Jianyang Li

A scalable graphene sulfur composite synthesis for rechargeable lithium batteries with good capacity and excellent columbic efficiency.

Sulfur nanoparticles wrapped with a conductive graphene framework was synthesized with a high sulfur loading through a scalable one-step process. The graphene-coated sulfur nanostructured composite, when used as cathode for lithium sulfur battery, shows a reversible capacity of 808 mAh g(-1) at a rate of 210 mA g(-1) and an average columbic efficiency of ∼98.3% over 100 cycles. It is found that graphene oxide (GO) with a porous structure offers flexible confinement function that helps prevent the loss of active materials, thus extending the cycling life of the electrode. Moreover, reduced graphene oxide provides a conductive network surrounding the sulfur particles, which facilitates both electron transport and ion transportation. This novel one-step, all-solution-based process is scalable and provides a promising approach for potential industrial applications.

Life Cycle Environmental Impact of High-Capacity Lithium Ion Battery with Silicon Nanowires Anode for Electric Vehicles

Although silicon nanowires (SiNW) have been widely studied as an ideal material for developing high-capacity lithium ion batteries (LIBs) for electric vehicles (EVs), little is known about the environmental impacts of such a new EV battery pack during its whole life cycle. This paper reports a life cycle assessment (LCA) of a high-capacity LIB pack using SiNW prepared via metal-assisted chemical etching as anode material. The LCA study is conducted based on the average U.S. driving and electricity supply conditions. Nanowastes and nanoparticle emissions from the SiNW synthesis are also characterized and reported. The LCA results show that over 50% of most characterized impacts are generated from the battery operations, while the battery anode with SiNW material contributes to around 15% of global warming potential and 10% of human toxicity potential. Overall the life cycle impacts of this new battery pack are moderately higher than those of conventional LIBs but could be actually comparable when considering the uncertainties and scale-up potential of the technology. These results are encouraging because they not only provide a solid base for sustainable development of next generation LIBs but also confirm that appropriate nanomanufacturing technologies could be used in sustainable product development.

A Multilayered Silicon-Reduced Graphene Oxide Electrode for High Performance Lithium-Ion Batteries

A multilayered structural silicon-reduced graphene oxide electrode with superior electrochemical performance was synthesized from bulk Si particles through inexpensive electroless etching and graphene self-encapsulating approach. The prepared composite electrode presents a stable charge-discharge performance with high rate, showing a reversible capacity of 2787 mAh g(-1) at a charging rate of 100 mA g(-1), and a stable capacity over 1000 mAh g(-1) was retained at 1 A g(-1) after 50 cycles with a high columbic efficiency of 99% during the whole cycling process. This superior performance can be attributed to its novel multilayered structure with porous Si particles encapsulated, which can effectively accommodate the large volume change during the lithiation process and provide increased electrical conductivity. This facile low-cost approach offers a promising route to develop an optimized carbon encapsulated Si electrode for future industrial applications.

Enhanced photovoltaic performance of perovskite CH₃NH₃PbI₃ solar cells with freestanding TiO₂ nanotube array films.

Freestanding TiO2 nanotube array films are fabricated and first applied as electrodes in perovskite CH3NH3PbI3 sensitized solar cells. The device demonstrates improved light absorption with more than 90% of light absorbed in the whole visible range and a reduced charge recombination rate, leading to a significant improvement of the photocurrent and efficiency. This study suggests a promising way of improving the conversion efficiency of perovskite solar cells through novel electrodes.

Effects of amorphous and crystalline MoO3 coatings on the Li-ion insertion behavior of a TiO2 nanotube anode for lithium ion batteries

Amorphous and crystalline MoO3 coatings are synthesized on anodic TiO2 nanotube arrays by electrodeposition, as a self-standing, binder-free anode material in Li-ion batteries for enhancing the Li-ion insertion performance. The amorphous MoO3 layer is uniform and conformal with a thickness of 10 nm, and is converted into crystalline nanoparticles via thermal treatment. Our results show that both the coated TiO2 nanotubes deliver much higher areal capacities than bare nanotubes or a dense crystalline α-MoO3 film, while the crystalline α-MoO3 coating greatly increases the areal capacity of TiO2 nanotubes compared to the amorphous. The results are obtained at 1340 μA h cm−2 initial capacity for nanotubes with a crystalline coating, 977 μA h cm−2 for those with an amorphous coating and 342 μA h cm−2 for the bare ones. The significant enhancement is due to a combination of MoO3 with high specific capacity and TiO2 nanotube arrays with large surface area allowing uniform MoO3 deposition and rapid ionic transfer. Crystalline α-MoO3 is better than amorphous MoO3 and the coating medium is discussed in terms of chemical state, crystal defects, capacitive contributions and the charge–discharge kinetics in coated TiO2 nanotube electrodes.

Carbon nanotube-assisted growth of single-/multi-layer SnS2 and SnO2 nanoflakes for high-performance lithium storage

SnS2 nanoparticles and SnS2 nanoflake/CNTs composite are prepared by a low-cost facile hydrothermal method for their use in rechargeable Li-ion batteries. It is found that the presence of multi-walled CNTs during synthesis greatly affects the morphology of as-formed SnS2 nanostructures, and circinal single-layer and multilayer SnS2 nanoflakes enwrapped by CNTs are produced. The composite is further oxidized to porous SnO2 nanoflake/CNTs hybrid by annealing at 500 °C in air. The formation mechanism of SnS2/CNTs and SnO2/CNTs composites is examined. All the three materials are used as the anode in Li-ion batteries. The SnS2/CNTs composite delivers stronger cycling stability than the pure SnS2 anode. In tests the former exhibits excellent capacity retention of 91.5% at 100 mA g−1 over 50 cycles, while the latter displays 66.8%. The rate capability of SnS2/CNTs composite is much better than pure SnS2 as well. Redox reaction characteristics and Li-ion transfer kinetics at the two SnS2 anodes are studied by differential capacity plots and electrochemical impedance spectroscopy. It is discovered that the SnS2/CNTs composite with larger surface area allows faster Li-ion transfer kinetics, effective cushion of volume changes, and thus gains the improved Li-ion intercalation behaviours. The capacity of the tin-based anode can be further raised by transformation to a SnO2/CNTs hybrid that also delivers excellent rate and cycling performances.

3D Edge-Enriched Fe3C@C Nanocrystals with a Core-Shell Structure Grown on Reduced Graphene Oxide Networks for Efficient Oxygen Reduction Reaction

The design of highly active, stable, and low-cost oxygen reduction reaction (ORR) electrocatalysts to replace platinum-based materials is crucial to the development of renewable energy technologies. Herein, novel 3D edge-enriched Fe3 C@C nanocrystals with a core-shell structure grown on reduced graphene oxide (rGO) networks (Fe3 C@C/rGO) are reported as highly efficient and stable electrocatalysts for the ORR. The rGO nanosheets act as a host and provide vital support for local growth of edge-enriched Fe3 C@C nanocrystals, leading to a large surface area of 263 m2  g-1 and superstable hybrid structure. The unique structural design of the Fe3 C@C/rGO hybrid enables fast mass transport and a substantial number of exposed active edge sites for electrocatalytic reaction. The Fe3 C@C/rGO hybrid exhibits excellent ORR catalytic activity, with a high positive onset potential close to 1.0 V, a Tafel slope of 65 mV dec-1 , and excellent durability with only about 8 % current density decay at 0.8 V after 20 000 s continuous operation, which is superior to that of commercial Pt/C catalyst in an alkaline electrolyte.