Abstract. Atmospheric oxidation capacity is the basis for converting freshly emitted substances into secondary products and is dominated by reactions involving hydroxyl radicals (OH) during daytime. In this study, we present in situ measurements of ROx radical (hydroxy OH, hydroperoxy HO2, and organic peroxy RO2) precursors and products; the measurements are carried out in four Chinese megacities (Beijing, Shanghai, Guangzhou, and Chongqing) during photochemically polluted seasons. The atmospheric oxidation capacity is evaluated using an observation-based model and radical chemistry precursor measurements as input. The radical budget analysis illustrates the importance of HONO and HCHO photolysis, which account for ∼50 % of the total primary radical sources. The radical propagation is efficient due to abundant NO in urban environments. Hence, the production rate of secondary pollutants, that is, ozone (and fine-particle precursors (H2SO4, HNO3, and extremely low volatility organic compounds, ELVOCs) is rapid, resulting in secondary air pollution. The ozone budget demonstrates its high production in urban areas; also, its rapid transport to downwind areas results in rapid increase in local ozone concentrations. The O3–NOx–VOC (volatile organic compound) sensitivity tests show that ozone production is VOC-limited and that alkenes and aromatics should be mitigated first for ozone pollution control in the four studied megacities. In contrast, NOx emission control (that is, a decrease in NOx) leads to more severe ozone pollution. With respect to fine-particle pollution, the role of the HNO3–NO3 partitioning system is investigated using a thermal dynamic model (ISORROPIA 2). Under high relative humidity (RH) and ammonia-rich conditions, nitric acid converts into nitrates. This study highlights the efficient radical chemistry that maintains the atmospheric oxidation capacity in Chinese megacities and results in secondary pollution characterized by ozone and fine particles.

During the COVID-19 lockdown period (from January 23 to February 29, 2020), ambient PM 2.5 concentrations in the Yangtze River Delta (YRD) region were observed to be much lower, while the maximum daily 8 h average (MDA8) O 3 concentrations became much higher compared to those before the lockdown (from January 1 to 22, 2020). Here, we show that emission reduction is the major driving force for the PM 2.5 change, contributing to a PM 2.5 decrease by 37% to 55% in the four YRD major cities (i.e., Shanghai, Hangzhou, Nanjing, and Hefei), but the MDA8 O 3 increase is driven by both emission reduction (29%–52%) and variation in meteorological conditions (17%– 49%). Among all pollutants, reduction in emissions mainly of primary PM contributes to a PM 2.5 decrease by 28% to 46%, and NOx emission reduction contributes 7% to 10%. Although NOx emission reduction dominates the MDA8 O 3 increase (38%–59%), volatile organic compounds (VOCs) emission reduction lead to a 5% to 9% MDA8 O 3 decrease. Increased O 3 promotes secondary aerosol formation and partially offsets the decrease of PM 2.5 caused by the primary PM emission reductions. The results demonstrate that more coordinated air pollution control strategies are needed in YRD.

Over the past six decades, ferroelectric ceramics including lead or lead-free oxide-based solid solutions, such as Pb(Zr,Ti)O 3 (PZT), BaTiO 3 (BT), etc., have been predominating in the piezoelectric materials and devices field and market. [1][2][3][4] However, their piezoelectricity is far inferior to that of recently developed relaxor ferroelectric-PbTiO 3 solid solution single crystals. [5][6][7][8][9][10] Under an applied stress or electric field bias the piezoelectric performance of the ceramics could be improved, but the increase in the piezoelectric constant d 33 is limited. [11][12][13][14] On the other hand, the relaxor-based piezocrystals suffer from a low Curie temperature, an even lower depoling temperature, and a low coercive field, making them unsuitable for high-temperature and high-power applications. Here, we report novel ferroelectric ceramics (0.95-x)BiScO 3 -xPbTiO 3 -0.05Pb(Sn 1/3 Nb 2/3 )O 3 (BS-xPT-PSN) of complex perovskite structure with compositions near the morphotropic phase boundary (MPB), which exhibit a piezoelectric coefficient d 33 = 555 pC/N, a large-signal coefficient * 33 d  1200 pm/V at temperature, and a high Curie temperature T C of 408 o C. More interestingly, this ternary exhibits a giant and stable piezoelectric response at 200 o C with a large-signal * 33 d  2500 pm/V, matching that of the costly relaxor-based piezoelectric single crystals at room temperature. The mechanisms of such giant piezoelectricity and its characteristic temperature dependence are attributed to the spontaneous polarization rotation and extension under an This article is protected by copyright. All rights reserved. 3 electric field and the MPB-related phase transition. Our findings reveal that the BS-xPT-PSN ceramics constitute a new family of high-performance piezoelectric materials suitable for electromechanical transducers that can be operated at high temperatures (at 200 ºC, or

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Abstract. A high-resolution air pollutant emission inventory for the Yangtze River Delta (YRD) region was updated for 2017 using emission factors and chemical speciation based mainly on local measurements in this study. The inventory included 424 non-methane volatile organic compounds (NMVOCs) and 43 fine particulate matter (PM2.5) species from 259 specific sources. The total emissions of SO2, NOx, CO, NMVOCs, PM10, PM2.5, and NH3 in the YRD region in 2017 were 1552, 3235, 38 507, 4875, 3770, 1597, and 2467 Gg, respectively. SO2 and CO emissions were mainly from boilers, accounting for 49 % and 73 % of the total. Mobile sources dominated NOx emissions, contributing 57 % of the total. NMVOC emissions, mainly from industrial sources, made up 61 % of the total. Dust sources accounted for 55 % and 28 % of PM10 and PM2.5 emissions, respectively. Agricultural sources accounted for 91 % of NH3 emissions. Major PM2.5 species were OC, Ca, Si, PSO4, and EC, accounting for 9.0 %, 7.0 %, 6.4 %, 4.6 %, and 4.3 % of total PM2.5 emissions, respectively. The main species of NMVOCs were aromatic hydrocarbons, making up 25.3 % of the total. Oxygenated volatile organic compounds (OVOCs) contributed 21.9 % of the total NMVOC emissions. Toluene had the highest comprehensive contribution to ozone (O3) and secondary organic aerosol (SOA) formation potentials, while other NMVOCs included 1,2,4-trimethylbenzene, m,p-xylene, propylene, ethene, o-xylene, and ethylbenzene. Industrial process and solvent-use sources were the main sources of O3 and SOA formation potential, followed by motor vehicles. Among industrial sources, chemical manufacturing, rubber and plastic manufacturing, appliance manufacturing, and textiles made significant contributions. This emission inventory should provide scientific guidance for future control of air pollutants in the YRD region of China.