The layered square-planar nickelates, Nd_n+1Ni_nO_2n+2, are an appealing system to tune the electronic properties of square-planar nickelates via dimensionality; indeed, superconductivity was recently observed in Nd₆Ni₅O₁₂ thin films. Here, we investigate the role of epitaxial strain in the competing requirements for the synthesis of the n = 3 Ruddlesden-Popper compound, Nd₄Ni₃O₁₀, and subsequent reduction to the square-planar phase, Nd₄Ni₃O₈. We synthesize our highest quality Nd₄Ni₃O₁₀ films under compressive strain on LaAlO₃ (001), while Nd₄Ni₃O₁₀ on NdGaO₃ (110) exhibits tensile strain-induced rock salt faults but retains bulk-like transport properties. A high density of extended defects forms in Nd₄Ni₃O₁₀ on SrTiO₃ (001). Films reduced on LaAlO₃ become insulating and form compressive strain-induced c-axis canting defects, while Nd₄Ni₃O₈ films on NdGaO₃ are metallic. This work provides a pathway to the synthesis of Nd_n+1Ni_nO_2n+2 thin films and sets limits on the ability to strain engineer these compounds via epitaxy.

The rare-earth nickelates possess a diverse set of collective phenomena including metal-to-insulator transitions, magnetic phase transitions, and upon chemical reduction, superconductivity. Here, we demonstrate epitaxial stabilization of layered nickelates in the Ruddlesden-Popper form ${\mathrm{Nd}}_{n+1}{\mathrm{Ni}}_n{\mathrm{O}}_{3n+1}$ using molecular beam epitaxy. By optimizing the stoichiometry of the parent perovskite ${\mathrm{NdNiO}}_3$, we can reproducibly synthesize the $n=1-5$ member compounds. X-ray absorption spectroscopy at the O $K$ and Ni $L$ edges indicate systematic changes in both the nickel-oxygen hybridization level and nominal nickel filling from $3d^8$ to $3d^7$ as we move across the series from $n=1$ to $\infty$. The $n=3-5$ compounds exhibit weakly hysteretic metal-to-insulator transitions with transition temperatures that depress with increasing order toward ${\mathrm{NdNiO}}_3$ $(n=\infty )$.

Developing novel antimicrobials capable of controlling multidrug-resistant bacterial pathogens is essential to restrict the use of antibiotics. Bacteriophages (phages) constitute a major resource that can be harnessed as an alternative to traditional antimicrobial therapies. Phage ZCSE2 was isolated among several others from raw sewage but was distinguished by broad-spectrum activity against Salmonella serovars considered pathogenic to humans and animals. Lytic profiles of ZCSE2 against a panel of Salmonella were determined together with low temperature activity and pH stability. The morphological features of the phage and host infection processes were characterized using a combination of transmission electron and atomic force microscopies. Whole genome sequencing of ZCSE2 produced a complete DNA sequence of 53,965 bp. No known virulence genes were identified in the sequence data, making ZCSE2 a good candidate for phage-mediated biological control purposes. ZCSE2 was further tested against S. Enteritidis in liquid culture and was observed to reduce the target bacterium to below the limits of detection from initial concentrations of 10⁷–10⁸ Colony Forming Units (CFU)/mL. With a broad host-range against pathogenic Salmonella serovars, phage ZCSE2 constitutes a potential tool against a major cause of human and animal disease.