Solar RRL最新文献

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A Metal-Free Boron Carbon Nitride (BCN) Photocatalyst for Enhanced CO2-to-CH4 Conversion by Surface Electronic Tuning 无金属硼碳氮化(BCN)光催化剂表面电子调谐增强co2到ch4的转化
IF 6 3区 工程技术
Solar RRL Pub Date : 2025-03-24 DOI: 10.1002/solr.202500037
Hansong Zhang, Xinyue Han, Jingming Zhu, Siyu Lou, Pengfei Song, Yannick J. Dappe, Zhenhuai Yang, Yongjie Wang, Jiaqi Zhu
{"title":"A Metal-Free Boron Carbon Nitride (BCN) Photocatalyst for Enhanced CO2-to-CH4 Conversion by Surface Electronic Tuning","authors":"Hansong Zhang,&nbsp;Xinyue Han,&nbsp;Jingming Zhu,&nbsp;Siyu Lou,&nbsp;Pengfei Song,&nbsp;Yannick J. Dappe,&nbsp;Zhenhuai Yang,&nbsp;Yongjie Wang,&nbsp;Jiaqi Zhu","doi":"10.1002/solr.202500037","DOIUrl":"https://doi.org/10.1002/solr.202500037","url":null,"abstract":"<p>Graphitic carbon nitride (g-C<sub>3</sub>N<sub>4</sub>) has emerged as an attractive metal-free photocatalyst due to its numerous advantages like tunable surface chemistry, Earth abundance, and nontoxicity. Unfortunately, its photocatalytic efficiency has been seriously limited by charge carrier recombination and low reaction dynamics. Here, we report a metal-free BCN photocatalyst achieving highly selective CO<sub>2</sub>-to-CH<sub>4</sub> conversion under visible light without requiring any metal cocatalyst. The exfoliated CN nanosheets can enrich the reaction interface with protons to accelerate the protonation of CO intermediate to further produce CH<sub>4</sub>. Moreover, B doping not only introduces more reactive defects but also tunes its electronic structure with a more negative conduction band for rapid electron extraction and enhance CO<sub>2</sub>-to-CH<sub>4</sub> conversion. Photocatalytic measurements show that CH<sub>4</sub> production rate and CH<sub>4</sub>/CO ratio are 24 and 13 times higher than those of bulk CN, respectively. The CH<sub>4</sub> production rate can also reach 130 and 31 times higher than that of few-layer g-C<sub>3</sub>N<sub>4</sub> (FL-CN) and Cu/FL-CN, respectively. The electron selectivity toward CH<sub>4</sub> generation on BCN photocatalysts can reach ≈90%. Furthermore, sunlight driving CO<sub>2</sub>-to-CH<sub>4</sub> conversion on such BCN photocatalysts has also been demonstrated. This work offers new insights for the design of customized multifunctional 2D materials for solar-driven CO<sub>2</sub> conversion to CH<sub>4</sub>.</p>","PeriodicalId":230,"journal":{"name":"Solar RRL","volume":"9 8","pages":""},"PeriodicalIF":6.0,"publicationDate":"2025-03-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143865694","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Recombination Effects of Urbach Tails as Trap States in Cu(In, Ga)Se2 Solar Cells Probed by Temperature-Dependent Junction-Transient Spectroscopies 温度相关结态-瞬态光谱探测Cu(in, Ga)Se2太阳能电池中Urbach尾作为陷阱态的重组效应
IF 6 3区 工程技术
Solar RRL Pub Date : 2025-03-24 DOI: 10.1002/solr.202400925
Cheuk Kai Gary Kwok, Naoki Masuko, Shogo Ishizuka, Roland Scheer, Muhammad Monirul Islam, Takeaki Sakurai
{"title":"Recombination Effects of Urbach Tails as Trap States in Cu(In, Ga)Se2 Solar Cells Probed by Temperature-Dependent Junction-Transient Spectroscopies","authors":"Cheuk Kai Gary Kwok,&nbsp;Naoki Masuko,&nbsp;Shogo Ishizuka,&nbsp;Roland Scheer,&nbsp;Muhammad Monirul Islam,&nbsp;Takeaki Sakurai","doi":"10.1002/solr.202400925","DOIUrl":"https://doi.org/10.1002/solr.202400925","url":null,"abstract":"<p>Recombination centers such as carrier traps due to point defects have long been known as one major limitation to the device efficiency of solar cells. Realizing the origin and the mechanism of the trapping and recombination processes enables a smart design strategy of high-performance photovoltaic (PV) technologies. Thin film Cu(In, Ga)Se<sub>2</sub> solar cells have been commercially used in the PV community due to their high power conversion efficiency, cost-effectiveness, and chemical stability. In this work, we explore the roles of subgap defect states in carrier trapping, in particular effects of Urbach tails in terms of the recombination mechanism, in Cu(In, Ga)Se<sub>2</sub> solar cells via junction-transient spectroscopic techniques. The temperature-dependent Urbach energy (<i>E</i><sub>U</sub>) was extracted from transient photocapacitance (TPC) and transient photocurrent (TPI) measurements. Thermal quenching behavior is observed at ~220 K for slightly different optimum Ga concentrations, with activation energies of 0.2–0.3 eV obtained from the thermal quenching model. The thermal and optical activation processes along the defect states are further interpreted using a 1D configuration coordinate model which takes the electron–phonon interaction into consideration.</p>","PeriodicalId":230,"journal":{"name":"Solar RRL","volume":"9 8","pages":""},"PeriodicalIF":6.0,"publicationDate":"2025-03-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/solr.202400925","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143865692","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synthesis and Photovoltaic Characterization of Cs3Sb2Br9 Thin Films Cs3Sb2Br9薄膜的合成及光伏表征
IF 6 3区 工程技术
Solar RRL Pub Date : 2025-03-21 DOI: 10.1002/solr.202400815
Wenqi Yan, Nadja Glück, Wenxin Mao, Sebastian O. Fürer, Saripally Sudhaker Reddy, Anthony S. R. Chesman, Alexandr N. Simonov, Udo Bach
{"title":"Synthesis and Photovoltaic Characterization of Cs3Sb2Br9 Thin Films","authors":"Wenqi Yan,&nbsp;Nadja Glück,&nbsp;Wenxin Mao,&nbsp;Sebastian O. Fürer,&nbsp;Saripally Sudhaker Reddy,&nbsp;Anthony S. R. Chesman,&nbsp;Alexandr N. Simonov,&nbsp;Udo Bach","doi":"10.1002/solr.202400815","DOIUrl":"https://doi.org/10.1002/solr.202400815","url":null,"abstract":"<p>Inorganic antimony halides with the general formula A<sub>3</sub>Sb<sub>2</sub>X<sub>9</sub> have emerged as promising materials for photovoltaic applications due to their low toxicity and high stability. However, achieving high-quality thin-film morphology with this class of materials remains challenging, which adversely affects performance of the solar cell devices. In this work, a facile synthesis procedure is demonstrated for the fabrication of highly crystalline and pinhole-free Cs<sub>3</sub>Sb<sub>2</sub>Br<sub>9</sub> thin films by introducing a post-annealing process in a solvent-rich atmosphere. Stability of the resulting Cs<sub>3</sub>Sb<sub>2</sub>Br<sub>9</sub> films on a timescale of 3 days under ambient conditions at 60% relative humidity is demonstrated. Photovoltaic performance of the Cs<sub>3</sub>Sb<sub>2</sub>Br<sub>9</sub> films is assessed using a standard <i>n-i-p</i> configuration, which produces a power conversion efficiency of 0.173% ± 0.014% under simulated 1 sun irradiation, which represents an improvement compared to the lower efficiency (0.053% ± 0.006%) observed in Cs<sub>3</sub>Sb<sub>2</sub>Br<sub>9</sub> films prepared using conventional methods.</p>","PeriodicalId":230,"journal":{"name":"Solar RRL","volume":"9 8","pages":""},"PeriodicalIF":6.0,"publicationDate":"2025-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/solr.202400815","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143865651","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Nonbonded Electronic Coupling between Au and Phenolic Hydroxyl Groups in Resorcinol-Formaldehyde Resin: Enhanced Interfacial Charge Transfer and H2O2 Photosynthesis 间苯二酚-甲醛树脂中Au和酚羟基之间的非键电子耦合:增强界面电荷转移和H2O2光合作用
IF 6 3区 工程技术
Solar RRL Pub Date : 2025-03-20 DOI: 10.1002/solr.202500087
Yuyang Tang, Wuming Wang, Jiaqi Ran, Cheng Peng, Wenhai Chu
{"title":"Nonbonded Electronic Coupling between Au and Phenolic Hydroxyl Groups in Resorcinol-Formaldehyde Resin: Enhanced Interfacial Charge Transfer and H2O2 Photosynthesis","authors":"Yuyang Tang,&nbsp;Wuming Wang,&nbsp;Jiaqi Ran,&nbsp;Cheng Peng,&nbsp;Wenhai Chu","doi":"10.1002/solr.202500087","DOIUrl":"https://doi.org/10.1002/solr.202500087","url":null,"abstract":"<p>Harnessing sunlight for the direct generation of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) from water and air presents a significant challenge in sustainable chemistry.Resorcinol-formaldehyde (RF) resins, as emerging donor–acceptor (D-A) polymeric photocatalysts, encounter limitations stemming from inefficient charge transfer. This study introduces the design and synthesis of noble metal (Au, Ag, and Pt) nanoparticle-modified RF resins, with a specific focus on Au-RF due to its exceptional photocatalytic activity. The electronic coupling at the interface between Au nanoparticles and the C<span></span>O bonds of phenolic hydroxyl groups in RF resin facilitates efficient charge transfer, leading to a remarkable improvement in photocatalytic performance, which is attributed to interfacial interactions rather than surface plasmon resonance effects. The optimized Au-RF composite demonstrates a record photocatalytic H<sub>2</sub>O<sub>2</sub> production rate of 252.28 μmol g<sup>−1</sup> h<sup>−1</sup> with a solar-chemical conversion efficiency of 1.23% after 6 h, significantly surpassing that of the pristine RF resin. This research paves the way for the development of efficient D-A polymeric photocatalysts for sustainable H<sub>2</sub>O<sub>2</sub> production under solar irradiation.</p>","PeriodicalId":230,"journal":{"name":"Solar RRL","volume":"9 9","pages":""},"PeriodicalIF":6.0,"publicationDate":"2025-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143909481","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Photothermal Promotion of Uranium Extraction from Seawater with Self-Supporting Functionalized Polyurethane Sponge 光热促进自支撑功能化聚氨酯海绵从海水中提取铀
IF 6 3区 工程技术
Solar RRL Pub Date : 2025-03-18 DOI: 10.1002/solr.202500011
Xinyu Kong, Zewen Shen, Huihui Jin, Hao Pan, Hongliang Bao, Chumin Yan, Yezi Hu, Guixia Zhao, Xiangke Wang, Xiubing Huang
{"title":"Photothermal Promotion of Uranium Extraction from Seawater with Self-Supporting Functionalized Polyurethane Sponge","authors":"Xinyu Kong,&nbsp;Zewen Shen,&nbsp;Huihui Jin,&nbsp;Hao Pan,&nbsp;Hongliang Bao,&nbsp;Chumin Yan,&nbsp;Yezi Hu,&nbsp;Guixia Zhao,&nbsp;Xiangke Wang,&nbsp;Xiubing Huang","doi":"10.1002/solr.202500011","DOIUrl":"https://doi.org/10.1002/solr.202500011","url":null,"abstract":"<p>Extracting uranium from seawater at an ultralow concentration (3.3 ppb) is a promising approach for the sustainable development of nuclear energy, which presents a critical obstacle. Herein, we report a photothermal-promoted extraction strategy by utilizing a self-supporting covalent organic polymer-based sponge (named TpPa-SO<sub>3</sub>H@PU sponge) composed of black polyurethane sponge substrate and <i>β</i>-ketoenamine covalent organic polymer with sulfonic acid groups. The adequate water transport induced by photothermal conversion significantly improves the mass transfer of uranyl ions. Compared with the dark condition, a 25.8% increase of uranyl extraction capacity, up to 36.4 mg g<sup>−1</sup>, is achieved under simulated sunlight irradiation. In 1 L of seawater, 83.8% of uranyl is extracted after exposure to natural sunlight for 48 h. Furthermore, 20 mL of concentrated solution containing 1 ppm uranyl is obtained from 9 L seawater after nine consecutive extraction-elution cycles. These results demonstrate that TpPa-SO<sub>3</sub>H@PU sponge holds significant potential for practical uranium extraction from seawater under natural sunlight.</p>","PeriodicalId":230,"journal":{"name":"Solar RRL","volume":"9 8","pages":""},"PeriodicalIF":6.0,"publicationDate":"2025-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143865841","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Medium-Bandgap Acceptors for Efficient Ternary Organic Solar Cells Achieved by End-Group Engineering 端基工程制备高效三元有机太阳能电池的中带隙受体
IF 6 3区 工程技术
Solar RRL Pub Date : 2025-03-18 DOI: 10.1002/solr.202500088
Long Chen, Yuanyuan Liu, Hong-Jian Deng, Yu-Jie Zhou, Wen-Rui Liu, Zheng-Chun Yin, Shi-Qi Ye, Zhi-Wei Xu, Qun Zhang, Guan-Wu Wang
{"title":"Medium-Bandgap Acceptors for Efficient Ternary Organic Solar Cells Achieved by End-Group Engineering","authors":"Long Chen,&nbsp;Yuanyuan Liu,&nbsp;Hong-Jian Deng,&nbsp;Yu-Jie Zhou,&nbsp;Wen-Rui Liu,&nbsp;Zheng-Chun Yin,&nbsp;Shi-Qi Ye,&nbsp;Zhi-Wei Xu,&nbsp;Qun Zhang,&nbsp;Guan-Wu Wang","doi":"10.1002/solr.202500088","DOIUrl":"https://doi.org/10.1002/solr.202500088","url":null,"abstract":"<p>The ternary strategy has been evidenced as one of the most crucial methods to improve the photovoltaic performance of organic solar cells. However, the selection and design of the third components are decisive factors facilitating the progress of ternary organic solar cells (TOSCs). In this study, focuses are concentrated on the D18-Cl:N3 binary host device by developing a weakly electron-withdrawing end group and synthesizing a guest acceptor, BTP-CM, which holds a similar backbone to N3. The structure resemblance ensures good compatibility of the molecule with N3, which improves charge transport and reduces charge recombination. Thereby, the D18-Cl:N3:BTP-CM-based TOSC exhibits an improved power conversion efficiency to 18.32%, compared to 17.13% of the binary device. This work provides an effective strategy for the design of guest acceptors, which aims to introduce new weakly electron-withdrawing end groups to obtain molecules with complementary absorptions and matched energy levels while preserving the molecular backbone of the host acceptor.</p>","PeriodicalId":230,"journal":{"name":"Solar RRL","volume":"9 9","pages":""},"PeriodicalIF":6.0,"publicationDate":"2025-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143909668","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Modulating Internal Residual Stress for Efficient and Durable Flexible Perovskite Solar Cells 高效耐用柔性钙钛矿太阳能电池的内部残余应力调节
IF 6 3区 工程技术
Solar RRL Pub Date : 2025-03-18 DOI: 10.1002/solr.202500052
Gan Zuo, Peide Zhu, Jie Zeng, Deng Wang, Wenbo Peng, Gang Liu, Xingzhu Wang, Yong Zhang, Baomin Xu
{"title":"Modulating Internal Residual Stress for Efficient and Durable Flexible Perovskite Solar Cells","authors":"Gan Zuo,&nbsp;Peide Zhu,&nbsp;Jie Zeng,&nbsp;Deng Wang,&nbsp;Wenbo Peng,&nbsp;Gang Liu,&nbsp;Xingzhu Wang,&nbsp;Yong Zhang,&nbsp;Baomin Xu","doi":"10.1002/solr.202500052","DOIUrl":"https://doi.org/10.1002/solr.202500052","url":null,"abstract":"<p>Flexible perovskite solar cells (F-PSCs) are promising due to their low cost and versatility. However, the thermal instability of flexible substrates often results in internal defects and residual stress during the formation of perovskite films. To address this issue, cellulose diacetate (CDA), a green and eco-friendly material derived from natural plant fibers, is used. CDA not only enhanced the quality of the perovskite films but also reduced the generation of internal residual stress. Furthermore, it effectively passivates defects that arise during the annealing process. As a result, a power conversion efficiency of 24.68% on flexible substrate, which is one of the highest values in the F-PSCs, is achieved. The incorporation of CDA also lead to a more uniform stress distribution in the films during bending, significantly improving the long-term environmental stability of the flexible devices. This sustainable fiber-based approach provides a new direction for the advancement of flexible solar cells.</p>","PeriodicalId":230,"journal":{"name":"Solar RRL","volume":"9 9","pages":""},"PeriodicalIF":6.0,"publicationDate":"2025-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143909667","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Scalable Passivation of Perovskite Solar Cells Using Evaporated CsPbCl3 利用蒸发态 CsPbCl3 对过氧化物太阳能电池进行可扩展的钝化处理
IF 6 3区 工程技术
Solar RRL Pub Date : 2025-03-16 DOI: 10.1002/solr.202500042
Youpeng Wang, You Gao, Pengfei Liu, Chen Jia, Jin Si, Jiuda Wen, Zetong Sunli, Xiaona Du, Ying Zhao, Xiaodan Zhang, Biao Shi
{"title":"Scalable Passivation of Perovskite Solar Cells Using Evaporated CsPbCl3","authors":"Youpeng Wang,&nbsp;You Gao,&nbsp;Pengfei Liu,&nbsp;Chen Jia,&nbsp;Jin Si,&nbsp;Jiuda Wen,&nbsp;Zetong Sunli,&nbsp;Xiaona Du,&nbsp;Ying Zhao,&nbsp;Xiaodan Zhang,&nbsp;Biao Shi","doi":"10.1002/solr.202500042","DOIUrl":"https://doi.org/10.1002/solr.202500042","url":null,"abstract":"<p>The suboptimal interfacial quality between the perovskite absorption layer and the electron-transport layer constrains the performance of perovskite solar cells. Introducing an interface passivation layer is generally recognized as an effective method for addressing this issue. A uniform passivation film with a large area can be prepared using an evaporation technique. In this study, we designed and fabricated an inorganic CsPbCl<sub>3</sub> passivation layer by the coevaporation of PbCl<sub>2</sub> and CsCl. The evaporated passivator exhibited excellent interface passivation effects and a relatively low thickness sensitivity to device performance. As a result, the open-circuit voltage of perovskite solar cells with a 1.68 eV perovskite absorber was improved by nearly 100 mV, and the device efficiency achieved was 21.84%, ranking as the highest efficiency based on the hybrid evaporation-solution method. The proposed passivation approach has potential applications in large-area perovskite solar cells.</p>","PeriodicalId":230,"journal":{"name":"Solar RRL","volume":"9 8","pages":""},"PeriodicalIF":6.0,"publicationDate":"2025-03-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143865990","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Investigation of Potential-Induced Degradation in Perovskite Solar Cells under Inert Conditions 惰性条件下钙钛矿太阳能电池电位诱导降解的研究
IF 6 3区 工程技术
Solar RRL Pub Date : 2025-03-16 DOI: 10.1002/solr.202400923
Robbe Breugelmans, Stijn Lammar, Aranzazu Aguirre, Tom Aernouts, Bart Vermang, Michaël Daenen
{"title":"Investigation of Potential-Induced Degradation in Perovskite Solar Cells under Inert Conditions","authors":"Robbe Breugelmans,&nbsp;Stijn Lammar,&nbsp;Aranzazu Aguirre,&nbsp;Tom Aernouts,&nbsp;Bart Vermang,&nbsp;Michaël Daenen","doi":"10.1002/solr.202400923","DOIUrl":"https://doi.org/10.1002/solr.202400923","url":null,"abstract":"<p>Perovskite solar cells (PSCs) have emerged as a promising photovoltaic technology due to their remarkable efficiency advancements. However, their commercialization is hindered by stability challenges, including sensitivity to environmental conditions and a critical degradation mechanism known as potential-induced degradation (PID). PID can significantly impair PSC performance within hours under operational conditions. This study investigates PID in 48 triple-cation p-i-n PSCs over 313 h in an inert environment, excluding additional stressors like moisture and oxygen. The PID-stressed devices degraded to 79% of their initial efficiency, primarily driven by losses in short-circuit current density. Time-of-flight secondary ion mass spectroscopy revealed sodium ion migration from soda-lime glass substrates into the perovskite layer. Interestingly, photoluminescence and X-ray diffraction analyses detected no measurable differences between PID-stressed and reference devices, contradicting prior literature that associates PID with perovskite segregation and decomposition. These findings challenge the conventional understanding of PID, suggesting that environmental factors such as oxygen and moisture might exacerbate degradation effects. This work provides critical insights into the intrinsic mechanisms of PID under controlled conditions and highlights the need for further research into the interplay between PID and environmental stressors to guide the development of more stable PSC technologies.</p>","PeriodicalId":230,"journal":{"name":"Solar RRL","volume":"9 7","pages":""},"PeriodicalIF":6.0,"publicationDate":"2025-03-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143761937","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
ZIF-67 Anchored Mn0.5Cd0.5S Constructs S-Scheme Heterojunctions to Facilitate Photocatalytic Hydrogen Production ZIF-67锚定Mn0.5Cd0.5S构建s型异质结促进光催化制氢
IF 6 3区 工程技术
Solar RRL Pub Date : 2025-03-12 DOI: 10.1002/solr.202500038
Kang Liu, Fei Jin, Jieyuan Du, Peizhen Wang, Guoping Jiang, Zhiliang Jin
{"title":"ZIF-67 Anchored Mn0.5Cd0.5S Constructs S-Scheme Heterojunctions to Facilitate Photocatalytic Hydrogen Production","authors":"Kang Liu,&nbsp;Fei Jin,&nbsp;Jieyuan Du,&nbsp;Peizhen Wang,&nbsp;Guoping Jiang,&nbsp;Zhiliang Jin","doi":"10.1002/solr.202500038","DOIUrl":"https://doi.org/10.1002/solr.202500038","url":null,"abstract":"<p>Photocatalytic hydrogen production is regarded as one of the most promising approaches for solar energy utilization due to its reliance on renewable energy sources, environmental friendliness, and generation of clean energy. In this field, Mn<sub>0.5</sub>Cd<sub>0.5</sub>S demonstrates considerable potential, but its severe stacking issue and insufficient exposure of active sites restrict its application. Although Mn<sub>0.5</sub>Cd<sub>0.5</sub>S demonstrates considerable potential, its severe stacking issue and insufficient exposure of active sites restrict its application. In this research, by combining Mn<sub>0.5</sub>Cd<sub>0.5</sub>S with dodecahedral ZIF-67 and optimizing the interfacial electronic structure, a uniform distribution of Mn<sub>0.5</sub>Cd<sub>0.5</sub>S on the surface of ZIF-67 was successfully accomplished. Synthesis of composite materials effectively mitigated the agglomeration phenomenon of Mn<sub>0.5</sub>Cd<sub>0.5</sub>S and constructed an S-scheme heterostructure of Mn<sub>0.5</sub>Cd<sub>0.5</sub>S/ZIF-67. The resulting composite achieved a hydrogen yield of 677.4 μmol in a lactic acid system, 6.8 times higher than that of pure Mn<sub>0.5</sub>Cd<sub>0.5</sub>S. This notable enhancement is attributed to the increased specific surface area of the composite, facilitating greater exposure of the active sites and improving charge transfer efficiency. In situ X-ray photoelectron spectroscopy analysis revealed the underlying electron transfer mechanism, while EPR studies confirmed the enhanced redox capacity of the composite, further supporting its superior performance in hydrogen production. This research offers new insights into morphology and interface engineering for Mn<sub>0.5</sub>Cd<sub>0.5</sub>S-based materials.</p>","PeriodicalId":230,"journal":{"name":"Solar RRL","volume":"9 8","pages":""},"PeriodicalIF":6.0,"publicationDate":"2025-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143865648","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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