Ultraviolet and visible integrated photonics enable applications in quantum information, sensing, and spectroscopy, among others. Few materials support low-loss photonics into the UV, and the relatively low refractive index of known depositable materials limits the achievable functionality. Here, we present a high-index integrated photonics platform based on HfO2and Al2O3composites deposited via atomic layer deposition (ALD) with low loss in the visible and near UV. We show that Al2O3incorporation dramatically decreases bulk loss compared to pure HfO2, consistent with inhibited crystallization due to the admixture of Al2O3. Composites exhibit refractive indexnfollowing the average of that of HfO2and Al2O3, weighted by the HfO2fractional compositionx. Atλ = 375 nm, composites withx = 0.67 exhibitn = 2.01, preserving most of HfO2’s significantly higher index, and 3.8(7) dB/cm material loss. We further present fully etched and cladded waveguides, grating couplers, and ring resonators, realizing a single-mode waveguide loss of 0.25(2) dB/cm inferred from resonators of 2.6 million intrinsic quality factor atλ = 729 nm, 2.6(2) dB/cm atλ = 405 nm, and 7.7(6) dB/cm atλ = 375 nm. We measure the composite’s thermo-optic coefficient (TOC) to be 2.44(3) × 10−5RIU/°C nearλ = 397 nm. This work establishes (HfO2)x(Al2O3)1−xcomposites as a platform amenable to integration for low-loss, high-index photonics spanning the UV to NIR.
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This content will become publicly available on May 23, 2026
Poorly quantified trends in ammonium nitrate remain critical to understand future urban aerosol control strategies
Despite decades of progress in reducing nitrogen oxide (NOx) emissions, ammonium nitrate (AN) remains the primary inorganic component of particulate matter (PM) in Los Angeles (LA). Using aerosol mass spectrometry over multiple years in LA illustrates the controlling dynamics of AN and their evolution over the past decades. These data suggest that much of the nitric acid (HNO3) production required to produce AN in LA occurs during the nighttime via heterogeneous hydrolysis of N2O5. Further, we show that US Environmental Protection Agency–codified techniques for measuring total PM2.5fail to quantify the AN component, while low-cost optical sensors demonstrate good agreement. While previous studies suggest that declining NOxhas reduced AN, we show that HNO3formation is still substantial and leads to the formation of many tens of micrograms per cubic meter of AN aerosol. Continued focus on reductions in NOxwill help meet the PM2.5standards in the LA basin and many other regions.
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- Award ID(s):
- 2131914
- PAR ID:
- 10629755
- Publisher / Repository:
- American Association for the Advancement of Science (AAAS)
- Date Published:
- Journal Name:
- Science Advances
- Volume:
- 11
- Issue:
- 21
- ISSN:
- 2375-2548
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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