This review investigates strategies for employing μ-IMERs for continuous biocatalysis via a top-down approach.

Food production in green crops is severely limited by low activity and poor specificity of D-ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCO) in natural photosynthesis (NPS). This work presents a scientific solution to overcome this problem by immobilizing RuBisCO into a microfluidic reactor, which demonstrates a continuous production of glucose precursor at 13.8 μmol g −1 RuBisCO min −1 from CO 2 and ribulose-1,5-bisphosphate. Experiments show that the RuBisCO immobilization significantly enhances enzyme stabilities (7.2 folds in storage stability, 6.7 folds in thermal stability), and also improves the reusability (90.4% activity retained after 5 cycles of reuse and 78.5% after 10 cycles). This work mimics the NPS pathway with scalable microreactors for continuous synthesis of glucose precursor using very small amount of RuBisCO. Although still far from industrial production, this work demonstrates artificial synthesis of basic food materials by replicating the light-independent reactions of NPS, which may hold the key to food crisis relief and future space colonization.

No abstract

D‐π‐A type 4‐((9‐phenylcarbazol‐3‐yl)ethynyl)‐N‐dodecyl‐1,8‐naphthalimide (CZNI) with a large dipole moment of 8.49 D and A‐π‐A type bis[(4,4′‐1,8‐naphthalimide)‐N‐dodecyl]ethyne (NINI) with a negligible dipole moment of 0.28 D, were smartly designed and synthesized to demonstrate the evidence of a molecular dipole as the dominant mechanism for controlling charge separation of organic semiconductors. In aqueous solution, these two novel naphthalimides can self‐assemble to form nanoribbons (NRs) that present significantly different traces of exciton dissociation dynamics. Upon photoexcitation of NINI‐NRs, no charge‐separated excitons (CSEs) are formed due to the large exciton binding energy, accordingly there is no hydrogen evolution. On the contrary, in the photoexcited CZNI‐NRs, the initial bound Frenkel excitons are dissociated to long‐lived CSEs after undergoing ultrafast charge transfer within ca. 1.25 ps and charge separation within less than 5.0 ps. Finally, these free electrons were injected into Pt co‐catalysts for reducing protons to H2 at a rate of ca. 417 μmol h−1 g−1, correspondingly an apparent quantum efficiency of ca. 1.3 % can be achieved at 400 nm.

We report a one-step strategy for the formation of an artificial photosystem I, with an enhanced coenzyme regeneration rate.

We consider a one-period two-echelon supply chain composed of a lossaverse supplier with yield randomness and a loss-averse retailer with demand uncertainty. At the beginning of the selling season, the retailer orders from the supplier via the wholesale price contract, and then the supplier makes his production decision. We derive the loss-averse retailer's optimal ordering policy and the lossaverse supplier's optimal production policy under these conditions. In addition, we discuss the effect of loss aversion on both parties' decision making and show how loss aversion contributes to decision bias. Furthermore, we find that the loss-averse retailer's optimal order quantity may increase in wholesale price and decrease in retail price which is differ from the risk-neutral case where the optimal order quantity is always decreasing in wholesale price and increasing in retail price. Finally, numerical examples are presented to illustrate how loss aversion and yield variance contribute to the supply chain performance.

Chloroplast of plants is a natural microfluidic reactor for natural photosynthesis, in which, the multi-enzymatic Calvin cycle is the key. In chloroplast, the Calvin cycle enzymes are reportedly attached to...

This paper reports a tunable in-plane optofluidic lens by continuously tuning a silicone oil-air interface from concave to convex using the dielectrophoresis (DEP) force. Two parallel glasses are bonded firmly on two sides by NOA 81(Norland Optical Adhesive 81) spacers, forming an open microfluidic channel. An ITO (indium tin oxide) strip and another unpatterned ITO layer are deposited on two glasses as the top and bottom electrodes. Initially, a capillary concave liquid-air interface is formed at the end of the open channel. Then the DEP force is enabled to continuously deform the interface (lens) from concave to convex. In the experiment, the focal length gradually decreases from about -1 mm to infinite and then from infinite to around + 1 mm when the driving voltage is increased from 0 V to 260 V. Particularly, the longitudinal spherical aberration (LSA) is effectively suppressed to have LSA < 0.04 when the lens is operated in the focusing state. This work is the first study of in-plane tunable lenses using the DEP force and possesses special merits as compared to the other reported tunable lenses that are formed by pumping different liquids or by temperature gradient, such as wide tunability, no need for continuous supply of liquids, low power consumption (~81 nJ per switching) due to the capacitor-type driving, and the use of only one type of liquid. Besides, its low aberration makes it favorable for light manipulation in microfluidic networks.