Dongchang Chen

Nickel-cobalt hydroxide nanosheets coated on NiCo2O4 nanowires grown on carbon fiber paper for high-performance pseudocapacitors.

A series of flexible nanocomposite electrodes were fabricated by facile electro-deposition of cobalt and nickel double hydroxide (DH) nanosheets on porous NiCo2O4 nanowires grown radially on carbon fiber paper (CFP) for high capacity, high energy, and power density supercapacitors. Among different stoichiometries of CoxNi1-xDH nanosheets studied, Co0.67Ni0.33 DHs/NiCo2O4/CFP hybrid nanoarchitecture showed the best cycling stability while maintaining high capacitance of ∼1.64 F/cm(2) at 2 mA/cm(2). This hybrid composite electrode also exhibited excellent rate capability; the areal capacitance decreased less than 33% as the current density was increased from 2 to 90 mA/cm(2), offering excellent specific energy density (∼33 Wh/kg) and power density (∼41.25 kW/kg) at high cycling rates (up to150 mA/cm(2)).

Hybrid Composite Ni(OH)(2)@NiCo2O4 Grown on Carbon Fiber Paper for High-Performance Supercapacitors

We have successfully fabricated and tested the electrochemical performance of supercapacitor electrodes consisting of Ni(OH)2 nanosheets coated on NiCo2O4 nanosheets grown on carbon fiber paper (CFP) current collectors. When the NiCo2O4 nanosheets are replaced by Co3O4 nanosheets, however, the energy and power density as well as the rate capability of the electrodes are significantly reduced, most likely due to the lower conductivity of Co3O4 than that of NiCo2O4. The 3D hybrid composite Ni(OH)2/NiCo2O4/CFP electrodes demonstrate a high areal capacitance of 5.2 F/cm(2) at a cycling current density of 2 mA/cm(2), with a capacitance retention of 79% as the cycling current density was increased from 2 to 50 mA/cm(2). The remarkable performance of these hybrid composite electrodes implies that supercapacitors based on them have potential for many practical applications.

Crosslinking Graphene Oxide into Robust 3D Porous N‐Doped Graphene

3D N-doped graphene crosslinked by covalent bonds is fabricated through thermal treatment of graphene oxide with a nitrogen-contained resin. The material possesses a hierarchical porous architecture, robust mechanical stability, and abundant N-doped properties. As an electrode material for supercapacitors, this multifunctional material exhibits an unprecedented specific capacitance, high rate capability, and excellent long-term cycle stability.

Dramatically enhanced reversibility of Li2O in SnO2-based electrodes: the effect of nanostructure on high initial reversible capacity

The formation of irreversible Li2O during discharge is believed to be the main cause of large capacity loss and low Coulombic efficiency of oxide negative electrodes for Li batteries. This assumption may have misguided the development of high-capacity SnO2-based anodes in recent years. Here we demonstrated that contrary to this perception, Li2O can indeed be highly reversible in a SnO2 electrode with controlled nanostructure and achieved an initial Coulombic efficiency of ∼95.5%, much higher than that previously believed to be possible (52.4%). In situ spectroscopic and diffraction analyses corroborate highly reversible electrochemical cycling, suggesting that the interfaces and grain boundaries of nano-sized SnO2 may suppress the coarsening of Sn and enable the conversion between Li2O and Sn to amorphous SnO2 when de-lithiated. These results provide important insight into the rational design of high-performance oxide electrodes for Li-ion batteries.

Oxygen- and Nitrogen-Enriched 3D Porous Carbon for Supercapacitors of High Volumetric Capacity.

Efficient utilization and broader commercialization of alternative energies (e.g., solar, wind, and geothermal) hinges on the performance and cost of energy storage and conversion systems. For now and in the foreseeable future, the combination of rechargeable batteries and electrochemical capacitors remains the most promising option for many energy storage applications. Porous carbonaceous materials have been widely used as an electrode for batteries and supercapacitors. To date, however, the highest specific capacitance of an electrochemical double layer capacitor is only ∼200 F/g, although a wide variety of synthetic approaches have been explored in creating optimized porous structures. Here, we report our findings in the synthesis of porous carbon through a simple, one-step process: direct carbonization of kelp in an NH3 atmosphere at 700 °C. The resulting oxygen- and nitrogen-enriched carbon has a three-dimensional structure with specific surface area greater than 1000 m(2)/g. When evaluated as an electrode for electrochemical double layer capacitors, the porous carbon structure demonstrated excellent volumetric capacitance (>360 F/cm(3)) with excellent cycling stability. This simple approach to low-cost carbonaceous materials with unique architecture and functionality could be a promising alternative to fabrication of porous carbon structures for many practical applications, including batteries and fuel cells.

A tailored double perovskite nanofiber catalyst enables ultrafast oxygen evolution

Rechargeable metal–air batteries and water splitting are highly competitive options for a sustainable energy future, but their commercialization is hindered by the absence of cost-effective, highly efficient and stable catalysts for the oxygen evolution reaction. Here we report the rational design and synthesis of a double perovskite PrBa0.5Sr0.5Co1.5Fe0.5O5+δ nanofiber as a highly efficient and robust catalyst for the oxygen evolution reaction. Co-doping of strontium and iron into PrBaCo2O5+δ is found to be very effective in enhancing intrinsic activity (normalized by the geometrical surface area, ∼4.7 times), as validated by electrochemical measurements and first-principles calculations. Further, the nanofiber morphology enhances its mass activity remarkably (by ∼20 times) as the diameter is reduced to ∼20 nm, attributed to the increased surface area and an unexpected intrinsic activity enhancement due possibly to a favourable eg electron filling associated with partial surface reduction, as unravelled from chemical titration and electron energy-loss spectroscopy.

Carbon fiber paper supported hybrid nanonet/nanoflower nickel oxide electrodes for high-performance pseudo-capacitors

A composite electrode consisting of hybrid nanonet/nanoflower NiO deposited on carbon fiber paper scaffolds demonstrates a much-improved areal capacitance (0.93 F cm−2) while maintaining high rate capability and excellent cycling life. These performance characteristics are attributed to the unique electrode architecture and the nanostructures of NiO. While the nanonet NiO with a high surface area greatly facilitates the redox reactions for charge storage, the porous nanoflowers further extend the active sites for the redox reactions, leading to fast Faradic reactions for efficient energy storage.

High-temperature surface enhanced Raman spectroscopy for in situ study of solid oxide fuel cell materials

In situ probing of surface species and incipient phases is vital to unraveling the mechanisms of chemical and energy transformation processes. Here we report Ag nanoparticles coated with a thin-film SiO2 shell that demonstrate excellent thermal robustness and chemical stability for surface enhanced Raman spectroscopy (SERS) study of solid oxide fuel cell materials under in situ conditions (at ∼400 °C).

A robust and active hybrid catalyst for facile oxygen reduction in solid oxide fuel cells

The sluggish oxygen reduction reaction (ORR) greatly reduces the energy efficiency of solid oxide fuel cells (SOFCs). Here we report our findings in dramatically enhancing the ORR kinetics and durability of the state-of-the-art La0.6Sr0.4Co0.2Fe0.8O3 (LSCF) cathode using a hybrid catalyst coating composed of a conformal PrNi0.5Mn0.5O3 (PNM) thin film with exsoluted PrOx nanoparticles. At 750 °C, the hybrid catalyst-coated LSCF cathode shows a polarization resistance of ∼0.022 Ω cm2, about 1/6 of that for a bare LSCF cathode (∼0.134 Ω cm2). Further, anode-supported cells with the hybrid catalyst-coated LSCF cathode demonstrate remarkable peak power densities (∼1.21 W cm−2) while maintaining excellent durability (0.7 V for ∼500 h). Near Ambient X-ray Photoelectron Spectroscopy (XPS) and Near Edge X-Ray Absorption Fine Structure (NEXAFS) analyses, together with density functional theory (DFT) calculations, indicate that the oxygen-vacancy-rich surfaces of the PrOx nanoparticles greatly accelerate the rate of electron transfer in the ORR whereas the thin PNM film facilitates rapid oxide-ion transport while drastically enhancing the surface stability of the LSCF electrode.

Deformable fibrous carbon supported ultrafine nano-SnO2 as a high volumetric capacity and cyclic durable anode for Li storage

Multidimensional fibrous carbon scaffolds, derived from carbonized filter papers (CFPs), were used to support SnO2 nanocrystals (NCs, with a size of 4–5 nm) to form a free-standing SnO2NC@CFP hybrid anode for Li-ion batteries. The SnO2NC particles are well accreted on the surfaces of 1D carbon fibers and 2D ultrathin carbon sheets while maintaining 3D interconnected pores of the carbon matrices for fast ionic transport. The SnO2NC@CFP hybrid electrode exhibits long-term higher energy density than the commercial graphite anode, and excellent rate capability, mainly due to good dispersion of SnO2 in the multidimensional conductive carbon. In particular, the reversible deformation of the flexible fibrous carbon matrices, as inferred from in situ Raman spectroscopy and SEM image analysis, facilitates stress release from the active SnO2NCs during discharge–charge cycling while maintaining the structural integrity of the self-supported SnO2NC@CFP anode. These demonstrate that the rational combination of the multidimensional architecture of deformable carbon with nanoscale active materials is ideally suited for high-performance Li-ion batteries.