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Schematic diagram representation the introduction of selenium and iron synergistically modulate the d-band center of Ni 3 S 2 to enhance oxygen evolution reaction (OER) and urea oxidation reaction (UOR). [Display omitted] • The introduction of selenium and iron synergistically modulated the d-band center of Ni 3 S 2 , resulting in the enhanced catalytic activity for the oxygen evolution reaction (OER) and urea oxidation reaction (UOR). • By adjusting the position of the d-band center, it is possible to optimize the adsorption and desorption energies of SeFe-Ni 3 S 2 towards urea molecules, as well as the overpotential for OER (η OER) and the limiting potential for UOR (U L). • The synthesized SeFe-Ni 3 S 2 presents as 3.9 nm lamellar structure with a larger specific surface area leading to the exposure of more active sites. Efficient production of green hydrogen energy is crucial in addressing the energy crisis and environmental concerns. The oxygen evolution reaction (OER) poses a challenge in conventional overall water electrolysis due to its slow thermodynamically process. Urea oxidation reaction (UOR) offers an alternative anodic oxidation method that is highly efficient and cost-effective, with favorable thermodynamics and sustainability. Recently, there has been limited research on bifunctional catalysts that exhibit excellent activity for both OER and UOR reactions. In this study, we developed a selenium and iron co-doped nickel sulfide (SeFe-Ni 3 S 2) catalyst that demonstrated excellent Tafel slopes of 53.9 mV dec−1 and 16.4 mV dec−1 for OER and UOR, respectively. Density Functional Theory (DFT) calculations revealed that the introduction of metal (iron) and nonmetallic elements (selenium) was found to coordinate the d-band center, resulting in improved adsorption/desorption energies of the catalysts and reduced the overpotentials and limiting potentials for OER and UOR, respectively. This activity enhancement can be attributed to the altered electronic coordination structure after the introduction of selenium (Se) and iron (Fe), leading to an increase in the intrinsic activity of the catalyst. This work offers a new strategy for bifunctional catalysts for OER and UOR, presenting new possibilities for the future development of hydrogen production and novel energy conversion technologies. It contributes towards the urgent search for technologies that efficiently produce green hydrogen energy, providing potential solutions to mitigate the energy crisis and protect the environment. [ABSTRACT FROM AUTHOR]

[Display omitted] Carbon dots (CDs) emerge as promising luminescent materials for potential applications in optoelectronics on basis of their merits including low cost, eco-friendliness and strong, color-tunable photoluminescence (PL). However, the research on solid-state emissive CDs is still at the primary stage because of the aggregation-caused quenching (ACQ) of PL and their poor film-formation ability. In this work, we produce CDs with branched-polyethylenimine (b-PEI) chemically functionalized on the surfaces. The thus newly synthesized P-CDs successfully overcome the bottleneck of ACQ effect and display efficient red and NIR emission in aggregate state. Under the excitation of 520 nm, a strong red emission (maxima of 640 nm) with a high photoluminescence quantum yield (PLQY) of 21% was observed for the P-CDs in neat film. Moreover, this design strategy endows the P-CDs with good film-formation ability via solution spin-coating, which significantly increases its value for the film-based optoelectronic devices. [ABSTRACT FROM AUTHOR]

• A universal strategy to solve interfacial detachment of solid EDLCs. • Significantly reduced interfacial impedance. • Optimizing solvated structures of Hybrid ILs. • Excellent cycling stability of EDLCs at high temperature. The growing application domain of energy storage devices (ESDs) is leading research to temperature tolerant supercapacitors. To realize reliable and safe devices, high modulus solid electrolytes are favored by most researchers. However, the inferior infiltrating ability of such electrolytes usually results in poor electrochemical performances of the ESDs. Herein, we adopted a hierarchical optimization strategy to address the aforementioned interfacial issues. Continuous ionic percolation throughout the hierarchical pores of the 3D electrode was formed by in-situ introducing an ionogel buffer layer. Benefiting from this, the rate of ions diffusing within electrodes was increased by 5 times. Furthermore, the kinetics of ions entering into nanopores was improved via introducing small size ions into ionic liquids (ILs) and adjusting the solvated structures. Both the capacity and rate performance of the electrochemical double layer capacitors (EDLCs) were improved. Additionally, the buffer layer exhibited sufficient thermostability to cooperate with poly(ether ether ketone) (PEEK)-based solid electrolyte. Consequently, the EDLCs exhibited excellent cycling stability (79% capacitance retention after 5000 cycles) at 120 °C and delivered a maximum energy density of 46.9 Wh kg−1 with a power density of 926.9 W kg−1. Our strategy is believed to be effective to cooperate with various solid electrolyte systems and offer a general design principle for durable and high performance EDLCs. [ABSTRACT FROM AUTHOR]

In recent years, shape control has received the most attention in the exploration of Pd nanocrystals (NCs). However, exploring an efficient approach for the systematic production of Pd NCs under similar reaction conditions still presents a significant challenge, which is significantly important to clearly explain the effectiveness of morphology on the catalytic activity of Pd NCs. We designed and accomplished a facile strategy for the morphology transformation between Pd nanosheets and Pd nanotetrahedra by simply controlling the reaction temperature. A growth mechanism was proposed based on TEM images of the time-dependent morphology evolution. The Pd nanosheets and Pd nanotetrahedra exhibit higher activity for the methanol oxidation reaction (MOR) and oxygen reduction reaction (ORR) compared with the benchmark Pd/C catalysts, and their activities are dependent on the morphology. In particular, Pd nanosheets show an increased activity by 3.81 (MOR) and 2.86 (ORR) times due to their large specific surface area and exposed facets. [ABSTRACT FROM AUTHOR]

Abstract: In this study, we have developed a simple and green method for one-pot synthesis of ultrathin gold nanocrystals attached to graphene through photo irradiation. High-yield ultrathin Au nanocrystals are distributed on the reduced graphene oxide, immediately followed by the deoxygenation of graphene oxide in the absence of chemical reductants and surfactants. The procedure has been thoroughly completed and the products have been analyzed by transmission electron microscopy (TEM), atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), etc. The results show that both graphene oxide and photo irradiation play essential roles in the formation of ultrathin Au nanocrystals. The nanohybrids also display excellent electro-catalytical performance to methanol oxidation. This study not only has potential in the applications of bio-sensing and fuel cells, but also provides new procedures for the preparation of metal/graphene nanomaterials. [Copyright &y& Elsevier]

Abstract: A novel hedgehog-like core/shell structure, consisting of a high density of vertically aligned graphene sheets and a thin graphene shell/a copper core (VGs-GS/CC), has been synthesized via a simple one-step synthesis route using radio-frequency plasma-enhanced chemical vapor deposition (RF-PECVD). Scanning and transmission electron microscopy investigations show that the morphology of this core/shell material could be controlled by deposition time. For a short deposition time, only multilayer graphene shell tightly surrounds the copper particle, while as the deposition time is relative long, graphene sheets extend from the surface of GS/CC. The GS can protect CC particles from oxidation. The growth mechanism for the obtained GS/CC and VGs-GS/CC has been revealed. Compared to VGs, VGs-GS/CC material exhibits a better electron field emission property. This investigation opens a possibility for designing a core/shell structure of different carbon–metal hybrid materials for a wide variety of practical applications. [Copyright &y& Elsevier]

Abstract: A hybrid material of graphene oxide (GO) sheets beaded with ZnO nanoparticles was prepared. The material extends over a few hundred square nanometers, in which the ZnO nanoparticles (average diameter (∼5nm)) are dispersed evenly on the GO sheet. Both the surface photovoltage or surface photocurrent intensity for the material are much stronger than for pure ZnO nanoparticles, meaning that the free charge carriers can effectively be transferred from ZnO nanoparticles to GO sheets, which can serve as a probe to monitor the electron transfer from excited ZnO to GO. Anchoring ZnO nanoparticles on two dimensional carbon nanostructures such as GO can pave a way towards the design of ordered nanostructure assemblies that can harvest light energy efficiently. [Copyright &y& Elsevier]

Abstract: In this work, graphite encapsulated Fe nanoparticles and thin carbon nanotubes (CNTs) supported on the pristine CNTs, respectively, were synthesized using plasma enhanced chemical vapor deposition via efficiently controlling the flow rate of discharging CH4 and H2 gas. The properties of the obtained hybrid materials were characterized with superconducting quantum interference and field emission measurements. The results showed that the encapsulated Fe nanoparticles had diameters ranging from 1 to 30nm, and this hybrid nanocomposite exhibited a ferromagnetic behavior at room temperature. Thin CNTs with an average diameter of 6nm were attached to the surface of the prepared CNTs, which exhibited a lower turn-on field and higher emission current density than the pristine CNTs. The Fe nanoparticles either encapsulated with graphite or used as catalyst for thin CNTs growth were all originated from the pyrolysis of ferrocene. [Copyright &y& Elsevier]