| 1. |
- Luo, Yifei, et al.
(författare)
-
Technology Roadmap for Flexible Sensors
- 2023
-
Ingår i: ACS Nano. - : American Chemical Society. - 1936-0851 .- 1936-086X. ; 17:6, s. 5211-5295
-
Forskningsöversikt (refereegranskat)abstract
- Humans rely increasingly on sensors to address grand challenges and to improve quality of life in the era of digitalization and big data. For ubiquitous sensing, flexible sensors are developed to overcome the limitations of conventional rigid counterparts. Despite rapid advancement in bench-side research over the last decade, the market adoption of flexible sensors remains limited. To ease and to expedite their deployment, here, we identify bottlenecks hindering the maturation of flexible sensors and propose promising solutions. We first analyze challenges in achieving satisfactory sensing performance for real-world applications and then summarize issues in compatible sensor-biology interfaces, followed by brief discussions on powering and connecting sensor networks. Issues en route to commercialization and for sustainable growth of the sector are also analyzed, highlighting environmental concerns and emphasizing nontechnical issues such as business, regulatory, and ethical considerations. Additionally, we look at future intelligent flexible sensors. In proposing a comprehensive roadmap, we hope to steer research efforts towards common goals and to guide coordinated development strategies from disparate communities. Through such collaborative efforts, scientific breakthroughs can be made sooner and capitalized for the betterment of humanity.
|
|
| 2. |
- Wang, Chaoqian, et al.
(författare)
-
A stepwise microwave synergistic pyrolysis approach to produce sludge-based biochars : Feasibility study simulated by laboratory experiments
- 2020
-
Ingår i: Fuel. - : Elsevier. - 0016-2361 .- 1873-7153. ; 272, s. 1-10
-
Tidskriftsartikel (refereegranskat)abstract
- A stepwise microwave synergistic pyrolysis (SMSP) approach is proposed as a new way to relieve disposal problems of the sewage sludge. Here the sludge is first pre-pyrolyzed by a conventional heating stage, and then rapidly pyrolyzed by a microwave-induced heating stage without any extra microwave absorbers or blending needed. Under simulated process pyrolysis conditions, the dried sludge, intermediate and final sludge-based biochar samples were prepared in the laboratory. Their chemical composition, microstructure and morphology, and leaching toxicity of heavy metals were carefully characterized and analyzed by various techniques such as proximate and ultimate analysis, X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, Brunauer-Emmett-Teller (BET), and scanning electron microscope equipped with energy-dispersive x-ray spectroscopy (SEM-EDX). Results showed that the pre-pyrolytic biochar can be rapidly heated up to 1100 °C within 5 min under microwave irradiation. The pre-pyrolytic stage increased the carbonization and ash enrichment degree of the sludge which itself acted as a good microwave absorber while achieving a quick temperature rise under microwave irradiation. The ash remaining ratio and the specific surface area of the biochar derived from the SMSP approach (labelled as SBC2) are increased by 6.46% and 16.17% respectively, compared with the conventional biochar sample (SBC1). And SBC2 still had diverse surface functional groups kept after SMSP. The residual ratios of Ni, Cu, Zn, Pb, Cr and Cd in SBC2 was more noticeable than in SBC1 but the leaching ratios quite the contrary. Vitrification is also well proved by the increment of quartz peak detected by XRD tests, and the formation of melted glassy spheres with elemental composition of Si, Ca, Al observed by SEM-EDX. It can favorably increase solidification level and decrease leaching toxicity of heavy metals in the SBC2. The feasibility of this proposed SMSP concept has been positively supported by our experimental results. The properties of the sludge-based biochar produced from the SMSP approach also show great potential to be utilized as precursors to produce various adsorbents.
|
|
| 3. |
- Zhang, Xiaorong, et al.
(författare)
-
Review of chemical looping process for carbonaceous feedstock Conversion : Rational design of oxygen carriers
- 2022
-
Ingår i: Fuel. - : Elsevier. - 0016-2361 .- 1873-7153. ; 325
-
Forskningsöversikt (refereegranskat)abstract
- The chemical looping partial oxidation (CLPO) process as a technology of chemical looping process (CLP) is recognized as a potential strategy for the efficient and clean conversion of fuels into syngas/H2. Herein, in view of the importance of low-cost high-performance metal oxides as oxygen carriers (OCs) for this conversion, we systematically review the classification and CLPO applications of such OCs and discuss the improvement of OC reactivity and stability via the creation of metal–metal or metal–support synergism, the generation of oxygen vacancies, and the enhancement of deactivation resistance. Further, we present the results of theoretical and experimental characterizations probing ion diffusion and surface reactions to provide insights into the related reaction mechanisms and touch on the challenges and opportunities of developing metal oxides with excellent reactivity and long-term cycling stability in CLP. Thus, this review facilitates the design and performance regulation of OCs for future energy conversion systems.
|
|
| 4. |
- Gao, Lihua, et al.
(författare)
-
Interfacial phenomenon and Marangoni convection of Fe–C melt on coke substrate under in situ observation
- 2023
-
Ingår i: Scientific Reports. - : Springer Nature. - 2045-2322. ; 13:1
-
Tidskriftsartikel (refereegranskat)abstract
- The interfacial phenomenon between liqiuid iron and coke is important for determining the melting efficiency in the blast furnace iron-making process. In this study, the interaction observed in the case of the iron-carbon (Fe–C) melt on coke substrate was investigated using a high-temperature vacuum wettability test equipment. The Fe–C melt did not wet and spread on the coke substrate with different graphitization degrees (r 0) at a high temperature of 1450 °C. The contact angles changed from 124.5° to 105.3°, and the r 0 increased from 9.30 to 50.00%, thus indicating a nonwetting state. The deepening of graphitization decreased the contact angle. Thereby, increasing the contact area between liquid iron and the carbonaceous material, which facilitated carbon dissolution. The irregular movements of Fe–C melt were observed in situ during the wetting process. The horizontal force of the droplet caused by interfacial tension and the contact angle; the Marangoni convection owing to the gradient of carbon concentration; and the impulse force caused by the generation, aggregation, and release of SiO bubbles at the interface were attributed to the driving force.
|
|
| 5. |
- Li, Gang, et al.
(författare)
-
Selective Electrochemical Alkaline Seawater Oxidation Catalyzed by Cobalt Carbonate Hydroxide Nanorod Arrays with Sequential Proton-Electron Transfer Properties
- 2021
-
Ingår i: ACS Sustainable Chemistry and Engineering. - : American Chemical Society (ACS). - 2168-0485. ; 9:2, s. 905-913
-
Tidskriftsartikel (refereegranskat)abstract
- Seawater oxygen evolution is one of the promising energy conversion technologies for large-scale renewable energy storage. It requires efficient catalysts to accelerate the oxygen evolution reaction (OER) for sustained water oxidation, avoiding chlorine evolution under acidic conditions or hypochlorite formation in alkaline solutions. Conventional metal oxide-based OER catalysts follow the adsorbate evolution mechanism that involves concerted proton-electron transfer steps at the active sites. Thus, on the scale of reversible hydrogen electrode, their catalytic activity is independent of the pH of electrolytes. In the present study, nanostructured cobalt carbonate hydroxide (CoCH) with sequential proton-electron transfer properties was tested as a catalyst for seawater oxygen evolution. CoCH exhibited pH-dependent water oxidation activities, thereby providing larger potential and current operating windows for selective water oxidation compared to the catalysts with pH-independent OER activities. The operating window can be further expanded by increasing the pH of the electrolyte.
|
|
| 6. |
- Li, Wenlong, et al.
(författare)
-
A bio-inspired coordination polymer as outstanding water oxidation catalyst via second coordination sphere engineering
- 2019
-
Ingår i: Nature Communications. - : NATURE PUBLISHING GROUP. - 2041-1723. ; 10
-
Tidskriftsartikel (refereegranskat)abstract
- First-row transition metal-based catalysts have been developed for the oxygen evolution reaction (OER) during the past years, however, such catalysts typically operate at overpotentials (eta) significantly above thermodynamic requirements. Here, we report an iron/ nickel terephthalate coordination polymer on nickel form (NiFeCP/NF) as catalyst for OER, in which both coordinated and uncoordinated carboxylates were maintained after electrolysis. NiFeCP/NF exhibits outstanding electro-catalytic OER activity with a low overpotential of 188 mV at 10 mA cm(-2) in 1.0 KOH, with a small Tafel slope and excellent stability. The pH-independent OER activity of NiFeCP/NF on the reversible hydrogen electrode scale suggests that a concerted proton-coupled electron transfer (c-PET) process is the rate-determining step (RDS) during water oxidation. Deuterium kinetic isotope effects, proton inventory studies and atom-proton-transfer measurements indicate that the uncoordinated carboxylates are serving as the proton transfer relays, with a similar function as amino acid residues in photosystem II (PSII), accelerating the proton-transfer rate.
|
|
| 7. |
- Liu, Wenlong, et al.
(författare)
-
On the calculation of electric diffusion coefficient of radiation belt electrons with in situ electric field measurements by THEMIS
- 2016
-
Ingår i: Geophysical Research Letters. - 0094-8276 .- 1944-8007. ; 43:3, s. 1023-1030
-
Tidskriftsartikel (refereegranskat)abstract
- Based on 7years' observations from Time History of Events and Macroscale Interactions during Substorms (THEMIS), we investigate the statistical distribution of electric field Pc5 ULF wave power under different geomagnetic activities and calculate the radial diffusion coefficient due to electric field, , for outer radiation belt electrons. A simple empirical expression of is also derived. Subsequently, we compare to previous D-LL models and find similar Kp dependence with the model, which is also based on in situ electric field measurements. The absolute value of is constantly higher than , probably due to the limited orbital coverage of CRRES. The differences between and the commonly used and models are significant, especially in Kp dependence and energy dependence. Possible reasons for these differences and their implications are discussed. The diffusion coefficient provided in this paper, which also has energy dependence, will be an important contributor to quantify the radial diffusion process of radiation belt electrons.
|
|
| 8. |
- Lu, Yang, et al.
(författare)
-
Precise tuning of interlayer electronic coupling in layered conductive metal-organic frameworks
- 2022
-
Ingår i: Nature Communications. - : Nature Portfolio. - 2041-1723. ; 13:1
-
Tidskriftsartikel (refereegranskat)abstract
- Layered metal-organic frameworks attract interests for optoelectronics and spintronics. Here, the authors report a strategy to tune interlayer charge transport and thermoelectric properties via side-chain induced control of the layer spacing. Two-dimensional conjugated metal-organic frameworks (2D c-MOFs) have attracted increasing interests for (opto)-electronics and spintronics. They generally consist of van der Waals stacked layers and exhibit layer-depended electronic properties. While considerable efforts have been made to regulate the charge transport within a layer, precise control of electronic coupling between layers has not yet been achieved. Herein, we report a strategy to precisely tune interlayer charge transport in 2D c-MOFs via side-chain induced control of the layer spacing. We design hexaiminotriindole ligands allowing programmed functionalization with tailored alkyl chains (HATI_CX, X = 1,3,4; X refers to the carbon numbers of the alkyl chains) for the synthesis of semiconducting Ni-3(HATI_CX)(2). The layer spacing of these MOFs can be precisely varied from 3.40 to 3.70 angstrom, leading to widened band gap, suppressed carrier mobilities, and significant improvement of the Seebeck coefficient. With this demonstration, we further achieve a record-high thermoelectric power factor of 68 +/- 3 nW m(-1) K-2 in Ni-3(HATI_C3)(2), superior to the reported holes-dominated MOFs.
|
|
| 9. |
- Wang, Longguang, et al.
(författare)
-
NTIRE 2023 Challenge on Stereo Image Super-Resolution : Methods and Results
- 2023
-
Ingår i: IEEE Computer Society Conference on Computer Vision and Pattern Recognition Workshops (CVPRW). - Vancover : Institute of Electrical and Electronics Engineers (IEEE). - 9798350302493 - 9798350302509 ; , s. 1346-1372
-
Konferensbidrag (övrigt vetenskapligt/konstnärligt)abstract
- In this paper, we summarize the 2nd NTIRE challenge on stereo image super-resolution (SR) with a focus on new solutions and results. The task of the challenge is to super-resolve a low-resolution stereo image pair to a high-resolution one with a magnification factor of x4. Compared with single image SR, the major challenge of this challenge lies in how to exploit additional information in another viewpoint and how to maintain stereo consistency in the results. This challenge has 3 tracks, including one track on distortion (e.g., PSNR) and bicubic degradation, one track on perceptual quality (e.g., LPIPS) and bicubic degradation, as well as another track on real degradations. In total, 175, 93, and 103 participants were successfully registered for each track, respectively. In the test phase, 21, 17, and 12 teams successfully submitted results with PSNR (RGB) scores better than the baseline. This challenge establishes a new benchmark for stereo image SR.
|
|
| 10. |
- Wu, Yue, et al.
(författare)
-
Photoswitching between black and colourless spectra exhibits resettable spatiotemporal logic
- 2016
-
Ingår i: Materials Horizons. - : Royal Society of Chemistry. - 2051-6347 .- 2051-6355. ; 3:2, s. 124-129
-
Tidskriftsartikel (refereegranskat)abstract
- Logic is the key to computing. Traditionally, logic devices have been fabricated by the top-down approach, whose dimensions are drastically limited. The ultimate goal is to use molecular tailorability to design logics using the "bottom-up'' approach. Here we report an unprecedented photochromic molecule that undergoes unimolecular logic switching when excited anywhere in the entire UV-visible spectrum, thus a bottom-up, all-photonic, molecular logic gate. Specifically, these molecular photonic logics embedded in the polymer thin films function as the "AND'' or "OR'' gate at different temporal responses. To achieve high information-processing density, moreover, a ternary flip-flap-flop gate is realized in the molecular logic because the fact that this photochromic molecule can be photoswitched anywhere in its UV-vis spectrum enabled three different lasers (532, 473, and 561 nm) as the inputs to deliver the complex logic optical outputs.
|
|
