摘要：Phase transformation of two-dimensional(2D)nanomaterials can lead to significant changes in electronic and optical properties,which enables the development of novel *** strategies for phase engineering of 2D nanomaterials have drawn considerable attention in recent *** review focuses on the state-of-the-art progress in the phase transformation of 2D nanomaterials and their catalytic ***,the basic concepts of phase transformation and the outstanding electronic and optical properties induced by phase transformation are briefly ***,different strategies for achieving phase transformation are discussed in detail and classified into several types based on their characteristics,including(i)doping,(ii)external fields,(iii)optical irradiation,(iv)strain effect,(v)high-energy particle excitation,and(vi)thermal *** applications of 2D nanomaterials in catalysis based on phase transformation have also been ***,a summary of the technical challenges to phase control in 2D nanomaterials and potential opportunities for developing novel applications is presented.

摘要：数字微镜器件(DMD)的近红外光谱仪,具有波长重复性好、分辨率高和抗振动性好等优点,广泛应用于食品安全和农业生产等领域的研究。随着DMD的微小型近红外光谱仪发展逐渐趋于成熟,仪器的成本和性能仍然是研发的关键。尽管大部分将重点放在了软件开发和检测方法的研究,而仪器硬件的处理速度至关重要。只有确保光谱仪能够快速准确的采集并传输数据,才能有效实现光谱分析。在多数研究中,阿达玛矩阵的生成和解码工作通常由上位机完成,并通过FLASH存储的方式导入模板。这种方式可能会限制采集一幅完整光谱数据的时间效率。为了提高光谱采集速度和信噪比,提出一种高速驱动DMD和快速数据采集的方法,并基于DMD微小型近红外光谱仪设计一套硬件电路系统。采用现场可编辑门阵列(FPGA)和ARM的架构,创新性地实现了奇偶阿达玛模板的生成与解码过程在嵌入式系统底层执行,加快了光谱分析的速度并提高信噪比。通过与市面上DMD型光谱仪对比,研究结果显示,所研发的光谱仪完成单次光谱的采集时间仅需214 ms,相比商用DMD型光谱仪,采集效率提升了4倍。在同等3 s的采集时间内,所研发光谱仪的信噪比为4600,相比商用DMD型光谱仪,信噪比提升了1.5倍。通过所研发的光谱仪对油菜籽样品进行光谱扫描,分析了油菜籽的脂肪、蛋白质和水分的含量,并采用偏最小二乘回归(PLSR)建立了相应的模型。油菜籽脂肪含量的校正相关系数为0.9865、预测相关系数为0.9672;蛋白质含量的校正相关系数为0.9854、预测相关系数系数为0.9636;水分含量的校正相关系数为0.9875、预测相关系数为0.9614。模型评估的结果表明,该光谱仪能够满足油菜籽成分检测的需求,验证该光谱仪在商业领域具有重要的应用价值。

摘要：许多具有d^(6)和d^(8)电子构型的第二和第三周期过渡金属配合物具有长寿命的金属中心到配体的电荷转移(MLCT)激发态,表现出优异的光化学和光物理性能。然而,这类金属普遍昂贵且在地壳中的丰度很低。因此,开发新型廉价和丰产第一周期过渡金属光功能配合物具有重要的理论研究意义和实际应用价值。其中,具有3d^(6)电子构型的Fe(Ⅱ)和3d^(5)电子构型的Fe(Ⅲ)光功能配合物引起了众多关注。其主要挑战为通过有效的配体设计调控Fe(Ⅱ)配合物的MLCT激发态,以及实现Fe(Ⅲ)配合物配体到金属的电荷转移(LMCT)激发态发光。近年来,相关研究取得了突破性的进展,具有较长MLCT激发态寿命的Fe(Ⅱ)配合物和LMCT发光的Fe(Ⅲ)配合物被陆续开发出来,并成功应用于光化学领域。在此,我们从配合物和配体设计出发,总结了Fe(Ⅱ)和Fe(Ⅲ)配合物激发态调控的最新进展。此外,我们还讨论了Fe(Ⅱ)/Fe(Ⅲ)配合物在光化学领域的潜在应用。

摘要：Conjugated polymers exhibit exceptional adaptability in flexible thin-film transistors,owing to their inherent flexibility and high charge ***,achieving conjugated polymers that demonstrate both high mobility and stability under mechanical stress,such as bending or stretching,remains a significant *** this study,we synthesized an ethylene-bridged conjugated polymer,PDPPVIDT,derived from methyl-side diketopyrrolopyrrole(DPP)and indacenodithiophene(IDT)aldehydes,using an environmentally friendly Knoevenagel condensation reaction under mild conditions,resulting in a moderate yield with promising *** characterization techniques revealed enhanced backbone planarity with stableπ-πstacking,while thin films of PDPPVIDT displayed a nearamorphous nature due to the conformational isomerism of the ethylene *** structure enables simultaneous charge transport and ***,flexible organic thinfilm transistor(OTFT)devices based on PDPPVIDT demonstrated excellent hole mobility(μh)reaching up to 1.70 cm^(2) V^(−1) s^(−1),along with high mechanical bending *** work underscores the potential of vinyl-bridged donor-acceptor conjugated polymers,highlighting the industrial adaptability of their production process and offering new insights for the design and synthesis of future flexible electronic materials.

摘要：生物乙醇是重要的生物质平台分子,全球年产能约9000万吨,且乙醇分子化学键丰富,是化学键构成最具代表性的最小的含氧化合物分子,为其高值化转化提供了丰富的反应路径,近年来,引起科学界的广泛关注.本文对乙醇经O-H键定点活化、α-C-H键定点活化,O-H键/α-C-H键同时活化制备高附加值化学品的催化剂设计进行了介绍;对乙醇催化转化在催化剂理性设计、催化剂机理研究以及未来规模化放大等方面进行了展望.

摘要：Covalent organic frameworks(COFs)are garnering significant interest in photocatalytic CO_(2) ***,their limited efficiency in separating photogenerated carriers and the scarcity of catalytic sites lead to suboptimal photocatalytic *** we develop a molecular engineering approach to design a pyrene-based COF(PyTa-H COF)confined cobalt single atoms photocatalyst(Co SACs)for CO_(2) *** moiety is introduced to enhance visible-light harvesting capability and improve charge separation in the ***,Co SACs enhance the photocatalytic activity by accelerating the migration of photo-induced carriers and reducing the reaction energy of the rate-determining ***,PyTa-H@Co achieves a CO production rate of 18.36 mmol g^(−1) h^(−1) and a selectivity of 94%in 4 h under visible light irradiation,which is comparable to the reported best-performing *** functional theory calculations reveal that the Co SACs greatly stabilize*COOH and significantly reduce the energy of the decisive step,leading to outstanding photocatalytic *** work,through molecular engineering design,highlights the critical relationship between catalyst structure and function in enhancing photocatalytic efficiency.

摘要：Constructing an information storage or communication system, where countless pieces of information canbe hidden like a canvas and revealed on demand throughspecific stimuli or decoding rules, is significant. In the presentstudy, we developed a hydrogel canvas that leverages noncovalentinteractions to induce phase separation in the polymer matrix, creating various “paintings”, including custommessages, using different chemical inks. Our strategy focuseson designing small molecule inks, with varying affinities withthe hydrogel and specific responsiveness to stimuli, to achievemultiple changes such as color shifts, fluorescence emission,and dynamic optical image evolution. This skips the typicaldesign approaches, such as incorporating responsive fluorophoresinto polymers for color emission through grafting orcopolymerization, and thus avoids the complex processes involved in modifying and synthesizing functional polymers,along with the uncertainties in material properties that theseprocesses bring.

摘要：Untreated urea-rich wastewater exerts severeadverse impacts on both the environment and human health,prompting extensive attention towards the urea oxidationreaction (UOR) as a sustainable technology to generate cleanenergy in recent years. UOR has a thermodynamic advantageover oxygen evolution reaction (OER) (1.23 V vs reversiblehydrogen electrode, RHE) and only requires 0.37 V (vs RHE),which is considered as an effective alternative to H_(2) production by water electrolysis. However, the inevitable kineticslowness and complex adsorption/desorption during the processhinder its practical application. Most traditional catalystsutilized for the UOR are comprised of precious metals, resulting in limited economic viability. Inspired by natural ureases, Ni-based catalysts have emerged as promisingalternatives owing to their rich deposits, low cost, and theregulated d orbitals of transition metal Ni, demonstratingconsiderable potential for UOR. Currently, numerous studieshave explored Ni-based hydroxides, oxides, chalcogenides, andphosphides in alkaline solutions. In this review, we will explorethe UOR reaction mechanism and summarize the catalystdesign strategies of various Ni-based catalysts recently, especially Ni-MOF, which has been rarely discussed before. Then,the broad prospects of UOR in practical applications aresummarized. Finally, based on the design strategies and performance comparisons discussed above, the challenges andprospects facing the future development of Ni-based electrocatalysts for the UOR will be presented.

摘要：新兴污染物因具有环境持久性、生物累积性、生物毒性以及在环境中痕量存在等特点而备受全球众多国家关注。因此,对环境、食品以及生物样品中的新兴污染物进行高灵敏检测至关重要。传统样品前处理技术存在耗时长、吸附剂用量大,以及对不稳定污染物的分析准确性差等缺点,因此,亟需开发设计具有高选择性、高传质效率的新型材料作为前处理技术的吸附剂,以实现新兴污染物的高选择、高灵敏检测。共价有机骨架材料(COFs),特别是功能化的COFs材料,因具有比表面积大、结构可设计、稳定且构筑基元丰富等诸多优点而被广泛用于新兴污染物的富集。该文主要综述了近年来功能化COFs材料的合成策略及其作为样品前处理吸附剂在环境、食品和生物样品中新兴污染物中的分析应用,并对该类材料的未来发展趋势进行了展望。

摘要：从2000年开始，VASTO就洞察到必须在原有基础上深化品牌，使其个性更为突出，才有机会一争天下。国内常见的时装广告创意水准不高，品牌缺乏个性和生命力：最常见的明星广告，从天皇巨星到小小演员人人有份：而富丽堂皇的环境。世界大都会也是常见的背景。常看到的用词亦不外乎贵族、气派、品位、高贵等陈词滥调。究其原因，其实是自身品牌没有思想的结果，就算有时碰运气碰到一些好东西，也没有办法抽出它的DNA去继续发展。