Minimizing Voltage Losses via Synergistically Reducing Hetero-Interface Energy Offset for High Efficiency Perovskite Solar Cells.

The open circuit voltage (VOC) losses at multiple interfaces within perovskite solar cells (PSCs) limit the improvements in power conversion efficiency (PCE). Herein, a tailored strategy is proposed to reduce the energy offset at both hetero-interfaces within PSCs to decrease the VOC losses. For the interface of perovskite and electron transport layer where exists a mass of defects, it uses the pyromellitic acid to serve as a molecular bridge, which reduces non-radiative recombination and energy level offset. For the interface of perovskite and hole transport layer, which includes a passivator of PEAI, the detrimental effect (negative shift of work function) of PEAI passivation and optimizing the interface energy level alignment are neutralized by incorporating (2-(4-(bis(4-methoxyphenyl)amino)phenyl)-1-cyanovinyl)phosphonic acid. Owing to synergistically reduced hetero-interface energy offset, the PSCs achieve a PCE of 25.13%, and the VOC is increased from 1.134 to 1.174 V. In addition, the resulting PSCs possess enhanced stability, the unencapsulated PSCs can maintain ≈96% and ≈97% of their initial PCE after 2000 h of aging under ambient conditions and 210 h under operation conditions.

21.83% incident light can circumvent a 6.6 × 6.6 cm2 obstruction by introducing a layer of bubbles into the photovoltaic glass.

Obstruction is inevitable and will significantly impact the actual output performance of photovoltaic modules, even jeopardize their operational safety. We introduced a layer of bubbles into photovoltaic glass. These bubbles can alter the path of incident light, while the internal reflection at the glass/air interface enables the redirected light rays to have longer lateral propagation distance, circumventing the obstructions. The optimized photovoltaic glass with a bubble diameter of 1.8 mm and a surface density of 16 cm-2 enables the light intensity underneath a 6.6 × 6.6 cm2 obstruction to reach 21.83% of the incident light intensity. This enhancement permits a partial shading of the photovoltaic module, increasing its output power by ∼20.8% and decreasing the reverse bias voltage on the shaded cell by ∼1.4 V.

Inhibition of ion diffusion/migration in perovskite p-n homojunction by polyetheramine insert layer to enhance stability of perovskite solar cells with p-n homojunction structure.

Perovskite p-n homojunctions (PHJ) have been confirmed to play a crucial role in facilitating carrier separation/extraction in the perovskite absorption layer and provide an additional built-in potential, which benefits the inhibition of carrier recombination in perovskite solar cells (PSCs) and ultimately improves device performance. However, the diffusion and migration of ions between n-type and p-type perovskite films, particularly under operational and heating conditions, lead to the degradation of PHJ structures and limit the long-term stability of PSCs with PHJ structure (denoted as PHJ-PSCs). In this study, we propose an insert layer strategy by directly introducing an ultra-thin polyetheramine (PEA) layer between the n-type and p-type perovskite films to address those challenges arising from ion movements. Femtosecond transient absorption (fs-TAS) and photoluminescence (PL) measurements demonstrate that the PHJ (without and with the insert layer) enhances carrier separation/extraction compared to the single n-type perovskite film. Monitoring the evolution of bromine element distribution reveals that the insert layer can efficiently suppress ion diffusion between perovskite films, even under long-term illumination and heating conditions. Consequently, an efficiency of 23.53% with excellent long-term operational stability is achieved in the optimized PHJ-PSC with the insert layer.

Cascade Reaction in Organic Hole Transport Layer Enables Efficient Perovskite Solar Cells.

The doped organic hole transport layer (HTL) is crucial for achieving high-efficiency perovskite solar cells (PSCs). However, the traditional doping strategy undergoes a time-consuming and environment-dependent oxidation process, which hinders the technology upgrades and commercialization of PSCs. Here, we reported a new strategy by introducing a cascade reaction in traditional doped Spiro-OMeTAD, which can simultaneously achieve rapid oxidation and overcome the erosion of perovskite by 4-tert-butylpyridine (tBP) in organic HTL. The ideal dopant iodobenzene diacetate was utilized as the initiator that can react with Spiro to generate Spiro⋅+ radicals quickly and efficiently without the participation of ambient air, with the byproduct of iodobenzene (DB). Then, the DB can coordinate with tBP through a halogen bond to form a tBP-DB complex, minimizing the sustained erosion from tBP to perovskite. Based on the above cascade reaction, the resulting Spiro-based PSCs have a champion PCE of 25.76 % (certificated of 25.38 %). This new oxidation process of HTL is less environment-dependent and produces PSCs with higher reproducibility. Moreover, the PTAA-based PSCs obtain a PCE of 23.76 %, demonstrating the excellent applicability of this doping strategy on organic HTL.

Oriented Molecular Bridge Constructs Homogeneous Buried Interface for Perovskite Solar Cells with Efficiency Over 25.3.

Buried interface optimization matters the efficiency improvement of planar perovskite solar cells (PSCs), and the molecular bridge is reported to be an effective approach. Herein, a molecular bridge is constructed at buried interface using 4-chloro-3-sulfamoylbenzoic acid (CSBA), and its preferred arrangement is systematically investigated. It is elucidated that the CSBA molecular is prone to be orientationally absorbed on TiO2 surface through COOH-Ti, and then connect with perovskite through S═O-Pb, resulting in a feasible oriented molecular bridge. Contributing to the passivated interfacial defects, optimized interfacial energy level, and released perovskite tensile stress, resulting from the oriented CSBA molecular bridge, the PSCs with an active area of 0.08 cm2 achieve a certified power conversion efficiency (PCE) of 25.32%, the highest among the TiO2-based planar PSCs. Encouragingly, the PSCs with an active area of 1 cm2 achieve a champion PCE of 24.20%, significantly promoting the efficiency progress of large-area PSCs. In addition, the PSCs with oriented CSBA molecular bridge possess enhanced stability, the unencapsulated PSCs can maintain ≈91% and ≈85% of their initial PCE after 3000 h aging under ambient condition and 1200 h aging under exposure to UV irradiation.

Enhanced Resonance for Facilitated Modulation of Large-Area Perovskite Films with Stable Photovoltaics.

Upscaling efficient and stable perovskite films is a challenging task in the industrialization of perovskite solar cells partly due to the lack of high-performance hole transport materials (HTMs), which can simultaneously promote hole transport and regulate the quality of perovskite films especially in inverted solar cells. Here, a novel HTM based on N-C = O resonance structure is designed for facilitating the modulation of the crystallization and bottom-surface defects of perovskite films. Benefiting from the resonance interconversion (N-C = O and N+ = C-O- ) in donor-resonance-donor (D-r-D) architecture and interactions with uncoordinated Pb2+ in perovskite, the resulting D-r-D HTM with two donor units exhibits not only excellent hole extraction and transport capacities, but also efficient crystallization modulation of perovskite for high-quality photovoltaic films in large area. The D-r-D HTM-based large-area (1.02 cm2 ) devices exhibit high power conversion efficiencies (PCEs) up to 21.0%. Moreover, the large-area devices have excellent photo-thermal stability, showing only a 2.6% reduction in PCE under continuous AM 1.5G light illumination at elevated temperature (≈65 °C) for over 1320 h without encapsulation.

Multifunctional Role of Ag-Substitution in Enhancing the Photoelectrochemical Properties of LaFeO3 Photocathodes.

Earth-abundant LaFeO3 is a promising p-type semiconductor for photoelectrochemical cells due to its stable photoresponses, high photovoltages and appropriate band alignments, but the photoelectrochemical properties of LaFeO3 , especially the incident-photon-to-current conversion efficiency, need to be further improved. Herein, we propose to partially substitute La3+ of LaFeO3 with Ag+ to enhance the photoelectrochemical performance of LaFeO3 . The combined experimental and computational studies show that Ag-substitution improves surface charge transfer kinetics through introducing active electronic states and increasing electrochemically active surface areas. Furthermore, Ag-substitution decreases grain boundary number and increases majority carrier density, which promotes bulk charge transports. Ag-substitution also reduces the bandgap energy, increasing the flux of carriers involved in photoelectrochemical reactions. As a result, after 8 % Ag-substitution, the photocurrent density of LaFeO3 is enhanced by more than 6 times (-0.64 mA cm-2 at 0.5 V vs RHE) in the presence of oxygen, which is the highest photocurrent gain compared with other cation substitution or doping. The corresponding photocurrent onset potential also demonstrates a positive shift of 30 mV. This work highlights the versatile effects of Ag-substitution on the photoelectrochemical properties of LaFeO3 , which can provide useful insights into the mechanism of enhanced photoelectrochemical performance by doping or substitution.

Quantification of cardiac iron in patients with thalassemia with 3-T MRI calibrated by 1.5-T MRI.

BACKGROUND: Due to the small sample size of many studies, it remained unclear what standardized reference range the T2* cutoff at 3 T would be used to assess the severity of cardiac iron load. In addition, the number of patients with moderate to severe cardiac iron load was small in some studies, especially the sample of patients with severe cardiac iron load. PURPOSE: To explore the feasibility, reproducibility, and reliability of using T2* values in quantifying cardiac iron load in patients with thalassemia at 3 T. MATERIAL AND METHODS: A total of 122 patients with thalassemia underwent cardiac T2* imaging at both 1.5 T and 3 T. Cardiac R2* (1000/T2*) values of the 100 patients at 3 T were fitted against the values at 1.5 T using linear regression and the prediction equation was derived. The remaining 22 cases were used to test the prediction accuracy of the equation. RESULTS: The combined R2* values exhibited a strong linear relationship between 1.5 T and 3 T (r = 0.830，P<0.001). At the center, it had a slope of 1.348 and an intercept of 37.279. According to the equation, the truncated T2* values of cardiac iron overload and cardiac heavy iron overload at 3 T were <10 ms and <6 ms, respectively. The two truncated T2* values were used to diagnose different levels of cardiac iron overloaded of 22 patients at 3 T; the accuracy rates were 95.5% and 100.0%, respectively. CONCLUSION: T2* quantification of cardiac iron load at 3 T MRI resulted to be feasible, reproducible, and reliable.

Multifunctional Resonance Bridge-Mediated Dynamic Modulation of Perovskite Films For Enhanced Intrinsic Stability of Photovoltaics.

The improving intrinsic stability, determining the life span of devices, is a challenging task in the industrialization of inverted perovskite solar cells. The most important prerequisite for boosting intrinsic stability is high-quality perovskite films deposition. Here, a molecule, N-(2-pyridyl)pivalamide (NPP) is utilized, as a multifunctional resonance bridge between poly(triarylamine) (PTAA) and perovskite film to regulate the perovskite film quality and promote hole extraction for enhancing the device intrinsic stability. The pyridine groups in NPP couple with the phenyl groups in PTAA through π-π stacking to improve hole extraction capacities and minimize interfacial charge recombination, and the resonance linkages (NCO) in NPP dynamically modulate the perovskite buried defects through strong PbO bonds based on the fast self-adaptive tautomerization between resonance forms (NCO and N+ CO- ). Because of the combined effect of the reduction defect density and improved energy level in the perovskite buried interfaces as well as the optimized crystal orientation in perovskite film enabled by the NPP substrate, the devices based on NPP-grown perovskite films show an efficiency approaching 20% with negligible hysteresis. More impressively, the unencapsulated device displays start-of-the-art intrinsic photostability, operating under continuous 1-sun illumination for 2373 h at 65 °C without loss of PCE.

In situ surface regulation of 3D perovskite using diethylammonium iodide for highly efficient perovskite solar cells.

Surface passivation by constructing a 2D/3D structure is considered to be an effective strategy for suppressing non-radiative recombination and improving the device efficiency and stability. Herein, the 2D perovskite is formed in situ on the surface of a 3D perovskite via chemical interactions between diethylammonium iodide (DAI) and Pb-I octahedra, which greatly reduces the deep level defects and non-radiative recombination. Moreover, the 2D/3D structure can regulate the energy level alignment, enhance the charge extraction, and improve the open-circuit voltage. Finally, compared with the control device, the power conversion efficiency (PCE) of the DAI-treated device increases from 21.58 to 23.50%. The unencapsulated devices stored in air for more than 500 hours can still retain 97% of their initial PCE, revealing good long-term placement stability. This work provides a promising strategy to fabricate efficient PSCs through the in situ construction of 2D/3D perovskite heterojunctions.

Battery-Type-Behavior-Retention Ni(OH)2-rGO Composite for an Ultrahigh-Specific-Capacity Asymmetric Electrochemical Capacitor Electrode.

Nanosized battery-type materials applied in electrochemical capacitors can effectively reduce a series of problems caused by low conductivity and large volume changes. However, this approach will lead to the charging and discharging process being dominated by capacitive behavior, resulting in a serious decline in the specific capacity of the material. By controlling the material particles to an appropriate size and a suitable number of nanosheet layers, the battery-type behavior can be retained to maintain a large capacity. Here, Ni(OH)2, which is a typical battery-type material, is grown on the surface of reduced graphene oxide to prepare a composite electrode. By controlling the dosage of the nickel source, the composite material with an appropriate Ni(OH)2 nanosheet size and a suitable number of layers was prepared. The high-capacity electrode material was obtained by retaining the battery-type behavior. The prepared electrode had a specific capacity of 397.22 mA h g-1 at 2 A g-1. After the current density was increased to 20 A g-1, the retention rate was as high as 84%. The prepared asymmetric electrochemical capacitor had an energy density of 30.91 W h kg-1 at a power density of 1319.86 W kg-1 and the retention rate could reach 79% after 20,000 cycles. We advocate an optimization strategy that retains the battery-type behavior of electrode materials by increasing the size of nanosheets and the number of layers, which can significantly improve the energy density while combining the advantage of the high rate capability of the electrochemical capacitor.

Strategy of Voltage Match on the Maximum Power Point for a High-Efficiency Photorechargeable Device.

A photorechargeable device can generate power from sunlight and store it in one device, which has a broad application prospect in the future. However, if the working state of the photovoltaic part in the photorechargeable device deviates from the maximum power point, its actual power conversion efficiency will reduce. The strategy of voltage match on the maximum power point is reported to achieve a high overall efficiency (ηoa) of the photorechargeable device assembled by a passivated emitter and rear cell (PERC) solar cell and Ni-based asymmetric capacitors. According to matching the voltage of the maximum power point of the photovoltaic part, the charging characteristics of the energy storage part are adjusted to realize a high actual power conversion efficiency of the photovoltaic part (ηpv). The ηpv of a Ni(OH)2-rGO-based photorechargeable device is 21.53%, and the ηoa is up to 14.55%. This strategy can promote further practical application for the development of photorechargeable devices.

Pristine GaFeO3 Photoanodes with Surface Charge Transfer Efficiency of Almost Unity at 1.23 V for Photoelectrochemical Water Splitting.

Oxide-based photoelectrodes commonly generate deep trap states associated with various intrinsic defects such as vacancies, antisites, and dislocations, limiting their photoelectrochemical properties. Herein, it is reported that rhombohedral GaFeO3 (GFO) thin-film photoanodes exhibit defect-inactive features, which manifest themselves by negligible trap-states-associated charge recombination losses during photoelectrochemical water splitting. Unlike conventional defect-tolerant semiconductors, the origin of the defect-inactivity in GFO is the strongly preferred antisite formation, suppressing the generation of other defects that act as deep traps. In addition, defect-inactive GFO films possess really appropriate oxygen vacancy concentration for the oxygen evolution reaction (OER). As a result, the as-prepared GFO films achieve the surface charge transfer efficiency (ηsurface ) of 95.1% for photoelectrochemical water splitting at 1.23 V versus RHE without any further modification, which is the highest ηsurface reported of any pristine inorganic photoanodes. The onset potential toward the OER remarkably coincides with the flat band potential of 0.43 V versus RHE. This work not only demonstrates a new benchmark for the surface charge transfer yields of pristine metal oxides for solar water splitting but also enriches the arguments for defect tolerance and highlights the importance of rational tuning of oxygen vacancies.

Decoupling the impact of bulk and surface point defects on the photoelectrochemical properties of LaFeO3 thin films.

Point defects (PDs) play a key role in the properties of semiconductor photoelectrodes, from doping density to carrier mobility and lifetime. Although this issue has been extensively investigated in the context of photovoltaic absorbers, the role of PDs in photoelectrodes for solar fuels remains poorly understood. In perovskite oxides such as LaFeO3 (LFO), PDs can be tuned by changing the cation ratio, cation substitution and oxygen content. In this paper, we report the first study on the impact of bulk and surface PDs on the photoelectrochemical properties of LFO thin films. We independently varied the La : Fe ratio, within 10% of the stoichiometric value, in the bulk and at the surface by tuning the precursor composition as well as selective acid etching. The structure and composition of thin films deposited by sol-gel methods were investigated by SEM-EDX, ICP-OES, XPS and XRD. Our analysis shows a correlation between the binding energies of Fe 2p3/2 and O 1s, establishing a link between the oxidation state of Fe and the covalency of the Fe-O bond. Electrochemical studies reveal the emergence of electronic states close to the valence band edge with decreasing bulk Fe content. DFT calculations confirm that Fe vacancies generate states located near the valence band, which act as hole-traps and recombination sites under illumination. Dynamic photocurrent responses associated with oxygen reduction and hydrogen evolution show that the stoichiometric La : Fe ratio provides the most photoactive oxide; however, this can only be achieved by independently tuning the bulk and surface compositions of the oxide.

Improving carrier separation at the TiO2/CsPbIBr2 interface by gradient Sn-doping.

Subhani et al. found that Sm-doping in CsPbIBr2 decreased its bandgap from 2.05 eV to 1.8 eV; thus, the efficiency of CsPbIBr2 solar cells was improved by ∼30%. However, Sm is a vital strategic resource with high costs. Metal Sn is much more abundant and cheaper than Sm; meanwhile, it has been proven that Sn can adjust the bandgap of CsPbIBr2 in a broader range, 2.05 eV to 1.64 eV. Therefore, Sn-doping in CsPbIBr2 may improve the efficiency of CsPbIBr2 solar cells, even to a greater extent. In this work, we established the TiO2/CsPbIBr2 interface model by gradient Sn-doping in CsPbIBr2 and investigated the impacts of such gradient doping on the carrier separation behaviors at the TiO2/CsPbIBr2 interface from the aspects of the cross-interface electric field, bandgap, and band matching, based on first-principles calculations. It is found that gradient Sn-doping can transfer more electrons from TiO2 to perovskites, thus creating an enhanced cross-interface electric field conducive to the separation of carriers at the TiO2/CsPbIBr2 interface. Affected by the existence of the interface, the bandgap of each perovskite layer gradually increases as it moves away from the interface; in addition, due to the gradient Sn-doping, the steps between the bandgaps of adjacent perovskite layers become smaller and more uniform, which is favorable for the separation of electrons. In summary, gradient Sn-doping can improve the carrier separation at the TiO2/CsPbIBr2 interface.

A green and sustainable strategy toward lithium resources recycling from spent batteries.

Recycling lithium from spent batteries is challenging because of problems with poor purity and contamination. Here, we propose a green and sustainable lithium recovery strategy for spent batteries containing LiFePO4, LiCoO2, and LiNi0.5Co0.2Mn0.3O2 electrodes. Our proposed configuration of "lithium-rich electrode || LLZTO@LiTFSI+P3HT || LiOH" system achieves double-side and roll-to-roll recycling of lithium-containing electrode without destroying its integrity. The LiTFSI+P3HT-modified LLZTO membrane also solves the H+/Li+ exchange problem and realizes a waterproof protection of bare LLZTO in the aqueous working environment. On the basis of these advantages, our system shows high Li selectivity (97%) and excellent Faradaic efficiency (≥97%), achieving high-purity (99%) LiOH along with the production of H2. The Li extraction processes for spent LiFePO4, LiNi0.5Co0.2Mn0.3O2, and LiCoO2 batteries is shown to be economically feasible. Therefore, this study provides a previously unexplored technology with low energy consumption as well as high economic and environmental benefits to realize sustainable lithium recycling from spent batteries.

Dopamine Hydrochloride-Assisted Synergistic Modulation of Perovskite Crystallization and Sn2+ Oxidation for Efficient and Stable Lead-free Solar Cells.

Tin perovskites have received great concern in solar cell research owing to their favorable optoelectronic performance and environmental friendliness. However, due to their poor crystallization and easy oxidation, the performance improvement for tin-based perovskite solar cells (TPSCs) is rather challenging. Herein, reductive 3-hydroxytyramine hydrochloride (DACl) with NH2·HCl and phenol groups as co-additives with SnF2 is added into the precursor to modulate perovskite crystallization and inhibit Sn2+ oxidation for high-performance TPSCs. The Lewis base group of NH2 HCl in DACl could bind to perovskite lattices to modulate the crystallization with suppressed defects in the bulk and grain boundary, whereas reductive phenol groups effectively constrain the Sn2+ oxidation. Moreover, the undissociated DACl decreases the supersaturated concentration of tin perovskite solution and creates a pre-nucleation site for rapid nucleation to further regulate crystallization. Consequently, the DACl-derived TPSCs achieve a high power-conversion efficiency (PCE) that reaches up to 11%. More impressively, the device remains at 84% of the initial PCE after full-sun illumination in N2 over 600 h without being encapsulated. This DACl-based synergistic modulation of a lead-free perovskite demonstrates a feasible approach using one molecule with different functional groups to manipulate crystallization, Sn2+ oxidation, and defect reparation of tin perovskite films, providing a critical guideline for constructing high-quality perovskites by multifunctional additives with high photovoltaic performance.

Constructing Soft Perovskite-Substrate Interfaces for Dynamic Modulation of Perovskite Film in Inverted Solar Cells with Over 6200 Hours Photostability.

High-performance perovskite solar cells (PSCs) depend heavily on the quality of perovskite films, which is closely related to the lattice distortion, perovskite crystallization, and interfacial defects when being spin-coated and annealed on the substrate surface. Here, a dynamic strategy to modulate the perovskite film formation by using a soft perovskite-substrate interface constructed by employing amphiphilic soft molecules (ASMs) with long alkyl chains and Lewis base groups is proposed. The hydrophobic alkyl chains of ASMs interacted with poly(triarylamine) (PTAA) greatly improve the wettability of PTAA to facilitate the nucleation and growth of perovskite crystals, while the Lewis base groups bound to perovskite lattices significantly passivate the defects in situ. More importantly, this soft perovskite-substrate interface with ASMs between PTAA and perovskite film can dynamically match the lattice distortion with reduced interfacial residual strain upon perovskite crystallization and thermal annealing owing to the soft self-adaptive long-chains, leading to high-quality perovskite films. Thus, the inverted PSCs show a power conversion efficiency approaching 20% with good reproducibility and negligible hysteresis. More impressively, the unencapsulated device exhibits state-of-the-art photostability, retaining 84% of its initial efficiency under continuous simulated 1-sun illumination for more than 6200 h at elevated temperature (≈65 °C).

Impact of Precursor Concentration on Perovskite Crystallization for Efficient Wide-Bandgap Solar Cells.

High-crystalline-quality wide-bandgap metal halide perovskite materials that achieve superior performance in perovskite solar cells (PSCs) have been widely explored. Precursor concentration plays a crucial role in the wide-bandgap perovskite crystallization process. Herein, we investigated the influence of precursor concentration on the morphology, crystallinity, optical property, and defect density of perovskite materials and the photoelectric performance of solar cells. We found that the precursor concentration was the key factor for accurately controlling the nucleation and crystal growth process, which determines the crystallization of perovskite materials. The precursor concentration based on Cs0.05FA0.8MA0.15Pb(I0.84Br0.16)3 perovskite was controlled from 0.8 M to 2.3 M. The perovskite grains grow larger with the increase in concentration, while the grain boundary and bulk defect decrease. After regulation and optimization, the champion PSC with the 2.0 M precursor concentration exhibits a power conversion efficiency (PCE) of 21.13%. The management of precursor concentration provides an effective way for obtaining high-crystalline-quality wide-bandgap perovskite materials and high-performance PSCs.

Polyethylene Oxide as a Multifunctional Binder for High-Performance Ternary Layered Cathodes.

Nickel cobalt manganese ternary cathode materials are some of the most promising cathode materials in lithium-ion batteries, due to their high specific capacity, low cost, etc. However, they do have a few disadvantages, such as an unstable cycle performance and a poor rate performance. In this work, polyethylene oxide (PEO) with high ionic conductance and flexibility was utilized as a multifunctional binder to improve the electrochemical performance of LiNi0.6Co0.2Mn0.2O2 cathode materials. Scanning electron microscopy showed that the addition of PEO can greatly improve the adhesion of the electrode components and simultaneously enhance the integrity of the electrode. Thus, the PEO-based electrode (20 wt% PEO in PEO/PVDF) shows a high electronic conductivity of 19.8 S/cm, which is around 15,000 times that of the pristine PVDF-based electrode. Moreover, the PEO-based electrode exhibits better cycling stability and rate performance, i.e., the capacity increases from 131.1 mAh/g to 147.3 mAh/g at 2 C with 20 wt% PEO addition. Electrochemical impedance measurements further indicate that the addition of the PEO binder can reduce the electrode resistance and protect the LiNi0.6Co0.2Mn0.2O2 cathode materials from the liquid electrolyte attack. This work offers a simple yet effective method to improve the cycling performance of the ternary cathode materials by adding an appropriate amount of PEO as a binder in the electrode fabrication process.