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A key challenge in millimeter-wave and terahertz wireless networks is blockage of the line-of-sight path between a base station and a user. User and environmental mobility can lead to blockage of highly directional beams by intervening people or objects, yielding link disruptions and poor quality of service. Here, we propose a solution to this problem which leverages the fact that, in such scenarios, users are likely to be located within the electromagnetic near field of the base station, which opens the possibility to engineer wave fronts for link maintenance. We show that curved beams, carrying data at high bit rates, can realize a link by curving around an intervening obstacle. We develop a model to analyze and experimentally evaluate the bandwidth limitations imposed by the use of self accelerating beams. We also demonstrate that such links employ the full aperture of the transmitter, even those portions which have no direct line of sight to the receiver, emphasizing that ray optics fails to capture the behavior of these near-field wave fronts. This approach, which is ideally suited for use at millimeter-wave and terahertz frequencies, opens vast new possibilities for wave front management in directional wireless networks.

By combining the unique characteristics of molecular bottlebrushes (MBBs) and the properties of stimuli‐responsive polymers, we show that MBBs with randomly grafted poly(n‐butyl acrylate) and pH‐responsive poly(2‐(N,N‐diethylamino)ethyl methacrylate) (PDEAEMA) side chains are efficient and robust pH‐responsive emulsifiers. Water‐in‐toluene emulsions were formed at pH 4.0 and disrupted by increasing the pH to 10.0. The emulsion generation and disruption was reversible over the ten cycles investigated, and the bottlebrushes remained intact. The exceptional emulsion stability stemmed from the high interfacial binding energy of MBBs, imparted by their large molecular size and Janus architecture at the interface, as evidenced by the interfacial jamming and wrinkling of the assemblies upon reducing the interfacial area. At pH 10.0, PDEAEMA became water‐insoluble, and the MBBs desorbed from the interface, causing de‐emulsification. Consequently, we have shown that the judicious design of MBBs can generate properties of particle emulsifiers from their large size, while the responsiveness of the MBBs enables more potential applications.

By combining the unique characteristics of molecular bottlebrushes (MBBs) and the properties of stimuli‐responsive polymers, we show that MBBs with randomly grafted poly(n‐butyl acrylate) and pH‐responsive poly(2‐(N,N‐diethylamino)ethyl methacrylate) (PDEAEMA) side chains are efficient and robust pH‐responsive emulsifiers. Water‐in‐toluene emulsions were formed at pH 4.0 and disrupted by increasing the pH to 10.0. The emulsion generation and disruption was reversible over the ten cycles investigated, and the bottlebrushes remained intact. The exceptional emulsion stability stemmed from the high interfacial binding energy of MBBs, imparted by their large molecular size and Janus architecture at the interface, as evidenced by the interfacial jamming and wrinkling of the assemblies upon reducing the interfacial area. At pH 10.0, PDEAEMA became water‐insoluble, and the MBBs desorbed from the interface, causing de‐emulsification. Consequently, we have shown that the judicious design of MBBs can generate properties of particle emulsifiers from their large size, while the responsiveness of the MBBs enables more potential applications.

Abstract. New particle formation (NPF) and subsequent particle growth are importantsources of condensation nuclei (CN) and cloud condensation nuclei (CCN).While many observations have shown positive contributions of NPF to CCN atlow supersaturation, negative NPF contributions were often simulated inpolluted environments. Using the observations in a coastal city of Qingdao,Beijing, and Gucheng in north China, we thoroughly evaluate the simulatednumber concentrations of CN and CCN using an NPF-explicit parameterizationembedded in the WRF-Chem model. For CN, the initial simulation shows largebiases of particle number concentrations at 10–40 and 40–100 nm. Byadjusting the process of gas–particle partitioning, including the massaccommodation coefficient (MAC) of sulfuric acid, the phase changes in primary organic aerosol emissions, and the condensational amount of nitric acid, the improvement of the particle growth process yields substantially reduced overestimation of CN. Regarding CCN, secondary organic aerosol (SOA) formed from the oxidation of semi-volatile and intermediate-volatility organic compounds (S/IVOCs) is called SI-SOA, the yield of which is an important contributor. At default settings, the SI-SOA yield is too high without considering the differences in precursor oxidation rates. Lowering the SI-SOA yield under linear H2SO4 nucleation scheme results in much-improved CCN simulations compared to observations. On the basis of the bias-corrected model, we find substantially positive contributions of NPF to CCN at low supersaturation (∼ 0.2 %) over broad areas of China, primarily due to competing effects of increasing particle hygroscopicity, a result of reductions in SI-SOA amount, surpassing that of particle size decreases. The bias-corrected model is robustly applicable to other schemes, such as the quadratic H2SO4 nucleation scheme, in terms of CN and CCN, though the dependence of CCN on SI-SOA yield is diminished likely due to changes in particle composition. This study highlights potentially much larger NPF contributions to CCN on a regional and even global basis.