBs. Here, a class of low‐temperature organic/inorganic hybrid cathode materials for LIBs, prepared by grafting a conducting polymer coating on the surface of 3 µm sized LiNi0.6Co0.2Mn0.2O2 (LNCM‐3) material particles via a greener diazonium soft‐chemistry method is reported. Specifically, LNCM‐3 particles are uniformly coated with a thin polyphenylene film via the spontaneous reaction between LNCM‐3 and C6H5N2+BF4−. Compared with the uncoated one, the polyphenylene‐coated LNCM‐3 (polyphenylene/LNCM‐3) has shown much improved low‐temperature discharge capacity (≈148 mAh g−1 at 0.1 C, −20 °C), outstanding rate capability (≈105 mAh g−1 at 1 C, −20 °C), and superior low‐temperature long‐term cycling stability (capacity retention is up to 90% at 0.5 C over 1150 cycles). The low‐temperature performance of polyphenylene/LNCM‐3 is the best among the reported state‐of‐the art cathode materials for LIBs. The present strategy opens up a new avenue to construct advanced cathode materials for wider range applications.