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The Intel Optane DC Persistent Memory Module (AEP), which is the first commercial available Non-Volatile Memory (NVM) product, offers comparable performance with DRAM while providing larger capacities and data persistence. Existing researches that substitute NVM with DRAM or hybridize them are either emulator-based or focused on how to improve the energy efficiency for writes. Unfortunately, the energy efficiency of the real AEP system is less explored. Based on real AEP, we observe that even though eliminating the DRAM-like refresh energy consumptions, AEP consumes significant different energy at different performance levels. Specifically, requests with time intervals (dispersed) underperform in both performance and energy efficiency when compared with the case of requests without time intervals (compact). This disparity and parallelism exploitation potentials motivate us to propose Sprint-AEP, an energy-efficiency-oriented scheduling method for AEP-equipped servers. Sprint-AEP fully activates adequate AEPs to serve most of the requests by deferring the write requests and prefetching the hottest data. The remaining AEPs will stay in idle mode with a low idle power to save energy. Besides, we also utilize the read parallelism to accelerate the sync and prefetching processes. Compared with energy-unaware AEP usages, our experimental results show that Sprint-AEP saves up to 26% energy with little performance degradation. 

A novelC₃symmetric 1,1’‐bi‐2‐naphthol‐based Schiff base (R,R,R)‐6has been synthesized which shows highly selective fluorescence enhancement with Zn²⁺among 21 metal cations examined. Its sensitivity and selectivity are found to be greater than other relatedC₂(1) andC₁[(R)‐9] symmetric compounds in the fluorescent recognition of Zn²⁺. The mechanistic study reveals that the selective fluorescence enhancement of the probe can be attributed to the formation of a unimolecular multidentate 6‐coordinated Zn²⁺complex.

 

2,2’‐Diformyl‐1,1’‐binaphthyl is found to exhibit highly enantioselective fluorescence enhancement in the presence of various β‐amino alcohols and base. It provides a new method to determine the enantiomeric composition of those substrates and has potential for high throughput analysis. Based on detailed spectroscopic analyses, it is proposed that a stereoselective cyclization of a β‐amino alcohol with the probe should occur to form a rigid macrocyclic intermediate, contributing to the greatly enhanced fluorescence.