The discovery of highly efficient photocatalysts for water splitting remains a challenge of high importance. Here, we report a series of novel organic conjugated polymers (OCPs) that contain complexed non-noble metals for photocatalytic hydrogen evolution. The conjugated chromophore polymers were synthesized by a Heck coupling between ferrocene and phenantholine derivatives, which absorb broadly, even up to the near-IR region. The photocatalyst performances were investigated for hydrogen evolution by using Fe 3 (CO) 12 as a water reduction catalyst. H 2 evolution rates up to 212.4 mmol h À1 , with an apparent quantum yield of 10.3 % at 380 nm, were obtained with a photocatalyst polymer based on alternating ferrocene and 4,7-bisphenyl-1,10-phenanthroline units. The high activity is likely due to favorable electron transfer and coordination of Fe 3 (CO) 12 with phenanthroline in the supramolecular OCPs.Limited fossil fuel reserves and serious environmental pollution require an urgent search for renewable green power sources. [1] Hydrogen gas generated by photochemical water splitting is a highly attractive option. To realize a light-driven hydrogenbased economy, the development of efficient, safe and cheap photocatalysts are required, but still remains a big challenge. During the past few decades, inorganic materials based on metals with d 0 or d 10 electronic configurations have been developed for water splitting, such as TiO 2 , [2] ZrO 2 , [3] CdS [4] and so on. [5] But their relatively limiting properties has impelled the development of metal-free photocatalysts for water splitting.Graphitic carbon nitride polymer (g-C 3 N 4 ) was discovered by Xinchen Wang's group in 2009, which shows activities for photocatalytic water splitting, and opens new prospects for the search of efficient and stable organic conjugated polymer photocatalysts. [6] The well-known advantage of organic conjugated photocatalysts is that their structures are easy to systematically adjust at the molecular level, so their physicochemical properties can be easily tuned. As a typical example, Cooper synthesized a series of pyrene-based microporous OCPs by adjusting the type and proportion of co-monomers. [7] Interestingly, the optical gap of these co-polymers was between 1.94-2.95 eV, and the hydrogen evolution rate (HER) was up to 17.4 mmolh À1 under visible light, rather than ultraviolet irradiation, in the presence of sacrificial agents. Subsequently, Cooper developed a series of planarized conjugated polymer photocatalysts by introducing bridging fluorene units in linear phenylenes. [8] The visible-lightdriven HER rose to 116 mmolh À1 when Pt was added as a cocatalyst, which was further enhanced to 145 mmolh À1 with l > 295 nm, and the apparent quantum yield (AQY) was up to 2.3 % at l = 420 nm. Recently, Hao Chen and co-workers have introduced diethynylbenzene into the backbone of linear polymers, which extended the absorption edge and showed an optimal HER of 180.7 mmolh À1 (AQY = 4.2 % at l = 420 nm) under l > 420 nm irradiation, ev...