Recent Trends on the Dehydrogenation Catalysis of Liquid Organic Hydrogen Carrier (LOHC): A Review

Considering the expansion of the use of renewable energy in the future, the technology to store and transport hydrogen will be important. Hydrogen is gaseous at an ambient condition, diffuses easily, and its energy density is low. So liquid organic hydrogen carriers (LOHCs) have been proposed as a way to store hydrogen in high density. LOHC can store, transport, and use hydrogen at high density by hydrogenation and dehydrogenation cycles. In this review, we will focus on typical LOHCs, methylcyclohexane (MCH), 18H-dibenzyltoluene (DBT), and 12H-N-ethylcarbazole (NECZ), and summarize recent developments in dehydrogenation catalytic processes, which are key in this cycle.


Introduction
In order to achieve carbon neutrality by 2050, we need to flexibly change our social systems of energy and materials around the world. In the field of energy, solar cells are becoming more widespread and less costly, and electricity derived from a variety of renewable energy sources such as wind power is being expanded. These are great energy sources if they can be used immediately on the spot, but on the other hand, transporting the electricity over long distances via copper wires is highly impairing, and it is difficult to store the electricity on a large scale. Since the time and place of generation of renewable energy is in a different phase from that of the users, we need to think of ways to use renewable energy while shifting time and place. Figure 1 compares the energy densities of hydrogen gas, some liquid organic hydrogen carriers, batteries, synthetic fuels, etc., with respect to volume and weight [1,2]. As can be seen from this figure, batteries can store less energy per weight than synthetic fuels and hydrogen. The simplest option is to convert electricity to hydrogen. If conduits exist to transport hydrogen, it is desirable to transport it directly through pipelines. On the other hand, pipelines to transport hydrogen are difficult to achieve in some cases due to the physical properties of hydrogen (i.e. it is easy to diffuse and leak, etc.). In such cases, one possible solution is to confine the hydrogen in the form of an energy carrier. So far, ammonia, hydrazine, FT (Fischer Tropsch) fuel, methanol, ethanol, formic acid, and organic hydrides have been proposed as energy carriers to store hydrogen. Among these, organic hydrides are expected to be used in a wide variety of applications because of their excellent long-term storage properties and stability at room temperature [1]. In this review, we will focus on dehydrogenation catalysts for these various organic hydrides and summarize their current status and issues.

Catalysts for Dehydrogenation of Methylcyclohexane
Among various organic hydrides, methylcyclohexane (MCH) is said to be promising in terms of its high affinity with conventional petroleum refining and transport/storage/ distribution. Table 1 compares the physical and chemical properties of organic hydride with gaseous hydrogen and ammonia [1,2]. When MCH is used as a liquid organic hydrogen carrier (LOHC), the dehydrogenation reaction of MCH to toluene shown in the Eq. 1 must be carried out efficiently and selectively over a metal catalyst.
Many studies have been published on catalytic MCH dehydrogenation [2]. Dehydrogenation catalysts basically consist of fine particles of the active metal dispersed on a catalyst support like alumina. In such supported metal catalysts, the morphology of the active metal particles, the metal-support interaction, and the acidity of the support material are important factors. These determine the dehydrogenation activity, selectivities to products, and the catalyst (1) stability. Since the dehydrogenation to toluene and the demethylation of toluene (i.e. a side reaction) proceed simultaneously on the metal surface, the morphology and electronic state control of the supported metal are important factors.
Wolf and Petersen conducted a study of dehydrogenation of MCH using a 0.6% platinum catalyst on γ-alumina in 1977 [3]. The reaction temperature was 623 K, and the effect of partial pressure of hydrogen on the hydrogen poisoning was discussed. Furthermore, Corma et al. compared three different samples of platinum-loaded NaY zeolite catalysts with different degrees of metal dispersion to study the correlation between the catalyst structure and catalytic activity  [4]. Coughlin et al. studied the effect of sulfur coexistence and showed that a little pre-sulfurization of the catalyst increased the yield of toluene on the Pt catalyst [5]. Furthermore, they studied the effect of small amounts of sulfur in detail, and showed that carbon deposition was greatly suppressed by the presence of small amounts of hydrogen sulfide [6]. In the same year, Touzani et al. investigated the kinetics and showed that the dehydrogenation rate of MCH depends only on the partial pressure of MCH [7]. Thus, by the early 1980s, the basic knowledge about dehydrogenation catalysis of MCH had been established. Subsequently, there were a series of reports on the process and demonstrations. Yolcular et al. found that even nickel catalysts can also show stable activity for the dehydrogenation of MCH [8]. Shukla et al. reported the performance of lanthanum oxide and perovskite as supports of Pt clusters [9]. The kinetic model is discussed in detail in literature [10], and it is shown that the reaction is well explained when non-Langmuir adsorption isotherms are used. Furthermore, Ali et al. showed that dehydrogenation beyond equilibrium was possible using a catalytic reactor with a palladium-silver tubular membrane to separate the produced hydrogen in-situ. Using a pre-sulfurized catalyst, conversions of four times the equilibrium value were obtained over a period of 300 h at temperatures as low as 573 K [11]. Okada et al. introduces a pre-sulfurized catalyst that can show high activity and stability over a long period, taking advantage of the MCH dehydrogenation technology for hydrogen stations [12]. Based on this knowledge in the past masterpieces, we will discuss the recent research trends for these 5 years in Pt-based catalysts and other metal catalysts, and catalytic processes for dehydrogenation of MCH in this section.

Recent Reports on Pt-based Catalysts for MCH Dehydrogenation
Pt-based catalysts are the most widely studied catalysts because of their ability to activate C-H bonds and their high dehydrogenation activity compared to other metal catalysts.
The basic policy to enhance the performance of Pt-based catalysts is to increase the number of active sites by increasing the dispersion of supported Pt and to control the electronic state of Pt. The specific methods include the design of the support material and bimetallization by adding different metals. The addition of different metals can change the structure (geometrical factor) and electronic state (electronic factor) of Pt sites and improve the catalytic performance compared to monometallic Pt catalysts. A variety of second metal-Pt bimetallic catalysts have been studied as dehydrogenation catalysts for various hydrocarbons [2,13,14] (see Table 2). Recently, Yan et al. [15] reported that the addition of Sn to Pt/Mg-Al-O catalyst significantly enhanced the MCH dehydrogenation activity, which was attributed to the electron donation from Sn to Pt and the adjustment of the interaction of MCH and the resulting toluene with the Pt surface. On the other hand, when excess Sn is added, the surface Pt sites are diluted by the formation of Pt-Sn alloy, and the activity decreases. Such a decrease in the conversion rate due to the dilution of Pt sites by the excess of the second metal was also observed in Pt/Mo-SiO 2 catalysts. Nakano et al. found that adding a small amount of Mn to Pt/Al 2 O 3 suppressed the demethylation reaction of toluene without reducing the MCH conversion [13]. Manabe et al. [14] attributed this suppression of the side reaction to the selective coating of MnO x on the coordination unsaturated sites of Pt, which was revealed by a combination of XAFS measurements and DFT calculations. Also, the MCH dehydrogenation performance of Cu-Pt bimetallic catalysts has been investigated in detail; Zhang et al. [16] found that the Cu addition improved the MCH conversion of Pt/Silicalite-1 (S-1) from 17.7 to 59.4% under the same conditions, and the toluene selectivity was 99.6%. The high conversion rate was attributed to the improvement of Pt dispersion and sintering resistance by alloying with Cu. It was also experimentally shown that the electron density of Pt may be relatively reduced by intermetallic electron transfer. It is believed that excessive hydrogenation and hydrogenolysis are suppressed on the Pt with low electron density, resulting in high selectivity. As for the catalyst support, the most basic support is Al 2 O 3 [13,14,[17][18][19][20], and as other options, Mg-Al-O [15,21], USY zeolite [22], TiO 2 [17,23], TiO 2 -Al 2 O 3 [17,20], and Silicalite-1 [16] are reported. In addition to the role of high dispersion of Pt particles, the support material is also expected to suppress the aggregation of Pt particles by strong metal-support interaction (SMSI) (anchoring effect) and electron transfer between Pt and support. Wang et al. reported that Pt/Ce-Mg-Al-O, which is Mg-Al-O combined with a small amount of Ce, shows high MCH dehydrogenation activity with a conversion rate of 98.5% [21]. The addition of CeO 2 to the support has been found to improve the dispersion of Pt particles. Although the surface area of TiO 2 is lower than that of Al 2 O 3 and zeolite, it has been reported that TiO 2 has a strong interaction with Pt and has several interesting support effects. Nagatake et al. found that Pt/ TiO 2 is a more stable dehydrogenation catalyst than Pt/Al 2 O 3 because it is less susceptible to the reaction inhibition effect of adsorption of product toluene [23]. The effect of electron donation from TiO 2 to Pt has been reported by Sugiura et al. [20] and Yang [17]. Sugiura et al. focused on the relationship between methane by-products and Pt electronic state on Pt/ TiO 2 -Al 2 O 3 , and found that the greater the electron donation from TiO 2 to Pt, the more the demethylation of toluene is suppressed.
As for the precious metal catalyst other than Pt, Cromwell et al. [22] reported that monometallic Ir catalyst showed better dehydrogenation performance than Pt catalyst. Under the reaction conditions of 523 K, 3 MPa total hydrogen pressure, and WHSV = 92.4/h, Ir/USY was about 11 times higher in toluene yield than Pt/USY. However, the Ir/USY catalyst showed 0% toluene selectivity (89% cyclohexane selectivity) when the reaction temperature was raised to 573 K. This was attributed to the preferential dealkylation of MCH molecules due to the acidic nature of the USY support. Although the Ir catalyst was shown to be superior to the Pt catalyst in this reaction condition, Ir is a noble metal like Pt, so the cost advantage is low. If the amount of Ir used can be reduced while maintaining catalytic performance exceeding that of Pt by appropriate selection of support materials and catalyst design such as bimetallicization by adding a second metal, Ir may become a superior alternative to Pt.  [24]. The conversion on other monometallic catalysts was less than 1%. For improving the activity of Ni-catalyst, a second metal was added as the bimetallic Ni (Ni-Ag, Ni-Zn, Ni-Sn. and Ni-In) catalyst, The performance of bimetallic Ni (Ni-Ag, Ni-Zn, Ni-Sn, and Ni-In) catalysts was improved by adding secondary metals. From the DFT calculations [18], it is concluded that the Zn coating of the low coordination sites, where C-C cleavage occurs preferentially, suppresses the demethylation reaction, and achieves high selectivity.

Recent Reports on the Kinetics and Reaction Mechanism on the MCH Dehydrogenation
In the use of precious metals such as Pt and Ir, and base metals such as Ni, kinetics and reaction mechanisms are important in considering activity and selectivity as a catalyst. Akram et al. [19] used a number of kinetic equations derived from power-law kinetics and Langmuir-Hinshelwood-Hougen-Watson (LHHW) kinetics to determine the kinetic models for MCH dehydrogenation over monometallic and bimetallic Pt-supported-Al 2 O 3 catalysts. They show that the kinetic model based on the single-site surface reaction mechanism [Eqns. (2)(3)(4)(5)(6)] best reproduces the experimental data and that the "the loss of first molecular hydrogen" step in Eq. 3 is the rate-limiting step.
Here, σ denotes the active site of the catalyst. It is also mentioned that the final product, toluene, inhibits the reaction due to its strong adsorption on the catalyst surface. Similar observations on the rate-limiting step of the reaction have been made by several groups in experimental kinetic investigations combined with kinetics modeling [25][26][27][28]. In addition, density functional theory (DFT) studies of the dehydrogenation of MCH to toluene on a Pt (111) surface have shown that the first dehydrogenation step, which has the highest energy barrier, may determine the overall rate of the reaction [29,30].
Thus, several studies support the view that the first dehydrogenation step from MCH (C 7 H 14 ) to methylcyclohexene (C 7 H 12 ) is the rate-limiting step in the MCH dehydrogenation reaction on Pt surfaces, while other views have been proposed. Zhao et al. [31] investigated the dehydrogenation reactivity of Pt 13 clusters supported on alumina (100) surface using density functional theory (DFT) and ab-initio molecular dynamics. The optimal reaction pathway was found to be a combination of six C-H bond cleavage and H diffusion and cluster reconstruction steps. As a result, the C-H bond dissociation (the third C-H dissociation) step of C 7 H 12 was the most energetic one at the reaction temperature of 625 K. This finding suggests that the active site reconstruction itself should be considered as an elementary reaction and that the conventional Langmuir-Hinshelwood type theory may not be directly applicable. In the catalytic MCH dehydrogenation process, a number of side reactions can also proceed. Since the presence of by-products other than hydrogen and toluene has a significant impact on the stability and economics of the process operation, it is desirable to minimize the byproducts as much as possible and proceed with the dehydrogenation to toluene in a highly selective manner. In particular, methane by-products reduce the purity of the exit gas hydrogen, and coke formation causes irreversible degradation of the dehydrogenation catalyst activity. Alhumaidan (Fig. 2), and revealed the effect of side reactions on the long-term deactivation of the catalyst [32]. They evaluated the operating parameters (the reactor space-time (W/F), pressure, temperature, and H 2 /MCH ratio) that affect the by-product yields. Among the many side reactions, benzene formation was reported to be the most productive and sensitive to operating parameters. The rate of demethylation of toluene to form benzene increased significantly with increasing the reaction temperature and pressure. In a practical LOHC system based on the MCH-toluene-H 2 cycle, the demethylation of toluene is considered to be the most critical side reaction because the system needs to be operated at relatively high temperature and pressure. It was also shown that the demethylation reaction and the formation of coke precursor (cyclopentadiene, etc.) can be reduced by coexisting H 2 in the feed at a moderate ratio. In order to increase the feasibility of the process, it is important to develop a highly engineered catalytic process that can suppress side reactions and selectively promote the dehydrogenation of MCH to toluene.

Application of a Membrane Reactor
Since MCH dehydrogenation is a highly endothermic reaction, a high operating temperature is required due to the limitation of thermodynamic equilibrium in the case of a typical fixed bed reactor. In addition, a separation system is required to increase the purity of the outlet gas, which increases the cost of the process. Membrane reactor (MR) technology has received much attention as an approach to solve these drawbacks. Membrane reactors can shift the equilibrium of dehydrogenation to the product side by selectively separating H 2 from the reaction zone in-situ. As a result, higher MCH conversions can be achieved at lower temperatures than in conventional fixed bed reactors, and the separation process in the subsequent stages can be simplified. In fact, Kreuder et al. [33] have successfully tested MCH dehydrogenation in a planar fixed-bed microreactor ( Fig. 3) with microstructured channels combining a catalystfilled bed and a Pd membrane. Simulation studies have also been conducted to predict the reaction behavior and optimize the reactor for various forms of MR [34,35]. Byun et al. [36] compared the technical and economic aspects of the MCH dehydrogenation reaction using MR and a conventional packed-bed reactor (PBR). The cost estimation based on the process simulation shows that the unit H 2 production cost of PBR is 11.76, 9.50, 8.50, and 8.08 dollars and that of MR is 9.37, 7.43, 6.58, and 6.23 dollars for H 2 production capacities of 30, 100, 300, and 700 m 3 /h, respectively.

Application of an Electric Field for Catalytic MCH Dehydrogenation
Since MCH dehydrogenation is an endothermic reaction, it is necessary to provide heat for the reaction. If the reaction can be driven by low-temperature waste heat (< 473 K) that exists in the H 2 utilization area, it will be possible to construct a hydrogen supply chain with less energy loss as a whole. However, conventional catalytic processes cannot achieve sufficient hydrogen yield at low temperatures due to both of the kinetic limitation and the thermodynamic  equilibrium constraint. To solve this problem, unconventional MCH dehydrogenation processes have been proposed in which a weak electric field is applied to the catalyst bed [37][38][39]. It has been reported that the application of a weak electric field to a catalyst such as Pt/CeO 2 or Pt/TiO 2 greatly enhances the dehydrogenation activity and results in MCH conversions that exceed thermodynamic equilibrium. The selectivity of toluene in this reaction is more than 99%, and the MCH dehydrogenation reaction is stable and highly selective with no or less deactivation over time. Takise et al. [37,38] have conducted various kinetic analyses to elucidate the detailed mechanism of the electric field MCH dehydrogenation reaction. The dependence of the reaction rate on the partial pressures of the reactants (MCH) and products (toluene and H 2 ) was evaluated, and it was found that the dehydrogenation rate in the conventional thermally catalyzed reaction is negatively dependent on the H 2 partial pressure, while it is positively dependent in the catalytic reaction under an electric field. In addition, kinetic analysis using isotopic substrates (D 2 and C 7 D 14 ) shows that the rate constant increases with the use of isotopic substrates (k D /k H > 1), indicating a reverse isotope effect in the catalytic reaction under the electric field. This suggests that the dehydrogenation reaction is promoted by H 2 or its derived species present in the system. Based on a series of kinetic analyses, we speculate that the activation of the MCH molecule occurs thanks to collisions with H + conducting across the catalyst surface. It is concluded that the dehydrogenation proceeds via the intermediate [C 7 H 13 -H-H] + due to the collision of conduction H + and MCH on the catalyst with the applied electric field. Since the C-H bond dissociation via a triatomic intermediate such as C-H-H + is irreversible, we consider that the MCH dehydrogenation reaction, which does not follow the conventional thermodynamic equilibrium theory, is driven by the electric field applied catalytic reaction. The application of the catalytic reaction under the electric field has demonstrated that it drives the irreversible MCH dehydrogenation reaction in the low-temperature range. In addition to the design of optimal catalyst materials, further research on the design of electric-field catalytic reactors for the scale-up of the process is expected in the future.

Catalytic Dehydrogenation of Other LOHCs
There is a wide range of LOHC candidates other than the methylcyclohexane being considered to date, and it is necessary to carefully determine which LOHC systems are most promising for later social implementation. Niermann et al.
[40] presented a LOHC system employing seven different LOHCs (12H-N-ethylcarbazole, 18H-dibenzyltoluene, 1,2-dihydro-1,2-azaborine, formic acid, methanol, naphthalene, toluene). The suitability of the LOHC system for transportation and storage applications was evaluated from both technical and economic points of view. As a result, 18H-dibenzyltoluene (18H-DBT) was shown to be an inexpensive LOHC option for storage and transportation along with methanol and toluene. In addition, 12H-N-ethylcarbazole (12H-NECZ) has been evaluated as a promising material for mobility applications [1]. Therefore, in this section, we will focus on DBT and NECZ, and the catalytic dehydrogenation studies of their hydrogenated products, 18H-DBT and 12H-NECZ, will be described in detail below (see Tables 3 and 4). 1 3

Recent Reports on the Catalytic Dehydrogenation of 18H-dibenzyltoluene
Pt-based catalysts have been the most studied catalysts for the dehydrogenation of 18H-DBT. In fact, the most active catalysts reported in recent years are Pt-based catalysts ( Table 3). The theoretical investigation using DFT calculations by Ouma et al. [41] shows that the activation energy for 18H-DBT dehydrogenation is lower on the Pt surface than on the Pd surface. Modisha et al. [42] investigated the 18H-DBT dehydrogenation performance of Pt/Al 2 O 3 , Pd/ Al 2 O 3 and Pt-Pd/Al 2 O 3 catalysts. The dehydrogenation rates obtained for Pt, Pd, and Pt-Pd catalysts were 82, 11, and 6%, respectively, at 593 K, and the monometallic Pt catalyst was reported to be significantly superior. However, Pt/ Al 2 O 3 has a relatively high concentration of methane as a by-product during the reaction. It is known that methane mixed in hydrogen fuel gas is difficult to remove and causes a decrease in the power output when fed to the fuel cell [43]. Therefore, it is desirable to develop more selective catalysts that can suppress side reactions. Auer et al. [44] found that sulfur coating of the low-coordination sites of Pt particles on Pt/Al 2 O 3 can suppress the side reactions. They also believe that the turnover rate of the reaction is improved as a result of the enhanced desorption of the dehydrogenation product, DBT, due to the change in the electronic state of Pt caused by the sulfur modification. In recent years, several studies on monometallic Pt catalysts supported on various support materials have been reported [45][46][47][48]. Lee et al. [45] synthesized Pt/Al 2 O 3 and Pt/CeO 2 using the glycine nitrate process (GNP) and investigated the dehydrogenation activity of 18H-DBT. The conversions of Pt/CeO 2 and Pt/ Al 2 O 3 were 80.5%/2.5 h and 3.5%/2.5 h, respectively, and Pt/CeO 2 showed very high activity. The Pt/CeO 2 synthesized by the GNP method has a relatively large support surface area and pore size. It is considered that these features of catalyst resulted in the improved Pt dispersion and better diffusion of 18H-DBT molecules in the catalyst particles. They mention the need for more detailed studies on the diffusion of 18H-DBT into the catalyst particle pores due to the larger molecular size of 18H-DBT than MCH. Shi et al. [46] have also studied the effect of surface hydroxyl groups and the surface oxygen vacancies (SOV) on the reversible hydrogenation and dehydrogenation reactivity of 18H-DBT using Pt/Al 2 O 3 with controlled surface hydroxyl groups and SOV by a plasma treatment method. It was found that the surface hydroxyl groups increase the degree of reduction of the supported Pt by promoting hydrogen spillover, thereby improving the hydrogenation and dehydrogenation activities. It was also shown that increasing SOV increased the percentage of low-coordinated Pt, which promoted side reactions.
These findings indicate that controlling the surface properties of the support is an effective approach for designing high-performance 18H-DBT dehydrogenation catalysts.

Recent Reports on the Catalytic Dehydrogenation of 12H-N-ethylcarbazole (12H-NECZ)
Although 12H-NECZ is inferior to cycloalkanes in terms of H 2 weight density, it can be a promising candidate for LOHC from the viewpoint of energy efficiency because of its ability to perform hydrogenation/dehydrogenation cycles at low temperatures below 473 K. The bottleneck in the LOHC cycle using NECZ is the dehydrogenation of the hydride 12H-NECZ [49]. Therefore, the development of dehydrogenation catalysts with high activity and selectivity has become an important research topic. Yang et al. [50] studied the dehydrogenation of 12H-NECZ using noble metal catalysts supported on Al 2 O 3 and reported that the catalytic activity follows the order of Pd > Pt > Ru > Rh > Au. In the study of graphene-supported noble metal catalysts by Wang et al. [51] reported in 2018, the dehydrogenation activity was also found to be Pd > Pt > Rh > Ru > Au. Pd is expected to be a promising catalyst for the dehydrogenation of 12H-NECZ, and in fact, recent reports on the dehydrogenation of 12H-NECZ (including some 12H-N-propylcarbazole (12H-NPCZ)) have focused on Pd base catalysts ( The high activity was attributed to the reduction of Pd particle size by Cu addition (geometric effect). In addition, when the replacement ratio of Pd with Cu is more than 50%, electron transfer from Pd to Cu starts to occur and the dehydrogenation activity decreases (electronic effect). In addition to the active metal, the support material is also considered to be a factor that affects the catalytic activity. Feng et al. [56] investigated the 12H-NECZ dehydrogenation activity of Pd nanoparticle catalysts supported on four different supports (activated carbon, Al 2 O 3 , TiO 2 , and SiO 2 ) and reported that the order of dehydrogenation activity was Pd/C > Pd/Al 2 O 3 > Pd/TiO 2 > Pd/ SiO 2 . The kinetic analysis indicates that the rate-limiting step of the dehydrogenation reaction may be different for each carrier. It was confirmed that the state of supported Pd, such as particle size and degree of reduction, varies greatly depending on the support. Jiang et al. [49] compared the dehydrogenation performance of precious metal catalysts supported on TiO 2 and found that Pt/TiO 2 showed higher activity and selectivity than Pd/TiO 2 and Pd/Al 2 O 3 . We believe that the electron transfer from TiO 2 to Pd is the reason for the higher performance of the Pd catalyst, but further studies are needed to clarify the effect in more detail.

Conclusion
In this review, recent trends on the catalytic dehydrogenation of MCH and other LOHCs are summarized. LOHCs are very good candidates for storing hydrogen stably even at an ambient condition. In the hydrogenation-dehydrogenation cycle of LOHC, the hydrogenation step is exothermic and rather easy, so the dehydrogenation of LOHC (endothermic) is important. It requires external heat, so high energy efficiency is anticipated. Also, a selective and stable reaction process is desired. For these purposes, designing a metal catalyst with analytical feedback and a computational prediction is very important. Further investigation for enhancing the dehydrogenation at low temperature is also required, including the utilization of membrane and/or electric field.

Conflict of interest
The authors have no conflicts of interest to declare that are relevant to the content of this article.
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http:// creat iveco mmons. org/ licen ses/ by/4. 0/.