Growing interests have been devoted to the design of polymer acceptors as potential replacement for fullerene derivatives for high-performance all polymer solar cells (all-PSCs). One key factor that is limiting the efficiency of all-PSCs is the low fill factor (FF) (normally <0.65), which is strongly correlated with the mobility and film morphology of polymer:polymer blends. In this work, we find a facile method to modulate the crystallinity of the well-known naphthalene diimide (NDI) based polymer N2200, by replacing a certain amount of bithiophene (2T) units in the N2200 backbone by single thiophene (T) units and synthesizing a series of random polymers PNDI-Tx, where x is the percentage of the single T. The acceptor PNDI-T10 is properly miscible with the low band gap donor polymer PTB7-Th, and the nanostructured blend promotes efficient exciton dissociation and charge transport. Solvent annealing (SA) enables higher hole and electron mobilities, and further suppresses the bimolecular recombination. As expected, the PTB7-Th:PNDI-T10 solar cells attain a high PCE of 7.6%, which is a 2-fold increase compared to that of PTB7-Th:N2200 solar cells. The FF of 0.71 reaches the highest value among all-PSCs to date. Our work demonstrates a rational design for fine-tuned crystallinity of polymer acceptors, and reveals the high potential of all-PSCs through structure and morphology engineering of semicrystalline polymer:polymer blends.

No abstract

High-performance ternary all-polymer solar cells with outstanding efficiency of 9.0% are realized by incorporating two donor and one acceptor polymers with complementary absorption and proper energy level alignment.

Solar‐driven interfacial evaporation is an emerging technology with a strong potential for applications in water distillation and desalination. However, the high‐cost, complex fabrication, leaching, and disposal of synthetic materials remain the major roadblocks toward large‐scale applications. Herein, the benefits offered by renewable bacterial cellulose (BC) are considered and an all‐cellulose‐based interfacial steam generator is developed. In this monolithic design, three BC‐based aerogels are fabricated and integrated to endow the 3D steam generator with well‐defined hybrid structures and several self‐contained properties of lightweight, efficient evaporation, and good durability. Under 1 sun, the interfacial steam generator delivers high water evaporation rates of 1.82 and 4.32 kg m−2 h−1 under calm and light air conditions, respectively. These results are among the best‐performing interfacial steam generators, and surpass a majority of devices constructed from cellulose and other biopolymers. Importantly, the first example of integrating solar‐driven interfacial evaporation with water wave detection is also demonstrated by introducing a self‐powered triboelectric nanogenerator (TENG). This work highlights the potential of developing biopolymer‐based, eco‐friendly, and durable steam generators, not merely scaling up sustainable clean water production, but also discovering new functions for detecting wave parameters of surface water.