We collected information on demographic characteristics, exposure history, and illness timelines of laboratory-confirmed cases of NCIP that had been reported by January 22, 2020. We described characteristics of the cases and estimated the key epidemiologic time-delay distributions. In the early period of exponential growth, we estimated the epidemic doubling time and the basic reproductive number. RESULTSAmong the first 425 patients with confirmed NCIP, the median age was 59 years and 56% were male. The majority of cases (55%) with onset before January 1, 2020, were linked to the Huanan Seafood Wholesale Market, as compared with 8.6% of the subsequent cases. The mean incubation period was 5.2 days (95% confidence interval [CI], 4.1 to 7.0), with the 95th percentile of the distribution at 12.5 days. In its early stages, the epidemic doubled in size every 7.4 days. With a mean serial interval of 7.5 days (95% CI, 5.3 to 19), the basic reproductive number was estimated to be 2.2 (95% CI, 1.4 to 3.9). CONCLUSIONSOn the basis of this information, there is evidence that human-to-human transmission has occurred among close contacts since the middle of December 2019. Considerable efforts to reduce transmission will be required to control outbreaks if similar dynamics apply elsewhere. Measures to prevent or reduce transmission should be implemented in populations at risk. (Funded by the Ministry of Science and Technology of China and others.) a bs tr ac t Early Transmission Dynamics

2 Molecular design of non-fullerene acceptors (NFAs) is of vital importance for highefficiency organic solar cells. The branched alkyl chain modification is often regarded as a counter-intuitive approach as which may introduce undesirable steric hindrance that reduces charge transport in NFAs. Here we show the design and synthesis of a highly efficient NFA family by substituting the beta position of thiophene unit on Y6-based A-DAD-A backbone with branched alkyl chains. It was found that such modification of different alkyl chain length could completely change the molecular packing behavior of NFAs, leading to improved structure order and charge transport in thin films. Unprecedented efficiency of 18.32% (certified value of 17.9%) with a fill factor of 81.5% is achieved for single-junction organic solar cells. This work reveals the importance of branched alkyl chain topology in tuning the molecular packing and blend morphology that leads to improved organic photovoltaic performance.

The JUNO experiment locates in Jinji town, Kaiping city, Jiangmen city, Guangdong province. The geographic location is east longitude 112 • 31'05' and North latitude 22 • 07'05'. The experimental site is 43 km to the southwest of the Kaiping city, a county-level city in the prefecture-level city Jiangmen in Guangdong province. There are five big cities, Guangzhou, Hong Kong, Macau, Shenzhen, and Zhuhai, all in ∼200 km drive distance, as shown in figure 3.

In organic photovoltaics, morphological control of donor and acceptor domains on the nanoscale is key for efficient exciton diffusion and dissociation, carrier transport, and suppression of recombination losses. To realise this, here, we demonstrated a double-fibril network based on ternary donor:acceptor morphology with multi-length scales constructed by combining ancillary conjugated polymer crystallizers and non-fullerene acceptor filament assembly. Using this approach, we achieved an average power conversion efficiency of 19.3% (certified 19.2%). The success lies in the good match between the photoelectric parameters and the morphological characteristic lengths, which utilizes the excitons and free charges efficiently. This strategy leads to enhanced exciton diffusion length (hence exciton dissociation yield) and reduced recombination rate, hence minimizing photon-to-electron losses in the ternary devices as compared to their binary counterparts. The double-fibril network morphology strategy minimizes losses and maximizes the power output, offering the possibility towards 20% power conversion efficiencies in single-junction organic photovoltaics. MainOrganic semiconductors offer the advantage of high optical absorption and tunable energy levels, enabling thin-film solar cells with high light-to-electron conversion efficiencies over a wide range of wavelengths [1][2][3][4] . Desipte recent progresses, the performance of organic solar cells (OSCs) is still limited by non-ideal exciton and charge transport, which depend not only on the electronic structure of organic semiconductors but also on the nanostructure that is formed by material crystallization and phase separation in a bulk heterojunction (BHJ) setting [5][6][7][8] . A suitable sized phase-separated morphology that balances crystalline region and mixing domain on the nanoscale is therefore needed to further push the power conversion efficiency (PCE) of OSCs, however it is a