A Yolk–Shell Structured Silicon Anode with Superior Conductivity and High Tap Density for Full Lithium‐Ion Batteries

The poor cycling stability resulting from the large volume expansion caused by lithiation is a critical issue for Si‐based anodes. Herein, we report for the first time of a new yolk–shell structured high tap density composite made of a carbon‐coated rigid SiO₂ outer shell to confine multiple Si NPs (yolks) and carbon nanotubes (CNTs) with embedded Fe₂O₃ nanoparticles (NPs). The high tap density achieved and superior conductivity can be attributed to the efficiently utilised inner void containing multiple Si yolks, Fe₂O₃ NPs, and CNTs Li⁺ storage materials, and the bridged spaces between the inner Si yolks and outer shell through a conductive CNTs “highway”. Half cells can achieve a high area capacity of 3.6 mAh cm^?2 and 95 % reversible capacity retention after 450 cycles. The full cell constructed using a Li‐rich Li₂V₂O₅ cathode can achieve a high reversible capacity of 260 mAh g^?1 after 300 cycles.     

A Sodiophilic Interphase‐Mediated,Dendrite‐Free Anode with Ultrahigh Specific Capacity for Sodium‐Metal Batteries

Despite efforts to stabilize sodium metal anodes and prevent dendrite formation, achieving long cycle life with high areal capacities remains difficult owing to a combination of complex failure modes that involve retardant uneven sodium nucleation and subsequent dendrite formation. Now, a sodiophilic interphase based on oxygen‐functionalized carbon nanotube networks is presented, which concurrently facilitates a homogeneous sodium nucleation and a dendrite‐free, lateral growth behavior upon recurring sodium plating/stripping processes. This sodiophilic interphase renders sodium anodes with an ultrahigh capacity of 1078 mAh g^?1 (areal capacity of 10 mAh cm^?2), approaching the theoretical capacity of 1166 mAh g^?1 of pure sodium, as well as a long cycle life up to 3000 cycles. Implementation of this anode allows for the construction of a sodium–air battery with largely enhanced cycling performance owing to the oxygen functionalization‐mediated, dendrite‐free sodium morphology.     

Facile One‐Pot,One‐Step Synthesis of a Carbon Nanoarchitecture for an Advanced Multifunctonal Electrocatalyst

A one‐pot/one‐step synthesis strategy was developed for the preparation of a nitrogen‐doped carbon nanoarchitecture with graphene‐nanosheet growth on the inner surface of carbon nanotubes (CNTs). The N‐graphene/CNT hybrids exhibit outstanding electrocatalytic activity for several important electrochemical reactions as a result of their unique morphology and defect structures, such as high but uniform nitrogen doping, graphene insertion into CNTs, considerable surface area, and the presence of iron nanoparticles. The high‐yield synthetic process features high efficiency, low‐cost, straightforward operation, and simple equipment.     

A One‐Dimensional Fluidic Nanogenerator with a High Power Conversion Efficiency

Electricity generation from flowing water has been developed for over a century and plays a critical role in our lives. Generally, heavy and complex facilities are required for electricity generation, while using these technologies for applications that require a small size and high flexibility is difficult. Here, we developed a fluidic nanogenerator fiber from an aligned carbon nanotube sheet to generate electricity from any flowing water source in the environment as well as in the human body. The power conversion efficiency reached 23.3 %. The fluidic nanogenerator fiber was flexible and stretchable, and the high performance was well‐maintained after deformation over 1 000 000 cycles. The fiber also offered unique and promising advantages, such as the ability to be woven into fabrics for large‐scale applications.     

Covalently Grafting Cobalt Porphyrin onto Carbon Nanotubes for Efficient CO2 Electroreduction

Molecular complexes with inexpensive transition‐metal centers have drawn extensive attention, as they show a high selectivity in the electrochemical conversion of CO₂ to CO. In this work, we propose a new strategy to covalently graft cobalt porphyrin onto the surface of a carbon nanotube by a substitution reaction at the metal center. Material characterization and electrochemical studies reveal that the porphyrin molecules are well dispersed at a high loading of 10 wt. %. As a result, the turnover frequency for CO formation is improved by a factor of three compared to traditional physically‐mixed catalysts with the same cobalt content. This leads to an outstanding overall current density of 25.1 mA cm^?2 and a Faradaic efficiency of 98.3 % at 490 mV overpotential with excellent long‐term stability. This work provides an effective pathway for the improvement of the performance of electrocatalysts that could inspire rational design of molecular catalysts in the future.     

Assembly of Ring‐Shaped Phosphorus within Carbon Nanotube Nanoreactors

A phosphorus allotrope that has not been observed so far, ring‐shaped phosphorus consisting of alternate P₈ and P₂ structural units, has been assembled inside multi‐walled carbon nanotube nanoreactors with inner diameters of 5–8 nm by a chemical vapor transport and reaction of red phosphorus at 500 °C. The ring‐shaped nanostructures with surrounding graphene walls are stable under ambient conditions. The nanostructures were characterized by high‐resolution transmission electron microscopy, scanning transmission electron microscopy, energy‐dispersive X‐ray spectroscopy, Raman scattering, attenuated total reflectance Fourier transform infrared spectroscopy, and X‐ray photoelectron spectroscopy.