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Supplementary Table 11: Key clinical data for the CRC cohort showing overall survival (OS)

Supplementary Table 7: Key clinical data for different types of kidney cancer and metastasis

Supplementary Table 2: Clinical-pathological data for colorectal cancer patients used for genomic analysis and validation Supplementary Table 3: Clinical-pathological data for colorectal liver metastasis patients used for genomic analysis and validation Supplementary Table 4: Clinical-pathological data for renal cancer patients used for genomic analysis and validation

Supplementary Table 9: Key clinical data for clear cell RCC cohort 2 showing overall survival (OS)

The structure and molecular signature of tumor-associated vasculature are distinct from those of the host tissue, offering an opportunity to selectively target the tumor blood vessels. To identify tumor-specific endothelial markers, we performed a microarray on tumor-associated and nonmalignant endothelium collected from patients with renal cell carcinoma (RCC), colorectal carcinoma, or colorectal liver metastasis. We identified a panel of genes consistently upregulated by tumor blood vessels, of which melanoma cell adhesion molecule (MCAM) and its extracellular matrix interaction partner laminin alpha 4 (LAMA4) emerged as the most consistently expressed genes. This result was subsequently confirmed by immunohistochemical analysis of MCAM and LAMA4 expression in RCC and colorectal carcinoma blood vessels. Strong MCAM and LAMA4 expression was also shown to predict poor survival in RCC, but not in colorectal carcinoma. Notably, MCAM and LAMA4 were enhanced in locally advanced tumors as well as both the primary tumor and secondary metastases. Expression analysis in 18 different cancers and matched healthy tissues revealed vascular MCAM as highly specific in RCC, where it was induced strongly by VEGF, which is highly abundant in this disease. Lastly, MCAM monoclonal antibodies specifically localized to vessels in a murine model of RCC, offering an opportunity for endothelial-specific targeting of anticancer agents. Overall, our findings highlight MCAM and LAMA4 as prime candidates for RCC prognosis and therapeutic targeting. Cancer Res; 76(8); 2314–26. ©2016 AACR.

Supplementary Table 8: Key clinical data for clear cell RCC cohort 1, showing overall survival (OS)

Supplementary Table 1: Primer sequences for RTqPCR using the Roche Exiqon probe library system. Supplementary Figure 1. Representative images demonstrative of scoring for staining intensity. Images are of MCAM staining in RCC at a weak (i-ii) or strong (iii-iv) level with associated H&E images (v,vi,vii,viii) . Scale bar = 50 μm.

Supplementary Table 5: Matrix metallopeptidase regulation across tissue types (Gene expression comparison shown as Log2 fold change) Supplementary Table 6: Collagen regulation across tissue types (Gene expression comparison shown as Log2 fold change)

The rapid growth, demand, and production of batteries to meet various emerging applications, such as electric vehicles and energy storage systems, will result in waste and disposal problems in the next few years as these batteries reach end-of-life. Battery reuse and recycling are becoming urgent worldwide priorities to protect the environment and address the increasing need for critical metals. As a review article, this paper reveals the current global battery market and global battery waste status from which the main battery chemistry types and their management, including reuse and recycling status, are discussed. This review then presents details of the challenges, opportunities, and arguments on battery second-life and recycling. The recent research and industrial activities in the battery reuse domain are summarized to provide a landscape picture and valuable insight into battery reuse and recycling for industries, scientific research, and waste management.

Redox flow batteries are being utilised as an attractive electrochemical energy storage technology for electricity from renewable generation. At present, the global installed capacity of redox flow battery is 1100 MWh. There are several parameters that significantly govern redox flow battery performance amongst which electrode activation, electrode material, felt compression, electrolyte additive, electrolyte temperature, membrane, and flow field design are notable. This review article presents an overview of the influence of individual components by comparing the performance of a parametrically modified cell with a default cell, which has 0% felt compression, inactivated electrode, zero electrolyte additives, and ambient condition operation. From the reviewed studies, electrode activation (thermal, chemical, laser perforation) and felt compression were identified as the most significant parameters. Electrolyte additive and flow field design were identified to be reasonably significant. Electrolyte temperature and membrane type were identified as the least significant amongst all the parameters. Based on this survey, a parametric matrix has been outlined that will aid researchers to identify appropriate parameters to focus research efforts onto improved redox flow battery performance.

The electrodeposition of lithium metal from room temperature ionic liquid (RTIL) electrolytes consisting of N-propyl-N-methylpyrrolidinium bis(fluorosulfonyl)imide (Pyr13[FSI]) with LiFSI, LiTFSI, LiBF4, LiPF6 or LiAsF6 salts onto Pt and Li electrodes was undertaken to identify mechanistic details. Cyclic voltammetry at both Pt and Li electrodes is complicated by the chemical reaction between fresh/electrodeposited Li metal and electrolyte to form a solid-electrolyte interphase (SEI). As such, all electrolyte systems depict quasi-reversible cycling, owing to the concomitant chemical breakdown of the electrolyte and deposition of a passivation product onto the electrode surface. The rate at which the SEI forms can be observed through cyclic voltammetric scan rate studies. Chronoamperometry data supports the cyclic voltammetry studies and indicates that an instantaneous nucleation and growth type mechanism is taking place at all potentials as determined through modelling the current-time transients utilising the Hills-Scharifker theory. We show herein that these RTIL based electrolytes can be cycled effectively in an order of stability of salt inclusion as follows: LiBF4 > LiFSI > LiAsF6 > LiTFSI > LiPF6.

Suppressing dendrite formation at lithium metal anodes during cycling is critical for the implementation of future lithium metal-based battery technology. Here we report that it can be achieved via the facile process of immersing the electrodes in ionic liquid electrolytes for a period of time before battery assembly. This creates a durable and lithium ion-permeable solid–electrolyte interphase that allows safe charge–discharge cycling of commercially applicable Li|electrolyte|LiFePO4 batteries for 1,000 cycles with Coulombic efficiencies >99.5%. The tailored solid–electrolyte interphase is prepared using a variety of electrolytes based on the N-propyl-N-methylpyrrolidinium bis(fluorosulfonyl)imide room temperature ionic liquid containing lithium salts. The formation is both time- and lithium salt-dependant, showing dynamic morphology changes, which when optimized prevent dendrite formation and consumption of electrolyte during cycling. This work illustrates that a simple, effective and industrially applicable lithium metal pretreatment process results in a commercially viable cycle life for a lithium metal battery., Suppressing dendrite formation at lithium anodes during cycling is critical to development of lithium battery technology. Here, the authors show that immersion of lithium electrodes in ionic liquid electrolytes prior to battery assembly produces a durable and lithium ion permeable solid-electrolyte interphase.

Despite the high theoretical capacity of Si anodes, the electrochemical performance of Si anodes is hampered by severe volume changes during lithiation and delithiation, leading to poor cyclability and eventual electrode failure. Nanostructured silicon and its nanocomposite electrodes could overcome this problem holding back the deployment of Si anodes in lithium-ion batteries (LIBs) by providing facile strain relaxation, short lithium diffusion distances, enhanced mass transport, and effective electrical contact. Here, the recent progress in nanostructured Si-based anode materials such as nanoparticles, nanotubes, nanowires, porous Si, and their respective composite materials and fabrication processes in the application of LIBs have been reviewed. The ability of nanostructured Si materials in addressing the above mentioned challenges have been highlighted. Future research directions in the field of nanostructured Si anode materials for LIBs are summarized.

The lithium–sulfur (Li–S) battery in which the ionic liquid (IL) C4mpyr-TFSI is a major component of the electrolyte has attracted much attention by researchers due to the ability of the IL to suppress the polysulfide shuttle effect, combined with advantageous properties of thermal, chemical and electrochemical stability. In a largely parallel stream of research, LiNO3 has come to be known as an additive for improving Li–S battery performance through its influence on protecting the lithium anode and beneficial interaction with the polysulfide shuttle. In this work a deeper understanding is sought of the combined effects of LiNO3 and C4mpyr-TFSI on the factors that impact Li–S cell performance. Specifically, we investigate the formation of the protective surface film on lithium anode and results are compared with those for a typical organic electrolyte for the Li–S battery, DOL:DME. Electrochemical impedance spectroscopy (EIS) confirms that the LiNO3 additive is vital to achieving acceptable levels of performance with the organic electrolyte. Although LiNO3 improves the performance of a battery assembled with IL containing electrolyte, it shows a higher impact in the organic electrolyte based battery. Furthermore X-ray photoelectron spectroscopy (XPS) spectra confirm the participation of C4mpyr-TFSI on the formation of the interphase layer on the anode.

The electrochemical behaviour and electrical performance are investigated for a series of lithium-sulfur (Li-S) cells in which the electrolyte solutions are organic solvent-ionic liquid mixtures that are based on the 1-butyl-1-methylpyrrolidinium (C4mpyr) cation with a range of anions. In each case, performance is compared with cells that are based on a standard mixed-ether organic electrolyte. The capacity of cells assembled with electrolytes containing 1-butyl-1-methylpyrrolidinium tris(pentafluoroethyl) trifluorophosphate (C4mpyr-FAP), 1-butyl-1-methylpyrrolidinium trifluoromethanesulfonate (C4mpyr-OTf), or 1-butyl-1-methylpyrrolidinium tricyanomethanide (C4mpyr-TCM) decline rapidly due to low conductivity, high polysulfide solubility and side reaction of electrolyte with electrodes, respectively. Our results confirm that polysulfide solubility is strongly controlled by the anion of the ionic liquid and verify that not all ionic liquids decrease polysulfide solubility. In agreement with previous reports, 1-butyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl) imide (C4mpyr-TFSI) shows the best compatibility in Li-S batteries and has a higher coulombic efficiency of greater than 99% over 100 cycles. Furthermore, impedance spectroscopy confirms that electrolyte composition influences the SEI layer formed on the lithium anode and its subsequent impedance.

The effect of ionic strength on the electrodeposition of silver has been investigated in acetonitrile (MeCN) containing TBAPF6 or in the ionic liquid [EMIm][OTf]. The use of an ionic liquid allows a greater ionic strength to be investigated as the solubility limits of supporting electrolytes in organic solvents can be overcome using neat ionic liquid. The SEM and XRD data show that polycrystalline silver is deposited in a fcc structure and that dendrite formation is retarded at high ionic strength. Electrochemical measurements undertaken in electrolytes of low ionic strength indicate that the deposition and growth of a few nuclei is preferred and leads to dendrite formation. However, at higher ionic strength, the deposition and growth of significantly more nuclei is observed and therefore dendrite growth rates and tip currents are lower leading to the deposition of spherical particulates. Crucially, the data shows that if the ionic strength of the electrolyte is controlled there are no differences between ionic liquids and molecular solvents for the electrodeposition of silver.

The structure and molecular signature of tumor-associated vasculature are distinct from those of the host tissue, offering an opportunity to selectively target the tumor blood vessels. To identify tumor-specific endothelial markers, we performed a microarray on tumor-associated and nonmalignant endothelium collected from patients with renal cell carcinoma (RCC), colorectal carcinoma, or colorectal liver metastasis. We identified a panel of genes consistently upregulated by tumor blood vessels, of which melanoma cell adhesion molecule (MCAM) and its extracellular matrix interaction partner laminin alpha 4 (LAMA4) emerged as the most consistently expressed genes. This result was subsequently confirmed by immunohistochemical analysis of MCAM and LAMA4 expression in RCC and colorectal carcinoma blood vessels. Strong MCAM and LAMA4 expression was also shown to predict poor survival in RCC, but not in colorectal carcinoma. Notably, MCAM and LAMA4 were enhanced in locally advanced tumors as well as both the primary tumor and secondary metastases. Expression analysis in 18 different cancers and matched healthy tissues revealed vascular MCAM as highly specific in RCC, where it was induced strongly by VEGF, which is highly abundant in this disease. Lastly, MCAM monoclonal antibodies specifically localized to vessels in a murine model of RCC, offering an opportunity for endothelial-specific targeting of anticancer agents. Overall, our findings highlight MCAM and LAMA4 as prime candidates for RCC prognosis and therapeutic targeting. Cancer Res; 76(8); 2314–26. ©2016 AACR.

The fabrication of a superhydrophobic nylon textile based on the organic charge-transfer complex CuTCNAQ (TCNAQ=11,11,12,12-tetracyanoanthraquinodimethane) is reported. The nylon fabric, which is metallized with copper, undergoes a spontaneous chemical reaction with TCNAQ dissolved in acetonitrile to form nanorods of CuTCNAQ that are intertwined over the entire surface of the fabric. This creates the necessary micro- and nanoscale roughness that often allows the Cassie-Baxter state to be obtained with high robustness, thereby achieving a superhydrophobic/superoleophilic surface without the need for a fluorinated surface. The material is characterized with SEM, FTIR spectroscopy, and X-ray photoelectron spectroscopy, and investigated for its ability to separate oil and water in two modes, namely through filtration and as an absorbent material. It is found that the fabric can separate dichloromethane, olive oil, and crude oil from water, and reduce the water content of the oil during the separation process. The fabric is reusable, highly durable, and tolerant to conditions such as seawater, hydrochloric acid, and extensive time periods on the shelf. Given that CuTCNAQ is a copper-based semiconductor, there may also be the possibility of other uses in areas such as photocatalysis and antibacterial applications.

As an anode material for lithium-ion batteries, titanium dioxide (TiO 2 ) shows good gravimetric performance (336 mAh g -1 for LiTiO 2 ) and excellent cyclability. To address the poor rate behavior, slow lithium-ion (Li + ) diffusion, and high irreversible capacity decay, TiO 2 nanomaterials with tuned phase compositions and morphologies are being investigated. Here, a promising material is prepared that comprises a mesoporous "yolk-shell" spherical morphology in which the core is anatase TiO 2 and the shell is TiO 2 (B). The preparation employs a NaCl-assisted solvothermal process and the electrochemical results indicate that the mesoporous yolk-shell microspheres have high specific reversible capacity at moderate current (330.0 mAh g -1 at C/5), excellent rate performance (181.8 mAh g -1 at 40C), and impressive cyclability (98% capacity retention after 500 cycles). The superior properties are attributed to the TiO 2 (B) nanosheet shell, which provides additional active area to stabilize the pseudocapacity. In addition, the open mesoporous morphology improves diffusion of electrolyte throughout the electrode, thereby contributing directly to greatly improved rate capacity.