Project description:Today's best perovskite solar cells use a mixture of formamidinium and methylammonium as the monovalent cations. With the addition of inorganic cesium, the resulting triple cation perovskite compositions are thermally more stable, contain less phase impurities and are less sensitive to processing conditions. This enables more reproducible device performances to reach a stabilized power output of 21.1% and ∼18% after 250 hours under operational conditions. These properties are key for the industrialization of perovskite photovoltaics.
Project description:The advancement of perovskite solar cells (PVSCs) technology toward commercialized promotion needs high efficiency and optimum stability. By introducing a small molecular material such as tetratetracontane (TTC, CH3(CH2)42CH3) at the fullerene (C60)/perovskite interface of planar p-i-n PVSCs, we significantly reduced the interfacial traps, thereby suppressing electron recombination and facilitating electron extraction. Consequently, an improved efficiency of 20.05% was achieved with a high fill factor of 79.4%, which is one of the best performances for small molecular-modified PVSCs. Moreover, the hydrophobic TTC successfully protects the perovskite film from water damage. As a result, we realized a better long-term stability that maintains 87% of the initial efficiency after continuous exposure for 200 h in air.
Project description:Wide applications of personal consumer electronics have triggered tremendous need for portable power sources featuring light-weight and mechanical flexibility. Perovskite solar cells offer a compelling combination of low-cost and high device performance. Here we demonstrate high-performance planar heterojunction perovskite solar cells constructed on highly flexible and ultrathin silver-mesh/conducting polymer substrates. The device performance is comparable to that of their counterparts on rigid glass/indium tin oxide substrates, reaching a power conversion efficiency of 14.0%, while the specific power (the ratio of power to device weight) reaches 1.96 kW kg(-1), given the fact that the device is constructed on a 57-μm-thick polyethylene terephthalate based substrate. The flexible device also demonstrates excellent robustness against mechanical deformation, retaining >95% of its original efficiency after 5,000 times fully bending. Our results confirmed that perovskite thin films are fully compatible with our flexible substrates, and are thus promising for future applications in flexible and bendable solar cells.
Project description:The perovskite solar cells have demonstrated to be strong competitors for conventional silicon solar cells due to their remarkable power conversion efficiency. However, their structural instability is the biggest obstacle to commercialization. To address these issues, we prepared (CH3NH3)1-x (HC(NH2)2) x PbI3 (CH3NH3 = MA, HC(NH2)2 = FA) perovskite alloys that contain ethylammonium (EA, CH3CH2NH3 +) and benzylammonium (BA, C6H5CH2NH3 +) cations with no new additional two-dimensional (2D) perovskite phases. The crystal structures of alloy perovskites exhibit the cubic phase, which decreased the cation disorder and the intrinsic instability compared to 3D MAPbI3 perovskite. The band gaps of the alloy perovskites are almost the same as the corresponding 3D perovskites, which exhibit a high refractive index, a large absorption coefficient, and paramagnetic properties for the production of high performance photovoltaic devices. After we constructed the solar cell with the configuration of regular (n-i-p) solar cells using the alloy perovskites, the power conversion efficiencies (PCE) of the MA0.83EA0.17PbI3 perovskite solar cell showed the highest efficiency, which was 10.22%, under 1 sun illumination.
Project description:Advanced light management techniques can enhance the sunlight absorption of perovskite solar cells (PSCs). When located at the front, they may act as a UV barrier, which is paramount for protecting the perovskite layer against UV-enabled degradation. Although it was recently shown that photonic structures such as Escher-like patterns could approach the theoretical Lambertian-limit of light trapping, it remains challenging to also implement UV protection properties for these diffractive structures while maintaining broadband absorption gains. Here, we propose a checkerboard (CB) tile pattern with designated UV photon conversion capability. Through a combined optical and electrical modeling approach, this photonic structure can increase photocurrent and power conversion efficiency in ultrathin PSCs by 25.9% and 28.2%, respectively. We further introduce a luminescent down-shifting encapsulant that converts the UV irradiation into Visible photons matching the solar cell absorption spectrum. To this end, experimentally obtained absorption and emission profiles of state-of-the-art down-shifting materials (i.e., lanthanide-based organic-inorganic hybrids) are used to predict potential gains from harnessing the UV energy. We demonstrate that at least 94% of the impinging UV radiation can be effectively converted into the Visible spectral range. Photonic protection from high-energy photons contributes to the market deployment of perovskite solar cell technology, and may become crucial for Space applications under AM0 illumination. By combining light trapping with luminescent downshifting layers, this work unravels a potential photonic solution to overcome UV degradation in PSCs while circumventing optical losses in ultrathin cells, thus improving both performance and stability.
Project description:Nickel oxide (NiO) is one of the most promising and high-performing Hole Transporting Layer (HTL) in inverted perovskite solar cells due to ideal band alignment with perovskite absorber, wide band gap, and high mobility of charges. At the same time, however, NiO does not provide good contact and trap-free junction for hole collection. In this paper, we examine this problem by developing a double hole transport configuration with a copper iodide (CuI) interlayer for efficient surface passivation. Transient photo-current (TPC) measurements showed that Perovskite/HTL interface with CuI interlayer has an improved hole injection; CuI passivation reduces the concentration of traps and the parasitic charge accumulation that limits the flow of charges. Moreover, we found that CuI protect the HTL/perovskite interface from degradation and consequently improve the stability of the cell. The presence of CuI interlayer induces an improvement of open-circuit voltage VOC (from 1.02 V to 1.07 V), an increase of the shunt resistance RSH (100%), a reduction of the series resistance RS (-30%), and finally a +10% improvement of the solar cell efficiency.
Project description:The power conversion efficiency of perovskite polycrystalline thin film solar cells has rapidly increased in recent years, while the stability still lags behind due to its low thermal stability as well as the fast ion migration along the massive grain boundaries. Here, stable and efficient lateral-structure perovskite solar cells (PSCs) are achieved based on perovskite single crystals. By optimizing anode contact with a simple surface treatment, the open circuit voltage and fill factor dramatically increase and promote the efficiency of the devices exceeding 11% (0.05 to 1 Sun) compared to that of 5.9% (0.25 Sun) of the best lateral-structure single crystal PSCs previously reported. Devices show excellent operational stability and no degradation observed after 200 h continuous operation at maximum power point under 1 Sun illumination. Devices with scalable architectures are investigated by utilizing interdigital electrodes, which show huge potential to realize low cost and highly efficient perovskite photovoltaic devices.
Project description:Flexible perovskite solar cells (PSCs) have attracted tremendous attention due to their potential application in portable and wearable electronics. However, the photoelectric conversion efficiency (PCE) of flexible PSCs is still far lower than that of usual rigid PSCs. Moreover, the mechanical stability of flexible PSCs cannot meet the needs of commercial applications because of the cracking of perovskite grains caused by bending stress. Here, we introduced a spacer cation additive (2-(chloromethyl) pyridine hydrochloride, CPHC) within the perovskite organic precursor to improve the device PCE and its mechanical stability. We observed that the CPHC spacer cation additive could simultaneously facilitate the crystallization of perovskite and stitch the grain boundaries to improve the flexibility. Compared to the 17.64% PCE of the control devices, the target flexible PSCs achieved a more highly efficiency over 19% with an improved mechanical stability (87.2% of the initial PCE after the 1000 cycles with the bending radius R = 6 mm). In addition, compared to methylammonium or formamidinium cation, due to the stronger hydrophobic and larger activation energy barrier for the ion migration of the CPHC spacer cation, the device retained over 80% of the initial PCE after 30 days storage in an ambient environment.
Project description:Interfacial engineering is of great concern in photovoltaic devices. Metal halide perovskite solar cells (PSCs) have garnered much attention due to their impressive development in power conversion efficiencies (PCEs). Benefiting from high electron mobility and good energy-level alignment with perovskite, aqueous SnO2 as an electron transport layer has been widely used in n-i-p perovskite solar cells. However, the interfacial engineering of an aqueous SnO2 layer on PSCs is still an obscure and confusing process. Herein, we proposed the preparation of n-i-p perovskite solar cells with different concentrations of SnO2 as electron transport layers and achieved optimized PCE with an efficiency of 20.27%. I Interfacial engineering with regard to the SnO2 layer is investigated by observing the surface morphology, space charge-limited current (SCLC) with the use of an electron-only device, and time-resolved photoluminescence (TRPL) of perovskite films.
Project description:Perovskite materials are fascinating candidates for the next-generation solar devices. With long charge carrier lifetime, metal-halide perovskites are known to be good candidates for low-light harvesting. To match the irradiance spectra of indoor light, we configured a triple-cation perovskite material with appropriate content of bromide and chloride (FA0.45MA0.49Cs0.06Pb(I0.62Br0.32Cl0.06)3) to achieve an optimum band gap (Eg) of [Formula: see text]1.80 eV. With low photon flux at indoor condition, minimal recombination is highly desirable. To achieve such goal, we, for the first time, combined dual usage of antisolvent deposition and vacuum thermal annealing, namely VTA, to fabricate a high-quality perovskite film. VTA leads to compact, dense, and hard morphology while suppressing trap states at surfaces and grain boundaries, which are key culprits for exciton losses. With low-cost carbon electrode architecture, VTA devices exhibited average power conversion efficiency (PCE) of 27.7 ± 2.7% with peak PCE of 32.0% (Shockley-Queisser limit of 50-60%) and average open-circuit voltage (Voc) of 0.93 ± 0.02 V with peak Voc of 0.96 V, significantly more than those of control and the vacuum treatment prior to heat.