Memristor, which had been predicted a long time ago (Chua, L. O. IEEE Trans. Circuit Theory 1971, 18, 507), was recently invented (Strukov, D. B.; et al. Nature 2008, 453, 80). The introduction of a memristor is expected to open a new era for nonvolatile memory storage, neuromorphic computing, digital logic, and analog circuit. Furthermore, several breakthroughs were made for memristive phenomena and transistors with single-layer MoS2 (Sangwan, V. K.; et al. Nat. Nanotechnol. 2015, 10, 403. van der Zande, A. M.; et al. Nat. Mater. 2013, 12, 554. Liu, H.; et al. ACS Nano 2014, 8, 1031. Bessonov, A. A.; et al. Nat. Mater. 2015, 14, 199. Yuan, J.; et al. Nat. Nanotechnol. 2015, 10, 389). Herein, we demonstrate that 2H phase of bulk MoS2 possessed an ohmic feature, whereas 1T phase of exfoliated MoS2 nanosheets exhibited a unique memristive behavior due to voltage-dependent resistance change. Furthermore, an ideal odd-symmetric memristor with odd-symmetric I-V characteristics was successfully fabricated by the 1T phase MoS2 nanosheets via combining two asymmetric switches antiserially.

The large energy requirement of CO 2 reforming of methane (CRM) has obstructed its application. Solar energy is a solution for the issue. Different from efficient photocatalytic splitting of water, photocatalysis for CRM exhibits a very low efficiency and employs only ultraviolet (UV) light. This letter reports an efficient visible-light photocatalytic CRM by combining Pt/black TiO 2 catalyst with lightdiffuse-reflection-surface. Under visible light illumination by filtering UV light from AM 1.5G sunlight, H 2 and CO yields reached 71 and 158 mmol/h/g cat , with a quantum efficiency of 32.3% at 550 °C, and 129 and 370 mmol/h/g cat , with a quantum efficiency of 57.8% at 650 °C. Those yields are 3 orders of magnitude larger than the reported values.

Atomically thin graphene with a high-density of precise subnanometer pores represents the ideal membrane for ionic and molecular separations. However, a single large-nanopore can severely compromise membrane performance and differential etching between pre-existing defects/grain boundaries in graphene and pristine regions presents fundamental limitations. Here, we show for the first time that size-selective interfacial polymerization after high-density nanopore formation in graphene not only seals larger defects (>0.5 nm) and macroscopic tears but also successfully preserves the smaller subnanometer pores. Low-temperature growth followed by mild UV/ozone oxidation allows for facile and scalable formation of highdensity (4−5.5 × 10 12 cm −2 ) useful subnanometer pores in the graphene lattice. We demonstrate scalable synthesis of fully functional centimeter-scale nanoporous atomically thin membranes (NATMs) with water (∼0.28 nm) permeance ∼23× higher than commercially available membranes and excellent rejection to salt ions (∼0.66 nm, >97% rejection) as well as small organic molecules (∼0.7−1.5 nm, ∼100% rejection) under forward osmosis.

We report on a roll-to-roll manufacturing compatible isopropanol-assisted-hot-lamination process for facile fabrication of large-area nanoporous atomically thin graphene membranes (NATMs) for dialysis and molecular separations.