Acta Energiae Solaris Sinica•2026•DOI: 10.19912/j.0254-0096.tynxb.202608_9712
High-energy-consuming industrial parks account for 42% of China's industrial carbon emissions, with an emission intensity of 1.2 t CO2 per 10,000 CNY, necessitating innovative market mechanisms to reduce carbon costs. This study proposes an optimal scheduling model integrating short-term generation rights trading with a ladder-type carbon emission-green certificate hybrid market mechanism for a system comprising a concentrated solar power (CSP) plant, wind power, photovoltaic (PV) generation, and a self-owned power plant in a high-energy-consuming park. The CSP thermal energy storage (TES) system enables energy time-shifting and electro-thermal coupling, constructing a multi-energy complementary power coordination model to smooth wind/PV fluctuations and enhance consumption. A joint short-term generation rights trading strategy is designed, dynamically matching renewable output with the self-owned plant's regulation demand through a generation rights-carbon quota-green certificate conversion mechanism. Simulation on a high-energy-consuming park in Jiuquan, Gansu Province, demonstrates that the proposed method effectively reduces carbon emissions and improves renewable energy consumption. The introduction of the CSP plant further lowers total park costs, achieving dual optimization of environmental and economic benefits. The model is linearized using the big-M method, transforming a mixed-integer nonlinear programming problem into a mixed-integer linear programming problem for solution. This approach addresses the mismatch between medium-to-long-term generation rights trading and short-term supply-demand fluctuations, as well as the lack of linkage among generation rights, carbon, and green certificate trading, thereby synergizing emission reduction incentives with power trading objectives.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4494-9
Superionic conductors exhibit high cation mobility arising from weak binding and continuous transport pathways, atomistically characterized by extensive structural disorder and partial occupancy akin to amorphization. This disorder, whether confined to a cation sublattice or extended to full amorphization, strongly impedes lattice thermal transport, rendering these materials intrinsically ideal thermal insulators. This work investigates Ag26I18W4O16, a superionic conductor tunable from fully amorphous to single-crystalline states, as a model system to probe the impact of disorder and amorphization on thermal transport. Extensive Ag+ disorder, in both crystalline and amorphous phases, reduces thermal conductivity to approximately the theoretical lower bound of 0.16 W/m-K with virtually no temperature dependence, while concurrently achieving the lowest mean sound velocity ever recorded for a dense solid. Pair distribution function (PDF) analysis of synchrotron X-ray total scattering data indicates that short-range disorder (< 5 Å), rather than long-range periodicity, governs thermal insulation performance in both phases. These findings suggest a design strategy reconciling structural stability with glass-like thermal insulation.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4197-4
Deep-blue organic light-emitting diodes (OLEDs) remain the most challenging primary-color emitters due to stringent exciton energy requirements. We strategically designed two innovative deep-blue emitters, SCZ-4AnCN and STPA-4AnCN, via systematic functionalization of an anthracene core with arylamino-decorated spirofluorene donors and cyano-substituted phenyl acceptors. Comprehensive theoretical and experimental analyses demonstrate that these spirofluorene-anthracene hybrids adopt precisely engineered distorted configurations, effectively suppressing detrimental intermolecular π–π stacking in condensed phases. The sp3-hybridized bridgehead carbons in spirofluorene units play a pivotal role by simultaneously restricting π-conjugation extension and fine-tuning donor–acceptor interactions, thereby stabilizing the lowest excited singlet (S1) state with dominant local excitation (LE) character. This molecular engineering yields exceptional deep-blue emission with remarkable efficiency. Notably, the materials exhibit unique high-lying reverse intersystem crossing (hRISC) behavior, enabling efficient triplet harvesting. Optimized doped devices incorporating SCZ-4AnCN achieve outstanding performance, including a maximum external quantum efficiency (EQE_max) exceeding 10% and CIE coordinates (0.154, 0.052) approaching the BT.2020 blue standard. Nondoped devices maintain impressive performance with an EQE_max of 7.51% and superior operational stability, demonstrating less than 10% efficiency roll-off at 1000 cd m−2. This work validates anthracene-based molecular architectures for deep-blue electroluminescence and establishes a transformative design paradigm for next-generation OLED emitters.
Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2025010201
The Guanzhong region, traversed by the Wei River Basin, is one of the most industrially, agriculturally, and medically advanced and densely populated areas in Northwest China, has seen increasing attention paid to the pollution of perfluoroalkyl substances (PFASs) in its surface water environment. This study systematically investigated the pollution characteristics of PFASs in the surface water of this region and their ecological and health risks. By optimizing the online solid-phase extraction-liquid chromatography-tandem quadrupole mass spectrometry (Online SPE-LC/MS/MS), efficient detection of 19 PFASs was achieved, with the method detection limits ranging from 0.2 ng·L−1 to 0.3 ng·L−1, linear correlation coefficients all ≥ 0.990, and spiked recoveries between 75.2% and 130.0%. Monitoring data indicated that PFBA, PFPeA, PFHxA and PFOS, short-chain perfluorinated compounds, were the main pollutants in this region, with high detection frequencies and concentrations, but the overall content was lower than that in most areas of China. The concentrations of PFASs in surface water showed significant seasonal variations, with the highest concentrations during the dry season (∑19PFASs:126.1 — 2584.3 ng·L−1), followed by the normal season (∑19PFASs:3.5—3567.6 ng·L−1), and the lowest during the wet season (∑19PFASs:26.3—294.6 ng·L−1). Ecological risk assessment showed that, except for PFDoDA in the dry season, the ecological risk quotient (RQ) of all other PFASs was < 1. Although the water of the Wei River is not used as direct drinking water, health risk assessment indicated that all PFASs posed low risks, with only PFOA and PFOS showing potential risks (HR > 0.1) to adults and children at some sites during dry/normal seasons. This study provides a scientific basis for PFASs pollution control in the Wei River Basin.
Chinese Journal of Environmental Engineering•2026•DOI: 10.12030/j.cjee.202510041
This study presents a full-scale engineering practice of retrofitting an idle upflow anaerobic sludge blanket (UASB) reactor into an aerobic granular sludge (AGS) system for treating low-strength municipal wastewater. The design capacity was 20,000 m3/d (maximum 24,000 m3/d), achieving separate treatment of industrial and domestic wastewater to reduce operational costs. Systematic analysis covered hydraulic capacity enhancement, effluent quality, pollutant removal efficiencies, sludge granulation progress, and operational costs. Results showed rapid start-up: the system reached 75% of design capacity by day 10 and 90% by day 26. During a 4-month operation, average removal efficiencies for COD, NH4+-N, TN, and SS were 83.2%, 97.0%, 75.9%, and 94.4%, respectively, even under low influent BOD5/TN ratios (typically below 4). Granulation progressed quickly: by day 44, average particle size was 2.6 times that of the inoculum and over 4 times that of flocs, with granules (>200 μm) accounting for 17.3%; by day 110, these values increased to 3.2 times and 5 times, with granule proportion reaching 33.4%. Compared to the previous year (June–August), the AGS process reduced electricity consumption, chemical consumption, and sludge production by 77.3%, 25.4%, and 30.4%, respectively, while saving 65.6% of footprint. This ten-thousand-ton case provides a practical basis for AGS technology application in China.
Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2025111403
Sediments from the Hengyang reach of the Xiangjiang River were analyzed for concentrations, chemical fractions, and sources of 14 heavy metals (As, Se, Cd, Sb, Pb, Tl, Bi, Co, Ni, Mn, Zn, V, Cr, Cu). Mean concentrations of As, Se, Cd, Sb, Pb, Tl, and Bi exceeded local background values, with Cd, Se, Bi, and As showing pronounced enrichment. Spatial heterogeneity was marked, with higher levels downstream; overall concentrations were lower than previously reported. Sequential extraction revealed that Sb, Bi, Se, Tl, Cu, As, V, Cr, and Ni were predominantly in the residual fraction (F4), while Zn, Cd, Pb, and Mn had higher extractable fractions (F1+F2+F3), with bioavailable fractions generally elevated downstream. Geo-accumulation index (Igeo) indicated no contamination by Co, Zn, V, or Cr, but varying degrees of contamination by Mn, Ni, As, Se, Cd, Sb, Pb, Tl, Bi, and Cu, with pollution severity order: Se>Cd>Bi>As>Sb>Pb>Tl>Ni>Cu>Mn>Zn>Cr>Co>V. Enrichment factors showed significant enrichment for Cd, Sb, and Bi, moderate for Pb, and low for others. Potential ecological risk index (RI) revealed Cd as the primary contributor (87.49% of total risk), with overall moderate risk at downstream sites and slight risk across the entire section. Source apportionment using PCA and PMF identified three sources: industrial and traffic mixed source (57.60%), natural source (16.00%), and industrial-natural mixed source (26.40%). These findings enhance understanding of heavy metal pollution mechanisms in the Hengyang section and recommend priority control of industrial and traffic emissions, with focus on Cd mobility, to support sediment remediation strategies.
SCIENCE CHINA Materials•2025•DOI: 10.1007/s40843-025-3577-4
Broad-absorbing materials, characterized by tunable absorption across ultraviolet to mid-infrared spectral regions, have emerged as a crucial class of optoelectronic materials. Significant advances have been achieved in organic and inorganic materials; however, current enhancement strategies remain largely platform-specific and are not guided by a unified physical framework. To address this gap, this review introduces a three-factor physical model grounded in the theory of transition probability, thereby providing a consistent theoretical basis for understanding how electronic transitions are modulated across orbital, vibrational, and spin dimensions. Structure-mechanism-performance relationships are systematically examined in classic material platforms. In addition, the contributions of external-field enhancement mechanisms, such as plasmonic resonance, to spectral broadening and local-field enhancement are discussed. Based on clear mechanistic insight and targeted materials design, recent advances in integrating broad-absorbing materials into broadband photodetectors are highlighted, emphasizing their practical relevance. The review examines the three core challenges and mechanism-driven design strategies for high-performance broadband optoelectronic systems, providing an instructive outlook for future advancements.
SCIENCE CHINA Materials•2025•DOI: 10.1007/s40843-025-3593-5
Organic ultrathin crystals, comprising monolayers or a few molecular layers, exhibit outstanding optoelectronic properties and have shown great promise for constructing advanced functional neuromorphic devices. However, scalable growth of high-quality organic ultrathin crystals and their seamless concurrent integration with charge trapping layers for multi-mode neuromorphic devices, that required in future high-density neuromorphic integration, remain challenging. Here, we present a scalable one-step fabrication strategy based on solution shearing, where spontaneous vertical phase separation of a small-molecule/polymer (Ph-BTBT-10/PS) blend enables the simultaneous formation of high-quality ultrathin Ph-BTBT-10 crystals and an electret PS charge-trapping layer. The PS electret layer serves a dual function: it facilitates the formation of ultrathin, highly ordered Ph-BTBT-10 crystals; meanwhile, its gate-tunable electron-trapping capability enables dynamic switching between photo-switching and photo-synaptic modes within a single device. As a photodetector, the device exhibits exceptional performance, including a responsivity of 4.7 × 10^4 A/W, specific detectivity of 2.2 × 10^17 Jones, and photosensitivity of 1.5 × 10^8. Under negative gate bias, light-triggered switching behavior enables logic gate demonstration, while under positive gate modulation, photonic synaptic behavior successfully emulates key biological functions, including excitatory post-synaptic current (EPSC), paired-pulse facilitation (PPF), short-term plasticity (STP) to long-term plasticity (LTP) transition, dynamic learning-forgetting processes, and image processing. Moreover, the system exhibits excellent compatibility with low-voltage flexible substrates and further demonstrates its application in low-consumption flexible neuromorphic devices. This work provides a scalable route toward high-performance, multifunctional neuromorphic optoelectronics based on organic ultrathin crystals, and advances the integration of flexible electronics and brain-inspired computing.
SCIENCE CHINA Materials•2025•DOI: 10.1007/s40843-025-3563-0
Organic cocrystals have become increasingly prevalent in various research domains owing to simple preparation, cost-effectiveness, and highly tunable properties. Strong charge transfer (CT) interactions in cocrystals render them promising candidates for high-efficiency photothermal conversion materials. However, the majority of reported organic photothermal cocrystals exhibit planar and rigid π-conjugated structures, which restrict molecular vibrations while simultaneously impeding non-radiative dissipation processes—ultimately hindering the enhancement of photothermal conversion performance. Herein, we design a novel non-planar photothermal NMTQ cocrystal, which shows a broadband absorption range of 220–2000 nm and high photothermal conversion efficiencies from ultraviolet (UV) to near-infrared (NIR)-II region. Quantum chemical calculations demonstrate that the distorted butterfly-like conformation in NMTQ is conducive to non-radiative transitions via higher non-adiabatic couplings (NACs) and lower spatial overlap integral (Sr). An interfacial solar evaporation system was constructed using NMTQ cocrystals, achieving an evaporation rate of 2.158 kg m−2 h−1 with 94.96% solar-to-vapor conversion efficiency under 1 Sun irradiation. The photothermal platform demonstrated simultaneous contaminant removal functionality, establishing a sustainable strategy for clean water production through rational photothermal material design.
SCIENCE CHINA Materials•2025•DOI: 10.1007/s40843-025-3549-6
Intramolecular noncovalent conformational locks (NoCLs) have emerged as a potent strategy for engineering high-performance organic/polymeric semiconductors (OPSs) by suppressing non-radiative decay. While the impact of NoCLs on small molecules is well-documented, their influence on the physicochemical properties of conjugated polymers (CPs) remains poorly understood due to the structural complexity, low crystallinity, and poor solubility of CPs. This study addresses that gap by integrating theoretical calculations with advanced experimental techniques—temperature-dependent absorption spectroscopy, cryogenic electron microscopy (cryo-EM), dynamic light scattering (DLS), small-angle neutron scattering (SANS), and freeze-drying transmission electron microscopy (TEM). The results demonstrate that incorporating NoCLs into CP backbones increases chain rigidity, enhances intermolecular interactions, promotes the formation of pre-aggregates with optimal length, and improves charge transport. These findings provide a mechanistic framework for designing high-performance CPs, overcoming the limitations of conventional characterization methods that are restricted to small molecules. The work establishes a correlative link between NoCL-induced conformational locking and macroscopic transport properties, offering a rational design pathway for next-generation organic optoelectronic devices.
SCIENCE CHINA Materials•2025•DOI: 10.1007/s40843-025-3542-8
Rechargeable sodium-chlorine (Na/Cl2) batteries derived from thionyl chloride (SOCl2) primary systems offer high theoretical energy density and wide-temperature operation, but their reversibility is constrained by chlorine shuttle and unstable sodium-metal interfaces. Dai et al. demonstrate a Na/Cl2 battery using multi-walled carbon nanotubes (MWCNTs) as the cathode host, a sodium-metal anode, and a SOCl2-based electrolyte containing AlCl3, potassium bis(fluorosulfonyl)imide (KFSI), and NaCl additives. The cell delivers an initial discharge capacity of 5400 mAh g−1 (carbon mass basis), a reversible capacity of 3500 mAh g−1, and a discharge plateau near 3.9 V at room temperature, sustaining over 140 cycles at rates up to 2 C with near 100% Coulombic efficiency. The dual-function KFSI additive suppresses sodium dendrites via electrostatic shielding from the lower K+/K redox potential and forms a NaF/KF-rich solid-electrolyte interphase. In situ Raman spectroscopy reveals reversible SCl2 and S2Cl2 formation at the end of charge, contributing an additional ~3.9 V plateau, while the main Cl−/Cl2 redox plateau remains at ~3.55 V. Cryogenic transmission electron microscopy shows NaCl nanocrystals deposited within the hollow cores of MWCNTs, and electron energy loss spectroscopy confirms uniform chlorine distribution on nanotube surfaces in the charged state. A high defect density (Raman D/G ratio = 1.01) and large pore volume (2.48 cm3 g−1) are identified as critical enablers of superior battery performance.