Dynamic Channel Modeling for Indoor Millimeter-Wave Propagation Channels Based on Measurements

In this contribution, a recently conducted measurement campaign for indoor millimeter-wave propagation channels is introduced. A vector network analyzer (VNA)-based channel sounder was exploited to record the channel characteristics at the frequency band from 28-30 GHz. A virtual uniform circular array (UCA) with a radius of 0.25m was formed using a rotator with 360 steps. Moreover, by taking advantage of fiber-optic technique applied in the channel sounder, measurements at 50 positions were performed from an indoor hall to an indoor corridor along a long pre-defined route. A low-complexity highresolution propagation estimation (HRPE) algorithm is exploited to estimate the propagation parameters of multipath components (MPCs). Based on the HRPE estimation results, a novel clustering identification and tracking algorithm is proposed to trace clusters. Composite channel characteristics, cluster-level characteristics and dynamic (or birth-death) behaviours of the clusters are investigated, which constitute a dynamic model for the indoor millimeter-wave channel

Dynamic mmWave Channel Emulation in a Cost-Effective MPAC with Dominant-Cluster Concept

Millimeter-Wave (mmWave) massive multiple-input multiple-output (MIMO) has been considered as a key enabler for the fifth-generation (5G) communications. It is essential to design and test mmWave 5G devices under various realisticscenarios since the radio propagation channels pose intrinsic limitations on the performance. This requires emulating realistic dynamic mmWave channels in a reproducible manner in laboratories, which is the goal of this paper. In this contribution, we first illustrate the dominant-cluster(s) concept, where thenon-dominant clusters in the mmWave channels are pruned, for mmWave 5G devices applying massive MIMO beamforming. This demonstrates the importance and necessity to accurately emulate the mmWave channels at a cluster level rather than the composite-channel level. Thus, an over-the-air (OTA) emulationstrategy for dynamic mmWave channels is proposed based on the concept of dominant-cluster(s) in a sectored multiprobe anechoic chamber (SMPAC). The key design parameters including the probe number and the angular spacing of probes are investigated through comprehensive simulations. A cost-effective switch circuit is also designed for this purpose and validated in the simulation. Furthermore, a dynamic mmWave channel measured in an indoor scenario at 28-30 GHz is presented, where the proposed emulation strategy is also validated by reproducing the measured reality

Dynamic mmWave Channel Emulation in a Cost-Effective MPAC with Dominant-Cluster Concept

Millimeter-Wave (mmWave) massive multiple-input multiple-output (MIMO) has been considered as a key enabler for the fifth-generation (5G) communications. It is essential to design and test mmWave 5G devices under various realistic scenarios, since the radio propagation channels pose intrinsic limitations on the performance. This requires emulating realistic dynamic mmWave channels in a reproducible manner in laboratories, which is the goal of this paper. In this contribution, we firstly illustrate the dominant-cluster(s) concept, where the non-dominant clusters in the mmWave channels are pruned, for mmWave 5G devices applying massive MIMO beamforming. This demonstrates the importance and necessity to accurately emulate the mmWave channels at a cluster level rather than the composite-channel level. Thus, an over-the-air (OTA) emulation strategy for dynamic mmWave channels is proposed based on the concept of dominant-cluster(s) in a sectored multiprobe anechoic chamber (SMPAC). The key design parameters including the probe number and the angular spacing of probes are investigated through comprehensive simulations. A cost-effective switchcircuit is also designed for this purpose and validated in the simulation. Furthermore, a dynamic mmWave channel measured in an indoor scenario at 28-30 GHz is presented, where the proposed emulation strategy is also validated by reproducing the measured reality.Comment: Accepted by IEEE Transactions on Antennas and Propagatio

Development of a growth-coupled selection platform for directed evolution of heme biosynthetic enzymes in Corynebacterium glutamicum

Heme is an important tetrapyrrole compound, and has been widely applied in food and medicine industries. Although microbial production of heme has been developed with metabolic engineering strategies during the past 20 years, the production levels are relatively low due to the multistep enzymatic processes and complicated regulatory mechanisms of microbes. Previous studies mainly adopted the strategies of strengthening precursor supply and product transportation to engineer microbes for improving heme biosynthesis. Few studies focused on the engineering and screening of efficient enzymes involved in heme biosynthesis. Herein, a growth-coupled, high-throughput selection platform based on the detoxification of Zinc-protoporphyrin IX (an analogue of heme) was developed and applied to directed evolution of coproporphyrin ferrochelatase, catalyzing the insertion of metal ions into porphyrin ring to generate heme or other tetrapyrrole compounds. A mutant with 3.03-fold increase in kcat/KM was selected. Finally, growth-coupled directed evolution of another three key enzymes involved in heme biosynthesis was tested by using this selection platform. The growth-coupled selection platform developed here can be a simple and effective strategy for directed evolution of the enzymes involved in the biosynthesis of heme or other tetrapyrrole compounds

Quantifying Inactive Lithium in Lithium Metal Batteries

Inactive lithium (Li) formation is the immediate cause of capacity loss and catastrophic failure of Li metal batteries. However, the chemical component and the atomic level structure of inactive Li have rarely been studied due to the lack of effective diagnosis tools to accurately differentiate and quantify Li+ in solid electrolyte interphase (SEI) components and the electrically isolated unreacted metallic Li0, which together comprise the inactive Li. Here, by introducing a new analytical method, Titration Gas Chromatography (TGC), we can accurately quantify the contribution from metallic Li0 to the total amount of inactive Li. We uncover that the Li0, rather than the electrochemically formed SEI, dominates the inactive Li and capacity loss. Using cryogenic electron microscopies to further study the microstructure and nanostructure of inactive Li, we find that the Li0 is surrounded by insulating SEI, losing the electronic conductive pathway to the bulk electrode. Coupling the measurements of the Li0 global content to observations of its local atomic structure, we reveal the formation mechanism of inactive Li in different types of electrolytes, and identify the true underlying cause of low Coulombic efficiency in Li metal deposition and stripping. We ultimately propose strategies to enable the highly efficient Li deposition and stripping to enable Li metal anode for next generation high energy batteries

Arabidopsis R-SNARE Proteins VAMP721 and VAMP722 Are Required for Cell Plate Formation

Background: Cell plate formation during plant cytokinesis is facilitated by SNARE complex-mediated vesicle fusion at the cell-division plane. However, our knowledge regarding R-SNARE components of membrane fusion machinery for cell plate formation remains quite limited. Methodology/Principal Findings: We report the in vivo function of Arabidopsis VAMP721 and VAMP722, two closely sequence-related R-SNAREs, in cell plate formation. Double homozygous vamp721vamp722 mutant seedlings showed lethal dwarf phenotypes and were characterized by rudimentary roots, cotyledons and hypocotyls. Furthermore, cell wall stubs and incomplete cytokinesis were frequently observed in vamp721vamp722 seedlings. Confocal images revealed that green fluorescent protein-tagged VAMP721 and VAMP722 were preferentially localized to the expanding cell plates in dividing cells. Drug treatments and co-localization analyses demonstrated that punctuate organelles labeled with VAMP721 and VAMP722 represented early endosomes overlapped with VHA-a1-labeled TGN, which were distinct from Golgi stacks and prevacuolar compartments. In addition, protein traffic to the plasma membrane, but not to the vacuole, was severely disrupted in vamp721vamp722 seedlings by subcellular localization of marker proteins. Conclusion/Significance: These observations suggest that VAMP721 and VAMP722 are involved in secretory trafficking to the plasma membrane via TGN/early endosomal compartment, which contributes substantially to cell plate formatio