Polymer electrolyte membrane water electrolysis (PEMWE) has been regarded as a promising technology for renewable hydrogen production. However, acidic oxygen evolution reaction (OER) catalysts with long‐term stability impose a grand challenge in its large‐scale industrialization. In this review, critical factors that may lead to catalyst's instability in couple with potential solutions are comprehensively discussed, including mechanical peeling, substrate corrosion, active‐site over‐oxidation/dissolution, reconstruction, oxide crystal structure collapse through the lattice oxygen‐participated reaction pathway, etc. Last but not least, personal prospects are provided in terms of rigorous stability evaluation criteria, in situ/operando characterizations, economic feasibility and practical electrolyzer consideration, highlighting the ternary relationship of structure evolution, industrial‐relevant activity and stability to serve as a roadmap towards the ultimate application of PEMWE.
2015) Design of exponential control charts based on average time to signal using a sequential sampling schemeExponential charts based on time-between-events (TBE) data are widely investigated and applied in various fields. The average time to signal (ATS) is used instead of the average run length to evaluate the performance of TBE charts, since the ATS involves both the number and the time of samples inspected until a signal occurs. An ATS-unbiased exponential control chart is proposed when the in-control parameter is known. Considering the need in practice to start monitoring a production process as soon as possible, a sequential sampling scheme is adopted and the in-control parameter is estimated by an unbiased and consistent estimator. Some specific guidelines to stop updating control limits are obtained from the relationship between the phase I sample size and the actual false alarm rate. Finally, two real examples are given to illustrate the implementation and efficiency of the proposed method.
concentration has increased from ≈277 ppm in 1750, prior to Industrial Revolution, to ≈410 ppm in 2019 and the average annual growth of carbon emission in 2018 and 2019 is greater than its 10-year average. [1] Thus, it is urgent to search for renewable and zero-carbon energy sources as alternatives to replace fossil fuels. [2] Although solar, wind and tidal energy are abundant and sustainable, their intermittent and weather-dependent limitations require development and deployment of highly efficient energy conversion and storage systems at large scale to bridge the time gap between supply and demand. [3] An attractive solution is to convert the electrical energy derived from the aforementioned renewable energy sources into chemical energy in the form of hydrogen. [4,5] Pure or mixed hydrogen is playing important roles in transportation, industrial sectors, and chemical transformation processes. [6] However, at present, 95% of hydrogen is still produced by reforming of fossil fuels that emits significant amount of CO 2 and only 4% is through water electrolysis, mainly owing to the much higher production cost of the latter. [7] Therefore, crucial to enable this sustainable vision is to improve the efficiency and scalability of water electrolysis technology.
Self-propelled droplet jumping plays a crucial role in numerous applications such as condensation heat transfer, self-cleaning, and water harvesting. Compared to individual droplet jumping, the coalescence-induced droplet jumping in a domino manner has attracted more attention due to its potential for the high performance of droplet mobility and heat transfer. However, there is an apparent gap in the current literature regarding the demonstration of the advantage of this preferred droplet transport in a well-controlled way. In this study, we report the attainment of droplet jumping relay by designing a nanosheet-covered superhydrophobic surface with V-shaped macrogrooves (Groove-SHS). We find that the macrogroove arrays can significantly modify the droplet dynamics in the presence of a non-condensable gas (NCG) by coupling rapid droplet growth and efficient droplet removal by jumping relay. The condensate droplets formed through the NCG diffusion layer on top of the cones and between the grooves serve as more efficient conduits for heat transfer. The droplets with higher mobility formed on the bottom of the grooves can undergo a series of coalescence which results in the preferred droplet jumping relay. Such a droplet jumping relay can induce a considerable vibration for triggering the removal of droplets on top of the cones. The condensation performance of the Groove-SHS is increased by 60% compared to that of the flat superhydrophobic surface due to the synergistic effect of rapid droplet growth and efficient droplet removal facilitated by the integration of the droplet jumping relay. The mechanisms revealed in this work pave the way for dropwise condensation enhancement.
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