Interface Engineering Overall Seawater Splitting of Self-Supporting CeOx@NiCo2O4 Arrays.

Exploring advanced electrocatalysts for overall seawater splitting is of great significance for large-scale green hydrogen production in which interface engineering has been considered as an effective strategy to enhance the intrinsic activities of the electrocatalysts. In this work, CeOx-modified NiCo2O4 nanoneedle arrays are designed and constructed in situ grown on Ni foam (NF) through a facile two-step synthesis method. Density functional theory calculations reveal that the strong interaction between CeOx and NiCo2O4 can regulate the electronic states of metal surfaces and optimize the electronic structures of the materials, essentially improving the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) properties. Specifically, in alkaline electrolytes, CeOx@NiCo2O4/NF exhibits superior electrocatalytic activities and stabilities, requiring overpotentials of 238 mV for the OER and 144 mV for the HER to achieve a current density of 10 mA cm-2. When applied to a simulated seawater splitting device, the CeOx@NiCo2O4/NF also maintains a battery voltage of 1.66 V to reach 10 mA cm-2 and exhibits good stability for over 60 h, with high faradic efficiencies (FEs) close to 100% for both the OER and HER.

Cold-plasma activation converting conductive agent in spent Li-ion batteries to bifunctional oxygen reduction/evolution electrocatalyst for zinc-air batteries.

Considerable amount of high-value transition metals components can be recycled in spent ternary lithium-ion batteries. In this study, we utilized the conductive agent carbon black, obtained from the leaching waste resulting from the chemical recovery of spent lithium-nickel-manganese-cobalt (NCM) oxide cathode materials. This process allows us to create valuable bifunctional catalysts for the oxygen reduction reaction and oxygen evolution reaction (ORR/OER), facilitated by a facile cold plasma activation method, as a part of lithium batteries circular economy. The activated conductive agent (RCA-30) exhibited an ORR half-wave potential of 0.74 V (vs. RHE) in 0.1 mol/L KOH solution, and an OER overpotential of 360 mV at 10 mA cm-2 in 1 mol/L KOH electrolyte, owing to nitrogen doping of carbon black and activation of surface metal oxides. The complete zinc-air batteries incorporating the activated catalysts at the cathode exhibited an open circuit potential of up to 1.48 V and sustained cycling for 100 h at a current density of 5 mA cm-2. Additionally, the activated catalysts contributed to a power density of 92 mW cm-2 and a full discharge capacity of 640 mAh/g.

A green aqueous binder to enhance the electrochemical performance of Li-rich disordered rock salt cathode material.

Li-rich disordered rock-salt oxides (DRX) are considered an attractive cathode material in the future battery field due to their excellent energy density and specific capacity. Nevertheless, anionic redox provides high capacity while causing O2 over-oxidation to O2, resulting in voltage hysteresis and capacity decay. Herein, the crystal structure of Li1.3Mn0.4Ti0.3O1.7F0.3 (LMTOF) cathode is stabilized by using sodium carboxymethylcellulose (CMC) binders replacing traditional polyvinylidene difluoride (PVDF) binders. The electrochemical impedance spectroscopy (EIS) and galvanostatic intermittent titration technique (GITT) reveal that the CMC-based LMTOF electrode has higher electronic conductivity and lithium-ion diffusion kinetics. Moreover, CMC has been demonstrated to improve the O2- reversibility, reduce the amounts of byproducts from electrolyte decomposition and suppress transition metal dissolution by Na+/Li+ exchange reaction. Furthermore, the CMC-based LMTOF electrode also exhibits less volume change upon lithiation/delithiation processes compared to the PVDF-based electrode, resulting in enhanced structural stability during cycling. Benefiting from these features, the CMC binders can effectively improve the cycling life and rate performance of the LMTOF cathode, and the CMC-based LMTOF electrode shows good capacity retention of 94.5 % after 30 cycles at 20 mA/g and 66.7 % after 100 cycles at 200 mA/g. This finding indicates that CMC as a binder can efficiently stabilize the structure and improve the electrochemical performance of Li-rich disordered rock-salt oxides cathode, making it possible for practical Li-ion battery applications.

Interface engineering and nanoconfinement strategies to synergistically enhance hydrogen evolution in acidic and basic media.

As a potential catalyst for hydrogen evolution reaction (HER), tungsten nitride (W2N) has attracted extensive attention, due to its Pt-like characteristic. Nevertheless, insufficient active sites, slow electron transfer, and lack of scale-up nano-synthesis methods significantly limit its practical application. Constructing multi-component active centers and interface-rich heterojunctions to increase exposed active sites and modulate interface electrons is a very effective modification strategy. Therefore, a nano-heterostructure formed from tungsten nitride, tungsten phosphide and tungsten encapsulated in N, P co-doped carbon nanofiber (W2N/WP/W@NPC) was synthesized by a flexible and scalable electrospinning technology. Experimental results reveal that abundant heterojunctions are formed, electron transfer occurs between tungsten nitride and tungsten phosphide, and carbon nanofibers play a confinement role. The optimized W2N/WP/W@NPC-3 electrocatalyst demonstrates excellent HER catalytic activity and robust stability in both acidic and base media. Furthermore, the overall water splitting performance is tested using W2N/WP/W@NPC as the cathode through a two-electrode electrolyzer, which also exhibits impressive electrochemical performance.

Conductive Robust Interfaces with Fluoro-Borate Based Electrolyte Additive for 4.6 V Well-Cycled LiNi0.90 Co0.06 Mn0.04 O2 ||Li Batteries.

Owing to the outstanding comprehensive properties of high energy density, excellent cycling ability, and reasonable cost, Ni-rich layered oxides (NCM) are the most promising cathode for lithium-ion batteries (LIBs). To further enhance the specific capacity of Ni-rich layered oxides, it is necessary to increase the cut-off voltage to a higher level. However, a higher cut-off voltage can lead to substantial structural changes and trigger interface side reactions, presenting significant challenges for practical applications (cycle life and safety). Herein, to solve above issues, tris(hexafluoroisopropyl)borate (TFPB) is introduced as a high voltage electrolyte additive for LiNi0.90 Co0.06 Mn0.04 O2 cathode. Based on detail in situ/ex situ characterization, this study proves that TFPB forms a protective solid-state interphase (SEI) layer on the Li-anode. Additionally, derivatives of TFPB are easily oxidatively decomposed to create a dense cathode electrolyte interphase (CEI) film on the cathode. This CEI film effectively prevents the continuous oxidation of the electrolyte and mitigates the adverse effects of HF on the battery. Benefit from the protective SEI and CEI layer, the LiNi0.90 Co0.06 Mn0.04 O2 ||Li battery with a TFPB-containing electrolyte maintains an unprecedented level of performance, with a capacity retention of 89.1% after 100 cycles under the ultrahigh cut-off voltage of 4.6 V (vs Li/Li+ ).

InSb/InP Core-Shell Colloidal Quantum Dots for Sensitive and Fast Short-Wave Infrared Photodetectors.

Colloidal quantum dot (CQD) technology is considered the main contender toward a low-cost high-performance optoelectronic technology platform for applications in the short-wave infrared (SWIR) to enable 3D imaging, LIDAR night vision, etc. in the consumer electronics and automotive markets. In order to unleash the full potential of this technology, there is a need for a material that is environmentally friendly, thus RoHS compliant, and possesses adequate optoelectronic properties to deliver high-performance devices. InSb CQDs hold great potential in view of their RoHS-compliant nature and─in principle─facile access to the SWIR. However, to date progress in realizing high-performance optoelectronic devices, including photodetectors (PDs), has been limited. Here, we have developed a synthesis method for producing size-tunable InSb CQDs with distinct excitonic peaks spanning a wide range from 900 to 1750 nm. To passivate the surface defects and enhance the photoluminescence (PL) efficiency of InSb CQDs, we further designed an InSb/InP core-shell structure. By employing the InSb/InP core-shell CQDs in a photodiode device stack, we report on robust InSb CQD SWIR photodetectors that exhibit an external quantum efficiency (EQE) of 25% at 1240 nm, a wide linear dynamic range exceeding 128 dB, a photoresponse time of 70 ns, and a specific detectivity of 4.4 × 1011 jones.

Enhancing Electrochemical Performance of Aluminum-Oxygen Batteries with Graphene Aerogel Cathode.

Aluminum-oxygen batteries (AOBs) own the benefits of high energy density (8.14 kWh kg-1 ), low cost, and high safety. However, the design of a cathode with high surface area, structure integrity, and good catalytic performance is still challenging for rechargeable AOBs. Herein, the fabrication of a robust self-supporting cathode using 3D graphene aerogel (3DGA) for rechargeable AOBs is demonstrated. Electroanalysis showed that the 3DGA presented good catalytic activity in both oxygen reduction and evolution reactions, which allowed the AOB to operate for >90 cycles with low overpotentials at a current density of 0.2 mA cm-2 , and a high Coulombic efficiency of ca. 99% using ionic liquid as electrolyte. In comparison, the cell with the carbon paper cathode can only cycle for 50 rounds. The excellent cyclic performance can be attributed to the porous structure, large surface area, good electric conductivity, and catalytic activity of the 3DGA, which is prospective to be applied for other metal-air batteries, fuel cells, and supercapacitors.

A Stress Self-Adaptive Silicon/Carbon "Ordered Structures" to Suppress the Electro-Chemo-Mechanical Failure: Piezo-Electrochemistry and Piezo-Ionic Dynamics.

Construction of ordered structures that respond rapidly to environmental stimuli has fascinating possibilities for utilization in energy storage, wearable electronics, and biotechnology. Silicon/carbon (Si/C) anodes with extremely high energy densities have sparked widespread interest for lithium-ion batteries (LIBs), while their implementation is constrained via mechanical structure deterioration, continued growth of the solid electrolyte interface (SEI), and cycling instability. In this study, a piezoelectric Bi0.5 Na0.5 TiO3 (BNT) layer is facilely deposited onto Si/C@CNTs anodes to drive piezoelectric fields upon large volume expansion of Si/C@CNTs electrode materials, resulting in the modulation of interfacial Li+ kinetics during cycling and providing an electrochemical reaction with a mechanically robust and chemically stable substrate. In-depth investigations into theoretical computation, multi-scale in/ex situ characterizations, and finite element analysis reveal that the improved structural stability, suppressed volume variations, and controlled ion transportation are responsible for the improvement mechanism of BNT decorating. These discoveries provide insight into the surface coupling technique between mechanical and electric fields to control the interfacial Li+ kinetics behavior and improve structural stability for alloy-based anodes, which will also spark a great deal attention from researchers and technologists in multifunctional surface engineering for electrochemical systems.

Mnx+ Substitution to Improve Na3V2(PO4)2F3-Based Electrodes for Sodium-Ion Battery Cathode.

Na3V2(PO4)2F3 (NVPF) is an extremely promising sodium storage cathode material for sodium-ion batteries because of its stable structure, wide electrochemical window, and excellent electrochemical properties. Nevertheless, the low ionic and electronic conductivity resulting from the insulated PO43- structure limits its further development. In this work, the different valence states of Mnx+ ions (x = 2, 3, 4) doped NVPF were synthesized by the hydrothermal method. A series of tests and characterizations reveals that the doping of Mn ions (Mn2+, Mn3+, Mn4+) changes the crystal structure and also affects the residual carbon content, which further influences the electrochemical properties of NVPF-based materials. The sodiation/desodiation mechanism was also investigated. Among them, the as-prepared NVPF doped with Mn2+ delivers a high reversible discharge capacity (116.2 mAh g-1 at 0.2 C), and the capacity retention of 67.7% after 400 cycles at 1 C was obtained. Such excellent performance and facile modified methods will provide new design ideas for the development of secondary batteries.

Engineering Crystal Growth and Surface Modification of Na3 V2 (PO4 )2 F3 Cathode for High-Energy-Density Sodium-Ion Batteries.

Na3 V2 (PO4 )2 F3 (NVPF) is a suitable cathode for sodium-ion batteries owing to its stable structure. However, the large radius of Na+ restricts diffusion kinetics during charging and discharging. Thus, in this study, a phosphomolybdic acid (PMA)-assisted hydrothermal method is proposed. In the hydrothermal process, the NVPF morphologies vary from bulk to cuboid with varying PMA contents. The optimal channel for accelerated Na+ transmission is obtained by cuboid NVPF. With nitrogen-doping of carbon, the conductivity of NVPF is further enhanced. Combined with crystal growth engineering and surface modification, the optimal nitrogen-doped carbon-covered NVPF cuboid (c-NVPF@NC) exhibits a high initial discharge capacity of 121 mAh g-1 at 0.2 C. Coupled with a commercial hard carbon (CHC) anode, the c-NVPF@NC||CHC full battery delivers 118 mAh g-1 at 0.2 C, thereby achieving a high energy density of 450 Wh kg-1 . Therefore, this work provides a novel strategy for boosting electrochemical performance by crystal growth engineering and surface modification.

Interfacial Reviving of the Degraded LiNi0.8 Co0.1 Mn0.1 O2 Cathode by LiPO3 Repair Strategy.

Nickel-rich cathode materials, owing to their high energy density and low cost, are considered to be one of the cathodes with the most potential in next-generation lithium-ion batteries. Unfortunately, this kind of cathode with highly active surface is easy to react with H2 O and CO2 when exposed to ambient air, resulting in the formation of lithium impurities and interfacial phase transition as well as deterioration of the electrochemical properties. In this work, the evolution mechanism of the structure and interface of LiNi0.8 Co0.1 Mn0.1 O2 during air-exposure is systematically investigated. Furthermore, a facile reviving strategy is proposed to restore the degraded LiNi0.8 Co0.1 Mn0.1 O2 by using LiPO3 as the repair agent. The lithium impurities on the surface of the degraded sample can transform into the repair/coating layer, and part of the rock salt phase on the subsurface can revive to layered phase after repair heat treatment. As a result, the optimized cathode delivers an initial discharge capacity of 198.3 mAh g-1 at 0.1C and a capacity retention of 85.5% after 50 cycles. Although slightly lower than the bare sample (201 mAh g-1 and 88%), they are obviously higher than the exposed samples (166.5 mAh g-1 and 40.4%). The regenerated electrochemical properties should be attributed to the multifunctional repair layer that can efficiently reduce the surface lithium impurities, prevent the corrosion of electrolyte, and improve the interfacial Li+ diffusion kinetics. This work can effectively reduce the waste of the degraded Ni-rich ternary materials and realize the transformation of "waste" into wealth.

Novel PETEA-based grafted gel polymer electrolyte with excellent high-rate cycling performance for LiNi0.5Co0.2Mn0.3O2 lithium-ion batteries.

Due to the higher specific capacity and operating voltage platform of the ternary cathode material (LiCoxNiyMn1-x-yO2), it has a specific market application in the electric vehicle (EV) industry. Gel polymer electrolytes (GPEs) have proven to be an effective method of resolving this issue. As a result of its high conductivity and safety performance, pentaerythritol tetraacrylate (PETEA) is a promising gel polymer electrolyte. Butyl methacrylate (BMA) was successfully grafted onto PETEA to decrease its stiffness in this study. Surprisingly, after cycling for 100 cycles at a rate of 2 C, the cycle retention rate of the half-cell of NCM523/GPE/Li reached 63.9%, whereas the utilization of liquid electrolyte ceased to function normally. The successfully prepared PETEA-g-BMA GPE by in-situ thermal polymerization formed a three-dimensional network structure. The PETEA-g-BMA GPE effectively protected the structure of the cathode material during the lithium-ion charging and discharging process, inhibited the occurrence of side reactions, and minimized the risk of thermal runaway. The straightforward preparation process and low cost make industrial applications a possibility in the future.

Cross-Linked Sodium Alginate-Sodium Borate Hybrid Binders for High-Capacity Silicon Anodes in Lithium-Ion Batteries.

Silicon is considered one of the most promising next-generation anode materials for lithium-ion batteries. It has the advantages of high theoretical specific capacity (4200 mAh·g-1), which is 10 times larger than that of a commercial graphite anode (372 mAh·g-1). However, there are some problems such as the pulverization of the electrode and an unstable solid electrolyte interphase (SEI) layer aroused by the huge bulk effect (>300%) of Si during the repeated lithiation/delithiation process. A binder plays a vital role in the conventional lithium-ion batteries that can effectively relieve the bulk expansion stress of a silicon anode. In this work, the inorganic cross-linker sodium borate (SB) and the commonly used binder sodium alginate (SA) were condensed through an esterification reaction and the reaction product was marked as SA-SB. It is found that the mechanical robustness and the peel strength of SA-SB are improved after cross-linking, which is conducive to maintaining the structural stability of the silicon anode in long cycle life. In consequence, the capacity retention of the silicon anode using the SA-SB binder (64.1%) is higher than that of SA (50.6%) after 100 cycles at 0.2 A·g-1.

Interface-Driven Pseudocapacitance Endowing Sandwiched CoSe2/N-Doped Carbon/TiO2 Microcubes with Ultra-Stable Sodium Storage and Long-Term Cycling Stability.

Cobalt diselenide (CoSe2) has drawn great concern as an anode material for sodium-ion batteries due to its considerable theoretical capacity. Nevertheless, the poor cycling stability and rate performance still impede its practical implantation. Here, CoSe2/nitrogen-doped carbon-skeleton hybrid microcubes with a TiO2 layer (denoted as TNC-CoSe2) are favorably prepared via a facile template-engaged strategy, in which a TiO2-coated Prussian blue analogue of Co3[Co(CN)6]2 is used as a new precursor accompanied with a selenization procedure. Such structures can concurrently boost ion and electron diffusion kinetics and inhibit the structural degradation during cycling through the close contact between the TiO2 layer and NC-CoSe2. Besides, this hybrid structure promotes the superior Na-ion intercalation pseudocapacitance due to the well-designed interfaces. The as-prepared TNC-CoSe2 microcubes exhibit a superior cycling capability (511 mA h g-1 at 0.2 A g-1 after 200 cycles) and long cycling life (456 mA h g-1 at 6.4 A g-1 for 6000 cycles with a retention of 92.7%). Coupled with a sodium vanadium fluorophosphate (Na3V2(PO4)2F3)@C cathode, this assembled full cell displays a specific capacity of 281 mA h g-1 at 0.2 A g-1 for 100 cycles. This work can be potentially used to improve other metal selenide-based anodes for rechargeable batteries.

Dual-Element-Modified Single-Crystal LiNi0.6Co0.2Mn0.2O2 as a Highly Stable Cathode for Lithium-Ion Batteries.

Single-crystalline LiNi0.6Co0.2Mn0.2O2 cathodes have received great attention due to their high discharge capacity and better electrochemical performance. However, the single-crystal materials are suffering from severe lattice distortion and electrode/electrolyte interface side reactions when cycling at high voltage. Herein, a unique single-crystal LiNi0.6Co0.2Mn0.2O2 with Al and Zr doping in the bulk and a self-formed coating layer of Li2ZrO3 in the surface has been constructed by a facile strategy. The optimized cathode material exhibits excellent structural stability and cycling performance at room/elevated temperatures after long-term cycling. Specifically, even after 100 cycles (1C, 3.0-4.4 V) at 50 °C, the capacity retention for the Al and Zr co-doped sample reaches 92.1%, which is much higher than those of the single Al-doped (85.4%), single Zr-doped (87.1%), and bare samples (76.3%). The characterization results and first-principles calculations reveal that the excellent electrochemical properties are attributed to the stable structure and interface, in which the Al and Zr co-doping hinders cation mixing and suppresses detrimental phase transformations to reduce internal stress and mitigate microcracks, and the coating layer of Li2ZrO3 can protect the surface and suppress interfacial parasitic reactions. Overall, this work provides important insights into how to simultaneously build a stable bulk structure and interface for the single-crystal NCM cathode via a facile preparation process.

NaOH-Intercalated Iron Chalcogenides (Na1-xOH)Fe1-yX (X = Se, S): Ion-Exchange Synthesis and Physical Properties.

The discovery of the (Li1-xFexOH)FeSe superconductor has aroused significant interest in metal hydroxide-intercalated iron chalcogenides. However, all efforts made to intercalate NaOH between FeSe and FeS layers have failed so far. Here we report two NaOH-intercalated iron chalcogenides (Na1-xOH)Fe1-yX (X = Se, S) that were synthesized by a low-temperature hydrothermal ion-exchange method. Their crystal structures were solved through single-crystal X-ray diffraction and refined against powder X-ray and neutron diffraction data. Different from the (Li1-xFexOH)FeX superconductors that crystallize in a tetragonal space group P4/nmm with Z = 2, (Na1-xOH)Fe1-yX belong to an orthorhombic space group Cmma with Z = 4. The structural solution also reveals that there are vacancies in both Na and Fe sites and there are not iron ions in the (Na1-xOH) layer. This is probably why both Fe(II) and Fe(III) species exist in the title compounds, as detected by X-ray photoelectron spectroscopy. Based on magnetization and electrical resistivity measurements, the two compounds were found to be paramagnetic semiconductors. The absence of superconductivity should be closely related to the iron vacancies in the Fe1-yX layer. Theoretical calculations suggest that inducing superconductivity in (Na1-xOH)Fe1-ySe is promising due to the similarity of the electronic structures between stoichiometric (NaOH)FeSe and the (Li1-xFexOH)FeSe superconductor.

Blue-AsP monolayer as a promising anode material for lithium- and sodium-ion batteries: a DFT study.

Based on first-principle calculations, we proposed a one two-dimensional (2D) blue AsP (b-AsP) monolayer as an ideal anode material for lithium/sodium-ion (Li/Na-ion) batteries for the first time. The b-AsP monolayer possesses thermal and dynamic stabilities. The system undergoes the transition from semiconductor to metal after Li/Na atoms are embedded, which ensures good electric transportation. Most remarkably, our results indicate that the b-AsP monolayer exhibits high theoretical capacities of 1011.2 mA h g-1 (for Li) and 1769.6 mA h g-1 (for Na), low average open circuit voltages of 0.17 eV for Li4AsP and 0.14 eV for Na7AsP systems and ultrafast diffusivity with the low energy barriers of 0.17/0.15 eV and 0.08/0.07 eV of the P/As sides for Li and Na, respectively. Given these exceptional properties, the synthesis of a buckled b-AsP monolayer is desired to achieve a promising electrode material for Li- and Na-ion batteries.

Pomegranate-Like Structured Si@SiOx Composites With High-Capacity for Lithium-Ion Batteries.

Silicon anodes with an extremely high theoretical specific capacity of 4,200 mAh g-1 have been considered as one of the most promising anode materials for next-generation lithium-ion batteries. However, the large volume expansion during lithiation hinders its practical application. In this work, pomegranate-like Si@SiOx composites were prepared using a simple spray drying process, during which silicon nanoparticles reacted with oxygen and generated SiOx on the surface. The thickness of the SiOx layer was tuned by adjusting the drying temperature. In the unique architecture, the SiOx which serves as the protection layer and the void space in pomegranate-like structure could alleviate the volume expansion during repeated lithium insertion/extraction. As a lithium-ion battery anode, pomegranate-like Si@SiOx composites dried at 180°C delivered a high specific capacity of 1746.5 mAh g-1 after 300 cycles at 500 mA g-1.

In situ Measuring Film-Depth-Dependent Light Absorption Spectra for Organic Photovoltaics.

Organic donor-acceptor bulk heterojunction are attracting wide interests for solar cell applications due to solution processability, mechanical flexibility, and low cost. The photovoltaic performance of such thin film is strongly dependent on vertical phase separation of each component. Although film-depth-dependent light absorption spectra measured by non-in situ methods have been used to investigate the film-depth profiling of organic semiconducting thin films, the in situ measurement is still not well-resolved. In this work, we propose an in situ measurement method in combination with a self-developed in situ instrument, which integrates a capacitive coupled plasma generator, a light source, and a spectrometer. This in situ method and instrument are easily accessible and easily equipped in laboratories of the organic electronics, which could be used to conveniently investigate the film-depth-dependent optical and electronic properties.

Fabrication of SiOx-G/PAA-PANi/Graphene Composite With Special Cross-Doped Conductive Hydrogels as Anode Materials for Lithium Ion Batteries.

Silicon oxides (SiOx) have been considered to be the likeliest material to substitute graphite anode for lithium-ion batteries (LIBs) due to its high theoretical capacity, appropriate working potential plus rich abundance. Nevertheless, the two inherent disadvantages of volume expansion and low electrical conductivity of SiOx have been a main obstacle to its application. Here, SiOx-G/PAA-PANi/graphene composite has been successfully synthesized by in-situ polymerization, in which SiOx-G particles linked together by a graphene-doped polyacrylic acid-polyaniline conductive flexible hydrogel and SiOx-G is encapsulated inside the conductive hydrogel. We demonstrate that SiOx-G/PAA-PANi/graphene composite possesses a discharge-specific capacity of 842.3 mA h g-1 at a current density of 500 mA g-1 after a cycle life of 100 cycles, and a good initial coulombic efficiency (ICE) of 74.77%. The superior performance probably due to the lithium ion transmission rate and the electric conductivity enhanced by the three-dimensional (3D) structured conductive polymer hydrogel.