The present invention relates to a graphene photodetector, in particular to a graphene photodetector exploiting the photo-conversion mechanism based on photo-thermoelectric and photo-voltaic effect.
Graphene photodetectors offer several advantages in a range of applications, in particular for high speed data and telecommunication applications due to the graphene properties.
Graphene is a one-atom-thick layer of carbon having a two-dimensional hexagonal structure with sp2 hybridization. The valence and the conduction band of this material meet in six points in the reciprocal space called Dirac points.
Graphene has a low density of states linearly varying with the energy of the electronic states and vanishing at the Dirac point. Such a feature enables an easy tuneability of the chemical potential (low gate voltage is required to shift the chemical potential if compared to other materials like Silicon) and all the material properties associated with it (e.g., electrical conductivity, Seebeck coefficient, optical absorption, etc.) by means of field effect. This feature is referred to as electrostatic doping.
The optical absorption spectrum for graphene spans from the UV to the far IR and the charge carriers' mobility in graphene can exceed 100.000 cm2/Vs even at room temperature when the material is properly encapsulated (e.g., in hBN).
The fast carrier dynamics of optically excited carriers upon optical excitation owing to the short relaxation time (of the order of picoseconds) and the small electronic heat capacitance enables the realization of photodetectors having opto-electronic bandwidths larger than 100 GHz.
In addition, graphene can be grown by chemical vapor deposition (CVD) on a proper substrate (e.g., copper) and transferred on virtually any photonic substrate.
Use of graphene photodetectors based on the photo-thermoelectric effect, mainly allows for direct optical power to voltage conversion, zero dark current, and ultra-fast operation.
Photo-thermal effect (PTE) is based on an increase of the temperature of the electronic system following the absorption of optical power. In PTE based graphene photodetectors, the electromotive force is generated by the Seebeck effect caused by the spatial gradient of the electronic temperature in graphene in presence of a spatially non-homogeneous Seebeck coefficient.
For a better understanding of this concept, if it is assumed that a laser beam excites an active graphene layer which has a spatially homogeneous chemical potential and thus a Seebeck coefficient (property depending on the chemical potential) constant along the channel, the hot carriers optically excited within the laser spot region (i.e., electrons and holes found at higher temperature with respect to the lattice after illumination), radially diffuse from the center of the excitation region to the sides. In this condition hot electrons (or holes depending on the sign of the Seebeck coefficient) diffuse in opposite directions giving rise to a zero net photocurrent. To the contrary, if a step change of the chemical potential (and consequently of the Seebeck coefficient) is induced at the center of the excitation region, hot electrons or holes will diffuse in the same direction giving rise to a net photocurrent. Since the photo response is directly generated by a thermoelectric effect, differently from other effects (photo-conductive and photo-bolometric effect, for example), the photo-thermoelectric effect does not require a bias applied to the active graphene layer and, thus, operates in absence of dark current.
Both the photo-voltaic and the photo-thermoelectric effect require, for different reasons, a non-homogeneous chemical potential, i.e., a pn junction. There are remarkable differences between the graphene pn homojunctions (where the junction is made only of graphene) and the classical semiconductor-based diodes.
The first difference is that a classical semiconductor requires physical doping to realize a pn junction. Differently, the easy tuneability of graphene chemical potential through field effect enables the realization of electrostatically induced pn homojunctions by using proper gating structures. Several gating configurations are reported in literature combining top gate configurations (gate electrodes are placed on top of the active graphene layer) and bottom gate configurations (gate electrodes are placed under the active graphene layer). Just as an example, reference is made in the following to the top split gate and the bottom split gate configuration.
In a split gate configuration two gate electrodes separated by a small gap (usually less than 300 nm) are used to induce in the active layer a spatial doping profile with opposite sign in the two sides of the junction. Two examples of top and bottom split gate configuration related to waveguide integrated graphene photodetectors are shown in
In
In the top split gate configuration of
A main object of the invention is to provide a graphene photodetector to overcome the limits highlighted with reference to known solutions.
This object and others that will be more apparent hereinafter are achieved by a graphene photodetector made in accordance with the appended claims.
According to one aspect of the disclosed subject matter, the invention relates to a graphene photodetector comprising:
In some embodiments, the width of said channel can be further preferably comprised between 250 nm and 450 nm.
In some embodiments, the thickness of the first and second metal electrode, defining the height of the channel cross-section, is comprised between 70 nm and 200 nm.
In some embodiments, the thickness of the first and second metal electrode is preferably 100 nm.
In some embodiments, the thickness of the gate dielectric layer is comprised between 10 nm and 40 nm.
In some embodiments, the thickness of the dielectric layer is preferably 20 nm.
In some embodiments, the first and/or the second metal electrode are made of one or more of the following metals: Gold, Silver, Aluminum, Titanium nitride (TIN), or alloy thereof.
In some embodiments, the distance between the first and the second metal electrode, defining the width of the channel cross-section, is constant in the longitudinal extension of the channel.
In some embodiments, the constant width of the channel cross section is comprised between 250 nm and 450 nm.
In some embodiments, the width of the channel is periodically variable in the longitudinal extension of the channel, with sections having a minimum width alternating with sections having a maximum width, and in which the width varies gradually between the minimum value and the maximum value, and vice versa, along said longitudinal direction.
In some embodiments, the minimum width is comprised between 100 nm and 250 nm and the maximum width is comprised between 450 nm and 600 nm
In some embodiments, the number of channel sections having the minimum width is comprised between two and five.
In some embodiments, in said channel three sections having the minimum width are provided.
In some embodiments, between two sections of minimum and maximum width, adjacent to each other, the opposite surfaces of the channel are angled at an angle between 4° and 23° degrees, with respect to the longitudinal extension direction of the channel.
In some embodiments, the optical mode of the dielectric waveguide has to be quasi-Transverse-Electric (quasi-TE).
In some embodiments, said channel can be realized by using more than one graphene layer, preferably two graphene layers. Preferably the two layers of graphene are superimposed on each other.
Further features and advantages of the invention will be made clearer by the detailed description hereinafter of some of its preferred embodiments illustrated, by way of non-limiting example, with reference to the accompanying drawings, in which:
With initial reference to
The photodetector 1 comprises a first graphene absorption layer 2 (having a planar configuration depicted with a dashed line) connected to a first metal electrode 3 at a first end 2a of the first graphene layer 2 and to a second metal electrode 4 at a second end 2b of the first graphene layer 2 opposite to the first end 2a. The first and second metal electrode 3, 4 are referred to as source and drain, respectively.
The contact between the graphene layer 2 and each of the metal electrode 3, 4 ensures the appropriate electrical connection to conduct and detect the photocurrent produced in the photodetector.
The first 3 and/or the second metal electrode 4 are preferably made of one or more of the following metals: Gold, Silver, Aluminum, Titanium nitride (TiN), or alloy thereof.
The first and second metal electrode 3, 4 further define on the first graphene layer 2 a channel 5 operating as a plasmonic waveguide, as clearly disclosed in the following.
The first and second metal electrode 3,4 are spaced apart and the distance between the first and the second metal electrode, indicated d1, defines the width of the channel cross-section.
The thickness of the first and second metal electrode, indicated tm, defines the height of the channel cross-section and is preferably comprised between 70 nm and 200 nm, and more preferably is 100 nm.
Preferably the distance d1 between the first and second metal electrode 3,4 is comprised between 100 nm and 600 nm, and more preferably is comprised between 250 nm and 450 nm.
The photodetector 1 further comprises a gate dielectric layer 6 interposed between the first graphene layer 2 and a second graphene layer 7 (also depicted with a dashed line), such a configuration realizing a capacitor, where the dielectric layer 6 is placed on the opposite side of the channel 5 with respect to the first graphene layer 2. Preferably the dielectric layer 6 is made of SiN or Al2O3.
The first and second graphene layer 2, 7 are preferably planar and parallel to each other, the distance between them being defined by the thickness of the dielectric layer 6, indicated tdiel.
The second graphene layer 7 is used for electrical gating and comprises a first and a second gate electrode, indicated 8,9, which are located proximate to the first metal electrode 3 and the second metal electrode 4, respectively, in at least partial overlapping with the first graphene layer 2.
Preferably the first and second gate electrode 8,9 are spaced apart with a distance d2 and have a configuration centered with respect to the channel 5, as clearly shown in
Preferably, the distance d2, between the gating electrodes 8,9 is at least 60% of the distance between said first and second metal electrode 3,4, and more preferably the distance d2 is comprised between 100 nm and 300 nm. In this range, more preferably the value of d2 is 150 nm.
As further disclosed below, the metal electrodes 3,4 on top of the first graphene layer 2, defining the active channel 5, are provided to either collect the photocurrent and to confine the light at the metal-graphene interface. Control of the electrostatic doping in the active channel, by changing the graphene chemical potential (applying an external voltage to the gating electrodes) is achieved by using a so called bottom split gate geometry obtained by the gating electrodes 8,9 of the second graphene layer 4.
The photodetector 1 further comprises a photonic dielectric waveguide 10 with a planarized cladding 11 disposed underneath the dielectric layer 6, with the first and second gating electrode 8, 9 remaining interposed between the dielectric layer 6 and the cladding 11. The waveguide 10 includes a core 12, preferably a silicon core, embedded in the cladding 11, preferably a SiO2 cladding.
The waveguide 10, preferably configured in a rectangular cross-section, is located centrally with respect to the active graphene channel 5. The dielectric spacer thickness between the waveguide 10 and the graphene gate electrodes is indicated by tclad. Preferably the waveguide 10 can have a rectangular cross section of 220 nm by 480 nm.
Referring to the top view of
According to one embodiment of the invention, shown in the top view of
According to another embodiment of the invention, shown in the top view of
Preferably the minimum width d1′ is comprised between 100 nm and 300 nm and the maximum width d1″ is comprised between 450 nm and 600 nm. Preferably, the number of channel sections having the minimum width d1′ may be comprised between two and five, and more preferably three channel sections having the minimum width d1′ may be provided in the longitudinal extension of the channel.
In
A small tapering angle α (see
The thickness tdiel of the gate dielectric layer is chosen small enough to maximize the optical absorption in the active graphene channel. However, the thickness tdiel is preferably chosen to be at least 20 nm to prevent current leakage between the active channel and the gate electrodes.
The graphene-based photodetector of the claimed subject matter is proposed for exploiting the photo-conversion mechanisms (photovoltaic and photo-thermoelectric effect) occurring at the metal/graphene interface. Photovoltaic and photo-thermoelectric mechanism at the metal/graphene interface can be exploited to generate a photocurrent. Differently from the devices of the prior art, described with reference to
The geometry of the photodetector is shown in
In order to excite the plasmonic mode the optical mode of the dielectric waveguide has to be quasi-Transverse-Electric (quasi-TE).
The light from the dielectric waveguide 10 is coupled to the plasmonic mode of the Metal-Insulator-Metal (MIM) waveguide on top of the active graphene channel 5. Most of the optical power is absorbed at the graphene/metal interface at the edge of the metal contacts. Referring to
In
As described above, with reference to the prior art solutions, a graphene layer interposed between the dielectric waveguide and the active graphene layer is detrimental because it would absorb a large amount of the optical power reducing the responsivity of the photodetector. In the proposed invention this problem is strongly mitigated. As a matter of fact, the use of a plasmonic waveguide enhances the electric field in the active graphene layer. Moreover, graphene optical absorption linearly scales with the number of layers. By using two graphene layers the active channel has a larger absorption with respect to gates.
In the graph of
As to the graphene active channel, the major drawbacks of small gaps between the metal electrodes are the large absorption in metals and the non-trivial control of graphene chemical potential between the two metal electrodes. With small gaps, as it has been observed by the Applicant with a gap of 20 nm, the chemical potential in the gap is almost constant and does not vary from the left contact to the right contact. Since the gap region of the channel is the region where the largest part of the optical power is absorbed, if it not possible to control the chemical potential in the gap, it is not possible to maximize the PTE and PV photo-response. As a consequence of that, the voltage responsivity is poor. However, thanks to the field enhancement obtained in the gap, the embodiment with tapered sections has the advantage of increasing the amount of optical power absorbed in the active graphene channel. Two embodiments of the photodetectors can be compared: 1—a realization of photodetector having a constant width of 300 nm and 2—a photodetector with tapered sections having for instance a minimum width d1′ equal to 250 nm and a maximum width d1″ equal to 600 nm. In the realization constant width photodetector the absorbed optical power is less compared to the case of photodetector with periodically tapered width. Moreover, thanks to a minimum gap width (>100 nm), in the periodically tapered realizations the optical power is not confined only in the gap but a relevant part of the absorption occurs also in sections of the taper having larger width.
Optical power absorption in regions where the width is larger than 100 nm allows a more accurate control the chemical potential. This permits a better optimization of the PTE and PV effect and therefore the responsivity of the detector can be optimized.
For such reasons the solution with tapered sections and relatively large gap (>100 nm) represents the optimum design and the optimal range for d1′ and d1″ (see
In the graph of
Number | Date | Country | Kind |
---|---|---|---|
102021000032822 | Dec 2021 | IT | national |
Filing Document | Filing Date | Country | Kind |
---|---|---|---|
PCT/EP2022/086960 | 12/20/2022 | WO |