High‐voltage Li‐metal batteries (LMBs) are regarded as next‐generation high‐energy‐density storage devices to apply to extensive fields such as electric vehicles, space explorations, subsea operations, and grid‐scale storages. Unfortunately, their practical applications are restricted by some defects of commercial carbonate electrolytes including flammability, low oxidation stability, narrow temperature operation window, and Li dendrites growth. Herein, a novel ultralow‐concentration electrolyte (ULCE, 0.1 m) is fabricated by dissolving lithium difluoro(oxalato)borate in N‐methyl‐N‐methoxyethyl‐pyrrolidinium bis(trifluoromethylsulfonyl)imide ([MEMP][TFSI]) ionic liquid and 1,1,2,2‐tetrafluoroethyl‐2,2,3,3‐tetrafluoropropylether. This advanced ULCE exhibits impressive merits including low cost, non‐flammability, wide operation temperature (−100 to +70 °C), and high electrochemical window (5.75 V). Meanwhile, it helps to suppress Li dendrite growth due to the combined effect of the cation shielding by MEMP+ cations and robust solid electrolyte interphase formed by the preferential decomposition of DFOB− and TFSI− anions. The LiNi0.6Co0.2Mn0.2O2 (NCM622)/Li cell with ULCE shows outstanding performance under a high voltage of 4.5 V and a wide temperature range from −60 to 70 °C. This work provides a distinctive sight to design advanced electrolyte for lower cost, safe, and wide‐temperature high‐energy‐density LMBs.

Phytate ( myo -inositol hexakisphosphate salts) can constitute a large fraction of the organic P in soils. As a more recalcitrant form of soil organic P, up to 51 million metric tons of phytate accumulate in soils annually, corresponding to ∼65% of the P fertilizer application. However, the availability of phytate is limited due to its strong binding to soils via its highly-phosphorylated inositol structure, with sorption capacity being ∼4 times that of orthophosphate in soils. Phosphorus (P) is one of the most limiting macronutrients for agricultural productivity. Given that phosphate rock is a finite resource, coupled with the increasing difficulty in its extraction and geopolitical fragility in supply, it is anticipated that both economic and environmental costs of P fertilizer will greatly increase. Therefore, optimizing the use of soil phytate-P can potentially enhance the economic and environmental sustainability of agriculture production. To increase phytate-P availability in the rhizosphere, plants and microbes have developed strategies to improve phytate solubility and mineralization by secreting mobilizing agents including organic acids and hydrolyzing enzymes including various phytases. Though we have some understanding of phytate availability and phytase activity in soils, the limiting steps for phytate-P acquisition by plants proposed two decades ago remain elusive. Besides, the relative contribution of plant- and microbe-derived phytases, including those from mycorrhizas, in improving phytate-P utilization is poorly understood. Hence, it is important to understand the processes that influence phytate-P acquisition by plants, thereby developing effective molecular biotechnologies to enhance the dynamics of phytate in soil. However, from a practical view, phytate-P acquisition by plants competes with soil P fixation, so the ability of plants to access stable phytate must be evaluated from both a plant and soil perspective. Here, we summarize information on phytate availability in soils and phytate-P acquisition by plants. In addition, agronomic approaches and biotechnological strategies to improve soil phytate-P utilization by plants are discussed, and questions that need further investigation are raised. The information helps to better improve phytate-P utilization by plants, thereby reducing P resource inputs and pollution risks to the wider environment.

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Phytate as a root exudate is rare in plants as it mainly serves as a P storage in the seeds; however, As-hyperaccumulator Pteris vittata effectively secretes phytate and utilizes phytate-P, especially under As exposure. This study investigated the effects of As on its phytate and phytase exudation and the impacts of As and/ or phytate on each other's uptake in P. vittata through two hydroponic experiments. Under 10−100 μM arsenate (AsV), the exudation of phytate and phytase by P. vittata was increased by 50− 72% to 20.4−23.4 μmol h −1 g −1 and by 28−104% to 18.6−29.5 nmol h −1 plant −1 , but they were undetected in non-hyperaccumulator Pteris ensiformis at 10 μM AsV. Furthermore, compared to 500 μM phytate, the phytate concentration in the growth media was reduced by 69% to 155 μM, whereas the P and As contents in P. vittata fronds and roots were enhanced by 68−134% and 44−81% to 2423−2954 and 82−407 mg kg −1 under 500 μM phytate plus 50 μM AsV. The increased P/As uptake in P. vittata was probably attributed to 3.0−4.5-fold increase in expressions of P transporters PvPht1;3−1;4. Besides, under As exposure, plant P may be converted to phytate in P. vittata roots, thereby increasing phytate's contents by 84% to 840 mg kg −1 . Overall, our results suggest that As-induced phytate/phytase exudation and phytate-P uptake stimulate its growth and As hyperaccumulation by P. vittata.

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