位敏型近贴聚焦光电倍增管的研制

报导了具有４×４矩阵阳极的位敏近贴聚焦光电倍增管的最新研究成果，以及它的基本工作原理、设计计算、性能和工艺技术难点。该管的主要技术性能指标与国外同类产品Ｒ１７１２－０１，Ｒ１７１２－０４水平相当。     

Mesoporous Carbon Nanofibers Embedded with MoS2 Nanocrystals for Extraordinary Li‐Ion Storage

MoS₂ nanocrystals embedded in mesoporous carbon nanofibers are synthesized through an electrospinning process followed by calcination. The resultant nanofibers are 100–150 nm in diameter and constructed from MoS₂ nanocrystals with a lateral diameter of around 7 nm with specific surface areas of 135.9 m² g^?1. The MoS₂@C nanofibers are treated at 450 °C in H₂ and comparison samples annealed at 800 °C in N₂. The heat treatments are designed to achieve good crystallinity and desired mesoporous microstructure, resulting in enhanced electrochemical performance. The small amount of oxygen in the nanofibers annealed in H₂ contributes to obtaining a lower internal resistance, and thus, improving the conductivity. The results show that the nanofibers obtained at 450 °C in H₂ deliver an extraordinary capacity of 1022 mA h g^?1 and improved cyclic stability, with only 2.3 % capacity loss after 165 cycles at a current density of 100 mA g^?1, as well as an outstanding rate capability. The greatly improved kinetics and cycling stability of the mesoporous MoS₂@C nanofibers can be attributed to the crosslinked conductive carbon nanofibers, the large specific surface area, the good crystallinity of MoS₂, and the robust mesoporous microstructure. The resulting nanofiber electrodes, with short mass‐ and charge‐transport pathways, improved electrical conductivity, and large contact area exposed to electrolyte, permitting fast diffusional flux of Li ions, explains the improved kinetics of the interfacial charge‐transfer reaction and the diffusivity of the MoS₂@C mesoporous nanofibers. It is believed that the integration of MoS₂ nanocrystals and mesoporous carbon nanofibers may have a synergistic effect, giving a promising anode, and widening the applicability range into high performance and mass production in the Li‐ion battery market.     

A Robust Ion‐Conductive Biopolymer as a Binder for Si Anodes of Lithium‐Ion Batteries

Binders have been reported to play a key role in improving the cycle performance of Si anode materials of lithium‐ion batteries. In this study, the biopolymer guar gum (GG) is applied as the binder for a silicon nano­particle (SiNP) anode of a lithium‐ion battery for the first time. Due to the large number of polar hydroxyl groups in the GG molecule, a robust interaction between the GG binder and the SiNPs is achieved, resulting in a stable Si anode during cycling. More specifically, the GG binder can effectively transfer lithium ions to the Si surface, similarly to polyethylene oxide solid electrolytes. When GG is used as a binder, the SiNP anode can deliver an initial discharge capacity as high as 3364 mAh g^?1, with a Coulombic efficiency of 88.3% at the current density of 2100 mA g^?1, and maintain a capacity of 1561 mAh g^?1 after 300 cycles. The study shows that the electrochemical performance of the SiNP anode with GG binder is significantly improved compared to that of a SiNP anode with a sodium alginate binder, and it demonstrates that GG is a promising binder for Si anodes of lithium‐ion batteries.     

Interpenetrated Gel Polymer Binder for High‐Performance Silicon Anodes in Lithium‐ion Batteries

Silicon has attracted ever‐increasing attention as a high‐capacity anode material in Li‐ion batteries owing to its extremely high theoretical capacity. However, practical application of silicon anodes is seriously hindered by its fast capacity fading as a result of huge volume changes during the charge/discharge process. Here, an interpenetrated gel polymer binder for high‐performance silicon anodes is created through in‐situ crosslinking of water‐soluble poly(acrylic acid) (PAA) and polyvinyl alcohol (PVA) precursors. This gel polymer binder with deformable polymer network and strong adhesion on silicon particles can effectively accommodate the large volume change of silicon anodes upon lithiation/delithiation, leading to an excellent cycling stability and high Coulombic efficiency even at high current densities. Moreover, high areal capacity of ～4.3 mAh/cm² is achieved based on the silicon anode using the gel PAA–PVA polymer binder with a high mass loading. In view of simplicity in using the water soluble gel polymer binder, it is believed that this novel binder has a great potential to be used for high capacity silicon anodes in next generation Li‐ion batteries, as well as for other electrode materials with large volume change during cycling.     

Unusual Formation of ZnCo2O4 3D Hierarchical Twin Microspheres as a High‐Rate and Ultralong‐Life Lithium‐Ion Battery Anode Material

A facile two‐step strategy involving a polyol method and subsequent thermal annealing treatment is successfully developed for the large‐scale preparation of ZnCo₂O₄ various hierarchical micro/nanostructures (twin mcrospheres and microcubes) without surfactant assistance. To the best of our knowledge, this is the first report on the synthesis of ZnCo₂O₄ mesoporous twin microspheres and microcubes. More significantly, based on the effect of the reaction time on the morphology evolution of the precursor, a brand‐new crystal growth mechanism, multistep splitting then in situ dissolution recrystallization accompanied by morphology and phase change, is first proposed to understand the formation of the 3D twin microshperes, providing new research opportunity for investigating the formation of novel micro/nanostructures. When evaluated as anode materials for lithium‐ion batteries (LIBs), ZnCo₂O₄ hierarchical microstructures exhibit superior capacity retention, excellent cycling stability at the 5 A g^?1 rate for 2000 cycles. Surprisingly, the ZnCo₂O₄ twin microspheres show an exceptionally high rate capability up to the 10 A g^?1 rate. It should be noted that such super‐high rate performance and cycling stability at such high charge/discharge rates are significantly higher than most work previously reported on ZnCo₂O₄ micro/nanostructures and ZnCo₂O₄‐based heterostructures. The ZnCo₂O₄ 3D hierarchical micro/nanostructures demonstrate the great potential as negative electrode materials for high‐performance LIBs.     

Dendrite‐Free Lithium Plating Induced by In Situ Transferring Protection Layer from Separator

Lithium (Li) metal anodes are regarded as a promising pathway to meet the rapidly growing requirements on high energy density cells, owing to their highest gravimetric capacity (3840 mAh g^?1) and their lowest redox potential. The application of Li metal anodes, however, is still hindered by undesired dendrites formation and endless consumption of liquid electrolyte due to a continuous reaction on interface of electrolyte/Li‐metal without a stable solid–electrolyte–interface (SEI) layer. A stable protection layer is formed on Li metal anode by in situ transferring the coating layer from polymer separator. The Li anode protection strategy is developed with an in situ formed protection layer transferred through the reduction of a coating layer on polymer separator. A PbZr_0.52Ti_0.48O₃ (PZT) coating layer on polypropylene (PP) separator is reduced by Li metal anode to produce a Pb metal containing composite layer, which could form Pb–Li alloy and adhere to the surface of Li metal anode after the reaction and improves the Li plating/stripping efficiency owing to the formation of a more homogenized electric field. Both the Li/Li symmetric cells and LiFePO₄/Li cells with this PZT precoated PP separators exhibit significantly improved Coulombic efficiency and cycling life.     

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.     

Lithiophilic MXene-Guided Lithium Metal Nucleation and Growth Behavior

The positive effects of a lithiophilic substrate on the electrochemical performance of lithium metal anodes are confirmed in several reports, while the understanding of lithiophilic substrate-guided lithium metal nucleation and growth behavior is still insufficient. In this study, the effect of a lithiophilic surface on lithium metal nucleation and growth behaviors is investigated using a large-area Ti₃C₂T_x MXene substrate with a large number of oxygen and fluorine dual heteroatoms. The use of the MXene substrate results in a high lithium-ion concentration as well as the formation of uniform solid–electrolyte-interface (SEI) layers on the lithiophilic surface. The solid–solid interface (MXene-SEI layer) significantly affects the surface tension of the deposited lithium metal nuclei as well as the nucleation overpotential, resulting in the formation of uniformly dispersed lithium nanoparticles ( ≈ 10–20 nm in diameter) over the entire MXene surface. The primary lithium nanoparticles preferentially coalesce and agglomerate into larger secondary particles while retaining their primary particle shapes. Subsequently, they form close-packed structures, resulting in a dense metal layer composed of particle-by-particle microstructures. This distinctive lithium metal deposition behavior leads to highly reversible cycling performance with high Columbic efficiencies >  99.0% and long cycle lives of over 1000 cycles.     

Engineering Carbon Distribution in Silicon-Based Anodes at Multiple Scales

The successful commercialization of promising silicon-based anode materials has been hampered by their poor cycling stability caused by the huge volume change. Integration of the carbon matrix with silicon-based (C/Si-based) anode materials has been demonstrated to be a powerful solution to achieve satisfactory electrochemical performance. This minireview aims to outline recent developments on C/Si-based composites, with the emphasis on the importance of carbon distribution at multiple scales. In addition, the forms of the carbon framework (carbon sources and doping of heteroatoms) have been summarized. Particularly, a novel C/Si-based hybrid with carbon distributed at the atomic scale has been highlighted.