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Coralloid-Pt nanodendrites decorated nanoporous gold films (NPG-Ptx) were fabricated through underpotential deposition/in-situ reduction replacement (UPD/IRR) strategy and exhibit significantly enhanced ORR activities. Ab initio density functional theory (DFT) studies further demonstrate the ORR mechanism of NPG-Ptx. [Display omitted] • Coralloid-Pt nanodendrites decorated nanoporous gold films (NPG-Ptx) were fabricated through underpotential deposition/in-situ reduction replacement (UPD/IRR) strategy. • The NPG-Ptx (x = 1 ∼ 4) exhibit significantly enhanced ORR activities in acidic media. • The DFT studies demonstrate the ORR mechanism and rate-determining step of NPG-Ptx follow the free energy diagrams. • The PDOS results indicate a relatively stronger O 2 reaction capacity on Pt side than Pt top. Deposition of trace amounts of Pt onto nanoporous gold ligaments (NPG-Pt) has demonstrated promising performance of low-Pt electrocatalysts for oxygen reduction reaction (ORR); however, improving the activity of ORR remains challenging because of the difficulty in understanding the electronic effect between Pt and NPG as well as the absence of ORR mechanism studies on NPG-Pt. Here we show that NPG-Ptx (x = 1 ∼ 4), unique coralloid-Pt nanodendrites decorated nanoporous gold films through underpotential deposition/in-situ reduction replacement (UPD/IRR) strategy, exhibit significantly enhanced ORR activities. Among them, NPG-Pt3 exhibits the best ORR activity compared with the others and Pt/C in acidic media. Density functional theory (DFT) studies demonstrate the ORR mechanism and rate-determining step of NPG-Ptx follow the free energy diagrams. Furthermore, the projected density of state (PDOS) results reveal a relatively weaker O 2 reaction capacity on the top side of Pt (Pt top) than the side site (Pt side) for NPG-Ptx. The increase of d -band center for NPG-Ptx pushes up the energy of the antibonding state above the Fermi level, and then the backflow of electrons into the system makes the energy more stable, optimizing the ORR activity. These results provide new inspirations for the development of low-Pt electrocatalysts for energy technologies in a rational manner. [ABSTRACT FROM AUTHOR]

[Display omitted] • Ru-doped SrFe 1-x Ru x O 3-δ perovskite oxides were successfully fabricated through a modified sol–gel method. • The SrFe 0.7 Ru 0.3 O 3-δ exhibits significantly enhanced bifunctional electrocatalytic activities for HER and OER in alkaline electrolytes. • The DFT studies demonstrate Ru doping optimizes the electronic structure of SrFe 0.7 Ru 0.3 O 3-δ and thus improves the charge transfer efficiency. • An electrolyzer with SFR30 as both the anode and cathode catalysts requires only a cell voltage of 1.58 V vs. RHE to drive a current density of 10 mA cm−2 in an alkaline medium. Recently, perovskite oxides have acquired a rapidly growing research interest in energy storage and conversion systems, especially the electrolysis of water. Rational doping is an extremely effective strategy to enhance the hydrogen evolution reaction/oxygen evolution reaction (HER/OER) of the perovskite oxides. Herein, a series of novel bi-functional electrocatalysts were synthesized by doping Ru in SrFeO 3-δ perovskite oxide (SrFe 1-x Ru x O 3-δ , x = 0, 0.15, 0.30, 0.45) which exhibit remarkable enhancements of HER/OER activities and long-term stabilities in the alkaline solution (1.0 M KOH). Among them, SrFe 0.7 Ru 0.3 O 3-δ (SFR30) shows the best electrocatalytic activities for overall water splitting, exhibiting low overpotentials for HER (∼41 mV) and OER (∼334 mV) at −10 and 10 mA cm−2, respectively, generating current densities of 10 mA cm−2 in alkaline electrolytic cell using the potential of 1.58 V. In addition, the SFR30 electrocatalyst exhibits remarkable stability which can be operated continuously for 96 h without significant delay. Density functional theory (DFT) calculations indicate that Ru doping can effectively modulate the adsorption of intermediates on the active sites to achieve excellent electrocatalytic performance. Many new prospects have been opened for the development of bi-functional electrocatalysts for overall water splitting. [ABSTRACT FROM AUTHOR]

[Display omitted] • Hierarchical 1D/2D Ni(OH) 2 /PCC is fabricated via a facile hydrothermal route as the positive electrode. • The porous corn stigma-derived carbon with the 3D open framework is preparated as the negative electrode. • Explore the excellent electrochemical performance of 1D/2D Ni(OH) 2 /PCC by DFT. • The hybrid supercapacitor displays supeiror energy and power density. Enhancing the energy density of supercapacitors is of great scientific and technological importance, producing a larger energy density than traditional symmetrical carbon supercapacitors. Herein, a hybrid supercapacitor based on an activated corn stigma-derived carbon (PCC) electrode combined with a large-capacity faradic 1D nanofiber/2D nanosheet Ni(OH) 2 electrode is designed to fulfill this goal. Benefiting from the highly conductive, porous construction, and 3D open framework of PCC electrode couple with unique hierarchical 1D nanofiber/2D nanosheet Ni(OH) 2 , such 1D/2D Ni(OH) 2 /PCC electrode is capable of increasing accessible active sites, shortening ion-diffusion path, and accelerating mass transfer. More importantly, DFT calculations unveil that 1D/2D Ni(OH) 2 /PCC composites own high electrical conductivity and OH– adsorption energy. Therefore, the specific capacity of the 1D/2D Ni(OH) 2 /PCC composite electrode reaches 655.9C g−1 at the current density of 1 A/g. Moreover, such hybrid 1D/2D Ni(OH) 2 /PCC||PCC supercapacitor show an outstanding energy density and power density of 38.6 Wh kg−1, and 1.03 kW kg−1, respectively. This work provides the possibility of fabricating hierarchical hydroxide/bio-carbon as a better electrode for high-energy–density electrochemical supercapacitors. [ABSTRACT FROM AUTHOR]

[Display omitted] • Hierarchical NiC 2 O 4 /Ni(OH) 2 nanospheres are synthesized via a simple two-step hydrothermal method as the positive electrode. • The porous biomass-derived carbon with the honeycomb structure is obtained from pine petals as the negative electrode. • Hierarchical NiC 2 O 4 /Ni(OH) 2 nanospheres and the porous biomass-derived carbon possess a high specific capacity. • The hybrid supercapacitor exhibits excellent energy and power density. The high-performance hybrid supercapacitor (HSC) with high power capability and stable cyclability is intensively pursued as a next-generation energy storage device. Here, a kind of hierarchical NiC 2 O 4 /Ni(OH) 2 nanospheres, consisting of subunits of NiC 2 O 4 nanorods and Ni(OH) 2 nanospheres, are synthesized via a two-step hydrothermal method. The hierarchical NiC 2 O 4 /Ni(OH) 2 nanosphere positive electrode, benefiting from the synergistic effect of unique hierarchical structure and built-in electric fields, significantly boosting electron transmission capability and accelerating the ion/electron transfer rate, delivers an excellent specific capacity of 668 C g−1 at 1 A g−1. In addition, the porous biomass-derived carbon (PBC) with the honeycomb structure from pine petals as the negative electrode shows a remarkable electrochemical performance, exhibiting a specific capacitance of 249.7 F g−1 at 1 A g−1. As such, an assembled HSC of NiC 2 O 4 /Ni(OH) 2 ||PBC based on hierarchical NiC 2 O 4 /Ni(OH) 2 nanospheres positive electrode and PBC negative electrode display a conspicuous energy density of 31.07 Wh kg−1, and a power density of 833.47 W kg−1 at a maximum potential window of 1.7 V. This innovative hierarchical engineering of double nickel-based composites with bio-carbon provides an advanced enlightenment for high-performance HSCs. [ABSTRACT FROM AUTHOR]