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A conventional dual-winding (DW) motor has two internal windings consisting of a master part and a slave part, each connected to a different electronic control unit (ECU) to realize a redundant system. However, existing DW motors have a problem related to heat generation in both the healthy mode and the faulty mode of the motor operation. In the healthy mode, unexpected overloads can cause both windings to burn out simultaneously due to equal heat distribution. If the current sensor fails to measure correctly, the motor may exceed the designed current density of 4.7 [Arms/mm2] under air-cooling conditions, further increasing burnout risk. External factors such as excessive load cycles or extreme heat conditions can further exacerbate this issue. In the faulty mode, the motor requires double the current to generate maximum torque, leading to rapid temperature increases and a high risk of overheating. To address these challenges, this paper proposes the design of a thermal fault-tolerant asymmetric dual-winding (ADW) motor, which improves heat management in both healthy and faulty modes for autonomous vehicles. A lumped-parameter thermal network (LPTN) with a piecewise stator-housing model (PSMs) was employed to evaluate the coil temperature during faulty operation. An optimal design approach, incorporating kriging modeling, Design of Experiments (DOE), and a genetic algorithm (GA), was also utilized. The results confirm that the proposed ADW motor design effectively reduces the risk of simultaneous burnout in the healthy mode and overheating in the faulty mode, offering a robust solution for autonomous vehicle applications. [ABSTRACT FROM AUTHOR]

Hydrogen (H2) gas, with its high calorimetric combustion energy and cleanness, is a green source of energy and an alternative to fossil fuels. However, it has a small kinetic diameter, with high diffusivity and a highly explosive nature. Hence, the reliable detection of H2 gas is essential in various fields such as fuel cells. Herein, we decorated ZnO nanoparticles (NPs) with Pd noble metal NPs, using UV irradiation to enhance their H2 gas-sensing performance. The synthesized materials were fully characterized in terms of their phases, morphologies, and chemical composition. Then, the sensing layer was deposited on the electrode-patterned glass substrate to make a transparent sensor. The fabricated transparent gas sensor was able to detect H2 gas at various temperatures and humidity levels. At 250 °C, the sensor exhibited the highest response to H2 gas. As a novelty of the present study, we successfully detected H2 gas in mixtures of H2/benzene and H2/toluene gases. The enhanced H2 gas response was related to the catalytic effect of Pd, the formation of heterojunctions between Pd and ZnO, the partial reduction of ZnO to Zn in the presence of H2 gas, and the formation of PdHx. With a high performance in a high response, good selectivity, and repeatability, we believe that the sensor developed in this study can be a good candidate for practical applications where the detection of H2 is necessary. [ABSTRACT FROM AUTHOR]

Flexible optoelectronics is the need of the hour as the market moves toward wearable and conformable devices. Crystalline π-conjugated materials offer high performance as active materials compared to their amorphous counterpart, but they are typically brittle. This poses a significant challenge that needs to be overcome to unfold their potential in optoelectronic devices. Unveiling the molecular packing topology and identifying interaction descriptors that can accommodate strain offers essential guiding principles for developing conjugated materials as active components in flexible optoelectronics. The molecular packing and interaction topology of eight crystal systems of dicyano-distyrylbenzene derivatives are investigated. Face-to-face π-stacks in an inclined orientation relative to the bending surface can accommodate expansion and compression with minimal molecular motion from their equilibrium positions. This configuration exhibits good compliance towards mechanical strain, while a similar structure with a criss-cross arrangement capable of distributing applied strain equally in opposite directions enhances the flexibility. Molecular arrangements that cannot reversibly undergo expansion and compression exhibit brittleness. In the isometric CT crystals, the disproportionate strength of the interactions along the bending plane and orthogonal directions makes these materials sustain a moderate bending strain. These results provide an updated explanation for the elastic bending in semiconducting π-conjugated crystals., (© 2024 Wiley-VCH GmbH.)