The need for moving electricity generation to a sustainable model requires the development of low cost ubiquitous photovoltaics (PVs) to harvest the planet’s primary energy source, the Sun. Building upon the successes of Si-based and CdTe-based PV technologies, PVs with lower-embodied energy and requiring lower carbon dioxide equivalent to produce will be required to meet long-term sustainability goals. In particular, thin-film technologies, such as high-efficiency metal halide perovskite (MHP) PV modules, provide avenues to reduced embodied energy, lower energy payback times, and enabling energy-dense tandems [H. M. Wikoff et al., Joule 6(7), 1710–1725 (2022) and V. Fthenakis, Renewable Sustainable Energy Rev. 13(9), 2746–2750 (2009)]. The ability to improve efficiency and lower energy payback time of next generation thin-film PV modules is a critical foundation for green H2 and electrification more broadly. In this regard, Pb-based MHP-PVs have separated themselves as a result of the high-efficiencies that can be realized across a range of electronic gaps. Questions regarding Pb-based MHP-PVs that are often asked, as the challenges of efficiency and reliability are met, revolve around the “problem” of the Pb content. Specifically, “does Pb toxicity preclude MHP-PV modules from being deployed at the TW scale?” To provide this sense of scale, in 2021, the United States burned 10.5 quads of coal, with 90% of that used for electricity generation. Given the energy content of coal of 29 MJ/kg and a residual lead content in that coal of 30 mg/kg, electricity generation from coal resulted in more lead emitted into the atmosphere than what would be required to produce over 2 TW of MHP-PV name plate capacity (assuming a 20% module efficiency and an ∼700 nm active layer). This amounts to more PV power than has been deployed across all PV technologies and geographies to date. This only includes US coal consumption; the rest of the world would be much larger. This example illustrates the scale of the material usage relative to the energy production. Imagine a power-generation technology that offsets these Pb emissions from coal and essentially sequesters this Pb content between two sheets of impermeable glass. Why should we let Pb’s history of misuse prevent it from being included in next generation PV modules that can enable a sustainable energy future?
{"title":"Leaving in the lead: Priorities for perovskite photovoltaics","authors":"Joseph J. Berry, M. D. Irwin","doi":"10.1063/5.0150167","DOIUrl":"https://doi.org/10.1063/5.0150167","url":null,"abstract":"The need for moving electricity generation to a sustainable model requires the development of low cost ubiquitous photovoltaics (PVs) to harvest the planet’s primary energy source, the Sun. Building upon the successes of Si-based and CdTe-based PV technologies, PVs with lower-embodied energy and requiring lower carbon dioxide equivalent to produce will be required to meet long-term sustainability goals. In particular, thin-film technologies, such as high-efficiency metal halide perovskite (MHP) PV modules, provide avenues to reduced embodied energy, lower energy payback times, and enabling energy-dense tandems [H. M. Wikoff et al., Joule 6(7), 1710–1725 (2022) and V. Fthenakis, Renewable Sustainable Energy Rev. 13(9), 2746–2750 (2009)]. The ability to improve efficiency and lower energy payback time of next generation thin-film PV modules is a critical foundation for green H2 and electrification more broadly. In this regard, Pb-based MHP-PVs have separated themselves as a result of the high-efficiencies that can be realized across a range of electronic gaps. Questions regarding Pb-based MHP-PVs that are often asked, as the challenges of efficiency and reliability are met, revolve around the “problem” of the Pb content. Specifically, “does Pb toxicity preclude MHP-PV modules from being deployed at the TW scale?” To provide this sense of scale, in 2021, the United States burned 10.5 quads of coal, with 90% of that used for electricity generation. Given the energy content of coal of 29 MJ/kg and a residual lead content in that coal of 30 mg/kg, electricity generation from coal resulted in more lead emitted into the atmosphere than what would be required to produce over 2 TW of MHP-PV name plate capacity (assuming a 20% module efficiency and an ∼700 nm active layer). This amounts to more PV power than has been deployed across all PV technologies and geographies to date. This only includes US coal consumption; the rest of the world would be much larger. This example illustrates the scale of the material usage relative to the energy production. Imagine a power-generation technology that offsets these Pb emissions from coal and essentially sequesters this Pb content between two sheets of impermeable glass. Why should we let Pb’s history of misuse prevent it from being included in next generation PV modules that can enable a sustainable energy future?","PeriodicalId":178574,"journal":{"name":"APL Energy","volume":"2 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"131588979","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
R. Chiara, G. Accorsi, A. Listorti, M. Coduri, Clarissa Coccia, C. Tedesco, M. Morana, L. Malavasi
We report here a novel series of halide alloyed Ge-containing 2D perovskites including decylammonium as organic spacer, namely DA2Ge(Br1−xIx)4. This system forms a continuous solid solution on the halide site with a modulation of the bandgap from 2.74 to 2.17 eV with a rapid decrease up to x = 0.5 followed by a plateau. Iodide-rich compositions show enhanced broad room temperature (RT) photoluminescence (PL) that narrows at low temperature with maximum quantum yields for mixed compositions. The replacement of Ge with Pb and Sn in DA2GeBr4 and DA2GeI4 provides a tuning of the bandgap in the whole visible spectrum with a marked blue-shift when lead is present and, opposite, a red-shift for Sn replacement. The RT PL progressively broadens moving from Pb to Sn and to Ge covering an emission range from 400 to 800 nm. Finally, the air stability of lead-free 2D perovskites of this work has been determined indicating its improvement by increasing the hardness of the halide.
{"title":"Halide alloying and role of central atom on the structural and optical properties of decylammonium germanium 2D perovskites","authors":"R. Chiara, G. Accorsi, A. Listorti, M. Coduri, Clarissa Coccia, C. Tedesco, M. Morana, L. Malavasi","doi":"10.1063/5.0146748","DOIUrl":"https://doi.org/10.1063/5.0146748","url":null,"abstract":"We report here a novel series of halide alloyed Ge-containing 2D perovskites including decylammonium as organic spacer, namely DA2Ge(Br1−xIx)4. This system forms a continuous solid solution on the halide site with a modulation of the bandgap from 2.74 to 2.17 eV with a rapid decrease up to x = 0.5 followed by a plateau. Iodide-rich compositions show enhanced broad room temperature (RT) photoluminescence (PL) that narrows at low temperature with maximum quantum yields for mixed compositions. The replacement of Ge with Pb and Sn in DA2GeBr4 and DA2GeI4 provides a tuning of the bandgap in the whole visible spectrum with a marked blue-shift when lead is present and, opposite, a red-shift for Sn replacement. The RT PL progressively broadens moving from Pb to Sn and to Ge covering an emission range from 400 to 800 nm. Finally, the air stability of lead-free 2D perovskites of this work has been determined indicating its improvement by increasing the hardness of the halide.","PeriodicalId":178574,"journal":{"name":"APL Energy","volume":"107 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"132509219","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Alan B. Kaplan, Q. Burlingame, Rudolph Holley, Y. Loo
Perovskite CsPbI3 is a promising photovoltaic absorber material, thanks to its ideal bandgap for Si-tandem solar cell applications and its excellent thermochemical stability compared with hybrid organic–inorganic perovskites. However, CsPbI3 has its own stability challenges as its photoactive β- and γ-polymorphs are thermodynamically unstable at room temperature compared with the yellow non-perovskite δ-phase. Stabilizing CsPbI3 has, thus, been the subject of considerable research in recent years. While some approaches, such as alloying with halides and reducing crystalline domain size, have proven effective in improving phase stability, these benefits have, thus far, come at the expense of photovoltaic efficiency compared with the state-of-the-art CsPbI3 solar cells. In this perspective, we discuss the progress and limitations of inorganic perovskite stabilization techniques and look forward at how to achieve inorganic perovskite solar cells with both commercially viable efficiencies and lifetimes.
{"title":"Prospects for inorganic CsPbI3 perovskite solar cells with commercially viable lifetimes","authors":"Alan B. Kaplan, Q. Burlingame, Rudolph Holley, Y. Loo","doi":"10.1063/5.0147116","DOIUrl":"https://doi.org/10.1063/5.0147116","url":null,"abstract":"Perovskite CsPbI3 is a promising photovoltaic absorber material, thanks to its ideal bandgap for Si-tandem solar cell applications and its excellent thermochemical stability compared with hybrid organic–inorganic perovskites. However, CsPbI3 has its own stability challenges as its photoactive β- and γ-polymorphs are thermodynamically unstable at room temperature compared with the yellow non-perovskite δ-phase. Stabilizing CsPbI3 has, thus, been the subject of considerable research in recent years. While some approaches, such as alloying with halides and reducing crystalline domain size, have proven effective in improving phase stability, these benefits have, thus far, come at the expense of photovoltaic efficiency compared with the state-of-the-art CsPbI3 solar cells. In this perspective, we discuss the progress and limitations of inorganic perovskite stabilization techniques and look forward at how to achieve inorganic perovskite solar cells with both commercially viable efficiencies and lifetimes.","PeriodicalId":178574,"journal":{"name":"APL Energy","volume":"48 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"129587553","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"APL Energy. Bridging the gap between fundamental research and technological innovation","authors":"M. Lira-Cantú","doi":"10.1063/5.0153209","DOIUrl":"https://doi.org/10.1063/5.0153209","url":null,"abstract":"","PeriodicalId":178574,"journal":{"name":"APL Energy","volume":"15 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"131102135","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
M. Sha, Bili Zhu, Qian Wang, Ping Deng, Xunfan Liao, Hang Yin, Xiaotao Hao
All-polymer solar cells (all-PSCs) have attracted enormous attention and achieved significant progress in recent years due to their long-term stability and excellent film stretchability. However, the problem of morphology control in bulk-heterojunction (BHJ) films due to highly entangled polymeric chains hinders the further improvement of device performance. In this work, we obtained fine-tuned photoactive layer morphology through reconstructed microstructure induced by steric effects to realize an improved device performance in ternary all-PSCs. The large tetrahexylphenyl substituents on the backbone of naphthalene diimide–indacenodithienothiophene based copolymer acceptor BL-102 bring forth the steric-hindrance effect and influence intermolecular interactions. Therefore, the copolymer BL-102 delivers the property of suppressed self-aggregation, causing reconstructed crystalline features and morphology in blending films. The ternary devices tended to reduce the excessive phase separation by suppressing the aggregation of original polymers but to promote intermixing behaviors. Therefore, the optimal BHJ film manifested a well-formed bi-continuous interpenetrating nanoscale network with a larger π–π stacking coherence length and ordered face-on molecular orientation. Hence, a faster electron transfer (ET) and hole transfer (HT) process combined with balanced charge carrier mobilities can be achieved to enhance the overall device performance. This work provides an effective method to regulate the photoactive layer morphology of all-PSCs through structurally steric hindrance effects and demonstrate the significance of ternary-blending strategy induced nanoscale morphology modulation for fabricating highly efficient all-PSCs.
{"title":"Crystallinity and phase separation induced morphological modulation for efficient ternary all-polymer solar cells","authors":"M. Sha, Bili Zhu, Qian Wang, Ping Deng, Xunfan Liao, Hang Yin, Xiaotao Hao","doi":"10.1063/5.0131128","DOIUrl":"https://doi.org/10.1063/5.0131128","url":null,"abstract":"All-polymer solar cells (all-PSCs) have attracted enormous attention and achieved significant progress in recent years due to their long-term stability and excellent film stretchability. However, the problem of morphology control in bulk-heterojunction (BHJ) films due to highly entangled polymeric chains hinders the further improvement of device performance. In this work, we obtained fine-tuned photoactive layer morphology through reconstructed microstructure induced by steric effects to realize an improved device performance in ternary all-PSCs. The large tetrahexylphenyl substituents on the backbone of naphthalene diimide–indacenodithienothiophene based copolymer acceptor BL-102 bring forth the steric-hindrance effect and influence intermolecular interactions. Therefore, the copolymer BL-102 delivers the property of suppressed self-aggregation, causing reconstructed crystalline features and morphology in blending films. The ternary devices tended to reduce the excessive phase separation by suppressing the aggregation of original polymers but to promote intermixing behaviors. Therefore, the optimal BHJ film manifested a well-formed bi-continuous interpenetrating nanoscale network with a larger π–π stacking coherence length and ordered face-on molecular orientation. Hence, a faster electron transfer (ET) and hole transfer (HT) process combined with balanced charge carrier mobilities can be achieved to enhance the overall device performance. This work provides an effective method to regulate the photoactive layer morphology of all-PSCs through structurally steric hindrance effects and demonstrate the significance of ternary-blending strategy induced nanoscale morphology modulation for fabricating highly efficient all-PSCs.","PeriodicalId":178574,"journal":{"name":"APL Energy","volume":"25 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"130123035","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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