Integration of graphene with Si microelectronics is very appealing by offering a potentially broad range of new functionalities. New materials to be integrated with the Si platform must conform to stringent purity standards. Here, we investigate graphene layers grown on copper foils by chemical vapor deposition and transferred to silicon wafers by wet etching and electrochemical delamination methods with respect to residual submonolayer metallic contaminations. Regardless of the transfer method and associated cleaning scheme, time-of-flight secondary ion mass spectrometry and total reflection X-ray fluorescence measurements indicate that the graphene sheets are contaminated with residual metals (copper, iron) with a concentration exceeding 10¹³ atoms/cm². These metal impurities appear to be partially mobile upon thermal treatment, as shown by depth profiling and reduction of the minority charge carrier diffusion length in the silicon substrate. As residual metallic impurities can significantly alter electronic and electrochemical properties of graphene and can severely impede the process of integration with silicon microelectronics, these results reveal that further progress in synthesis, handling, and cleaning of graphene is required to advance electronic and optoelectronic applications.

We report an all-fiber Tm-doped fiber laser mode-locked by graphene saturable absorber. The laser emits 1.2 ps pulses at 1884 nm center wavelength with 4 nm of bandwidth and 20.5 MHz mode spacing. The graphene layers were grown on copper foils by chemical vapor deposition (CVD) and transferred onto the fiber connector end. Up to date this is the shortest reported pulse duration achieved from a Tm-doped laser mode-locked by graphene saturable absorber. Such cost-effective and stable fiber lasers might be considered as sources for mid-infrared spectroscopy and remote sensing.

Graphene is considered a record-performance nonlinear-optical material on the basis of numerous experiments. The observed strong nonlinear response ascribed to the refractive part of graphene’s electronic third-order susceptibility χ⁽³⁾ cannot, however, be explained using the relatively modest χ⁽³⁾ value theoretically predicted for the 2D material. Here we solve this long-standing paradox and demonstrate that, rather than χ⁽³⁾-based refraction, a complex phenomenon which we call saturable photoexcited-carrier refraction is at the heart of nonlinear-optical interactions in graphene such as self-phase modulation. Saturable photoexcited-carrier refraction is found to enable self-phase modulation of picosecond optical pulses with exponential-like bandwidth growth along graphene-covered waveguides. Our theory allows explanation of these extraordinary experimental results both qualitatively and quantitatively. It also supports the graphene nonlinearities measured in previous self-phase modulation and self-(de)focusing (Z-scan) experiments. This work signifies a paradigm shift in the understanding of 2D-material nonlinearities and finally enables their full exploitation in next-generation nonlinear-optical devices.

In this paper a stretched-pulse, mode-locked Er-doped fiber laser based on graphene saturable absorber (SA) is presented. A 60 layer graphene/polymer composite was used as a SA. The all-fiber dispersion managed laser resonator with the repetition frequency of 21.15 MHz allows for Gaussian pulses generation with the full width at half maximum (FWHM) of 48 nm. The generated chirped pulses were compressed outside the cavity to the 88 fs using a piece of standard single mode fiber. The average output power and pulse energy were of 1.5 mW and 71 pJ, respectively.

We experimentally demonstrate a negative Kerr nonlinearity for quasiundoped graphene. Hereto, we introduce the method of chirped-pulse-pumped self-phase modulation and apply it to graphene-covered silicon waveguides at telecom wavelengths. The extracted Kerr-nonlinear index for graphene equals $n_{2,\mathrm{gr}}=-{10}^{-13}{\mathrm{m}}^2/\mathrm{W}$. Whereas the sign of $n_{2,\mathrm{gr}}$ turns out to be negative in contrast to what has been assumed so far, its magnitude is in correspondence with that observed in earlier experiments. Graphene’s negative Kerr nonlinearity strongly impacts how graphene should be exploited for enhancing the nonlinear response of photonic (integrated) devices exhibiting a positive nonlinearity. It also opens up the possibility of using graphene to annihilate unwanted nonlinear effects in such devices, to develop unexplored approaches for establishing Kerr processes, and to extend the scope of the “periodic poling” method often used for second-order nonlinearities towards third-order Kerr processes. Because of the generic nature of the chirped-pulse-pumped self-phase modulation method, it will allow fully characterizing the Kerr nonlinearity of essentially any novel (2D) material.

We demonstrate an experimental study on the influence of the parameters of a graphene-based saturable absorber (SA) on the performance of mode-locked Er- and Tm-doped fiber lasers. We have fabricated a set of saturable absorbers with different number of graphene layers: 9, 12, 24, 37 and 48. Each SA was characterized in terms of nonlinear optical parameters (modulation depth, saturation intensity, saturation fluence) and tested in two state-of-the-art, low-power Er- and Tm-doped fiber lasers. Our results show, that in the Er-laser the broadest output spectrum (11 nm) and shortest pulses (345 fs) are generated using 37 layers of graphene in the SA. In case of a Tm-laser, the best performance (737 fs pulses with 5.82 nm bandwidth) was achieved with 24 layers. Additionally, we show that the modulation depth of a 9-layer SA is insufficient to initiate mode-locking in both lasers. This is the first reported comprehensive study on controlling of the parameters of a SA by scaling the number of graphene layers.