AN INFORMATIVE PIPELINING WITH SCHEDULING REGULATOR TO SUPPORT RECOVERY

Within this work, we apply Razor to hardware accelerators that find growing application in System-on-Nick designs rich in-performance needs that must definitely be delivered under stringent power budgets. We exploit these traits usual for DSP and image-processing accelerators to apply Razor recovery in manner that's amenable to RTL validation and verification. We describe the implementation and plastic measurement is a result of a Razor-based hardware loop-accelerator (RZLA), applying the Sobel edge-recognition formula. Unlike microprocessors, the RZLA pipeline is data path-dominated with statically-scheduled control which has queue-based storage structures that are simply extended to aid check-pointing and recovery. The RFF is deployed along with an amount-sensitive latch-insertion based formula to deal with the minimum-delay constraint contained in all Razor systems. This formula enables using the time period for timing speculation resulting in robust error recognition and correction across a large dynamic current- and frequency-scaling range

Synthesis of Hierarchically Porous SnO2 Microspheres and Performance Evaluation as Li-Ion Battery Anode by Using Different Binders

We have prepared nanoporous SnO2 hollow microspheres (HMS) by employing the resorcinol-formaldehyde (RF) gel method. Further, we have investigated the electrochemical property of SnO2−HMS as negative electrode material in rechargeable Li-ion batteries by employing three different binderspolyvinylidene difluoride (PVDF), Na salt of carboxy methyl cellulose (Na-CMC), and Na-alginate. At 1C rate, SnO2 electrode with Na-alginate binder exhibits discharge capacity of 800 mA h g−1, higher than when Na- CMC (605 mA h g−1) and PVDF (571 mA h g−1) are used as binders. After 50 cycles, observed discharge capacities were 725 mA h g−1, 495 mA h g−1, and 47 mA h g−1, respectively, for electrodes with Na-alginate, Na-CMC, and PVDF binders that amounts to a capacity retention of 92%, 82%, and 8% . Electrochemical impedance spectroscopy (EIS) results confirm that the SnO2 electrode with Na-alginate as binder had much lower charge transfer resistance than the electrode with Na-CMC and PVDF binders. The superior electrochemical property of the SnO2 electrode containing Na-alginate can be attributed to the cumulative effects arising from integration of nanoarchitecture with a suitable binder; the hierarchical porous structure would accommodate large volume changes during the Li interaclation− deintercalation process, and the Na-alginate binder provides a stronger adhesion betweeen electrode film and current collecto

Synthesis of Hierarchically Porous SnO₂ Microspheres and Performance Evaluation as Li-Ion Battery Anode by Using Different Binders

We have prepared nanoporous SnO₂ hollow microspheres (HMS) by employing the resorcinol-formaldehyde (RF) gel method. Further, we have investigated the electrochemical property of SnO₂–HMS as negative electrode material in rechargeable Li-ion batteries by employing three different binderspolyvinylidene difluoride (PVDF), Na salt of carboxy methyl cellulose (Na-CMC), and Na-alginate. At 1C rate, SnO₂ electrode with Na-alginate binder exhibits discharge capacity of 800 mA h g^–1, higher than when Na-CMC (605 mA h g^–1) and PVDF (571 mA h g^–1) are used as binders. After 50 cycles, observed discharge capacities were 725 mA h g^–1, 495 mA h g^–1, and 47 mA h g^–1, respectively, for electrodes with Na-alginate, Na-CMC, and PVDF binders that amounts to a capacity retention of 92%, 82%, and 8% . Electrochemical impedance spectroscopy (EIS) results confirm that the SnO₂ electrode with Na-alginate as binder had much lower charge transfer resistance than the electrode with Na-CMC and PVDF binders. The superior electrochemical property of the SnO₂ electrode containing Na-alginate can be attributed to the cumulative effects arising from integration of nanoarchitecture with a suitable binder; the hierarchical porous structure would accommodate large volume changes during the Li interaclation–deintercalation process, and the Na-alginate binder provides a stronger adhesion betweeen electrode film and current collector