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Fabrication processes for all-inorganic CsPbBr3 perovskite solar cells 全无机CsPbBr3钙钛矿太阳能电池的制备工艺
Q1 Chemistry Pub Date : 2023-08-22 DOI: 10.1002/eom2.12407
Jin Ho Park, Young Seon Yoon, Jin Young Kim

All-inorganic perovskite solar cells have shown great potential owing to their superior stability against thermal stress and moisture compared to organic–inorganic perovskite solar cells. However, there are some remaining issues in the all-inorganic perovskite solar cell fabrication process, such as the low solubility of the perovskite precursors and the occurrence of the secondary phases. In this review, we focus on all-inorganic CsPbBr3 perovskite solar cells and categorize them based on their fabrication process. Various processes and strategies that have been developed to solve the aforementioned issues including the general process of multistep spin coating are thoroughly investigated. Finally, a summary of the various processes for the all-inorganic CsPbBr3 perovskite solar cells and an outlook for the development of highly efficient all-inorganic perovskite solar cells are proposed.

与有机-无机钙钛矿太阳能电池相比,全无机钙钛矿太阳能电池由于其优越的抗热应力和湿度稳定性而显示出巨大的潜力。然而,在全无机钙钛矿太阳能电池的制备过程中还存在着钙钛矿前驱体溶解度低和二次相的存在等问题。本文综述了全无机CsPbBr3钙钛矿太阳能电池,并根据其制备工艺对其进行了分类。本文深入研究了为解决上述问题而开发的各种工艺和策略,包括多步旋转涂层的一般工艺。最后,总结了全无机CsPbBr3钙钛矿太阳能电池的各种工艺,并对高效全无机钙钛矿太阳能电池的发展进行了展望。
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引用次数: 0
Rational design of bi‐phase CaV2O6/NaV6O15 cathode materials for long‐life aqueous zinc batteries 长寿命锌水电池用双相CaV2O6/NaV6O15正极材料的合理设计
Q1 Chemistry Pub Date : 2023-08-22 DOI: 10.1002/eom2.12409
Y. Liu, Yi Liu, Xiang Wu
Vanadium‐based compounds with various crystal structures are highly promising cathode materials for aqueous zinc‐based batteries. However, their further development is limited due to the low electrical conductivity, slow zinc ion diffusion, and weak structural stability. It is a feasible strategy to resolve above mentioned issues through surface modification. Herein, we design bi‐phase coexisting CaV2O6/NaV6O15 nanobelt structures with abundant interfaces, which provide more reactive sites than single‐phase ones. The samples as the electrode materials deliver a specific capacity of 312 mAh g−1 at 5 A g−1 after 2000 cycles. They still keep a capacity of 231 mAh g−1 at 10 A g−1 with a cycle life of 6500 times.image
具有多种晶体结构的钒基化合物是极有前途的锌基水性电池正极材料。然而,由于其电导率低、锌离子扩散缓慢、结构稳定性弱,限制了其进一步发展。通过表面改性是解决上述问题的可行策略。在此,我们设计了具有丰富界面的双相共存的CaV2O6/NaV6O15纳米带结构,该结构比单相结构提供了更多的反应位点。作为电极材料的样品在5ag−1下经过2000次循环后的比容量为312 mAh g−1。它们在10a g−1时仍然保持231 mAh g−1的容量,循环寿命为6500次
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引用次数: 2
A self‐adhesive bark veneer for all‐natural plywood 用于全天然胶合板的自粘树皮单板
Q1 Chemistry Pub Date : 2023-08-14 DOI: 10.1002/eom2.12405
Zhongxuan Wu, Yan Zhan, Shuaiming He, Panpan Yue, Guanghui Song, J. Rao, Zi-wen Lv, Bo Jiang, Baozhong Lü, Gegu Chen, Feng Peng
The commercial plywood is mainly made of high‐value wood veneer and formaldehyde‐based adhesives, which pose a major risk to human health and environmental protection. Here, we report an all‐natural plywood made of self‐adhesive bark veneer directly from hardy rubber trees (HRT) via delignification, epoxidation reaction and densification. The resulting bark veneer is demonstrated with sandwich structures featuring natural integration between cellulose and biopolymer Eucommia ulmoides gum (EUG). The intrinsic EUG act as a potential strong “self‐adhesive” and water‐proofing agent, leading to bark veneer with high hardness, excellent hydrophobicity, wear resistance, and low thermal conductivity. Furthermore, we can produce the self‐adhesive plywood on a large scale directly from HRT bark using this approach without any adhesives, endowing it with environmental friendliness, safety in use, and health benefits of human beings. Combining its efficient and low‐cost production, the bark veneer shows great promise in fabricating high‐performance and environmentally sustainable plywood.image
商用胶合板主要由高价值木单板和甲醛基粘合剂制成,对人类健康和环境保护构成重大风险。在这里,我们报道了一种由耐寒橡胶树(HRT)通过脱木素、环氧化反应和致密化直接制成的自粘树皮单板制成的全天然胶合板。所得到的树皮单板具有三明治结构,其特征在于纤维素和生物聚合物杜仲胶(EUG)之间的自然整合。固有的EUG作为一种潜在的强“自粘”和防水剂,使树皮单板具有高硬度、优异的疏水性、耐磨性和低导热性。此外,我们可以在不使用任何粘合剂的情况下,使用这种方法直接从HRT树皮大规模生产自粘胶合板,使其具有环境友好性、使用安全性和对人类健康的益处。树皮单板结合其高效和低成本的生产,在制造高性能和环境可持续的胶合板方面显示出巨大的前景。图片
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引用次数: 0
Chelating resin encapsulation for reduced Pb leakage in perovskite solar cells 螯合树脂封装降低钙钛矿太阳能电池铅泄漏
Q1 Chemistry Pub Date : 2023-08-04 DOI: 10.1002/eom2.12400
Qingrui Wang, Zhenhua Lin, Yumeng Xu, Boyao Zhang, Xing Guo, Zhaosheng Hu, Yue Hao, Jingjing Chang

Although perovskite solar cells have achieved efficiency over 25%, the toxic of Pb content remains severe problem given its commercial prospect. Especially when the devices suffer harsh weather, the Pb content can easily leak out to soil and water. Chelating resins (CRs) exhibit excellent superiority in treating waste water in industrial field, since the functional groups in CRs can adsorb divalent metal ion to soften and purify waste water. Herein, an iminodiacetic acid (IDA)-CR is introduced as encapsulation over perovskite solar cells for the first time. The IDA-CR exhibits high surface area and excellent adsorption capability. Qualitative and quantitative analysis of Pb leakage are studied, and the devices with encapsulation of IDA-CR can detain over 90% of Pb compared with control devices without encapsulation after immersed in deionized water for 12 h even in acid situation or after heating. This IDA-CR method provides a new strategy towards environmental and biological-friendly perovskite optoelectronic devices.

尽管钙钛矿太阳能电池的效率已超过25%,但鉴于其商业前景,铅含量的毒性仍然是一个严重的问题。特别是当设备遭受恶劣天气时,铅含量很容易泄漏到土壤和水中。螯合树脂在处理工业废水方面表现出优异的优越性,因为螯合树脂中的官能团可以吸附二价金属离子来软化和净化废水。本文首次引入亚氨基二乙酸(IDA)-CR作为钙钛矿太阳能电池的封装。IDA-CR表现出高表面积和优异的吸附能力。对铅泄漏进行了定性和定量分析,在去离子水中浸泡12小时后,与未封装的对照装置相比,封装IDA‐CR的装置可滞留90%以上的铅 h即使在酸性条件下或加热后。这种IDA-CR方法为环境和生物友好的钙钛矿光电器件提供了一种新的策略
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引用次数: 0
Irreversible phase back conversion of α-FAPbI3 driven by lithium-ion migration in perovskite solar cells 钙钛矿太阳能电池中锂离子迁移驱动的α-FAPbI3的不可逆相反转换
Q1 Chemistry Pub Date : 2023-08-02 DOI: 10.1002/eom2.12398
Seung-Gu Choi, Jin-Wook Lee

Typically n-i-p structured perovskite solar cells (PSCs) incorporate 2,2′,7,7′-tetrakis (N,N-di-p-methoxyphenyl amine)-9,9′-spirobifluorene (spiro-OMeTAD) as the hole-transporting material. Chemical doping of spiro-OMeTAD involves a lithium bis(trifluoromethyl sulfonyl)imide dopant, causing complex side-reactions that affect the device performance, which are not fully understood. Here, we investigate the aging-dependent device performance of widely used formamidinium lead triiodide (FAPbI3)-based PSCs correlated with lithium-ion (Li+) migration. Comprehensive analyses reveal that Li+ ions migrate from spiro-OMeTAD to perovskite, SnO2, and their interfaces to induce the phase-back conversion of α-FAPbI3 to δ-FAPbI3, generation and migration of iodine defects, and de-doping of spiro-OMeTAD. The rapid performance drop of FAPbI3-based PSCs, even aging under dark conditions, is attributed to a series of these processes. This study identifies the hidden side effects of Li+ ion migration in FAPbI3-based PSCs that can guide further work to maximize the operational stability of PSCs.

通常,n‐i‐p结构钙钛矿太阳能电池(PSC)包含2,2′,7,7′-四(n,n‐二‐p‐甲氧基苯基胺)-9,9′-螺二芴(螺-OMeTAD)作为空穴传输材料。spiro‐OMeTAD的化学掺杂涉及双(三氟甲基磺酰基)酰亚胺锂掺杂剂,导致影响器件性能的复杂副反应,这一点尚不完全清楚。在这里,我们研究了广泛使用的三碘化甲脒铅(FAPbI3)基PSCs与锂离子(Li+)迁移相关的老化相关器件性能。综合分析表明,Li+离子从spiro‐OMeTAD迁移到钙钛矿、SnO2及其界面,以诱导α‐FAPbI3向δ‐FAPbI3的相反转换、碘缺陷的产生和迁移以及spiro‐OMeTAD的去掺杂。基于FAPbI3的PSC的性能快速下降,甚至在黑暗条件下老化,都归因于一系列这些过程。这项研究确定了基于FAPbI3的PSCs中Li+离子迁移的隐藏副作用,可以指导进一步的工作,最大限度地提高PSCs的操作稳定性。图片
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引用次数: 0
Aesthetic and efficient perovskite/Si tandem solar cells using luminescent down-shifting textured anti-reflection films 使用发光下移纹理防反射膜的美观高效的钙钛矿/Si串联太阳能电池
Q1 Chemistry Pub Date : 2023-08-02 DOI: 10.1002/eom2.12399
Eui Dae Jung, Chan Ul Kim, Young Wook Noh, Seong Kuk Seo, Young Im Noh, Kyoung Jin Choi, Myoung Hoon Song

Perovskite-based tandem cells are emerging as new photovoltaic (PV) cells with a high efficiency that exceeds the efficiency limit of single-junction cells. Building-integrated PVs that require high efficiency are attractive, but aesthetics play key roles in these urban applications. One of the most challenging problems with respect to aesthetic PV cells is the efficiency loss due to color tuning. Here, we demonstrate for the first time lossless full-color tunable PV cells based on the use of textured luminescent down-shifting (LDS) films with LDS dyes with ultraviolet-selective absorption. The LDS anti-reflection (AR) films improve the perovskite/Si tandem cell efficiency by reducing the loss of parasitic UV absorption of the layers above the perovskite film due to LDS effect and the loss due to cell reflection due to the textured surface. Therefore, color tuning with LDS AR films can be used to produce highly aesthetic and efficient PV cells for urban applications.

钙钛矿基串联电池是新兴的新型光伏电池,其高效率超过了单结电池的效率极限。需要高效率的建筑集成光伏很有吸引力,但美学在这些城市应用中起着关键作用。美学PV电池最具挑战性的问题之一是由于颜色调整导致的效率损失。在这里,我们首次展示了无损全彩可调光伏电池,该电池基于使用具有紫外选择性吸收的发光下移(LDS)染料的纹理发光下移(LDS)薄膜。LDS抗反射(AR)膜通过减少由于LDS效应而导致的钙钛矿/硅串联电池的寄生紫外吸收损失和由于纹理表面导致的电池反射损失,提高了钙钛矿/硅串联电池的效率。因此,使用LDS AR薄膜进行颜色调整可用于生产高度美观和高效的光伏电池,用于城市应用
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引用次数: 2
Stay healthy under global warming: A review of wearable technology for thermoregulation 全球变暖下保持健康:可穿戴体温调节技术综述
Q1 Chemistry Pub Date : 2023-07-21 DOI: 10.1002/eom2.12396
Ronghui Wu, Ting-Hsuan Chen, Po-Chun Hsu

Global warming has been affecting human health, including direct mortality and morbidity from extreme heat, storms, drought, and indirect infectious diseases. It is not only “global” but extremely “personal”—it is a matter of life and death for many of us. In this perspective, we propose the use of wearable technologies for localized personal thermoregulation as an innovative method to reduce the impact on health and enable wider adaptability to extreme thermal environments. The state-of-the-art thermoregulation methods and wearable sensing technologies are summarized. In addition, the feasibility of thermoregulation technology in preventive medicine for promoting health under climate change is comprehensively discussed. Further, we provide an outlook on health-oriented closed loop that can be achieved based on parallel thermoregulation and multiple data inputs from the physiological, environmental, and psychological cues, which could promote individuals and the public to better adapt to global warming.

全球变暖一直在影响人类健康,包括酷热、风暴、干旱和间接传染病造成的直接死亡和发病率。这不仅是“全球性的”,而且是极其“个人化的”——这对我们许多人来说是生死攸关的问题。从这个角度来看,我们建议使用可穿戴技术进行局部个人体温调节,作为一种创新方法,以减少对健康的影响,并使其能够更广泛地适应极端热环境。综述了最新的温度调节方法和可穿戴传感技术。此外,还全面讨论了体温调节技术在气候变化下促进健康的预防医学中的可行性。此外,我们对以健康为导向的闭环进行了展望,该闭环可以基于平行的体温调节和来自生理、环境和心理线索的多个数据输入来实现,这可以促进个人和公众更好地适应全球变暖。
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引用次数: 0
CoNiFe-layered double hydroxide decorated Co-N-C network as a robust bi-functional oxygen electrocatalyst for zinc-air batteries CoNiFe -层状双氢氧化物修饰Co - N - C网络作为锌-空气电池的强大双功能氧电催化剂
Q1 Chemistry Pub Date : 2023-07-21 DOI: 10.1002/eom2.12394
Yasir Arafat, Yijun Zhong, Muhammad R. Azhar, Mohammad Asif, Moses O. Tadé, Zongping Shao

Rechargeable zinc-air batteries (ZABs) are cost-effective energy storage devices and display high-energy density. To realize high round-trip energy efficiency, it is critical to develop durable bi-functional air electrodes, presenting high catalytic activity towards oxygen evolution/reduction reactions together. Herein, we report a nanocomposite based on ternary CoNiFe-layered double hydroxides (LDH) and cobalt coordinated and N-doped porous carbon (Co-N-C) network, obtained by the in-situ growth of LDH over the surface of ZIF-67-derived 3D porous network. Co-N-C network contributes to the oxygen reduction reaction activity, while CoNiFe-LDH imparts to the oxygen evolution reaction activity. The rich active sites and enhanced electronic and mass transport properties stemmed from their unique architecture, culminated into outstanding bi-functional catalytic activity towards oxygen evolution/reduction in alkaline media. In ZABs, it displays a high peak power density of 228 mW cm−2 and a low voltage gap of 0.77 V over an ultra-long lifespan of 950 h.

可充电锌空气电池(ZABs)是一种具有高性价比和高能量密度的储能装置。为了实现高往返能量效率,开发耐用的双功能空气电极是关键,同时对析氧/还原反应具有高催化活性。在此,我们报道了一种基于三元conive层状双氢氧化物(LDH)和钴配位n掺杂多孔碳(Co-N-C)网络的纳米复合材料,该复合材料是通过在zif -67衍生的三维多孔网络表面原位生长LDH而获得的。Co-N-C网络对氧还原反应活性有贡献,CoNiFe-LDH网络对析氧反应活性有贡献。丰富的活性位点和增强的电子和质量输运特性源于其独特的结构,最终形成了在碱性介质中对氧析出/还原的杰出双功能催化活性。在ZABs中,它显示出228 mW cm−2的峰值功率密度和0.77 V的低电压间隙,并具有950 h的超长寿命。
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引用次数: 0
Ligand chemistry for surface functionalization in MXenes: A review MXenes表面功能化的配体化学研究进展
Q1 Chemistry Pub Date : 2023-07-19 DOI: 10.1002/eom2.12395
Sungmin Jung, Ujala Zafar, L. Satish Kumar Achary, Chong Min Koo

Surface chemistry of MXenes is of significant interest due to its potential to control their final optoelectronic and physicochemical properties, and address the oxidation and dispersion stabilities of MXenes. Surface chemistry of MXenes can be manipulated by either MXene synthesis via chemical etching or post surface functionalization method. Although numerous reviews have explored MXene synthesis methods, there has been a lack of focus on post surface functionalization. This review aims to fill this gap by summarizing recent advancements in the MXene surface functionalization chemistry, and elucidating mechanisms, properties, and future perspectives of functionalized MXenes. We discuss organic ligand molecules, such as organic salts, catechols, phosphonates, carboxylates, and silanes, which can be employed to surface-functionalize MXene through covalent or non-covalent bond interaction. This comprehensive review offers valuable insights for scientists and engineers in utilizing functionalized MXenes across diverse applications, including EMI shielding, energy storage, electronics, optoelectronics, and sensors.

MXenes的表面化学具有重要的意义,因为它有可能控制其最终的光电和物理化学性质,并解决MXenes的氧化和分散稳定性。MXene的表面化学性质可以通过化学蚀刻法或表面后功能化法合成。虽然已经有许多综述探讨了MXene的合成方法,但缺乏对表面后功能化的关注。本文旨在通过总结MXene表面功能化化学的最新进展,阐明功能化MXene的机制、性质和未来前景来填补这一空白。我们讨论了有机配体分子,如有机盐、儿茶酚、膦酸盐、羧酸盐和硅烷,它们可以通过共价键或非共价键相互作用使MXene表面功能化。这篇全面的综述为科学家和工程师在各种应用中利用功能化MXenes提供了有价值的见解,包括EMI屏蔽,储能,电子,光电子和传感器。
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引用次数: 1
Simulation model of a non-contact triboelectric nanogenerator based on electrostatic induction 基于静电感应的非接触摩擦电纳米发电机仿真模型
Q1 Chemistry Pub Date : 2023-07-02 DOI: 10.1002/eom2.12392
Jing You, Jiajia Shao, Yahua He, Xin Guo, K. W. See, Zhong Lin Wang, Xiaolin Wang

Based on the coupling effects of contact electrification and electrostatic induction, a triboelectric nanogenerator (TENG) can convert mechanical energy into electric power, which is at the cutting edge of alternative energy technology. Although a considerable number of TENGs with different configurations have been designed, some of them however, which only depend on the electrostatic induction effect have not received enough attention. Here, a non-contact TENG model consists of copper rings and charged dielectric sphere is presented, which is aimed at exploring the working process of TENGs caused by electrostatic induction. Two classical models, including vertical and horizontal double copper rings models are also proposed. Relevant advanced and accurate models of TENGs have been established through the finite element method. We anticipate that the constructed model and theoretical analysis are helpful for the design of non-contact model TENGs with complicated geometric construction, and expand their applications in various fields.

摩擦电纳米发电机(TENG)利用接触通电和静电感应的耦合效应,将机械能转化为电能,是替代能源技术的前沿。虽然已经设计了相当数量的不同结构的teng,但其中一些仅依赖于静电感应效应的teng并没有得到足够的重视。本文提出了一种由铜环和带电介质球组成的非接触式TENG模型,旨在探索静电感应引起的TENG的工作过程。提出了两种经典模型,包括垂直和水平双铜环模型。通过有限元方法建立了相应的先进、精确的TENGs模型。我们期望所建立的模型和理论分析有助于具有复杂几何结构的非接触模型teng的设计,并扩大其在各个领域的应用。
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引用次数: 0
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