Hongyang Zhao

Bio: Hongyang Zhao is an academic researcher from Xi'an Jiaotong University. The author has contributed to research in topics: Anode & Cathode. The author has an hindex of 32, co-authored 70 publications receiving 2376 citations. Previous affiliations of Hongyang Zhao include Hunan University & Xinjiang University.

Phosphorization boosts the capacitance of mixed metal nanosheet arrays for high performance supercapacitor electrodes.

Abstract: Binary transition metal phosphides hold immense potential as innovative electrode materials for constructing high-performance energy storage devices. Herein, porous binary nickel-cobalt phosphide (NiCoP) nanosheet arrays anchored on nickel foam (NF) were rationally designed as self-supported binder-free electrodes with high supercapacitance performance. Taking the combined advantages of compositional features and array architectures, the nickel foam supported NiCoP nanosheet array (NiCoP@NF) electrode possesses superior electrochemical performance in comparison with Ni-Co LDH@NF and NiCoO2@NF electrodes. The NiCoP@NF electrode shows an ultrahigh specific capacitance of 2143 F g-1 at 1 A g-1 and retained 1615 F g-1 even at 20 A g-1, showing excellent rate performance. Furthermore, a binder-free all-solid-state asymmetric supercapacitor device is designed, which exhibits a high energy density of 27 W h kg-1 at a power density of 647 W kg-1. The hierarchical binary nickel-cobalt phosphide nanosheet arrays hold great promise as advanced electrode materials for supercapacitors with high electrochemical performance.

A general salt-resistant hydrophilic/hydrophobic nanoporous double layer design for efficient and stable solar water evaporation distillation

Abstract: A novel and elegant hydrophilic/hydrophobic nanoporous double layer structure was designed and developed for efficient long-term water desalination. It contained a hydrophobic salt-resistant hierarchical layer of well-defined Cu2SnSe3 (or Cu2ZnSnSe4) nanosphere arrays for broad solar harvesting and water vapor evaporation, and a hydrophilic filter membrane for continuous water supply and vapor generation. The as-fabricated self-floatable devices achieve remarkable solar water evaporation performances (average evaporation rate: 1.657 kg m−2 h−1 and solar thermal conversion efficiency: 86.6% under one sun) with super stability for water distillation from seawater and wastewater containing organic dyes, heavy metals and bacteria.

Hydrothermal synthesis of nitrogen-doped graphene hydrogels using amino acids with different acidities as doping agents

Abstract: A one-pot hydrothermal route was developed for the preparation of nitrogen-doped graphene (NG) hydrogels using graphene oxide (GO) as a raw material and nine amino acids with different acidities (acidic, neutral and basic) as doping agents. The morphology, structure and composition of the prepared NG using three amino acids (DL-aspartic acid, acidic; L-glycine, neutral; L-arginine, basic) were characterized by SEM, nitrogen physisorption, Raman and XPS spectroscopy. Acidic amino acids yielded NG with a cross-linked 3D network with a large specific surface area of 367.1 m2 g−1, while NG arising from the use of basic amino acids showed a tightly stacked structure with a much smaller surface area of 10.5 m2 g−1. The charged amino acids, and the ensuing electrostatic interactions between the amino acid and GO, affect the morphology of NG, and ultimately affect its electrochemical performance. The samples prepared using acidic amino acids, with the lowest surface N content (1.0%) but the largest surface area, displayed high specific capacitance of 246 F g−1 at 3 A g−1. The microstructure, surface area and effective nitrogen content, mainly the pyridinic nitrogen group related to pseudocapacitance, play important roles in the capacitive performance of the NG samples.

MOF-derived porous Ni2P nanosheets as novel bifunctional electrocatalysts for the hydrogen and oxygen evolution reactions

Abstract: Transition metal phosphides (TMPs) are considered to be highly-efficient electrochemical catalysts, which have extraordinary capabilities to relieve the energy crisis and have gradually become prime candidates for application in energy conversion and storage devices. In this contribution, we report the preparation of porous Ni2P nanosheets in a controllable manner using NiO–MOF-74 as precursors, followed by a conventional phosphorization strategy. The porous Ni2P nanosheets exhibit excellent electrocatalytic performance towards the hydrogen evolution reaction (HER) with a low overpotential of 168 mV at a current density of 10 mA cm−2 in 1.0 M KOH and a small Tafel slope of 63 mV dec−1. The overpotential and Tafel slope of porous Ni2P nanosheets for the oxygen evolution reaction (OER) are 320 mV (10 mA cm−2) and 105 mV dec−1, respectively. In addition, both the HER and OER measurements demonstrate that porous Ni2P nanosheets have superior electrochemical stability in alkaline solution. The desirable electrocatalytic properties of the porous Ni2P nanosheets may be due to their larger surface area and favorable electrical conductivity. The porous structures of the Ni2P nanosheets provide pathways for electron conduction, which facilitates electron transfer and accelerates bubble (H2 and O2) diffusion on the surface of the electrode.

Electrochromic Poly(chalcogenoviologen)s as Anode Materials for High-Performance Organic Radical Lithium-Ion Batteries

Abstract: A series of electrochromic electron-accepting poly(chalcogenoviologen)s with multiple, stable, and reversible redox centers were used as anodic materials in organic radical lithium-ion batteries (ORLIBs). The introduction of heavy atoms (S, Se, and Te) into the viologen scaffold significantly improved the capacity and cycling stability of the ORLIBs. Notably, the poly(Te-BnV) anode was able to intercalate 20 Li ions and showed higher conductivity and insolubility in the electrolyte, thus contributing to a reversible capacity of 502 mAh g-1 at 100 mA g-1 when the Coulombic efficiency approached 100 %. The charged/discharged state of flexible electrochromic batteries fabricated from these anodic materials could be monitored visually owing to the unique electrochromic and redox properties of the materials. This study opens a promising avenue for the development of organic polymer-based electrodes for flexible hybrid visual electronics.

Sodium-ion batteries: present and future

Abstract: Energy production and storage technologies have attracted a great deal of attention for day-to-day applications. In recent decades, advances in lithium-ion battery (LIB) technology have improved living conditions around the globe. LIBs are used in most mobile electronic devices as well as in zero-emission electronic vehicles. However, there are increasing concerns regarding load leveling of renewable energy sources and the smart grid as well as the sustainability of lithium sources due to their limited availability and consequent expected price increase. Therefore, whether LIBs alone can satisfy the rising demand for small- and/or mid-to-large-format energy storage applications remains unclear. To mitigate these issues, recent research has focused on alternative energy storage systems. Sodium-ion batteries (SIBs) are considered as the best candidate power sources because sodium is widely available and exhibits similar chemistry to that of LIBs; therefore, SIBs are promising next-generation alternatives. Recently, sodiated layer transition metal oxides, phosphates and organic compounds have been introduced as cathode materials for SIBs. Simultaneously, recent developments have been facilitated by the use of select carbonaceous materials, transition metal oxides (or sulfides), and intermetallic and organic compounds as anodes for SIBs. Apart from electrode materials, suitable electrolytes, additives, and binders are equally important for the development of practical SIBs. Despite developments in electrode materials and other components, there remain several challenges, including cell design and electrode balancing, in the application of sodium ion cells. In this article, we summarize and discuss current research on materials and propose future directions for SIBs. This will provide important insights into scientific and practical issues in the development of SIBs.

Mn3O4-Graphene Hybrid as a High Capacity Anode Material for Lithium Ion Batteries

Abstract: We developed two-step solution-phase reactions to form hybrid materials of Mn3O4 nanoparticles on reduced graphene oxide (RGO) sheets for lithium ion battery applications. Mn3O4 nanoparticles grown selectively on RGO sheets over free particle growth in solution allowed for the electrically insulating Mn3O4 nanoparticles wired up to a current collector through the underlying conducting graphene network. The Mn3O4 nanoparticles formed on RGO show a high specific capacity up to ~900mAh/g near its theoretical capacity with good rate capability and cycling stability, owing to the intimate interactions between the graphene substrates and the Mn3O4 nanoparticles grown atop. The Mn3O4/RGO hybrid could be a promising candidate material for high-capacity, low-cost, and environmentally friendly anode for lithium ion batteries. Our growth-on-graphene approach should offer a new technique for design and synthesis of battery electrodes based on highly insulating materials.

Nanoarchitectonics for Transition-Metal-Sulfide-Based Electrocatalysts for Water Splitting.

Abstract: Heterogenous electrocatalysts based on transition metal sulfides (TMS) are being actively explored in renewable energy research because nanostructured forms support high intrinsic activities for both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). Herein, it is described how researchers are working to improve the performance of TMS-based materials by manipulating their internal and external nanoarchitectures. A general introduction to the water-splitting reaction is initially provided to explain the most important parameters in accessing the catalytic performance of nanomaterials catalysts. Later, the general synthetic methods used to prepare TMS-based materials are explained in order to delve into the various strategies being used to achieve higher electrocatalytic performance in the HER. Complementary strategies can be used to increase the OER performance of TMS, resulting in bifunctional water-splitting electrocatalysts for both the HER and the OER. Finally, the current challenges and future opportunities of TMS materials in the context of water splitting are summarized. The aim herein is to provide insights gathered in the process of studying TMS, and describe valuable guidelines for engineering other kinds of nanomaterial catalysts for energy conversion and storage technologies.

Review on recent advances in nitrogen-doped carbons: preparations and applications in supercapacitors

Abstract: It is of great interest to develop new carbon-based materials as electrodes for supercapacitors because the conventional electrodes of activated carbons in supercapacitors cannot meet the ever-increasing demands for high energy and power densities for electronic devices. Due to their high electronic conductivity and improved hydrophilic properties, together with their easy syntheses and functionalization, N-doped carbons have shown a great potential in energy storage and conversion applications. In this review, after a brief introduction of electrochemical capacitors, we summarize the advances, in the recent six years, in the preparation methods of N-doped carbons for applications in supercapacitors. We also discuss and predict futuristic research trends towards the design and syntheses of N-doped carbons with unique properties for electrochemical energy storage.