Halide perovskites enable polaritonic XY spin Hamiltonian at room temperature.

Exciton polaritons, the part-light and part-matter quasiparticles in semiconductor optical cavities, are promising for exploring Bose-Einstein condensation, non-equilibrium many-body physics and analogue simulation at elevated temperatures. However, a room-temperature polaritonic platform on par with the GaAs quantum wells grown by molecular beam epitaxy at low temperatures remains elusive. The operation of such a platform calls for long-lifetime, strongly interacting excitons in a stringent material system with large yet nanoscale-thin geometry and homogeneous properties. Here, we address this challenge by adopting a method based on the solution synthesis of excitonic halide perovskites grown under nanoconfinement. Such nanoconfinement growth facilitates the synthesis of smooth and homogeneous single-crystalline large crystals enabling the demonstration of XY Hamiltonian lattices with sizes up to 10 × 10. With this demonstration, we further establish perovskites as a promising platform for room temperature polaritonic physics and pave the way for the realization of robust mode-disorder-free polaritonic devices at room temperature.

Observation of Rydberg exciton polaritons and their condensate in a perovskite cavity.

The condensation of half-light half-matter exciton polaritons in semiconductor optical cavities is a striking example of macroscopic quantum coherence in a solid-state platform. Quantum coherence is possible only when there are strong interactions between the exciton polaritons provided by their excitonic constituents. Rydberg excitons with high principal value exhibit strong dipole-dipole interactions in cold atoms. However, polaritons with the excitonic constituent that is an excited state, namely Rydberg exciton polaritons (REPs), have not yet been experimentally observed. Here, we observe the formation of REPs in a single crystal CsPbBr3 perovskite cavity without any external fields. These polaritons exhibit strong nonlinear behavior that leads to a coherent polariton condensate with a prominent blue shift. Furthermore, the REPs in CsPbBr3 are highly anisotropic and have a large extinction ratio, arising from the perovskite's orthorhombic crystal structure. Our observation not only sheds light on the importance of many-body physics in coherent polariton systems involving higher-order excited states, but also paves the way for exploring these coherent interactions for solid-state quantum optical information processing.

Recovery and dormancy of nitrogen removal characteristics in the pilot-scale denitrification-partial nitrification-Anammox process for landfill leachate treatment.

The pilot-scale partial nitrification-anaerobic ammonia oxidation (PN-Anammox) process for landfill leachate treatment has been running stably for 2 years. The degradation characteristics of nitrogen removal performance of PN-Anammox in this system were discussed during shutdown, and different recovery strategies were analyzed from the perspective of economy and easy implementation. The results showed that during the 166 d dormancy period, the decrease in Anammox bacteria activity occurred earlier than that of Anammox bacteria, and both tended to slow down after 128 d. The recovery strategy of simulated wastewater was the fastest, followed by the pretreated landfill leachate recovery strategy with inoculation of some corresponding functional sludges, while the worst strategy was the direct pretreated landfill leachate recovery strategy. The recovery start-up of the pilot-scale PN-Anammox process further showed that microbial activities were difficult to recover simultaneously during operation using raw wastewater directly due to the presence of high NH4+-N levels and the coupling process, which easily led to the accumulation of NH4+-N or NO2-N, thereby inhibiting microbial activity. The addition of some functional bacteria was more conducive to the rapid recovery of microbial activity. This study provides a new strategy for the rapid recovery of microbial activity for the engineering application of the PN-Anammox process.

Room-temperature polariton quantum fluids in halide perovskites.

Quantum fluids exhibit quantum mechanical effects at the macroscopic level, which contrast strongly with classical fluids. Gain-dissipative solid-state exciton-polaritons systems are promising emulation platforms for complex quantum fluid studies at elevated temperatures. Recently, halide perovskite polariton systems have emerged as materials with distinctive advantages over other room-temperature systems for future studies of topological physics, non-Abelian gauge fields, and spin-orbit interactions. However, the demonstration of nonlinear quantum hydrodynamics, such as superfluidity and Cerenkov flow, which is a consequence of the renormalized elementary excitation spectrum, remains elusive in halide perovskites. Here, using homogenous halide perovskites single crystals, we report, in both one- and two-dimensional cases, the complete set of quantum fluid phase transitions from normal classical fluids to scatterless polariton superfluids and supersonic fluids-all at room temperature, clear consequences of the Landau criterion. Specifically, the supersonic Cerenkov wave pattern was observed at room temperature. The experimental results are also in quantitative agreement with theoretical predictions from the dissipative Gross-Pitaevskii equation. Our results set the stage for exploring the rich non-equilibrium quantum fluid many-body physics at room temperature and also pave the way for important polaritonic device applications.

[Improved on Nitrogen Removal of Anaerobic Ammonia Oxidation by Coupling Element Sulfur-based Autotrophic Short-cut Denitrification].

In order to enhance the removal of NO3--N in the ANAMMOX process, an element sulfur-based autotrophic short-cut denitrification (short-cut S0-SADN) was introduced by adding elemental sulfur to an ANAMMOX continuous flow reactor. The effects of different influent NH4+-N/NO2--N ratios on the nitrogen conversion and NO2--N competitive characteristics in the coupled system were investigated at (33±2)℃ and a pH of 7.8-8.2. The results showed that under different influent NH4+-N/NO2--N ratios (1:1.3, 1:1.5, 1:1, and 1:1.1), the average total nitrogen (TN) removal efficiency of the coupled system reached 96.78%, 97.21%, 94.68%, and 97.72%, respectively, which were much higher than the highest TN removal efficiency of the ANAMMOX theory (89%). Among them, the stable operation of deep nitrogen removal of the short-cut S0-SADN coupled with ANAMMOX was successfully achieved with an influent NH4+-N/NO2--N ratio of 1:1 or 1:1.1. Under the optimal influent NH4+-N/NO2--N ratio of 1:1.1, the concentrations of influent NH4+-N and NO2--N were 240 mg·L-1 and 265 mg·L-1, respectively, the TN removal rate reached 1.50 kg·(m3·d)-1, and the TN removal efficiency of ANAMMOX and S0-SADN pathways were stable at (95.68±1.22)% and (2.04±0.77)%, respectively. During the entire operational process, ANAMMOX always occupied an absolute advantage in the competition of substrate NO2--N, and the activity of ANAMMOX bacteria (NH4+-N/VSS) was stable at (0.166±0.008)kg·(kg·d)-1.

H2O2-activated triplet-triplet annihilation upconversion via modulation of the fluorescence quantum yields of the triplet acceptor and the triplet-triplet-energy-transfer efficiency.

Oxidation-activatable triplet­triplet annihilation (TTA) upconversion was achieved with 9,10-bis(diphenylphosphino)-anthracene (BDPPA, nonfluorescent) as an activatable triplet acceptor/emitter, which can be oxidized to BDPPA-O (highly fluorescent) by H2O2 under mild conditions, and thus TTA upconversion was switched on by H2O2.