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David J. Dvorak

Publications and source records attributed to David J. Dvorak.

3 recordsLinked to original sources

Advancing the Pareto front for thin-film materials using a self-driving laboratory

Useful materials must satisfy multiple objectives, where the optimization of one objective is often at the expense of another. The Pareto front reports the optimal trade-offs between competing objectives. Here we report a self-driving laboratory, "Ada", that defines the Pareto front of conductivities and processing temperatures for palladium films formed by combustion synthesis. Ada identified previously untested combustion synthesis conditions that resulted in the discovery of lower processing temperatures (below 200 °C) relative to the prior art for this technique (250 °C), a temperature difference that makes the coating of different commodity plastic materials possible (e.g., Nafion, polyethersulfone). These conditions enabled us to use combustion synthesis to spray coat uniform palladium films with moderate conductivity (1.1 $\times$ 10$^5$ S m$^{-1}$) at 191 °C. Spray coating at 226 °C yielded films with conductivities (2.0 $\times$ 10$^6$ S m$^{-1}$) comparable to those of sputtered films (2.0 to 5.8 $\times$ 10$^6$ S m$^{-1}$). This work shows how self-driving laboratories can discover materials satisfying multiple objectives.

cond-mat.mtrl-sci

Self-driving laboratory for accelerated discovery of thin-film materials

Discovering and optimizing commercially viable materials for clean energy applications typically takes over a decade. Self-driving laboratories that iteratively design, execute, and learn from material science experiments in a fully autonomous loop present an opportunity to accelerate this research. We report here a modular robotic platform driven by a model-based optimization algorithm capable of autonomously optimizing the optical and electronic properties of thin-film materials by modifying the film composition and processing conditions. We demonstrate this platform by using it to maximize the hole mobility of organic hole transport materials commonly used in perovskite solar cells and consumer electronics. This demonstration highlights the possibilities of using autonomous laboratories to discover organic and inorganic materials relevant to materials sciences and clean energy technologies.

physics.app-ph

Dopant-free molecular hole transport material that mediates a 20% power conversion efficiency in a perovskite solar cell

Organic molecular hole-transport materials (HTMs) are appealing for the scalable manufacture of perovskite solar cells (PSCs) because they are easier to reproducibly prepare in high purity than polymeric and inorganic HTMs. There is also a need to construct PSCs without dopants and additives to avoid formidable engineering and stability issues. We report here a power conversion efficiency (PCE) of 20.6% with a molecular HTM in an inverted (p-i-n) PSC without any dopants or interlayers. This new benchmark was made possible by the discovery that annealing a spiro-based dopant-free HTM (denoted DFH) containing redox-active triphenyl amine (TPA) units undergoes preferential molecular organization normal to the substrate. This structural order, governed by the strong intermolecular interactions of the DFH dioxane groups, affords high intrinsic hole mobility (1x10-3 cm2 V-1 s-1). Annealing films of DFH also enables the growth of large perovskite grains (up to 2 um) that minimize charge recombination in the PSC. DFH can also be isolated at a fraction of the cost of any other organic HTM.

physics.chem-ph