• Energy Research

Lithium (Li) pulverization and associated large volume expansion during cycling is one of the most critical barriers for the safe operation of Li-metal batteries. Here, we report an approach to minimize the Li pulverization using an electrolyte based on a fluorinated orthoformate solvent. The solid–electrolyte interphase (SEI) formed in this electrolyte clearly exhibits a monolithic feature, which is in sharp contrast with the widely reported mosaic- or multilayer-type SEIs that are not homogeneous and could lead to uneven Li stripping/plating and fast Li and electrolyte depletion over cycling. The highly homogeneous and amorphous SEI not only prevents dendritic Li formation, but also minimizes Li loss and volumetric expansion. Furthermore, this new electrolyte strongly suppresses the phase transformation of the LiNi0.8Co0.1Mn0.1O2 cathode (from layered structure to rock salt) and stabilizes its structure. Tests of high-voltage Li||NMC811 cells show long-term cycling stability and high rate capability, as well as reduced safety concerns. Parasitic reactions between Li metal and electrolytes need to be mitigated in Li-metal batteries. Here, the authors report the use of a fluorinated orthoformate-based electrolyte, leading to a monolithic solid–electrolyte interphase and subsequently a high-performance Li-metal battery.

Co-deposition of carbon atoms with hydrogen isotopes and hydrogenated carbon radicals and molecules is recognized as the main mechanism for tritium retention in the graphite walls of the previous tokamak fusion devices. Significant tritium retention would be a serious concern for safe and economic long-term operation of future fusion test reactors and fusion energy systems. Similar deposits are observed on the surface of the engineered components in a tritium-producing assembly, known as a Tritium-Producing Burnable Absorber Rod (TPBAR). Characterization of the deposits can help understand the tritium transport, accumulation history and distribution in TPBARs. This study reports our recent results from the carbonaceous deposits formed on an aluminide-coated cladding in the lower plenum of a TPBAR following thermal neutron irradiation. The observed deposits are amorphous in nature, consisting of flakes of interconnected nanoscale features. They contain primarily double-bonded carbon (e.g., alkene) and carbonyl carbon, as well as a minor fraction of aliphatic carbon, all of which are likely tritiated. A similar co-deposition process that occurred in previous fusion devices is responsible for the formation and growth of the carbonaceous deposits.

Cobalt (Co)-free ultrahigh-nickel (Ni) layered oxides exhibit dual competitive advantages in reducing the cathode cost and boosting the energy density, promising the sustainable development of batt...