Dec 4, 2024
3:30pm - 3:45pm
Hynes, Level 1, Room 109
Talisi Meyer1,Kevin Jiang1,Ching Chun Peng1,Reilly Lynch1,Richard Robinson1
Cornell University1
Talisi Meyer1,Kevin Jiang1,Ching Chun Peng1,Reilly Lynch1,Richard Robinson1
Cornell University1
The thiospinel group of nickel cobalt sulfides (Ni<i>x</i>Co3–<i>x</i>S4) are promising materials for energy applications such as supercapacitors, fuel cells, and solar cells. Solution-processible nanoparticles of Ni<i>x</i>Co3–<i>x</i>S4 have advantages of low cost and fabrication of high-performance energy devices due to their high surface-to-volume ratio, which increases the electrochemically active surface area and shortens the ionic diffusion path. The current approaches to synthesize Ni<i>x</i>Co3–<i>x</i>S4 nanoparticles are often based on hydrothermal or solvothermal methods that are difficult to scale up safely and efficiently and that preclude monitoring the reaction through aliquots, making optimization of size and dispersity challenging, typically resulting in aggregated nanoparticles with polydisperse sizes.<br/><br/>In this talk, I will discuss our scalable “heat-up” method to colloidally synthesize Ni<i>x</i>Co3–<i>x</i>S4 nanoparticles that are smaller than 15 nm in diameter with less than 15% in size dispersion, using two inexpensive, earth-abundant sulfur sources. The synthesis leverages the amino acid l-cysteine ethyl ester and elemental sulfur to provide tunable compositional control, yielding gram-scale quantities, and is applicable to multiple ternary metal sulfide systems. Our method provides a reliable synthetic pathway to produce phase-pure, low-dispersity, gram-scale nanoparticles of ternary metal sulfides. This method enhances the current capabilities of Ni<i>x</i>Co3–<i>x</i>S4 nanoparticles to meet the performance demands to improve renewable energy technologies.