► A new Bayesian inference based two-stage support vector regression approach. ► Strong ability to identify and reconcile biased measurements under uncertainty. ► High accuracy and robustness for ...soft sensor predictions in batch bioprocess. ► Improved performance than SVR method in handling process uncertainty. ► Applied to fed-batch penicillin cultivation process with satisfactory results.
Inherent process and measurement uncertainty has posed a challenging issue on soft sensor development of batch bioprocesses. In this paper, a new soft sensor modeling framework is proposed by integrating Bayesian inference strategy with two-stage support vector regression (SVR) method. The Bayesian inference procedure is first designed to identify measurement biases and misalignments via posterior probabilities. Then the biased input measurements are calibrated through Bayesian estimation and the first-stage SVR model is thus built for output measurement reconciliation. The inferentially calibrated input and output data can be further used to construct the second-stage SVR model, which serves as the main model of soft sensor to predict new output measurements. The Bayesian inference based two-stage support vector regression (BI-SVR) approach is applied to a fed-batch penicillin cultivation process and the obtained soft sensor performance is compared to that of the conventional SVR method. The results from two test cases with different levels of measurement uncertainty show significant improvement of the BI-SVR approach over the regular SVR method in predicting various output measurements.
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GEOZS, IJS, IMTLJ, KILJ, KISLJ, NUK, OILJ, PNG, SAZU, SBCE, SBJE, UL, UM, UPCLJ, UPUK
Abstract
Na-ion cathode materials operating at high voltage with a stable cycling behavior are needed to develop future high-energy Na-ion cells. However, the irreversible oxygen redox reaction at ...the high-voltage region in sodium layered cathode materials generates structural instability and poor capacity retention upon cycling. Here, we report a doping strategy by incorporating light-weight boron into the cathode active material lattice to decrease the irreversible oxygen oxidation at high voltages (i.e., >4.0 V vs. Na
+
/Na). The presence of covalent B–O bonds and the negative charges of the oxygen atoms ensures a robust ligand framework for the NaLi
1/9
Ni
2/9
Fe
2/9
Mn
4/9
O
2
cathode material while mitigating the excessive oxidation of oxygen for charge compensation and avoiding irreversible structural changes during cell operation. The B-doped cathode material promotes reversible transition metal redox reaction enabling a room-temperature capacity of 160.5 mAh g
−1
at 25 mA g
−1
and capacity retention of 82.8% after 200 cycles at 250 mA g
−1
. A 71.28 mAh single-coated lab-scale Na-ion pouch cell comprising a pre-sodiated hard carbon-based anode and B-doped cathode material is also reported as proof of concept.
Replacement of CC unit with its isoelectronic BN unit in aromatics provides a new class of molecules with appealing properties, which have attracted great attention recently. In this Concept, we ...focus on BN‐substituted polycyclic aromatics with fused structures, and review their synthesis, photophysical, and redox properties, as well as their applications in organic electronics. We also present challenging synthetic targets, large BN‐ substituted polycyclic aromatics, such as regioregular BN heterosuperbenzenes, which can be viewed as BN‐doped nanographenes. Finally, we propose an atomically precise bottom‐up synthesis of structurally well‐defined BN‐doped graphenes.
A new super hero! BN substitution in aromatic systems could provide a new family of interesting compounds. In this Concept, the development of BN‐substituted polycyclic aromatics is reported, and their synthesis, properties and electronic applications are summarized. From monocyclic BN‐substituted benzene to polycyclic BN heteroaromatics (like BN heterosuperbenzene), the possible ways to structurally well‐defined BN‐doped graphenes are proposed.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SBCE, SBMB, UL, UM, UPUK
The predictive model based soft sensor technique has become increasingly important to provide reliable online measurements, facilitate advanced process control and optimization, and improve product ...quality in process industries. The conventional soft sensors are normally single-model based and thus may not be appropriate for processes with shifting operating phases or conditions and the underlying changing dynamics. In this study, a multiway Gaussian mixture model (MGMM) based adaptive kernel partial least-squares (AKPLS) method is proposed to handle online quality prediction of batch or semibatch processes with multiple operating phases. The three-dimensional measurement data are first preprocessed and unfolded into two-dimensional matrix. Then, the multiway Gaussian mixture model is estimated in order to identify and isolate different operating phases. Further, the process and quality measurements are separated into multiple segments corresponding to those identified phases, and the various localized kernel PLS models are built in the high-dimensional nonlinear feature space to characterize the shifting dynamics across different operating phases. Using Bayesian inference strategy, each process measurement sample of a new batch is classified into a particular phase with the maximal posterior probability, and thus, the local kernel PLS model representing the identical phase can be adaptively chosen for online quality variable prediction. The presented soft sensor modeling method is applied to a simulated multiphase penicillin fermentation process, and the computational results demonstrate that the proposed MGMM-AKPLS approach is superior to the conventional kernel PLS model in terms of prediction accuracy and model reliability.
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IJS, KILJ, NUK, PNG, UL, UM
Sodium‐ion batteries have gained much attention for their potential application in large‐scale stationary energy storage due to the low cost and abundant sodium sources in the earth. However, the ...electrochemical performance of sodium‐ion full cells (SIFCs) suffers severely from the irreversible consumption of sodium ions of cathode during the solid electrolyte interphase (SEI) formation of hard carbon anode. Here, a high‐efficiency cathode sodiation compensation reagent, sodium oxalate (Na2C2O4), which possesses both a high theoretical capacity of 400 mA h g−1 and a capacity utilization as high as 99%, is proposed. The implementation of Na2C2O4 as sacrificial sodium species is successfully realized by decreasing its oxidation potential from 4.41 to 3.97 V through tuning conductive additives with different physicochemical features, and the corresponding mechanism of oxidation potential manipulation is analyzed. Electrochemical results show that in the full cell based on a hard carbon anode and a P2‐Na2/3Ni1/3Mn1/3Ti1/3O2 cathode with Na2C2O4 as a sodium reservoir to compensate for sodium loss during SEI formation, the capacity retention is increased from 63% to 85% after 200 cycles and the energy density is improved from 129.2 to 172.6 W h kg−1. This work can provide a new avenue for accelerating the development of SIFCs.
The development of sodium‐ion batteries has been hindered so far by the irreversible consumption of sodium ions of the cathode during the solid electrolyte interphase formation. Therefore, in search of a safe, cost‐effective, and highly efficient cathode sodiation reagent, the feasibility of Na2C2O4 as a sodium reservoir source for enhancing the performance of sodium‐ion batteries is investigated.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SBCE, SBMB, UL, UM, UPUK
Chemical modification of electrode materials by heteroatom dopants is crucial for improving storage performance in rechargeable batteries. Electron configurations of different dopants significantly ...influence the chemical interactions inbetween and the chemical bonding with the host material, yet the underlying mechanism remains unclear. We revealed competitive doping chemistry of Group IIIA elements (boron and aluminum) taking nickel‐rich cathode materials as a model. A notable difference between the atomic radii of B and Al accounts for different spatial configurations of the hybridized orbital in bonding with lattice oxygen. Density functional theory calculations reveal, Al is preferentially bonded to oxygen and vice versa, and shows a much lower diffusion barrier than BIII. In the case of Al‐preoccupation, the bulk diffusion of BIII is hindered. In this way, a B‐rich surface and Al‐rich bulk is formed, which helps to synergistically stabilize the structural evolution and surface chemistry of the cathode.
A model study has been performed on Group IIIA element (boron and aluminum) co‐doped high‐nickel layered oxide cathode materials to understand competitive doping chemistry. A notable difference between the atomic radii of B and Al accounts for different spatial configurations of the hybridized orbital in bonding with lattice oxygen, resulting in the formation of a B‐rich surface and an Al‐rich bulk.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SBCE, SBMB, UL, UM, UPUK
In the past several decades, conducting polymers have achieved remarkable progress and have been widely applied as the active materials for optoelectronics. So far, p-type conducting polymers exhibit ...high conductivities over 1000 S cm–1 and thermoelectric performance comparable to that of inorganic materials; however, only a few n-type conducting polymers showed conductivities over 1 S cm–1 after doping. The low conductivity of n-type conducting polymers is considered as the major barrier for further enhancing their thermoelectric performances. In this perspective, we highlight the scientific and engineering challenges to enhance the conductivity of n-type polymer thermoelectric materials, including n-doping efficiency in n-type polymers, factors influencing charge carrier mobilities after doping, and stability of n-type conducting polymers. Recent development and strategies to address these issues and enhance the conductivity of n-type conjugated polymers are summarized and discussed, providing materials and device engineering guidelines for the future high-performance polymer thermoelectric materials research and development.
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IJS, KILJ, NUK, PNG, UL, UM
Layered transition metal oxide P2‐Na2/3Ni1/3Mn2/3O2 usually suffers from large‐volume phase transitions and different Na‐vacancy ordering during sodium (de)intercalation, incurring rapid capacity ...decline and poor rate capability. Herein, an effective strategy based on synergetic effect of selected multiple metal ions is designed for P2‐type cathodes with improved performance. The role of tetravalent titanium provides high redox potential, inactive divalent magnesium stabilizes the structure, and the monovalent lithium smooths the electrochemical curves. The combined analysis of in operando X‐ray diffraction, in operando X‐ray absorption spectroscopy and density functional theory calculations demonstrates the contribution of multi‐metal ions converts the unfavorable and large‐volume P2 to O2 transition into a moderate “Z”‐intergrowth structure by increasing the energy barrier of transition metal slab gliding. As a consequence, the resultant P2‐Na0.7Li0.03Mg0.03Ni0.27Mn0.6Ti0.07O2 electrode delivers a reversible capacity of 134 mAh g−1, a working voltage of 3.57 V, excellent cycling stability (82% of capacity retention after 200 cycles), and superior rate performance (110 mAh g−1 at 4 C). Full cells fabricated with a hard carbon anode achieve an energy density of 296 Wh kg−1. This study presents a route to rationally design cathode materials with this functionalization to improve the cell performance for sodium‐ion batteries.
Herein, a co‐substitution strategy is proposed for P2‐Na2/3Ni1/3Mn2/3O2 to realize high‐energy sodium‐ion batteries. On account of the synergetic effects of Li+ (suppressing Na‐vacancy ordering), Ti4+ (increasing redox potential), and Mg2+ (stabilizing structure), the as‐obtained Na0.7Li0.03Mg0.03Ni0.27Mn0.6Ti0.07O2 electrode demonstrates moderate phase transition behavior and superior electrochemical performance.
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FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SBCE, SBMB, UL, UM, UPUK
Mitofusin-2 (MFN2) is a dynamin-like GTPase that plays a central role in regulating mitochondrial fusion and cell metabolism. Mutations in MFN2 cause the neurodegenerative disease Charcot-Marie-Tooth ...type 2A (CMT2A). The molecular basis underlying the physiological and pathological relevance of MFN2 is unclear. Here, we present crystal structures of truncated human MFN2 in different nucleotide-loading states. Unlike other dynamin superfamily members including MFN1, MFN2 forms sustained dimers even after GTP hydrolysis via the GTPase domain (G) interface, which accounts for its high membrane-tethering efficiency. The biochemical discrepancy between human MFN2 and MFN1 largely derives from a primate-only single amino acid variance. MFN2 and MFN1 can form heterodimers via the G interface in a nucleotide-dependent manner. CMT2A-related mutations, mapping to different functional zones of MFN2, lead to changes in GTP hydrolysis and homo/hetero-association ability. Our study provides fundamental insight into how mitofusins mediate mitochondrial fusion and the ways their disruptions cause disease.
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