MXenes for Solar Cells

This review summarizes applications and developments of MXenes in solar cells by far. The issues needing to be addressed for performance improvement of the related solar cells are discussed. Suggestions are given for pushing exploration of MXenes’ application in solar cells. This review summarizes applications and developments of MXenes in solar cells by far. The issues needing to be addressed for performance improvement of the related solar cells are discussed. Suggestions are given for pushing exploration of MXenes’ application in solar cells. Application of two-dimensional MXene materials in photovoltaics has attracted increasing attention since the first report in 2018 due to their metallic electrical conductivity, high carrier mobility, excellent transparency, tunable work function and superior mechanical property. In this review, all developments and applications of the Ti3C2Tx MXene (here, it is noteworthy that there are still no reports on other MXenes’ application in photovoltaics by far) as additive, electrode and hole/electron transport layer in solar cells are detailedly summarized, and meanwhile, the problems existing in the related studies are also discussed. In view of these problems, some suggestions are given for pushing exploration of the MXenes’ application in solar cells. It is believed that this review can provide a comprehensive and deep understanding into the research status and, moreover, helps widen a new situation for the study of MXenes in photovoltaics.

To comprehensively understand the achievements and meanwhile to provide insights and valuable suggestions for the following development, a timely summary and discussion of the related studies is highly necessary. In this review, we first categorize the roles of Ti 3 C 2 T x played in the reported solar cells and then follow the roles to introduce the achievements and analyze the existing problems limiting device performance improvement. Finally, a perspective to outlook the further development of the MXenes' application in solar cells is given.
As summarized in Fig. 1, the roles of the Ti 3 C 2 T x MXene in application of solar cells can be categorized into three kinds, i.e., additive [51], electrode [52] and HTL/ETL [53]. In the meantime, the corresponding type of the solar cells is also summarized for each role played by Ti 3 C 2 T x . Moreover, it is noted that the corresponding areas of the roles and the solar cells in Fig. 1 are in direct proportion to the number of the reports/publications. One thus can conclude that the Ti 3 C 2 T x MXene is mainly applied in perovskite and organic solar cells (OSCs). In the following part, the review will be extended following the role of the Ti 3 C 2 T x MXene.

Additive in Perovskite Materials, ETLs/HTLs
In 2018, Guo et al. first reported addition of Ti 3 C 2 T x into the MAPbI 3 -based perovskite absorber [51], initiating exploration of the MXenes' application in solar cells. Their study indicates that addition of Ti 3 C 2 T x can retard the nucleation process of MAPbI 3 (see the schematic diagram in Fig. 2a), resulting in the enlarged crystal size. Moreover, the Ti 3 C 2 T x additive is highly beneficial to accelerate the electron transfer, like a "carrier bridge" [54][55][56][57], through the grain boundary, which is further confirmed by the lower charge transfer resistance for the Ti 3 C 2 T x -added device as indicated by the electrochemical impedance spectra exhibited in Fig. 2b. Thanks to these effects, the average power conversion efficiency (PCE) increases from 15.18% to 16.80%. (Note: all PCEs in this review were measured at AM 1.5G illumination.) In 2019, Agresti et al. reported the WF adjustment of the MAPbI 3 films and thus optimization of the energy-level alignment for improving the performance of the related solar cells by adding the Ti 3 C 2 T x MXene [58]. It was found that the WF of the perovskite films could be effectively tuned from 4.72 to 4.37 eV without affecting other intrinsic electronic properties such as bandgap, the relative position of the valance band to the Fermi level and film morphology. The PCE of the Ti 3 C 2 T x -incorporated MAPbI 3 -based solar cells can be improved by 26.5% after simultaneously introducing Ti 3 C 2 T x addition in the ETL, as compared to the control one without Ti 3 C 2 T x . Recently, Zhang et al. reported surface decoration of MAPbBr 3 nanocrystals by few-layer Ti 3 C 2 T x MXene nanosheets to form the perovskite/ MXene heterostructure via in situ solution growth, as shown in Fig. 2c [59]. The facilitated electron injection from the MAPbBr 3 nanocrystals to the Ti 3 C 2 T x MXene because of the matched energy levels, as indicated in Fig. 2d, is beneficial to performance improvement for the related solar cells.
Very recently, Chen et al. first reported employment of ultrathin Ti 3 C 2 T x quantum dots (TQDs) to engineer the CsFAMA (FA: CH(NH 2 ) 2 ) perovskite absorber and the perovskite/TiO 2 ETL interface, as indicated in Fig. 2e [60]. Thanks to the improved crystallinity of the perovskite for the reference device and long-time ambient and light stability. It is notable that the improved performance and stability are also partly contributed by the addition of Cu 1.8 S in the HTL facilitating the perovskite crystallinity and the increased hole extraction at the perovskite/Spiro-OMeTAD HTL interface because of the matched energylevel alignment, as indicated in Fig. 2f. Besides addition in the active layer, embedding the Ti 3 C 2 T x MXene in ETLs/HTLs has also been reported. In 2019, Yang et al. reported modification of the SnO 2 ETL by adding 1.0 wt‰ Ti 3 C 2 T x for the MAPbI 3 -based PSCs (Fig. 3a, b for the schematized architecture and cross-sectional SEM image of the device). Thanks to the facilitated electron transport and enhanced hole blocking because of the optimized energy-level alignment due to Ti 3 C 2 T x addition (Fig. 3c), PCE increases to 18.34% from 17.23% for the control device without Ti 3 C 2 T x addition [61]. Huang et al. further advanced the Ti 3 C 2 T x MXene-added SnO 2 ETL by introducing TiO 2 with a suitable crystal phase for forming an effective heterojunction structure, named a multi-dimensional conductive network (MDCN) structure, as exhibited in Fig. 3d, e. Owing to the matched energy-level alignment (Fig. 3f) of the ETL with the (FAPbI 3 ) 0.97 (MAPbBr 3 ) 0.03 photoactive and FTO transparent conductive layers, a PCE increment from 16.83% (SnO 2 ETL) to 19.14% is achieved. Moreover, the MDCN-incorporated device exhibits high toleration to moisture and maintains ~ 85% of the initial performance for more than 45 days in 30-40% humidity air due to an oxygen vacancy scramble effect [62].
Besides modification of the MAPbI 3 photoactive layer using Ti 3 C 2 T x , Agresti et al. also incorporated Ti 3 C 2 T x into the TiO 2 ETL to finely tune its WF, i.e., from 3.91 to 3.85 eV that benefits for tuning the interface energy-level alignment between the perovskite absorber and the TiO 2 ETL, thus reducing the barrier height and enhancing charge transfer [58]. Based on dual addition and optimization in both the MAPbI 3 photoactive and TiO 2 electron transport layers, the device delivers a PCE of 20.14%, ~ 26.5% higher than that of the control device without Ti 3 C 2 T x addition. Moreover, it was found that the Ti 3 C 2 T x addition reduces hysteresis in the current density-voltage (J-V) curves and meanwhile enhances long-time exposure stability of the PSCs. Very recently, this group further investigated the MAPbI 3 perovskite/Ti 3 C 2 T x -based MXene interface using density functional theory calculations, and the results show that the interface WF exhibits a strong nonlinear behavior when the relative concentrations of OH-, O-and F-terminating groups are varied, providing a deep insight regarding the energy-level alignment for high-performance device fabrication [63]. Similarly, adding the Ti 3 C 2 T x MXene into HTLs also can improve device performance. Recently, Hou et al. reported modification of the conductive polymer, PEDOT:PSS (poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate)), normally as the HTL in OSCs using the Ti 3 C 2 T x MXene nanosheets [64]. As demonstrated in Fig. 4a, after adding the MXene nanosheets, more charge transfer channels between PEDOT nanocrystals can be formed. In the meantime, the conformational transformation of PEDOT from a coil structure to a linear/expansion coil structure can be induced, hence leading to the improved electrical conductivity for the modified PEDOT:PSS, as verified by the conductivity measurement shown in Fig. 4b. Using the modified PEDOT:PSS as the HTL, the OSCs based on the non-fullerene PBDB-T:ITIC system were constructed, as schematized in Fig. 4c. Thanks to the improved electrical conductivity and matched energy-level alignment with the neighboring components ( Fig. 4d) for the Ti 3 C 2 T x -modified PEDOT:PSS, a PCE of 11.02% is achieved as compared to 9.72% for the control device using pure PEDOT:PSS as the HTL. When using the PM6:Y6 system as the active layer, a PCE of 14.55% can be delivered for the case of employing the Ti 3 C 2 T x -modified PEDOT:PSS HTL as compared to 13.10% for the control device using pure PEDOT:PSS. Moreover, appropriate addition of the Ti 3 C 2 T x MXene nanosheets can improve the performance stability, as indicated in Fig. 4e. Moreover, they also tried to add the Ti 3 C 2 T x MXene nanosheets in zinc oxide (ZnO) to fabricate a novel ZnO/ Ti 3 C 2 T x hybrid ETL by precisely controlling the amount of Ti 3 C 2 T x in the sol-gel ZnO precursor solution [65]. The nanosheets act as the "electron bridges," as aforementioned [54,55], between the ZnO nanocrystals, thus providing additional charge transport pathways. Meanwhile, the Ti 3 C 2 T x MXene passivates the surface of the ZnO nanocrystals by forming the Zn-O-Ti bonding, through which electrons can transfer. This ZnO/Ti 3 C 2 T x hybrid ETL with excellent optical and electrical properties was applied in fullerene (PBDB-T:ITIC and PM6:Y6) and non-fullerene (PTB7:PC 71 BM) OSCs (Fig. 4f, g for the architecture and energy-level alignment of the device), and the improved PCEs of 12.20%, 16.51% and 9.36% from 10.56%, 14.99% and 8.18% for the control devices using the pristine ZnO ETLs were achieved by the solar cells based on the PBDB-T:ITIC, PM6:Y6 and PTB7:PC 71 BM photoactive layers, respectively. Moreover, the improved stability for the devices using the ZnO/Ti 3 C 2 T x hybrid ETLs was observed, as shown in Fig. 4h.

Electrode
The newly reported electrical conductivity of the Ti 3 C 2 T x MXene has reached as high as 15,100 S cm -1 [66], and moreover, high transparency, outstanding flexibility and adjustable WF are associated with it [67][68][69]. All these properties make Ti 3 C 2 T x suitable as electrodes in optoelectronic devices including solar cells. In the following, the review will be expanded in the sequence of the perovskite-based, organic, Si wafer-based and dyesensitized solar cells.
In 2019, Gao et al. reported use of Ti 3 C 2 T x MXene materials as the back electrode in noble-metal-free MAPbI 3 -based PSCs through a simple hot-pressing method, and Fig. 5a-c shows the preparation procedure, cross-sectional SEM image and energy-level alignment of each component for the devices [52]. One notes that as the back electrode, the Ti 3 C 2 T x MXene can facilitate hole injection from the MAPbI 3 photoactive layer, and the device delivers a PCE of up to 13.83%, ~ 27.2% higher than that of the control device using the carbon electrode. Moreover, thanks to the seamless interfacial contact, the device exhibits improved stability compared with the control one. Recently, Mi et al. employed a mixed electrode consisting of carbon, carbon nanotube (CNT) and Ti 3 C 2 T x in CsPbBr 3 -based PSCs, and Fig. 5d shows the device architecture and the cross-sectional SEM images of the mixed electrode. As indicated in Fig. 5e, the devices using the Ti 3 C 2 T x -incorporated electrodes exhibit improved performance compared with the devices employing the electrodes without Ti 3 C 2 T x [70].
In 2019, Tang et al. combined Ti 3 C 2 T x nanosheets with Ag nanowire networks to fabricate the transparent, highly conductive and flexible hybrid electrodes for flexible OSCs that are based on different combinations of organic active materials including PTB7-Th:PC 71 BM, PBDB-T:ITIC and PBDB-T:ITIC:PC 71 BM [71]. This MXene/Ag nanowire hybrid electrode, prepared via a simple and scalable solution-processed method as shown in Fig. 6a, exhibits excellent performance. The flexible ternary (PBDB-T:ITIC:PC 71 BM) OSCs using this hybrid transparent electrode deliver a champion PCE of 8.30% and meanwhile exhibit robust mechanical performance, i.e., 84.6% retention of the initial PCE after 1000 bending and unbending cycles to a 5-mm bending radius.
Recently, Qin et al. reported utilization of the Ti 3 C 2 T x MXene thin film as a common electrode to fabricate the MXene-based all-solution-processed semitransparent flexible photovoltaic (PV) supercapacitor by integrating a flexible OSC and a transparent MXene supercapacitor in the vertical direction [72]. Figure 6b shows the schematic of the preparation (left), optical photograph (upper right) and cross-sectional demonstration (lower right) of the transparent flexible electrode, and the device configuration and working principle are shown in Fig. 6c. The flexible OSCs with Ti 3 C 2 T x as the transparent electrode can deliver a high PCE of 13.6%, comparable with that of the control device using an ITO electrode. The PV supercapacitor exhibits an average visible transmission of 33.5% and the maximum storage efficiency and overall efficiency of up to 88% and 2.2%, respectively. In addition, this strategy is suitable for blading, printing and roll-to-roll manufacturing, which is promising for the production of cost-efficient flexible PV supercapacitors to satisfy the increasing energy demands for portable, wearable and miniature electronic devices. In 2019, Fu et al. drop-casted the Ti 3 C 2 T x MXene solution on the groove surface of the n + -Si emitter as the back electrode in an n + -n-p + Si solar cell (see Fig. 7a-c for the device architecture, groove surface before and after MXene coating) [73]. The ohmic contact between Ti 3 C 2 T x and n + -Si (see Fig. 7d for the energy-level alignment) facilitates electron transfer from the n + -Si emitter and thus suppresses charge carrier recombination, resulting in good output of the short-circuit current density (J sc ) and open-circuit voltage (V oc ). Moreover, it was found that the rapid thermal annealing (RTA) treatment of 30 s can further improve the electrical contact and physical adhesion between the MXene coating and the n + -Si substrate, leading to the reduced series resistance (it can be concluded from the increased slope for the J-V curves around V oc in Fig. 7e and also verified by the resistance measurement, as exhibited in Fig. 7f) and thus a remarkable improvement of PCE to 11.5%. In some cases, MXenes serve both the electrode and the component of forming the Schottky junction with Si. For example, Yu et al. reported a Schottky junction solar cell fabricated based on Ti 3 C 2 T x and n-Si, where the Ti 3 C 2 T x electrode meanwhile serves as a transparent conducting film for charge collection, as shown in Fig. 10a (later) [74]. For this content, we would like to more detailedly discuss in the following part of MXenes as HTLs/ETLs.
The Ti 3 C 2 T x MXene was also employed to fabricate the counter electrode (CE) in quantum dot-sensitized solar cells (QDSCs). In 2019, Chen et al. reported a composite CE consisting of hydrothermally grown CuSe nanoparticles on Ti 3 C 2 T x MXene nanosheets that were screenprinted onto a graphite sheet [75]. This composite CE possesses the better electrical conductivity for electron transfer and a larger specific surface area to provide more active sites for polysulfide electrolyte reduction, as compared to CuSe-and Ti 3 C 2 T x -based CEs, respectively. The PCE of 5.12% can be achieved by the device using the CuSe/Ti 3 C 2 T x composite CE with an optimal mass ratio. As a comparison, the devices using the CuSe-and Ti 3 C 2 T x -based CEs deliver the PCE of 3.47% and 2.04%, CEs via a facile ion-exchange method at room temperature, exhibiting a significantly faster electrocatalytic rate toward the polysulfide reduction than pure CuS [76]. The QDSC based on this composite CE delivers an overall PCE of 5.11%, which is 1.5 times obtained from the device using the pure CuS CE. The performance enhancement is mainly attributed to the combined advantages of the excellent conductivity of the Ti 3 C 2 skeleton and the abundant catalytically active sites of the CuS nanoparticles.

HTL/ETL
Owing to the easily tunable WF, the Ti 3 C 2 T x MXene can also be applied as an HTL or ETL, and the related reports in PSCs, OSCs and crystalline Si solar cells can be found. In 2019, Chen et al. reported insertion of Ti 3 C 2 T x nanosheets between the CsPbBr 3 active layer and the carbon electrode as the HTL [77], as indicated in Fig. 8a. The electron potential barrier because of the inserted Ti 3 C 2 T x layer (Fig. 8b, c) effectively blocks the transfer of electrons from CsPbBr 3 to the carbon electrode and thus mitigates the electron-hole recombination. In addition, the CsPbBr 3 grains can be well passivated by the functional groups in Ti 3 C 2 T x , thus reducing the trap defects in the CsPbBr 3 film and improving the perovskite film quality. A high initial PCE of 9.01% is obtained for the PSCs with long-term stability for more than 1900 h in a moisture environment and over 600 h under thermal conditions.
In the same year, employing the Ti 3 C 2 T x layer as a novel ETL for MAPbI 3 -based PSCs was reported by Yang et al. [78], and Fig. 8d, e shows the device architecture and crosssectional SEM image of the solar cell. Under the assistance of ultraviolet-ozone (UV-O 3 ) treatment, the Fermi level of Ti 3 C 2 T x could be downshifted from − 5.52 to − 5.62 eV, as indicated in Fig. 8f, and meanwhile, the interface properties between Ti 3 C 2 T x and MAPbI 3 were improved because of the formation of the additional oxide-like Ti-O bonds on the surface of Ti 3 C 2 T x (Ti 3 C 2 O 2 ). Thanks to the enhanced hole blocking because of the downshifted Fermi level of Ti 3 C 2 T x and meanwhile to the improved MAPbI 3 /Ti 3 C 2 T x interface, a champion PCE of 17.17% was thus achieved for the device employing the Ti 3 C 2 T x MXene film with 30 min UV-O 3 treatment. However, the device using Ti 3 C 2 T x without UV-O 3 treatment only delivers the 5.00% PCE. Further investigations verified that the charge transfer was truly enhanced for the case with the optimal UV-O 3 treatment of 30 min, as indicated by the EIS measurement. In addition, UV-O 3 treatment to Ti 3 C 2 T x also contributes to improve the device stability.
Recently, Wang et al. reported a perovskite solar cell with a thin Ti 3 C 2 T x MXene layer inserted between the F-doped SnO 2 (FTO) electrode and the SnO 2 ETL [79], and Fig. 8g, i shows the architecture and cross-sectional SEM image of the device. As indicated in Fig. 8h, the inserted MXene thin layer is favorable to form matched energy-level alignment between FTO and the SnO 2 ETL, thus facilitating electron transport from SnO 2 to FTO. Meanwhile, the strong interaction and electron hybridization between MXene and SnO 2 can be introduced (see Fig. 8i for the simulated structure), thus leading to the enhanced electron mobility in SnO 2 . Moreover, the surface of the SnO 2 ETL becomes more hydrophobic and smoother than the case without MXene, which is beneficial for growing high-quality perovskite layers. It was also found that compared with the case without MXene, non-radiative recombinations were significantly suppressed by the MXene-modified SnO 2 ETL together with the remarkably improved homogeneity and reduced carrier transport loss (Fig. 8i). Thanks to these synergetic effects introduced by the MXene thin layer, the related device delivers a stabilized PCE of 20.65% (< 19.00% for the control device without MXene) with an ultralow saturated current density and negligible hysteresis.
In 2019, Yu et al. reported utilization of the UV-O 3 treatment or N 2 H 4 treatment to increase or decrease the WF of Ti 3 C 2 T x (in a range between 4.08 and 4.95 eV) because of the oxidation or reduction of the C element, respectively [53]. As shown in Fig. 9a, the Ti 3 C 2 T x MXenes with different WFs can be used as either the HTLs or ETLs for the OSCs employing PBDB-T:ITIC as the photoactive layer. The PCEs of 9.06% and 9.02% were obtained for the cases using Ti 3 C 2 T x as electron and hole-collection buffer layers, respectively (Fig. 9b). Moreover, it was found that V oc increases with the treatment duration, as exhibited in Fig. 9c. In the same year, Hou et al. also reported employment of Ti 3 C 2 T x as the HTLs in PBDB-T:ITIC-based OSCs to facilitate hole transport and collection, benefiting from the outstanding metallic conductivity of Ti 3 C 2 T x , improved interface contact and matched energy-level alignment as exhibited in Fig. 9d [80]. It is notable that evident enhancement of PCE can be achieved for the devices using Ti 3 C 2 T x as the HTLs compared with the control one only using ITO (PCE: 4.21%). Moreover, the optimal Ti 3 C 2 T x -based device also outperforms the state-of-the-art PEDOT:PSS-based device, i.e., 10.53% vs. 10.11% (see Fig. 9e for the device performance comparison). Meanwhile, the Ti 3 C 2 T x -based devices also exhibit the improved long-term stability under the atmosphere condition without any encapsulations, as indicated in Fig. 9f.
As briefly aforementioned, in 2019, Yu et al. reported a novel solar cell formed by depositing the Ti 3 C 2 T x MXene on n-Si, where Ti 3 C 2 T x serves as both the electrode for hole collection and the component to form the Schottky junction with n-Si [74], as demonstrated in Fig. 10a. Figure 10b shows the illuminated J-V curves for the devices prepared by depositing MXene using floating and oven transfer methods, respectively, with the initial efficiencies of 0.58% and 4.20%. Moreover, as exhibited in Fig. 10c, the PCE of the as-prepared device by oven transfer can be further improved, i.e., > 9% by a two-step chemical treatment using HCl and AuCl 3 in sequence and > 10% by further introducing a PDMS antireflection layer. More investigations indicate that the SiO 2 thin layer formed between Ti 3 C 2 T x and n-Si during oven transfer plays the key role to suppress carrier recombinations and thus to achieve the higher device performance as compared to the floating method. For the improved device performance by the two-step chemical treatment, it can be attributed to the increased conductivity for the MXene layer due to the doping effect introduced by HCl, the increased Schottky barrier height (note: The WF of the MXene layer increases from 4.80 to 4.84 and further to 4.93 eV for the pristine, HCl-and AuCl 3 -treated samples) and enhanced charge transfer because of the formed Au nanoparticles from AuCl 3 .

Conclusion and Prospect
In this review, all applications and developments of the Ti 3 C 2 T x MXene in solar cells since the first report in 2018 are detailedly summarized. As can be seen, the Ti 3 C 2 T x MXene mainly plays three roles, i.e., additive, electrode and charge (electron or hole) transport layer, and the type of the applied solar cells includes perovskite (mainly), organic (mainly), silicon wafer-based and quantum dotsensitized solar cells. (Note: The functions in different roles for MXenes applied in solar cells are briefly summarized in Table 1, and meanwhile, the key device parameters are compiled in Tables 2, 3 and 4, according to the roles played by the Ti 3 C 2 T x MXene.) Moreover, there is one report regarding a hybrid device combining electricity generation and storage, i.e., the so-called PV supercapacitor in which all electrodes are Ti 3 C 2 T x , and the organic PV device and supercapacitor share one common electrode [72]. Generally speaking, report of MXenes in application of solar cells just began since the last quarter of 2018, and the related study is still in its infant stage mainly focusing on exploration of the feasibility in varying solar cells. Device performance including PCE and stability still has plenty of room for improvement [81]. Moreover, the influence of Accelerating the electron transfer, like an "electron" bridge Improving crystallinity of the perovskite materials Tuning the work function of the carrier transport materials and other properties such as conductivity Passivating the surface and engineering interface Electrode Metallic conductivity, high transparency, outstanding flexibility and adjustable work functions To form hybrid electrodes with other conducting nanomaterials, such as carbon nanotubes or metallic nanowires HTL/ETL Easily tunable work functions and carrier conducting properties  On the other hand, the properties of MXenes including morphology, conductivity, transparency, terminating groups, WF and stability are sensitive to the fabrication process. In the meantime, considering the application scenarios, i.e., solar cells, developing the fabrication methods of MXenes with accurately controllable properties, large scale and low cost is necessary [85][86][87]. Moreover, besides applications in solar cells, other optoelectronic devices such as light-emitting diodes and photodetectors can find more innovations because of the unique optical, electrical and mechanical properties of MXenes. Another issue needing to be concerned is the stability of MXenes if they were exposed to air for a long time due to oxidation, which would increase their resistance and thus reduce the device performance. Thus, appropriate passivation and/or encapsulation is necessary for stable working of the related devices [88][89][90][91]. In addition, F-free synthesis of the Ti 3 C 2 T x MXene with high purity has attracted significant attention because of the high safety and environmental friendliness.
There exist more than 100 stoichiometric MXene compositions and a limitless number of solid solutions, which would provide not only unique combinations of properties but also plenty of ways to tune them by changing the ratios of M or X elements [92]. To date, only the first discovered MXene, Ti 3 C 2 T x , has been applied in the PV field, while other types of MXenes have rarely been reported in application of solar cells. The large underexplored family of MXenes with unique properties make us believe that many exciting discoveries are to come. We optimistically expect that MXenes-based PV devices could achieve a great progress in the near future with further efforts by the researchers in this area.
Based on the above discussion and analysis, several suggestions are given for pushing exploration of MXene's applications in solar cells: (1) deep understanding into the adjustment and optimization of the Fermi level and the electrical properties for Ti 3 C 2 T x MXene materials terminated with varying functional groups based on theoretical prediction and experimental examination for better guiding experimental realization of high-performance solar cells; (2) further improvement of device performance such as PCE and stability based on (1), optimization of each interface in solar cells and incorporation of additional light management structures/components; (3) development of the related flexible PV devices considering the good flexibility of the MXene materials; (4) exploration of novel multifunctional integrated devices such as PV supercapacitors/secondary batteries and self-powered sensors considering the advantages of high transparency, abundant electrochemical active sites and remarkable adjustment of the electrical properties by functional groups for MXenes; and (5) in-depth study of the mechanism of the degraded performance for MXenes in air, exploration of the appropriate passivation and/or encapsulation measures and development of fabrication approaches suitable for solar cell applications. Moreover, besides the further development of the Ti 3 C 2 T x MXene, exploring other suitable MXenes applicable in solar cells is necessary to enrich the related studies and thus to find more opportunities to realize PV devices and/or integrated devices with high performance-to-cost ratios.