In Situ Observation of the Electrochemical Lithiation of a Single SnO2 Nanowire Electrode

Fragile Tin Oxide Electrodes While tin oxide has a high energy density, and would thus make an attractive anode material for a Li-ion battery, it undergoes significant volume changes when Li is intercalated. The large strains cause cracking, pulverization, and a resultant loss of electrical conduction. Huang et al. (p. 1515; see the Perspective by Chiang) used in situ transmission electron microscopy on a single tin oxide nanowire to identify the physical changes that occur during intercalation and observed a moving cloud of dislocations that separated the reacted and unreacted sections. Upon completion of the electrochemical charging, the nanowire showed up to 90% elongation and a 35% increase in diameter. Transmission electron microscopy reveals dimensional changes in a tin oxide nanowire as it intercalates lithium. We report the creation of a nanoscale electrochemical device inside a transmission electron microscope—consisting of a single tin dioxide (SnO2) nanowire anode, an ionic liquid electrolyte, and a bulk lithium cobalt dioxide (LiCoO2) cathode—and the in situ observation of the lithiation of the SnO2 nanowire during electrochemical charging. Upon charging, a reaction front propagated progressively along the nanowire, causing the nanowire to swell, elongate, and spiral. The reaction front is a “Medusa zone” containing a high density of mobile dislocations, which are continuously nucleated and absorbed at the moving front. This dislocation cloud indicates large in-plane misfit stresses and is a structural precursor to electrochemically driven solid-state amorphization. Because lithiation-induced volume expansion, plasticity, and pulverization of electrode materials are the major mechanical effects that plague the performance and lifetime of high-capacity anodes in lithium-ion batteries, our observations provide important mechanistic insight for the design of advanced batteries.