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Theory predicts that rising CO₂increases global photosynthesis, a process known as CO₂fertilization, and that this is responsible for much of the current terrestrial carbon sink. The estimated magnitude of the historic CO₂fertilization, however, differs by an order of magnitude between long-term proxies, remote sensing-based estimates and terrestrial biosphere models. Here we constrain the likely historic effect of CO₂on global photosynthesis by combining terrestrial biosphere models, ecological optimality theory, remote sensing approaches and an emergent constraint based on global carbon budget estimates. Our analysis suggests that CO₂fertilization increased global annual terrestrial photosynthesis by 13.5 ± 3.5% or 15.9 ± 2.9 PgC (mean ± s.d.) between 1981 and 2020. Our results help resolve conflicting estimates of the historic sensitivity of global terrestrial photosynthesis to CO₂and highlight the large impact anthropogenic emissions have had on ecosystems worldwide.

 

Using transdimensional plasmonic materials (TDPM) within the framework of fluctuational electrodynamics, we demonstrate nonlocality in dielectric response alters near-field heat transfer at gap sizes on the order of hundreds of nanometers. Our theoretical study reveals that, opposite to the local model prediction, propagating waves can transport energy through the TDPM. However, energy transport by polaritons at shorter separations is reduced due to the metallic response of TDPM stronger than that predicted by the local model. Our experiments conducted for a configuration with a silica sphere and a doped silicon plate coated with an ultrathin layer of platinum as the TDPM show good agreement with the nonlocal near-field radiation theory. Our experimental work in conjunction with the nonlocal theory has important implications in thermophotovoltaic energy conversion, thermal management applications with metal coatings, and quantum-optical structures. 

The study of cell-cell interaction in high-throughput is critically important in many biological systems, including oncology, immunology, and tissue engineering. However, the passive co-encapsulation of one type A cell and one type B cell per single droplet, termed 1-1-1 encapsulation, has been dictated by double Poisson distribution, which yields only ~5% efficiency with common cell loading density. Such low efficiency makes it impractical for biological analyses at scale. Here, we demonstrate a passive 1-1-1 co-encapsulation microfluidic device that leverages close packing of cells with hydrodynamic sheath flow to achieve over two-fold improvement compared to the double Poisson model. 

Self-healing triboelectric nanogenerators (SH-TENGs) with fast self-healing, high output performance, and wearing comfort have wide and promising applications in wearable electronic devices. This work presents a high-performance hydrogel-based SH-TENG, which consists of a high dielectric triboelectric layer (HDTL), a self-healing hydrogel electrode layer (SHEL), and a physical cross-linking layer (PCLL). Carbon nanotubes (CNTs), obtained by a chemical vapor deposition (CVD) method, were added into polydimethylsiloxane (PDMS) to produce the HDTL. Compared with pure PDMS, the short-circuit transferred charge (44 nC) and the open circuit voltage (132 V) are doubled for PDMS with 0.01 wt% CNTs. Glycerin, polydopamine particles (PDAP) and graphene were added to poly (vinyl alcohol) (PVA) to prepare the self-healing hydrogel electrode layer. SHEL can physically self-heal in ~1 min when exposed to air. The self-healing efficiency reaches up to 98%. The PCLL is made of poly(methylhydrosiloxane) (PMHS) and PDMS. It forms a good physical bond between the hydrophilic hydrogel and hydrophobic PDMS layers. The electric output performance of the SH-TENG can reach 94% of the undamaged one in 1 min. The SH-TENG (6 × 6 cm2) exhibits good stability and superior electrical performance, enabling it to power 37 LEDs simultaneously.