Novel silicon carbide/polypyrrole composites; preparation and physicochemical properties

Novel silicon carbide/polypyrrole (SiC/PPy) conducting composites were prepared using silicon carbide as inorganic substrate. The surface modification of SiC was performed in aqueous solution by oxidative polymerization of pyrrole using ferric chloride as oxidant. Elemental analysis was used to determine the mass loading of polypyrrole in the SiC/PPy composites. Scanning electron microscopy showed the surface modification of SiC by PPy. PPy in composites was confirmed by the presence of PPy bands in the infrared spectra of SiC/PPy containing various amounts of conducting polymer. The conductivity of SiC/PPy composites depends on PPy content on the surface. The composite containing 35 wt.% PPy showed conductivity about 2 S cm⁻¹, which is in the same range as the conductivity of pure polypyrrole powder prepared under the same conditions using the same oxidant. PPy in the composites was clearly detected by X-ray photoelectron spectroscopy (XPS) measurements by its N1s and Cl2p peaks. High resolution scans of the C1s regions distinguished between silicon carbide and polypyrrole carbons. The fraction of polypyrrole at the composite surface was estimated from the silicon and nitrogen levels. The combination of XPS and conductivity measurements suggests that the surface of the SiC/PPy composites is polypyrrole-rich for a conducting polymer mass loading of at least 12.6 wt.%.     

Fabrication of multiwalled carbon nanotubes/polypyrrole/Prussian blue ternary composite nanofibers and their application for enzymeless hydrogen peroxide detection

In this article, Prussian blue (PB) covered multiwalled carbon nanotubes (MWCNTs)/polypyrrole (PPy) ternary composite nanofibers with good dispersibility in water and ethanol have been prepared by directly mixing ferric-(III) chloride and potassium ferricyanide in the presence of MWCNT/PPy coaxial nanofibers under ambient conditions. Transmission electron microscopy shows that the as-synthesized PB nanoparticles covered on the surface of MWCNT/PPy nanofibers. Fourier-transform infrared spectroscopy, UV–Visible spectroscopy, and X-ray diffraction patterns have been used to characterize the obtained MWCNT/PPy/PB ternary composite nanofibers. The MWCNT/PPy/PB ternary composite nanofibers exhibit good electrocatalytic response to detection of H₂O₂ and provide a new material to modify electrode for amperometric biosensors.     

Formulated quasi-solid state electrolyte based on polypyrrole/polyaniline–polyurethane nanocomposite for dye-sensitized solar cell

A polymer-based quasi-solid state electrolyte using polyurethane (PU) matrix was applied for dye-sensitized solar cell (DSSC). To further improve the performance of the electrolyte, 10 wt% of conductive polymer [polypyrrole (PPy) and polyaniline (PANi)] nanoparticles were introduced into the matrix. The samples were named PU-10%PPy and PU-10%PANi, and characterized using ATR–FTIR, TEM, DLS, a transmitted light microscope, a reflected light microscope, and TGA. The formulated polymeric nanocomposites were immersed in the liquid electrolyte and the polymer matrix absorbency, conductivity (σ), ion diffusion coefficient (D_ff), and photovoltaic performance in the DSSC were measured. Polymer matrix absorbency and D_ff of PU-10%PPy (1.72 g g^?1, 1.52 µcm² s^?1) and PU-10%PANi (1.74 g g^?1, 1.31 µcm² s^?1) were lower than the PU matrix (2.01 g g^?1, 1.68 µcm² s^?1). However, the conductivity of PU-10%PPy and PU-10%PANi was higher than the PU matrix (2.64, 2.69, and 2.59 mS cm^?1, respectively). The efficiency of the DSSC based on PU-10%PANi was the highest, with open circuit voltage of 709 mV, short circuit current of 3.67 mA cm^?2, fill factor of 0.62, and light-to-energy conversion efficiency of 2.68%.     

Synthesis and characterization of conductive polypyrrole/multi-walled carbon nanotubes composites with improved solubility and conductivity

High conductivity and solubility of polypyrrole (PPy)/multi-walled carbon nanotubes (MWCNT) composites has been successfully synthesized by in situ chemical oxidation polymerization using various concentrations of cationic polyelectrolyte poly(styrenesulfonate) (PSS) and ammonium peroxodisulfate (APS). Raman spectroscopy, FTIR, EPR, FESEM and HRTEM were used to characterize their structure and morphology. These images of FESEM and HRTEM showed that the fabricated PPy/MWCNT composites are one-dimensional core-shell structures with the average thickness of the PPy/MWCNT composites without PSS is about 250 nm and considerably decreases to 100–150 nm by adding the PSS content. The results of Raman spectrum, FTIR and UV–Vis indicate the synthesized PPy/MWCNT composites are in the doped state. The conductivities of PPy/MWCNT composites synthesized with the weight ratio of PSS/pyrrole monomer at 0.5 are about two times of magnitude higher than that of PPy/MWCNT composites without PSS. These results are perhaps due to the part of cationic electrolyte served as a dopant can be incorporated to the PPy structure to improve the conductivity of fabricated PPy/MWCNT composites.     

Enhancing the thermoelectric performance by defect structures induced in p-type polypyrrole-polyaniline nanocomposite for room-temperature thermoelectric applications

Organic thermoelectric materials mainly conducting polymers are green materials that can convert heat energy into electrical energy and vice versa at room temperature. In the present work, we investigated the thermoelectric properties of polymer nanocomposite of polypyrrole (PPy) and polyaniline (PANI) (PPy/PANI) by varying the pyrrole: aniline monomer ratios (60:40, 50:50, and 40:60). The PPy/PANI composite is prepared by in-situ chemical polymerization of PPy on PANI dispersion. It has been observed that the combination of two conducting polymers has enhanced the electrical and thermal properties in the PPy/PANI composite due to the strong π–π stacking and H-bonding interaction between the conjugated structure of PPy and conjugated structure of PANI. The maximum electrical conductivity of 14.7 S m^?1 was obtained for composite with high pyrrole content, whereas the maximum Seebeck coefficient of 29.5 μV K^?1 was obtained for composite with high aniline content at 366 K. Consequently, the PPy/PANI composite with pyrrole to aniline monomer ratio of 60:40 exhibits the optimal electrical conductivity, Seebeck coefficient, and high power factor. As a result, the maximum power factor of 2.24 nWm^?1 K^?2 was obtained for the PPy/PANI composite at 60:40 pyrrole to aniline monomer ratio, which is 29 times and 65.8 times higher than PPy (0.077 nWm^?1 K^?2) and PANI (0.034 nWm^?1 K^?2), respectively.

     

Characterization of copper manganite oxide-polypyrrole composite electrodes cathodically polarized in acidic medium

We have studied the electrochemical behaviour induced by polarization in sandwich-type composite electrodes with the structure GC/PPy/PPy(Ox)/PPy where GC stands for glassy carbon, PPy for polypyrrole and Ox for Cu_1.4Mn_1.6O₄ nanoparticles. The electrodes were polarized at ?0.45 V/SCE in 0.15 M KCl aqueous solution at pH 2.2 either saturated in Ar or O₂ at 25 °C. The changes occurring on these electrodes were studied using X-ray photoelectron spectroscopy (XPS) and X-ray absorption spectroscopy (EXAFS and XANES) techniques. In previous work we have shown that when the oxide particles are incorporated into the PPy matrix the Cu⁺ present in the initial oxide suffers dismutation to give Cu²⁺ and metallic Cu. In this work we show that the polarized electrodes also reveal the presence of metallic Cu and Cu²⁺. The data also show that the oxide particles embedded in the polarized electrodes contain Mn³⁺ and Mn⁴⁺, although the Mn³⁺/Mn⁴⁺ ratio is different from that found in the fresh electrodes. The Cl 2p XPS data show that in the electrode polarized in O₂ there is an enhancement of the Cl covalent contribution that appears at 200.8 eV (which is already present in the fresh electrode although with a very small intensity). This result suggests that the oxygen reduction reaction leads to an increase of the OH^? concentration inside the composite electrode that explains the charge transport in PPy at negative potentials.     

Synthesis of polypyrrole/Fe-kanemite nanocomposite through in situ polymerization: effect of iron exchange,acid treatment,and CO<Subscript>2</Subscript> adsorption properties

This paper focuses on the synthesis of polypyrrole/Fe-kanemite nanocomposites by in situ polymerization of pyrrole. Different percentages of PPy/Fe-kan have been prepared and tested for the CO₂ adsorption. Fe-exchanged kanemite was prepared using various iron contents and used as an oxidant for the preparation of PPy/Fe-kan nanocomposite. The obtained materials were characterized using various techniques such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy, ultraviolet–visible (UV–vis), thermogravimetric analysis TGA, energy dispersive X-ray analysis, scanning and transmission electronic microscopy (SEM, TEM). Based on the XRD and UV–vis analysis, the exchange process leads to the formation of various iron species on the external and internal surface. The thermal stability of PPy/Fe-kan was improved and increased in the following order PPy/Fe-kan (1%) > PPy/Fe-kan (3%) > PPy/Fe-kan (5%) > PPy/Fe-kan (10%) > PPy. SEM and TEM analysis show that the nanocomposite particles have spherical morphology with a high dispersion of the Fe-kanemite in the polymer matrix. CO₂ adsorption at 0 and 15 °C was carried using a volumetric method, and the recorded isotherm indicated that the CO₂ adsorption capacity of PPy/Fe-kan can be enhanced through modification by polypyrrole. The unmodified Na-kanemite has low CO₂ adsorption capacity around 0.05 mmol g^?1 at 15 °C, while the PPy/Fe-kan (5%) nanocomposite presented the best CO₂ adsorption capacity around 1.7 mmol g^?1 at 0 °C under low pressure that is mainly attributable to physical adsorption.     

High‐Performance Sb/Sb2O3 Anode Materials Using a Polypyrrole Nanowire Network for Na‐Ion Batteries

Three‐dimensional porous Sb/Sb₂O₃ anode materials are successfully fabricated using a simple electrodeposition method with a polypyrrole nanowire network. The Sb/Sb₂O₃–PPy electrode exhibits excellent cycle performance and outstanding rate capabilities; the charge capacity is sustained at 512.01 mAh g^?1 over 100 cycles, and 56.7% of the charge capacity at a current density of 66 mA g^?1 is retained at 3300 mA g^?1. The improved electrochemical performance of the Sb/Sb₂O₃–PPy electrode is attributed not only to the use of a highly porous polypyrrole nanowire network as a substrate but also to the buffer effects of the Sb₂O₃ matrix on the volume expansion of Sb. Ex situ scanning electron microscopy observation confirms that the Sb/Sb₂O₃–PPy electrode sustains a strong bond between the nanodeposits and polypyrrole nanowires even after 100 cycles, which maintains good electrical contact of Sb/Sb₂O₃ with the current collector without loss of the active materials.     

Polypyrrole Serving as Multifunctional Surface Modifier for Photoanode Enables Efficient Photoelectrochemical Water Oxidation

Conjugated polymer polypyrrole (PPy) with high electrical conductivity and excellent photothermal effect has been adopted as multifunctional surface modifier on ternary metal sulfide (CdIn₂S₄, CIS) photoanode for photoelectrochemical (PEC) water splitting for the first time. As a p-type conducting polymer, PPy forms p–n junction with n-type CIS to relieve the bulk carrier recombination. Besides, the incorporation of Ni ions into PPy matrix further enhances the surface charge carrier transfer at photoanode/electrolyte interfaces. Furthermore, the excellent photothermal effect of PPy produces heat under near-infrared (NIR) irradiation, which can elevate the temperature of CIS photoanode in situ and further enhance the PEC performance. As a result, the optimum CIS/Ni-PPy photoanode shows an obviously enhanced photocurrent density of 6.07 mA cm^?2 at 1.23 V versus reversible hydrogen electrode under the irradiation of AM 1.5G combined with NIR light, which is the highest among all the CIS based photoanodes reported to date. The synergetic effect of Ni-PPy significantly suppresses the bulk recombination, decreases the carrier transfer resistance, and accelerates the surface water oxidation dynamics, resulting in high carrier injection efficiency over 80% in the measured potential range. The universality of the multifunctional surface modifier strategy has also been confirmed on metal oxide photoanode.     

Surface characterizations of conductive poly(methyl methacrylate)/polypyrrole composites

The composites of poly(methyl methacrylate) and polypyrrole (PMMA/PPy) were prepared by a chemical oxidation of pyrrole in a PMMA latex medium resulting in a network like structure of polypyrrole embedded in the insulating polymer matrix. Water was used as the dispersion medium. The content of polypyrrole was determined by elemental analysis as varying from 0.25 wt.% to 10 wt.%. The electrical conductivity of prepared composites depends on the concentration of polypyrrole and reached values of between 1 × 10_{– 9} S/cm to 0.1 S/cm The surface of powder form of PMMA/PPy composites was characterized by X-ray photoelectron spectroscopy (XPS) and by scanning electron microscopy (SEM). The antistatic properties of compression moulding form of composites were tested.     

Synthesis,characterization, and voltammetric hydrogen peroxide sensing on novel monometallic (Ag,Co/MWCNT) and bimetallic (AgCo/MWCNT) alloy nanoparticles

Multiwall carbon nanotube supported (MWCNT) Ag, Co, and Ag-Co alloy nanocatalysts were synthesized at varying metal loadings by borohydride reduction methods without stabilizers to obtain enhanced hydrogen peroxide sensitivity. The resulting materials were characterized employing Scanning electron microscopy (SEM), Energy dispersive X-ray spectroscopy (EDX), and X-ray diffraction (XRD). For electrochemical measurements carried out cyclic voltammetry (CV) and differential pulse voltammetry (DPV), glassy carbon electrode (GCE) was modified with Ag/MWCNT, Co/MWCNT, and Ag-Co/MWCNT alloy nanoparticles. Ag-Co/MWCNT/GCE exhibited the highest performance toward electrochemical oxidation of H₂O₂ in 0.1 M phosphate buffered solution (PBS). Furthermore, the sensitivity and the limit of detection values for Ag-Co/MWCNT/GCE were obtained as 57.14 µA cm^?2 mM^?1and 0.74 µM, respectively. However, the sensitivity values for Ag/MWCNT/GCE, and Co/MWCNT/GCE are 41.66 and 13.88 µA cm^?2 mM^?1, respectively. The LOD values were predicted as 1.84 µM for Ag/MWCNT/GCE and 3.3 µM for Co/MWCNT/GCE.

In addition, the interference experiment indicated that the Ag-Co/MWCNT alloy nanoparticles have good selectivity toward H₂O₂.     

Bacterial cellulose membranes coated by polypyrrole/copper oxide as flexible supercapacitor electrodes

The developments of flexible supercapacitors are of great importance to the growing demand of portable electronic products. In the present work, we have successfully prepared bacterial cellulose (BC) membranes coated by polypyrrole (PPy) and copper oxide (CuO) as flexible composite electrodes for supercapacitor applications. The highest electrical conductivity value of 7.4 S cm^?1 was achieved using copper acetate aqueous solution with concentration of 1 wt%. Electrochemical measurements proved that the supercapacitors using the PPy/CuO/BC electrodes had a specific capacitance of 601 F g^?1 with an energy density of 48.2 Wh kg^?1 and a power density of 85.8 W kg^?1 at a current density of 0.8 mA cm^?2. The specific capacitance was kept at 385 F g^?1 after 300 cycles. The introduction of the CuO nanoparticles gave rise to the improved capacitance.     

Conducting‐Polymer Nanotubes Improve Electrical Properties,Mechanical Adhesion,Neural Attachment,and Neurite Outgrowth of Neural Electrodes

An in vitro comparison of conducting‐polymer nanotubes of poly(3,4‐ethylenedioxythiophene) (PEDOT) and poly(pyrrole) (PPy) and to their film counterparts is reported. Impedance, charge‐capacity density (CCD), tendency towards delamination, and neurite outgrowth are compared. For the same deposition charge density, PPy films and nanotubes grow relatively faster vertically, while PEDOT films and nanotubes grow more laterally. For the same deposition charge density (1.44 C cm^?2), PPy nanotubes and PEDOT nanotubes have lower impedance (19.5 ± 2.1 kΩ for PPy nanotubes and 2.5 ± 1.4 kΩ for PEDOT nanotubes at 1 kHz) and higher CCD (184 ± 5.3 mC cm^?2 for PPy nanotubes and 392 ± 6.2 mC cm^?2 for PEDOT nanotubes) compared to their film counterparts. However, PEDOT nanotubes decrease the impedance of neural‐electrode sites by about two orders of magnitude (bare iridium 468.8 ± 13.3 kΩ at 1 kHz) and increase capacity of charge density by about three orders of magnitude (bare iridium 0.1 ± 0.5 mC cm^?2). During cyclic voltammetry measurements, both PPy and PEDOT nanotubes remain adherent on the surface of the silicon dioxide while PPy and PEDOT films delaminate. In experiments of primary neurons with conducting‐polymer nanotubes, cultured dorsal root ganglion explants remain more intact and exhibit longer neurites (1400 ± 95 µm for PPy nanotubes and 2100 ± 150 µm for PEDOT nanotubes) than their film counterparts. These findings suggest that conducting‐polymer nanotubes may improve the long‐term function of neural microelectrodes.     

Highly compressible graphene/polypyrrole aerogel for superelastic pseudocapacitors

Highly compressible graphene aerogel are proposed as the promising electrode materials for compression-tolerant electrochemical capacitors. Herein, the polypyrrole (PPy) was introduced into the compressible graphene aerogel to further improve its specific capacitance and compression-tolerant ability. As-prepared graphene/PPy aerogel withstands 95% repeated compression cycling without any structure collapse. The gravimetric capacitance of the superelastic pseudocapacitors based on graphene/PPy aerogel electrodes reaches 335 F g^?1 and can retain 97% even under 95% compressive strain. And a volumetric capacitance of 108 F cm^?3 is achieved due to the significantly increased density of the electrodes under 95% strain. This value of the volumetric capacitance can be preserved by 85% after 3500 charge/discharge cycles with various compression conditions. This work will pave the way for advanced applications in the area of compressible energy-storage devices.     

Conducting polymer‐coated, palladium‐functionalized multi‐walled carbon nanotubes for the electrochemical sensing of hydroxylamine

Electrochemical sensors of hydroxylamine were fabricated on glassy carbon electrodes (GCEs) by the electropolymerization of 3,4‐ethylenedioxypyrrole (EDOP) and 3,4‐ethylenedioxythiophene (EDOT) on palladium (Pd) nanoparticles attached to thiolated multi‐walled carbon nanotubes (MWCNTs), denoted as PEDOP/MWCNT‐Pd/GCE and PEDOT/MWCNT‐Pd/GCE. The sensors were characterized by field emission scanning electron microscopy and electrochemical impedance spectroscopy. They showed strong catalytic activity toward the oxidation of hydroxylamine. Cyclic voltammetry and amperometry were used to characterize the sensors' performances. The detection limits of hydroxylamine by PEDOP/MWCNT‐Pd/GCE and PEDOT/MWCNT‐Pd/GCE were 0.22 and 0.24 μM (S/N = 3), respectively. The sensors' sensitivity, selectivity, and stability were also investigated.     

Polypyrrole/multiwall carbon nanotube nanocomposites electropolymerized on copper substrate

Polypyrrole/multiwall carbon nanotube (PPy/MWCNT) nanocomposites were successfully synthesized by electropolymerization of MWCNT-dispersed pyrrole solution on the surface of copper electrodes. The obtained nanocomposites were characterized with scanning electron microscopy (SEM), linear sweep voltammetry (LSV) and thermal gravimetric analysis (TGA). Polypyrrole structures which embraced the MWCNTs led to the formation of nanocomposite striated parallel walls. MWCNTs acted as appropriate substrates for electrodeposition of polypyrrole particulate structures and high yield synthesis of PPy was observed on them. Smooth PPy/MWCNT nanocomposite films were obtained on Cu electrodes by decreasing the potential scan rate. Thermogravimetric analysis showed that MWCNTs increased the thermal stability of polypyrrole.     

Electrodeposition and Characterization of Co Particles on Ultrathin Polypyrrole Films

Ultrathin polypyrrole (PPy) films with the thicknesses of 20, 50, and 100 nm were prepared by electropolymerization. Co particles with a charge density in the range of 125–1,250 mC cm^?2 were grown on these ultrathin PPy films. Current time transients were used to investigate the electrochemical properties. It was observed that the deposition of Co becomes more difficult as the PPy film gets thicker. The chemical structure of PPy films in the reduced and oxidized forms and a PPy film with Co particles were examined with Fourier transform infrared spectroscopy (FTIR). The characteristic peaks of the oxidized PPy film were observed. The intensity and position of some peaks changed, and new peaks appeared for the reduced PPy film, possibly as a result of undoping of the PPy film. There are further differences in the spectrum of Co on PPy. The morphology of the films was studied by scanning electron microscopy (SEM). It was found that the morphology was affected by both the PPy film thickness and the Co charge density. Magnetic measurements were made by vibrating sample magnetometry (VSM). The magnetic moment of the samples increases with both decreasing PPy film thickness and increasing charge density due to increased Co deposition. For all samples, the easy axis is parallel to the film plane.     

Electrodeposition of platinum nanoparticles on polypyrrole-functionalized graphene

In this study, the new electrocatalyst of platinum support on polypyrrole-functionalized graphene (GNS–PPy/PtNPs) is reported. The polypyrrole-functionalized graphene (GNS–PPy) is constructed first with graphene nanosheets (GNS) and polypyrrole (PPy) particles by constant potential deposition. And then PtNPs are deposited on the surface of GNS–PPy by cyclic voltammetry. The as-prepared GNS–PPy/PtNPs is characterized by scanning electron microscopy, energy-dispersive spectroscopy, X-ray powder diffraction, X-ray photoelectron spectroscopy, and Raman spectroscopy. The prepared GNS–PPy/PtNPs catalyst is employed for methanol oxidation reactions. Compared with GNS/PtNPs and PPy/PtNPs, the GNS–PPy/PtNPs has higher catalytic activity (508 mA/mg), better stability, and stronger poisoning-tolerance (I _f/I _b = 4.18) due to high dispersion of PtNPs on large surface of GNS–PPy as well as synergic effect among the GNS, PPy particles, and PtNPs. The experimental results indicate that GNS–PPy/PtNPs may be an ideal candidate catalyst for direct methanol fuel cell.     

Corrosion protection of cold-rolled steel with alkyd paint coatings composited with submicron-structure types polypyrrole-modified nano-size alumina and carbon nanotubes

This paper is focused on studying corrosion protection of cold-rolled steel with alkyd paint coatings comprising nano-size alumina and either polystyrene-sulphonate (PSS) modified or sulphonated multi-walled carbon nanotube (MWCNT) supported polypyrrole (PPy). Single layer coatings (in thickness of 40 ± 5 μm) comprising PPy deposited alumina and PSS modified MWCNT supported PPy afforded viable protection during the 1 M sodium chloride test. The coatings containing PSS modified and weakly sulphonated MWCNTs (at volume fractions of 9.9 × 10⁻⁴ and 2.5 × 10⁻⁴) with PPy volume fractions of 3.5 × 10⁻³ and 2.5 × 10⁻³ provided effective corrosion prevention during the 1 M sodium chloride and hydrochloric acid solution tests. While inhibitor particles were characterised by infrared spectroscopy, corrosion products formed at the paint–steel interface were studied by X-ray photoelectron spectroscopy. Apart from the electron microscopy observations, rheology study of three-dimensional structure of the inhibitor particles was performed in dispersions at similar compositions to those used for the paint formulations. Thus, protection mechanism relating to both types of immersion tests is discussed in terms of properties of the inhibitor particles and their microstructure in the coatings.     

Metal‐Tuned Acetylene Linkages in Hydrogen Substituted Graphdiyne Boosting the Electrochemical Oxygen Reduction

Different from graphene with the highly stable sp²‐hybridized carbon atoms, which shows poor controllability for constructing strong interactions between graphene and guest metal, graphdiyne has a great potential to be engineered because its high‐reactive acetylene linkages can effectively chelate metal atoms. Herein, a hydrogen‐substituted graphdiyne (HsGDY) supported metal catalyst system through in situ growth of Cu₃Pd nanoalloys on HsGDY surface is developed. Benefiting from the strong metal‐chelating ability of acetylenic linkages, Cu₃Pd nanoalloys are intimately anchored on HsGDY surface that accordingly creates a strong interaction. The optimal HsGDY‐supported Cu₃Pd catalyst (HsGDY/Cu₃Pd‐750) exhibits outstanding electrocatalytic activity for the oxygen reduction reaction (ORR) with an admirable half‐wave potential (0.870 V), an impressive kinetic current density at 0.75 V (57.7 mA cm^?2) and long‐term stability, far outperforming those of the state‐of‐the‐art Pt/C catalyst (0.859 V and 15.8 mA cm^?2). This excellent performance is further highlighted by the Zn–air battery using HsGDY/Cu₃Pd‐750 as cathode. Density function theory calculations show that such electrocatalytic performance is attributed to the strong interaction between Cu₃Pd and C?C bonds of HsGDY, which causes the asymmetric electron distribution on two carbon atoms of C?C bond and the strong charge transfer to weaken the shoulder‐to‐shoulder π conjugation, eventually facilitating the ORR process.