Abstract:Engineering the interface between the active layer and the electrodes has proven to be a promising strategy to enhance the power conversion efficiency (PCE) of hybrid perovskite solar cells (PeSCs). Here, we present an effective approach to achieve highly efficient PeSCs by inserting an easy-accessible hexamethonium bromide (HMB)-doped [6,6]-phenyl-C-butyric acid methyl ester (PCBM) film between the active perovskite layer and the Ag cathode. This doped interfacial layer delivers several remarkable features fo… Show more
“…For instance, we have demonstrated a series of n-doped cathode interfacial layer materials for PeSC, and significant advancement in device efficiency and stability has been made. [19][20][21][22][23][24] In this study, for the first time, we propose a facile strategy to increase the performance and stability of PeSC by incorporating tri(ethylene glycol) divinyl ether (TEGDVE; see Figure 1a for its chemical structure) as the additive and dopant for methylammonium lead iodide (MAPbI 3 ) perovskite active layer and alcoholsoluble nonfullerene amine-functionalized perylene diimide (PDIN; see Figure 1a for its chemical structure) cathode interfacial layer, respectively. The perovskite layer is fabricated by the two-step sequential deposition method (Figure 1a) based on our previous study, [19][20][21][22][23][24] except that TEGDVE additive is incorporated into moniumiodide (MAI) solution in this work.…”
Section: Doi: 101002/pssa202300128mentioning
confidence: 99%
“…For instance, we have demonstrated a series of n‐doped cathode interfacial layer materials for PeSC, and significant advancement in device efficiency and stability has been made. [ 19–24 ]…”
In this study, a facile and promising strategy is presented to enhance the performance and stability of perovskite solar cells (PeSC) by incorporating tri(ethylene glycol) divinyl ether (TEGDVE) as the additive and dopant for perovskite active layer and amine‐functionalized perylene diimide (PDIN) cathode interfacial layer, respectively. The results indicate that the electron‐donating oxygen atoms of TEGDVE can interact with undercoordinated Pb2+ via the formation of coordination bond, which synchronously passivates the defects within perovskite film and manipulates the crystallization kinetics. Additionally, the vinyl functional groups on TEGDVE can undergo thermal cross‐linking reaction and form three‐dimensional polymer network, enabling perovskite film to possess good optoelectronic properties and enhanced moisture stability. In addition, the incorporation of TEGDVE can induce n‐doping of PDIN due to its adequate electron donation capability offered by oxygen atoms. With these appealing features, the resulting device delivers not only high power conversion efficiency up to 20.90% but also satisfied ambient stability, greatly outperforming those of the PeSC without TEGDVE. This work provides a new avenue to improve the efficiency and stability of PeSC based on a facile strategy. The findings present a significant step towards the practical applications of this emerging technology.
“…For instance, we have demonstrated a series of n-doped cathode interfacial layer materials for PeSC, and significant advancement in device efficiency and stability has been made. [19][20][21][22][23][24] In this study, for the first time, we propose a facile strategy to increase the performance and stability of PeSC by incorporating tri(ethylene glycol) divinyl ether (TEGDVE; see Figure 1a for its chemical structure) as the additive and dopant for methylammonium lead iodide (MAPbI 3 ) perovskite active layer and alcoholsoluble nonfullerene amine-functionalized perylene diimide (PDIN; see Figure 1a for its chemical structure) cathode interfacial layer, respectively. The perovskite layer is fabricated by the two-step sequential deposition method (Figure 1a) based on our previous study, [19][20][21][22][23][24] except that TEGDVE additive is incorporated into moniumiodide (MAI) solution in this work.…”
Section: Doi: 101002/pssa202300128mentioning
confidence: 99%
“…For instance, we have demonstrated a series of n‐doped cathode interfacial layer materials for PeSC, and significant advancement in device efficiency and stability has been made. [ 19–24 ]…”
In this study, a facile and promising strategy is presented to enhance the performance and stability of perovskite solar cells (PeSC) by incorporating tri(ethylene glycol) divinyl ether (TEGDVE) as the additive and dopant for perovskite active layer and amine‐functionalized perylene diimide (PDIN) cathode interfacial layer, respectively. The results indicate that the electron‐donating oxygen atoms of TEGDVE can interact with undercoordinated Pb2+ via the formation of coordination bond, which synchronously passivates the defects within perovskite film and manipulates the crystallization kinetics. Additionally, the vinyl functional groups on TEGDVE can undergo thermal cross‐linking reaction and form three‐dimensional polymer network, enabling perovskite film to possess good optoelectronic properties and enhanced moisture stability. In addition, the incorporation of TEGDVE can induce n‐doping of PDIN due to its adequate electron donation capability offered by oxygen atoms. With these appealing features, the resulting device delivers not only high power conversion efficiency up to 20.90% but also satisfied ambient stability, greatly outperforming those of the PeSC without TEGDVE. This work provides a new avenue to improve the efficiency and stability of PeSC based on a facile strategy. The findings present a significant step towards the practical applications of this emerging technology.
“…For the blade-coated devices, the devices were fabricated according to our previous study. [43] Briefly,P bI 2 (15 mL) complex solution (1.1 m in anhydrous dimethylformamide) was dispensed from as yringe under the edge of the blade fixed at 100 mma bove the substrate surface, and the blade was dragged at ac onstant speed of 70 mm s À1 .I t should be noted that the substrates were heated at an elevated temperature of 80 8Cd uring the blade deposition to obtain compact film with good uniformity.F APbI 3 crystallization was achieved by dipping the PbI 2 -coated samples into the FAIs olution (20 mg mL À1 in anhydrous 2-propanol). The as-deposited perovskite films were subsequently thermally annealed at 150 8Cf or 10 min.…”
Here, efficient and stable vacuum-free processed perovskite solar cells (PSCs) are demonstrated by employing solutionprocessed molybdenum tris-[1-(trifluoroethanoyl)-2-(trifluoromethyl)ethane-1,2-dithiolene] (Mo(tfd-COCF ) )-doped poly(3,4-ethylenedioxythiophene) (PEDOT) film as hole transport layer (HTL). Our results indicate that the incorporation of Mo(tfd-COCF ) dopant can induce p-doping through charge transfer from the highest occupied molecular orbital (HOMO) level of the PEDOT host to the electron affinity of Mo(tfd-COCF ) , leading to an increase in conductivity by more than three orders of magnitude. With this newly developed p-doped film as HTL in planar heterojunction PSCs, a high power conversion efficiency (PCE) up to 18.47 % can be achieved, which exceeds that of the device with commonly used HTL 2,2',7,7'-tetrakis(N,N-di-p-methoxyphenyl-amine)9,9'-spirobifluorene (spiro-OMeTAD). Taking the advantage of the high conductivity of this doped film, a prominent PCE as high as 15.58 % is also demonstrated even when a large HTL thickness of 220 nm is used. Importantly, the high quality film of this HTL is capable of acting as an effective passivation layer to keep the underlying perovskite layer intact during solution-processed Ag-nanoparticles layer deposition. The resulting vacuum-free PSCs deliver an impressive PCE of 14.81 %, which represents the highest performance ever reported for vacuum-free PSCs. Furthermore, the resulting devices show good ambient stability without encapsulation.
“…23 In another study, PC 61 BM was doped with hexamethonium bromide (HMB), which delivered PCE ∼18.0% in PSCs, that demonstrated a shelf life of >1100 h under an inert atmosphere without light. 24 Recently, Z. Xing et al have introduced a new set of pyrrolidinofullerene derivatives as ETLs in p–i–n PSCs and reported a PCE of 20%. 25 The designed ETLs enabled long-term ambient stability for ∼1056 h ( T 80 ) in air but without light illumination.…”
In this contribution, we report the synthesis and structural characterization of a series of fullerene derivatives and their further systematic investigation as promising ETL (electron transport layer) materials in p-i-n...
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